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US20190314620A1 - Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures - Google Patents

️Thu Oct 17 2019

Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures Download PDF

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Publication number

US20190314620A1

US20190314620A1 US16/424,735 US201916424735A US2019314620A1 US 20190314620 A1 US20190314620 A1 US 20190314620A1 US 201916424735 A US201916424735 A US 201916424735A US 2019314620 A1 US2019314620 A1 US 2019314620A1 Authority

United States

Prior art keywords

balloon

stent

catheter

nasal cavity

devices

Prior art date

2004-04-21

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Abandoned

Application number

US16/424,735

Inventor

John Y. Chang

Joshua Makower

Julia D. Vrany

Amrish J. WALKE

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Acclarent Inc

Original Assignee

Acclarent Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2004-04-21

Filing date

2019-05-29

Publication date

2019-10-17

2004-04-21 Priority claimed from US10/829,917 external-priority patent/US7654997B2/en

2004-09-17 Priority claimed from US10/944,270 external-priority patent/US20060004323A1/en

2019-05-29 Application filed by Acclarent Inc filed Critical Acclarent Inc

2019-05-29 Priority to US16/424,735 priority Critical patent/US20190314620A1/en

2019-10-17 Publication of US20190314620A1 publication Critical patent/US20190314620A1/en

2020-01-21 Priority to US16/747,590 priority patent/US11529502B2/en

Status Abandoned legal-status Critical Current

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- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0058—Additional features; Implant or prostheses properties not otherwise provided for
- A61F2250/0067—Means for introducing or releasing pharmaceutical products into the body
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M2025/0177—Introducing, guiding, advancing, emplacing or holding catheters having external means for receiving guide wires, wires or stiffening members, e.g. loops, clamps or lateral tubes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M2025/1043—Balloon catheters with special features or adapted for special applications
- A61M2025/1072—Balloon catheters with special features or adapted for special applications having balloons with two or more compartments
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M2025/1043—Balloon catheters with special features or adapted for special applications
- A61M2025/1079—Balloon catheters with special features or adapted for special applications having radio-opaque markers in the region of the balloon
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M2025/1043—Balloon catheters with special features or adapted for special applications
- A61M2025/109—Balloon catheters with special features or adapted for special applications having balloons for removing solid matters, e.g. by grasping or scraping plaque, thrombus or other matters that obstruct the flow
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M29/00—Dilators with or without means for introducing media, e.g. remedies
- A61M29/02—Dilators made of swellable material
- A61M2029/025—Dilators made of swellable material characterised by the guiding element
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2210/00—Anatomical parts of the body
- A61M2210/06—Head
- A61M2210/0681—Sinus (maxillaris)
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2210/00—Anatomical parts of the body
- A61M2210/10—Trunk
- A61M2210/1025—Respiratory system
- A61M2210/1028—Larynx
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1006—Balloons formed between concentric tubes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1011—Multiple balloon catheters

Definitions

the present invention relates generally to medical devices and methods and more particularly to minimally invasive, devices, systems and methods for treating sinusitis and other ear, nose & throat disorders.
the nose is responsible for warming, humidifying and filtering inspired air and for conserving heat and moisture from expired air.
the nose is formed mainly of cartilage, bone, mucous membranes and skin.
the bones in the nose contain a series of cavities known as paranasal sinuses that are connected by passageways.
the paranasal sinuses include frontal sinuses, ethmoid sinuses, sphenoid sinuses and maxillary sinuses.
the paranasal sinuses are lined with mucous-producing epithelial tissue and ultimately opening into the nasal cavity. Normally, mucous produced by the epithelial tissue slowly drains out of each sinus through an opening known as an ostium. If the epithelial tissue of one of these passageways becomes inflamed for any reason, the cavities which drain through that passageway can become blocked. This blockage can be periodic (resulting in episodes of pain) or chronic.
This interference with drainage of mucous can result in mucosal congestion within the paranasal sinuses.
Chronic mucosal congestion of the sinuses can cause damage to the epithelium that lines the sinus with subsequent decreased oxygen tension and microbial growth (e.g., a sinus infection).
sinusitis refers generally to any inflammation or infection of the paranasal sinuses caused by bacteria, viruses, fungi (molds), allergies or combinations thereof. It has been estimated that chronic sinusitis (e.g., lasting more than 3 months or so) results in 18 million to 22 million physician office visits per year in the United States.
one of the ways to treat sinusitis is by restoring the lost mucous flow.
the initial therapy is drug therapy using anti-inflammatory agents to reduce the inflammation and antibiotics to treat the infection.
a large number of patients do not respond to drug therapy.
the gold standard for patients with chronic sinusitis that do not respond to drug therapy is a corrective surgery called Functional Endoscopic Sinus Surgery.
an endoscope In FESS, an endoscope is inserted into the nose and, under visualization through the endoscope, the surgeon may remove diseased or hypertrophic tissue or bone and may enlarge the ostia of the sinuses to restore normal drainage of the sinuses. FESS procedures are typically performed with the patient under general anesthesia.
FESS continues to be the gold standard therapy for surgical treatment of severe sinus disease
FESS does have several shortcomings.
FESS can cause significant post-operative pain.
FESS procedures are associated with significant postoperative bleeding and, as a result, nasal packing is frequently placed in the patient's nose for some period of time following the surgery. Such nasal packing can be uncomfortable and can interfere with normal breathing, eating, drinking etc.
Some patients remain symptomatic even after multiple FESS surgeries.
FESS procedures are associated with risks of iatrogenic orbital, intracranial and sinonasal injury. Many otolaryngologists consider FESS an option only for patients who suffer from severe sinus disease (e.g., those showing significant abnormalities under CT scan).
FESS procedures can be bloody and painful relates to the fact that instruments having straight, rigid shafts are used. In order to target deep areas of the anatomy with such straight rigid instrumentation, the physician needs to resect and remove or otherwise manipulate any anatomical structures that may lie in the direct path of the instruments, regardless of whether those anatomical structures are part of the pathology.
U.S. Pat. No. 2,525,183 discloses an inflatable pressure device which can be inserted following sinus surgery and inflated within the sinus.
the patent does not disclose device designs and methods for flexibly navigating through the complex nasal anatomy to access the natural ostia of the sinuses.
the discussion of balloon materials is also fairly limited to thin flexible materials like rubber which are most likely to be inadequate for dilating the bony ostia of the sinus.
United States patent publication number 2004/0064150 A1 discloses balloon catheters formed of a stiff hypotube to be pushed into a sinus.
the balloon catheters have a stiff hypotube with a fixed pre-set angle that enables them to be pushed into the sinus.
the prior art discloses the use of dilating balloons for sinus treatments, it does not disclose the various means for navigation through the complex anatomy without significant manipulation of non-pathogenic anatomical regions that obstruct direct access to the sinus openings. Further, the prior art only discloses balloons of relatively simple shapes or materials for dilating sinus openings. Further, this art does not sufficiently elaborate beyond endoscopy on other means for imaging or tracking the position of such devices within the sinus anatomy.
the present invention provides methods, devices and systems for diagnosing and/or treating sinusitis or other conditions of the ear, nose or throat.
one or more flexible or rigid elongate devices as described herein are inserted in to the nose, nasopharynx, paranasal sinus, middle ear or associated anatomical passageways to perform an interventional or surgical procedure.
Examples of procedures that may be performed using these flexible catheters or other flexible elongate devices include but are not limited to: remodeling or changing the shape, size or configuration of a sinus ostium or other anatomical structure that affects drainage from one or more paranasal sinuses; cutting, ablating, debulking, cauterizing, heating, freezing, lasing, forming an osteotomy or trephination in or otherwise modifying bony or cartilaginous tissue within paranasal sinus or elsewhere within the nose; removing puss or aberrant matter from the paranasal sinus or elsewhere within the nose; scraping or otherwise removing cells that line the interior of a paranasal sinus; delivering contrast medium; delivering a therapeutically effective amount of a therapeutic substance; implanting a stent, tissue remodeling device, substance delivery implant or other therapeutic apparatus; cutting, ablating, debulking, cauterizing, heating, freezing, lasing, dilating or otherwise modifying tissue such as nasal polyps, abberant or enlarged tissue, abnormal
Introducing devices may be used to facilitate insertion of working devices (e.g. catheters e.g. balloon catheters, tissue cutting or remodeling devices, guidewires, devices for implanting elements like stents, electrosurgical devices, energy emitting devices, devices for delivering diagnostic or therapeutic agents, substance delivery implants, scopes etc) into the paranasal sinuses and other structures in the ear, nose or throat.
working devices e.g. catheters e.g. balloon catheters, tissue cutting or remodeling devices, guidewires, devices for implanting elements like stents, electrosurgical devices, energy emitting devices, devices for delivering diagnostic or therapeutic agents, substance delivery implants, scopes etc
apparatus and methods for navigation and imaging of the interventional devices within the sinuses using endoscopic including stereo endoscopic, fluoroscopic, ultrasonic, radiofrequency localization, electromagnetic, magnetic and other radiative energy based modalities.
imaging and navigation technologies may also be referenced by computer directly or indirectly to pre-existing or simultaneously created 3-D or 2-D data sets which help the doctor place the devices within the appropriate region of the anatomy.
FIG. 1 shows a schematic diagram of a system for catheter-based minimally invasive sinus surgery of the present invention being used to perform a sinus surgery procedure on a human patient.
FIG. 1A is an enlarged view of portion “IA” of FIG. 1 .
FIGS. 2A through 2D are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a guide and thereafter dilating or remodeling the ostial opening into the paranasal sinus.
FIGS. 2E through 2H are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a steerable guide and thereafter.
FIGS. 2I through 2L are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using an introducing device in the form of a guidewire with a preset shape.
FIGS. 2M through 2O are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a balloon catheter that has a guide protruding from its distal end.
FIGS. 2P through 2X are partial sagittal sectional views through a human head showing various steps of a method of accessing an ethmoid sinus through a natural or artificially created opening of the ethmoid sinus.
FIGS. 2Y through 2AC are partial coronal sectional views through a human head showing various steps of a method for treating a mucocele in a frontal sinus.
FIGS. 3A through 3C are partial coronal sectional views through a human head showing various steps of a method of accessing a paranasal sinus through an artificially created opening of the paranasal sinus.
FIG. 4A shows a partial longitudinal sectional view of a system for dilating a sinus ostium or other intranasal anatomical structure, such system comprising three progressively larger dilators useable in sequence.
FIGS. 4B through 4E show various steps of a method of dilating a nasal cavity using a working device comprising a balloon catheter with a pressure-expandable stent.
FIG. 4F shows a partial perspective view of a working device that comprises a side suction and/or side cutter.
FIG. 4G shows a partial perspective view of a working device that comprises a rotating cutter to cut away tissue.
FIGS. 4H and 4I show various steps of a method of dilating the ostium of a paranasal sinus or other nasal passageway using a mechanical dilator.
FIGS. 4J and 4K show perspective views of a mechanical dilator comprising a screw mechanism.
FIGS. 4L and 4M show sectional views of a mechanical dilator that comprises a pushable member.
FIGS. 4N and 4O show sectional views of a mechanical dilator that comprises a pullable member.
FIGS. 4P and 4Q show sectional views of a mechanical dilator that comprises a hinged member.
FIGS. 4R through 4W are schematic diagrams of alternative configurations for the distal portions of mechanical dilators of the types shown in FIGS. 4H through 4Q .
FIG. 5A shows a perspective view of a balloon that comprises a conical proximal portion, a conical distal portion and a cylindrical portion between the conical proximal portion and the conical distal portion.
FIG. 5B shows a perspective view of a conical balloon.
FIG. 5C shows a perspective view of a spherical balloon.
FIG. 5D shows a perspective view of a conical/square long balloon.
FIG. 5E shows a perspective view of a long spherical balloon.
FIG. 5F shows a perspective view of a bi-lobed “dog bone” balloon.
FIG. 5G shows a perspective view of an offset balloon.
FIG. 5H shows a perspective view of a square balloon.
FIG. 5I shows a perspective view of a conical/square balloon.
FIG. 5J shows a perspective view of a conical/spherical long balloon.
FIG. 5K shows a perspective view of an embodiment of a tapered balloon.
FIG. 5L shows a perspective view of a stepped balloon.
FIG. 5M shows a perspective view of a conical/offset balloon.
FIG. 5N shows a perspective view of a curved balloon.
FIG. 5O shows a partial perspective view of a balloon catheter device comprising a balloon for delivering diagnostic or therapeutic substances.
FIG. 5P shows a partial perspective view of a balloon/cutter catheter device comprising a balloon with one or more cutter blades.
FIG. 5Q shows a perspective view of a balloon catheter device comprising a balloon with a reinforcing braid attached on the external surface of the balloon.
FIG. 5R shows a partial sectional view of a balloon catheter wherein inflation ports are located near the distal end of the balloon.
FIG. 5S shows a partial sectional view of an embodiment of a balloon catheter comprising multiple balloons inflated by a single lumen.
FIG. 5T shows a partial sectional view of a balloon catheter comprising multiple balloons inflated by multiple lumens.
FIGS. 5U through 5AB show perspective and sectional views of various embodiments of balloon catheters having sensors mounted thereon or therein.
FIG. 6A shows a partial perspective view of a shaft design useable in the various devices disclosed herein, wherein the shaft comprises an external spiral wire.
FIG. 6B shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a stiffening wire.
FIG. 6C shows a partial perspective view of an embodiment of a shaft design for the various devices disclosed herein, wherein the shaft comprises stiffening rings.
FIG. 6D shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises controllable stiffening elements.
FIG. 6E shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a hypotube.
FIG. 6F shows a partial perspective cut-away view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a braid.
FIG. 6F ′ is an enlarged side view of the braid of the device of FIG. 6F .
FIG. 6G shows a partial perspective view of an embodiment of a device comprising a shaft having a plastically deformable region.
FIG. 6H shows a partial perspective view of a device comprising a shaft having a flexible element.
FIG. 6I shows a partial perspective view of a shaft comprising a malleable element.
FIG. 6J shows a partial perspective view of the shaft of FIG. 6I in a bent configuration.
FIG. 6K shows a cross sectional view through plane 6 K- 6 K of FIG. 6I .
FIG. 6L shows a partial sectional view of an embodiment of a controllably deformable shaft.
FIG. 6M shows a partial sectional view of the controllably deformable shaft of FIG. 6L in a deformed state.
FIG. 6N shows a perspective view of a balloon catheter comprising a rigid or semi-rigid member.
FIGS. 6O through 6Q show sectional views of a balloon catheter that comprises an insertable and removable element.
FIG. 7A shows a cross sectional view through a balloon catheter shaft comprising two cylindrical lumens.
FIG. 7B shows a cross sectional view through a balloon catheter shaft comprising an inner lumen and an annular outer lumen disposed about the inner lumen.
FIG. 7C shows a cross sectional view through a balloon catheter shaft which comprises a first tubular element with a first lumen, a second tubular element with a second lumen and a jacket surrounding the first and second tubular elements.
FIG. 7D shows a cross sectional view through a balloon catheter shaft comprising three lumens.
FIG. 7E shows a cross sectional view through a balloon catheter shaft comprising a cylindrical element, a tubular element that has a lumen and a jacket surrounding the cylindrical element and the tubular element.
FIG. 7F shows a cross sectional view of through a balloon catheter shaft comprising an embedded braid.
FIG. 7G shows a partial perspective view of a catheter shaft comprising a zipper lumen with a guide extending through a portion of the zipper lumen.
FIG. 7H shows a cross sectional view through line 7 H- 7 H of FIG. 7G .
FIG. 7I shows is a partial longitudinal sectional view of a catheter shaft comprising a rapid exchange lumen with a guide extending through the rapid exchange lumen.
FIG. 7J shows a cross sectional view of the catheter shaft of FIG. 7I through line 7 J- 7 J.
FIG. 7K shows a cross sectional view of the catheter shaft of FIG. 7I through line 7 K- 7 K.
FIG. 7L is a partial perspective view of a balloon catheter device of the present invention comprising a through-lumen and a balloon inflation lumen within the shaft of the catheter.
FIG. 7M is a cross sectional view through line 7 M- 7 M of FIG. 7L .
FIG. 7N is a cross sectional view through line 7 N- 7 N of FIG. 7L .
FIG. 7O is a partial perspective view of another balloon catheter device of the present invention comprising a through lumen within the shaft of the catheter and a balloon inflation tube disposed next to and optionally attached to the catheter shaft.
FIG. 7P is a cross sectional view through line 7 P- 7 P of FIG. 7O .
FIG. 7Q is a cross sectional view through line 7 Q- 7 Q of FIG. 7O .
FIG. 8A shows a partial perspective view of a catheter shaft comprising distance markers.
FIG. 8B shows a partial perspective view of a catheter shaft comprising one type of radiopaque markers.
FIG. 8C shows a partial perspective view of a catheter shaft comprising another type of radiopaque markers.
FIG. 8D shows a partial perspective view of a balloon catheter comprising an array of radiopaque markers arranged on the outer surface of the balloon.
FIG. 8E shows a partial perspective view of a balloon catheter comprising an array of radiopaque markers arranged on an inner surface of the balloon.
FIG. 8E ′ is a longitudinal sectional view of FIG. 8E .
FIGS. 1 and IA provide a general showing of a minimally invasive surgery system of the present invention comprising a C-arm fluoroscope 1000 that is useable to visualize a first introducing device 1002 (e.g., a guide catheter or guide tube), a second introducing device 1004 (e.g., a guidewire or elongate probe) and a working device 1006 (e.g., a balloon catheter, other dilation catheter, debrider, cutter, etc.).
a first introducing device 1002 e.g., a guide catheter or guide tube
a second introducing device 1004 e.g., a guidewire or elongate probe
a working device 1006 e.g., a balloon catheter, other dilation catheter, debrider, cutter, etc.
2A-8E ′ show certain non-limiting examples of the introducing devices 1002 (e.g., a guide catheter or guide tube), 1004 (guides, guidewires, elongate probes, etc.) and working devices 1006 (e.g., a balloon catheters, other dilation catheters, debrider, cutters, etc.) that may be useable in accordance with this invention.
the devices 1002 , 1004 , 1006 may be radiopaque and/or may incorporate radiopaque markers such that C-arm fluoroscope 1000 may be used to image and monitor the positioning of the devices 1002 , 1004 , 1006 during the procedure.
the devices 1002 , 1004 , 1006 may incorporate and/or may be used in conjunction with one or more endoscopic devices, such as the typical rigid or flexible endoscopes or stereo endocscopes used by otolaryngologists during FESS procedures.
some embodiments of the devices 1002 , 1004 , 1006 may incorporate sensors which enable the devices 1002 , 1004 , 1006 to be used in conjunction with image guided surgery systems or other electro-anatomical mapping/guidance systems including but not limited to: VectorVision (BrainLAB AG); HipNav (CASurgica); CBYON Suite (CBYON); InstaTrak, FluoroTrak, ENTrak (GE Medical); StealthStation Treon, iOn (Medtronic); Medivision; Navitrack (Orthosoft); OTS (Radionics); VISLAN (Siemens); Stryker Navigation System (Stryker Leibinger); Voyager, Z-Box (Z-Kat Inc.) and NOGA and CARTO systems (Johnson & Johnson).
VectorVision BrainLAB AG
HipNav CASurgica
CBYON Suite CBYON
InstaTrak FluoroTrak
ENTrak GE Medical
StealthStation Treon iOn (Medtronic); Medi
interventional navigation systems can also be used in conjunction with the devices and methods.
Further non-fluoroscopic interventional imaging technologies including but not limited to: OrthoPilot (B. Braun Aesculap); PoleStar (Odin Medical Technologies; marketed by Medtronic); SonoDoppler, SonoWand (MISON); CT Guide, US Guide (UltraGuide) etc. may also be used in conjunction with the devices and methods.
Guidance under magnetic resonance is also feasible if the catheter is modified to interact with the system appropriately.
the devices and methods of the present invention relate to the accessing and dilation or modification of sinus ostia or other passageways within the ear nose and throat. These devices and methods may be used alone or may be used in conjunction with other surgical or non-surgical treatments, including but not limited to the delivery or implantation of devices and drugs or other substances as described in copending U.S. patent application Ser. No. 10/912,578 entitled Implantable Devices and Methods for Delivering Drugs and Other Substances to Treat Sinusitis and Other Disorders filed on Aug. 4, 2004, the entire disclosure of which is expressly incorporated herein by reference.
FIGS. 2A through 2D are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a guide catheter.
a first introducing device in the form of a guide catheter 200 is introduced through a nostril and through a nasal cavity NC to a location close to an ostium SSO of a sphenoid sinus SS.
the guide catheter 200 may be flexible. Flexible devices are defined as devices with a flexural stiffness less than about 200 pound-force per inch over a device length of one inch.
the guide catheter 200 may be straight or it may incorporate one or more preformed curves or bends.
the deflection angle of the curve or bend may be in the range of up to 135°.
Examples of specific deflection angles formed by the curved or bent regions of the guide catheter 200 are 0°, 30°, 45°, 60°, 70°, 90°, 120° and 135°.
Guide catheter 200 can be constructed from suitable elements like Pebax, Polyimide, Braided Polyimide, Polyurethane, Nylon, PVC, Hytrel, HDPE, PEEK, metals like stainless steel and fluoropolymers like PTFE, PFA, FEP and EPTFE.
Guide catheter 200 can have a variety of surface coatings e.g.
a second introduction device comprising a guidewire 202 is introduced through the first introduction device (i.e., the guide catheter 200 ) so that the guidewire 202 enters the sphenoid sinus SS through the ostium SSO.
Guidewire 202 may be constructed and coated as is common in the art of cardiology.
a working device 204 for example a balloon catheter is introduced over guidewire 202 into the sphenoid sinus SS. Thereafter, in FIG. 2D , the working device 204 is used to perform a diagnostic or therapeutic procedure.
the procedure is dilation of the sphenoid sinus ostium SSO, as is evident from FIG. 2D .
the present invention may also be used to dilate or modify any sinus ostium or other man-made or naturally occurring anatomical opening or passageway within the nose, paranasal sinuses, nasopharynx or adjacent areas.
guide catheter 200 , guidewire 202 and working device 204 are withdrawn and removed.
a guidewire 202 may be steerable (e.g. torquable, actively deformable) or shapeable or malleable.
Guidewire 202 may comprise an embedded endoscope or other navigation or imaging modalities including but not limited to fluoroscopic, X-ray radiographic, ultrasonic, radiofrequency localization, electromagnetic, magnetic, robotic and other radiative energy based modalities.
some of the figures show optional scopes SC is dotted lines. It is to be appreciated that such optional scopes SC may comprise any suitable types of rigid or flexible endoscopes and such optional scopes SC may be separate from or incorporated into the working devices and/or introduction devices of the present invention.
FIGS. 2E through 2H are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a steerable catheter.
an introducing device in the form of a steerable catheter 206 is introduced through a nostril.
examples of a device which has a steerable tip with functionality similar to that described here include but are not limited to the NaviportTM manufactured by Cardima, Inc. in Fremont, Calif.; Attain Prevail and Attain Deflectable catheters manufactured by Medtronic; Livewire Steerable Catheters manufactured by St.
Steerable catheter 206 comprises a proximal portion, a distal portion and a controllably deformable region between the proximal portion and the distal portion.
the steerable catheter 206 is steered through the nasal anatomy so that the distal portion of steerable catheter 206 is near an ostium SSO of a sphenoid sinus SS.
a working device in the form of a balloon catheter 208 is introduced through steerable catheter 206 so that it enters sphenoid sinus SS through the ostium SSO. Thereafter, balloon catheter 208 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO.
balloon catheter 208 is used to dilate the ostium SSO.
steerable catheter 206 and balloon catheter 208 are withdrawn from the nasal anatomy.
a first introduction device in the form of a steerable catheter 206 is used to effect insertion and operative positioning of the working device (which in this example is balloon catheter 208 ).
a second introduction device e.g., an elongate guide member, guidewire, elongate probe, etc.
the working device 208 could then be advanced over such second introduction device to the desired operative location.
FIGS. 2I through 2L are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using an introducing device in the form of a guidewire with a preset shape.
an introducing device in the form of a guidewire 210 with a preset shape is introduced in a nasal cavity.
Guidewire 210 comprises a proximal portion and a distal portion and is shaped such that it can easily navigate through the nasal anatomy.
guidewire 210 is substantially straight.
guidewire 210 comprises an angled, curved or bent region between the proximal portion and the distal portion.
Examples of the deflection angle of the angled, curved or bent regions are 0°, 30°, 45°, 60°, 70°, 90°, 120° and 135°.
guidewire 210 is advanced through the nasal anatomy so that the distal tip of guidewire enters a sphenoid sinus SS through an ostium SSO.
a working device in the form of a balloon catheter 212 is advanced along guidewire 210 into the sphenoid sinus SS.
the working device will have a guidewire lumen extending through or formed in or on at least a portion of the working device 212 to facilitate advancement of the working device 212 over the guidewire 212 in the manner well understood in the art of interventional medicine.
the position of balloon catheter 212 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO.
the balloon catheter 212 may be radiopaque and/or may incorporate one or more visible or imageable markers or sensors.
balloon catheter 212 is used to dilate the ostium SSO.
guidewire 210 and balloon catheter 212 are withdrawn from the nasal anatomy.
balloon catheter 212 is shapeable or malleable.
FIGS. 2M through 2O are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a balloon catheter comprising a steering wire at its distal end.
a working device comprising a balloon catheter 214 comprising a proximal portion and distal portion is introduced in a nasal cavity.
Balloon catheter 214 comprises a steering wire 216 at its distal end.
balloon catheter 214 is advanced through the nasal anatomy into a sphenoid sinus SS through a sphenoid sinus ostium SSO.
balloon catheter 214 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO.
balloon catheter 214 is used to dilate the ostium SSO.
balloon catheter 214 is withdrawn from the nasal anatomy.
steering wire 216 can be retracted into or advanced from balloon catheter 214 .
the retraction or advancement of steering wire can be controlled by several means like a thumb wheel, a slide, a button hooked up to electronic motor and a trigger.
steering wire 216 may be hollow or may incorporate one or more lumen(s) to enable it to introduce or remove devices or diagnostic or therapeutic agents, examples of which are described in copending U.S.
FIGS. 2P through 2X are partial sagittal sectional views through a human head showing various steps of a method for accessing an ethmoid sinus through a natural or artificially created opening of the ethmoid sinus.
an introducing device in the form of a guide catheter 218 is introduced in an ethmoid sinus ES.
Ethmoid sinus ES comprises multiple ethmoid air cells EAC.
a guidewire 220 is introduced through guide catheter into a first EAC.
a balloon catheter 222 is introduced over guidewire 220 into the first EAC.
balloon catheter 222 is inflated to dilate the structures of ES.
guide catheter 218 , guidewire 220 and balloon catheter 222 are withdrawn leaving a first new passage in the ES.
the newly created passage in the ES facilitates drainage of the mucous through the ES.
FIG. 2U only balloon catheter 222 is withdrawn.
the position of guide catheter 218 is adjusted and guidewire 220 is introduced into a second EAC.
balloon catheter 222 is introduced over guidewire 220 into the second EAC.
balloon catheter 222 is inflated to dilate the structures of ES.
guide catheter 218 , guidewire 220 and balloon catheter 222 are withdrawn leaving a second new passage in the ES.
the second new passage in the ES further facilitates drainage of the mucous through the ES.
This method of dilating the structures of ES can be repeated to create multiple new passages in the ES.
FIGS. 2Y through 2AC are partial coronal sectional views through a human head showing various steps of a method for treating a mucocele in a frontal sinus.
an introducing device in the form of a guide catheter 224 is introduced in a frontal sinus FS through the nasal cavity NC.
Frontal sinus FS has a mucocele MC to be treated.
a penetrating device 226 comprising a sharp tip 228 is introduced through guide catheter 224 such that penetrating device 226 punctures the MC at least partially.
a balloon catheter 230 is introduced over penetrating device 226 into the MC. Thereafter, in FIG. 2AB , balloon catheter 230 is inflated to rupture the MC and allow the drainage of contents of the MC.
penetrating device 226 and balloon catheter 230 are withdrawn.
the methods disclosed herein may also comprise the step of cleaning or lavaging anatomy within the nose, paranasal sinus, nasopharynx or nearby structures including but not limited to irrigating and suctioning.
the step of cleaning the target anatomy can be performed before or after a diagnostic or therapeutic procedure.
the methods of the present invention may also include one or more preparatory steps for preparing the nose, paranasal sinus, nasopharynx or nearby structures for the procedure, such as spraying or lavaging with a vasoconstricting agent (e.g., 0.025-0.5% phenylephyrine or Oxymetazoline hydrochloride (Neosynephrine or Afrin) to cause shrinkage of the nasal tissues, an antibacterial agent (e.g., provodine iodine (Betadine), etc. to cleanse the tissues, etc.
a vasoconstricting agent e.g., 0.025-0.5% phenylephyrine or Oxymetazoline hydrochloride (Neosynephrine or Afrin)
an antibacterial agent e.g., provodine iodine (Betadine)
Betadine provodine iodine
FIGS. 3A through 3C are partial coronal sectional views through a human head showing various steps of a method of accessing a paranasal sinus through an artificially created opening of the paranasal sinus.
a puncturing device 300 is inserted through a nostril and used to create an artificial opening in a maxillary sinus.
puncturing devices well known in the art like needles including needles, needles with bent shafts, dissectors, punches, drills, corers, scalpels, burs, scissors, forceps and cutters.
FIG. 3B puncturing device 300 is withdrawn and a working device for example a balloon catheter 302 is introduced through the artificial opening into the maxillary sinus.
a working device for example a balloon catheter 302 is introduced through the artificial opening into the maxillary sinus.
balloon catheter 302 is used to dilate the artificially created opening in the maxillary sinus. After this step, the balloon catheter 302 is withdrawn.
the puncturing device 300 may have a lumen through which an introduction device (e.g., a guidewire or other elongate probe or member), may be inserted into the maxillary sinus and the puncturing device 300 may then be removed leaving such introduction device (e.g., a guidewire or other elongate probe or member) in place.
an introduction device e.g., a guidewire or other elongate probe or member
the working device e.g., balloon catheter 302
the working device may incorporate a lumen or other structure that allows the working device (e.g., balloon catheter 300 ) to be advanced over the previously inserted introduction device (e.g., a guidewire or other elongate probe or member).
FIG. 4A shows a sectional view of an example of a working device comprising a set of three sequential dilators: a first sequential dilator 402 , a second sequential dilator 404 and a third sequential dilator 406 .
the D 3 of third sequential dilator 406 is greater than the diameter D 2 of second sequential dilator 404 which in turn is greater than the diameter D 1 of first sequential dilator 402 .
the sequential dilators may comprise one or more bent or angled regions.
the sequential dilators can be constructed from a variety of biocompatible materials like stainless steel 316. A variety of other metals, polymers and materials can also be used to construct the sequential dilators.
FIGS. 4B through 4E show various steps of a method of dilating a nasal cavity using a working device comprising a balloon catheter with a pressure-expandable stent.
an introducing device e.g. a guidewire 416 is introduced into a nasal cavity e.g. an ostium of a sinus.
a balloon catheter 418 is introduced over guidewire 416 into the nasal cavity.
Balloon catheter 418 comprises a pressure-expandable stent 420 .
the position of balloon catheter 418 is adjusted so that pressure-expandable stent 420 is located substantially within the target anatomy where the stent is to be deployed.
FIG. 4B an introducing device e.g. a guidewire 416 is introduced into a nasal cavity e.g. an ostium of a sinus.
Balloon catheter 418 comprises a pressure-expandable stent 420 .
the position of balloon catheter 418 is adjusted so that pressure-exp
stent 420 like metallic tube designs, polymeric tube designs, chain-linked designs, spiral designs, rolled sheet designs, single wire designs etc. These designs may have an open celled or closed celled structure.
fabrication methods can be used for fabricating stent 420 including but not limited to laser cutting a metal or polymer element, welding metal elements etc.
a variety of materials can be used for fabricating stent 420 including but not limited to metals, polymers, foam type materials, plastically deformable materials, super elastic materials etc. Some non-limiting examples of materials that can be used to construct the stent are silicones e.g. silastic, polyurethane, gelfilm and polyethylene. A variety of features can be added to stent 420 including but not limited to radiopaque coatings, drug elution mechanisms etc.
FIG. 4F shows a partial perspective view of an embodiment of a working device comprising a side suction and/or cutting device 422 comprising a device body 424 having a side opening 426 .
Cutting device 422 is advanced into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned so that side opening 426 is adjacent to matter (e.g., a polyp, lesion, piece of debris, tissue, blood clot, etc.) that is to be removed.
Cutting device 422 is rotated to cut tissue that has been positioned in the side opening 426 .
Cutting device 422 may incorporate a deflectable tip or a curved distal end which may force side opening 426 against the tissue of interest.
this cutting device 422 may have an optional stabilizing balloon incorporated on one side of cutting device 422 to press it against the tissue of interest and may also contain one or more on-board imaging modalities such as ultrasound, fiber or digital optics, OCT, RF or electro-magnetic sensors or emitters, etc.
on-board imaging modalities such as ultrasound, fiber or digital optics, OCT, RF or electro-magnetic sensors or emitters, etc.
FIG. 4G shows a partial perspective view of an embodiment of a working device comprising a rotating cutter device to cut away tissue.
Rotating cutter device 428 comprises a rotating member 430 enclosed in an introducing device 432 .
Rotating member 430 comprises a rotating blade 434 located near the distal region of rotating member 430 .
Rotating blade 434 may be retractable into rotating member 430 .
Rotating cutter device 428 is inserted in a passageway 436 such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned so that rotating blade 434 is adjacent to matter (e.g., a polyp, lesion, piece of debris, tissue, blood clot, etc.) that is to be removed.
matter e.g., a polyp, lesion, piece of debris, tissue, blood clot, etc.
rotating member 430 is rotated to cause rotating blade 434 to remove tissue.
rotating member 430 can be retracted into introducing device 432 .
rotating cutter device 428 may comprise a mechanism for suction or irrigation near the distal end of rotating cutter device 428 .
FIGS. 4H and 4I show various steps of a method of dilating a nasal cavity using a working device comprising a mechanical dilator 408 .
Mechanical dilator 408 comprises an outer member 410 , an inner member 412 and one or more elongate bendable members 414 .
Inner member 412 can slide within outer member 410 .
the proximal ends of bendable members 414 are attached to distal end of outer member 410 and the distal ends of bendable members 414 are attached to distal end of inner member 412 .
mechanical dilator 408 is inserted into an opening in the nasal anatomy e.g. an ostium of a sinus.
Mechanical dilator 408 is positioned in the opening such that bendable members 414 are within the opening in the nasal anatomy.
relative motion of outer member 410 and inner member 412 causes the distal end of outer member 410 to come closer to the distal end of inner member 412 .
bendable members 414 to come into contact with the opening in the nasal anatomy and exert an outward pressure to dilate the opening.
Various components of mechanical dilator 408 like outer member 410 , inner member 412 and bendable members 414 can be constructed from suitable biocompatible materials like stainless steel 316.
outer member 410 is substantially rigid and inner member 412 is flexible. Outer member 410 can be substantially straight or may comprise one or more bent or angled regions. Inner member 412 may comprise one or more lumens.
FIGS. 4J and 4K illustrate a perspective view of a design of a mechanical dilator comprising a screw mechanism.
FIG. 4J shows the mechanical dilator comprising an outer member 438 and an inner screw member 440 .
Inner screw member 440 is connected to outer member 438 through a first pivot 442 located on the distal end of outer member 438 .
the distal end of inner screw member 440 is connected to a second pivot 444 .
the mechanical dilator further comprises one or more bendable members 446 .
the distal end of bendable members 446 is attached to second pivot 444 and the proximal end of bendable members 446 is attached to first pivot 442 .
inner screw member 440 is rotated in one direction.
Outer member 438 can be substantially straight or may comprise one or more bent or angled regions.
Inner screw member 440 may comprise one or more lumens.
FIGS. 4L and 4M illustrate sectional views of a design of a mechanical dilator comprising a pushable member.
FIG. 4L shows the mechanical dilator comprising an outer member 448 comprising one or more bendable regions 449 on the distal end of outer member 448 .
Mechanical dilator further comprises an inner pushable member 450 comprising an enlarged region 452 on the distal end of inner pushable member 450 .
inner pushable member 450 is pushed in the distal direction. This exerts an outward force on bendable regions 449 causing bendable regions 449 to bend in a radial direction exerting an outward force. This force can be used to dilate or displace portions of the anatomy.
Outer member 448 can be substantially straight or may comprise one or more bent or angled regions.
Inner pushable member 450 may comprise one or more lumens.
FIGS. 4N and 4O illustrate sectional views of a design of a mechanical dilator comprising a pullable member.
FIG. 4N shows the mechanical dilator comprising an outer member 454 comprising one or more bendable regions 456 on the distal end of outer member 454 .
Mechanical dilator further comprises an inner pullable member 458 comprising an enlarged region 460 on the distal end of inner pullable member 458 .
inner pullable member 458 is pulled in the proximal direction. This exerts an outward force on bendable regions 456 causing bendable regions 456 to bend in a radial direction exerting an outward force. This force can be used to dilate or displace portions of the anatomy.
Outer member 454 can be substantially straight or may comprise one or more bent or angled regions.
Inner pullable member 458 may comprise one or more lumens.
FIGS. 4P and 4Q illustrate sectional views of a design of a mechanical dilator comprising a hinged member.
FIG. 4P shows the mechanical dilator comprising an outer member 462 comprising one or more bendable regions 464 located on the distal end of outer member 462 .
the mechanical dilator also comprises an inner member 466 located within outer member 462 .
inner member 466 is tubular.
the distal end of inner member 466 comprises one or more first hinges 468 .
First hinges 468 are hinged to the proximal ends of one or more moving elements 470 .
Distal ends of moving elements 470 are hinged to one or more second hinges 472 located on the inner surface of outer member 462 .
FIG. 4P shows the mechanical dilator comprising an outer member 462 comprising one or more bendable regions 464 located on the distal end of outer member 462 .
the mechanical dilator also comprises an inner member 466 located within outer member 4
inner member 466 is pushed in the distal direction. This causes moving elements 470 to exert an outward radial force on bendable regions 464 causing bendable regions 464 to bend in an outward radial direction with an outward force. This outward force can be used to dilate or displace portions of the anatomy.
Outer member 462 can be substantially straight or may comprise one or more bent or angled regions.
Inner member 466 may comprise one or more lumens.
FIGS. 4R through 4W illustrate examples of configurations of mechanical dilators in FIGS. 4H through 4Q .
FIG. 4R shows a sectional view of a mechanical dilator comprising an inner member 474 , an outer stationary member 476 and an outer bendable member 478 .
movement of inner member 474 displaces outer bendable member 478 in the radial direction with a force. This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force in a particular radial direction.
FIG. 4S ′ shows a partial perspective view of the outer stationary member 476 of FIG. 4R .
FIG. 4T shows a sectional view of a mechanical dilator comprising an inner member 480 , a first outer hemi-tubular member 482 and a second outer hemi-tubular member 484 .
movement of inner member 480 displaces first outer hemi-tubular member 482 and second outer hemi-tubular member 484 in the radial direction with a force.
This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force in two diametrically opposite regions.
FIG. 4U ′ shows a partial perspective view of the first outer hemi-tubular member 482 and the second outer hemi-tubular member 484 of FIG. 4T .
FIG. 4V shows a sectional view of a mechanical dilator comprising an inner member 486 , a first outer curved member 488 and a second outer curved member 490 .
movement of inner member 486 displaces first outer curved member 488 and second outer curved member 490 in the radial direction with a force.
This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force over smaller areas in two diametrically opposite regions.
FIG. 4W ′ shows a partial perspective view of the first outer curved member 488 and the second outer curved member 490 of FIG. 4V .
Similar designs for mechanical dilators in FIGS. 4H through 4Q are possible using three or more displaceable members.
the inner member in the mechanical dilators disclosed herein may be replaced by a balloon for displacing the outer members to exert an outward radial force.
Several other designs of the working device may also be used including but not limited to cutters, chompers, rotating drills, rotating blades, tapered dilators, punches, dissectors, burs, non-inflating mechanically expandable members, high frequency mechanical vibrators, radiofrequency ablation devices, microwave ablation devices, laser devices (e.g. CO 2 , Argon, potassium titanyl phosphate, Holmium:YAG and Nd:YAG laser devices), snares, biopsy tools, scopes and devices that introduce diagnostic or therapeutic agents.
cutters chompers, rotating drills, rotating blades, tapered dilators, punches, dissectors, burs, non-inflating mechanically expandable members, high frequency mechanical vibrators, radiofrequency ablation devices, microwave ablation devices, laser devices (e.g. CO 2 , Argon, potassium titanyl phosphate, Holmium:YAG and Nd:YAG laser devices), snares, biopsy tools, scopes and devices that introduce diagnostic or therapeutic
FIG. 5A shows a perspective view of an embodiment of a balloon comprising a conical proximal portion, a conical distal portion and a cylindrical portion between the conical proximal portion and the conical distal portion.
FIGS. 5B to 5N show perspective views of several alternate embodiments of the balloon.
FIG. 5B shows a conical balloon
FIG. 5C shows a spherical balloon
FIG. 5D shows a conical/square long balloon
FIG. 5E shows a long spherical balloon
FIG. 5F shows a dog bone balloon
FIG. 5G shows a offset balloon
FIG. 5H shows a square balloon
FIG. 5I shows a conical/square balloon
FIG. 5J shows a conical/spherical long balloon
FIG. 5K shows a tapered balloon
FIG. 5L shows a stepped balloon
FIG. 5M shows a conical/offset balloon
FIG. 5N shows a curved balloon
the balloons disclosed herein can be fabricated from biocompatible materials including but not limited to polyethylene terephthalate, Nylon, polyurethane, polyvinyl chloride, crosslinked polyethylene, polyolefins, HPTFE, HPE, HDPE, LDPE, EPTFE, block copolymers, latex and silicone.
the balloons disclosed herein can be fabricated by a variety of fabrication methods including but not limited to molding, blow molding, dipping, extruding etc.
the balloons disclosed herein can be inflated with a variety of inflation media including but not limited to saline, water, air, radiographic contrast materials, diagnostic or therapeutic substances, ultrasound echogenic materials and fluids that conduct heat, cold or electricity.
FIG. 5O shows a partial perspective view of an embodiment of a balloon catheter device 500 comprising a balloon for delivering diagnostic or therapeutic substances.
Balloon catheter device 500 comprises a flexible catheter 502 having a balloon 504 thereon.
the catheter device 500 is advanced, with balloon 504 deflated, into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned with the deflated balloon 504 situated within an ostium, passageway or adjacent to tissue or matter that is to be dilated, expanded or compressed (e.g., to apply pressure for hemostasis, etc.).
the balloon 504 may be inflated to dilate, expand or compress the ostium, passageway, tissue or matter. Thereafter the balloon 504 may be deflated and the device 500 may be removed.
This balloon 504 may also be coated, impregnated or otherwise provided with a medicament or substance that will elute from the balloon into the adjacent tissue (e.g., bathing the adjacent tissue with drug or radiating the tissue with thermal or other energy to shrink the tissues in contact with the balloon 504 ).
the balloon may have a plurality of apertures or openings through which a substance may be delivered, sometimes under pressure, to cause the substance to bathe or diffuse into the tissues adjacent to the balloon.
radioactive seeds, threads, ribbons, gas or liquid, etc. may be advanced into the catheter shaft 502 or balloon 504 or a completely separate catheter body for some period of time to expose the adjacent tissue and to achieve a desired diagnostic or therapeutic effect (e.g. tissue shrinkage, etc.).
FIG. 5P shows a partial perspective view of an embodiment of a balloon/cutter catheter device 506 comprising a flexible catheter 508 having a balloon 510 with one or more cutter blades 512 formed thereon.
the device 506 is advanced, with balloon 510 deflated, into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned with the deflated balloon 510 situated within an ostium, passageway or adjacent to tissue or matter that is to be dilated, expanded or compressed and in which it is desired to make one or more cuts or scores (e.g.
the balloon 510 is inflated to dilate, expand or compress the ostium, passageway, tissue or matter and causing the cutter blade(s) 512 to make cut(s) in the adjacent tissue or matter. Thereafter the balloon 510 is deflated and the device 506 is removed.
the blade may be energized with mono or bi-polar RF energy or otherwise heated such that it will cut the tissues while also causing hemostasis and/or to cause thermal contraction of collagen fibers or other connective tissue proteins, remodeling or softening of cartilage, etc.
FIGS. 5Q and 6F show perspective views of an embodiment of a balloon catheter device 514 comprising a flexible catheter 516 having a balloon 518 with one or more reinforcing means 520 thereon.
reinforcing means 520 is a braid attached on the external surface of balloon 518 .
the reinforcing braid can be constructed from suitable materials like polymer filaments (e.g. PET or Kevlar filaments), metallic filaments (e.g. SS316 or Nitinol filaments) and metallic or non-metallic meshes or sheets.
FIG. 6F ′ shows a perspective view of a reinforcing braid that can be used with the balloon catheter device in FIGS. 5Q and 6F .
FIG. 5R shows a partial sectional view of an embodiment of a balloon catheter 522 comprising a shaft 524 and a balloon 526 .
Shaft 524 comprises a balloon inflation lumen.
the distal portion of balloon inflation lumen terminates in inflation ports 528 located near the distal end of balloon 526 .
FIGS. 5S through 5T illustrate designs of balloon catheters comprising multiple balloons.
FIG. 5S shows a partial sectional view of an embodiment of a balloon catheter 530 comprising a shaft 532 with a lumen 533 .
Lumen 533 opens into three orifices located on shaft 532 namely a first orifice 534 , a second orifice 536 and a third orifice 538 .
the three orifices are used to inflate three balloons.
First orifice 534 inflates a first balloon 540
second orifice 536 inflates a second balloon 542
third orifice 538 inflates third balloon 544 .
first balloon 540 and third balloon 544 are inflated with a single lumen and second balloon 542 is inflated with a different lumen.
first balloon 540 , second balloon 542 and third balloon 544 interconnected and are inflated with a single lumen.
a valve mechanism allows first balloon and second balloon to inflate before allowing second balloon to inflate.
FIG. 5T shows a partial sectional view of an embodiment of a balloon catheter 546 comprising a shaft 548 comprising a first inflation lumen 550 , a second inflation lumen 552 and a third inflation lumen 554 .
the three inflation lumens are used to inflate three non-connected balloons.
First inflation lumen 550 inflates a first balloon 556
second inflation lumen 552 inflates a second balloon 558
third inflation lumen 554 inflates a third balloon 560 .
FIGS. 5U through 5AB illustrate perspective and sectional views of various embodiments of a balloon catheter comprising sensors.
FIG. 5U shows a partial perspective view of a balloon catheter comprising an outer member 562 , an inner member 564 and a balloon 566 attached to distal region of outer member 562 and distal region of inner member 564 .
the balloon catheter further comprises a first sensor 568 located on the distal region of outer member 562 and a second sensor 570 located on the distal region of inner member 564 .
FIG. 5V shows a crossection through plane 5 V- 5 V in FIG. 5U .
Outer member 562 comprises a first sensor lumen 572 to receive the lead from first sensor 568 .
Inner member 564 comprises a second sensor lumen 574 to receive the lead from second sensor 570 .
Inner member 564 further comprises a circular lumen 576 .
Outer member 562 and inner member 564 enclose an annular lumen 578 .
annular lumen 578 is a balloon inflation lumen.
FIG. 5W shows a partial perspective view of a balloon catheter comprising an outer member 580 , an inner member 582 and a balloon 584 attached to distal region of outer member 580 and distal region of inner member 582 .
the balloon catheter further comprises a first sensor 586 located on the distal region of inner member 582 and a second sensor 588 located on the distal region of inner member 582 distal to first sensor 586 .
FIG. 5X shows a cross section through plane 5 X- 5 X in FIG. 5W .
Inner member 582 comprises a first sensor lumen 590 to receive the lead from first sensor 586 and a second sensor lumen 592 to receive the lead from second sensor 588 .
Inner member 582 further comprises a circular lumen 594 .
Outer member 580 and inner member 582 enclose an annular lumen 596 .
annular lumen 596 is a balloon inflation lumen.
FIG. 5Y shows a partial perspective view of a balloon catheter comprising an outer member 598 , an inner member 600 and a balloon 602 attached to distal region of outer member 598 and distal region of inner member 600 .
the balloon catheter further comprises a first sensor 604 located on the distal region of outer member 598 and a second sensor 606 located on the distal region of outer member 598 distal to first sensor 604 .
FIG. 5Z shows a cross section through plane 5 Z- 5 Z in FIG. 5Y .
Outer member 598 comprises a first sensor lumen 608 to receive the lead from first sensor 604 and a second sensor lumen 610 to receive the lead from second sensor 606 .
Inner member 600 comprises a circular lumen 612 .
Outer member 598 and inner member 600 enclose an annular lumen 614 .
annular lumen 614 is a balloon inflation lumen.
FIG. 5AA shows a partial perspective view of a balloon catheter comprising an outer member 616 , an inner member 618 and a balloon 620 attached to distal region of outer member 616 and distal region of inner member 618 .
the balloon catheter further comprises a first sensor 624 located on the distal region of outer member 616 and a second sensor 626 located on the distal region of inner member 618 .
Second sensor 626 comprises a lead 628 .
FIG. 5AB shows a cross section through plane 5 AB- 5 AB in FIG. 5AA .
Outer member 616 comprises a first sensor lumen 630 to receive the lead from first sensor 624 .
Inner member 618 comprises a circular lumen 632 .
Lead 628 from second sensor 626 is attached on the outer surface of inner member 618 and is oriented parallel to inner member 618 .
Outer member 616 and inner member 618 enclose an annular lumen 634 .
annular lumen 634 is a balloon inflation lumen.
the sensors mentioned in FIGS. 5U through 5AB can be electromagnetic sensors or sensors including but not limited to location sensors, magnetic sensors, electromagnetic coils, RF transmitters, mini-transponders, ultrasound sensitive or emitting crystals, wire-matrices, micro-silicon chips, fiber-optic sensors, etc.
FIGS. 6A through 6G illustrate partial perspective views of several embodiments of shaft designs for the various devices disclosed herein. These shaft designs are especially useful for devices that encounter high torque or high burst pressures or require enhanced pushability, steerability and kink resistance.
FIG. 6A shows a partial perspective view of an embodiment of a shaft 602 comprising a spiral element 604 wound around the shaft.
Spiral element 604 can be made of suitable materials like metals (e.g. SS316L, SS304) and polymers.
spiral element 604 is in the form of round wire of diameter between 0.04 mm to 0.25 mm.
spiral element is in the form of flat wire of cross section dimensions ranging from 0.03 mm ⁇ 0.08 mm to 0.08 mm ⁇ 0.25 mm.
FIG. 6B shows a partial perspective view of an embodiment of a shaft 606 comprising a reinforcing filament 608 .
Reinforcing filament 608 is substantially parallel to the axis of shaft 606 .
Shaft 606 with reinforcing filament 608 can be covered with a jacketing layer.
Reinforcing filament 608 can be made of suitable materials like metals, polymers, glass fiber etc. Reinforcing filament 608 can also have shape memory characteristics.
reinforcing filament 608 is embedded in shaft 606 .
reinforcing filament is introduced through a lumen in shaft 606 .
Shaft 606 may comprise more than one reinforcing filament 608 .
FIG. 6C shows a partial perspective view of an embodiment of a shaft 610 comprising one of more stiffening rings 612 along the length of shaft 610 .
FIG. 6D shows a partial perspective view of an embodiment of a shaft 614 comprising a series of controllably stiffening elements 616 along the length of the shaft.
Shaft 614 further comprises a tension wire 618 that runs through controllably stiffening elements 616 and is attached to the most distal stiffening element. The tension in tension wire 618 causes controllably stiffening elements 616 to come into contact with each other with a force.
Friction between controllably stiffening elements 616 causes shaft 614 to have a certain stiffness. Increasing the tension in tension wire 618 increases the force with which controllably stiffening elements 616 come into contact with each other. This increases the friction between controllably stiffening elements 616 which in turn increases the stiffness of shaft 614 . Similarly, reducing the tension in tension wire 618 reduces the stiffness of shaft 614 .
Controllably stiffening elements 616 can be made from suitable materials like metal, polymers and composites. In one embodiment, controllably stiffening elements 616 are separated from each other by one or more springs. Tension wire 618 can be made from metals like SS316.
FIG. 6E shows a partial perspective view of an embodiment of a shaft 620 comprising a hypotube 622 .
hypotube 622 is located on the exterior surface of shaft 620 .
hypotube 622 is embedded in shaft 620 .
Hypotube 620 can be made of metals like stainless steel 316 or suitable polymers.
FIGS. 6F and 6F ′ show a partial perspective view of an embodiment of a shaft 624 comprising a reinforcing element 626 in the form of a reinforcing braid or mesh located on the outer surface of shaft 624 .
Reinforcing element 626 can be made of suitable materials like polymer filaments (e.g.
the braid pattern can be regular braid pattern, diamond braid pattern, diamond braid pattern with a half load etc.
the outer surface of reinforcing element 626 is covered with a jacketing layer.
FIG. 6G shows a partial perspective view of an embodiment of a device comprising a shaft 628 comprising a proximal portion 630 , a distal portion 632 , a working element 634 and a plastically deformable region 636 located between the proximal portion 630 and distal portion 632 .
Plastically deformable region 636 can be deformed by a physician to adjust the angle between proximal portion 630 and distal portion 632 . This enables the devices to be used for several different anatomical regions of the same patient. Also, such devices can be adjusted for optimal navigation through a patient's anatomy.
shaft 628 comprises multiple plastically deformable regions.
plastically deformable region 636 is located within working element 634 .
Such a design comprising one or more plastically deformable regions can be used for any of the devices mentioned herein like catheters with working elements, guide catheters, guide catheters with a pre-set shape, steerable guide catheters, steerable catheters, guidewires, guidewires with a pre-set shape, steerable guidewires, ports, introducers, sheaths etc.
FIG. 6H shows a partial perspective view of an embodiment of a device comprising a shaft with a flexible element.
the design is illustrated as a shaft 638 comprising a proximal portion 640 , a distal portion 642 and a working element 644 (e.g. a balloon).
Shaft 638 further comprises a flexible element 646 located between proximal portion 640 and distal portion 642 .
This design enables proximal portion 640 to bend with respect to distal portion 642 making it easier to navigate through the complex anatomy and deliver working element 644 to the desired location.
shaft 638 comprises multiple flexible elements.
flexible element 646 is located within working element 644 .
Such a design comprising one or more flexible elements can be used for any of the devices mentioned herein like catheters with working elements, guide catheters, guide catheters with a pre-set shape, steerable guide catheters, steerable catheters, guidewires, guidewires with a pre-set shape, steerable guidewires, ports, introducers, sheaths etc.
FIGS. 6I through 6K illustrate an example of a shaft comprising a malleable element.
FIG. 6I shows a partial perspective view of an embodiment of a shaft 648 comprising malleable element 650 and a lumen 652 wherein shaft 648 is in a substantially straight configuration.
Malleable element 650 is embedded in shaft 648 such that the axis of malleable element 650 is substantially parallel to the axis of shaft 648 .
FIG. 6J shows a partial perspective view of the embodiment of FIG. 6I in a bent configuration.
FIG. 6K shows a cross sectional view through plane 6 K- 6 K of FIG. 6I showing shaft 648 comprising malleable element 650 and a lumen 652 .
shaft 648 comprises more than one malleable element.
FIGS. 6L through 6M show an embodiment of a controllably deformable shaft.
FIG. 6L shows a partial sectional view of an embodiment of a controllably deformable shaft 654 comprising a pull wire 656 attached to a pull wire terminator 658 located near the distal end of shaft 654 .
FIG. 6M shows a partial sectional view of the controllably deformable shaft 654 of FIG. 6L in a bent orientation when pull wire 656 is pulled in the proximal direction.
the deformation can be varied by varying the location of pull wire terminator 658 and the stiffness of various sections of shaft 658 .
the stiffness of a section of shaft 658 can be varied by adding reinforcing coatings, external or internal reinforcing coils, reinforcing fabric, reinforcing meshes and reinforcing wires, hinged elements, embedded filaments, reinforcing rings etc.
FIG. 6N shows a perspective view of a balloon catheter comprising a rigid or semi-rigid member.
the balloon catheter comprises a rigid or semi-rigid member 660 and a balloon 662 located on the distal region of rigid or semi-rigid member 660 .
Rigid or semi-rigid member 660 may comprise one or more lumens.
Rigid or semi-rigid member 660 may comprise one or more bent, curved or angled regions.
Balloon 662 is inflated by a balloon inflation tube 664 comprising a hub 666 at the proximal end of balloon inflation tube 664 .
balloon inflation tube 664 is fully attached along its length to rigid or semi-rigid member 660 .
balloon inflation tube 664 is partially attached along its length to rigid or semi-rigid member 660 .
FIGS. 6O through 6Q illustrate sectional views of a balloon catheter comprising an insertable and removable element.
FIG. 6O shows a balloon catheter 668 comprising a balloon 670 , a first lumen 672 and a balloon inflation lumen 674 opening into balloon 670 through an inflation port 676 .
FIG. 6P shows an insertable element 678 having a proximal end 680 and a distal end 682 .
distal end 682 ends in a sharp tip for penetrating tissue.
insertable element 678 comprises one or more bent, angled or curved regions 684 .
Insertable element 678 can be fabricated from a variety of materials to obtain properties including but not limited to rigidity, shape memory, elasticity, ability to be plastically deformed etc. In FIG. 6Q , insertable element 678 is inserted into balloon catheter 668 through first lumen 672 . This combination can be used to perform a diagnostic or therapeutic procedure. Insertable element 678 may be removed during or after the procedure.
FIGS. 7A through 7K show cross sectional views of several embodiments of lumen orientation in the devices disclosed herein.
FIG. 7A shows a cross sectional view of an embodiment of a shaft 702 comprising a first lumen 704 and a second lumen 706 .
first lumen 704 is a guidewire lumen and second lumen 706 is an inflation lumen.
FIG. 7B shows a cross sectional view of an embodiment of a shaft 708 comprising a first lumen 710 and a annular second lumen 712 such that second annular lumen 712 is substantially coaxial with first lumen 710 .
first lumen 710 is a guidewire lumen and annular second lumen 712 is an inflation lumen.
FIG. 7A shows a cross sectional view of an embodiment of a shaft 702 comprising a first lumen 704 and a second lumen 706 .
first lumen 704 is a guidewire lumen and second lumen 706 is an inflation lumen.
FIG. 7C shows a cross sectional view of an embodiment of a shaft 714 comprising a first tubular element 716 comprising a first lumen 718 , a second tubular element 720 comprising a second lumen 722 and a jacket 724 surrounding first tubular element 716 and second tubular element 720 .
first lumen 718 is a guidewire lumen
second lumen 722 is an inflation lumen.
FIG. 7D shows a cross sectional view of an embodiment of a shaft 726 comprising a first lumen 728 , a second lumen 730 and a third lumen 732 .
first lumen 728 is a guidewire lumen
second lumen 730 is an irrigation/aspiration lumen
third lumen 732 is an inflation lumen.
FIG. 7E shows a cross sectional view of an embodiment of a shaft 734 comprising a cylindrical element 736 , a tubular element 738 comprising a lumen 740 and a jacket 742 surrounding cylindrical element 736 and tubular element 738 .
first lumen 748 is lined with a suitable coating 758 like hydrophilic lubricious coating, hydrophobic lubricious coating, abrasion resisting coating etc.
first lumen 748 is a guidewire lumen and second lumen 750 is an inflation lumen.
the lumens disclosed herein can be lined with suitable coatings like hydrophilic lubricious coatings, hydrophobic lubricious coatings, abrasion resisting coatings, radiopaque coatings, echogenic coatings etc.
FIG. 7G shows a partial perspective view of an embodiment of a shaft 754 * comprising a first lumen 756 * and a zipper lumen 758 *.
Zipper lumen 758 * allows a device like a guidewire 760 * to be easily introduced into or removed from shaft 754 *.
FIG. 7H shows a cross sectional view through plane 7 H- 7 H in FIG. 7G showing the orientations of first lumen 756 * and zipper lumen 758 *.
FIG. 7I shows a cross sectional view of an embodiment of a shaft 762 comprising a first lumen 764 and a rapid exchange lumen 766 .
Rapid exchange lumen 766 extends from the distal end of shaft 762 to a proximal region. Rapid exchange lumen 766 enables shaft 762 to be easily and quickly introduced or removed over an exchange device like a guidewire 768 .
FIG. 7J shows a cross sectional view through plane 7 J- 7 J in FIG. 7I showing first lumen 764 and rapid exchange lumen 766 .
FIG. 7K shows a cross sectional view through plane 7 K- 7 K in FIG. 7I showing first lumen 764 .
FIGS. 7L through 7Q shows perspective and sectional views of lumens for the devices disclosed herein that are not present throughout the length of the devices.
FIG. 7L shows a perspective view of a balloon catheter comprising a shaft 770 , a balloon 772 and a lumen 774 that is present throughout shaft 770 .
the balloon catheter further comprises a balloon inflation lumen 776 that opens into balloon 772 .
the distal end of balloon inflation lumen 776 is plugged with a plug 778 .
FIG. 7M shows a crossection through plane 7 M- 7 M in FIG. 7L showing shaft 770 comprising lumen 774 and balloon inflation lumen 776 .
FIG. 7N shows a crossection through plane 7 N- 7 N in FIG.
FIG. 7L shows shaft 770 comprising lumen 774 and plug 778 .
FIG. 7O shows a perspective view of a balloon catheter comprising a shaft 780 , a balloon 782 and a lumen 786 that is present throughout shaft 780 .
the balloon catheter further comprises a balloon inflation lumen 784 .
the distal end of balloon inflation lumen 784 opens into balloon 782 .
FIG. 7P shows a crossection through plane 7 P- 7 P in FIG. 7O showing shaft 780 comprising lumen 786 and balloon inflation lumen 784 .
FIG. 7Q shows a crossection through plane 7 Q- 7 Q in FIG. 7O showing shaft 780 comprising lumen 786 .
FIGS. 8A through 8E show partial perspective views of several embodiments of markers that may be present on the elements of the devices mentioned herein.
FIG. 8A shows a partial perspective view of an embodiment of a shaft 800 comprising a plurality of distance markers 802 located along the length of shaft 800 .
FIG. 8B shows a partial perspective view of an embodiment of a shaft 804 comprising a plurality of radiographic markers 806 located along the length of shaft 804 .
FIG. 8C shows a partial perspective view of an embodiment of a shaft 808 comprising a plurality of ring shaped radiographic markers 810 located along the length of shaft 808 .
FIG. 8D shows a partial perspective view of an embodiment of a balloon catheter 812 comprising a shaft 814 and a balloon 816 .
Balloon 816 comprises a plurality of radiographic markers 818 located on the outer surface of the balloon 816 .
markers 818 may be in a linear arrangement, non-linear arrangement or any other configuration that performs the desired marking function (e.g., delineating the length and/or diameter of the balloon, marking the proximal and/or distal ends of the balloon, etc.).
FIGS. 8E and 8E ′ show partial perspective and longitudinal sectional views of an embodiment of a balloon catheter 820 comprising a shaft 822 and a balloon 824 .
Balloon 824 comprises a plurality of radiographic markers 826 located on the inner surface of the balloon 824 .
Such markers 826 may be in a linear arrangement, non-linear arrangement or any other configuration that performs the desired marking function (e.g., delineating the length and/or diameter of the balloon, marking the proximal and/or distal ends of the balloon, etc.).
the devices disclosed herein may also comprise several other types of markers like ultrasound markers, radiofrequency markers and magnetic markers.
the devices disclosed herein may also comprise one or more sensors like electromagnetic sensors, electrical sensors, magnetic sensors, light sensors and ultrasound sensors.
diagnostic or therapeutic substance as used herein is to be broadly construed to include any feasible drugs, prodrugs, proteins, gene therapy preparations, cells, diagnostic agents, contrast or imaging agents, biologicals, etc. Such substances may be in bound or free form, liquid or solid, colloid or other suspension, solution or may be in the form of a gas or other fluid or nan-fluid.
the substance delivered may comprise pharmaceutically acceptable salt or dosage form of an antimicrobial agent (e.g., antibiotic, antiviral, antiparasitic, antifungal, etc.), a corticosteroid or other anti-inflammatory (e.g., an NSAID), a decongestant (e.g., vasoconstrictor), a mucous thinning agent (e.g., an expectorant or mucolytic), an agent that prevents of modifies an allergic response (e.g., an antihistamine, cytokine inhibitor, leucotriene inhibitor, IgE inhibitor, immunomodulator), etc.
an antimicrobial agent e.g., antibiotic, antiviral, antiparasitic, antifungal, etc.
a corticosteroid or other anti-inflammatory e.g., an NSAID
a decongestant e.g., vasoconstrictor
a mucous thinning agent e.g., an expectorant or mu
nasal cavity used herein to be broadly construed to include any cavity that is present in the anatomical structures of the nasal region including the nostrils and paranasal sinuses.
trans-nasal means through a nostril.
any of the working devices and guide catheters described herein may be configured or equipped to receive or be advanced over a guidewire or other guide member (e.g., an elongate probe, strand of suure material, other elongate member) unless to do so would render the device inoperable for its intended purpose.
a guidewire or other guide member e.g., an elongate probe, strand of suure material, other elongate member
guidewires e.g., an elongate probe, strand of suure material, other elongate member
This may include the use of coils, tapered or non-tapered core wires, radioopaque tips and/or entire lengths, shaping ribbons, variations of stiffness.
these wires may possess dimensions of length between 5 and 75 cm and outer diameter between 0.005′′ and 0.050′′.
the devices disclosed herein may comprise an endoscope for visualization of the target anatomy.
the devices may also comprise ultrasound imaging modalities to image the anatomical passageways and other anatomical structures.
the devices disclosed herein may comprise one or more magnetic elements especially on the distal end of the devices. Such magnetic elements may be used to navigate through the anatomy by using external magnetic fields. Such navigation may be controlled digitally using a computer interface.
the devices disclosed herein may also comprise one or more markers (e.g. infra-red markers). The markers can be used to track the precise position and orientation of the devices using image guidance techniques.
imaging or navigating modalities including but not limited to fluoroscopic, radiofrequency localization, electromagnetic, magnetic and other radiative energy based modalities may also be used with the methods and devices disclosed herein.
imaging and navigation technologies may also be referenced by computer directly or indirectly to pre-existing or simultaneously created 3-D or 2-D data sets which help the doctor place the devices within the appropriate region of the anatomy.
the distal tip of devices mentioned herein may comprise a flexible tip or a soft, atraumatic tip. Also, the shaft of such devices may be designed for enhanced torquability.

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Abstract

Sinusitis and other disorders of the ear, nose and throat are diagnosed and/or treated using minimally invasive approaches with flexible or rigid instruments. Various methods and devices are used for remodeling or changing the shape, size or configuration of a sinus ostium or duct or other anatomical structure in the ear, nose or throat; implanting a device, cells or tissues; removing matter from the ear, nose or throat; delivering diagnostic or therapeutic substances or performing other diagnostic or therapeutic procedures. Introducing devices (e.g., guide catheters, tubes, guidewires, elongate probes, other elongate members) may be used to facilitate insertion of working devices (e.g. catheters e.g. balloon catheters, guidewires, tissue cutting or remodeling devices, devices for implanting elements like stents, electrosurgical devices, energy emitting devices, devices for delivering diagnostic or therapeutic agents, substance delivery implants, scopes etc.) into the paranasal sinuses or other structures in the ear, nose or throat.

Description

This application is a continuation of copending U.S. patent application Ser. No. 11/928,346 entitled Apparatus and Methods for Dilating and Modifying Ostia of Paranasal Sinuses and Other Intranasal or Paranasal Structures filed on Oct. 30, 2007 which is a continuation of copending U.S. patent application Ser. No. 10/944,270 entitled Apparatus and Methods for Dilating and Modifying Ostia of Paranasal Sinuses and Other Intranasal or Paranasal Structures filed on Sep. 17, 2004 which is a continuation-in-part of copending U.S. patent application Ser. No. 10/829,917 entitled “Devices, Systems and Methods for Diagnosing and Treating Sinusitis and Other Disorders of the Ears, Nose and/or Throat” filed on Apr. 21, 2004, the entire disclosure of which is expressly incorporated herein by reference.
The present invention relates generally to medical devices and methods and more particularly to minimally invasive, devices, systems and methods for treating sinusitis and other ear, nose & throat disorders.
The nose is responsible for warming, humidifying and filtering inspired air and for conserving heat and moisture from expired air. The nose is formed mainly of cartilage, bone, mucous membranes and skin.
The bones in the nose contain a series of cavities known as paranasal sinuses that are connected by passageways. The paranasal sinuses include frontal sinuses, ethmoid sinuses, sphenoid sinuses and maxillary sinuses. The paranasal sinuses are lined with mucous-producing epithelial tissue and ultimately opening into the nasal cavity. Normally, mucous produced by the epithelial tissue slowly drains out of each sinus through an opening known as an ostium. If the epithelial tissue of one of these passageways becomes inflamed for any reason, the cavities which drain through that passageway can become blocked. This blockage can be periodic (resulting in episodes of pain) or chronic. This interference with drainage of mucous (e.g., occlusion of a sinus ostium) can result in mucosal congestion within the paranasal sinuses. Chronic mucosal congestion of the sinuses can cause damage to the epithelium that lines the sinus with subsequent decreased oxygen tension and microbial growth (e.g., a sinus infection).
Sinusitis:
The term “sinusitis” refers generally to any inflammation or infection of the paranasal sinuses caused by bacteria, viruses, fungi (molds), allergies or combinations thereof. It has been estimated that chronic sinusitis (e.g., lasting more than 3 months or so) results in 18 million to 22 million physician office visits per year in the United States.
Patients who suffer from sinusitis typically experience at least some of the following symptoms:

- headaches or facial pain
- nasal congestion or post-nasal drainage
- difficulty breathing through one or both nostrils
- bad breath
- pain in the upper teeth

Thus, one of the ways to treat sinusitis is by restoring the lost mucous flow. The initial therapy is drug therapy using anti-inflammatory agents to reduce the inflammation and antibiotics to treat the infection. A large number of patients do not respond to drug therapy. Currently, the gold standard for patients with chronic sinusitis that do not respond to drug therapy is a corrective surgery called Functional Endoscopic Sinus Surgery.
Current and Proposed Procedures for Sinus Treatment
Functional Endoscopic Sinus Surgery
In FESS, an endoscope is inserted into the nose and, under visualization through the endoscope, the surgeon may remove diseased or hypertrophic tissue or bone and may enlarge the ostia of the sinuses to restore normal drainage of the sinuses. FESS procedures are typically performed with the patient under general anesthesia.
Although FESS continues to be the gold standard therapy for surgical treatment of severe sinus disease, FESS does have several shortcomings. For example, FESS can cause significant post-operative pain. Also, some FESS procedures are associated with significant postoperative bleeding and, as a result, nasal packing is frequently placed in the patient's nose for some period of time following the surgery. Such nasal packing can be uncomfortable and can interfere with normal breathing, eating, drinking etc. Also, some patients remain symptomatic even after multiple FESS surgeries. Additionally, some FESS procedures are associated with risks of iatrogenic orbital, intracranial and sinonasal injury. Many otolaryngologists consider FESS an option only for patients who suffer from severe sinus disease (e.g., those showing significant abnormalities under CT scan). Thus, patients with less severe disease may not be considered candidates for FESS and may be left with no option but drug therapy. One of the reasons why FESS procedures can be bloody and painful relates to the fact that instruments having straight, rigid shafts are used. In order to target deep areas of the anatomy with such straight rigid instrumentation, the physician needs to resect and remove or otherwise manipulate any anatomical structures that may lie in the direct path of the instruments, regardless of whether those anatomical structures are part of the pathology.
Balloon Dilation Based Sinus Treatment
Methods and devices for sinus intervention using dilating balloons have been disclosed in U.S. Pat. No. 2,525,183 (Robison) and United States Patent Publication No. 2004/0064150 A1 (Becker). For example, U.S. Pat. No. 2,525,183 (Robison) discloses an inflatable pressure device which can be inserted following sinus surgery and inflated within the sinus. The patent does not disclose device designs and methods for flexibly navigating through the complex nasal anatomy to access the natural ostia of the sinuses. The discussion of balloon materials is also fairly limited to thin flexible materials like rubber which are most likely to be inadequate for dilating the bony ostia of the sinus.
United States patent publication number 2004/0064150 A1 (Becker) discloses balloon catheters formed of a stiff hypotube to be pushed into a sinus. The balloon catheters have a stiff hypotube with a fixed pre-set angle that enables them to be pushed into the sinus. In at least some procedures wherein it is desired to position the balloon catheter in the ostium of a paranasal sinus, it is necessary to advance the balloon catheter through complicated or tortuous anatomy in order to properly position the balloon catheter within the desired sinus ostium. Also, there is a degree of individual variation in the intranasal and paranasal anatomy of human beings, thus making it difficult to design a stiff-shaft balloon catheter that is optimally shaped for use in all individuals. Indeed, rigid catheters formed of hypotubes that have pre-set angles cannot be easily adjusted by the physician to different shapes to account for individual variations in the anatomy. In view of this, the Becker patent application describes the necessity of having available a set of balloon catheters, each having a particular fixed angle so that the physician can select the appropriate catheter for the patient's anatomy. The requirement to test multiple disposable catheters for fit is likely to be very expensive and impractical. Moreover, if such catheter are disposable items (e.g., not sterilizable and reusable) the need to test and discard a number of catheters before finding one that has the ideal bend angle could be rather expensive.
Thus, although the prior art discloses the use of dilating balloons for sinus treatments, it does not disclose the various means for navigation through the complex anatomy without significant manipulation of non-pathogenic anatomical regions that obstruct direct access to the sinus openings. Further, the prior art only discloses balloons of relatively simple shapes or materials for dilating sinus openings. Further, this art does not sufficiently elaborate beyond endoscopy on other means for imaging or tracking the position of such devices within the sinus anatomy.
Thus, there is a need for new devices and methods for easily navigating the complex anatomy of the nasal cavities and paranasal sinuses and for treating disorders of the paranasal sinuses with minimal complications due to individual variations in anatomy and causing minimal trauma to or disruption of anatomical structures that are not pathogenic.
In general, the present invention provides methods, devices and systems for diagnosing and/or treating sinusitis or other conditions of the ear, nose or throat.
In accordance with the present invention, there are provided methods wherein one or more flexible or rigid elongate devices as described herein are inserted in to the nose, nasopharynx, paranasal sinus, middle ear or associated anatomical passageways to perform an interventional or surgical procedure. Examples of procedures that may be performed using these flexible catheters or other flexible elongate devices include but are not limited to: remodeling or changing the shape, size or configuration of a sinus ostium or other anatomical structure that affects drainage from one or more paranasal sinuses; cutting, ablating, debulking, cauterizing, heating, freezing, lasing, forming an osteotomy or trephination in or otherwise modifying bony or cartilaginous tissue within paranasal sinus or elsewhere within the nose; removing puss or aberrant matter from the paranasal sinus or elsewhere within the nose; scraping or otherwise removing cells that line the interior of a paranasal sinus; delivering contrast medium; delivering a therapeutically effective amount of a therapeutic substance; implanting a stent, tissue remodeling device, substance delivery implant or other therapeutic apparatus; cutting, ablating, debulking, cauterizing, heating, freezing, lasing, dilating or otherwise modifying tissue such as nasal polyps, abberant or enlarged tissue, abnormal tissue, etc.; grafting or implanting cells or tissue; reducing, setting, screwing, applying adhesive to, affixing, decompressing or otherwise treating a fracture; delivering a gene or gene therapy preparation; removing all or a portion of a tumor, removing a polyp; delivering histamine, an allergen or another substance that causes secretion of mucous by tissues within a paranasal sinus to permit assessment of drainage from the sinus; implanting a cochlear implant or indwelling hearing aid or amplification device, etc.
Still further in accordance with the invention, there are provided devices and systems for performing some or all of the procedures described herein. Introducing devices may be used to facilitate insertion of working devices (e.g. catheters e.g. balloon catheters, tissue cutting or remodeling devices, guidewires, devices for implanting elements like stents, electrosurgical devices, energy emitting devices, devices for delivering diagnostic or therapeutic agents, substance delivery implants, scopes etc) into the paranasal sinuses and other structures in the ear, nose or throat.
Still further in accordance with the invention, there are provided apparatus and methods for navigation and imaging of the interventional devices within the sinuses using endoscopic including stereo endoscopic, fluoroscopic, ultrasonic, radiofrequency localization, electromagnetic, magnetic and other radiative energy based modalities. These imaging and navigation technologies may also be referenced by computer directly or indirectly to pre-existing or simultaneously created 3-D or 2-D data sets which help the doctor place the devices within the appropriate region of the anatomy.
Further aspects, details and embodiments of the present invention will be understood by those of skill in the art upon reading the following detailed description of the invention and the accompanying drawings.
FIG. 1
shows a schematic diagram of a system for catheter-based minimally invasive sinus surgery of the present invention being used to perform a sinus surgery procedure on a human patient.
FIG. 1A
is an enlarged view of portion “IA” of
FIG. 1
.
FIGS. 2A through 2D
are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a guide and thereafter dilating or remodeling the ostial opening into the paranasal sinus.
FIGS. 2E through 2H
are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a steerable guide and thereafter.
FIGS. 2I through 2L
are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using an introducing device in the form of a guidewire with a preset shape.
FIGS. 2M through 2O
are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using a balloon catheter that has a guide protruding from its distal end.
FIGS. 2P through 2X
are partial sagittal sectional views through a human head showing various steps of a method of accessing an ethmoid sinus through a natural or artificially created opening of the ethmoid sinus.
FIGS. 2Y through 2AC
are partial coronal sectional views through a human head showing various steps of a method for treating a mucocele in a frontal sinus.
FIGS. 3A through 3C
are partial coronal sectional views through a human head showing various steps of a method of accessing a paranasal sinus through an artificially created opening of the paranasal sinus.
FIG. 4A
shows a partial longitudinal sectional view of a system for dilating a sinus ostium or other intranasal anatomical structure, such system comprising three progressively larger dilators useable in sequence.
FIGS. 4B through 4E
show various steps of a method of dilating a nasal cavity using a working device comprising a balloon catheter with a pressure-expandable stent.
FIG. 4F
shows a partial perspective view of a working device that comprises a side suction and/or side cutter.
FIG. 4G
shows a partial perspective view of a working device that comprises a rotating cutter to cut away tissue.
FIGS. 4H and 4I
show various steps of a method of dilating the ostium of a paranasal sinus or other nasal passageway using a mechanical dilator.
FIGS. 4J and 4K
show perspective views of a mechanical dilator comprising a screw mechanism.
FIGS. 4L and 4M
show sectional views of a mechanical dilator that comprises a pushable member.
FIGS. 4N and 4O
show sectional views of a mechanical dilator that comprises a pullable member.
FIGS. 4P and 4Q
show sectional views of a mechanical dilator that comprises a hinged member.
FIGS. 4R through 4W
are schematic diagrams of alternative configurations for the distal portions of mechanical dilators of the types shown in
FIGS. 4H through 4Q
.
FIG. 5A
shows a perspective view of a balloon that comprises a conical proximal portion, a conical distal portion and a cylindrical portion between the conical proximal portion and the conical distal portion.
FIG. 5B
shows a perspective view of a conical balloon.
FIG. 5C
shows a perspective view of a spherical balloon.
FIG. 5D
shows a perspective view of a conical/square long balloon.
FIG. 5E
shows a perspective view of a long spherical balloon.
FIG. 5F
shows a perspective view of a bi-lobed “dog bone” balloon.
FIG. 5G
shows a perspective view of an offset balloon.
FIG. 5H
shows a perspective view of a square balloon.
FIG. 5I
shows a perspective view of a conical/square balloon.
FIG. 5J
shows a perspective view of a conical/spherical long balloon.
FIG. 5K
shows a perspective view of an embodiment of a tapered balloon.
FIG. 5L
shows a perspective view of a stepped balloon.
FIG. 5M
shows a perspective view of a conical/offset balloon.
FIG. 5N
shows a perspective view of a curved balloon.
FIG. 5O
shows a partial perspective view of a balloon catheter device comprising a balloon for delivering diagnostic or therapeutic substances.
FIG. 5P
shows a partial perspective view of a balloon/cutter catheter device comprising a balloon with one or more cutter blades.
FIG. 5Q
shows a perspective view of a balloon catheter device comprising a balloon with a reinforcing braid attached on the external surface of the balloon.
FIG. 5R
shows a partial sectional view of a balloon catheter wherein inflation ports are located near the distal end of the balloon.
FIG. 5S
shows a partial sectional view of an embodiment of a balloon catheter comprising multiple balloons inflated by a single lumen.
FIG. 5T
shows a partial sectional view of a balloon catheter comprising multiple balloons inflated by multiple lumens.
FIGS. 5U through 5AB
show perspective and sectional views of various embodiments of balloon catheters having sensors mounted thereon or therein.
FIG. 6A
shows a partial perspective view of a shaft design useable in the various devices disclosed herein, wherein the shaft comprises an external spiral wire.
FIG. 6B
shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a stiffening wire.
FIG. 6C
shows a partial perspective view of an embodiment of a shaft design for the various devices disclosed herein, wherein the shaft comprises stiffening rings.
FIG. 6D
shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises controllable stiffening elements.
FIG. 6E
shows a partial perspective view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a hypotube.
FIG. 6F
shows a partial perspective cut-away view of a shaft design for the various devices disclosed herein, wherein the shaft comprises a braid.
FIG. 6F
′ is an enlarged side view of the braid of the device of
FIG. 6F
.
FIG. 6G
shows a partial perspective view of an embodiment of a device comprising a shaft having a plastically deformable region.
FIG. 6H
shows a partial perspective view of a device comprising a shaft having a flexible element.
FIG. 6I
shows a partial perspective view of a shaft comprising a malleable element.
FIG. 6J
shows a partial perspective view of the shaft of
FIG. 6I
in a bent configuration.
FIG. 6K
shows a cross sectional view through
plane
6K-6K of
FIG. 6I
.
FIG. 6L
shows a partial sectional view of an embodiment of a controllably deformable shaft.
FIG. 6M
shows a partial sectional view of the controllably deformable shaft of
FIG. 6L
in a deformed state.
FIG. 6N
shows a perspective view of a balloon catheter comprising a rigid or semi-rigid member.
FIGS. 6O through 6Q
show sectional views of a balloon catheter that comprises an insertable and removable element.
FIG. 7A
shows a cross sectional view through a balloon catheter shaft comprising two cylindrical lumens.
FIG. 7B
shows a cross sectional view through a balloon catheter shaft comprising an inner lumen and an annular outer lumen disposed about the inner lumen.
FIG. 7C
shows a cross sectional view through a balloon catheter shaft which comprises a first tubular element with a first lumen, a second tubular element with a second lumen and a jacket surrounding the first and second tubular elements.
FIG. 7D
shows a cross sectional view through a balloon catheter shaft comprising three lumens.
FIG. 7E
shows a cross sectional view through a balloon catheter shaft comprising a cylindrical element, a tubular element that has a lumen and a jacket surrounding the cylindrical element and the tubular element.
FIG. 7F
shows a cross sectional view of through a balloon catheter shaft comprising an embedded braid.
FIG. 7G
shows a partial perspective view of a catheter shaft comprising a zipper lumen with a guide extending through a portion of the zipper lumen.
FIG. 7H
shows a cross sectional view through
line
7H-7H of
FIG. 7G
.
FIG. 7I
shows is a partial longitudinal sectional view of a catheter shaft comprising a rapid exchange lumen with a guide extending through the rapid exchange lumen.
FIG. 7J
shows a cross sectional view of the catheter shaft of
FIG. 7I
through
line
7J-7J.
FIG. 7K
shows a cross sectional view of the catheter shaft of
FIG. 7I
through
line
7K-7K.
FIG. 7L
is a partial perspective view of a balloon catheter device of the present invention comprising a through-lumen and a balloon inflation lumen within the shaft of the catheter.
FIG. 7M
is a cross sectional view through
line
7M-7M of
FIG. 7L
.
FIG. 7N
is a cross sectional view through
line
7N-7N of
FIG. 7L
.
FIG. 7O
is a partial perspective view of another balloon catheter device of the present invention comprising a through lumen within the shaft of the catheter and a balloon inflation tube disposed next to and optionally attached to the catheter shaft.
FIG. 7P
is a cross sectional view through
line
7P-7P of
FIG. 7O
.
FIG. 7Q
is a cross sectional view through line 7Q-7Q of
FIG. 7O
.
FIG. 8A
shows a partial perspective view of a catheter shaft comprising distance markers.
FIG. 8B
shows a partial perspective view of a catheter shaft comprising one type of radiopaque markers.
FIG. 8C
shows a partial perspective view of a catheter shaft comprising another type of radiopaque markers.
FIG. 8D
shows a partial perspective view of a balloon catheter comprising an array of radiopaque markers arranged on the outer surface of the balloon.
FIG. 8E
shows a partial perspective view of a balloon catheter comprising an array of radiopaque markers arranged on an inner surface of the balloon.
FIG. 8E
′ is a longitudinal sectional view of
FIG. 8E
.
The following detailed description, the accompanying drawings and the above-set-forth Brief Description of the Drawings are intended to describe some, but not necessarily all, examples or embodiments of the invention. The contents of this detailed description do not limit the scope of the invention in any way.
A number of the drawings in this patent application show anatomical structures of the ear, nose and throat. In general, these anatomical structures are labeled with the following reference letters:


	Nasal Cavity	NC
	Nasopharynx	NP
	Frontal Sinus	FS
	Ethmoid Sinus	ES
	Ethmoid Air Cells	EAC
	Sphenoid Sinus	SS
	Sphenoid Sinus Ostium	SSO
	Maxillary Sinus	MS
	Mucocele	MC

FIGS. 1
and IA provide a general showing of a minimally invasive surgery system of the present invention comprising a C-
arm fluoroscope
1000 that is useable to visualize a first introducing device 1002 (e.g., a guide catheter or guide tube), a second introducing device 1004 (e.g., a guidewire or elongate probe) and a working device 1006 (e.g., a balloon catheter, other dilation catheter, debrider, cutter, etc.).
FIGS. 2A-8E
′ show certain non-limiting examples of the introducing devices 1002 (e.g., a guide catheter or guide tube), 1004 (guides, guidewires, elongate probes, etc.) and working devices 1006 (e.g., a balloon catheters, other dilation catheters, debrider, cutters, etc.) that may be useable in accordance with this invention. The
devices
1002, 1004, 1006 may be radiopaque and/or may incorporate radiopaque markers such that C-
arm fluoroscope
1000 may be used to image and monitor the positioning of the
devices
1002, 1004, 1006 during the procedure. In addition to or, as an alternative to the use of radiographic imaging, the
devices
1002, 1004, 1006 may incorporate and/or may be used in conjunction with one or more endoscopic devices, such as the typical rigid or flexible endoscopes or stereo endocscopes used by otolaryngologists during FESS procedures. Also, in addition to or as an alternative to radiographic imaging and/or endoscopic visualizations, some embodiments of the
devices
1002, 1004, 1006 may incorporate sensors which enable the
devices
1002, 1004, 1006 to be used in conjunction with image guided surgery systems or other electro-anatomical mapping/guidance systems including but not limited to: VectorVision (BrainLAB AG); HipNav (CASurgica); CBYON Suite (CBYON); InstaTrak, FluoroTrak, ENTrak (GE Medical); StealthStation Treon, iOn (Medtronic); Medivision; Navitrack (Orthosoft); OTS (Radionics); VISLAN (Siemens); Stryker Navigation System (Stryker Leibinger); Voyager, Z-Box (Z-Kat Inc.) and NOGA and CARTO systems (Johnson & Johnson). Commercially available interventional navigation systems can also be used in conjunction with the devices and methods. Further non-fluoroscopic interventional imaging technologies including but not limited to: OrthoPilot (B. Braun Aesculap); PoleStar (Odin Medical Technologies; marketed by Medtronic); SonoDoppler, SonoWand (MISON); CT Guide, US Guide (UltraGuide) etc. may also be used in conjunction with the devices and methods. Guidance under magnetic resonance is also feasible if the catheter is modified to interact with the system appropriately.
It is to be appreciated that the devices and methods of the present invention relate to the accessing and dilation or modification of sinus ostia or other passageways within the ear nose and throat. These devices and methods may be used alone or may be used in conjunction with other surgical or non-surgical treatments, including but not limited to the delivery or implantation of devices and drugs or other substances as described in copending U.S. patent application Ser. No. 10/912,578 entitled Implantable Devices and Methods for Delivering Drugs and Other Substances to Treat Sinusitis and Other Disorders filed on Aug. 4, 2004, the entire disclosure of which is expressly incorporated herein by reference.
FIGS. 2A through 2D
are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a guide catheter. In
FIG. 2A
, a first introducing device in the form of a
guide catheter
200 is introduced through a nostril and through a nasal cavity NC to a location close to an ostium SSO of a sphenoid sinus SS. The
guide catheter
200 may be flexible. Flexible devices are defined as devices with a flexural stiffness less than about 200 pound-force per inch over a device length of one inch. The
guide catheter
200 may be straight or it may incorporate one or more preformed curves or bends. In embodiments where the
guide catheter
200 is curved or bent, the deflection angle of the curve or bend may be in the range of up to 135°. Examples of specific deflection angles formed by the curved or bent regions of the
guide catheter
200 are 0°, 30°, 45°, 60°, 70°, 90°, 120° and 135°.
Guide catheter
200 can be constructed from suitable elements like Pebax, Polyimide, Braided Polyimide, Polyurethane, Nylon, PVC, Hytrel, HDPE, PEEK, metals like stainless steel and fluoropolymers like PTFE, PFA, FEP and EPTFE.
Guide catheter
200 can have a variety of surface coatings e.g. hydrophilic lubricious coatings, hydrophobic lubricious coatings, abrasion resisting coatings, puncture resisting coatings, electrically or thermal conductive coatings, radiopaque coatings, echogenic coatings, thrombogenicity reducing coatings and coatings that release drugs. In
FIG. 2B
, a second introduction device comprising a
guidewire
202 is introduced through the first introduction device (i.e., the guide catheter 200) so that the
guidewire
202 enters the sphenoid sinus SS through the ostium SSO.
Guidewire
202 may be constructed and coated as is common in the art of cardiology. In
FIG. 2C
, a working
device
204 for example a balloon catheter is introduced over
guidewire
202 into the sphenoid sinus SS. Thereafter, in
FIG. 2D
, the working
device
204 is used to perform a diagnostic or therapeutic procedure. In this particular example, the procedure is dilation of the sphenoid sinus ostium SSO, as is evident from
FIG. 2D
. However, it will be appreciated that the present invention may also be used to dilate or modify any sinus ostium or other man-made or naturally occurring anatomical opening or passageway within the nose, paranasal sinuses, nasopharynx or adjacent areas. After the completion of the procedure, guide
catheter
200, guidewire 202 and working
device
204 are withdrawn and removed. As will be appreciated by those of skill in the art, in this or any of the procedures described in this patent application, the operator may additionally advance other types of catheters or of the present invention, a
guidewire
202 may be steerable (e.g. torquable, actively deformable) or shapeable or malleable.
Guidewire
202 may comprise an embedded endoscope or other navigation or imaging modalities including but not limited to fluoroscopic, X-ray radiographic, ultrasonic, radiofrequency localization, electromagnetic, magnetic, robotic and other radiative energy based modalities. In this regard, some of the figures show optional scopes SC is dotted lines. It is to be appreciated that such optional scopes SC may comprise any suitable types of rigid or flexible endoscopes and such optional scopes SC may be separate from or incorporated into the working devices and/or introduction devices of the present invention.
FIGS. 2E through 2H
are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a steerable catheter. In
FIG. 2E
, an introducing device in the form of a
steerable catheter
206 is introduced through a nostril. Although commercially available devices are neither designed, nor easily usable for this technique in the sinuses, examples of a device which has a steerable tip with functionality similar to that described here include but are not limited to the Naviport™ manufactured by Cardima, Inc. in Fremont, Calif.; Attain Prevail and Attain Deflectable catheters manufactured by Medtronic; Livewire Steerable Catheters manufactured by St. Jude Medical Inc.; Inquiry™ Steerable Diagnostic Catheters manufactured by Boston Scientific; TargetCath™ manufactured by EBI; Safe-Steer Catheter manufactured by Intraluminal Therapeutics, Inc.; Cynosar manufactured by Catheter Research, Inc.; Torque Control Balloon Catheter manufactured by Cordis Corp. and DynamicDeca Steerable Catheter and Dynamic XT Steerable Catheter manufactured by A.M.I. Technologies Ltd, Israel.
Steerable catheter
206 comprises a proximal portion, a distal portion and a controllably deformable region between the proximal portion and the distal portion. In
FIG. 2F
, the
steerable catheter
206 is steered through the nasal anatomy so that the distal portion of
steerable catheter
206 is near an ostium SSO of a sphenoid sinus SS. In
FIG. 2G
, a working device in the form of a
balloon catheter
208 is introduced through
steerable catheter
206 so that it enters sphenoid sinus SS through the ostium SSO. Thereafter,
balloon catheter
208 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO. In
FIG. 2H
,
balloon catheter
208 is used to dilate the ostium SSO. After completion of the procedure,
steerable catheter
206 and
balloon catheter
208 are withdrawn from the nasal anatomy. In this example, only a first introduction device in the form of a
steerable catheter
206 is used to effect insertion and operative positioning of the working device (which in this example is balloon catheter 208). It will be appreciated, however, in some procedures, a second introduction device (e.g., an elongate guide member, guidewire, elongate probe, etc.) could be advanced through the lumen of the
steerable catheter
206 and the working
device
208 could then be advanced over such second introduction device to the desired operative location.
FIGS. 2I through 2L
are partial sagittal sectional views through a human head showing various steps of a method for gaining access to a paranasal sinus using an introducing device in the form of a guidewire with a preset shape. In
FIG. 2I
, an introducing device in the form of a
guidewire
210 with a preset shape is introduced in a nasal cavity.
Guidewire
210 comprises a proximal portion and a distal portion and is shaped such that it can easily navigate through the nasal anatomy. In one embodiment, guidewire 210 is substantially straight. In another embodiment, guidewire 210 comprises an angled, curved or bent region between the proximal portion and the distal portion. Examples of the deflection angle of the angled, curved or bent regions are 0°, 30°, 45°, 60°, 70°, 90°, 120° and 135°. In
FIG. 2J
, guidewire 210 is advanced through the nasal anatomy so that the distal tip of guidewire enters a sphenoid sinus SS through an ostium SSO. In
FIG. 2K
, a working device in the form of a
balloon catheter
212 is advanced along
guidewire
210 into the sphenoid sinus SS. Typically, as described more fully herebelow, the working device will have a guidewire lumen extending through or formed in or on at least a portion of the working
device
212 to facilitate advancement of the working
device
212 over the
guidewire
212 in the manner well understood in the art of interventional medicine. Thereafter, the position of
balloon catheter
212 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO. As described elsewhere in this application, the
balloon catheter
212 may be radiopaque and/or may incorporate one or more visible or imageable markers or sensors. In
FIG. 2L
,
balloon catheter
212 is used to dilate the ostium SSO. After completion of the procedure, guidewire 210 and
balloon catheter
212 are withdrawn from the nasal anatomy. In one embodiment,
balloon catheter
212 is shapeable or malleable.
FIGS. 2M through 2O
are partial sagittal sectional views through a human head showing various steps of a method of gaining access to a paranasal sinus using a balloon catheter comprising a steering wire at its distal end. In
FIG. 2M
, a working device comprising a
balloon catheter
214 comprising a proximal portion and distal portion is introduced in a nasal cavity.
Balloon catheter
214 comprises a
steering wire
216 at its distal end. In
FIG. 2N
,
balloon catheter
214 is advanced through the nasal anatomy into a sphenoid sinus SS through a sphenoid sinus ostium SSO. Thereafter, the position of
balloon catheter
214 is adjusted so that the balloon of the balloon catheter is located in the ostium SSO. In
FIG. 2O
,
balloon catheter
214 is used to dilate the ostium SSO. After completion of the procedure,
balloon catheter
214 is withdrawn from the nasal anatomy. In one embodiment,
steering wire
216 can be retracted into or advanced from
balloon catheter
214. The retraction or advancement of steering wire can be controlled by several means like a thumb wheel, a slide, a button hooked up to electronic motor and a trigger. In another embodiment,
steering wire
216 may be hollow or may incorporate one or more lumen(s) to enable it to introduce or remove devices or diagnostic or therapeutic agents, examples of which are described in copending U.S. patent application Ser. No. 10/912,578 entitled Implantable Devices and Methods for Delivering Drugs and Other Substances to Treat Sinusitis and Other Disorders filed on Aug. 4, 2004, the entire disclosure of which is expressly incorporated herein by reference.
FIGS. 2P through 2X
are partial sagittal sectional views through a human head showing various steps of a method for accessing an ethmoid sinus through a natural or artificially created opening of the ethmoid sinus. In
FIG. 2P
, an introducing device in the form of a
guide catheter
218 is introduced in an ethmoid sinus ES. Ethmoid sinus ES comprises multiple ethmoid air cells EAC. In
FIG. 2Q
, a
guidewire
220 is introduced through guide catheter into a first EAC. Thereafter, in
FIG. 2R
, a
balloon catheter
222 is introduced over
guidewire
220 into the first EAC. In
FIG. 2S
,
balloon catheter
222 is inflated to dilate the structures of ES. In
FIG. 2T
, guide
catheter
218, guidewire 220 and
balloon catheter
222 are withdrawn leaving a first new passage in the ES. The newly created passage in the ES facilitates drainage of the mucous through the ES. Alternatively, in
FIG. 2U
, only
balloon catheter
222 is withdrawn. The position of
guide catheter
218 is adjusted and
guidewire
220 is introduced into a second EAC. In
FIG. 2V
,
balloon catheter
222 is introduced over
guidewire
220 into the second EAC. In
FIG. 2W
,
balloon catheter
222 is inflated to dilate the structures of ES. In
FIG. 2X
, guide
catheter
218, guidewire 220 and
balloon catheter
222 are withdrawn leaving a second new passage in the ES. The second new passage in the ES further facilitates drainage of the mucous through the ES. This method of dilating the structures of ES can be repeated to create multiple new passages in the ES.
FIGS. 2Y through 2AC
are partial coronal sectional views through a human head showing various steps of a method for treating a mucocele in a frontal sinus. In
FIG. 2Y
, an introducing device in the form of a
guide catheter
224 is introduced in a frontal sinus FS through the nasal cavity NC. Frontal sinus FS has a mucocele MC to be treated. In
FIG. 2Z
, a penetrating
device
226 comprising a
sharp tip
228 is introduced through
guide catheter
224 such that penetrating
device
226 punctures the MC at least partially. In
FIG. 2AA
, a
balloon catheter
230 is introduced over penetrating
device
226 into the MC. Thereafter, in
FIG. 2AB
,
balloon catheter
230 is inflated to rupture the MC and allow the drainage of contents of the MC. In
FIG. 2AC
, penetrating
device
226 and
balloon catheter
230 are withdrawn.
The methods disclosed herein may also comprise the step of cleaning or lavaging anatomy within the nose, paranasal sinus, nasopharynx or nearby structures including but not limited to irrigating and suctioning. The step of cleaning the target anatomy can be performed before or after a diagnostic or therapeutic procedure.
The methods of the present invention may also include one or more preparatory steps for preparing the nose, paranasal sinus, nasopharynx or nearby structures for the procedure, such as spraying or lavaging with a vasoconstricting agent (e.g., 0.025-0.5% phenylephyrine or Oxymetazoline hydrochloride (Neosynephrine or Afrin) to cause shrinkage of the nasal tissues, an antibacterial agent (e.g., provodine iodine (Betadine), etc. to cleanse the tissues, etc.
FIGS. 3A through 3C
are partial coronal sectional views through a human head showing various steps of a method of accessing a paranasal sinus through an artificially created opening of the paranasal sinus. In
FIG. 3A
, a
puncturing device
300 is inserted through a nostril and used to create an artificial opening in a maxillary sinus. There are several puncturing devices well known in the art like needles including needles, needles with bent shafts, dissectors, punches, drills, corers, scalpels, burs, scissors, forceps and cutters. In
FIG. 3B
, puncturing
device
300 is withdrawn and a working device for example a
balloon catheter
302 is introduced through the artificial opening into the maxillary sinus. In
FIG. 3C
,
balloon catheter
302 is used to dilate the artificially created opening in the maxillary sinus. After this step, the
balloon catheter
302 is withdrawn. It will be appreciated that, in some embodiments, the
puncturing device
300 may have a lumen through which an introduction device (e.g., a guidewire or other elongate probe or member), may be inserted into the maxillary sinus and the
puncturing device
300 may then be removed leaving such introduction device (e.g., a guidewire or other elongate probe or member) in place. In such cases, the working device (e.g., balloon catheter 302) may incorporate a lumen or other structure that allows the working device (e.g., balloon catheter 300) to be advanced over the previously inserted introduction device (e.g., a guidewire or other elongate probe or member).
In the methods illustrated so far, balloon catheters were used only as an example for the several alternate working devices that could be used with this invention.
FIG. 4A
shows a sectional view of an example of a working device comprising a set of three sequential dilators: a first
sequential dilator
402, a second
sequential dilator
404 and a third
sequential dilator
406. The D3 of third
sequential dilator
406 is greater than the diameter D2 of second
sequential dilator
404 which in turn is greater than the diameter D1 of first
sequential dilator
402. The sequential dilators may comprise one or more bent or angled regions. The sequential dilators can be constructed from a variety of biocompatible materials like stainless steel 316. A variety of other metals, polymers and materials can also be used to construct the sequential dilators.
FIGS. 4B through 4E
show various steps of a method of dilating a nasal cavity using a working device comprising a balloon catheter with a pressure-expandable stent. In
FIG. 4B
, an introducing device e.g. a
guidewire
416 is introduced into a nasal cavity e.g. an ostium of a sinus. In
FIG. 4C
, a
balloon catheter
418 is introduced over
guidewire
416 into the nasal cavity.
Balloon catheter
418 comprises a pressure-
expandable stent
420. The position of
balloon catheter
418 is adjusted so that pressure-
expandable stent
420 is located substantially within the target anatomy where the stent is to be deployed. In
FIG. 4D
, the balloon of
balloon catheter
418 is expanded to deploy pressure-
expandable stent
420. In
FIG. 4E
,
balloon catheter
418 is withdrawn leaving pressure-
expandable stent
420 in the nasal cavity. Several types of stent designs can be used to construct
stent
420 like metallic tube designs, polymeric tube designs, chain-linked designs, spiral designs, rolled sheet designs, single wire designs etc. These designs may have an open celled or closed celled structure. A variety of fabrication methods can be used for fabricating
stent
420 including but not limited to laser cutting a metal or polymer element, welding metal elements etc. A variety of materials can be used for fabricating
stent
420 including but not limited to metals, polymers, foam type materials, plastically deformable materials, super elastic materials etc. Some non-limiting examples of materials that can be used to construct the stent are silicones e.g. silastic, polyurethane, gelfilm and polyethylene. A variety of features can be added to
stent
420 including but not limited to radiopaque coatings, drug elution mechanisms etc.
FIG. 4F
shows a partial perspective view of an embodiment of a working device comprising a side suction and/or cutting
device
422 comprising a
device body
424 having a
side opening
426. Cutting
device
422 is advanced into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned so that
side opening
426 is adjacent to matter (e.g., a polyp, lesion, piece of debris, tissue, blood clot, etc.) that is to be removed. Cutting
device
422 is rotated to cut tissue that has been positioned in the
side opening
426. Cutting
device
422 may incorporate a deflectable tip or a curved distal end which may force side opening 426 against the tissue of interest. Further, this
cutting device
422 may have an optional stabilizing balloon incorporated on one side of cutting
device
422 to press it against the tissue of interest and may also contain one or more on-board imaging modalities such as ultrasound, fiber or digital optics, OCT, RF or electro-magnetic sensors or emitters, etc.
FIG. 4G
shows a partial perspective view of an embodiment of a working device comprising a rotating cutter device to cut away tissue.
Rotating cutter device
428 comprises a rotating
member
430 enclosed in an introducing
device
432. Rotating
member
430 comprises a
rotating blade
434 located near the distal region of rotating
member
430.
Rotating blade
434 may be retractable into rotating
member
430.
Rotating cutter device
428 is inserted in a
passageway
436 such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned so that
rotating blade
434 is adjacent to matter (e.g., a polyp, lesion, piece of debris, tissue, blood clot, etc.) that is to be removed. Thereafter, rotating
member
430 is rotated to cause
rotating blade
434 to remove tissue. In one embodiment, rotating
member
430 can be retracted into introducing
device
432. In another embodiment,
rotating cutter device
428 may comprise a mechanism for suction or irrigation near the distal end of
rotating cutter device
428.
FIGS. 4H and 4I
show various steps of a method of dilating a nasal cavity using a working device comprising a
mechanical dilator
408.
Mechanical dilator
408 comprises an
outer member
410, an
inner member
412 and one or more elongate
bendable members
414.
Inner member
412 can slide within
outer member
410. The proximal ends of
bendable members
414 are attached to distal end of
outer member
410 and the distal ends of
bendable members
414 are attached to distal end of
inner member
412. In
FIG. 4H
,
mechanical dilator
408 is inserted into an opening in the nasal anatomy e.g. an ostium of a sinus.
Mechanical dilator
408 is positioned in the opening such that
bendable members
414 are within the opening in the nasal anatomy. In
FIG. 4I
, relative motion of
outer member
410 and
inner member
412 causes the distal end of
outer member
410 to come closer to the distal end of
inner member
412. This causes
bendable members
414 to bend such that the diameter of the distal region of
mechanical dilator
408 increases. This causes
bendable members
414 to come into contact with the opening in the nasal anatomy and exert an outward pressure to dilate the opening. Various components of
mechanical dilator
408 like
outer member
410,
inner member
412 and
bendable members
414 can be constructed from suitable biocompatible materials like stainless steel 316. A variety of other metals, polymers and materials can also be used to construct the various components of
mechanical dilator
408. In one embodiment,
outer member
410 is substantially rigid and
inner member
412 is flexible.
Outer member
410 can be substantially straight or may comprise one or more bent or angled regions.
Inner member
412 may comprise one or more lumens.
FIGS. 4J and 4K
illustrate a perspective view of a design of a mechanical dilator comprising a screw mechanism.
FIG. 4J
shows the mechanical dilator comprising an
outer member
438 and an
inner screw member
440.
Inner screw member
440 is connected to
outer member
438 through a
first pivot
442 located on the distal end of
outer member
438. The distal end of
inner screw member
440 is connected to a
second pivot
444. The mechanical dilator further comprises one or more
bendable members
446. The distal end of
bendable members
446 is attached to
second pivot
444 and the proximal end of
bendable members
446 is attached to
first pivot
442. In
FIG. 4K
,
inner screw member
440 is rotated in one direction. This causes
second pivot
444 to come closer to
first pivot
442. This causes
bendable members
446 to bend in the radial direction exerting an outward radial force. This force can be used to dilate or displace portions of the anatomy.
Outer member
438 can be substantially straight or may comprise one or more bent or angled regions.
Inner screw member
440 may comprise one or more lumens.
FIGS. 4L and 4M
illustrate sectional views of a design of a mechanical dilator comprising a pushable member.
FIG. 4L
shows the mechanical dilator comprising an
outer member
448 comprising one or more
bendable regions
449 on the distal end of
outer member
448. Mechanical dilator further comprises an inner
pushable member
450 comprising an
enlarged region
452 on the distal end of inner
pushable member
450. In
FIG. 4M
, inner
pushable member
450 is pushed in the distal direction. This exerts an outward force on
bendable regions
449 causing
bendable regions
449 to bend in a radial direction exerting an outward force. This force can be used to dilate or displace portions of the anatomy.
Outer member
448 can be substantially straight or may comprise one or more bent or angled regions. Inner
pushable member
450 may comprise one or more lumens.
FIGS. 4N and 4O
illustrate sectional views of a design of a mechanical dilator comprising a pullable member.
FIG. 4N
shows the mechanical dilator comprising an
outer member
454 comprising one or more
bendable regions
456 on the distal end of
outer member
454. Mechanical dilator further comprises an inner
pullable member
458 comprising an
enlarged region
460 on the distal end of inner
pullable member
458. In
FIG. 4O
, inner
pullable member
458 is pulled in the proximal direction. This exerts an outward force on
bendable regions
456 causing
bendable regions
456 to bend in a radial direction exerting an outward force. This force can be used to dilate or displace portions of the anatomy.
Outer member
454 can be substantially straight or may comprise one or more bent or angled regions. Inner
pullable member
458 may comprise one or more lumens.
FIGS. 4P and 4Q
illustrate sectional views of a design of a mechanical dilator comprising a hinged member.
FIG. 4P
shows the mechanical dilator comprising an
outer member
462 comprising one or more
bendable regions
464 located on the distal end of
outer member
462. The mechanical dilator also comprises an
inner member
466 located within
outer member
462. In one embodiment,
inner member
466 is tubular. The distal end of
inner member
466 comprises one or more first hinges 468. First hinges 468 are hinged to the proximal ends of one or more moving
elements
470. Distal ends of moving
elements
470 are hinged to one or more
second hinges
472 located on the inner surface of
outer member
462. In
FIG. 4Q
,
inner member
466 is pushed in the distal direction. This causes moving
elements
470 to exert an outward radial force on
bendable regions
464 causing
bendable regions
464 to bend in an outward radial direction with an outward force. This outward force can be used to dilate or displace portions of the anatomy.
Outer member
462 can be substantially straight or may comprise one or more bent or angled regions.
Inner member
466 may comprise one or more lumens.
FIGS. 4R through 4W
illustrate examples of configurations of mechanical dilators in
FIGS. 4H through 4Q
.
FIG. 4R
shows a sectional view of a mechanical dilator comprising an
inner member
474, an outer
stationary member
476 and an outer
bendable member
478. In
FIG. 4S
, movement of
inner member
474 displaces outer
bendable member
478 in the radial direction with a force. This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force in a particular radial direction.
FIG. 4S
′ shows a partial perspective view of the outer
stationary member
476 of
FIG. 4R
.
FIG. 4T
shows a sectional view of a mechanical dilator comprising an
inner member
480, a first outer hemi-
tubular member
482 and a second outer hemi-
tubular member
484. In
FIG. 4U
, movement of
inner member
480 displaces first outer hemi-
tubular member
482 and second outer hemi-
tubular member
484 in the radial direction with a force. This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force in two diametrically opposite regions.
FIG. 4U
′ shows a partial perspective view of the first outer hemi-
tubular member
482 and the second outer hemi-
tubular member
484 of
FIG. 4T
.
FIG. 4V
shows a sectional view of a mechanical dilator comprising an inner member 486, a first outer curved member 488 and a second outer curved member 490. In
FIG. 4W
, movement of inner member 486 displaces first outer curved member 488 and second outer curved member 490 in the radial direction with a force. This force can be used to dilate or displace portions of the anatomy. This configuration is useful to exert force over smaller areas in two diametrically opposite regions.
FIG. 4W
′ shows a partial perspective view of the first outer curved member 488 and the second outer curved member 490 of
FIG. 4V
. Similar designs for mechanical dilators in
FIGS. 4H through 4Q
are possible using three or more displaceable members. The inner member in the mechanical dilators disclosed herein may be replaced by a balloon for displacing the outer members to exert an outward radial force.
Several other designs of the working device may also be used including but not limited to cutters, chompers, rotating drills, rotating blades, tapered dilators, punches, dissectors, burs, non-inflating mechanically expandable members, high frequency mechanical vibrators, radiofrequency ablation devices, microwave ablation devices, laser devices (e.g. CO₂, Argon, potassium titanyl phosphate, Holmium:YAG and Nd:YAG laser devices), snares, biopsy tools, scopes and devices that introduce diagnostic or therapeutic agents.
FIG. 5A
shows a perspective view of an embodiment of a balloon comprising a conical proximal portion, a conical distal portion and a cylindrical portion between the conical proximal portion and the conical distal portion.
FIGS. 5B to 5N
show perspective views of several alternate embodiments of the balloon.
FIG. 5B
shows a conical balloon,
FIG. 5C
shows a spherical balloon,
FIG. 5D
shows a conical/square long balloon,
FIG. 5E
shows a long spherical balloon,
FIG. 5F
shows a dog bone balloon,
FIG. 5G
shows a offset balloon,
FIG. 5H
shows a square balloon,
FIG. 5I
shows a conical/square balloon,
FIG. 5J
shows a conical/spherical long balloon,
FIG. 5K
shows a tapered balloon,
FIG. 5L
shows a stepped balloon,
FIG. 5M
shows a conical/offset balloon and
FIG. 5N
shows a curved balloon.
The balloons disclosed herein can be fabricated from biocompatible materials including but not limited to polyethylene terephthalate, Nylon, polyurethane, polyvinyl chloride, crosslinked polyethylene, polyolefins, HPTFE, HPE, HDPE, LDPE, EPTFE, block copolymers, latex and silicone. The balloons disclosed herein can be fabricated by a variety of fabrication methods including but not limited to molding, blow molding, dipping, extruding etc.
The balloons disclosed herein can be inflated with a variety of inflation media including but not limited to saline, water, air, radiographic contrast materials, diagnostic or therapeutic substances, ultrasound echogenic materials and fluids that conduct heat, cold or electricity.
The balloons in this invention can also be modified to deliver diagnostic or therapeutic substances to the target anatomy. For example,
FIG. 5O
shows a partial perspective view of an embodiment of a
balloon catheter device
500 comprising a balloon for delivering diagnostic or therapeutic substances.
Balloon catheter device
500 comprises a
flexible catheter
502 having a
balloon
504 thereon. The
catheter device
500 is advanced, with
balloon
504 deflated, into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned with the deflated
balloon
504 situated within an ostium, passageway or adjacent to tissue or matter that is to be dilated, expanded or compressed (e.g., to apply pressure for hemostasis, etc.). Thereafter, the
balloon
504 may be inflated to dilate, expand or compress the ostium, passageway, tissue or matter. Thereafter the
balloon
504 may be deflated and the
device
500 may be removed. This
balloon
504 may also be coated, impregnated or otherwise provided with a medicament or substance that will elute from the balloon into the adjacent tissue (e.g., bathing the adjacent tissue with drug or radiating the tissue with thermal or other energy to shrink the tissues in contact with the balloon 504). Alternatively, in some embodiments, the balloon may have a plurality of apertures or openings through which a substance may be delivered, sometimes under pressure, to cause the substance to bathe or diffuse into the tissues adjacent to the balloon. Alternatively, in some embodiments, radioactive seeds, threads, ribbons, gas or liquid, etc. may be advanced into the
catheter shaft
502 or
balloon
504 or a completely separate catheter body for some period of time to expose the adjacent tissue and to achieve a desired diagnostic or therapeutic effect (e.g. tissue shrinkage, etc.).
The balloons in this invention can have a variety of surface features to enhance the diagnostic or therapeutic effects of a procedure. For example,
FIG. 5P
shows a partial perspective view of an embodiment of a balloon/
cutter catheter device
506 comprising a
flexible catheter
508 having a
balloon
510 with one or
more cutter blades
512 formed thereon. The
device
506 is advanced, with
balloon
510 deflated, into a passageway such as a nostril, nasal cavity, meatus, ostium, interior of a sinus, etc. and positioned with the deflated
balloon
510 situated within an ostium, passageway or adjacent to tissue or matter that is to be dilated, expanded or compressed and in which it is desired to make one or more cuts or scores (e.g. to control the fracturing of tissue during expansion and minimize tissue trauma etc.). Thereafter, the
balloon
510 is inflated to dilate, expand or compress the ostium, passageway, tissue or matter and causing the cutter blade(s) 512 to make cut(s) in the adjacent tissue or matter. Thereafter the
balloon
510 is deflated and the
device
506 is removed. The blade may be energized with mono or bi-polar RF energy or otherwise heated such that it will cut the tissues while also causing hemostasis and/or to cause thermal contraction of collagen fibers or other connective tissue proteins, remodeling or softening of cartilage, etc.
The balloons in this invention can have a variety of reinforcing means to enhance the balloon properties. For example,
FIGS. 5Q and 6F
show perspective views of an embodiment of a
balloon catheter device
514 comprising a
flexible catheter
516 having a
balloon
518 with one or more reinforcing means 520 thereon. In this example, reinforcing means 520 is a braid attached on the external surface of
balloon
518. The reinforcing braid can be constructed from suitable materials like polymer filaments (e.g. PET or Kevlar filaments), metallic filaments (e.g. SS316 or Nitinol filaments) and metallic or non-metallic meshes or sheets. A variety of other reinforcing means can be used including but not limited to reinforcing coatings, external or internal reinforcing coils, reinforcing fabric, reinforcing meshes and reinforcing wires, reinforcing rings, filaments embedded in balloon materials etc.
FIG. 6F
′ shows a perspective view of a reinforcing braid that can be used with the balloon catheter device in
FIGS. 5Q and 6F
.
The balloons in this invention can have a variety of inflation means to enhance the balloon properties.
FIG. 5R
shows a partial sectional view of an embodiment of a
balloon catheter
522 comprising a
shaft
524 and a
balloon
526.
Shaft
524 comprises a balloon inflation lumen. The distal portion of balloon inflation lumen terminates in
inflation ports
528 located near the distal end of
balloon
526. Thus, when
balloon catheter
522 is inserted in an orifice and
balloon
526 is inflated, the distal portion of
balloon
526 inflates earlier than the proximal portion of
balloon
526. This prevents
balloon
526 from slipping back out of the orifice.
FIGS. 5S through 5T
illustrate designs of balloon catheters comprising multiple balloons.
FIG. 5S
shows a partial sectional view of an embodiment of a
balloon catheter
530 comprising a
shaft
532 with a
lumen
533.
Lumen
533 opens into three orifices located on
shaft
532 namely a
first orifice
534, a
second orifice
536 and a
third orifice
538. The three orifices are used to inflate three balloons.
First orifice
534 inflates a
first balloon
540,
second orifice
536 inflates a
second balloon
542 and
third orifice
538 inflates
third balloon
544. In one embodiment,
first balloon
540 and
third balloon
544 are inflated with a single lumen and
second balloon
542 is inflated with a different lumen. In another embodiment,
first balloon
540,
second balloon
542 and
third balloon
544 interconnected and are inflated with a single lumen. A valve mechanism allows first balloon and second balloon to inflate before allowing second balloon to inflate.
Alternatively, the balloons can be inflated by separate lumens.
FIG. 5T
shows a partial sectional view of an embodiment of a
balloon catheter
546 comprising a
shaft
548 comprising a first inflation lumen 550, a
second inflation lumen
552 and a
third inflation lumen
554. The three inflation lumens are used to inflate three non-connected balloons. First inflation lumen 550 inflates a
first balloon
556,
second inflation lumen
552 inflates a
second balloon
558 and
third inflation lumen
554 inflates a
third balloon
560.
The devices disclosed herein may comprise one or more navigation or visualization modalities.
FIGS. 5U through 5AB
illustrate perspective and sectional views of various embodiments of a balloon catheter comprising sensors.
FIG. 5U
shows a partial perspective view of a balloon catheter comprising an
outer member
562, an
inner member
564 and a
balloon
566 attached to distal region of
outer member
562 and distal region of
inner member
564. The balloon catheter further comprises a
first sensor
568 located on the distal region of
outer member
562 and a
second sensor
570 located on the distal region of
inner member
564.
FIG. 5V
shows a crossection through
plane
5V-5V in
FIG. 5U
.
Outer member
562 comprises a
first sensor lumen
572 to receive the lead from
first sensor
568.
Inner member
564 comprises a
second sensor lumen
574 to receive the lead from
second sensor
570.
Inner member
564 further comprises a
circular lumen
576.
Outer member
562 and
inner member
564 enclose an
annular lumen
578. In one embodiment,
annular lumen
578 is a balloon inflation lumen.
FIG. 5W
shows a partial perspective view of a balloon catheter comprising an
outer member
580, an
inner member
582 and a
balloon
584 attached to distal region of
outer member
580 and distal region of
inner member
582. The balloon catheter further comprises a
first sensor
586 located on the distal region of
inner member
582 and a
second sensor
588 located on the distal region of
inner member
582 distal to
first sensor
586.
FIG. 5X
shows a cross section through
plane
5X-5X in
FIG. 5W
.
Inner member
582 comprises a
first sensor lumen
590 to receive the lead from
first sensor
586 and a
second sensor lumen
592 to receive the lead from
second sensor
588.
Inner member
582 further comprises a
circular lumen
594.
Outer member
580 and
inner member
582 enclose an
annular lumen
596. In one embodiment,
annular lumen
596 is a balloon inflation lumen.
FIG. 5Y
shows a partial perspective view of a balloon catheter comprising an
outer member
598, an
inner member
600 and a
balloon
602 attached to distal region of
outer member
598 and distal region of
inner member
600. The balloon catheter further comprises a
first sensor
604 located on the distal region of
outer member
598 and a
second sensor
606 located on the distal region of
outer member
598 distal to
first sensor
604.
FIG. 5Z
shows a cross section through
plane
5Z-5Z in
FIG. 5Y
.
Outer member
598 comprises a
first sensor lumen
608 to receive the lead from
first sensor
604 and a
second sensor lumen
610 to receive the lead from
second sensor
606.
Inner member
600 comprises a
circular lumen
612.
Outer member
598 and
inner member
600 enclose an
annular lumen
614. In one embodiment,
annular lumen
614 is a balloon inflation lumen.
The leads from the sensors may be attached on the surface of an element of the balloon catheter without being enclosed in a lumen.
FIG. 5AA
shows a partial perspective view of a balloon catheter comprising an
outer member
616, an
inner member
618 and a
balloon
620 attached to distal region of
outer member
616 and distal region of
inner member
618. The balloon catheter further comprises a
first sensor
624 located on the distal region of
outer member
616 and a
second sensor
626 located on the distal region of
inner member
618.
Second sensor
626 comprises a
lead
628.
FIG. 5AB
shows a cross section through plane 5AB-5AB in
FIG. 5AA
.
Outer member
616 comprises a
first sensor lumen
630 to receive the lead from
first sensor
624.
Inner member
618 comprises a
circular lumen
632. Lead 628 from
second sensor
626 is attached on the outer surface of
inner member
618 and is oriented parallel to
inner member
618.
Outer member
616 and
inner member
618 enclose an
annular lumen
634. In one embodiment,
annular lumen
634 is a balloon inflation lumen. The sensors mentioned in
FIGS. 5U through 5AB
can be electromagnetic sensors or sensors including but not limited to location sensors, magnetic sensors, electromagnetic coils, RF transmitters, mini-transponders, ultrasound sensitive or emitting crystals, wire-matrices, micro-silicon chips, fiber-optic sensors, etc.
FIGS. 6A through 6G
illustrate partial perspective views of several embodiments of shaft designs for the various devices disclosed herein. These shaft designs are especially useful for devices that encounter high torque or high burst pressures or require enhanced pushability, steerability and kink resistance.
FIG. 6A
shows a partial perspective view of an embodiment of a
shaft
602 comprising a
spiral element
604 wound around the shaft.
Spiral element
604 can be made of suitable materials like metals (e.g. SS316L, SS304) and polymers. In one embodiment,
spiral element
604 is in the form of round wire of diameter between 0.04 mm to 0.25 mm. In another embodiment, spiral element is in the form of flat wire of cross section dimensions ranging from 0.03 mm×0.08 mm to 0.08 mm×0.25 mm.
FIG. 6B
shows a partial perspective view of an embodiment of a
shaft
606 comprising a reinforcing
filament
608. Reinforcing
filament
608 is substantially parallel to the axis of
shaft
606.
Shaft
606 with reinforcing
filament
608 can be covered with a jacketing layer. Reinforcing
filament
608 can be made of suitable materials like metals, polymers, glass fiber etc. Reinforcing
filament
608 can also have shape memory characteristics. In one embodiment, reinforcing
filament
608 is embedded in
shaft
606. In another embodiment, reinforcing filament is introduced through a lumen in
shaft
606.
Shaft
606 may comprise more than one reinforcing
filament
608.
FIG. 6C
shows a partial perspective view of an embodiment of a
shaft
610 comprising one of more stiffening rings 612 along the length of
shaft
610.
FIG. 6D
shows a partial perspective view of an embodiment of a
shaft
614 comprising a series of controllably stiffening
elements
616 along the length of the shaft.
Shaft
614 further comprises a
tension wire
618 that runs through controllably stiffening
elements
616 and is attached to the most distal stiffening element. The tension in
tension wire
618 causes controllably stiffening
elements
616 to come into contact with each other with a force. Friction between controllably stiffening
elements
616 causes
shaft
614 to have a certain stiffness. Increasing the tension in
tension wire
618 increases the force with which controllably stiffening
elements
616 come into contact with each other. This increases the friction between controllably stiffening
elements
616 which in turn increases the stiffness of
shaft
614. Similarly, reducing the tension in
tension wire
618 reduces the stiffness of
shaft
614.
Controllably stiffening elements
616 can be made from suitable materials like metal, polymers and composites. In one embodiment, controllably stiffening
elements
616 are separated from each other by one or more springs.
Tension wire
618 can be made from metals like SS316.
Tension wire
618 may also be used to cause the device to actively bend or shorten in response to tension.
FIG. 6E
shows a partial perspective view of an embodiment of a
shaft
620 comprising a
hypotube
622. In one embodiment, hypotube 622 is located on the exterior surface of
shaft
620. In another embodiment, hypotube 622 is embedded in
shaft
620.
Hypotube
620 can be made of metals like stainless steel 316 or suitable polymers.
FIGS. 6F and 6F
′ show a partial perspective view of an embodiment of a
shaft
624 comprising a reinforcing
element
626 in the form of a reinforcing braid or mesh located on the outer surface of
shaft
624. Reinforcing
element
626 can be made of suitable materials like polymer filaments (e.g. PET or Kevlar filaments), metallic wires e.g. SS316 wires etc. The braid pattern can be regular braid pattern, diamond braid pattern, diamond braid pattern with a half load etc. In one embodiment, the outer surface of reinforcing
element
626 is covered with a jacketing layer.
The shafts of various devices disclosed herein may be non homogenous along their length. Examples of such shafts are illustrated in
FIGS. 6G through 6H
.
FIG. 6G
shows a partial perspective view of an embodiment of a device comprising a
shaft
628 comprising a
proximal portion
630, a
distal portion
632, a working
element
634 and a plastically
deformable region
636 located between the
proximal portion
630 and
distal portion
632. Plastically
deformable region
636 can be deformed by a physician to adjust the angle between
proximal portion
630 and
distal portion
632. This enables the devices to be used for several different anatomical regions of the same patient. Also, such devices can be adjusted for optimal navigation through a patient's anatomy. In one embodiment,
shaft
628 comprises multiple plastically deformable regions. In another embodiment plastically
deformable region
636 is located within working
element
634. Such a design comprising one or more plastically deformable regions can be used for any of the devices mentioned herein like catheters with working elements, guide catheters, guide catheters with a pre-set shape, steerable guide catheters, steerable catheters, guidewires, guidewires with a pre-set shape, steerable guidewires, ports, introducers, sheaths etc.
FIG. 6H
shows a partial perspective view of an embodiment of a device comprising a shaft with a flexible element. The design is illustrated as a
shaft
638 comprising a
proximal portion
640, a
distal portion
642 and a working element 644 (e.g. a balloon).
Shaft
638 further comprises a
flexible element
646 located between
proximal portion
640 and
distal portion
642. This design enables
proximal portion
640 to bend with respect to
distal portion
642 making it easier to navigate through the complex anatomy and deliver working
element
644 to the desired location. In one embodiment,
shaft
638 comprises multiple flexible elements. In another embodiment,
flexible element
646 is located within working
element
644. Such a design comprising one or more flexible elements can be used for any of the devices mentioned herein like catheters with working elements, guide catheters, guide catheters with a pre-set shape, steerable guide catheters, steerable catheters, guidewires, guidewires with a pre-set shape, steerable guidewires, ports, introducers, sheaths etc.
FIGS. 6I through 6K
illustrate an example of a shaft comprising a malleable element.
FIG. 6I
shows a partial perspective view of an embodiment of a
shaft
648 comprising
malleable element
650 and a
lumen
652 wherein
shaft
648 is in a substantially straight configuration.
Malleable element
650 is embedded in
shaft
648 such that the axis of
malleable element
650 is substantially parallel to the axis of
shaft
648.
FIG. 6J
shows a partial perspective view of the embodiment of
FIG. 6I
in a bent configuration.
FIG. 6K
shows a cross sectional view through
plane
6K-6K of
FIG. 6I showing shaft
648 comprising
malleable element
650 and a
lumen
652. In one embodiment,
shaft
648 comprises more than one malleable element.
FIGS. 6L through 6M
show an embodiment of a controllably deformable shaft.
FIG. 6L
shows a partial sectional view of an embodiment of a controllably
deformable shaft
654 comprising a
pull wire
656 attached to a
pull wire terminator
658 located near the distal end of
shaft
654.
FIG. 6M
shows a partial sectional view of the controllably
deformable shaft
654 of
FIG. 6L
in a bent orientation when
pull wire
656 is pulled in the proximal direction. The deformation can be varied by varying the location of
pull wire terminator
658 and the stiffness of various sections of
shaft
658. The stiffness of a section of
shaft
658 can be varied by adding reinforcing coatings, external or internal reinforcing coils, reinforcing fabric, reinforcing meshes and reinforcing wires, hinged elements, embedded filaments, reinforcing rings etc.
FIG. 6N
shows a perspective view of a balloon catheter comprising a rigid or semi-rigid member. The balloon catheter comprises a rigid or
semi-rigid member
660 and a
balloon
662 located on the distal region of rigid or
semi-rigid member
660. Rigid or
semi-rigid member
660 may comprise one or more lumens. Rigid or
semi-rigid member
660 may comprise one or more bent, curved or angled regions.
Balloon
662 is inflated by a balloon inflation tube 664 comprising a
hub
666 at the proximal end of balloon inflation tube 664. In one embodiment, balloon inflation tube 664 is fully attached along its length to rigid or
semi-rigid member
660. In another embodiment, balloon inflation tube 664 is partially attached along its length to rigid or
semi-rigid member
660.
FIGS. 6O through 6Q
illustrate sectional views of a balloon catheter comprising an insertable and removable element.
FIG. 6O
shows a
balloon catheter
668 comprising a
balloon
670, a
first lumen
672 and a
balloon inflation lumen
674 opening into
balloon
670 through an
inflation port
676.
FIG. 6P
shows an
insertable element
678 having a
proximal end
680 and a
distal end
682. In one embodiment,
distal end
682 ends in a sharp tip for penetrating tissue. In one embodiment,
insertable element
678 comprises one or more bent, angled or
curved regions
684.
Insertable element
678 can be fabricated from a variety of materials to obtain properties including but not limited to rigidity, shape memory, elasticity, ability to be plastically deformed etc. In
FIG. 6Q
,
insertable element
678 is inserted into
balloon catheter
668 through
first lumen
672. This combination can be used to perform a diagnostic or therapeutic procedure.
Insertable element
678 may be removed during or after the procedure.
FIGS. 7A through 7K
show cross sectional views of several embodiments of lumen orientation in the devices disclosed herein.
FIG. 7A
shows a cross sectional view of an embodiment of a
shaft
702 comprising a
first lumen
704 and a
second lumen
706. In one embodiment,
first lumen
704 is a guidewire lumen and
second lumen
706 is an inflation lumen.
FIG. 7B
shows a cross sectional view of an embodiment of a
shaft
708 comprising a
first lumen
710 and a annular
second lumen
712 such that second
annular lumen
712 is substantially coaxial with
first lumen
710. In one embodiment,
first lumen
710 is a guidewire lumen and annular
second lumen
712 is an inflation lumen.
FIG. 7C
shows a cross sectional view of an embodiment of a
shaft
714 comprising a first
tubular element
716 comprising a
first lumen
718, a second
tubular element
720 comprising a
second lumen
722 and a
jacket
724 surrounding first
tubular element
716 and second
tubular element
720. In one embodiment,
first lumen
718 is a guidewire lumen and
second lumen
722 is an inflation lumen.
FIG. 7D
shows a cross sectional view of an embodiment of a
shaft
726 comprising a
first lumen
728, a
second lumen
730 and a
third lumen
732. In one embodiment,
first lumen
728 is a guidewire lumen,
second lumen
730 is an irrigation/aspiration lumen and
third lumen
732 is an inflation lumen.
FIG. 7E
shows a cross sectional view of an embodiment of a
shaft
734 comprising a
cylindrical element
736, a
tubular element
738 comprising a
lumen
740 and a
jacket
742 surrounding
cylindrical element
736 and
tubular element
738.
FIG. 7F
shows a cross sectional view of an embodiment of a shaft 744 comprising a tubular member 746 comprising a first lumen 748 and a
second lumen
750; a first coating 752 located on the outer surface of tubular member 746; a
braid
754 located on the outer surface of first coating 752 and a
second coating
756 surrounding
braid
754. First lumen 748 is lined with a
suitable coating
758 like hydrophilic lubricious coating, hydrophobic lubricious coating, abrasion resisting coating etc. In one embodiment, first lumen 748 is a guidewire lumen and
second lumen
750 is an inflation lumen. The lumens disclosed herein can be lined with suitable coatings like hydrophilic lubricious coatings, hydrophobic lubricious coatings, abrasion resisting coatings, radiopaque coatings, echogenic coatings etc.
FIG. 7G
shows a partial perspective view of an embodiment of a
shaft
754* comprising a
first lumen
756* and a
zipper lumen
758*.
Zipper lumen
758* allows a device like a
guidewire
760* to be easily introduced into or removed from
shaft
754*.
FIG. 7H
shows a cross sectional view through
plane
7H-7H in
FIG. 7G
showing the orientations of
first lumen
756* and
zipper lumen
758*.
FIG. 7I
shows a cross sectional view of an embodiment of a
shaft
762 comprising a
first lumen
764 and a
rapid exchange lumen
766.
Rapid exchange lumen
766 extends from the distal end of
shaft
762 to a proximal region.
Rapid exchange lumen
766 enables
shaft
762 to be easily and quickly introduced or removed over an exchange device like a
guidewire
768.
FIG. 7J
shows a cross sectional view through
plane
7J-7J in
FIG. 7I
showing
first lumen
764 and
rapid exchange lumen
766.
FIG. 7K
shows a cross sectional view through
plane
7K-7K in
FIG. 7I
showing
first lumen
764.
FIGS. 7L through 7Q
shows perspective and sectional views of lumens for the devices disclosed herein that are not present throughout the length of the devices.
FIG. 7L
shows a perspective view of a balloon catheter comprising a
shaft
770, a
balloon
772 and a
lumen
774 that is present throughout
shaft
770. The balloon catheter further comprises a
balloon inflation lumen
776 that opens into
balloon
772. The distal end of
balloon inflation lumen
776 is plugged with a
plug
778.
FIG. 7M
shows a crossection through
plane
7M-7M in
FIG. 7L showing shaft
770 comprising
lumen
774 and
balloon inflation lumen
776.
FIG. 7N
shows a crossection through
plane
7N-7N in
FIG. 7L showing shaft
770 comprising
lumen
774 and plug 778.
FIG. 7O
shows a perspective view of a balloon catheter comprising a
shaft
780, a
balloon
782 and a
lumen
786 that is present throughout
shaft
780. The balloon catheter further comprises a
balloon inflation lumen
784. The distal end of
balloon inflation lumen
784 opens into
balloon
782.
FIG. 7P
shows a crossection through
plane
7P-7P in
FIG. 7O showing shaft
780 comprising
lumen
786 and
balloon inflation lumen
784.
FIG. 7Q
shows a crossection through plane 7Q-7Q in
FIG. 7O showing shaft
780 comprising
lumen
786.
FIGS. 8A through 8E
show partial perspective views of several embodiments of markers that may be present on the elements of the devices mentioned herein.
FIG. 8A
shows a partial perspective view of an embodiment of a
shaft
800 comprising a plurality of
distance markers
802 located along the length of
shaft
800.
FIG. 8B
shows a partial perspective view of an embodiment of a
shaft
804 comprising a plurality of
radiographic markers
806 located along the length of
shaft
804.
FIG. 8C
shows a partial perspective view of an embodiment of a
shaft
808 comprising a plurality of ring shaped
radiographic markers
810 located along the length of
shaft
808.
FIG. 8D
shows a partial perspective view of an embodiment of a
balloon catheter
812 comprising a
shaft
814 and a
balloon
816.
Balloon
816 comprises a plurality of
radiographic markers
818 located on the outer surface of the
balloon
816.
Such markers
818 may be in a linear arrangement, non-linear arrangement or any other configuration that performs the desired marking function (e.g., delineating the length and/or diameter of the balloon, marking the proximal and/or distal ends of the balloon, etc.).
FIGS. 8E and 8E
′ show partial perspective and longitudinal sectional views of an embodiment of a
balloon catheter
820 comprising a
shaft
822 and a
balloon
824.
Balloon
824 comprises a plurality of
radiographic markers
826 located on the inner surface of the
balloon
824.
Such markers
826 may be in a linear arrangement, non-linear arrangement or any other configuration that performs the desired marking function (e.g., delineating the length and/or diameter of the balloon, marking the proximal and/or distal ends of the balloon, etc.). The devices disclosed herein may also comprise several other types of markers like ultrasound markers, radiofrequency markers and magnetic markers. Similarly, the devices disclosed herein may also comprise one or more sensors like electromagnetic sensors, electrical sensors, magnetic sensors, light sensors and ultrasound sensors.
The term “diagnostic or therapeutic substance” as used herein is to be broadly construed to include any feasible drugs, prodrugs, proteins, gene therapy preparations, cells, diagnostic agents, contrast or imaging agents, biologicals, etc. Such substances may be in bound or free form, liquid or solid, colloid or other suspension, solution or may be in the form of a gas or other fluid or nan-fluid. For example, in some applications where it is desired to treat or prevent a microbial infection, the substance delivered may comprise pharmaceutically acceptable salt or dosage form of an antimicrobial agent (e.g., antibiotic, antiviral, antiparasitic, antifungal, etc.), a corticosteroid or other anti-inflammatory (e.g., an NSAID), a decongestant (e.g., vasoconstrictor), a mucous thinning agent (e.g., an expectorant or mucolytic), an agent that prevents of modifies an allergic response (e.g., an antihistamine, cytokine inhibitor, leucotriene inhibitor, IgE inhibitor, immunomodulator), etc. Other non-limiting examples of diagnostic or therapeutic substances that may be useable in this invention are described in copending U.S. patent application Ser. No. 10/912,578 entitled Implantable Devices and Methods for Delivering Drugs and Other Substances to Treat Sinusitis and Other Disorders filed on Aug. 4, 2004, the entire disclosure of which is expressly incorporated herein by reference.
The term “nasal cavity” used herein to be broadly construed to include any cavity that is present in the anatomical structures of the nasal region including the nostrils and paranasal sinuses.
The term “trans-nasal” means through a nostril.
Although the methods and devices disclosed herein are illustrated in conjunction with particular paranasal sinuses, it is understood that these methods and devices can be used in other paranasal sinuses as well as other anatomical passageways of the ear, nose or throat.
Optionally, any of the working devices and guide catheters described herein may be configured or equipped to receive or be advanced over a guidewire or other guide member (e.g., an elongate probe, strand of suure material, other elongate member) unless to do so would render the device inoperable for its intended purpose. Some of the specific examples described herein include guidewires, but it is to be appreciated that the use of guidewires and the incorporation of guidewire lumens is not limited to only the specific examples in which guidewires or guidewire lumens are shown. The guidewires used in this invention may be constructed and coated as is common in the art of cardiology. This may include the use of coils, tapered or non-tapered core wires, radioopaque tips and/or entire lengths, shaping ribbons, variations of stiffness. PTFE, silicone, hydrophilic coatings, polymer coatings, etc. For the scope of this invention, these wires may possess dimensions of length between 5 and 75 cm and outer diameter between 0.005″ and 0.050″.
Several modalities can be used with the devices and methods disclosed herein for navigation and imaging of the devices within the anatomy. For example, the devices disclosed herein may comprise an endoscope for visualization of the target anatomy. The devices may also comprise ultrasound imaging modalities to image the anatomical passageways and other anatomical structures. The devices disclosed herein may comprise one or more magnetic elements especially on the distal end of the devices. Such magnetic elements may be used to navigate through the anatomy by using external magnetic fields. Such navigation may be controlled digitally using a computer interface. The devices disclosed herein may also comprise one or more markers (e.g. infra-red markers). The markers can be used to track the precise position and orientation of the devices using image guidance techniques. Several other imaging or navigating modalities including but not limited to fluoroscopic, radiofrequency localization, electromagnetic, magnetic and other radiative energy based modalities may also be used with the methods and devices disclosed herein. These imaging and navigation technologies may also be referenced by computer directly or indirectly to pre-existing or simultaneously created 3-D or 2-D data sets which help the doctor place the devices within the appropriate region of the anatomy.
The distal tip of devices mentioned herein may comprise a flexible tip or a soft, atraumatic tip. Also, the shaft of such devices may be designed for enhanced torquability.
The embodiments herein have been described primarily in conjunction with minimally invasive procedures, but they can also be used advantageously with existing open surgery or laparoscopic surgery techniques.
It is to be appreciated that the invention has been described hereabove with reference to certain examples or embodiments of the invention but that various additions, deletions, alterations and modifications may be made to those examples and embodiments without departing from the intended spirit and scope of the invention. For example, any element or attribute of one embodiment or example may be incorporated into or used with another embodiment or example, unless to do so would render the embodiment or example unsuitable for its intended use. All reasonable additions, deletions, modifications and alterations are to be considered equivalents of the described examples and embodiments and are to be included within the scope of the following claims.

Claims (21)

11. A method, comprising:

(a) inserting a catheter into a nasal cavity of a patient, the catheter including a balloon and a stent positioned over the balloon;

(b) positioning the balloon and the stent in a targeted anatomical passageway in the nasal cavity

(c) expanding the balloon within the targeted anatomical passageway while the stent is positioned over the balloon, the stent engaging adjacent tissue in the targeted anatomical passageway; and

(d) removing the catheter from the nasal cavity, the stent remaining engaged with the adjacent tissue in the targeted anatomical passageway after the catheter is removed from the nasal cavity.

12. The method of

claim 11

, the balloon being in a non-expanded state during the act of inserting the catheter into the nasal cavity.

13. The method of

claim 11

, the targeted anatomical passageway comprising an ostium of a sinus.

14. The method of

claim 11

, the act of expanding the balloon resulting in dilation of the targeted anatomical passageway.

15. The method of

claim 11

, the stent including a therapeutic substance, such that the stent elutes the therapeutic substance while being engaged with the adjacent tissue in the nasal cavity after the catheter is removed from the nasal cavity.

16. The method of

claim 11

, the stent defining a cylindrical shape.

17. The method of

claim 11

, the stent being formed of a resilient material.

18. The method of

claim 11

, further comprising inserting an introducing device in the nasal cavity, the act of inserting the catheter into the nasal cavity comprising advancing the catheter along the introducing device.

19. The method of

claim 18

, the introducing device comprising a guidewire.

20. The method of

claim 11

, the stent comprising a metallic material.

21. The method of

claim 11

, the stent comprising a polymeric material.

22. The method of

claim 11

, the stent comprising a foam material.

23. The method of

claim 11

, the stent comprising a plastically deformable material.

24. The method of

claim 11

, the stent comprising a super elastic material.

25. The method of

claim 11

, the stent comprising a chain-link structure.

26. The method of

claim 11

, the stent comprising polyurethane.

27. The method of

claim 11

, the stent comprising polyethylene.

28. The method of

claim 11

, the stent comprising a radiopaque coating.

29. A method, comprising:

(a) inserting a catheter into a nasal cavity of a patient, the catheter including a balloon and a stent positioned over the balloon, the balloon and the stent each being in a non-expanded state during the act of inserting the catheter into the nasal cavity of the patient;

(b) positioning the balloon and the stent in a targeted anatomical passageway in the nasal cavity;

(c) expanding the balloon within the nasal cavity while the stent is positioned over the balloon in the targeted anatomical passageway, thereby expanding the stent, the expanded stent engaging adjacent tissue in the targeted anatomical passageway;

(d) transitioning the balloon to a non-expanded state, the expanded stent remaining engaged with the adjacent tissue in the targeted anatomical passageway during the act of transitioning the balloon to the non-expanded state; and

(e) removing the catheter from the nasal cavity with the balloon in the non-expanded state, the expanded stent remaining engaged with the adjacent tissue in the targeted anatomical passageway after the catheter is removed from the nasal cavity.

30. An apparatus, comprising:

(a) a catheter, the catheter comprising:

(i) a balloon, and

(ii) a shaft extending proximally from the balloon, the shaft having a length sufficient to enable positioning of the balloon in a targeted anatomical passageway in a nasal cavity of the patient while a proximal end of the shaft remains external to the patient; and

(b) a metallic stent, the metallic stent being configured to fit over the balloon of the catheter,

the balloon being operable to inflate to thereby transition the metallic stent from a contracted state to an expanded state,

the metallic stent in the expanded state being operable to bear against a sidewall of the targeted anatomical passageway in the nasal cavity.

US16/424,735 2004-04-21 2019-05-29 Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures Abandoned US20190314620A1 (en)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
US16/424,735 US20190314620A1 (en)	2004-04-21	2019-05-29	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US16/747,590 US11529502B2 (en)	2004-04-21	2020-01-21	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

Applications Claiming Priority (7)

Application Number	Priority Date	Filing Date	Title
US10/829,917 US7654997B2 (en)	2004-04-21	2004-04-21	Devices, systems and methods for diagnosing and treating sinusitus and other disorders of the ears, nose and/or throat
US10/944,270 US20060004323A1 (en)	2004-04-21	2004-09-17	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US11/928,346 US8172828B2 (en)	2004-04-21	2007-10-30	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US12/768,963 US8945088B2 (en)	2004-04-21	2010-04-28	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US14/566,845 US9713700B2 (en)	2004-04-21	2014-12-11	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US15/624,111 US20170348516A1 (en)	2004-04-21	2017-06-15	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US16/424,735 US20190314620A1 (en)	2004-04-21	2019-05-29	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

Related Parent Applications (1)

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US15/624,111 Continuation US20170348516A1 (en)	2004-04-21	2017-06-15	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

Related Child Applications (1)

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US16/747,590 Continuation US11529502B2 (en)	2004-04-21	2020-01-21	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

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US16/747,590 Expired - Lifetime US11529502B2 (en)	2004-04-21	2020-01-21	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

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US20200164188A1 (en)	2020-05-28

Publication	Publication Date	Title
US11511090B2 (en)	2022-11-29	Devices, systems and methods useable for treating sinusitis
US9713700B2 (en)	2017-07-25	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US11529502B2 (en)	2022-12-20	Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures

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US20190314620A1 - Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures - Google Patents

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