Systems and methods for transnasal dilation of passageways in the ear, nose or throat

Patent metadata

Field	Value
Publication number	US-9399121-B2
Application number	US-49622609-A
Country	US
Kind code	B2
Filing date	Jul 1, 2009
Priority date	Apr 21, 2004
Publication date	Jul 26, 2016
Grant date	Jul 26, 2016

Abstract

A dilation catheter device and system for dilating an opening in a paranasal sinus and/or other passageways within the ear, nose or throat is disclosed. A dilation catheter device and system is constructed in a manner that facilitates ease of use by the operator and, in at least some cases, allows the dilation procedure to be performed by a single operator. Additionally, the dilation catheter device and system may be useable in conjunction with an endoscope and/or a fluoroscope to provide for easy manipulation and positioning of the devices and real time visualization of the entire procedure or selected portions thereof. In some embodiments, shaft markers are disposed on a shaft of the dilation catheter and have a light color to contrast with a dark color of the dilation catheter shaft. The high contrast between the markers and catheter shaft allows for easy viewing of the markers in low light and operation conditions.

First claim

What is claimed:

1. A system for dilating an opening in a paranasal sinus, the system comprising:
(a) an endoscope;
(b) a guide catheter comprising a proximal end and a distal end; and
(c) a balloon dilation catheter configured to be advanced through the guide catheter, the balloon dilation catheter comprising:
(i) a catheter shaft having:
(A) a longitudinal axis,
(B) an inflation lumen,
(C) a distal end,
(D) a proximal end,
(E) a proximal shaft section, wherein the proximal shaft section comprises:
(1) an outer tube,
(2) an inner tube within the outer tube, wherein the inner tube includes an inflation lumen, and
(3) a middle tube between the inner tube and the outer tube, and

(F) a distal shaft section, wherein the distal shaft section comprises:
(1) a distal portion of the middle tube, and
(2) a distal portion of the inner tube, and

(G) a tapered section between the proximal shaft section and the distal shaft section,

(ii) an inflatable balloon disposed on the distal shaft section in fluid communication with the inflation lumen, wherein a distal end of the middle tube terminates within the inflatable balloon and the proximal end of the inflatable balloon is secured to the outer surface of the middle tube,
(iii) a first proximal shaft marker disposed on the proximal shaft section and having a lighter color than the catheter shaft, wherein the first proximal shaft marker is configured to be visualized directly at a location proximal to the proximal end of the guide catheter to allow a user to approximate a position of the balloon relative to the guide catheter, and
(iv) a first distal shaft marker disposed on the distal shaft section proximal to a proximal end of the balloon and having a lighter color than the catheter shaft, wherein the endoscope is configured to provide endoscopic visualization of the first distal shaft marker to enable a user to approximate a position of the balloon relative to an opening of a paranasal sinus.

2. The system of claim 1 , further comprising a second proximal shaft marker disposed on the proximal shaft section distally from the first proximal shaft marker and having a lighter color than the catheter shaft, wherein the first shaft marker has a greater length than the second shaft marker.

3. The system of claim 2 , wherein the length of the first proximal shaft marker is equal to a length from a proximal end of the balloon to the distal end of the catheter shaft, wherein the first shaft marker is spaced from the distal end of the catheter shaft such that it allows the user to approximate when the distal end of the shaft is located at the distal end of the guide catheter and when the proximal end of the balloon exits the guide catheter, and wherein the second proximal shaft marker allows the user to approximate when the distal end of the catheter shaft is located just proximal to a curve in the guide catheter.

4. The system of claim 1 , further comprising a second distal shaft marker disposed on the distal shaft section proximal to the first distal shaft marker and having a lighter color than the catheter shaft.

5. The system of claim 4 , wherein the first distal shaft marker is disposed at a known distance proximally from the proximal end of the balloon, and the second distal shaft marker is disposed at a known distance proximally from the first distal shaft marker, and wherein the first and second distal shaft marker have different appearances.

6. The system of claim 5 , wherein the first distal shaft marker is disposed approximately one centimeter from the proximal end of the balloon and the second distal shaft marker is disposed approximately two centimeters from the proximal end of the balloon.

7. The system of claim 4 , further comprising a third distal shaft marker disposed on the distal shaft section at the proximal end of the balloon.

8. The system of claim 1 , further comprising:
(a) a first radiopaque marker disposed on the distal shaft section within the balloon; and
(b) a second radiopaque marker disposed on the distal shaft section distally from the first
radiopaque marker within the balloon;
wherein the first and second radiopaque markers are disposed a distance apart from one another to indicate the effective length of the balloon.

9. The system of claim 1 , wherein the balloon further comprises an approximately triangular cross-sectional shape in a partially inflated state.

10. The system of claim 1 , wherein the balloon further comprises a balloon neck extending from the balloon and proximally along the catheter shaft.

11. The system of claim 10 , wherein the first proximal shaft marker is disposed on the distal shaft section and underneath the balloon neck.

12. The system of claim 1 , wherein the balloon dilation catheter further comprises a guidewire lumen.

13. The system of claim 1 , further comprising a guidewire that is advanceable through the guidewire lumen.

14. The system of claim 1 , wherein the-inflation fluid lumen is sized so that, after the balloon has been inflated to a working diameter, the balloon will deflate in less than 5 seconds with application of negative pressure to the inflation fluid lumen by a conventional balloon catheter inflation and deflation device.

15. The system of claim 1 , further comprising an irrigation catheter sized for advancement through the guide catheter into a paranasal sinus.

16. The system of claim 1 , wherein the guide catheter further comprises an anti-reflective coating or treatment.

17. The system of claim 1 , wherein the balloon dilation catheter further comprises an anti-reflective coating or treatment.

18. A method of operating a dilation system, the system comprising:
(a) an endoscope;
(b) a guide catheter comprising a proximal end and a distal end; and
(c) a balloon dilation catheter configured to be advanced through the guide catheter, the balloon dilation catheter comprising:
(i) a catheter shaft having a longitudinal axis, an inflation lumen, a distal end, a proximal end, a proximal shaft section that is substantially rigid, and a distal shaft section that is more flexible than the proximal shaft section, wherein the catheter shaft is dark in color,
(ii) an inflatable balloon disposed on the distal shaft section in fluid communication with the inflation lumen,
(iii) a first proximal shaft marker disposed on the proximal shaft section and having a lighter color than the catheter shaft, and
(iv) a first distal shaft marker disposed on the distal shaft section proximal to a proximal end of the balloon and having a lighter color than the catheter shaft,

wherein the method comprises:
(a) inserting the guide catheter into a nostril of the patient;
(b) advancing the guide catheter near a passageway of a paranasal sinus;
(c) advancing the balloon dilation catheter through the guide catheter;
(d) directly visualizing the first proximal shaft marker at a location proximal relative to the proximal end of the guide catheter to approximate a position of the balloon relative to the guide catheter;
(e) inserting the endoscope into the nostril of the patient; and
(f) endoscopically visualizing the first distal shaft maker relative to a passageway of the paranasal sinus.

Assignees

• Goldfarb Eric
• Chang John Y
• Facteau William M
• Lam Sivette
• Ha Hung V
• Kim Isaac J
• Muni Ketan P
• Acclarent Inc

Inventors

• Goldfarb Eric
• Chang John Y
• Facteau William M
• Lam Sivette
• Ha Hung V
• Kim Isaac J
• Muni Ketan P

Classifications

• A61B17/24 Primary

  for use in the oral cavity, larynx, bronchial passages or nose (for medical inspection of cavities or tubes in the body A61B1/00); Tongue scrapers · CPC title

• A61M2210/0681

  Sinus (maxillaris) · CPC title

• A61M2025/1079

  having radio-opaque markers in the region of the balloon · CPC title

• A61M25/1002

  characterised by balloon shape (A61M25/1006, A61M25/1009 take precedence) · CPC title

• A61M2025/1086

  having a special balloon surface topography, e.g. pores, protuberances, spikes or grooves · CPC title