IP Library Granted Patent US 10,716,920
Granted Patent B2
US 10,716,920 · App. 15/811,080 · Granted Jul 21, 2020

Transseptal puncture apparatus and method for using the same

Inventors: Paul Kurth (Santa Barbara, CA); Andrew Armour (Swarthmore, PA); Andrzej J. Chanduszko (Weymouth, MA); Carol A. Devellian (Topsfield, MA)
Assignee: AECORSIS B.V.
A61M25/09A61B17/0057A61B17/3468A61M25/09041A61B2017/00243A61B2017/00247A61B2017/00575A61B2017/00597A61B2017/00606A61B2017/00623A61B2017/00991A61B2017/06095A61B2017/22047A61M2025/0177
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Quick Facts
Patent No.
US 10,716,920
App. No.
15/811,080
Granted
Jul 21, 2020
Kind
B2
Abstract

Devices and methods for performing a transseptal puncture procedure using a device which includes either an untapered or tapered blunt end cannula disposed in an introducer carrying a sharp guidewire disposed longitudinally through the lumen of the blunt cannula, and a blunt end dilator wherein the guidewire is flexible and has an atraumatic shape at its tip. The cannula gives the more flexible introducer a defined shape and steerabilty allowing an ordinarily skilled physician to easily access a selected location on the septal wall of the heart for transseptal puncture and introducer placement thereacross without employing an exposed sharp end needle during the procedure.

Claims (41)

1. A method comprising:

telescopically disposing a blunt end cannula into a flexible introducer having an interior lumen, a distal curve, and a distal taper to define a predetermined shape and steerability to at least a distal portion of the introducer, where the flexible introducer has insufficient columnar strength and a shape ill-adapted for accessing a selected location on the cardiac septal wall of a patients heart when the cannula is not disposed within the interior lumen of the introducer and in dose proximity to the distal taper thereof, but is adapted to access the predetermined location on the cardiac septal wall when the cannula is disposed within the interior lumen of the introducer and in dose proximity to the distal taper thereof;

intravascularly accessing a right, atrium of a patient's heart with the introducer;

steering the distal taper of the introducer to the selected location on a septal wall of the heart to tent the septal wall at the selected location;

advancing a sharp ended floppy guidewire telescopically disposed within an interior lumen of the cannula while being supported by the cannula to provide sufficient columnar strength to the floppy guidewire to allow it to be pushed through the septal wall into a left atrium of the patients heart; and

advancing the sharp ended floppy guidewire beyond any support by the cannula to configure the sharp ended floppy guidewire into a prebiased atraumatic shape.

2. The method of claim 1 further comprising advancing the cannula through the septal wall over the guidewire.

3. The method of claim 2 further comprising advancing the introducer through the septal wall over the cannula.

4. The method of claim 1 further comprising advancing the introducer through the septal wall over the guidewire while leaving the cannula telescopically retained in the introducer.

5. The method of claim 1 where intravascularly accessing a right atrium of the patient's heart with the introducer comprises accessing the right atrium through a femoral vein.

6. The method of claim 1 where intravascularly accessing a right atrium of the patient's heart with the introducer comprises accessing the right atrium through a superior vena cava.

7. The method of claim 1 further comprising steering the distal taper of the introducer to a fossa ovalis using the blunt end cannula.

8. The method of claim 1 further comprising advancing the cannula through the septal wall over the sharp ended floppy guidewire.

9. A method comprising:

telescopically disposing a blunt end cannula into a flexible introducer having an interior lumen, a distal curve, and a distal taper to define a predetermined shape and steerability to at least a distal portion of the introducer, where the flexible introducer has insufficient columnar strength and a shape ill-adapted for accessing a selected location on a patient's tissue when the blunt end cannula is not disposed within the interior lumen of the introducer and in close proximity to the distal taper thereof, but is adapted to access the predetermined location on the patient's tissue when the blunt end cannula is disposed within the interior lumen of the introducer and in close proximity to the distal taper thereof;

providing a channel through the cannula in which to dispose an elongated medical device into the patient's heart;

providing sufficient columnar strength to the elongated medical device using the cannula to allow the elongated medical device to provide force against or push through the cardiac septal wall into the patient's heart;

intravascularly accessing the patient's tissue with the introducer; and

steering the distal taper of the introducer to the selected location on the patient's tissue to engage the tissue at the selected location.

10. The method of claim 9 where intravascularly accessing the patient's tissue with the introducer comprises accessing the cardiac septal wall of the patient's heart.

11. The method of claim 10 where intravascularly accessing the patient's heart with the introducer comprises accessing the right atrium through a femoral vein.

12. The method of claim 10 where intravascularly accessing the patient's heart with the introducer comprises accessing the right atrium through a superior vena cava.

13. The method of claim 9 further comprising advancing the elongated medical device beyond any support provided by the cannula while leaving the cannula retained in the introducer.

14. The method of claim 9 further comprising steering the distal taper of the introducer to a fossa ovalis using the cannula.

15. A method comprising:

telescopically disposing a blunt end cannula into a flexible introducer having an interior lumen, a distal curve, and a distal taper to define a predetermined shape and steerability to at least a distal portion of the introducer, where the flexible introducer has insufficient columnar strength and a shape ill-adapted for accessing a selected location of a patient's tissue when the cannula is not disposed within the interior lumen of the introducer and in close proximity to the distal taper thereof, but is adapted to access the predetermined location on the patient's tissue when the cannula is disposed within the interior lumen of the introducer and in close proximity to the distal taper thereof;

intravascularly accessing a patient's tissue with the introducer;

steering the distal taper of the introducer to the selected location on a patient's tissue at the selected location to engage the tissue;

advancing a sharp ended floppy guidewire telescopically disposed within an interior lumen of the cannula while being supported by the cannula to provide sufficient columnar strength to the floppy guidewire to allow it to be pushed through the patient's tissue; and

advancing the sharp ended floppy guidewire beyond any support by the cannula to configure the sharp ended floppy guidewire into a prebiased atraumatic shape.

16. A method comprising:

telescopically disposing a blunt end cannula into a flexible introducer having an interior lumen, a distal curve, and a distal taper to define a predetermined shape and steerability to at least a distal portion of the introducer, where the flexible introducer has insufficient columnar strength and shape for accessing a selected location on a patient's tissue when the blunt end cannula is not positioned within the interior lumen of the introducer and in close proximity to the distal taper thereof, but is able to access the predetermined location on the patient's tissue when the blunt end cannula is disposed within the interior lumen of the introducer and in close proximity to the distal taper thereof;

intravascularly accessing the patient's tissue with the introducer;

steering the distal taper of the introducer to the selected location on the patient's tissue to engage the tissue at the selected location;

providing a channel through the cannula in which to dispose an elongated medical device into the patient's heart; and

providing sufficient columnar strength to the elongated medical device using the cannula to allow the elongated medical device to provide force against or push through the cardiac septal wall into the patient's heart.

17. The method of claim 16 where intravascularly accessing the patient's tissue with the introducer comprises accessing the cardiac septal wall of the patient's heart.

18. The method of claim 17 where intravascularly accessing the patient's heart with the introducer comprises accessing the right atrium through a femoral vein.

19. The method of claim 17 where intravascularly accessing the patient's heart with the introducer comprises accessing the right atrium through a superior vena cava.

20. The method of claim 16 further comprising providing sufficient columnar strength to the elongated medical device using the cannula to allow the elongated medical device to provide force against or push through the cardiac septal wall into the patient's heart.

21. The method of claim 16 further comprising steering the distal taper of the introducer to a fossa ovalis using the cannula.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2022
From: BAYLIS MEDICAL COMPANY INC.
To: BOSTON SCIENTIFIC MEDICAL DEVICE LIMITED
Reel/Frame 060938/0731 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2020
From: PRESSURE PRODUCTS MEDICAL SUPPLIES, INC
To: BAYLIS MEDICAL COMPANY INC.
Reel/Frame 053094/0579 →
Continuity (3)
Division 14638537 · Mar 4, 2015
Continuation In Part 13428719 · Mar 23, 2012
Related Publication 20180064915A1 · Mar 8, 2018
Cited By (3)
US 12,213,727 US 12,708,354 US 12,708,431