Transseptal systems and methods

Patent metadata

Field	Value
Publication number	US-11806000-B2
Application number	US-202117554576-A
Country	US
Kind code	B2
Filing date	Dec 17, 2021
Priority date	Feb 15, 2021
Publication date	Nov 7, 2023
Grant date	Nov 7, 2023

Abstract

A transseptal system includes a needle, a guidewire, a handle, and a dilator. The handle defines a needle passage to slidably receive the needle, and a guidewire passage to slidably receive the guidewire. The dilator defines a lumen having a distal region and a proximal region. The dilator is coupled to the handle such that the lumen is open to the needle passage and the guidewire passage. The proximal region of the lumen is sized to simultaneously receive the needle body and the guidewire. The distal region is sized to slidably receive one of the needle and the guidewire on an individual basis. A transseptal puncture and access procedure can be performed, including puncturing tissue with the needle followed by immediate advancement of the guidewire into the accessed area, eliminating the need for multiple instrument exchanges during the procedure.

First claim

What is claimed is:

1. A transseptal system comprising:
a needle body defining a distal tip and an intermediate section proximal the distal tip;
a guidewire defining a leading end and an intermediate segment proximal the leading end;
a handle defining a needle passage and a guidewire passage, wherein the needle passage is sized to slidably receive the intermediate section of the needle body, and further wherein the guidewire passage is sized to slidably receive the intermediate segment of the guidewire;
a dilator body defining a distal end, a proximal end, and a lumen having a distal region open to the distal end and a proximal region open to the proximal end;
wherein the proximal end of the dilator body is coupled to the handle such that the lumen is open to the needle passage and the guidewire passage;
and further wherein the proximal region of the lumen is sized to simultaneously receive the intermediate section of the needle body and the intermediate segment of the guidewire;
and even further wherein the distal region of the lumen is sized to slidably receive the intermediate section of the needle body and the intermediate segment of the guidewire on an individual basis.

2. The transseptal system of claim 1 , wherein the dilator body defines a longitudinal axis, and further wherein a cross-sectional maximum outer dimension of the distal region of the lumen in a plane perpendicular to the longitudinal axis is less than a cross-sectional maximum outer dimension of the proximal region of the lumen in a plane perpendicular to the longitudinal axis.

3. The transseptal system of claim 1 , wherein a diameter of the intermediate section of the needle body and a diameter of the intermediate segment of the guidewire combine to define a maximum combined working dimension, and further wherein the dilator body defines a longitudinal axis, and even further wherein a cross-sectional maximum outer dimension of the distal region of the lumen in a plane perpendicular to the longitudinal axis is less than the maximum combined working dimension.

4. The transseptal system of claim 3 , wherein a cross-sectional maximum outer dimension of the proximal region of the lumen is greater than the maximum combined working dimension.

5. The transseptal system of claim 1 , wherein the transseptal system is configured to provide a first deployment state including:
the intermediate section of the needle body disposed within the lumen;
the distal tip of the needle body projecting beyond distal end of the dilator body; and
the leading end of the guidewire disposed within the proximal region of the lumen.

6. The transseptal system of claim 5 , wherein the transseptal system is configured to provide a second deployment state including:
the intermediate segment of the guidewire disposed within the lumen;
the leading end of the guidewire projecting beyond distal end of the dilator body; and
the distal tip of the needle body disposed within the proximal region of the lumen.

7. The transseptal system of claim 1 , wherein the needle passage extends from a proximal side to a distal side, the distal side intersecting, and open to, the guidewire passage.

8. The transseptal system of claim 1 , wherein the handle is provided as part of a handle assembly further including an actuator device connected to the handle and configured to retain the needle body.

9. The transseptal system of claim 8 , wherein the actuator device is slidably connected to the handle.

10. The transseptal system of claim 9 , wherein the actuator device includes a pusher body and a neck, and further wherein the head extends from the pusher body and is affixed to the needle body.

11. The transseptal system of claim 10 , wherein the pusher body is slidable relative to the handle between a forward position and a rearward position, and further wherein the transseptal system is configured such that in the forward position, the distal tip of the needle body is distal the distal end of the dilator body, and in the rearward position, the distal tip of the needle body is disposed within the proximal region of the lumen.

12. The transseptal system of claim 11 , wherein the handle assembly further includes a safety tab removably connected to the handle and arranged to prevent the pusher body from being directed to the forward position.

13. A transseptal system comprising:
a handle assembly including a handle defining a needle passage and a guidewire passage;
a dilator body defining a longitudinal axis, distal end, a proximal end, and a lumen having a distal region open to the distal end and a proximal region open to the proximal end, wherein a cross-sectional maximum outer dimension of the distal region of the lumen in a plane perpendicular to the longitudinal axis is less than a cross-sectional maximum outer dimension of the proximal region of the lumen in a plane perpendicular to the longitudinal axis;
wherein the proximal end of the dilator body is coupled to the handle such that the lumen is open to the needle passage and the guidewire passage; and
a needle body coupled to the handle assembly and slidably received within the needle passage and the lumen.

14. The transseptal system of claim 13 , further comprising a guidewire configured to be slidably received within the guidewire passage and the lumen.

15. A method of creating a transseptal passage, the method comprising:
advancing a dilator body over a guidewire to bring a distal end of the dilator body into contact with a first side of an atrial septum, the guidewire being slidably received within a lumen of the dilator body;
retracting the guidewire relative to the dilator body such that a leading end of the guidewire is located within the lumen;
forming a hole through the septum with a needle body while the leading end of the guidewire is maintained within lumen, including advancing the needle body along the lumen to cause a distal tip of the needle body to extend from the distal end of the dilator body and puncture through the first side of the atrial septum to an opposing, second side of the atrial septum;
retracting the needle body relative to the dilator body following the step of forming a hole such that the distal tip of the needle body is located within the lumen; and
advancing the guidewire relative to the dilator body such that the leading end of the guidewire extends distally beyond the distal end of the dilator body and the second side of the atrial septum.

16. The method of claim 15 , wherein during the step of advancing the dilator body over the guidewire, the distal tip of the needle body is located within the lumen.

17. The method of claim 15 , wherein during the step of retracting the guidewire relative to the dilator body, the distal tip of the needle body is located within the lumen.

18. The method of claim 15 , further comprising:
advancing a distal zone of the dilator body through the hole to dilate the hole following the step of advancing the needle body.

19. The method of claim 18 , further comprising:
withdrawing the dilator body and the needle body from the patient following the step of advancing the distal zone of the dilator body through the puncture hole;
wherein during the step of withdrawing, the guidewire remains within the patient and the leading end is located distally beyond the second side of the atrial septum.

20. The method of claim 19 , further comprising:
advancing a treatment device over the guidewire following the step of withdrawing the dilator body and the needle body.

Assignees

• Medtronic Inc

Inventors

• Howard Stephen A
• Knutsen Kevin A

Classifications

• A61B17/00234 Primary

  for minimally invasive surgery (A61B17/0218, A61B17/0469, A61B17/12013, A61B17/1285, A61B17/29, A61B17/320016 take precedence) · CPC title

• A61B17/3478 Primary

  Endoscopic needles, e.g. for infusion (biopsy needles A61B10/0233; catheters with injection needles A61M25/0067) · CPC title

• A61M25/09

  Guide wires · CPC title

• A61M29/00

  Dilators with or without means for introducing media, e.g. remedies · CPC title

• A61B2017/00247

  Making holes in the wall of the heart, e.g. laser Myocardial revascularization · CPC title