Method for intraluminally inducing cardioplegic arrest and catheter for use therein

• US 5,759,170 A
• Filed: 03/13/1996
• Issued: 06/02/1998
• Est. Priority Date: 11/30/1993
• Status: Expired due to Term

• Current Assignee: Edwards Lifesciences LLC (Edwards Lifesciences Corporation)
• Original Assignee: Heartport, Inc. (Johnson & Johnson)
• Inventors: Peters, William S.
• Primary Examiner(s): Buiz, Michael Powell
• Assistant Examiner(s): NGUYEN, ANH TUAN TUONG
• Application Number:
  US08/614,535
• Time in Patent Office: 811 Days
• Field of Search: 604/53, 604/4, 604/8, 604/96, 604/101, 604/102, 604/280, 604/171, 606/191, 606/192, 606/194, 606/198, 600/16-18
• US Class Current: 604/6.14
• CPC Class Codes: A61B 2018/00232 having an irregular shape
• CPC Class Codes: A61B 2018/00261 arranged in a line
• CPC Class Codes: A61M 2025/0031 characterized by lumina for withdrawing or delivering, i.e. used for extracorporeal circuit treatment
• CPC Class Codes: A61M 2025/028 having a mainly rigid support structure
• CPC Class Codes: A61M 2025/1052 for temporarily occluding a vessel for isolating a sector
• CPC Class Codes: A61M 2202/047 cardioplegic
• CPC Class Codes: A61M 2210/127 Aorta
• CPC Class Codes: A61M 25/0023 by the form of the lumen, e.g. cross-section, variable diameter
• CPC Class Codes: A61M 25/0026 Multi-lumen catheters with stationary elements catheter assemblies comprising a catheter in combination with a guide tube, sheath or sleeve A61M2025/0681; catheters comprising telescoping coaxial elements A61M2025/0175
• CPC Class Codes: A61M 25/0032 characterized by at least one unconventionally shaped lumen, e.g. polygons, ellipsoids, wedges or shapes comprising concave and convex parts
• CPC Class Codes: A61M 25/104 used for angioplasty
• CPC Class Codes: A61M 29/02 Dilators made of swellable material balloon catheters for angioplasty A61M25/104

Abstract

A process for inducing cardioplegic arrest of a heart in situ in a patient'"'"'s body, comprising maintaining the patient'"'"'s systemic circulation by peripheral cardiopulmonary by-pass, occluding the ascending aorta through a percutaneously placed arterial balloon catheter, venting the left side of the heart, and introducing a cardioplegic agent into the coronary circulation. This procedure readies the heart for a variety of surgical procedures that can be performed percutaneously through lumina in the catheter. An aortic catheter for use in the process is also described.

Claims

1. A catheter system for inducing cardioplegic arrest while circulation is supported by cardiopulmonary bypass, the system comprising:

an aortic catheter having a proximal end and a distal end, a first lumen, a second lumen, and a blood flow lumen each extending distally from the proximal end, a first occluding member coupled to the aortic catheter near the distal end and movable between a collapsed shape and an expanded shape, the first occluding member being configured to occlude a patient'"'"'s ascending aorta when in the expanded shape, a first outlet distal to the first occluding member coupled to the first lumen, a second outlet distal to the first occluding member coupled to the second lumen, and a blood outlet proximal to the first occluding member and coupled to the blood flow lumen, the aortic catheter having a length selected so that the occluding member is positionable in the ascending aorta with the proximal end extending to a peripheral artery;

a source of cardioplegic agent coupled to the first lumen; and

a bypass system having an inlet and an outlet, the outlet being coupled to the blood flow lumen for returning oxygenated blood to the patient.

2. The system of claim 1 further comprising:

a venous cannula for removing blood from a vein in the patient, the venous cannula having a proximal end, a distal end, a blood withdrawal lumen therebetween, and a length selected so as to extend into a first vessel selected from a superior vena cava and an inferior vena cava of the patient from a peripheral vein, the blood withdrawal lumen being coupled to the inlet of the bypass system.

3. The system of claim 2 wherein:

the first venous cannula includes at least a second occluding member near the distal end thereof sized and configured to occlude at least one of the superior vena cava and the inferior vena cava when in an expanded shape.