The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 29, 2023

Filed:

Aug. 06, 2019
Applicant:

University of Pittsburgh—of the Commonwealth System of Higher Education, Pittsburgh, PA (US);

Inventors:

Bryan W. Tillman, Pittsburgh, PA (US);

William W. Clark, Wexford, PA (US);

Sung Kwon Cho, Pittsburgh, PA (US);

Youngjae Chun, Pittsburgh, PA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61B 17/12 (2006.01); A61B 90/98 (2016.01); A61B 5/021 (2006.01); A61B 5/0215 (2006.01); A61F 2/966 (2013.01); G06K 7/10 (2006.01); A61B 90/00 (2016.01); A61B 17/00 (2006.01); A61F 2/07 (2013.01); A61F 2/95 (2013.01);
U.S. Cl.
CPC ...
A61B 17/12109 (2013.01); A61B 5/0215 (2013.01); A61B 5/02141 (2013.01); A61B 17/1204 (2013.01); A61B 17/12031 (2013.01); A61B 17/12036 (2013.01); A61B 17/12136 (2013.01); A61B 90/98 (2016.02); A61F 2/966 (2013.01); G06K 7/10366 (2013.01); A61B 2017/00115 (2013.01); A61B 2090/397 (2016.02); A61B 2090/3966 (2016.02); A61F 2/07 (2013.01); A61F 2002/9511 (2013.01);
Abstract

The present disclosure concerns embodiments of an implantable perfusion device that can be implanted in an injured blood vessel to control bleeding without occluding the vessel. In one specific implementation, the perfusion device can be implanted percutaneously into a patient's descending aorta to control bleeding at the site of a ruptured portion of the aorta (known as torso hemorrhage) while still allowing for the antegrade flow of blood from a location upstream of the ruptured portion of the aorta to a location downstream of the ruptured portion of the aorta. The perfusion device can be left inside the patient as the patient is transported to a medical facility where the injury can be repaired. Following repair of the vessel, the perfusion device can be withdrawn from the patient.


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