US 11,051,832 B2
Aspiration monitoring system and method
David M. Look, Newport Beach, CA (US); and Bradley S. Culbert, Mission Viejo, CA (US)
Assigned to Incuvate, LLC, Irvine, CA (US)
Filed by INCUVATE, LLC, Irvine, CA (US)
Filed on Jan. 4, 2019, as Appl. No. 16/239,679.
Application 16/239,679 is a continuation of application No. 15/388,716, filed on Dec. 22, 2016, granted, now 10,226,263.
Claims priority of provisional application 62/387,537, filed on Dec. 23, 2015.
Claims priority of provisional application 62/326,390, filed on Apr. 22, 2016.
Prior Publication US 2019/0133617 A1, May 9, 2019
This patent is subject to a terminal disclaimer.
Int. Cl. A61B 17/221 (2006.01); A61B 17/22 (2006.01); A61M 1/00 (2006.01); A61B 17/3207 (2006.01); A61B 17/00 (2006.01); A61B 90/00 (2016.01)
CPC A61B 17/22 (2013.01) [A61M 1/008 (2013.01); A61M 1/0031 (2013.01); A61B 17/320758 (2013.01); A61B 2017/00022 (2013.01); A61B 2017/22038 (2013.01); A61B 2017/22079 (2013.01); A61B 2017/320775 (2013.01); A61B 2090/064 (2016.02); A61M 1/0068 (2014.02); A61M 2205/3331 (2013.01); A61M 2205/52 (2013.01); A61M 2205/581 (2013.01); A61M 2205/582 (2013.01); A61M 2205/583 (2013.01); A61M 2210/12 (2013.01)] 20 Claims
OG exemplary drawing
1. A method for removing thromboembolic material from a blood vessel in a patient, the method comprising:
providing an aspiration catheter having an elongate shaft including an aspiration lumen having a proximal end and a distal end, the proximal end configured to couple to a vacuum source, the distal end having an orifice;
providing an elongate member configured for placement through the aspiration lumen of the aspiration catheter, the elongate member having a proximal portion configured to extend from the proximal end of the aspiration lumen;
inserting a distal portion of the elongate shaft of the aspiration catheter into a blood vessel of a subject and positioning the orifice into or adjacent thromboembolic material within the blood vessel of the subject;
inserting the elongate member into the aspiration lumen of the aspiration catheter;
coupling the proximal portion of the elongate member to a rotating device comprising a body and a rotator, the body configured to be gripped by a user and the rotator configured to rotate the elongate member when the rotating device is coupled to the elongate member;
applying a negative pressure to the aspiration lumen of the aspiration catheter to draw at least a portion of the thromboembolic material into the aspiration lumen;
rotating the elongate member within the aspiration lumen of the aspiration catheter with the rotating device;
monitoring the negative pressure with a pressure transducer; and
measuring one or more deviations in the negative pressure with a measurement device coupled to the pressure transducer.