TY - JOUR
T1 - Direct percutaneous left ventricular access and port closure
T2 - Pre-clinical feasibility
AU - Barbash, Israel M.
AU - Saikus, Christina E.
AU - Faranesh, Anthony Z.
AU - Ratnayaka, Kanishka
AU - Kocaturk, Ozgur
AU - Chen, Marcus Y.
AU - Bell, Jamie A.
AU - Virmani, Renu
AU - Schenke, William H.
AU - Hansen, Michael S.
AU - Slack, Michael C.
AU - Lederman, Robert J.
N1 - Funding Information:
This study was supported by the Division of Intramural Research, the National Heart, Lung, and Blood Institute , and National Institute of Health grants ( Z01-HL005062-08 , Z01-HL006039-01 , Z01-HL006040-01 , Z01-HL006041-01 ). AGA Medical supplied customized ventricular septal defect occluder devices but did not participate in the design, conduct, or analysis of the study.
PY - 2011/12
Y1 - 2011/12
N2 - This study sought to evaluate feasibility of nonsurgical transthoracic catheter-based left ventricular (LV) access and closure. Implanting large devices, such as mitral or aortic valve prostheses, into the heart requires surgical exposure and repair. Reliable percutaneous direct transthoracic LV access and closure would allow new nonsurgical therapeutic procedures. Percutaneous direct LV access was performed in 19 swine using real-time magnetic resonance imaging (MRI) and an "active" MRI needle antenna to deliver an 18-F introducer sheath. The LV access ports were closed percutaneously using a commercial ventricular septal defect occluder and an "active" MRI delivery cable for enhanced visibility. We used "permissive pericardial tamponade" (temporary fluid instillation to separate the 2 pericardial layers) to avoid pericardial entrapment by the epicardial disk. Techniques were developed in 8 animals, and 11 more were followed up to 3 months by MRI and histopathology. Imaging guidance allowed 18-F sheath access and closure with appropriate positioning of the occluder inside the transmyocardial tunnel. Of the survival cohort, immediate hemostasis was achieved in 8 of 11 patients. Failure modes included pericardial entrapment by the epicardial occluder disk (n = 2) and a true-apex entry site that prevented hemostatic apposition of the endocardial disk (n = 1). Reactive pericardial effusion (192 ± 118 ml) accumulated 5 ± 1 days after the procedure, requiring 1-time drainage. At 3 months, LV function was preserved, and the device was endothelialized. Direct percutaneous LV access and closure is feasible using real-time MRI. A commercial occluder achieved hemostasis without evident deleterious effects on the LV. Having established the concept, further clinical development of this approach appears realistic.
AB - This study sought to evaluate feasibility of nonsurgical transthoracic catheter-based left ventricular (LV) access and closure. Implanting large devices, such as mitral or aortic valve prostheses, into the heart requires surgical exposure and repair. Reliable percutaneous direct transthoracic LV access and closure would allow new nonsurgical therapeutic procedures. Percutaneous direct LV access was performed in 19 swine using real-time magnetic resonance imaging (MRI) and an "active" MRI needle antenna to deliver an 18-F introducer sheath. The LV access ports were closed percutaneously using a commercial ventricular septal defect occluder and an "active" MRI delivery cable for enhanced visibility. We used "permissive pericardial tamponade" (temporary fluid instillation to separate the 2 pericardial layers) to avoid pericardial entrapment by the epicardial disk. Techniques were developed in 8 animals, and 11 more were followed up to 3 months by MRI and histopathology. Imaging guidance allowed 18-F sheath access and closure with appropriate positioning of the occluder inside the transmyocardial tunnel. Of the survival cohort, immediate hemostasis was achieved in 8 of 11 patients. Failure modes included pericardial entrapment by the epicardial occluder disk (n = 2) and a true-apex entry site that prevented hemostatic apposition of the endocardial disk (n = 1). Reactive pericardial effusion (192 ± 118 ml) accumulated 5 ± 1 days after the procedure, requiring 1-time drainage. At 3 months, LV function was preserved, and the device was endothelialized. Direct percutaneous LV access and closure is feasible using real-time MRI. A commercial occluder achieved hemostasis without evident deleterious effects on the LV. Having established the concept, further clinical development of this approach appears realistic.
KW - hybrid surgical procedures
KW - interventional magnetic resonance imaging
KW - periventricular
KW - transcatheter aortic valve replacement
UR - http://www.scopus.com/inward/record.url?scp=84255172536&partnerID=8YFLogxK
U2 - 10.1016/j.jcin.2011.07.017
DO - 10.1016/j.jcin.2011.07.017
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C2 - 22192372
AN - SCOPUS:84255172536
SN - 1936-8798
VL - 4
SP - 1318
EP - 1325
JO - JACC: Cardiovascular Interventions
JF - JACC: Cardiovascular Interventions
IS - 12
ER -