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Improved outcomes in patients with severely depressed LVEF undergoing percutaneous coronary intervention with contemporary practices - 28/04/22

Doi : 10.1016/j.ahj.2022.02.006 
William W. O'Neill, MD a, , Mark Anderson, MD b, Daniel Burkhoff, MD, PhD c, Cindy L. Grines, MD d, Navin K. Kapur, MD e, Alexandra J. Lansky, MD f, Salvatore Mannino, DO g, James M. McCabe, MD h, Khaldoon Alaswad, MD a, Ramesh Daggubati, MD i, David Wohns, MD j, Perwaiz M. Meraj, MD k, Duane S. Pinto, MD l, Jeffrey J. Popma, MD l, Jeffrey W. Moses, MD m, Theodore L. Schreiber, MD n, E. Magnus Ohman, MD o
a Henry Ford Hospital, Detroit, MI 
b Hackensack University Medical Center, Hackensack, NJ 
c Cardiovascular Research Foundation, New York, NY 
d Northside Cardiovascular Institute, Atlanta, GA 
e Tufts Medical Center, Boston, MA 
f Yale New Haven Hospital, New Haven, CT 
g WellStar Kennestone Hospital, Marietta, GA 
h University of Washington Medical Center, Seattle, WA 
i WVU Heart and Vascular Institute, Morgantown, WV 
j Spectrum Health, Frederik Meijer Heart and Vascular Institute, Grand Rapids, MI 
k Northwell Health, Manhasset, Y 
l Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 
m Columbia University Medical Center, New York, NY 
n Ascension St. John Hospital and Medical Center, Detroit, MI 
o Duke University Medical Center, Durham, NC 

Reprint requests: William W. O'Neill, MD, Henry Ford Hospital, 2799 W Grand Blvd, K16-W1615, Detroit, MI 48202.Henry Ford Hospital2799 W Grand Blvd, K16-W1615DetroitMI48202

Riassunto

Background

Contemporary practices for hemodynamically supported high-risk percutaneous coronary intervention have evolved over the last decade. This study sought to compare outcomes of the prospective, multicenter, PROTECT III study to historic patients treated with Impella in the PROTECT II randomized controlled trial.

Methods

Of 1,134 patients enrolled in PROTECT III from March 2017 to March 2020, 504 were “PROTECT II-like” (met eligibility for PROTECT II randomized controlled trial) and are referred to as PROTECT III for comparative analysis. Major adverse cardiac and cerebrovascular events (MACCE), comprising all-cause mortality, stroke/transient ischemic attack, myocardial infarction, and repeat revascularization, were compared at hospital discharge and 90 days.

Results

Compared with PROTECT II (N = 216), PROTECT III patients were less often Caucasian (77.1% vs 83.8%, P = .045), with less prior CABG (13.7% vs 39.4%; P < .001) and prior myocardial infarction (40.7% vs 69.3%; P < .001). More PROTECT III patients underwent rotational atherectomy (37.1% vs 14.8%, P < .001) and duration of support was longer (median 1.6 vs 1.3 hours; p<0.001), with greater improvement achieved in myocardial ischemia jeopardy scores (7.0±2.4 vs 4.4±2.9; P < .001) and SYNTAX scores (21.4±10.8 vs 15.7±9.5; P < .001). In-hospital bleeding requiring transfusion was significantly lower in PROTECT III (1.8% vs 9.3%; P < .001), as was procedural hypotension (2.2% vs 10.1%; P < .001) and cardiopulmonary resuscitation or ventricular arrhythmia (1.6% vs 6.9%; P < .001). At 90 days, MACCE was 15.1% and 21.9% in PROTECT III and PROTECT II, respectively (p=0.037). Following propensity score matching, Kaplan-Meier analysis showed improved 90-day MACCE rates in PROTECT III (10.4% vs 16.9%, P = .048).

Conclusions

The PROTECT III study demonstrates improved completeness of revascularization, less bleeding, and improved 90-day clinical outcomes compared to PROTECT II for Impella-supported high-risk percutaneous coronary intervention among patients with severely depressed LVEF.

Il testo completo di questo articolo è disponibile in PDF.

Abbreviations : CABG, CAD, CHF, COPD, LVEF, MAP, MI, NYHA, SD, TIA


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© 2022  Pubblicato da Elsevier Masson SAS.
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P. 139-149 - Giugno 2022 Ritorno al numero
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