TY - JOUR
T1 - Impact of renin-angiotensin system inhibitors on mortality during the COVID Pandemic among STEMI patients undergoing mechanical reperfusion
T2 - Insight from an international STEMI registry
AU - De Luca, Giuseppe
AU - Cercek, Miha
AU - Okkels Jensen, Lisette
AU - Bushljetikj, Oliver
AU - Calmac, Lucian
AU - Johnson, Tom
AU - Gracida Blancas, Montserrat
AU - Ganyukov, Vladimir
AU - Wojakowski, Wojtek
AU - von Birgelen, Clemens
AU - IJsselmuiden, Alexander
AU - Tuccillo, Bernardo
AU - Versaci, Francesco
AU - Ten Berg, Jurrien
AU - Laine, Mika
AU - Berkout, Tim
AU - Casella, Gianni
AU - Kala, Petr
AU - López Ledesma, Bernabé
AU - Becerra, Victor
AU - Padalino, Roberto
AU - Santucci, Andrea
AU - Carrillo, Xavier
AU - Scoccia, Alessandra
AU - Amoroso, Giovanni
AU - Lux, Arpad
AU - Kovarnik, Tomas
AU - Davlouros, Periklis
AU - Gabrielli, Gabriele
AU - Flores Rios, Xacobe
AU - Bakraceski, Nikola
AU - Levesque, Sébastien
AU - Guiducci, Vincenzo
AU - Kidawa, Michał
AU - Marinucci, Lucia
AU - Zilio, Filippo
AU - Galasso, Gennaro
AU - Fabris, Enrico
AU - Menichelli, Maurizio
AU - Manzo, Stephane
AU - Caiazzo, Gianluca
AU - Moreu, Jose
AU - Sanchis Forés, Juan
AU - Donazzan, Luca
AU - Vignali, Luigi
AU - Teles, Rui
AU - Bosa Ojeda, Francisco
AU - Lehtola, Heidi
AU - Camacho-Freiere, Santiago
AU - Kraaijeveld, Adriaan
AU - Antti, Ylitalo
AU - Visconti, Gabriella
AU - Lozano Martínez-Luengas, Iñigo
AU - Scheller, Bruno
AU - Alexopulos, Dimitrios
AU - Moreno, Raul
AU - Kedhi, Elvin
AU - Uccello, Giuseppe
AU - Faurie, Benjamin
AU - Gutierrez Barrios, Alejandro
AU - Scotto Di Uccio, Fortunato
AU - Wilbert, Bor
AU - Cortese, Giuliana
AU - Dirksen, Maurits T
AU - Parodi, Guido
AU - Verdoia, Monica
N1 - Funding Information:
The study was promoted and partially funded by the Aging Project- Department of Excellence, Department of Translational Medicine, Eastern Piedmont University , Novara, Italy.
Publisher Copyright:
© 2021 The Authors
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/6
Y1 - 2021/6
N2 - Background: Concerns have been raised on a potential interaction between renin-angiotensin system inhibitors (RASI) and the susceptibility to coronavirus disease 2019 (COVID-19). No data have been so far reported on the prognostic impact of RASI in patients suffering from ST-elevation myocardial infarction (STEMI) during COVID-19 pandemic, which was the aim of the present study. Methods: STEMI patients treated with primary percutaneous coronary intervention (PPCI) and enrolled in the ISACS-STEMI COVID-19 registry were included in the present sub-analysis and divided according to RASI therapy at admission. Results: Our population is represented by 6095 patients, of whom 3654 admitted in 2019 and 2441 in 2020. No difference in the prevalence of SARSCoV2 infection was observed according to RASI therapy at admission (2.5% vs 2.1%, p = 0.5), which was associated with a significantly lower mortality (adjusted OR [95% CI]=0.68 [0.51–0.90], P = 0.006), confirmed in the analysis restricted to 2020 (adjusted OR [95% CI]=0.5[0.33–0.74], P = 0.001). Among the 5388 patients in whom data on in-hospital medication were available, in-hospital RASI therapy was associated with a significantly lower mortality (2.1% vs 16.7%, OR [95% CI]=0.11 [0.084–0.14], p < 0.0001), confirmed after adjustment in both periods. Among the 62 SARSCoV-2 positive patients, RASI therapy, both at admission or in-hospital, showed no prognostic effect. Conclusions: This is the first study to investigate the impact of RASI therapy on the prognosis and SARSCoV2 infection of STEMI patients undergoing PPCI during the COVID-19 pandemic. Both pre-admission and in-hospital RASI were associated with lower mortality. Among SARSCoV2-positive patients, both chronic and in-hospital RASI therapy showed no impact on survival.
AB - Background: Concerns have been raised on a potential interaction between renin-angiotensin system inhibitors (RASI) and the susceptibility to coronavirus disease 2019 (COVID-19). No data have been so far reported on the prognostic impact of RASI in patients suffering from ST-elevation myocardial infarction (STEMI) during COVID-19 pandemic, which was the aim of the present study. Methods: STEMI patients treated with primary percutaneous coronary intervention (PPCI) and enrolled in the ISACS-STEMI COVID-19 registry were included in the present sub-analysis and divided according to RASI therapy at admission. Results: Our population is represented by 6095 patients, of whom 3654 admitted in 2019 and 2441 in 2020. No difference in the prevalence of SARSCoV2 infection was observed according to RASI therapy at admission (2.5% vs 2.1%, p = 0.5), which was associated with a significantly lower mortality (adjusted OR [95% CI]=0.68 [0.51–0.90], P = 0.006), confirmed in the analysis restricted to 2020 (adjusted OR [95% CI]=0.5[0.33–0.74], P = 0.001). Among the 5388 patients in whom data on in-hospital medication were available, in-hospital RASI therapy was associated with a significantly lower mortality (2.1% vs 16.7%, OR [95% CI]=0.11 [0.084–0.14], p < 0.0001), confirmed after adjustment in both periods. Among the 62 SARSCoV-2 positive patients, RASI therapy, both at admission or in-hospital, showed no prognostic effect. Conclusions: This is the first study to investigate the impact of RASI therapy on the prognosis and SARSCoV2 infection of STEMI patients undergoing PPCI during the COVID-19 pandemic. Both pre-admission and in-hospital RASI were associated with lower mortality. Among SARSCoV2-positive patients, both chronic and in-hospital RASI therapy showed no impact on survival.
KW - COVID-19
KW - Mortality
KW - Percutaneous coronary intervention
KW - Renin-Angiotensin System inhibitors
KW - ST-segment elevation myocardial infarction
UR - http://www.scopus.com/inward/record.url?scp=85102599132&partnerID=8YFLogxK
U2 - 10.1016/j.biopha.2021.111469
DO - 10.1016/j.biopha.2021.111469
M3 - Article
C2 - 33740523
SN - 0753-3322
VL - 138
JO - Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie
JF - Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie
M1 - 111469
ER -