No harm from angiotensin-converting enzyme inhibitors or angiotensin receptor inhibitors in patients with COVID-19. Results of a prospective study on a hospital-based cohort

被引:3
|
作者
Anzola, Gian Paolo [1 ]
Bartolaminelli, Clara [2 ]
Gregorini, Gina Alessandra [3 ]
Coazzoli, Chiara [2 ]
Gatti, Francesca [4 ]
Mora, Alessandra [4 ]
Charalampakis, Dimitrios [4 ]
Palmigiano, Andrea [4 ]
De Simone, Michele [4 ]
Comini, Alice [4 ]
Dellaglio, Erica [4 ]
Cassetti, Salvatore [4 ]
Chiesa, Maurizio [4 ]
Spedini, Francesca [4 ]
D'Ottavi, Patrizia [2 ]
Savio, Maria Cristina [4 ]
机构
[1] San Camillo Hosp, Via Turati 47, I-25123 Brescia, Italy
[2] Terr Hlth Author, Brescia, Italy
[3] Univ Brescia, Brescia, Italy
[4] Gavardo Hosp, Emergency Dept, Brescia, Italy
关键词
COVID-19; angiotensin-converting enzyme inhibitors; angiotensin receptor inhibitors;
D O I
10.4081/itjm.2020.1313
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study aims to assess the effect of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor inhibitors (ARBs) on the course of COVID-19. It is a prospective study on 221 (M/F ratio= 143/78, mean age 72 +/- 13) consecutive hypertensive patients with COVID-19: 76 (34.4%) treated with ACEIs, 63 (28.5%) with ARBs and 82 (37.1%) with antihypertensives OTHER than ACEIs or ARBs. They were all followed up until discharge or death. BAD outcome was defined as the need for invasive mechanical ventilation or death. The three classes of medication were well balanced for confounding variables. BAD outcome was overall recorded in 63/221 (28%) patients, in 20/76 (26%) of ACEI, in 17/63 (27%) of ARB and in 26/82 (32%) of OTHER users, with no statistically significant difference in any comparison. These findings refute the hypothesis that treatment with ACEIs or ARBs may negatively affect the course of COVID-19.
引用
收藏
页码:162 / 166
页数:5
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