Mortality from angiotensin-converting enzyme-inhibitors and angiotensin receptor blockers in people infected with COVID-19: a cohort study of 3.7 million people.
Mortality from angiotensin-converting enzyme-inhibitors and angiotensin receptor blockers in people infected with COVID-19: a cohort study of 3.7 million people.
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DOI:
10.1093/fampra/cmac094
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发表时间:
2023-03-28
期刊:
影响因子:
2.2
通讯作者:
中科院分区:
文献类型:
--
作者:
Concerns have been raised that angiotensin-converting enzyme-inhibitors (ACE-I) and angiotensin receptor blockers (ARBs) might facilitate transmission of severe acute respiratory syndrome coronavirus 2 leading to more severe coronavirus disease (COVID-19) disease and an increased risk of mortality. We aimed to investigate the association between ACE-I/ARB treatment and risk of death amongst people with COVID-19 in the first 6 months of the pandemic. We identified a cohort of adults diagnosed with either confirmed or probable COVID-19 (from 1 January to 21 June 2020) using computerized medical records from the Oxford-Royal College of General Practitioners (RCGP) Research and Surveillance Centre (RSC) primary care database. This comprised 465 general practices in England, United Kingdom with a nationally representative population of 3.7 million people. We constructed mixed-effects logistic regression models to quantify the association between ACE-I/ARBs and all-cause mortality among people with COVID-19, adjusted for sociodemographic factors, comorbidities, concurrent medication, smoking status, practice clustering, and household number. There were 9,586 COVID-19 cases in the sample and 1,463 (15.3%) died during the study period between 1 January 2020 and 21 June 2020. In adjusted analysis ACE-I and ARBs were not associated with all-cause mortality (adjusted odds ratio [OR] 1.02, 95% confidence interval [CI] 0.85–1.21 and OR 0.84, 95% CI 0.67–1.07, respectively). Use of ACE-I/ARB, which are commonly used drugs, did not alter the odds of all-cause mortality amongst people diagnosed with COVID-19. Our findings should inform patient and prescriber decisions concerning continued use of these medications during the pandemic.
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DOI:
10.3399/bjgp20x713393
发表时间:
2020-12
期刊:
The British journal of general practice : the journal of the Royal College of General Practitioners
影响因子:
--
作者:
Joy M;Hobbs FR;Bernal JL;Sherlock J;Amirthalingam G;McGagh D;Akinyemi O;Byford R;Dabrera G;Dorward J;Ellis J;Ferreira F;Jones N;Oke J;Okusi C;Nicholson BD;Ramsay M;Sheppard JP;Sinnathamby M;Zambon M;Howsam G;Williams J;de Lusignan S
通讯作者:
de Lusignan S
影响因子:
8.5
作者:
de Lusignan S;McGee C;Webb R;Joy M;Byford R;Yonova I;Hriskova M;Matos Ferreira F;Elliot AJ;Smith G;Rafi I
通讯作者:
Rafi I
影响因子:
8.5
作者:
de Lusignan S;Liyanage H;McGagh D;Jani BD;Bauwens J;Byford R;Evans D;Fahey T;Greenhalgh T;Jones N;Mair FS;Okusi C;Parimalanathan V;Pell JP;Sherlock J;Tamburis O;Tripathy M;Ferreira F;Williams J;Hobbs FDR
通讯作者:
Hobbs FDR
DOI:
10.1152/ajplung.00498.2016
发表时间:
2018-01-01
影响因子:
4.9
作者:
Sodhi, Chhinder P.;Wohlford-Lenane, Christine;Jia, Hongpeng
通讯作者:
Jia, Hongpeng
影响因子:
4.5
作者:
de Lusignan, Simon;Sherlock, Julian;Joy, Mark
通讯作者:
Joy, Mark