scholarly journals Association between renin–angiotensin system antagonist use and mortality in heart failure with severe renal insufficiency: a prospective propensity score-matched cohort study

2015 ◽  
Vol 36 (34) ◽  
pp. 2318-2326 ◽  
Author(s):  
Magnus Edner ◽  
Lina Benson ◽  
Ulf Dahlström ◽  
Lars H. Lund
2020 ◽  
Vol 32 ◽  
pp. 120-130
Author(s):  
Ole Köhler-Forsberg ◽  
Liselotte Petersen ◽  
Michael Berk ◽  
Christiane Gasse ◽  
Søren Dinesen Østergaard

2018 ◽  
Vol 266 ◽  
pp. 180-186 ◽  
Author(s):  
Se Yong Jang ◽  
Shung Chull Chae ◽  
Myung Hwan Bae ◽  
Jang Hoon Lee ◽  
Dong Heon Yang ◽  
...  

2020 ◽  
Author(s):  
Shamil Haroon ◽  
Anuradhaa Subramanian ◽  
Jennifer Cooper ◽  
Astha Anand ◽  
Krishna Gokhale ◽  
...  

Abstract IntroductionRenin-angiotensin system (RAS) inhibitors have been postulated to influence susceptibility to Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). This study investigated whether there is an association between their prescription and the incidence of COVID-19 and all-cause mortality.MethodsWe conducted a propensity-score matched cohort study comparing the incidence of COVID-19 among patients with hypertension prescribed ACE inhibitors or ARBs to those treated with calcium channel blockers (CCBs) in a large UK-based primary care database (The Health Improvement Network). We estimated crude incidence rates for confirmed/suspected COVID-19 in each drug exposure group. We used Cox proportional hazards models to produce adjusted hazard ratios for COVID-19. We assessed all-cause mortality as a secondary outcome. ResultsThe incidence rate of COVID-19 among users of ACE inhibitors and CCBs was 9.3 per 1000 person-years (83 of 18,895 users [0.44%]) and 9.5 per 1000 person-years (85 of 18,895 [0.45%]), respectively. The adjusted hazard ratio was 0.92 (95% CI 0.68 to 1.26). The incidence rate among users of ARBs was 15.8 per 1000 person-years (79 out of 10,623 users [0.74%]). The adjusted hazard ratio was 1.38 (95% CI 0.98 to 1.95). There were no significant associations between use of RAS inhibitors and all-cause mortality. ConclusionUse of ACE inhibitors was not associated with the risk of COVID-19 whereas use of ARBs was associated with a statistically non-significant increase compared to the use of CCBs. However, no significant associations were observed between prescription of either ACE inhibitors or ARBs and all-cause mortality.


Cardiology ◽  
2010 ◽  
Vol 116 (4) ◽  
pp. 279-285 ◽  
Author(s):  
Sheng-Nan Chang ◽  
Jou-Wie Lin ◽  
Jyh-Ming Juang ◽  
Chai-Ti Tsai ◽  
Juey-Jen Hwang ◽  
...  

2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110414
Author(s):  
Jing Lin ◽  
Liu He ◽  
Qing Qiao ◽  
Xin Du ◽  
Chang-Sheng Ma ◽  
...  

Objective The effect of renin–angiotensin system inhibitors (RASIs) in patients with heart failure (HF) and atrial fibrillation (AF) remains unclear. This study aimed to investigate associations between RASI use and all-cause mortality and cardiovascular outcomes in patients with AF and HF. Methods Using data from the China Atrial Fibrillation Registry study, we included 938 patients with AF and HF with a left ventricular ejection fraction <50%. Cox regression models for RASIs vs. non-RASIs with all-cause mortality as the primary outcome were fitted in a 1:1 propensity score-matched cohort. A sensitivity analysis was performed by using a multivariable time-dependent Cox regression model. As an internal control, we assessed the relation between β-blocker use and all-cause mortality. Results During a mean follow-up of 35 months, the risk of all-cause mortality was similar in RASI users compared with non-users (hazard ratio: 0.92; 95% confidence interval: 0.67–1.26). Similar results were obtained in the sensitivity analysis. In contrast, β-blocker use was associated with significantly lower all-cause mortality in the same population. Conclusions RASI use was not associated with better outcomes in patients with AF and HF in this prospective cohort, which raises questions about their value in this specific subset. Trail Registration: ChiCTR-OCH-13003729.


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