TY - JOUR
T1 - Is the use of Renin-angiotensin System Inhibitors in Patients with Aortic Valve Stenosis Safe and of Prognostic benefit?
T2 - A systematic review and meta-analysis
AU - Andersson, Charlotte
AU - Abdulla, Jawdat
N1 - Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2016. For permissions please email: journals.permissions@oup.com.
PY - 2017/1
Y1 - 2017/1
N2 - BACKGROUND AND AIMS: Aortic valve stenosis (AVS) is associated with significant morbidity and mortality, especially in the presence of symptoms and echocardiographic signs of left ventricular remodeling (i.e., increase in left ventricular mass, left ventricular dilation, and systolic dysfunction). Renin-angiotensin system inhibitors (RASi) attenuate cardiac remodeling in various conditions, but the safety and efficacy of RASi in AVS is unsure. We performed a systematic review and meta-analysis to address these issues.METHODS AND RESULTS: We identified 3 smaller randomized clinical trials and 5 observational studies eligible for inclusion (Pubmed, EMBASE, and Cochrane library search criteria: aortic stenosis, aortic valve, angiotensin converting enzyme inhibitor in different combinations, published in English at any time up to April 1, 2016). Our analyses suggested that use of RASi was safe, with no observed increase in mortality risk (576/3389 patients receiving RASi vs. 1118/4384 controls died; relative risk 0.93 [95% confidence interval 0.78-1.11, p=0.44]). Use of RASi was also observed to lower the risk of aortic valve replacement (AVR) surgery (67/2913 patients with RASi vs. 154/3666 controls underwent AVR; relative risk 0.68 [95% confidence interval 0.51-0.91], p=0.01).CONCLUSIONS: In current clinical practice (based on published literature; mainly observational studies), use of RASi appears to be safe in patients with AVS and may reduce the need for AVR, but the evidence is overall weak. Large-scale randomized clinical trials are warranted to address whether prescription of RASi to treatment naïve patients may prevent disease progression, delay AVR surgery need, and lower the risk of mortality.
AB - BACKGROUND AND AIMS: Aortic valve stenosis (AVS) is associated with significant morbidity and mortality, especially in the presence of symptoms and echocardiographic signs of left ventricular remodeling (i.e., increase in left ventricular mass, left ventricular dilation, and systolic dysfunction). Renin-angiotensin system inhibitors (RASi) attenuate cardiac remodeling in various conditions, but the safety and efficacy of RASi in AVS is unsure. We performed a systematic review and meta-analysis to address these issues.METHODS AND RESULTS: We identified 3 smaller randomized clinical trials and 5 observational studies eligible for inclusion (Pubmed, EMBASE, and Cochrane library search criteria: aortic stenosis, aortic valve, angiotensin converting enzyme inhibitor in different combinations, published in English at any time up to April 1, 2016). Our analyses suggested that use of RASi was safe, with no observed increase in mortality risk (576/3389 patients receiving RASi vs. 1118/4384 controls died; relative risk 0.93 [95% confidence interval 0.78-1.11, p=0.44]). Use of RASi was also observed to lower the risk of aortic valve replacement (AVR) surgery (67/2913 patients with RASi vs. 154/3666 controls underwent AVR; relative risk 0.68 [95% confidence interval 0.51-0.91], p=0.01).CONCLUSIONS: In current clinical practice (based on published literature; mainly observational studies), use of RASi appears to be safe in patients with AVS and may reduce the need for AVR, but the evidence is overall weak. Large-scale randomized clinical trials are warranted to address whether prescription of RASi to treatment naïve patients may prevent disease progression, delay AVR surgery need, and lower the risk of mortality.
U2 - 10.1093/ehjcvp/pvw027
DO - 10.1093/ehjcvp/pvw027
M3 - Review
C2 - 27615013
VL - 3
SP - 21
EP - 27
JO - European Heart Journal - Cardiovascular Pharmacotherapy
JF - European Heart Journal - Cardiovascular Pharmacotherapy
SN - 2055-6837
IS - 1
ER -