Literature DB >> 27533962

ESC guidelines adherence is associated with improved survival in patients from the Norwegian Heart Failure Registry.

Jonathan De Blois1, Morten Wang Fagerland2, Morten Grundtvig3, Anne Grete Semb4, Lars Gullestad5, Arne Westheim6, Torstein Hole7, Dan Atar8, Stefan Agewall9.   

Abstract

AIMS: To assess the adherence to heart failure (HF) guidelines for angiotensin-converting enzyme-I (ACE-I), angiotensin II receptor blockers (ARB), and β-blockers and the possible association of ACE-I or ARB, β-blockers, and statins with survival in the large contemporary Norwegian Heart Failure Registry. METHODS AND
RESULTS: The study included 5761 outpatients who were diagnosed with HF of any aetiology (mean left ventricular ejection fraction 32% ± 11%) from January 2000 to January 2010 and followed up until death or February 2010. Adherence to treatment according to the guidelines was high. Cox regression analysis to identify risk factors for all-cause mortality, after adjustment for many factors, showed that ACE-I ≥ 50% of target dose, use of beta-blockers, and statins were significantly related to improved survival (P = 0.003, P < 0.001, and P < 0.001, respectively). Propensity scoring showed the same benefit for these variables.
CONCLUSIONS: Both multivariable and propensity scoring analyses showed survival benefits with β-blockers, statins, and adequate doses of ACE-I in this contemporary HF cohort. This study stresses the importance of guidelines adherence, even in the context of high levels of adherence to guidelines. Moreover, respecting the recommended target doses of ACE-I appears to have a crucial role in survival improvement and, in the multivariate Cox regression analysis, ARB treatment was not significantly associated with a lower all-cause mortality. Published on behalf of the European Society of Cardiology. All rights reserved. ©The Author 2015. For permissions please email: journals.permissions@oup.com.

Entities:  

Keywords:  ACE-I; Beta blockers; Guidelines; Heart failure

Mesh:

Substances:

Year:  2015        PMID: 27533962     DOI: 10.1093/ehjcvp/pvu010

Source DB:  PubMed          Journal:  Eur Heart J Cardiovasc Pharmacother


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