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December 17, 2010European Journal of Heart Failure127 citationsOpen Access

Direct Renin Inhibition in Addition to or as an Alternative to Angiotensin Converting Enzyme Inhibition in Patients with Chronic Systolic Heart Failure: Rationale and Design of the Aliskiren Trial to Minimize OutcomeS in Patients with HEart failuRE (ATMOSPHERE) Study

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HKHenry KrumBMBarry M. MassieWAWilliam T. Abraham

Key Result

Aliskiren monotherapy and aliskiren/enalapril combination therapy will be compared to enalapril monotherapy in approximately 7000 randomized patients for cardiovascular death or HF hospitalization.

Study Design

Type

RCT (n=7,000)

Randomization

1:1:1

Structured PICO

Does aliskiren monotherapy or aliskiren/enalapril combination therapy reduce cardiovascular death or HF hospitalization compared to enalapril monotherapy in patients with chronic systolic heart failure?

P
Population
Approximately 7000 patients with chronic systolic heart failure, NYHA functional class II-IV symptoms, elevated plasma levels of BNP, and tolerant to at least 10 mg or equivalent of enalapril.
I
Intervention
Aliskiren monotherapy or aliskiren/enalapril combination therapy
C
Comparator
Enalapril monotherapy
O
Outcome
Time to first occurrence of cardiovascular death or HF hospitalizationcomposite

The ATMOSPHERE study is designed to evaluate whether the direct renin inhibitor aliskiren, alone or in combination with enalapril, is superior or non-inferior to enalapril monotherapy in patients with chronic systolic heart failure.

Abstract

AIMS: The renin-angiotensin-aldosterone system (RAAS) represents a key therapeutic target in heart failure (HF) management. However, conventional agents that block this system induce a reflex increase in plasma renin activity (PRA), which may lead to RAAS 'escape'. Direct renin inhibitors (DRIs) have been developed that decrease PRA and thus may provide a greater RAAS blockade. Aliskiren is the first orally active DRI. Plasma levels of B-type natriuretic peptide (BNP) have been observed to be reduced with aliskiren compared with placebo. The aim of the Aliskiren Trial of Minimizing OutcomeS for Patients with HEart failuRE (ATMOSPHERE) study is to evaluate the effect of both aliskiren and enalapril monotherapy and aliskiren/enalapril combination therapy on cardiovascular death and HF hospitalization in patients with chronic systolic HF, NYHA functional class II-IV symptoms, and elevated plasma levels of BNP. Methods Patients tolerant to at least 10 mg or equivalent of enalapril will undergo an open-label run-in period where they receive enalapril then aliskiren. Approximately 7000 patients tolerating this run-in period will then be randomized 1:1:1 to aliskiren monotherapy, enalapril monotherapy, or the combination. The primary endpoints of ATMOSPHERE are (i) whether the aliskiren/enalapril combination is superior to enalapril monotherapy in delaying time to first occurrence of cardiovascular death or HF hospitalization and (ii) whether aliskiren monotherapy is superior or at least non-inferior to enalapril monotherapy on this endpoint. Perspective The ATMOSPHERE study will definitively determine the role of a DRI strategy additional to or as an alternative to conventional RAAS blockade in patients with chronic systolic HF.

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Cite This Study

Krum et al. (2010) conducted an RCT in Chronic systolic heart failure (n=7,000). Aliskiren monotherapy or aliskiren/enalapril combination therapy vs. Enalapril monotherapy was evaluated on Time to first occurrence of cardiovascular death or HF hospitalization. Aliskiren monotherapy and aliskiren/enalapril combination therapy will be compared to enalapril monotherapy in approximately 7000 randomized patients for cardiovascular death or HF hospitalization.

synapsesocial.com/papers/6a159d270c3a39952e9f895dhttps://doi.org/10.1093/eurjhf/hfq212
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