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Editorial
. 2016 Jun;3(2):65-70.
doi: 10.1002/ehf2.12092. Epub 2016 Apr 25.

Acute heart failure facts and numbers: acute heart failure populations

Affiliations
Editorial

Acute heart failure facts and numbers: acute heart failure populations

Julia Searle et al. ESC Heart Fail. 2016 Jun.

Abstract

Acute heart failure (AHF) is a life-threatening emergency, which largely profits from early diagnosis and treatment. The prevalence of AHF is difficult to assess, estimates range between 1 and 12% in the general population. Despite recent therapeutic advances, in-hospital mortality is high with estimates varying from 4 and 18% in different registries. Due to large differences in AHF definitions and selection criteria AHF populations vary in their characteristics and outcomes. This is especially true for randomized clinical trials and the external validity of some of these trials is questionable. Additionally, the timing of data collection and/or initiation of new therapies vary with the setting of trials. The aim of this article is to call attention to the difference in AHF populations and to emphasize the need for research to clearly define these populations. AHF populations from registries and clinical trials are the basis for evidence-based management strategies. It is important that these populations represent the patients in whom these strategies will be applied in routine care.

Keywords: AHF cohort; Acute Heart Failure; Emergency Department; randomized controlled Trial (RCT); registry.

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Figures

Figure 1
Figure 1
Screening results for a large, international, multicentre randomized clinical trial on patients with AHF from 1 March 2014 until 31 July 2015. Only 3% (n = 9) of all patients screened for eligibility (n = 352) were enrolled. *Other (n = 45) includes patients who met the following exclusion criteria: surgical intervention or neurological events within the previous 30 days, terminal stage of a malignant disease, infiltration in chest X‐ray, restricted medication, aortic valve stenosis, participation in another study, patient not willing or not able to give informed consent, body weight > 160 kg, and patients without acute dyspnoea. RCT, randomized controlled trial.

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