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Review
. 2021 Dec;8(6):4444-4453.
doi: 10.1002/ehf2.13646. Epub 2021 Oct 16.

'Time is prognosis' in heart failure: time-to-treatment initiation as a modifiable risk factor

Affiliations
Review

'Time is prognosis' in heart failure: time-to-treatment initiation as a modifiable risk factor

Amr Abdin et al. ESC Heart Fail. 2021 Dec.

Abstract

In heart failure (HF), acute decompensation can occur quickly and unexpectedly because of worsening of chronic HF or to new-onset HF diagnosed for the first time ('de novo'). Patients presenting with acute HF (AHF) have a poor prognosis comparable with those with acute myocardial infarction, and any delay of treatment initiation is associated with worse outcomes. Recent HF guidelines and recommendations have highlighted the importance of a timely diagnosis and immediate treatment for patients presenting with AHF to decrease disease progression and improve prognosis. However, based on the available data, there is still uncertainty regarding the optimal 'time-to-treatment' effect in AHF. Furthermore, the immediate post-worsening HF period plays an important role in clinical outcomes in HF patients after hospitalization and is known as the 'vulnerable phase' characterized by high risk of readmission and early death. Early and intensive treatment for HF patients in the 'vulnerable phase' might be associated with lower rates of early readmission and mortality. Additionally, in the chronic stable HF outpatient, treatments are often delayed or not initiated when symptoms are stable, ignoring the risk for adverse outcomes such as sudden death. Consequently, there is a dire need to better identify HF patients during hospitalization and after discharge and treating them adequately to improve their prognosis. HF is an urgent clinical scenario along all its stages and disease conditions. Therefore, time plays a significant role throughout the entire patient's journey. Therapy should be optimized as soon as possible, because this is beneficial regardless of severity or duration of HF. Time lavished before treatment initiation is recognized as important modifiable risk factor in HF.

Keywords: Heart failure; Prognosis; Treatment.

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Conflict of interest statement

A.A. received speaker's honoraria from Novartis and travel grants from Biotronik and Novartis. S.D.A. received honoraria for lectures and scientific advice from Vifor, Bayer, Boehringer Ingelheim, Novartis, Servier, Abbott, Actimed, Cardiac Dimensions, and Impulse Dynamics. J.B. received honoraria for lectures and scientific advice from Abbott, Adrenomed, Amgen, Applied Therapeutics, Array, AstraZeneca, Bayer, Boehringer Ingelheim, CVRx, G3 Pharma, Novartis, BI‐Lilly, and Janssen. A.J.S.C. received grants and personal fees from Vifor International and personal fees from AstraZeneca, Bayer, Boehringer Ingelheim, Menarini, Novartis, Nutricia, Servier, Vifor, Abbott, Actimed, Arena, Cardiac Dimensions, Corvia, CVRx, Enopace, ESN Cleer, Faraday, Gore, Impulse Dynamics, and Respicardia. I.K. reports personal fees from Akcea Therapeutics Germany GmbH, AstraZeneca, Bayer Vital GmbH, Boehringer Ingelheim, Bristol Myers Squibb Company, Hexal AG, Novartis, Pfizer Pharma GmbH, Servier Deutschland GmbH, Vifor, and Daiichi Sankyo Deutschland GmbH. M.L. reports personal fees from AstraZeneca, Bayer, Boehringer Ingelheim, Vifor Pharma, and Novartis. L.H.L. received grants and personal fees from Relypsa, Boehringer Ingelheim, and Novartis, grants from Boston Scientific, and personal fees from Merck, Vifor Fresenius, AstraZeneca, Bayer, Pharmacosmos, Abbott, Medscape, Myokardia, Sanofi, Lexicon, and Mundipharma. M.M. received personal fees and non‐financial support from Amgen, Abbott Vascular, and Bayer and personal fees from Servier, AstraZeneca, Edwards Therapeutics, Vifor Pharma, Actelion, LivaNova, and Windtree Therapeutics. W.M. received research grants from Novartis, Vifor, Medtronic, Biotronik, Abbott, and Boston Scientific. M.B. reports personal fees from Abbott, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Cytokinetics, Medtronic, Novartis, Servier, and Vifor.

Figures

Figure 1
Figure 1
In‐hospital mortality is high after acute decompensation (left, 4–6%). In the post‐discharge phase, rehospitalization rate (depicted by arrow) and death are higher (10–30% death or rehospitalization) than in the chronic outpatient heart failure population (40–50% 5 year mortality). The figure shows landmark heart failure trials during the period where patients were included in those studies (in‐hospital and pre‐discharge, early post‐hospitalization—vulnerable phase, and in the chronic phase). Also, this figure shows which trial did or did not meet its primary endpoints. Data taken from several studies., , , , , , , ,
Figure 2
Figure 2
(A) Association of door‐to‐furosemide time with probability of in‐hospital mortality. (B) Duration to time‐to‐first intravenous (IV) diuretic treatment on the intensive care unit (ICU), general ward, or emergency ward in North America (upper panel) Western Europe (middle panel) and Eastern Europe (lower panel). (C) Recommendation for a timely evaluation, diagnosis, and IV start of diuretic treatments after arrival in the emergency department (ED) after onset of acute heart failure (AHF) symptoms. Data taken from Matsue et al. and Filippatos et al.,
Figure 3
Figure 3
A schematic scheme of the association of outcomes, treatment initiation, missed opportunities, and potential benefits of early intervention in heart failure patients. Data taken from Böhm et al.

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