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Review
. 2024 Jan 16:13:2023-8-1.
doi: 10.7573/dic.2023-8-1. eCollection 2024.

Vulnerable period in heart failure: a window of opportunity for the optimization of treatment - a statement by Mexican experts

Affiliations
Review

Vulnerable period in heart failure: a window of opportunity for the optimization of treatment - a statement by Mexican experts

José Antonio Magaña Serrano et al. Drugs Context. .

Erratum in

Abstract

Acute heart failure (HF) is associated with poor prognosis. After the acute event, there is a vulnerable period during which the patient has a marked risk of readmission or death. Therefore, early optimization of treatment is mandatory during the vulnerable period. The objective of this article is to provide recommendations to address the management of patients with HF during the vulnerable period from a practical point of view. A group of Mexican experts met to prepare a consensus document. The vulnerable period, with a duration of up to 6 months after the acute event - either hospitalization, visit to the emergency department or the outpatient clinic/day hospital - represents a real window of opportunity to improve outcomes for these patients. To best individualize the recommendations, the management strategies were divided into three periods (early, intermediate and late vulnerable period), including not only therapeutic options but also evaluation and education. Importantly, the recommendations are addressed to the entire cardiology team, including physicians and nurses, but also other specialists implicated in the management of these patients. In conclusion, this document represents an opportunity to improve the management of this population at high risk, with the aim of reducing the burden of HF.

Keywords: acute; decompensation; heart failure; treatment; vulnerable period.

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Conflict of interest statement

Disclosure and potential conflicts of interest: JAMS: speaker, advisor and researcher for AstraZeneca, Bayer México S.A., M8, Novartis, Roche, Servier, Silanes. The author received no compensation or commercial guidance for the creation of this manuscript. JACL: speaker, advisor and researcher for AstraZeneca, Pfizer, Bayer México S.A., M8, Novartis, Roche, Silanes, Armstrong. The author received no compensation or commercial guidance for the creation of this manuscript. ACM has worked advising Bayer and other laboratories on issues regarding heart failure. JBIM is speaker or advisor for AstraZeneca, M8, Novartis, Servier, Merck. GHMZ is speaker or advisor for AstraZeneca, Bayer, Boehringer Ingelheim, Eli-Lilly, Novartis, Servier. LOD is speaker for Novartis, Amgen. GML is speaker or advisor for AstraZeneca, Bayer, Boehringer Ingelheim, Eli-Lilly, Novartis, Servier. LFAM has worked advising Bayer and other laboratories on issues regarding heart failure. PLNE: speaker for Menarini and Novartis. SACL, JEPB, EHHG, RPM declare no conflict of interest in relation to this article. None of the authors have received compensation or commercial guidance for the creation of this manuscript. The International Committee of Medical Journal Editors (ICMJE) Potential Conflicts of Interests form for the authors is available for download at: https://www.drugsincontext.com/wp-content/uploads/2023/12/dic.2023-8-1-COI.pdf

Figures

Figure 1
Figure 1
Evaluation of congestive symptoms. HF, heart failure.
Figure 2
Figure 2
Diuretic adjustment during acute HF episode.a aThe use of loop diuretics should be limited to the control of congestion. bIf the patient is already taking mineralocorticoid receptor antagonists (MRAs) and no marked deterioration of renal function or hyperkalaemia is observed, maintain MRA treatment. cConsider the introduction of MRAs in case of naive patients (or uptitration of MRA dosage if already taking) to increase diuresis. dConsider the introduction of MRAs in case of naive patients when reduction of loop diuretics dose starts, in patients without marked deterioration of renal function or hyperkalaemia.
Figure 3
Figure 3
Checklist in pre-discharge and early follow-up of patients with HF. ACEI, angiotensin-converting enzyme inhibitors; ARNI, angiotensin receptor-neprilysin inhibitor; BB, beta-blocker; MRA, mineralocorticoid receptor antagonist; SGLT2i, sodium–glucose cotransporter 2 inhibitors.
Figure 4
Figure 4
Comprehensive strategy for evaluation and management of patients with heart failure during the vulnerable period. CCT, cardiac computed tomography; CV, cardiovascular; DMHFD, disease-modifying HF drugs; EQ-5D, EuroQol-5D; HF, heart failure; KCCQ, Kansas City Cardiomyopathy Questionnaire; MLHFQ, Minnesota Living-With-Heart-Failure Questionnaire; MRI, magnetic resonance imaging; NM, nuclear medicine.

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