Blood Pressure Drops During Hospitalization for Acute Heart Failure Treated With Serelaxin: A Patient-Level Analysis of 4 Randomized Controlled Trials.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 22 2 2022
medline: 22 4 2022
entrez: 21 2 2022
Statut: ppublish

Résumé

Hypotensive events and drops in systolic blood pressure (SBP-drop) are frequent in patients hospitalized with acute heart failure. We investigated whether SBP-drops are associated with outcomes in patients treated with serelaxin. Patient-level retrospective analyses of 4 prospective trials investigating serelaxin in acute heart failure. Main inclusion criteria were SBP 125 to 180 mm Hg, pulmonary congestion, and elevated NT-proBNP (N-terminal pro-B-type natriuretic peptide). SBP-drops were prospectively defined as SBP<100 mm Hg, or, if SBP remained >100 mm Hg, a drop from baseline of 40 mm Hg from baseline. Outcomes were a short-term composite outcome (worsening heart failure, hospital readmission for heart failure or all-cause mortality through 14 days) and 180-day mortality. Overall, 2559/11 226 (23%) patients had an SBP-drop. SBP-drop, versus no SBP-drop, was associated with a worse outcome: cumulative incidence of 180-day mortality (11% versus 9%, hazard ratio [HR]. 1.21 [95% CI, 1.05-1.39]; SBP-drops in patients with acute heart failure and normal to high SBP at admission is associated with worse short- and long-term outcomes especially for SBP <100 mm Hg. However, in patients treated with the intravenous vasodilator serelaxin, SBP-drops seemed less harmful. URL: https://www. gov; Unique identifiers: NCT02064868, NCT02007720, NCT01870778, NCT00520806.

Sections du résumé

BACKGROUND
Hypotensive events and drops in systolic blood pressure (SBP-drop) are frequent in patients hospitalized with acute heart failure. We investigated whether SBP-drops are associated with outcomes in patients treated with serelaxin.
METHODS
Patient-level retrospective analyses of 4 prospective trials investigating serelaxin in acute heart failure. Main inclusion criteria were SBP 125 to 180 mm Hg, pulmonary congestion, and elevated NT-proBNP (N-terminal pro-B-type natriuretic peptide). SBP-drops were prospectively defined as SBP<100 mm Hg, or, if SBP remained >100 mm Hg, a drop from baseline of 40 mm Hg from baseline. Outcomes were a short-term composite outcome (worsening heart failure, hospital readmission for heart failure or all-cause mortality through 14 days) and 180-day mortality.
RESULTS
Overall, 2559/11 226 (23%) patients had an SBP-drop. SBP-drop, versus no SBP-drop, was associated with a worse outcome: cumulative incidence of 180-day mortality (11% versus 9%, hazard ratio [HR]. 1.21 [95% CI, 1.05-1.39];
CONCLUSIONS
SBP-drops in patients with acute heart failure and normal to high SBP at admission is associated with worse short- and long-term outcomes especially for SBP <100 mm Hg. However, in patients treated with the intravenous vasodilator serelaxin, SBP-drops seemed less harmful.
REGISTRATION
URL: https://www.
CLINICALTRIALS
gov; Unique identifiers: NCT02064868, NCT02007720, NCT01870778, NCT00520806.

Identifiants

pubmed: 35184572
doi: 10.1161/CIRCHEARTFAILURE.121.009199
doi:

Substances chimiques

Recombinant Proteins 0
Vasodilator Agents 0
serelaxin protein, human 0
Relaxin 9002-69-1

Banques de données

ClinicalTrials.gov
['NCT01870778', 'NCT02064868', 'NCT02007720', 'NCT00520806']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e009199

Auteurs

Johannes Grand (J)

Department of Cardiology Bispebjerg Hospital (J.G., K.M., A.S., O.W.N.), University of Copenhagen, Denmark.

Kristina Miger (K)

Department of Cardiology Bispebjerg Hospital (J.G., K.M., A.S., O.W.N.), University of Copenhagen, Denmark.

Ahmad Sajadieh (A)

Department of Cardiology Bispebjerg Hospital (J.G., K.M., A.S., O.W.N.), University of Copenhagen, Denmark.

Lars Køber (L)

Department of Cardiology, Rigshospitalet (L.K.), University of Copenhagen, Denmark.

Christian Torp-Pedersen (C)

Department of Cardiology, Hillerød Hospital, Denmark (C.T.-P.).

Georg Ertl (G)

German Comprehensive Heart Failure Center, Department of Internal Medicine I, University Hospital Würzburg (G.E.).

José López-Sendón (J)

IdiPaz Research Institute, Hospital La Paz, Autonomous University of Madrid, Spain (J.L.-S.).

Aldo Pietro Maggioni (A)

Associazione Nazionale Medicin Cardiologi Ospedalieri Research Center, Florence, Italy (A.P.M.).
Maria Cecilia Hospital, GVM Care & Research, Cotignola, Italy (A.P.M.).

John R Teerlink (JR)

Section of Cardiology, San Francisco Veterans Affairs Medical Center and School of Medicine, University of California San Francisco (J.R.T.).

Naoki Sato (N)

Department of Cardiovascular Medicine, Kawaguchi Cardiovascular and Respiratory Hospital, Saitama, Japan (N.S.).

Claudio Gimpelewicz (C)

Novartis Pharma AG, Basel, Switzerland (C.G., T.H.).

Marco Metra (M)

ASST Spedali Civili and Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Italy (M.M.).

Thomas Holbro (T)

Novartis Pharma AG, Basel, Switzerland (C.G., T.H.).

Olav W Nielsen (OW)

Department of Cardiology Bispebjerg Hospital (J.G., K.M., A.S., O.W.N.), University of Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences (O.W.N.), University of Copenhagen, Denmark.

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