Pulmonary artery pressure monitoring in chronic heart failure: effects across clinically relevant subgroups in the MONITOR-HF trial.

Randomized controlled trial pulmonary artery pressure quality of life sensor subgroups telemonitoring

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
11 May 2024
Historique:
received: 08 04 2024
revised: 03 05 2024
accepted: 09 05 2024
medline: 11 5 2024
pubmed: 11 5 2024
entrez: 11 5 2024
Statut: aheadofprint

Résumé

In patients with chronic heart failure (HF), the MONITOR-HF trial demonstrated the efficacy of pulmonary artery (PA)-guided HF therapy over standard of care in improving quality of life and reducing HF hospitalizations and mean PA pressure. This study aimed to evaluate the consistency of these benefits in relation to clinically relevant subgroups. The effect of PA-guided HF therapy was evaluated in the MONITOR-HF trial among predefined subgroups based on age, sex, atrial fibrillation, diabetes mellitus, left ventricular ejection fraction, HF aetiology, cardiac resynchronisation therapy, and implantable cardioverter defibrillator. Outcome measures were based upon significance in the main trial and included quality of life, clinical, and PA pressure endpoints, and were assessed for each subgroup. Differential effects in relation to the subgroups were assessed with interaction terms. Both unadjusted and multiple testing adjusted interaction terms were presented. The effects of PA monitoring on quality of life, clinical events, and PA pressure were consistent in the predefined subgroups, without any clinically relevant heterogeneity within or across all endpoint categories (all adjusted interaction P-values were nonsignificant). In the unadjusted analysis of the primary endpoint quality-of-life change, weak trends towards a less pronounced effect in older patients (Pinteraction = 0.03; adjusted Pinteraction = 0.33) and diabetics (Pinteraction = 0.01; adjusted Pinteraction = 0.06) were observed. However, these interaction effects did not persist after adjusting for multiple testing. This subgroup analysis confirmed the consistent benefits of PA-guided HF therapy observed in the MONITOR-HF trial across clinically relevant subgroups, highlighting its efficacy in improving quality of life, clinical, and PA pressure endpoints in chronic HF patients.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
In patients with chronic heart failure (HF), the MONITOR-HF trial demonstrated the efficacy of pulmonary artery (PA)-guided HF therapy over standard of care in improving quality of life and reducing HF hospitalizations and mean PA pressure. This study aimed to evaluate the consistency of these benefits in relation to clinically relevant subgroups.
METHODS METHODS
The effect of PA-guided HF therapy was evaluated in the MONITOR-HF trial among predefined subgroups based on age, sex, atrial fibrillation, diabetes mellitus, left ventricular ejection fraction, HF aetiology, cardiac resynchronisation therapy, and implantable cardioverter defibrillator. Outcome measures were based upon significance in the main trial and included quality of life, clinical, and PA pressure endpoints, and were assessed for each subgroup. Differential effects in relation to the subgroups were assessed with interaction terms. Both unadjusted and multiple testing adjusted interaction terms were presented.
RESULTS RESULTS
The effects of PA monitoring on quality of life, clinical events, and PA pressure were consistent in the predefined subgroups, without any clinically relevant heterogeneity within or across all endpoint categories (all adjusted interaction P-values were nonsignificant). In the unadjusted analysis of the primary endpoint quality-of-life change, weak trends towards a less pronounced effect in older patients (Pinteraction = 0.03; adjusted Pinteraction = 0.33) and diabetics (Pinteraction = 0.01; adjusted Pinteraction = 0.06) were observed. However, these interaction effects did not persist after adjusting for multiple testing.
CONCLUSIONS CONCLUSIONS
This subgroup analysis confirmed the consistent benefits of PA-guided HF therapy observed in the MONITOR-HF trial across clinically relevant subgroups, highlighting its efficacy in improving quality of life, clinical, and PA pressure endpoints in chronic HF patients.

Identifiants

pubmed: 38733175
pii: 7668040
doi: 10.1093/eurheartj/ehae323
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

P R D Clephas (PRD)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

V W Zwartkruis (VW)

Department of Cardiology, University Medical Centre Groningen, Groningen, Netherlands.

J Malgie (J)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

M W F van Gent (MWF)

Department of Cardiology, Albert Schweitzer Hospital, Dordrecht, Netherlands.

H P Brunner-La Rocca (HP)

Department of Cardiology, Maastricht University Medical Centre, Maastricht, Netherlands.

M K Szymanski (MK)

Department of Cardiology, University Medical Center Utrecht, Utrecht, Netherlands.

V P van Halm (VP)

Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, Netherlands.

M L Handoko (ML)

Department of Cardiology, University Medical Center Utrecht, Utrecht, Netherlands.

W Kok (W)

Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, Netherlands.

F W Asselbergs (FW)

Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, Netherlands.

R van Kimmenade (R)

Department of Cardiology, Radboud University Medical Centre, Nijmegen, Netherlands.

O Manintveld (O)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

N M D A van Mieghem (NMDA)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

S L M A Beeres (SLMA)

Department of Cardiology, Leiden University Medical Centre, Leiden, Netherlands.

M C Post (MC)

Department of Cardiology, University Medical Center Utrecht, Utrecht, Netherlands.
Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.

C J W Borleffs (CJW)

Department of Cardiology, HAGA Hospital, Den Haag, Netherlands.

R Tukkie (R)

Department of Cardiology, Spaarne Hospital, Haarlem, Netherlands.

A Mosterd (A)

Department of Cardiology, Meander Medical Centre, Amersfoort, Netherlands.

G C M Linssen (GCM)

Department of Cardiology, Hospital Group Twente, Almelo, Netherlands.

R F Spee (RF)

Department of Cardiology, Maxima Medical Centre, Veldhoven/Eindhoven, Netherlands.

M E Emans (ME)

Department of Cardiology, Ikazia hospital, Rotterdam, Netherlands.

T D J Smilde (TDJ)

Department of Cardiology, Scheeper Hospital TREANT, Emmen, Netherlands.

J van Ramshorst (J)

Department of Cardiology, Noordwest Hospital group, Alkmaar, Netherlands.

C Kirchhof (C)

Department of Cardiology, Alrijne Hospital, Leiderdorp, Netherlands.

F Feenema-Aardema (F)

Department of Cardiology, Medical Centre Leeuwarden, Leeuwarden, Netherlands.

C A da Fonseca (CA)

Department of Cardiology, Medical Centre Leeuwarden, Leeuwarden, Netherlands.

M van den Heuve (M)

Department of Cardiology, Department of Cardiology, Medisch Spectrum Twente, Enschede, Netherlands.

R Hazeleger (R)

Department of Cardiology, Vie Curi Hospital, Venlo, Netherlands.

M van Eck (M)

Department of Cardiology, Jeroen Bosch Hospital, 's-Hertogenbosch, Netherlands.

L van Heerebeek (L)

Department of Cardiology, OLVG Hospital, Amsterdam, Netherlands.

H Boersma (H)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

M Rienstra (M)

Department of Cardiology, University Medical Centre Groningen, Groningen, Netherlands.

R A de Boer (RA)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

J J Brugts (JJ)

Department of Cardiology, Thorax centre, Cardiovascular institute, Erasmus University Medical Center, Rotterdam, Netherlands.

Classifications MeSH