Effect of Chronic Digoxin Use on Mortality and Heart Failure Hospitalization in Pulmonary Arterial Hypertension.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
21 03 2023
Historique:
pubmed: 10 3 2023
medline: 23 3 2023
entrez: 9 3 2023
Statut: ppublish

Résumé

Background Digoxin acutely increases cardiac output in patients with pulmonary arterial hypertension (PAH) and right ventricular failure; however, the effects of chronic digoxin use in PAH are unclear. Methods and Results Data from the Minnesota Pulmonary Hypertension Repository were used. The primary analysis used likelihood of digoxin prescription. The primary end point was a composite of all-cause mortality or heart failure (HF) hospitalization. Secondary end points included all-cause mortality, HF hospitalization, and transplant-free survival. Multivariable Cox proportional hazards analyses determined the hazard ratios (HR) and 95% CIs for the primary and secondary end points. Among 205 patients with PAH in the repository, 32.7% (n=67) were on digoxin. Digoxin was more often prescribed to patients with severe PAH and right ventricular failure. After propensity score-matching, 49 patients were digoxin users, and 70 patients were nonusers; of these 31 (63.3%) in the digoxin group and 41 (58.6%) in nondigoxin group met the primary end point during a median follow-up time of 2.1 (0.6-5.0) years. Digoxin users had a higher combined all-cause mortality or HF hospitalization (HR, 1.82 [95% CI, 1.11-2.99]), all-cause mortality (HR, 1.92 [95% CI, 1.06-3.49]), HF hospitalization (HR, 1.89 [95% CI, 1.07-3.35]), and worse transplant-free survival (HR, 2.00 [95% CI, 1.12-3.58]) even after adjusting for patient characteristics and severity of PAH and right ventricular failure. Conclusions In this retrospective, nonrandomized cohort, digoxin treatment was associated with greater all-cause mortality and HF hospitalization, even after multivariate correction. Future randomized controlled trials should assess the safety and efficacy of chronic digoxin use in PAH.

Identifiants

pubmed: 36892094
doi: 10.1161/JAHA.122.027559
pmc: PMC10111549
doi:

Substances chimiques

Digoxin 73K4184T59

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e027559

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL162927
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL144472
Pays : United States
Organisme : NHLBI NIH HHS
ID : K24 HL159246
Pays : United States
Organisme : NHLBI NIH HHS
ID : K08 HL140100
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL158795
Pays : United States

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Auteurs

Kevin Y Chang (KY)

Cardiovascular Division, Department of Medicine University of Minnesota Minneapolis MN USA.

Katherine Giorgio (K)

Division of Epidemiology and Community Health, School of Public Health University of Minnesota Minneapolis MN USA.

Katlin Schmitz (K)

Cardiovascular Division, Department of Medicine University of Minnesota Minneapolis MN USA.

Rob F Walker (RF)

Division of Epidemiology and Community Health, School of Public Health University of Minnesota Minneapolis MN USA.

Kurt W Prins (KW)

Cardiovascular Division, Department of Medicine University of Minnesota Minneapolis MN USA.

Marc R Pritzker (MR)

Cardiovascular Division, Department of Medicine University of Minnesota Minneapolis MN USA.

Stephen L Archer (SL)

Department of Medicine Queen's University Kingston Ontario Canada.

Pamela L Lutsey (PL)

Division of Epidemiology and Community Health, School of Public Health University of Minnesota Minneapolis MN USA.

Thenappan Thenappan (T)

Cardiovascular Division, Department of Medicine University of Minnesota Minneapolis MN USA.

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Classifications MeSH