Efficacy and Safety of Direct Oral Anticoagulants for Stroke Prevention in Older Patients With Atrial Fibrillation: A Network Meta-Analysis of Randomized Controlled Trials.


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:
05 Dec 2023
Historique:
medline: 7 12 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: ppublish

Résumé

Although older patients with atrial fibrillation are at heightened risk of thromboembolic and bleeding events, their optimal treatment choice remains uncertain. This meta-analysis was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We searched the PubMed, EMBASE, and Cochrane databases for randomized controlled trials that compared thromboembolic or bleeding outcomes between a direct oral anticoagulant (DOAC) and a vitamin K antagonist (VKA) and reported outcomes for patients aged ≥75 years with atrial fibrillation. The efficacy outcome was the composite of stroke and systemic embolism. Safety outcomes included major bleeding, any clinically relevant bleeding, and intracranial hemorrhage. Each DOAC and VKA was compared pairwise in a network meta-analysis. High- and low-dose regimens and factor IIa and Xa inhibitors were also compared. Seven randomized controlled trials were included in the analysis. Stroke and systemic embolism risks did not differ significantly among DOACs. There were no significant differences in major bleeding between each DOAC and VKA. Intracranial hemorrhage risk was significantly lower with dabigatran, apixaban, and edoxaban than with VKA and rivaroxaban, which had similar risks. High-dose regimens led to lower risks of stroke or systemic embolism compared with VKA and low-dose regimens, with both doses having similar bleeding risks. In patients aged ≥75 years with atrial fibrillation, DOACs were associated with fewer thromboembolic events compared with VKA, whereas dabigatran, apixaban, and edoxaban were associated with lower risks of intracranial hemorrhage compared with VKA and rivaroxaban. URL: www.crd.york.ac.uk/prospero/. Unique identifier: CRD42022329557.

Sections du résumé

BACKGROUND BACKGROUND
Although older patients with atrial fibrillation are at heightened risk of thromboembolic and bleeding events, their optimal treatment choice remains uncertain.
METHODS AND RESULTS RESULTS
This meta-analysis was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We searched the PubMed, EMBASE, and Cochrane databases for randomized controlled trials that compared thromboembolic or bleeding outcomes between a direct oral anticoagulant (DOAC) and a vitamin K antagonist (VKA) and reported outcomes for patients aged ≥75 years with atrial fibrillation. The efficacy outcome was the composite of stroke and systemic embolism. Safety outcomes included major bleeding, any clinically relevant bleeding, and intracranial hemorrhage. Each DOAC and VKA was compared pairwise in a network meta-analysis. High- and low-dose regimens and factor IIa and Xa inhibitors were also compared. Seven randomized controlled trials were included in the analysis. Stroke and systemic embolism risks did not differ significantly among DOACs. There were no significant differences in major bleeding between each DOAC and VKA. Intracranial hemorrhage risk was significantly lower with dabigatran, apixaban, and edoxaban than with VKA and rivaroxaban, which had similar risks. High-dose regimens led to lower risks of stroke or systemic embolism compared with VKA and low-dose regimens, with both doses having similar bleeding risks.
CONCLUSIONS CONCLUSIONS
In patients aged ≥75 years with atrial fibrillation, DOACs were associated with fewer thromboembolic events compared with VKA, whereas dabigatran, apixaban, and edoxaban were associated with lower risks of intracranial hemorrhage compared with VKA and rivaroxaban.
REGISTRATION BACKGROUND
URL: www.crd.york.ac.uk/prospero/. Unique identifier: CRD42022329557.

Identifiants

pubmed: 38014696
doi: 10.1161/JAHA.123.030380
doi:

Substances chimiques

edoxaban NDU3J18APO
Rivaroxaban 9NDF7JZ4M3
Dabigatran I0VM4M70GC
Anticoagulants 0

Types de publication

Meta-Analysis Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e030380

Auteurs

Donna Shu-Han Lin (DS)

Division of Cardiology Department of Internal Medicine Shin Kong Wu Ho-Su Memorial Hospital Taipei Taiwan.
Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.

Hao-Yun Lo (HY)

Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.
Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Hsin-Chu Branch Hsinchu Taiwan.

Kuan-Chih Huang (KC)

Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.
Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Hsin-Chu Branch Hsinchu Taiwan.
Department of Internal Medicine National Taiwan University College of Medicine Taipei Taiwan.

Ting-Tse Lin (TT)

Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.
Department of Internal Medicine National Taiwan University College of Medicine Taipei Taiwan.

Jen-Kuang Lee (JK)

Division of Cardiology Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan.
Department of Internal Medicine National Taiwan University College of Medicine Taipei Taiwan.
Department of Laboratory Medicine National Taiwan University College of Medicine Taipei Taiwan.
Cardiovascular Center National Taiwan University Hospital Taipei Taiwan.
Telehealth Center National Taiwan University Hospital Taipei Taiwan.

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Classifications MeSH