Efficacy and Safety of Apixaban Versus Warfarin in Patients With Atrial Fibrillation and Extremes in Body Weight.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
14 05 2019
Historique:
pubmed: 19 2 2019
medline: 3 3 2020
entrez: 19 2 2019
Statut: ppublish

Résumé

Guidelines caution against the use of non-vitamin K antagonist oral anticoagulants in patients with extremely high (>120 kg) or low (≤60 kg) body weight because of a lack of data in these populations. In a post hoc analysis of ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation; n=18 201), a randomized trial comparing apixaban with warfarin for the prevention of stroke in patients with atrial fibrillation, we estimated the randomized treatment effect (apixaban versus warfarin) stratified by body weight (≤60, >60-120, >120 kg) using a Cox regression model and tested the interaction between body weight and randomized treatment. The primary efficacy and safety outcomes were stroke or systemic embolism and major bleeding. Of the 18 139 patients with available weight and outcomes data, 1985 (10.9%) were in the low-weight group (≤60 kg), 15 172 (83.6%) were in the midrange weight group (>60-120 kg), and 982 (5.4%) were in the high-weight group (>120 kg). The treatment effect of apixaban versus warfarin for the efficacy outcomes of stroke/systemic embolism, all-cause death, or myocardial infarction was consistent across the weight spectrum (interaction P value>0.05). For major bleeding, apixaban had a better safety profile than warfarin in all weight categories and even showed a greater relative risk reduction in patients in the low (≤60 kg; HR, 0.55; 95% CI, 0.36-0.82) and midrange (>60-120 kg) weight groups (HR, 0.71; 95% CI, 0.61-0.83; interaction P value=0.016). Our findings provide evidence that apixaban is efficacious and safe across the spectrum of weight, including in low- (≤60 kg) and high-weight patients (>120 kg). The superiority on efficacy and safety outcomes of apixaban compared with warfarin persists across weight groups, with even greater reductions in major bleeding in patients with atrial fibrillation with low to normal weight as compared with high weight. The superiority of apixaban over warfarin in regard to efficacy and safety for stroke prevention seems to be similar in patients with atrial fibrillation across the spectrum of weight, including in low- and very high-weight patients. Thus, apixaban appears to be appropriate for patients with atrial fibrillation irrespective of body weight. URL: https://www.clinicaltrials.gov . Unique identifier: NCT00412984.

Sections du résumé

BACKGROUND
Guidelines caution against the use of non-vitamin K antagonist oral anticoagulants in patients with extremely high (>120 kg) or low (≤60 kg) body weight because of a lack of data in these populations.
METHODS
In a post hoc analysis of ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation; n=18 201), a randomized trial comparing apixaban with warfarin for the prevention of stroke in patients with atrial fibrillation, we estimated the randomized treatment effect (apixaban versus warfarin) stratified by body weight (≤60, >60-120, >120 kg) using a Cox regression model and tested the interaction between body weight and randomized treatment. The primary efficacy and safety outcomes were stroke or systemic embolism and major bleeding.
RESULTS
Of the 18 139 patients with available weight and outcomes data, 1985 (10.9%) were in the low-weight group (≤60 kg), 15 172 (83.6%) were in the midrange weight group (>60-120 kg), and 982 (5.4%) were in the high-weight group (>120 kg). The treatment effect of apixaban versus warfarin for the efficacy outcomes of stroke/systemic embolism, all-cause death, or myocardial infarction was consistent across the weight spectrum (interaction P value>0.05). For major bleeding, apixaban had a better safety profile than warfarin in all weight categories and even showed a greater relative risk reduction in patients in the low (≤60 kg; HR, 0.55; 95% CI, 0.36-0.82) and midrange (>60-120 kg) weight groups (HR, 0.71; 95% CI, 0.61-0.83; interaction P value=0.016).
CONCLUSIONS
Our findings provide evidence that apixaban is efficacious and safe across the spectrum of weight, including in low- (≤60 kg) and high-weight patients (>120 kg). The superiority on efficacy and safety outcomes of apixaban compared with warfarin persists across weight groups, with even greater reductions in major bleeding in patients with atrial fibrillation with low to normal weight as compared with high weight. The superiority of apixaban over warfarin in regard to efficacy and safety for stroke prevention seems to be similar in patients with atrial fibrillation across the spectrum of weight, including in low- and very high-weight patients. Thus, apixaban appears to be appropriate for patients with atrial fibrillation irrespective of body weight.
CLINICAL TRIAL REGISTRATION
URL: https://www.clinicaltrials.gov . Unique identifier: NCT00412984.

Identifiants

pubmed: 30773022
doi: 10.1161/CIRCULATIONAHA.118.037955
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0
Pyrazoles 0
Pyridones 0
apixaban 3Z9Y7UWC1J
Warfarin 5Q7ZVV76EI

Banques de données

ClinicalTrials.gov
['NCT00412984']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2292-2300

Commentaires et corrections

Type : CommentIn

Auteurs

Stefan H Hohnloser (SH)

Johann Wolfgang Goethe University, Frankfurt, Germany (S.G.G.).

Marat Fudim (M)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

John H Alexander (JH)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

Daniel M Wojdyla (DM)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

Justin A Ezekowitz (JA)

University of Alberta, Alberta, Canada (J.A.E.).

Michael Hanna (M)

Bristol-Myers Squibb, Princeton, NJ (M.H.).

Dan Atar (D)

University of Oslo, Norway (D.A.).

Ziad Hijazi (Z)

Uppsala Clinical Research Center, Uppsala University, Sweden (Z.H., L.W.).

M Cecilia Bahit (MC)

Fundación INECO Rosario, Department of Cardiology, INECO Neurociencias Orono, Santa Fe, Argentina (M.C.B.).

Sana M Al-Khatib (SM)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

Jose Luis Lopez-Sendon (JL)

Hospital Universitario La Paz, Madrid, Spain (J.L.L.-S.).

Lars Wallentin (L)

Uppsala Clinical Research Center, Uppsala University, Sweden (Z.H., L.W.).

Christopher B Granger (CB)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (M.F., J.H.A., D.M.W., S.M.A.-K., C.B.G., R.D.L.).

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Classifications MeSH