Impact of type of anticoagulant on clinical outcomes in cancer patients who had atrial fibrillation.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
06 07 2023
Historique:
received: 24 01 2023
accepted: 02 07 2023
medline: 10 7 2023
pubmed: 7 7 2023
entrez: 6 7 2023
Statut: epublish

Résumé

To date, evidence on optimal anticoagulant options in patients with AF who concurrently have active cancer remains elusive. To describe anticoagulant patterns and clinical outcomes among patients with a concomitant diagnosis of AF and cancer. Data were obtained from the University of Utah and Huntsman Cancer Institute (HCI) Hospitals. Patients were included if they had diagnosis of AF and cancer. Outcome was type and pattern of anticoagulant. Clinical outcomes were stroke, bleeding and all-cause mortality. From October 1999 to December 2020, there were 566 AF patients who concurrently had active cancer. Mean age ± standard deviation was 76.2 ± 10.7 and 57.6% were males. Comparing to warfarin, patients who received direct oral anticoagulant (DOACs) were associated with similar risk of stroke (adjusted hazard ratio, aHR 0.8, 95% confidence interval [CI] 0.2-2.7, P = 0.67). On contrary, those who received low-molecular-weight heparin (LMWH) were associated with significantly higher risk of stroke comparing to warfarin (aHR 2.4, 95% CI 1.0-5.6, P = 0.04). Comparing to warfarin, DOACs and LMWH was associated with similar risk of overall bleeding with aHR 1.1 (95% CI 0.7-1.6, P = 0.73) and aHR 1.1 (95% CI 0.6-1.7, P = 0.83), respectively. Patients who received LMWH but not DOACs were associated with increased risk of death as compared to warfarin, aHR 4.5 (95% CI 2.8-7.2, P < 0.001) and 1.2 (95% CI 0.7-2.2, P = 0.47). In patients with active cancer and AF, LMWH, compared to warfarin, was associated with an increased risk of stroke and all-cause mortality. Furthermore, DOACs was associated with similar risk of stroke, bleeding and death as compared to warfarin.

Identifiants

pubmed: 37414965
doi: 10.1038/s41598-023-38071-3
pii: 10.1038/s41598-023-38071-3
pmc: PMC10325995
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI
Heparin, Low-Molecular-Weight 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10937

Informations de copyright

© 2023. The Author(s).

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Auteurs

Chatree Chai-Adisaksopha (C)

Department of Internal Medicine, Chiang Mai University, Chiang Mai, Thailand.

Alexandre H Watanabe (AH)

Department of Pharmacotherapy, Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, UT, USA.

Piyameth Dilokthornsakul (P)

Center for Medical and Health Technology Assessment (CM-HTA), Department of Pharmaceutical Care, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.

Leenhapong Navaravong (L)

Division of Cardiovascular Medicine, University of Utah, Salt Lake City, USA.

Daniel M Witt (DM)

Department of Pharmacotherapy, Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, UT, USA.

Nathorn Chaiyakunapruk (N)

Department of Pharmacotherapy, Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, UT, USA. nathorn.chaiyakunapruk@utah.edu.
IDEAS Center, Veterans Affairs Salt Lake City Healthcare System, Salt Lake City, UT, USA. nathorn.chaiyakunapruk@utah.edu.

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Classifications MeSH