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Real-World Risk of Gastrointestinal Bleeding for Direct Oral Anticoagulants and Warfarin Users: A Distributed Network Analysis Using a Common Data Model.
Cha, Jae Myung; Kim, Myoungsuk; Jo, Hyeong Ho; Seo, Won-Woo; Rhee, Sang Youl; Kim, Ji Hyun; Kim, Gwang Ha; Park, Junseok.
Afiliación
  • Cha JM; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul, Korea.
  • Kim M; Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul, Korea.
  • Jo HH; Department of Internal Medicine, Daegu Catholic University Medical Center, Daegu Catholic University School of Medicine, Daegu, Korea.
  • Seo WW; Department of Internal Medicine, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.
  • Rhee SY; Center for Digital Health, Kyung Hee University, Seoul, Korea.
  • Kim JH; Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea.
  • Kim GH; Department of Internal Medicine, Pusan National University Hospital, Pusan National University School, Busan, Korea.
  • Park J; Department of Internal Medicine, Soonchunhyang University Hospital, Soonchunhyang University School of Medicine, Seoul, Korea.
Gut Liver ; 18(5): 814-823, 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-38384200
ABSTRACT
Background/

Aims:

Early studies on direct oral anticoagulants (DOACs) reported a higher risk of gastrointestinal bleeding (GIB) compared with warfarin; however, recent studies have reported a reduced risk. Therefore, this study was designed to evaluate the risk of GIB in users of DOAC and warfarin.

Methods:

Using a common data model, we investigated the comparative risk of GIB in subjects from eight hospitals who were newly prescribed DOACs or warfarin. We excluded subjects who had a prior history of GIB or had been prescribed both medications. After propensity score matching, we analyzed 3,347 matched pairs of new DOAC and new warfarin users.

Results:

The risk of GIB in new DOAC users was comparable to that in new warfarin users (hazard ratio [HR], 0.95; 95% confidence interval [CI], 0.65 to 1.40; p=0.808). New DOAC users had a similar risk of GIB to new warfarin users among older patients >65 years (HR, 1.00; 95% CI, 0.69 to 1.52; p=0.997) and in older patients >75 years (HR, 1.21; 95% CI, 0.68 to 2.10; p=0.509). In addition, the risk of GIB was not significantly different between two groups according to sex. We also found that the risk of GIB in DOAC users was 26% lower in edoxaban or apixaban subgroups compared to rivaroxaban or dabigatran subgroups (HR, 0.74; 95% CI, 0.69 to 1.00; p=0.049).

Conclusions:

In real-world practice, the risk of GIB in new DOAC users is comparable to that in new warfarin users. In DOAC users, the risk of GIB was lower in edoxaban or apixaban subgroups than rivaroxaban or dabigatran subgroups.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirazoles / Warfarina / Dabigatrán / Hemorragia Gastrointestinal / Anticoagulantes Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Gut Liver Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pirazoles / Warfarina / Dabigatrán / Hemorragia Gastrointestinal / Anticoagulantes Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Gut Liver Año: 2024 Tipo del documento: Article
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