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Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort.

Publication ,  Journal Article
Butt, JH; Li, A; Xian, Y; Peterson, ED; Garcia, D; Torp-Pedersen, C; Køber, L; Fosbøl, EL
Published in: Am Heart J
October 2019

BACKGROUND: The purpose of the study was to examine the association between the type of preceding oral anticoagulant use (warfarin or direct oral anticoagulants [DOACs]) and in-hospital mortality among patients admitted with gastrointestinal bleeding. METHODS: In this observational cohort study, all patients admitted with a first-time gastrointestinal bleeding from January 2011 to March 2017 while receiving any oral anticoagulant therapy prior to admission were identified using data from Danish nationwide registries. The risk of in-hospital mortality according to type of oral anticoagulation therapy was examined by multivariable logistic regression models. RESULTS: Among 5,774 patients admitted with gastrointestinal bleeding (median age, 78 years [25th-75th percentile, 71-85 years]; 56.8% men), 2,038 (35.3%) were receiving DOACs and 3,736 (64.7%) were receiving warfarin prior to admission. The unadjusted in-hospital mortality rates were 7.5% for DOAC (7.2% for dabigatran, 6.4% for rivaroxaban, and 10.1% for apixaban) and 6.5% for warfarin. After adjustment for baseline demographic and clinical characteristics, there was no statistically significant difference in in-hospital mortality between prior use of any DOAC and warfarin (unadjusted odds ratio [OR] 1.18 [95% CI 0.95-1.45], adjusted OR 0.97 [95% CI 0.77-1.24]). Similar results were found for each individual DOAC as compared with warfarin (dabigatran: unadjusted OR 1.12 [95% CI 0.84-1.49], adjusted OR 0.96 [95% CI 0.71-1.30]); rivaroxaban: unadjusted OR 0.98 [95% CI 0.71-1.37], adjusted OR 0.84 [95% CI 0.59-1.21]; and apixaban: unadjusted OR 1.62 [95% CI 0.84-1.49], adjusted OR 1.22 [95% CI 0.83-1.79]). CONCLUSIONS: Among patients admitted with gastrointestinal bleeding, there was no statistically significant difference in in-hospital mortality between prior use of DOAC and warfarin.

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Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

October 2019

Volume

216

Start / End Page

117 / 124

Location

United States

Related Subject Headings

  • Warfarin
  • Vitamin K
  • United States
  • Rivaroxaban
  • Pyridones
  • Pyrazoles
  • Male
  • Logistic Models
  • Humans
  • Hospital Mortality
 

Citation

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Chicago
ICMJE
MLA
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Butt, J. H., Li, A., Xian, Y., Peterson, E. D., Garcia, D., Torp-Pedersen, C., … Fosbøl, E. L. (2019). Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort. Am Heart J, 216, 117–124. https://doi.org/10.1016/j.ahj.2019.07.012
Butt, Jawad H., Ang Li, Ying Xian, Eric D. Peterson, David Garcia, Christian Torp-Pedersen, Lars Køber, and Emil L. Fosbøl. “Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort.Am Heart J 216 (October 2019): 117–24. https://doi.org/10.1016/j.ahj.2019.07.012.
Butt JH, Li A, Xian Y, Peterson ED, Garcia D, Torp-Pedersen C, et al. Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort. Am Heart J. 2019 Oct;216:117–24.
Butt, Jawad H., et al. “Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort.Am Heart J, vol. 216, Oct. 2019, pp. 117–24. Pubmed, doi:10.1016/j.ahj.2019.07.012.
Butt JH, Li A, Xian Y, Peterson ED, Garcia D, Torp-Pedersen C, Køber L, Fosbøl EL. Direct oral anticoagulant- versus vitamin K antagonist-related gastrointestinal bleeding: Insights from a nationwide cohort. Am Heart J. 2019 Oct;216:117–124.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

October 2019

Volume

216

Start / End Page

117 / 124

Location

United States

Related Subject Headings

  • Warfarin
  • Vitamin K
  • United States
  • Rivaroxaban
  • Pyridones
  • Pyrazoles
  • Male
  • Logistic Models
  • Humans
  • Hospital Mortality