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Equivalent inpatient mortality among direct-acting oral anticoagulant and warfarin users presenting with major hemorrhage.
Bialkowski, Walter; Tan, Sylvia; Mast, Alan E; Kiss, Joseph E; Kor, Daryl; Gottschall, Jerome; Wu, Yanyun; Roubinian, Nareg; Triulzi, Darrell; Kleinman, Steve; Choi, Young; Brambilla, Donald; Zimrin, Ann.
Afiliación
  • Bialkowski W; Blood Research Institute, Versiti, WI, USA. Electronic address: walter.bialkowski@marquette.edu.
  • Tan S; Research Triangle International, MD, USA.
  • Mast AE; Blood Research Institute, Versiti, WI, USA.
  • Kiss JE; University of Pittsburgh, PA, USA.
  • Kor D; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, MN, USA.
  • Gottschall J; Blood Research Institute, Versiti, WI, USA.
  • Wu Y; Bloodworks Northwest, Washington, USA; School of Medicine, Yale University, CT, USA.
  • Roubinian N; Division of Research, Kaiser Permanente, California, USA.
  • Triulzi D; University of Pittsburgh, PA, USA.
  • Kleinman S; UBC School of Medicine, Victoria, BC, Canada.
  • Choi Y; School of Medicine, Yale University, CT, USA.
  • Brambilla D; Research Triangle International, MD, USA.
  • Zimrin A; School of Medicine, University of Maryland, MD, USA.
Thromb Res ; 185: 109-118, 2020 01.
Article en En | MEDLINE | ID: mdl-31794885
ABSTRACT

BACKGROUND:

Extrapolation of clinical trial results comparing warfarin and direct-acting oral anticoagulant (DOAC) users experiencing major hemorrhage to clinical care is challenging due to differences seen among non-randomized oral anticoagulant users, bleed location, and etiology. We hypothesized that inpatient all-cause-mortality among patients presenting with major hemorrhage differed based on the home-administered anticoagulant medication class, DOAC versus warfarin.

METHODS:

More than 1.5 million hospitalizations were screened and 3731 patients with major hemorrhage were identified in the REDS-III Recipient Database. Propensity score matching and stratification were used to account for potentially confounding factors.

RESULTS:

Inpatient all-cause-mortality was lower for DOAC (HR = 0.60, 95%CI 0.45-0.80, p = 0.0005) before accounting for confounding and competing events. Inpatient all-cause-mortality for 1266 propensity-score-matched patients compared using proportional hazards regression did not differ (HR = 0.84, 95%CI 0.58-1.22, p = 0.36). Inpatient all-cause-mortality in stratified analyses (warfarin as reference) produced HR = 0.69 (95%CI 0.31-1.55) for traumatic head injuries; HR = 1.10 (95%CI 0.62-1.95) for non-traumatic head injuries; HR = 0.62 (95%CI 0.20-1.94) for traumatic, non-head injuries; and HR = 0.69 (95%CI 0.29-1.63) for non-traumatic, non-head injuries. Mean time to discharge was shorter for DOAC (HR = 1.17, 95%CI 1.05-1.30, p = 0.0034) in the propensity score matched analysis. Plasma transfusion occurred in 42% of warfarin hospitalizations and 11% of DOAC hospitalizations. Vitamin K was administered in 63% of warfarin hospitalizations.

CONCLUSIONS:

After accounting for differences in patient characteristics, location of bleed, and traumatic injury, inpatient survival was no different in patients presenting with major hemorrhage while on DOAC or warfarin.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Accidente Cerebrovascular Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Thromb Res Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrilación Atrial / Accidente Cerebrovascular Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Thromb Res Año: 2020 Tipo del documento: Article