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Impact of concomitant fluconazole on direct oral anticoagulant bleeding risk.
Cid, Allison; Smetana, Megan E; Hebert, Courtney; Coe, Kelci; Smith, Jessica M.
Afiliação
  • Cid A; Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Smetana ME; Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Hebert C; Division of Infectious Diseases, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Coe K; Division of Infectious Diseases, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Smith JM; Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Pharmacotherapy ; 42(12): 880-889, 2022 12.
Article em En | MEDLINE | ID: mdl-36271717
ABSTRACT
STUDY

OBJECTIVE:

The aim of this study was to evaluate the effect on bleeding risk when fluconazole is administered concomitantly with direct oral anticoagulants (DOACs).

DESIGN:

This was a retrospective cohort study including hospitalized adult patients prescribed a DOAC with or without fluconazole.

SETTING:

The Ohio State University Wexner Medical Center, a tertiary care academic medical center with more than 1800 beds. PATIENTS Hospitalized patients ages 18-89 years who received apixaban or rivaroxaban with or without fluconazole from October 1, 2016, to September 30, 2021, were included. The minimum duration of DOAC or DOAC with fluconazole therapy was 48 h. Patients were excluded if they received fluconazole <400 mg daily or a DOAC at doses outside those recommended for atrial fibrillation or venous thromboembolism treatment or prophylaxis. Patients were matched based on DOAC received. INTERVENTION Patients who received a DOAC with fluconazole were compared with those receiving a DOAC alone. The primary outcome was a composite of major, clinically relevant nonmajor, and minor bleeding events at 30 days. MEASUREMENTS AND MAIN

RESULTS:

There were 216 patients included, 108 in the DOAC with fluconazole group and 108 in the DOAC alone group. More patients in the DOAC with fluconazole group experienced bleeding at 30 days compared with the DOAC alone group [35/108 (32%) vs. 21/108 (19%), respectively; p = 0.03]; however, after adjusting for proven confounding variables (hemoglobin and concomitant carvedilol) this was found not to be statistically significant [adjusted odds ratio 1.71, 95% confidence interval 0.85-3.40].

CONCLUSIONS:

Patients receiving a DOAC with fluconazole were not at significantly increased risk for bleeding at 30 days compared with those receiving a DOAC alone after controlling for confounding variables. As an increasing number of patients are prescribed DOACs, the results of this study may inform clinical decision-making on the safety of concomitant DOAC and fluconazole use.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fluconazol Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Pharmacotherapy Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fluconazol Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Pharmacotherapy Ano de publicação: 2022 Tipo de documento: Article