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  Poster Hall

Mon-59 - Evaluating bleed risk in hospitalized patients receiving apixiban with hypoalbuminemia

Scientific Poster Session III - Original Research

Original Research
  Monday, October 14, 2024
  01:00 PM–02:30 PM

Abstract

Introduction:

Rivaroxaban and apixaban exhibit high protein binding. Hypoalbuminemia could impact the pharmacodynamics of these medications, increasing bleed risk. Rivaroxaban has been associated with increased bleeding in patients with hypoalbuminemia however the effects in apixaban-treated patients remain unknown. This study evaluated hypoalbuminemia and bleeding risk in patients treated with apixaban.

Research Question or Hypothesis:

Does hypoalbuminemia increase bleeding risk in apixaban-treated patients?

Study Design:

IRB approved, retrospective cohort study

Methods:

Adult inpatients admitted from May-July 2023 were reviewed. Inclusion criteria were: apixaban =2.5 mg twice daily given inpatient for =48 hours or prescribed upon discharge and in patients with an albumin level drawn during index admission. Patients with a stroke or TIA within 14 days, bleeding with another anticoagulant, pregnancy, active COVID-19, cirrhosis, or thrombocytopenia were excluded. The primary endpoint assessed the impact of hypoalbuminemia (albumin =3g/dL) on International Society on Thrombosis and Hemostasis criteria bleeding rates in apixaban-treated patients. Bleeding risk was assessed using multivariable logistic regression with backwards stepwise elimination of variables with a p-value <0.2 on bivariate analysis. Alpha was set at <0.05 and SAS version 9.4 was used for analysis.

Results:

A total of 391 patients were included. Bleeding occurred in 49 (12.5%) patients. Albumin =3 g/dL was associated with a 2-fold increase in adjusted bleed risk (OR 2.002, 95% CI [1.003-3.996], p=0.0491). After backward stepwise elimination, gastroduodenal ulcer history (OR 1.428, 95% CI [1.003-2.032], p=0.0480) and proton pump inhibitor use (OR 2.278 [1.225-4.238], p=0.0093) were also associated with bleeding risk in the multivariable model.

Conclusion:

Albumin does not appear significantly associated with adjusted bleed risk in hospitalized patients receiving apixaban. The effect of hypoalbuminemia on apixaban’s clinical pharmacodynamics requires further investigation.

Presenting Author

Ashley Woodruff Pharm.D., BCPS
University at Buffalo School of Pharmacy and Pharmaceutical Sciences

Authors

Maya Chilbert Pharm.D., BCCP
University at Buffalo School of Pharmacy and Pharmaceutical Sciences

Bidoura Chowdhury PharmD Candidate
University at Buffalo School of Pharmacy and Pharmaceutical Sciences

Shiqi Zhang PharmD Candidate
University at Buffalo School of Pharmacy and Pharmaceutical Sciences