Costs and Healthcare Resource Utilization Associated with Idarucizumab or Andexanet Alfa Oral Anticoagulant Reversal in Patients Hospitalized with Life-Threatening Bleeds

Author:

Spyropoulos Alex C.123ORCID,Hartaigh Bríain Ó4,Cao Zhun5,Caberwal Harjeet4,Lipkin Craig5,Petrini Michaela4,Wang Cheng4

Affiliation:

1. Institute of Health System Science, Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY, USA

2. Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA

3. Department of Obstetrics and Gynecology, I.M. Sechenov First Moscow State Medical University, Moscow, Russia

4. Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA

5. Premier, Inc, Charlotte, NC, USA

Abstract

Purpose: To assess costs and healthcare resource utilization (HCRU) associated with the use of idarucizumab for the reversal of dabigatran and andexanet alfa for the reversal of direct oral Factor Xa inhibitors. Methods: This retrospective study utilizing Premier Healthcare Database (PHD) included patients aged ≥18 years on direct oral anticoagulants (DOACs) who experienced life-threatening bleeds, discharged from the hospital during 5/1/2018–6/30/2019, and received idarucizumab or andexanet alfa. Inverse of treatment probability weighting (IPTW) method was used to balance patient and clinical characteristics between treatment cohorts. Results: Idarucizumab patients were older than andexanet alfa patients (median age 81 vs 77 years; p < 0.001), and less likely to experience intracranial hemorrhage (ICH) (37.1%vs 73.8%; p  =  0.001). After IPTW adjustment, idarucizumab patients incurred lower mean total hospital costs ($30,413  ±  $33,028 vs $44,477  ±  $30,036; p < 0.001),and mean intensive care unit (ICU) cost ($25,114  ±  $30,433 vs $43,484  ±  $29,335; p < 0.001). Conclusions: Anticoagulant reversal therapy with idarucizumab was associated with significantly lower adjusted mean total hospital and ICU costs compared with andexanet alfa. However, a higher prevalence of ICH bleeds was noted in the andexanet alfa group. Trial Registration: Not applicable.

Funder

Boehringer Ingelheim

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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