Evaluating the impact of recombinant porcine factor VIII compared with activated recombinant factor VII on acquired hemophilia A outcomes

Author:

Batt Katharine12ORCID,Bullano Michael3ORCID,Schultz Bob G3ORCID,Liu Yanmei1,Kee Rebecca1,Harley Carolyn1,Cool Christina1ORCID

Affiliation:

1. Precision Value & Health, 60 E 42nd St #1325, New York, CA 10165, USA

2. Wake Forest Baptist School of Medicine, Department of Internal Medicine, Division of Hematology/Oncology, 1 Medical Center, Winston-Salem, NC 27157, USA

3. Takeda Pharmaceuticals USA, Inc., 95 Hayden Ave., Lexington, MA 02421, USA

Abstract

Objective: To compare mortality and readmission rates for patients with acquired hemophilia A (AHA) who were observed to use activated recombinant factor VII (rFVIIa) and/or recombinant porcine factor VIII (rpFVIII) during a hospital admission. Methods: The Medicare Limited Data Set was used for this analysis. Patients were selected into the study if they had a diagnosis of AHA and were treated with rpFVIII and/or rFVIIa between 1 January 2015 and 31 December 2019, among other criteria. Results: The probability of death or readmission with treatment within 12 months of a previous treatment was 40% lower in rpFVIII cases than rFVIIa cases (p = 0.047). Conclusion: Patients with AHA who received treatment with rpFVIII experienced significant declines in mortality and readmissions compared with patients treated with rFVIIa.

Funder

The Takeda Pharmaceutical Company

Publisher

Future Medicine Ltd

Subject

General Medicine

Reference17 articles.

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