Estimating the risk of thrombotic events in people with congenital hemophilia A using US claims data

Author:

Faghmous Imi12,Nissen Francis1ORCID,Kuebler Peter3,Flores Carlos4ORCID,Patel Anisha M5ORCID,Pipe Steven W6ORCID

Affiliation:

1. Real-World Data Oncology-Hematology, F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, Basel, 4070, Switzerland

2. Current affiliation: Health, Medicine & Life Sciences, University of Maastricht, Minderbroedersberg 4-6, 6211, LK Maastricht, The Netherlands

3. PHC Safety Interface, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

4. Evidence Strategy, Genesis Research Hoboken, 111 River St Ste 1120, Hoboken, NJ 07030, USA

5. US Medical Affairs, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA

6. Pediatrics and Pathology, University of Michigan, D4202 MPB, 1500 E Medical Center Drive, Ann Arbor, MI 48109-5718, USA

Abstract

Aim: Compare thrombotic risk in people with congenital hemophilia A (PwcHA) to the general non-hemophilia A (HA) population. Patients & methods: US claims databases were analyzed to identify PwcHA. Incidence rates of myocardial infarction, pulmonary embolism, ischemic stroke, deep vein thrombosis and device-related thrombosis were compared with a matched cohort without HA. Results: Over 3490 PwcHA were identified and 16,380 individuals matched. PwcHA had a similar incidence of myocardial infarction and pulmonary embolism compared with the non-HA population, but a slightly higher incidence of ischemic stroke and deep vein thrombosis. The incidence of device-related thrombosis was significantly higher in PwcHA. Conclusion: This analysis suggests that PwcHA are not protected against thrombosis, and provides context to evaluate thrombotic risk of HA treatments.

Funder

F. Hoffmann-La Roche

Publisher

Future Medicine Ltd

Subject

Health Policy

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