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Observational cohort study evaluates emicizumab's impact on bleeding rates in hemophilia A patients, suggesting effective long-term management.
Emicizumab prophylaxis has been approved in Canada for the prevention or reduction of bleeding episodes in people with congenital hemophilia A (PwHA). Using routinely collected health data from the Canadian Bleeding Disorders Registry (CBDR), this observational cohort study aimed to evaluate the long-term safety and effectiveness of emicizumab in PwHA. De-identified data from the CBDR were collected for PwHA who had received ≥1 dose of emicizumab from 2018 up to December 31, 2023. Intra-patient comparisons of annualized bleeding rates (ABRs) for all reported bleeds pre- and post-emicizumab were performed using a negative binomial regression model. Overall, 710 PwHA received ≥1 emicizumab dose and 539 (75.9%) had >1 year of emicizumab exposure. During the observational period, the safety profile was in keeping with previous reports; 34 adverse events were observed, including two thrombotic events (one unlikely related to emicizumab; one probably related to previous use of eptacog alfa and/or possibly related to previous emicizumab, and associated with a central venous access device). Over a median (Q1-Q3) follow-up time of 549 (374-690) days, 439 (61.8%) PwHA had no recorded bleeds. Mean ABR (95% confidence interval [CI]) decreased from 1.00 (0.87-1.14) pre-emicizumab to 0.47 (0.40-0.55) post-emicizumab (rate ratio [95% CI], 0.47 [0.41-0.55]; P < .001). A notable decrease in bleeds and sustained bleed control were observed in this population for up to a 5-year follow-up period. Continued follow-up will allow for greater quantification of this impact over time, providing valuable information to healthcare practitioners and regulatory authorities.
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Iorio et al. (2026) studied this question.
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