TY - JOUR
T1 - Inhibitors and mortality in persons with nonsevere hemophilia A in the United States
AU - Lim, Ming Y.
AU - Cheng, Dunlei
AU - Recht, Michael
AU - Kempton, Christine L.
AU - Key, Nigel S.
N1 - Funding Information:
M.Y.L. received a 2015 HTRS/ATHN DREAM Award from the Hemostasis and Thrombosis Research Society and the American Thrombosis and Hemostasis Network, which was supported by an independent medical educational grant from Shire.
Funding Information:
Conflict-of-interest disclosure: M.R. has acted as a paid consultant to Bioverativ/Sanofi, CSL Behring, Genentech, Kedrion, NovoNordisk, Pfizer, Shire/Takeda, and uniQure; in addition, his organization has received research support from Bioverativ/Sanofi, BioMarin, Genentech, NovoNordisk, Shire/Takeda, Spark Therapeutics, and uniQure; is on the Board of Directors of Foundation for Women and Girls with Blood Disorders and Partners in Bleeding Disorders; and is employed by the American Thrombosis and Hemostasis Network. C.L.K. received honoraria for participation in advisory boards with Spark Therapeutics, Pfizer, and Genentech and research support from Novo Nordisk. N.S.K. has received research funding from Takeda, Grifols, and Pfizer; in addition, he is on a steering committee for clinical trials for uniQure and grants review committee for NovoNordisk. The remaining authors declare no competing financial interests.
Publisher Copyright:
© 2020 by The American Society of Hematology
PY - 2020/10/13
Y1 - 2020/10/13
N2 - Although persons with nonsevere hemophilia A (NSHA) account for about one-half of the hemophilia A population, epidemiological data in this subset of individuals are scarce. We set out to describe the clinical characteristics of persons with NSHA with inhibitors, and to determine mortality rates, predictors of mortality, and primary causes of death in persons with NSHA in the United States over a 9-year period (2010-2018). We queried the American Thrombosis and Hemostasis Network dataset (ATHNdataset) for information on demographics, inhibitor status, and date and cause of death. A total of 6624 persons with NSHA (86.0% men; 14.0% women) were observed for an average of 8.5 years; total 56 119 person-years. The prevalence of inhibitors was 2.6% (n = 171), occurring at a median age of 13 years. At the end of follow-up, 136 persons died at a median age of 63 years; an age-adjusted mortality rate of 3.3 deaths per 1000 person-years. Three deaths occurred in inhibitor participants. Presence of inhibitors was not associated with increased mortality risk (hazard ratio [HR], 0.7, 95% confidence interval [CI], 0.2-2.3). Factors independently associated with increased risk of death (HR, 95% CI) were the following: age (10-year increase) (2.1, 2.0-2.4); male (2.6, 1.0-6.4); hepatitis C (2.2, 1.5-3.1); and HIV (3.6, 2.2-6.0). The most common primary cause of death was malignancy (n - 27, 20.0%). In persons with NSHA, the development of inhibitors occurred at an early age and was not associated with increased mortality.
AB - Although persons with nonsevere hemophilia A (NSHA) account for about one-half of the hemophilia A population, epidemiological data in this subset of individuals are scarce. We set out to describe the clinical characteristics of persons with NSHA with inhibitors, and to determine mortality rates, predictors of mortality, and primary causes of death in persons with NSHA in the United States over a 9-year period (2010-2018). We queried the American Thrombosis and Hemostasis Network dataset (ATHNdataset) for information on demographics, inhibitor status, and date and cause of death. A total of 6624 persons with NSHA (86.0% men; 14.0% women) were observed for an average of 8.5 years; total 56 119 person-years. The prevalence of inhibitors was 2.6% (n = 171), occurring at a median age of 13 years. At the end of follow-up, 136 persons died at a median age of 63 years; an age-adjusted mortality rate of 3.3 deaths per 1000 person-years. Three deaths occurred in inhibitor participants. Presence of inhibitors was not associated with increased mortality risk (hazard ratio [HR], 0.7, 95% confidence interval [CI], 0.2-2.3). Factors independently associated with increased risk of death (HR, 95% CI) were the following: age (10-year increase) (2.1, 2.0-2.4); male (2.6, 1.0-6.4); hepatitis C (2.2, 1.5-3.1); and HIV (3.6, 2.2-6.0). The most common primary cause of death was malignancy (n - 27, 20.0%). In persons with NSHA, the development of inhibitors occurred at an early age and was not associated with increased mortality.
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U2 - 10.1182/bloodadvances.2020002626
DO - 10.1182/bloodadvances.2020002626
M3 - Article
C2 - 33007074
AN - SCOPUS:85092288605
SN - 2473-9529
VL - 4
SP - 4739
EP - 4747
JO - Blood advances
JF - Blood advances
IS - 19
ER -