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ABSTRACT: Background
In patients with non-severe hemophilia A, we lack detailed knowledge on the timing of treatment with factor VIII (FVIII) concentrates. This knowledge could provide information about the expected treatment timing in patients with severe hemophilia A treated with non-replacement therapies.Objective
To assess the FVIII treatment history in patients with non-severe hemophilia A.Methods
Patients with non-severe hemophilia (baseline FVIII activity [FVIII:C] 2-40 IU/dL) were included from the INSIGHT study. The primary outcome was median age at first FVIII exposure (ED1). In a subgroup of patients for whom more detailed information was available, we analyzed the secondary outcomes: median age at first 20 EDs, annualized bleeding rate for all bleeds (ABR), joint bleeds (AJBR), and major spontaneous bleeds (ASmBR).Results
In the total cohort (n = 1013), median baseline FVIII activity was 8 IU/dL (interquartile range [IQR] 4-15) and the median age at ED1 was 3.7 years (IQR 1.4-7.7). Median age at ED1 rose from 2.5 years (IQR 1.2-5.7) in patients with FVIII:C 2-5 IU/dL to 9.7 years (IQR 4.8-16.0) in patients with FVIII:C 25-40 IU/dL. In the subgroup (n = 104), median age at ED1, ED5, ED10, and ED20 was 4.0 years (IQR 1.4-7.6), 5.6 years (IQR 2.9-9.3), 7.5 years (IQR 4.4-11.3), and 10.2 years (IQR 6.5-14.2), respectively. Median ABR, AJBR, and ASmBR were 1.1 (IQR 0.5-2.6), 0.3 (IQR 0.1-0.7), and 0 (IQR 0-0), respectively.Conclusion
This study demonstrates that in non-severe hemophilia A, the age at first FVIII exposure increases with baseline FVIII:C and that major spontaneous bleeds rarely occur.
SUBMITTER: Abdi A
PROVIDER: S-EPMC7756346 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature
Abdi Amal A Kloosterman Fabienne R FR Eckhardt Corien L CL Male Christoph C Castaman Giancarlo G Fischer Kathelijn K Beckers Erik A M EAM Kruip Marieke J H A MJHA Peerlinck Kathelijne K Mancuso Maria Elisa ME Santoro Cristina C Hay Charles R CR Platokouki Helen H van der Bom Johanna G JG Gouw Samantha C SC Fijnvandraat Karin K Hart Dan P DP
Journal of thrombosis and haemostasis : JTH 20200928 12
<h4>Background</h4>In patients with non-severe hemophilia A, we lack detailed knowledge on the timing of treatment with factor VIII (FVIII) concentrates. This knowledge could provide information about the expected treatment timing in patients with severe hemophilia A treated with non-replacement therapies.<h4>Objective</h4>To assess the FVIII treatment history in patients with non-severe hemophilia A.<h4>Methods</h4>Patients with non-severe hemophilia (baseline FVIII activity [FVIII:C] 2-40 IU/d ...[more]