血管性血友病因子
医学
荟萃分析
血管性血友病
去氨加压素
内科学
凝血病
胃肠病学
疾病
免疫学
血小板
作者
Sebastiaan Laan,Jessica Del Castillo,Suzanne C. Cannegieter,Karin Fijnvandraat,Marieke J. H. A. Kruip,Saskia le Cessie,Ruben Bierings,Jeroen Eikenboom,Iris van Moort
出处
期刊:Blood
[Elsevier BV]
日期:2025-01-24
卷期号:145 (16): 1814-1825
被引量:8
标识
DOI:10.1182/blood.2024026804
摘要
ABSTRACT: Desmopressin (1-desamino-8-d-arginine vasopressin [DDAVP]) can be used to prevent or stop bleeding. However, large interindividual variability is observed in DDAVP response and determinants are largely unknown. In this systematic review and meta-analysis, we aimed to identify the response to DDAVP and the factors that determine DDAVP response in patients. We included studies with patients with any bleeding disorder receiving DDAVP. First and second screening round and risk of bias assessment were performed by independent reviewers. The main outcome was proportion of patients with complete (factor level >50 U/dL) or partial (30-50 U/dL) response to DDAVP. Determinants of response including disease type, age, sex, von Willebrand factor (VWF) and factor VIII (FVIII) mutations, and baseline factor levels were investigated. In total, 591 articles were found and 103 were included. Of these, 71 articles (1772 patients) were suitable for the study's definition of response. Meta-analysis showed a pooled response proportion of 0.71 (0.64; 0.78) and a significant difference in response between disease subtypes. For hemophilia A, baseline FVIII activity (FVIII:C) was a borderline significant determinant of response. In patients with von Willebrand disease (VWD) type 1, VWF antigen (VWF:Ag), VWF activity, and FVIII:C were significant determinants. A large variation in response was observed for specific mutations in VWF and FVIII. Response to DDAVP varied between disease subtypes and was largely determined by the baseline levels of FVIII:C for hemophilia A and VWF:Ag for VWD. Our findings highlight the significant differences in response and emphasize the need for a standardized response definition and further research into response mechanisms.
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