Factor <scp>VII</scp> deficiency in China: Phenotype, genotype and current status of management
Cuiyun Qu, Wei Liu, Lingling Chen, Lei Zhang, Feng Xue, Renchi Yang
Abstract
Summary Congenital factor VII (FVII) deficiency is a rare bleeding disorder characterised by a wide molecular and clinical heterogeneity. We investigated the clinical phenotype of 193 patients and F7 genotype of 55/193 patients with FVII deficiency throughout China and showed their current status of management. The most frequent bleeding symptoms were epistaxis (44.6%), cutaneous (38.9%), oral cavity (40.4%) bleeding and menorrhagia (44.3% of females of reproductive age). Fatal central nervous system bleeding and disabling joint bleeding occurred in three patients each. The majority of patients (89.6%) had FVII activity (FVII:C) ≤10% and the proportion of symptomatic patients in this group (79.8%) was significantly higher than that in the groups with FVII:C >10%–25% (41.7%) and >25%–50% (37.5%) (χ 2 = 13.641, p = 0.001). Major bleeds occurred only in patients with FVII:C ≤10%. In total 55 patients underwent genotype analysis: most variants were missense (62.5%) and most patients had homozygous/compound heterozygous (85.4%) variants. Prothrombin complex concentrates (72.4%) were the most frequently used on‐demand replacement therapy. Prophylaxis before delivery decreased the risk of postpartum bleeding in women (χ 2 = 69.243, p = 0.000). Our study provides useful information on the phenotype, genotype and current status of FVII‐deficiency patients management and may promote further exploration and care of this population in the future.