Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study

P. D. James, J. Mahlangu, C. Bidlingmaier, M. E. Mingot-Castellano, M. Chitlur, P. F. Fogarty, A. Cuker, M. E. Mancuso, P. A. Holme, J. Grabell, N. Satkunam, W. M. Hopman, P. Mathew, Roshni Kulkarni, Alfonso Iorio, Keith Gomez, Raj Kasthuri, Rebecca Kruse-Jarres, Margareth Ozelo, Yasuaki ShidaGili Kenet, Global Emerging HEmostasis Experts Panel (GEHEP)

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: There has been increasing recognition in recent years that female carriers of haemophilia manifest abnormal bleeding; however, data on the use of bleeding assessment tools in this population are lacking. Aim: Our objective was to validate the ISTH-BAT in haemophilia carriers to describe bleeding symptoms and allow for comparisons with factor levels and other patient groups. Methods: This was a prospective, observational, cross-sectional study performed by members of Global Emerging HEmostasis Panel (GEHEP). Unselected consecutive haemophilia carriers were recruited and a CRF and the ISTH-BAT were completed by study personnel. Results: A total of 168 haemophilia carriers were enrolled: 155 haemophilia A and 13 haemophilia B. The mean age was 40 years (range: 20–82). Carriers had higher mean bleeding scores (BS) compared with age-matched controls (n = 46; 5.7 vs. 1.43; P < 0.0001) and Type 3 VWD OC (n = 32; 3.0; P = 0.009), but lower BS compared with women with Type 1 VWD (n = 83; 8.7; P < 0.0001). Fifteen carriers reported haemarthrosis, and of those six had normal FVIII/FIX levels. There was a significant but weak negative correlation between BS and factor level (Spearman's r2 = −0.36, P < 0.001). Conclusion: Our results show that haemophilia carriers experience abnormal bleeding, including haemarthrosis. Overall, BS in women with Type 1 VWD > haemophilia carriers > Type 3 VWD OC > controls. Understanding the performance of the ISTH-BAT in this population is a critical step in future research aimed at investigating the underlying pathophysiology of abnormal bleeding, with the ultimate goal of optimizing treatment.

Original languageEnglish
Pages (from-to)912-918
Number of pages7
JournalHaemophilia
Volume22
Issue number6
DOIs
Publication statusPublished - Nov 1 2016

Keywords

  • bleeding
  • haemophilia carriers
  • ISTH-BAT

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)

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