Women and girls with haemophilia: A retrospective cohort study in China

Author:

Zhang Wenhui1ORCID,Li Kuixing2ORCID,Poon Man‐Chiu3ORCID,Zhang Xinsheng4,Wu Jingsheng5,Zhao Xielan6,Zhou Min7,Wang Xuefeng8,Zhang Mei9,Xu Weiqun10,Yang Linhua11ORCID,Huang Meijuan12,Jin Chenghao13,Wang Xiaomin14,Zhang Donglei1,Chen Lingling1,Liu Wei1ORCID,Zhang Lei1,Xue Feng1ORCID,Yang Renchi1

Affiliation:

1. State Key Laboratory of Experimental Hematology National Clinical Research Center for Blood Diseases Haihe Laboratory of Cell Ecosystem Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Tianjin Key Laboratory of Gene Therapy for Blood Diseases CAMS Key Laboratory of Gene Therapy for Blood Diseases Tianjin China

2. Department of Haematology Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

3. Departments of Medicine Paediatrics and Oncology Cumming School of Medicine University of Calgary Calgary Alberta Canada

4. Shandong Blood Center Shandong Hemophilia Treatment Center Jinan China

5. The First Affiliated Hospital Chinese University of Science and Technology Hefei China

6. Xiangya Hospital Central South University Changsha China

7. Chengdu Women's and Children's Central Hospital Chengdu China

8. Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China

9. The First Affiliated Hospital of Xi'an Jiaotong University Xi'an China

10. Children's Hospital Zhejiang University School of Medicine Hangzhou China

11. The Second Hospital of Shanxi Medical University Taiyuan China

12. Fujian Medical University Union Hospital Fujian Institute of Haematology Fuzhou China

13. Jiangxi Provincial People's Hospital Department of Hematology Nanchang China

14. Xinjiang Uygur Autonomous Region People's Hospital Urumchi China

Abstract

AbstractIntroductionWomen and girls with haemophilia (WGH) may have spontaneous/traumatic bleeding similar to that in males with haemophilia, and in addition excessive bleeding during menstruation and delivery.AimTo characterize WGH in China and provide guidance for better management.MethodsWe retrospectively analysed the characteristics of WGH registered in the Haemophilia Treatment Center Collaborative Network of China (HTCCNC) Registry, including demographics, diagnosis and treatment, bleeding characteristics, obstetrical and gynaecological experiences, and surgical history.ResultsA total of 61 females had confirmed haemophilia. Diagnosis and treatment were typically delayed, longer in mild haemophilia than in severe and moderate. The most frequently reported bleeding manifestations were haemarthrosis in severe and moderate patients, and cutaneous bleeding in mild patients. Among 45 postmenarcheal WGH, 21 (46.7%) had history of heavy menstrual bleeding, but only three received treatments. Prenatal diagnosis and management of perinatal haemorrhage were inadequate. Of 34 deliveries in 30 women, nine deliveries were complicated by postpartum haemorrhage, and 22 offspring carried mutations causing haemophilia. Forty‐four surgical procedures were performed in 29 patients. Those procedures receiving preoperative coagulation factors coverage were significantly less likely to have excessive bleeding than those who did not (P = .003).ConclusionThis is the first and largest study describing WGH in China. There are currently deficiencies in the identification, diagnosis, and management of these patients. Improving health insurance policies, establishing haemophilia centres, and multidisciplinary teams for bleeding and perinatal or perioperative management will help reduce morbidity and mortality.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

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