Incidence and mortality rates of intracranial hemorrhage in hemophilia: a systematic review and meta-analysis

Author:

Zwagemaker Anne-Fleur1ORCID,Gouw Samantha C.1ORCID,Jansen Julie S.1,Vuong Caroline1,Coppens Michiel2ORCID,Hu Qun3,Feng Xiaoqin4,Kim Soon K.5,Van der Bom Johanna G.6ORCID,Fijnvandraat Karin1ORCID

Affiliation:

1. Department of Pediatric Hematology, Emma Children’s Hospital, and

2. Department of Vascular Medicine–Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands;

3. Department of Pediatrics, Tongji Hospital, Tongji Medical University, Wuhan, China;

4. Department of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China;

5. Department of Pediatrics, Inha University Hospital, Incheon, Korea; and

6. Department of Clinical Epidemiology, Leiden University Medical Center, Leiden University, Leiden, The Netherlands

Abstract

Abstract Intracranial hemorrhage (ICH) is a severe complication that is relatively common among patients with hemophilia. This systematic review aimed to obtain more precise estimates of ICH incidence and mortality in hemophilia, which may be important for patients, caregivers, researchers, and health policy makers. PubMed and EMBASE were systematically searched using terms related to “hemophilia” and “intracranial hemorrhage” or “mortality.” Studies that allowed calculation of ICH incidence or mortality rates in a hemophilia population ≥50 patients were included. We summarized evidence on ICH incidence and calculated pooled ICH incidence and mortality in 3 age groups: persons of all ages with hemophilia, children and young adults younger than age 25 years with hemophilia, and neonates with hemophilia. Incidence and mortality were pooled with a Poisson-Normal model or a Binomial-Normal model. We included 45 studies that represented 54 470 patients, 809 151 person-years, and 5326 live births of patients with hemophilia. In persons of all ages, the pooled ICH incidence and mortality rates were 2.3 (95% confidence interval [CI], 1.2-4.8) and 0.8 (95% CI 0.5-1.2) per 1000 person-years, respectively. In children and young adults, the pooled ICH incidence and mortality rates were 7.4 (95% CI, 4.9-11.1) and 0.5 (95% CI, 0.3-0.9) per 1000 person-years, respectively. In neonates, the pooled cumulative ICH incidence was 2.1% (95% CI, 1.5-2.8) per 100 live births. ICH was classified as spontaneous in 35% to 58% of cases. Our findings suggest that ICH is an important problem in hemophilia that occurs among all ages, requiring adequate preventive strategies.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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