The bleeding phenotype in people with nonsevere hemophilia.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 07 2022
Historique:
received: 17 03 2022
accepted: 28 04 2022
pubmed: 10 5 2022
medline: 28 7 2022
entrez: 9 5 2022
Statut: ppublish

Résumé

Detailed information on the onset, frequency, and severity of bleeding in nonsevere hemophilia is limited. We aimed to assess the bleeding phenotype of persons with nonsevere hemophilia and to analyze the association between baseline factor VIII/IX (FVIII/IX) levels and the joint bleeding rate. In the DYNAMO (Dynamic Interplay Between Bleeding Phenotype and Baseline Factor Level in Moderate and Mild Hemophilia A and B) study, an international multicenter cohort, we included males with nonsevere hemophilia (FVIII/IX, 0.02-0.35 IU/mL) aged 12 to 55 years. Information on age at first treated (joint) bleed, annual bleeding rates (ABRs), and annual joint bleeding rates (AJBRs) was collected from the medical files. The association between baseline FVIII/IX levels and the joint bleeding rate was assessed by using a frailty model for recurrent events. In total, 304 persons (70 with moderate hemophilia and 234 with mild hemophilia) were included. The median age was 38 years (interquartile range [IQR], 25-49 years), and the median baseline FVIII/IX level was 0.12 IU/mL (IQR, 0.05-0.21 IU/mL). In total, 245 (81%) persons had experienced at least 1 bleed, and 156 (51%) had experienced at least 1 joint bleed. The median age at first bleed and first joint bleed was 8 and 10 years, respectively. The median ABR and AJBR was 0.2 (IQR, 0.1-0.5) and 0.0 (IQR, 0.0-0.2). From baseline FVIII/IX levels 0.02 to 0.05 IU/mL to >0.25 IU/mL, the median ABR decreased from 0.6 (IQR, 0.2-1.4) to 0.1 (IQR, 0.0-0.2) and the AJBR from 0.2 (IQR, 0.0-0.4) to 0.0 (IQR, 0.0-0.0). Baseline FVIII/IX was inversely associated with the joint bleeding rate (P < .001). Low bleeding rates were observed in persons with nonsevere hemophilia. However, one-half of all adolescents and adults had experienced a joint bleed.

Identifiants

pubmed: 35533261
pii: 485196
doi: 10.1182/bloodadvances.2022007620
pmc: PMC9327532
doi:

Substances chimiques

Hemostatics 0
Factor IX 9001-28-9

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4256-4265

Informations de copyright

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Fabienne R Kloosterman (FR)

Emma Children's Hospital, Pediatric Hematology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.

Anne-Fleur Zwagemaker (AF)

Emma Children's Hospital, Pediatric Hematology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.

Catherine N Bagot (CN)

Department of Haematology, Glasgow Royal Infirmary, Glasgow, United Kingdom.

Erik A M Beckers (EAM)

Division of Hematology, Department of Internal Medicine, CARIM School for Cardiovascular Diseases, Maastricht University Medical Center, Maastricht, The Netherlands.

Giancarlo Castaman (G)

Department of Oncology, Center for Bleeding Disorders, Careggi University Hospital, Florence, Italy.

Marjon H Cnossen (MH)

Department of Pediatric Hematology, Erasmus University Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.

Peter W Collins (PW)

Cardiff Haemophilia Centre, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Charles Hay (C)

University Department of Haematology, The University of Manchester, Manchester Royal Infirmary, Manchester, United Kingdom.

Michel Hof (M)

Department of Epidemiology and Data Science, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.

Britta Laros-van Gorkom (B)

Department of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.

Frank W G Leebeek (FWG)

Department of Hematology, Erasmus University Medical Center, Erasmus MC, Rotterdam, The Netherlands.

Christoph Male (C)

Department of Pediatrics, Medical University of Vienna, Vienna, Austria.

Karina Meijer (K)

Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Ingrid Pabinger (I)

Clinical Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.

Susan Shapiro (S)

Department of Haematology, Oxford University Hospitals NHS Foundation, Oxford NIHR Biomedical Research Centre, Oxford, United Kingdom.
Radcliffe Department of Medicine, Oxford University, Oxford, United Kingdom.

Michiel Coppens (M)

Department of Vascular Medicine, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands; and.

Karin Fijnvandraat (K)

Emma Children's Hospital, Pediatric Hematology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.
Department of Molecular Cellular Hemostasis, Sanquin Research and Landsteiner Laboratory, Amsterdam, The Netherlands.

Samantha C Gouw (SC)

Emma Children's Hospital, Pediatric Hematology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.

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