Fabienne R. Kloosterman
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Fabienne R. Kloosterman has a total of 33 co-authors. Here are the top co-authors by number of shared publications:
- Samantha Claudia Gouw
Department of Pediatric Hematology, Amsterdam UMC location University of Amsterdam, Amsterdam, the Netherlands
4 shared publications - Anne-Fleur Zwagemaker
Amsterdam UMC University of Amsterdam, Emma Children's Hospital, Pediatric Hematology Amsterdam the Netherlands
3 shared publications - Karin Fijnvandraat
Amsterdam UMC, Pediatric Hematology, University of Amsterdam, Emma Children's Hospital, Amsterdam, Netherlands
3 shared publications - Michiel Coppens
Amsterdam UMC
3 shared publications - Catherine N. Bagot
Department of Haematology Glasgow Royal Infirmary Glasgow UK
2 shared publications - Erik A. M. Beckers
Department of Internal Medicine, Division Hematology, P. Debyelaan 25, Maastricht University Medical Center, Maastricht, 6229 HX, The Netherlands
2 shared publications
Latest Publications
- Open Access
- 31 August 2022
- Published by Elsevier in Research and Practice in Thrombosis and Haemostasis
- Vol. 6 (6) , e12777
Desmopressin for bleeding in non‐severe hemophilia A: Suboptimal use in a real‐world setting
- 31 August 2022
- Published by Elsevier in Research and Practice in Thrombosis and Haemostasis
- Vol. 6 (6) , e12777
Open AccessDesmopressin for bleeding in non‐severe hemophilia A: Suboptimal use in a real‐world setting
- Open Access
- 21 July 2022
- Published by American Society of Hematology in Blood Advances
- Vol. 6 (14) , 4256-4265
The bleeding phenotype in people with nonsevere hemophilia
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.
- 21 July 2022
- Published by American Society of Hematology in Blood Advances
- Vol. 6 (14) , 4256-4265
Open AccessThe bleeding phenotype in people with nonsevere hemophilia
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.
- Open Access
- 7 March 2022
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 20 (5) , 1126-1137
Joint status of patients with nonsevere hemophilia A
- 7 March 2022
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 20 (5) , 1126-1137
Open AccessJoint status of patients with nonsevere hemophilia A
- 23 September 2021
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 19 (10) , 2642-2644
The factor VIII treatment history of non‐severe hemophilia A—Response from original authors Abdi et al
- 23 September 2021
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 19 (10) , 2642-2644
The factor VIII treatment history of non‐severe hemophilia A—Response from original authors Abdi et al