Schutgens REG

No ORCID on file · 5 papers in corpus · active 2020-2026
2026
Haemophilia : the official journal of the World Federation of Hemophilia ·doi:10.1111/hae.70186

BackgroundGlanzmann thrombasthenia (GT) is an inherited platelet disorder resulting in severely reduced platelet aggregation and increased bleeding tendency. Pregnancy and childbirth in women with GT present significant challenges for both …

2025
British journal of haematology ·doi:10.1111/bjh.70056

To illustrate the challenges in the management of women with Glanzmann thrombasthenia (GT) planning a pregnancy, we conducted a literature review and present a case series of eight women giving detailed descriptions of reproductive health p…

2023
Research and practice in thrombosis and haemostasis ·doi:10.1016/j.rpth.2023.102229

BackgroundHeavy menstrual bleeding (HMB), self-reported by 37% of adolescents, can be the first sign of a bleeding disorder (BD) during adolescence. The Dutch general practitioner (GP) guideline demands laboratory diagnostics and referral f…

2022
Haemophilia : the official journal of the World Federation of Hemophilia ·doi:10.1111/hae.14492

AimCurrently, it is unknown which patient-reported outcomes are important for patients with autosomal inherited bleeding disorders. Therefore, the purpose of this study is to systematically review the available literature assessing patient-…

2020
Research and practice in thrombosis and haemostasis ·doi:10.1002/rth2.12281

BackgroundPatients with congenital blood platelet disorders (CPDs) demonstrate a predominantly mucocutaneous bleeding tendency. Repeated bleeds throughout life can have a significant impact on health status-related quality of life (HR-QoL),…