Volume 187, Issue 4 pp. 509-517
Research Paper

Bleeding and bruising in Osteogenesis Imperfecta: International Society on Thrombosis and Haemostasis bleeding assessment tool and haemostasis laboratory assessment in 22 individuals

Koert Gooijer

Corresponding Author

Koert Gooijer

Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands

Correspondence:

Koert Gooijer, Research Physican, Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands.

E-mail: [email protected]

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Jan M. M. Rondeel

Jan M. M. Rondeel

Department of Clinical Chemistry, Isala Hospital, Zwolle, The Netherlands

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Fleur S. van Dijk

Fleur S. van Dijk

Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands

North West Thames Regional Genetics Service, Ehlers-Danlos Syndrome National Diagnostic Service London, North West Health Care University NHS Trust, Harrow, Middlesex, UK

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Arjan G. J. Harsevoort

Arjan G. J. Harsevoort

Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands

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Guus J. M. Janus

Guus J. M. Janus

Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands

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Anton A. M. Franken

Anton A. M. Franken

Expert Centre for adults with Osteogenesis Imperfecta, Isala Hospital, Zwolle, The Netherlands

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First published: 14 July 2019
Citations: 19

Summary

Osteogenesis imperfecta (OI) is characterized by susceptibility to bone fractures. Other symptoms, such as easy bruising and bleeding complications during surgery necessitating transfusions, have also been reported. The aim of the cross-sectional pilot study was to assess the bleeding and bruising tendency in OI patients and to screen for possible underlying haematological disorders. Bleeding tendency was investigated using the International Society on Thrombosis and Haemostasis bleeding assessment tool (ISTH-BAT) in 22 adult OI patients. Laboratory testing was performed to investigate for bleeding disorders or abnormal coagulation. Four patients [OI type 1(n = 3), OI type 4(n = 1)] had a bleeding score (BS) fitting with a bleeding tendency, but without test results pointing to a coagulopathy. Two patients [OI type 1(n = 1), OI type 3 (n = 1)] without a bleeding tendency according to the BS had increased fibrinolysis. This is the second largest study to date addressing bleeding tendency in OI and the first study to use ISTH-BAT and elaborate laboratory testing for coagulopathies. Four patients had an increased bleeding tendency. However, laboratory testing demonstrated no bleeding disorder or abnormal coagulation. Increased fibrinolysis was demonstrated in two patients without bleeding tendency on BS. Vascular fragility as a cause of bleeding tendency in OI has been suggested earlier. Further research on bleeding tendency in OI is important.

Disclosure

The authors have stated that they have nothing to disclose and have no conflicts of interest.

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