Mode of delivery and risk of intracranial haemorrhage in newborns with severe haemophilia A: a multicentre study in Gulf region

Mode of delivery and risk of intracranial haemorrhage in newborns with severe haemophilia A: a multicentre study in Gulf region

Introduction The optimum mode of delivery in a known carrier of a haemophilia A is still an issue of debate. Aim This study was conducted to report a multicentre experience in Gulf Cooperation Council (GCC) on the incidence of intracranial haemorrhage (ICH) in newborns with severe haemophilia A deli...

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Veröffentlicht in:Haemophilia : the official journal of the World Federation of Hemophilia 2016-05, Vol.22 (3), p.e134-e138
Hauptverfasser: Nazir, H. F., Al Lawati, T., Beshlawi, I., AlSharidah, S., Elshinawy, M., Alkasim, F., Khanani, M. F., Tarawa, A., Al Subhi, T., Alrawas, A., Al Riyami, W., Al Kindi, S., Al Saadi, K., Al-Lamki, S., Wali, Y.
Format: Artikel
Sprache:eng
Schlagworte:
Adolescent
Cesarean Section - statistics & numerical data
Child
Child, Preschool
Childbirth & labor
Coagulation factors
Cohort Studies
Delivery, Obstetric - statistics & numerical data
Factor VIII deficiency
Female
Gulf region
haemophilia A
Hemophilia
Hemorrhage
Humans
Infant
Infant, Newborn
intracranial haemorrhage
Intracranial Hemorrhages - epidemiology
Male
Middle East - epidemiology
mode of delivery
Neonates
Patients
Pregnancy
Pregnancy Complications, Hematologic - epidemiology
Prospective Studies
Retrospective Studies
Risk
Vagina
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Beschreibung
Zusammenfassung:Introduction The optimum mode of delivery in a known carrier of a haemophilia A is still an issue of debate. Aim This study was conducted to report a multicentre experience in Gulf Cooperation Council (GCC) on the incidence of intracranial haemorrhage (ICH) in newborns with severe haemophilia A delivered by different modalities. Methods We have conducted a retrospective/prospective multicentre cohort study including a total of seven hospitals distributed in four GCC countries between 1998 and Jan 2015. A total of 163 patient with severe haemophilia A (factor VIII
ISSN:1351-8216
1365-2516
DOI:10.1111/hae.12842