Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/117277
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Type: Journal article
Title: Causes of stillbirth in a socioeconomically disadvantaged urban Australian population - a comprehensive analysis
Author: Wijs, L.
de Graaff, E.
Leemaqz, S.
Dekker, G.
Citation: The Journal of Maternal-Fetal and Neonatal Medicine, 2017; 30(23):2851-2857
Publisher: Taylor & Francis
Issue Date: 2017
ISSN: 1476-4954
1476-4954
Statement of
Responsibility: 
Laura Anna Wijs, Esti Charlotte de Graaff, Shalem Leemaqz and Gustaaf Dekker
Abstract: Introduction: The aim of this paper was to provide an in-depth analysis of all stillbirth causation over a period of 10 years in a busy maternity unit located in a socioeconomically disadvantaged urban area, with an emphasis on overlapping pathology. Materials and methods: A retrospective analysis of all structurally normal stillbirths in singleton pregnancies born during 2002–2012. The PSANZ stillbirth classification was used; per stillbirth subgroup main risk factors were evaluated. Results: Out of 130 cases, 43% showed overlapping pathologies. In the remaining 74 (56%) cases, the following single pathologies were found: IUGR 20 (15%), infection 12 (9%), abruption 8 (6%), placental thrombotic pathology 8 (6%), miscellaneous 6 stillbirths (5%), and 20 cases (15%) unexplained. Smoking was a risk factor for stillbirth associated with abruption (OR 3.639), infection (OR 2.271), and thrombotic pathology (OR 2.168). Drug use had an association with (placental) infection (OR 3.598). Obesity showed a significant association with IUGR (OR 3.782) and abruption (OR 9.040). Thrombophilia risk analysis for the overall group of stillbirths showed significant results for Protein S (OR 8.889) and homocysteine >90th centile (OR 2.087). Conclusions: Overlapping pathology was identified in 43% of stillbirths. Infection, IUGR, and abruption were the most important single cause of stillbirth.
Keywords: Australia
Stillbirth
causes
Rights: © 2016 Informa UK Limited, trading as Taylor & Francis Group
DOI: 10.1080/14767058.2016.1265933
Published version: http://dx.doi.org/10.1080/14767058.2016.1265933
Appears in Collections:Aurora harvest 3
Paediatrics publications

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