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Title: Severe spontaneous hemoperitoneum in pregnancy may be linked to in vitro fertilization in patients with endometriosis: a systematic review
Authors: Brosens, Ivo A.
Lier, Marit C.
Mijatovic, Velja
Benagiano, Giuseppe
First Published: 20-Jun-2016
Publisher: Elsevier for American Society for Reproductive Medicine
Citation: Fertility and Sterility, 2016, 106 (3), pp. 692-703
Abstract: Objective: To evaluate existing evidence of a possible association in women with endometriosis between controlled ovarian hyperstimulation plus embryo transfer (COH-ET) and the occurrence of spontaneous hemoperitoneum in pregnancy (SHiP). Design: Comprehensive review. Setting: Not applicable. Patient(s): None. Intervention(s): An electronic literature search up to February 2016 was conducted using Scopus and PubMed. Main Outcome Measure(s): The role of COH-ET in SHiP. Result(s): Controlled ovarian hyperstimulation plus embryo transfer may increase the severity or incidence of the rare condition known as SHiP. An analysis of published cases shows that bleeding often occurs from multiple or diffuse sites, mainly situated in the posterior pelvic cavity, making it difficult to control without interfering with the pregnancy itself. Spontaneous hemoperitoneum in pregnancy is linked to adverse perinatal outcomes, including stillbirth, neonatal mortality, and very low or low birth weight. In 14 cases a biopsy of the bleeding site was obtained, and in all cases, even in the absence of visible endometriosis, decidualization was documented. At present, the relatively small number of cases published prevents firm conclusions, although they are highly suggestive of a link between COH-ET in women with endometriosis and the occurrence and seriousness of SHiP. Conclusion(s): Spontaneous hemoperitoneum in pregnancy is a rare but potentially fatal complication for the pregnant woman and her unborn child. In vitro fertilization in women with severe endometriosis may be a risk factor for SHiP.
DOI Link: 10.1016/j.fertnstert.2016.05.025
ISSN: 0015-0282
eISSN: 1556-5653
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © the authors, 2016. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License (, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Appears in Collections:Published Articles, Dept. of Cancer Studies and Molecular Medicine

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