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Licensed Unlicensed Requires Authentication Published by De Gruyter August 19, 2017

Perinatal outcomes after previable preterm premature rupture of membranes before 24 weeks of gestation

  • Verena Kiver ORCID logo EMAIL logo , Vinzenz Boos , Anke Thomas , Wolfgang Henrich and Alexander Weichert

Abstract

Objective:

A current descriptive assessment of perinatal outcomes in pregnancies complicated by previable preterm premature rupture of membranes (pPPROM) at <24 weeks of gestation, after expectant treatment.

Study design:

Maternal and short-term neonatal data were collected for patients with pPPROM.

Results:

Seventy-three patients with 93 fetuses were hospitalized with pPPROM at 15–24 weeks’ gestation. Among these patients, 27.4% (n=20) chose pregnancy termination, 27.4% (n=20) miscarried and 45.2% (n=33) proceeded to live births. After a median latency period of 38 days, ranging from 1 to 126 days, 24 singletons and 20 multiples were live-born, of whom 79.5% (n=35) survived the perinatal period. The main neonatal sequelae were pulmonary hypoplasia (29.5%; n=13), connatal infection (56.8%; n=25), intraventricular hemorrhage (25%; n=11; resulting in five neonatal deaths) and Potter’s syndrome (15.9%; n=7). Nine newborns died, within an average of 2.8 days (range, 1–10 days). The overall neonatal survival rate was 51.5% – including miscarriages but not elective terminations. The intact survival rate was 45.5% of all live-born neonates.

Conclusions:

Even with limited treatment options, overall neonatal survival is increasing. However, neonatal mortality and morbidity rates remain high. The gestational age at membrane rupture does not predict neonatal outcome.

  1. Author’s statement

  2. Conflict of interest: Authors state no conflict of interest.

  3. Material and methods: Informed consent: Informed consent has been obtained from all individuals included in this study.

  4. Ethical approval: The research related to human subject use has complied with all the relevant national regulations, and institutional policies, and is in accordance with the tenets of the Helsinki Declaration, and has been approved by the authors’ institutional review board or equivalent committee.

  5. Disclosure statement: The authors report no conflict of interest. We have not disclosed any information that could reveal the identity of our patients. The authors affirm that this research was conducted in accordance with the ethical standards of all applicable national and institutional committees and of the World Medical Association’s Helsinki Declaration.

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Received: 2016-10-25
Accepted: 2017-7-11
Published Online: 2017-8-19
Published in Print: 2018-7-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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