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Outcomes in oligohydramnios: the role of etiology in predicting pulmonary morbidity/mortality

  • Ashley Hesson EMAIL logo and Elizabeth Langen
Published/Copyright: June 20, 2018

Abstract

Objective

Early-onset oligohydramnios is typically secondary to renal-urinary anomalies (RUA) or preterm premature rupture of membranes (PPROM). We compared neonatal pulmonary outcomes between these etiologies.

Methods

We conducted a retrospective cohort study of women with oligohydramnios identified before 24 completed weeks of gestation attributed to either PPROM or RUA. Patients were excluded if other fetal anomalies were noted. Respiratory morbidity was assessed by the need for oxygen at 36 corrected weeks or at hospital discharge.

Results

Of 116 eligible patients, 54 chose elective pregnancy termination. A total of 39.5% of PPROM (n=17/43) and 36.8% of RUA (n=7/19) pregnancies experienced pre-viable loss (P=1.00). Significantly fewer PPROM live births resulted in neonatal mortality (26.9% vs. 75.0%, P<0.01). There was no difference in respiratory morbidity (57.9% vs. 66.6%, P=1.00). The collective incidence of respiratory mortality and morbidity was not different between etiologies (P=0.06).

Conclusion

This analysis suggests that the prognoses for oligohydramnios due to pre-viable PPROM vs. renal anomalies are similarly grave, though RUA infants experienced a higher rate of neonatal respiratory mortality.


Corresponding author: Ashley Hesson, MD, PhD, University of Michigan Obstetrics and Gynecology, 1500 E. Medical Center Drive, L3211 UH South, Ann Arbor, MI 48109-5276, USA, Tel.: +1 716 348 9693

Acknowledgments

The authors would like to thank Marjorie C. Treadwell for her assistance in data collection and the attendees of the 2017 ACOG Annual Clinical and Scientific Meeting for their feedback on this project.

  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.

References

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Received: 2017-09-01
Accepted: 2018-02-06
Published Online: 2018-06-20
Published in Print: 2018-10-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

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