Startseite Obstetric outcomes of pregnancy complicated by urolithiasis: a retrospective cohort study
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Obstetric outcomes of pregnancy complicated by urolithiasis: a retrospective cohort study

  • Emily K. Clennon ORCID logo EMAIL logo , Bharti Garg , Brian D. Duty und Aaron B. Caughey
Veröffentlicht/Copyright: 18. August 2020

Abstract

Objectives

Evaluate the association between urolithiasis during pregnancy and obstetric outcomes outside the context of urological intervention.

Methods

We conducted a retrospective cohort study of singleton, non-anomalous gestations delivered at 23–42 weeks in California from 2007 to 2011. Maternal outcomes (preterm delivery [early (<32 weeks) and late (<37 weeks)], preeclampsia, gestational diabetes, cesarean deliveries, urinary tract infection [UTI] at delivery, chorioamnionitis, endomyometritis, and maternal sepsis) and newborn outcomes (seizure, respiratory distress syndrome, hypoglycemia, jaundice, and neonatal abstinence syndrome [NAS]) were compared using χ2-tests and multivariable logistic regression.

Results

A total of 2,013,767 pregnancies met inclusion criteria, of which 5,734 (0.28%) were complicated by urolithiasis. Stone disease during pregnancy was associated with 30% greater odds of each early (aOR 1.30; 95% CI 1.19–1.43) and late (aOR 1.29; 95% CI 1.18–1.41) preterm delivery. Cesarean delivery, UTI at delivery, gestational hypertension, gestational diabetes, preeclampsia, and sepsis were all significantly positively associated with urolithiasis. Odds of NAS (aOR 2.11; 95% CI 1.27–3.51) and jaundice were significantly greater in the neonates of stone-forming patients (aOR 1.08; 95% CI 1.01–1.16).

Conclusions

Urolithiasis during pregnancy was associated with 30% greater odds of preterm delivery and increased risk of myriad metabolic, hypertensive, and infectious disorders of gestation. Neonates born to stone-forming patients were more than twice as likely to develop neonatal abstinence syndrome but did not have significantly greater odds of complications of prematurity.


Corresponding author: Emily K. Clennon, MD, MPH, Oregon Health & Science University, Department of Urology, Portland, OR, USA, Phone: 217-369-5880, Fax: 503-494-2391, E-mail:

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Ethical approval: We obtained human subjects approval from the Oregon Health and Science University Institutional Review Board, the California Office of Statewide Health Planning and Development, and the California Committee for the Protection of Human Subjects.

  5. Disclosure: The views expressed in this article are the authors’ own and do not represent any official positions of Oregon Health and Science University.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jpm-2020-0199).

Received: 2020-05-04
Accepted: 2020-07-30
Published Online: 2020-08-18
Published in Print: 2021-01-26

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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  23. Acknowledgment
  24. Acknowledgment
Heruntergeladen am 10.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/jpm-2020-0199/html
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