CC BY-NC-ND 4.0 · AJP Rep 2020; 10(01): e62-e67
DOI: 10.1055/s-0040-1702935
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Clinical Utility of Weekly Laboratory Testing in the Outpatient Management of Preeclampsia and Gestational Hypertension

John A. Morgan
1   Department of Obstetrics and Gynecology, LSU Health Shreveport, Shreveport, Louisiana
,
Lauren E. McCalmont
1   Department of Obstetrics and Gynecology, LSU Health Shreveport, Shreveport, Louisiana
,
Craig V. Towers
2   Department of Obstetrics and Gynecology, The University of Tennessee Health Science Center, Knoxville, Tennessee
,
Melissa Davis
2   Department of Obstetrics and Gynecology, The University of Tennessee Health Science Center, Knoxville, Tennessee
,
Miriam Hankins
1   Department of Obstetrics and Gynecology, LSU Health Shreveport, Shreveport, Louisiana
,
Niyati Rangnekar
2   Department of Obstetrics and Gynecology, The University of Tennessee Health Science Center, Knoxville, Tennessee
,
Mary Ellen McNeal
2   Department of Obstetrics and Gynecology, The University of Tennessee Health Science Center, Knoxville, Tennessee
,
David F. Lewis
1   Department of Obstetrics and Gynecology, LSU Health Shreveport, Shreveport, Louisiana
› Author Affiliations
Funding No sources of funding were used for this study.
Further Information

Publication History

26 November 2019

05 December 2019

Publication Date:
04 March 2020 (online)

Abstract

Objective To investigate the utility of obtaining weekly laboratory testing in patients managed as an outpatient for gestational hypertension and preeclampsia without severe features.

Study Design A multisite retrospective cohort study was performed evaluating preterm women diagnosed with gestational hypertension/preeclampsia managed in an outpatient setting between gestational ages of 230/7 and 366/7. Patients were divided into two groups: weekly laboratory evaluation (laboratories group) and a no laboratories group. The primary study outcome was composite maternal morbidity including more than one of the following: development of severe features, HELLP syndrome, eclampsia, placental abruption, maternal intensive care unit admission, or maternal death.

Results A total of 204 patients were included in this study, laboratories group (n = 120) and no laboratories group (n = 84). The laboratories group was older (28.8 vs. 26.6 years, p = 0.02), had a higher rate of chronic hypertension (44 [36.7%] vs. 17 [20.2%], p = 0.01), and more often experienced the primary composite outcome (53 [44.2%] vs. 24 [28.5%], p = 0.02). No patients in our cohort were delivered for abnormal laboratory values.

Conclusion This study found that weekly laboratory testing may have minimal clinical utility in the outpatient management protocol in monitoring patients with mild gestational hypertension or preeclampsia. Delivery was guided by other clinical factors.

Disclosure

All authors report no conflicts of interest and have no financial disclosures to report.


Note

Oral presentation at the 86th Annual Meeting of the Central Association of Obstetricians and Gynecologists, October 19, 2019.


 
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