Management of Preeclampsia at Term
Management of preeclampsia at term (≥ 37 0/7 weeks) involves assessing the maternal-fetal status, preparing for delivery, and monitoring for disease severity and progression.
Delivery is indicated when preeclampsia is diagnosed at term regardless of the presence/absence of severe features. Approach to delivery depends on usual obstetric considerations: cervical status, fetal presentation, and maternal-fetal well-being. Vaginal delivery is preferred, provided usual contraindications are absent. Cesarean delivery is reserved for usual obstetric indications or if preeclampsia worsens resulting in maternal or fetal instability remote from delivery.
Critical to intrapartum and postpartum care is blood pressure monitoring which should occur minimally every hour, unless measurements of ≥ 160 or 110 mmHg systolic or diastolic respectively are encountered. Severe hypertension require increased frequency of evaluation and if persistent over 15 minutes, they require treatment with either IV labetalol or hydralazine, or oral short-acting nifedipine. Sample order sets exist which provide guidance on increasing dosages, timing between medication administration and blood pressure evaluations, plus additional supports (See Committee Opinion reference). In general, after administration of 3 doses of the initially selected agent, transition to a different agent, and emergency consultation with relevant specialists/subspecialists is recommended. If hypertension management requires acute IV treatment, it is often prudent to initiate oral labetalol or extended-release nifedipine to maintain blood pressures below the severe range. Intrapartum blood pressure management and consultation should not delay progress towards delivery. Fetal monitoring should be continuous.
In addition to evaluating and treating for severe-range blood pressures, monitoring for other severe features including signs/symptoms of organ dysfunction, is vital throughout the intra- and postpartum periods. Laboratory values and symptom assessment should be obtained every 6 hours with severe features; discontinuation can be considered after two normal sets with low threshold to obtain if clinical condition changes.
Patients with preeclampsia with severe features should be administered magnesium sulfate for seizure prevention. An initial IV loading dose is administered (4-6 grams bolus) followed by maintenance dosing (1-2 grams/hour); dose adjustments may be required with evidence of renal dysfunction. While the patient is receiving magnesium sulfate, it is important to monitor for magnesium toxicity (e.g.; absent deep tendon reflexes, respiratory depression). As magnesium sulfate is cleared renally, it is important to monitor urine output. Calcium gluconate (1 g IV) is the antidote for magnesium toxicity. Consider obtaining serum magnesium levels in patients with a BMI ≥ 30 kg/m2 to confirm levels are in the therapeutic range (4.8–8.4 mg/dL). Magnesium sulfate should continue until 24 hours after delivery or from the time of the last seizure, if eclampsia ensues. There are a few contraindications to magnesium; phenytoin can be considered for seizure prophylaxis in these instances.
Postpartum management includes: 1) monitoring for and treating severely elevated blood pressures; 2) continuing/initiating magnesium sulfate in the context of preeclampsia with severe features for 24 hours post-delivery; and 3) after discharge, assessing blood pressures and symptoms at 7-10 days. Close follow-up and medication management is imperative until the patient’s blood pressures normalize, or if a diagnosis of chronic hypertension is suspected, appropriate referral is made.
Roberts JM, August PA, Bakris G, et al; American College of Obstetricians and Gynecologists; Task Force on Hypertension in Pregnancy. Hypertension in Pregnancy: Report of the American College of Obstetricians and Gynecologists’ Task Force on Hypertension in Pregnancy. Obstet Gynecol. 2013 Nov;122(5):1122-31. doi: 10.1097/01.AOG.0000437382.03963.88.
El-Sayed YY, Borders AE, ACOG Committee on Obstetric Practice. Committee Opinion No. 692: Emergent Therapy for Acute-Onset, Severe Hypertension During Pregnancy and the Postpartum Period. Obstet Gynecol. 2017 Apr;129(4):e90-e95. doi: 10.1097/AOG.0000000000002019.
Initial Approval May 2018; Reaffirmed January 2020
********** Notice Regarding Use ************
The Society for Academic Specialists in General Obstetrics and Gynecology, Inc. (“SASGOG”) is committed to accuracy and will review and validate all Pearls on an ongoing basis to reflect current practice.
This document is designed to aid practitioners in providing appropriate obstetric and gynecologic care. Recommendations are derived from major society guidelines and high-quality evidence when available, supplemented by the opinion of the author and editorial board when necessary. It should not be construed as dictating an exclusive course of treatment or procedure to be followed.
Variations in practice may be warranted when, in the reasonable judgment of the treating clinician, such course of action is indicated by the condition of the patient, limitations of available resources, or advances in knowledge or technology. SASGOG reviews the articles regularly; however, its publications may not reflect the most recent evidence. While we make every effort to present accurate and reliable information, this publication is provided “as is” without any warranty of accuracy, reliability, or otherwise, either express or implied. SASGOG does not guarantee, warrant, or endorse the products or services of any firm, organization, or person. Neither SASGOG nor its respective officers, directors, members, employees, or agents will be liable for any loss, damage, or claim with respect to any liabilities, including direct, special, indirect, or consequential damages, incurred in connection with this publication or reliance on the information presented.
Copyright 2020 The Society for Academic Specialists in General Obstetrics and Gynecology, Inc. All rights reserved. No re-print, duplication or posting allowed without prior written consent.
Back to Search Results