eMedicine Specialties > Emergency Medicine > Obstetrics & Gynecology

Pregnancy, Eclampsia: Treatment & Medication

Author: Allysia M Guy, MD, Staff Physician, Department of Emergency Medicine, State University of New York Downstate Medical Center, Brooklyn, New York
Coauthor(s): Mark A Silverberg, MD, FACEP, MMB, Assistant Professor, Assistant Residency Director, Department of Emergency Medicine, State University of New York Downstate College of Medicine; Consulting Staff, Department of Emergency Medicine, Staten Island University Hospital, Kings County Hospital, University Hospital, State University of New York Downstate at Brooklyn
Contributor Information and Disclosures

Updated: Aug 11, 2009

Treatment

Prehospital Care

  • Emergency medical services personnel should (1) secure an intravenous line with a large-bore catheter, (2) initiate cardiac monitoring and administer oxygen, and (3) transport the patient in the left lateral decubitus position.
  • Supportive care includes airway support and attempted termination of any ongoing seizure with diazepam.

Emergency Department Care

  • Hospitalization, labor followed by delivery. In 1772, De la Motte recognized that prompt delivery of pregnant women with convulsions favored their recovery.9 Delivery is the only definitive treatment.
  • The initial step for supportive care is to maintain adequate oxygenation. Supportive care for eclampsia consists of close monitoring, invasive if clinically indicated; airway support; adequate oxygenation; anticonvulsant therapy; and BP control.
  • Intravenous magnesium sulfate is the initial drug administered to terminate seizures and lower BP. Seizures usually terminate after the loading dose of magnesium. A loading dose of 6 g (15-20 min) and a maintenance dose of 2 g per hour as a continuous intravenous solution. Once the seizures terminate, 85% of patients note improved blood pressure control.7,2 Note: Magnesium toxicity can cause coma, and, if mental status changes with these infusion rates, this should be considered.2
  • Severe hypertension must be addressed after magnesium infusions. Hydralazine or labetalol can then be administered IV for BP control. The goal is to maintain systolic BP between 140 and 160 mm Hg and diastolic BP between 90 and 110 mm Hg. Recommended intravenous bolus of hydralazine (5-10 mg) or labetalol (20-40 mg q15min prn). Other potent antihypertensive medications such as sodium nitroprusside or nitroglycerin can be used but are rarely required.2
  • Diuretics are used only in the setting of pulmonary edema.
  • Care must be taken not to decrease the BP too drastically; an excessive decrease can cause inadequate uteroplacental perfusion and fetal distress.9
  • Benzodiazepine or phenytoin can be used for seizures that are not responsive to magnesium sulfate.
  • Maintaining a diastolic BP of 90 mm Hg is the goal of antihypertensive therapy. Oral nifedipine (40-120 mg/d) with or without labetalol (600-2400 mg/d) is given to keep systolic BP between 140 and 155 mm Hg and diastolic pressure between 90 and 105 mm Hg.2
  • A dose of antenatal steroids may be administered in anticipation of emergent delivery when gestational age is less than 32 weeks. Betamethasone (12 mg IM q24h X 2 doses) or dexamethasone (6 mg IM q12h X 4 doses) is recommended.9,2
  • Several organizations have developed screening, treatment, and prevention guidelines for preeclampsia and eclampsia.10,11,12

Consultations

  • Recommend immediate consultation with in-house obstetrician and maternal fetal medicine for emergent delivery. ICU services may also be involved to facilitate close monitoring. 

Medication

The goal of therapy is to decrease BP, prevent or control convulsions, and deliver a viable neonate. The antihypertensive agent of choice is hydralazine. Alternative antihypertensives include labetalol, diazoxide, and occasionally, nitroprusside.

Anticonvulsants

Convulsive generalized status epilepticus in pregnancy jeopardizes both the mother and fetus. The anticonvulsant agent of choice is magnesium sulfate. However, when seizures continue after administration of magnesium, benzodiazepines are the drugs of choice.


Magnesium sulfate (MgSO4)

Used to treat and prevent seizures. May cause hyporeflexia, respiratory depression, and bradycardia. Monitor patient's reflexes and discontinue infusion if reflexes are absent or if magnesium level exceeds 6-8 mEq/L. Use IV/IM route for seizure prophylaxis in preeclampsia. When treating true eclampsia, use IV route for quicker action. Calcium gluconate 10% solution 10-20 mL IV can be given as an antidote for clinically significant hypermagnesemia. Discontinue as soon as desired effect is obtained. Repeat doses depend on continuing presence of patellar reflex and adequate respiratory function.

Adult

4 g IV initially, followed by 1-4 g IM q4h prn
Alternatively, 1-4 g/h continuous infusion

Pediatric

20-100 mg/kg/dose IV q4-6h prn; doses as high as 200 mg/kg/dose have been used in severe cases

Concurrent use with nifedipine may cause hypotension and neuromuscular blockade; may increase neuromuscular blockade seen with aminoglycoside use and potentiate neuromuscular blockade produced by tubocurarine, vecuronium, and succinylcholine; may increase CNS effects and toxicity of CNS depressants and betamethasone; may increase cardiotoxicity of ritodrine

Documented hypersensitivity; heart block; Addison disease; myocardial damage; severe hepatitis

Pregnancy

A - Fetal risk not revealed in controlled studies in humans

Precautions

May alter cardiac conduction, leading to heart block inpatients taking digitalis; respiratory rate, deep tendon reflex, and renal function should be monitored when electrolyte is administered parenterally; may produce significant hypertension or asystole; in overdose, calcium gluconate 10-20 mL IV of 10% solution can be given as antidote for clinically significant hypermagnesemia; use in eclampsia is reserved for immediate control of life-threatening convulsions


Diazepam (Valium)

For treatment of seizures resistant to magnesium sulfate. Depresses all levels of CNS (eg, limbic and reticular formation), possibly by increasing activity of GABA.

Adult

5-10 mg IV q10-20min; repeat in 2-4 h prn; not to exceed 30 mg in 8 h

Pediatric

0.05-0.3 mg/kg/dose IV over 2-3 min q15-30min; not to exceed 10 mg; repeat in 2-4 h prn

Increases toxicity of benzodiazepines in CNS with coadministration of phenothiazines, barbiturates, alcohols, and MAOIs

Documented hypersensitivity; narrow-angle glaucoma

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution with other CNS depressants, low albumin levels, or hepatic disease (may increase toxicity)

Antihypertensives

A systolic BP of 160-180 mm Hg or greater or a diastolic BP of 110 mm Hg or greater should be treated with IV antihypertensives to prevent cerebral hemorrhage. Hydralazine is the DOC for BP control in eclampsia. However, parenteral hydralazine is provided to pharmacists only through special emergency request. Therefore, be prepared to use other antihypertensive agents when hydralazine is not available immediately. Labetalol has alpha-adrenergic and beta-adrenergic blocking effects and can be used for rapid control of severe hypertension.

Other antihypertensive drugs have significant adverse effects and should not be used as primary agents. Diazoxide may cause hyperglycemia and inhibit labor. Nitroprusside may cause fetal cyanide toxicity. Diuretics should be avoided because of the relative intravascular volume depletion in the patient with eclampsia.


Hydralazine (Hydrea)

Decreases systemic resistance through direct vasodilation of arterioles.

Adult

5 mg IV initially, then 5-10 mg IV q20-30min prn; not to exceed 30 mg

Pediatric

0.1-0.2 mg/kg/dose IV q4-6h prn; not to exceed 20 mg or 1.7-3.5 mg/kg/d divided into 4-6 doses

MAOIs and beta-blockers may increase hydralazine toxicity; pharmacologic effects of hydralazine may be decreased by indomethacin

Documented hypersensitivity; mitral valve rheumatic heart disease

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Implicated in myocardial infarction; caution in suspected coronary artery disease


Labetalol (Normodyne)

Used as alternative to hydralazine in eclampsia. It blocks alpha-adrenergic, beta1-adrenergic, and beta2-aderenergic receptor sites.

Adult

20-30 mg IV over 2 min followed by 40-80 mg IV at 10-min intervals; not to exceed 300 mg/dose

Pediatric

Not established
Suggested dose: 0.4-1 mg/kg/h IV; not to exceed 3 mg/kg/h

Decreases effect of diuretics and increases toxicity of methotrexate, lithium, and salicylates; may diminish reflex tachycardia from nitroglycerin use, without interfering with hypotensive effects; cimetidine may increase labetalol blood levels; glutethimide may decrease labetalol effects by inducing microsomal enzymes

Documented hypersensitivity; cardiogenic shock; uncompensated congestive heart failure; bradycardia; pulmonary edema; reactive airway disease; atrioventricular block; severe bradycardia

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in impaired hepatic function; discontinue therapy with signs of liver dysfunction; in elderly patients, a lower response rate and higher incidence of toxicity may be observed


Diazoxide (Hyperstat)

Produces direct smooth-muscle relaxation of the peripheral arterioles, decreasing BP.

Adult

1-3 mg/kg IV as a single injection, not to exceed 150 mg/dose
Repeat dose in 5-15 min prn until BP is adequately reduced

Pediatric

Administer as in adults

May decrease serum hydantoins, possibly resulting in decreased anticonvulsant effects; thiazide diuretics may potentiate hyperuricemic and antihypertensive effects

Documented hypersensitivity; aortic coarctation; pheochromocytoma; arteriovenous shunts; aortic aneurysm

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Patients with diabetes mellitus may require treatment for hyperglycemia; when given prior to delivery, may produce fetal or neonatal hyperbilirubinemia, thrombocytopenia, altered carbohydrate metabolism, and other adverse reactions


Nitroprusside (Nitropress)

Used occasionally for treatment of eclampsia. It causes peripheral vasodilation by directly acting on venous and arteriolar smooth muscle, reducing peripheral resistance.

Adult

0.3-0.5 mcg/kg/min IV, increase in increments of 0.5 mcg/kg/min, titrate to desired hemodynamic effect; average dose is 3 mcg/kg/min

Pediatric

Administer as in adults

Documented hypersensitivity; subaortic stenosis; idiopathic hypertrophic; atrial fibrillation or flutter

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in increased intracranial pressure, hepatic failure, severe renal impairment, hypothyroidism; in renal or hepatic insufficiency, levels may increase and cause cyanide toxicity; can lower BP and should be used only in patients with mean arterial pressures >70 mm Hg

More on Pregnancy, Eclampsia

Overview: Pregnancy, Eclampsia
Differential Diagnoses & Workup: Pregnancy, Eclampsia
Treatment & Medication: Pregnancy, Eclampsia
Follow-up: Pregnancy, Eclampsia
References

References

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  2. Gabbe. Hypertension. In: Obstetrics: Normal and Problem Pregnancies. 5th ed. Churchill Livingstone, An Imprint of Elsevier; 2007:[Full Text].

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Further Reading

Keywords

eclampsia, hypertension of pregnancy, seizures in pregnancy, toxemia of pregnancy, coma in pregnancy, preeclampsia, hypertensive disorder, proteinuria

Contributor Information and Disclosures

Author

Allysia M Guy, MD, Staff Physician, Department of Emergency Medicine, State University of New York Downstate Medical Center, Brooklyn, New York
Disclosure: Nothing to disclose.

Coauthor(s)

Mark A Silverberg, MD, FACEP, MMB, Assistant Professor, Assistant Residency Director, Department of Emergency Medicine, State University of New York Downstate College of Medicine; Consulting Staff, Department of Emergency Medicine, Staten Island University Hospital, Kings County Hospital, University Hospital, State University of New York Downstate at Brooklyn
Mark A Silverberg, MD, FACEP, MMB is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Council of Emergency Medicine Residency Directors, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Michael S Beeson, MD, MBA, FACEP, Professor of Emergency Medicine, Northeastern Ohio Universities College of Medicine; Program Director, Emergency Medicine Residency, Summa Health System
Michael S Beeson, MD, MBA, FACEP is a member of the following medical societies: American College of Emergency Physicians, Council of Emergency Medicine Residency Directors, National Association of EMS Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Mark Zwanger, MD, MBA, Assistant Professor, Department of Emergency Medicine, Thomas Jefferson University
Mark Zwanger, MD, MBA is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and American Medical Association
Disclosure: Medicines Company Consulting fee Consulting; Pfizer Salary Employment

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Pamela L Dyne, MD, Professor of Clinical Medicine/Emergency Medicine, David Geffen School of Medicine at UCLA; Attending Physician, Department of Emergency Medicine, Olive View-UCLA Medical Center
Pamela L Dyne, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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