Hypertensive Disorders of Pregnancy

 

Am Fam Physician. 2016 Jan 15;93(2):121-127.

  Patient information: See related handout on high blood pressure during pregnancy, written by the authors of this article.

Author disclosure: No relevant financial affiliations.

Elevated blood pressure in pregnancy may represent chronic hypertension (occurring before 20 weeks' gestation or persisting longer than 12 weeks after delivery), gestational hypertension (occurring after 20 weeks' gestation), preeclampsia, or preeclampsia superimposed on chronic hypertension. Preeclampsia is defined as hypertension and either proteinuria or thrombocytopenia, renal insufficiency, impaired liver function, pulmonary edema, or cerebral or visual symptoms. Proteinuria is not essential for the diagnosis and does not correlate with outcomes. Severe features of preeclampsia include a systolic blood pressure of at least 160 mm Hg or a diastolic blood pressure of at least 110 mm Hg, platelet count less than 100 × 103 per μL, liver transaminase levels two times the upper limit of normal, a doubling of the serum creatinine level or level greater than 1.1 mg per dL, severe persistent right upper-quadrant pain, pulmonary edema, or new-onset cerebral or visual disturbances. Preeclampsia without severe features can be managed with twice-weekly blood pressure monitoring, antenatal testing for fetal well-being and disease progression, and delivery by 37 weeks' gestation. Preeclampsia with any severe feature requires immediate stabilization and inpatient treatment with magnesium sulfate, antihypertensive drugs, corticosteroids for fetal lung maturity if less than 34 weeks' gestation, and delivery plans. Preeclampsia can worsen or initially present after delivery. Women with hypertensive disorders should be monitored as inpatients or closely at home for 72 hours postpartum.

Hypertensive disorders affect up to 10% of pregnancies in the United States.1 Elevated blood pressure (BP) in pregnancy may represent chronic hypertension (occurring before 20 weeks' gestation or persisting longer than 12 weeks after delivery), gestational hypertension (occurring after 20 weeks' gestation), preeclampsia, or preeclampsia superimposed on chronic hypertension.1 National guidelines eliminate the requirement for proteinuria in the diagnosis of preeclampsia, recommend delivery at 37 weeks in women who have gestational hypertension or preeclampsia without severe features, recommend seizure prophylaxis with magnesium sulfate (MgSO4) only when preeclampsia has severe features, and call for increased awareness of postpartum hypertension risks.1

WHAT IS NEW ON THIS TOPIC: HYPERTENSIVE DISORDERS OF PREGNANCY

The U.S. Preventive Services Task Force recommends that pregnant women at high risk of preeclampsia take low-dose aspirin (81 mg per day) after 12 weeks' gestation.

Delivery is generally indicated at 37 weeks' gestation for women who have gestational hypertension or preeclampsia without severe features.

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SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendationEvidence ratingReferences

Women with gestational hypertension or preeclampsia without severe features should have planned delivery at 37 weeks' gestation.

B

1, 25

Magnesium sulfate is the treatment of choice to prevent eclamptic seizures (NNT = 100) and placental abruption (NNT = 100) in women who have preeclampsia with severe features.

A

23, 24, 29

Magnesium sulfate is more effective than diazepam (Valium) or phenytoin (Dilantin) for preventing recurrent eclamptic seizures and decreasing maternal mortality.

A

31, 32

Intravenous labetalol or hydralazine or oral nifedipine may be used to treat severe hypertension during pregnancy.

B

36

For women who have preeclampsia with severe features between 24 and 34 weeks' gestation, expectant management with close monitoring of the mother and fetus reduces neonatal complications and days in the intensive care unit.

B

40

Low-dose aspirin has small to moderate benefits in the prevention of preeclampsia among at-risk women (NNT = 72). The NNT falls to 19 among those at greatest risk.

A

50

Calcium supplementation may decrease the incidence of hypertension, preeclampsia, and mortality among high-risk women with low calcium intake. However, women in the United States or other developed countries are unlikely to benefit.

B

1, 52


NNT = number needed to treat.

A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendationEvidence ratingReferences

Women with gestational hypertension or preeclampsia without severe features should have planned delivery at 37 weeks' gestation.

B

1, 25

Magnesium sulfate is the treatment of choice to prevent eclamptic seizures (NNT = 100) and placental abruption (NNT = 100) in women who have preeclampsia with severe features.

A

23, 24, 29

Magnesium sulfate is more effective than diazepam (Valium) or phenytoin (Dilantin) for preventing recurrent eclamptic seizures and decreasing maternal mortality.

A

31, 32

Intravenous labetalol or hydralazine or oral nifedipine may be used to treat severe hypertension during pregnancy.

B

36

For women who have preeclampsia with severe features between 24 and 34 weeks' gestation, expectant management with close monitoring of the mother and fetus reduces neonatal complications and days in the intensive care unit.

B

40

Low-dose aspirin has small to moderate benefits in the prevention of preeclampsia among at-risk women (NNT = 72). The NNT falls to 19 among those at greatest risk.

A

50

Calcium supplementation may decrease the incidence of hypertension, preeclampsia, and mortality among high-risk women with low calcium intake. However, women in the United States or other developed countries are unlikely to benefit.

B

1, 52


NNT = number needed to treat.

A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.

Chronic Hypertension

Chronic hypertension is diagnosed by BP of at least 140/90 mm Hg on two occasions taken at least four hours apart at 20 weeks' gestation or earlier. Chronic hypertension is associated with preeclampsia, intrauterine growth restriction, and placental abruption. However, treating mild to moderately elevated BP does not benefit the fetus or prevent preeclampsia.24 Overtreatment may cause adverse perinatal outcomes resulting from placental hypoperfusion,5 so medication is reserved for women with BP persistently greater than 150/100 mm Hg.1,6,7 Women with chronic hypertension should be monitored for intrauterine growth restriction with serial ultrasonography after fetal viability, with intervals dependent on the severity of hypertension, comorbidities, and obstetric history.1

Methyldopa, labetalol, and nifedipine are the most commonly used oral agents to treat severe chronic hypertension in pregnancy.1 Angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers are contraindicated because of their association with intrauterine growth restriction, neonatal renal failure, oligohydramnios, and death.1 The beta blocker atenolol also may cause intrauterine growth restriction.1 Thiazide diuretics that were used before pregnancy may be continued, but should be stopped if preeclampsia develops to avoid worsening intravascular volume depletion.8,9 Women in active labor with uncontrolled severe chronic hypertension require rapid treatment, traditionally intravenous labetalol or hydralazine.9 Oral nifedipine may also be used; a small randomized controlled trial showed that it induces a faster response than intravenous labetalol.9,10

Gestational Hypertension

Women who develop hypertension after 20 weeks' gestation and who do not have proteinuria or other criteria for preeclampsia are diagnosed with gestational hypertension. This is a provisional diagnosis that includes women who eventually develop preeclampsia, those with unrecognized chronic hypertension (diagnosed by persistently elevated BP beyond 12 weeks postpartum), and women with transient hypertension of pregnancy. Approximately 50% of women diagnosed with gestational hypertension between 24 and 35 weeks' gestation ultimately develop preeclampsia.11 Management of gestational hypertension is similar to that of preeclampsia, with expectant monitoring and labor induction at 37 weeks' gestation (Figure 1).1

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Management of Gestational Hypertension and Preeclampsia Without Severe Features

Figure 1.

Algorithm for management of gestational hypertension or preeclampsia without severe features.

Reprinted with permission from American College of Obstetricians and Gynecologists. Hypertension in pregnancy. http://www.acog.org/Resources-And-Publications/Task-Force-and-Work-Group-Reports/Hypertension-in-Pregnancy. Accessed November 23, 2015.

Management of Gestational Hypertension and Preeclampsia Without Severe Features


Figure 1.

Algorithm for management of gestational hypertension or preeclampsia without severe features.

Reprinted with permission from American College of Obstetricians and Gynecologists. Hypertension in pregnancy. http://www.acog.org/Resources-And-Publications/Task-Force-and-Work-Group-Reports/Hypertension-in-Pregnancy. Accessed November 23, 2015.

Preeclampsia

Preeclampsia is a multiorgan disease process characterized by hypertension and proteinuria or one of the following features, which are diagnostic when they develop in the setting of new-onset hypertension after 20 weeks' gestation: thrombocytopenia, renal insufficiency, impaired liver function, pulmonary edema, or cerebral or visual symptoms. The etiology is becoming clearer with our understanding of the central role of placental angiogenic proteins, which negatively affect maternal endothelial function1,12  (Table 11317). Biomarkers and risk factors are only modestly predictive 1820  (Table 218,19).

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Table 1.

Pathophysiology of Preeclampsia

Abnormal placental implantation (defects in trophoblasts and spiral arterioles)13

Angiogenic factors (low level of placental growth factor)14

Genetic predisposition (maternal, paternal, thrombophilias)15

Immunologic phenomena16

Vascular endothelial damage17 and oxidative stress


Information from references 13 through 17.

Table 1.

Pathophysiology of Preeclampsia

Abnormal placental implantation (defects in trophoblasts and spiral arterioles)13

Angiogenic factors (low level of placental growth factor)14

Genetic predisposition (maternal, paternal, thrombophilias)15

Immunologic phenomena16

Vascular endothelial damage17 and oxidative stress


Information from references 13 through 17.

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Table 2.

Risk Factors for Preeclampsia

Risk factorRelative risk*

Antiphospholipid antibodies

10

Preeclampsia in a previous pregnancy (particularly if severe or before 32 weeks' gestation)

7

Diabetes mellitus (preexisting)

3

Family history of preeclampsia (first-generation relative)

3

Multiple gestation

3

Nulliparity

3

Elevated body mass index

2

Maternal age > 40 years

1.6

Chronic hypertension or renal disease

NA


NA = not available.

*—Compared with pregnant women without the risk factor.

Information from references 18 and 19.

Table 2.

Risk Factors for Preeclampsia

Risk factorRelative risk*

Antiphospholipid antibodies

10

Preeclampsia in a previous pregnancy (particularly if severe or before 32 weeks' gestation)

7

Diabetes mellitus (preexisting)

3

Family history of preeclampsia (first-generation relative)

3

Multiple gestation

3

Nulliparity

3

Elevated body mass index

2

Maternal age > 40 years

1.6

Chronic hypertension or renal disease

NA


NA = not available.

*—Compared with pregnant women without the risk factor.

Information from references 18 and 19.

DIAGNOSIS

Diagnosis of preeclampsia requires a systolic BP of at least 140 mm Hg or a diastolic BP of at least 90 mm Hg on at least two occasions, taken at least four hours apart, plus new-onset proteinuria or a severe feature 1  (Table 321). A single severe feature in combination with hypertension is sufficient for the diagnosis. Diagnostic criteria for proteinuria include at least 300 mg of protein in a 24-hour urine sample or a urinary protein/creatinine ratio of 0.3 or greater.1 Significant proteinuria is excluded if the protein/creatinine ratio is less than 0.19.22 Two urine dipstick measurements of at least 1+ (30 mg per dL) taken six hours apart suggest preeclampsia-level proteinuria; however, quantitative methods are preferred. Proteinuria is not essential for diagnosis if a severe feature is present. Urinary protein levels do not correlate with outcome severity and are not considered a severe feature.1

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Table 3.

Severe Features of Preeclampsia

Elevated blood pressure (systolic ≥ 160 mm Hg, diastolic ≥ 110 mm Hg)

Elevated creatinine level (> 1.1 mg per dL [97 μmol per L] or ≥ 2 times baseline)

Hepatic dysfunction (transaminase levels ≥ 2 times upper limit of normal) or right upper-quadrant or epigastric pain

New-onset headache or visual disturbances

Platelet count < 100 × 103 per μL (100 × 109 per L)

Pulmonary edema


Adapted with permission from Leeman L, Dresang L, Fontaine P. Chapter B: Medical complications of pregnancy. ALSO Provider Syllabus. American Academy of Family Physicians. February 2015:7.

Table 3.

Severe Features of Preeclampsia

Elevated blood pressure (systolic ≥ 160 mm Hg, diastolic ≥ 110 mm Hg)

Elevated creatinine level (> 1.1 mg per dL [97 μmol per L] or ≥ 2 times baseline)

Hepatic dysfunction (transaminase levels ≥ 2 times upper limit of normal) or right upper-quadrant or epigastric pain

New-onset headache or visual disturbances

Platelet count < 100 × 103 per μL (100 × 109 per L)

Pulmonary edema


Adapted with permission from Leeman L, Dresang L, Fontaine P. Chapter B: Medical complications of pregnancy. ALSO Provider Syllabus. American Academy of Family Physicians. February 2015:7.

Severe headache, visual disturbances, and hyperreflexia may signal impending eclamptic seizure. Increasing peripheral vascular resistance or myocardial dysfunction may lead to pulmonary edema. Decreased glomerular filtration rate may progress to oliguria and renal failure. Liver manifestations include elevated transaminase levels, subcapsular hemorrhage with right upper-quadrant pain, and capsular rupture with life-threatening intraabdominal bleeding. Preeclampsia-related coagulopathies include HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome and disseminated intravascular coagulation. Obstetric complications include intrauterine growth restriction, placental abruption, and fetal demise.

MANAGEMENT

Expectant management of preeclampsia without severe features may include twice-weekly BP monitoring, weekly laboratory tests (complete blood count and monitoring of creatinine levels, alanine transaminase, and/or aspartate transaminase levels), twice-weekly fetal nonstress testing, weekly amniotic fluid indices, and fetal growth ultrasonography every three weeks.1,6 Fetal umbilical artery Doppler ultrasonography is recommended if intrauterine growth restriction is present.1 Seizure prophylaxis with MgSO4 is not required unless severe features develop1 (number needed to treat [NNT] = 400 for asymptomatic women with BP less than 160/110 mm Hg, assuming that 50% of seizures are preventable23,24). Delivery timing involves balancing the risks of prematurity against worsening preeclampsia. To improve maternal outcomes, delivery is generally indicated at 37 weeks' gestation for women who have preeclampsia without severe features.1,25,26 Immediate delivery between between 34 weeks and 36 weeks, six days is not recommended because of an increase risk of neonatal respiratory distress syndrome.27

Women who have preeclampsia with severe features require hospitalization for careful monitoring. Treatment goals are fluid management, seizure prevention, lowering BP to prevent maternal end-organ damage, and expediting delivery based on disease severity and gestational age.1 Excessive fluid administration can result in pulmonary edema and ascites, whereas too little fluid can exacerbate intravascular volume depletion and end-organ ischemia. Urine output should be maintained above 30 mL per hour, and a Foley catheter should be used to monitor urine output if MgSO4 is administered.28 Total intravenous intake should be less than 100 mL per hour, and total combined oral and intravenous fluids should be less than 125 mL per hour.28

MgSO4 for Seizure Prophylaxis. MgSO4 helps prevent eclamptic seizures (NNT = 100) and placental abruption (NNT = 100) in women who have preeclampsia with severe features.29 It is more effective for preventing recurrent eclamptic seizures and decreasing maternal mortality than phenytoin (Dilantin), diazepam (Valium), or a combination of chlorpromazine, promethazine, and meperidine (Demerol).3032 BP is only mildly elevated in 30% to 60% of women with eclampsia.33 Those with preeclampsia without severe features should be monitored closely, and MgSO4 should be started if severe features develop1  (eTable A).

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eTable A.

Administration of Magnesium Sulfate for Severe Preeclampsia or Severe Gestational Hypertension

Administer loading dose of 4 to 6 g mixed in 100 mL of water, 5% dextrose solution, or 0.9% normal saline intravenously over 15 to 20 minutes, followed by a continuous infusion of 2 g per hour.

Monitor reflexes, mental status, respiratory status, and urine output.

Monitor magnesium levels (therapeutic range = 4 to 8 mg per dL) if patient has renal dysfunction, elevated creatinine levels, urine output < 30 mL per hour, loss of reflexes, or other symptoms.


Information from Sibai BM. Diagnosis, prevention, and management of eclampsia. Obstet Gynecol. 2005;105(2):402–410.

eTable A.

Administration of Magnesium Sulfate for Severe Preeclampsia or Severe Gestational Hypertension

Administer loading dose of 4 to 6 g mixed in 100 mL of water, 5% dextrose solution, or 0.9% normal saline intravenously over 15 to 20 minutes, followed by a continuous infusion of 2 g per hour.

Monitor reflexes, mental status, respiratory status, and urine output.

Monitor magnesium levels (therapeutic range = 4 to 8 mg per dL) if patient has renal dysfunction, elevated creatinine levels, urine output < 30 mL per hour, loss of reflexes, or other symptoms.


Information from Sibai BM. Diagnosis, prevention, and management of eclampsia. Obstet Gynecol. 2005;105(2):402–410.

Women with normal renal function do not require routine serum magnesium testing; however, testing should be performed every six hours in those with absent reflexes, elevated creatinine levels, or decreased urine output.33 Magnesium toxicity can lead to respiratory paralysis, central nervous system depression, and cardiac arrest. Vital functions are lost in a predictable sequence: if deep tendon reflexes are present, magnesium levels are rarely toxic. MgSO4 infusion should be discontinued and the serum magnesium level checked immediately if deep tendon reflexes are lost, respiratory rate decreases to less than 12 breaths per minute, or urine output is less than 30 mL per hour.33 Overdoses and maternal deaths have resulted from improper MgSO4 administration.34 The antidote for MgSO4 overdose is 1 g calcium gluconate administered intravenously over two minutes.28

Blood Pressure Management. The optimal BP for women with severe preeclampsia is unknown. Excessive lowering of BP may lead to uteroplacental insufficiency.2 It is recommended that systolic BP be maintained at less than 160 mm Hg and diastolic at less than 110 mm Hg. A retrospective review of 28 women with preeclampsia who had a stroke showed that more than 90% had systolic BP greater than 160 mm Hg, and 12.5% had diastolic BP greater than 110 mm Hg, which demonstrates the importance of pharmacologic treatment when either BP threshold is reached.35 Intravenous labetalol and hydralazine are commonly used for acute management and are equally effective36  (eTable B). Oral nifedipine is recommended as an alternative, particularly when urgent lowering of BP is needed and intravenous access has not been achieved.1,9,36

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eTable B.

Dosing of Hydralazine, Labetalol, and Nifedipine for Severe Preeclampsia

Hydralazine, 5 to 10 mg IV over 2 minutes. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after 20 minutes, administer an additional 10 mg IV. If above threshold BP after an additional 20 minutes, switch to IV labetalol.A1 May use constant IV infusion at rate of 0.5 to 10 mg per hour.A2

Labetalol, 20 mg IV initial dose. If the initial dose is not effective, double to 40 mg and then again to 80 mg at 10-minute intervals until target BP is reached. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after the 80-mg dose, switch to IV hydralazine.A3,A4 The maximal dosage of IV labetalol is 220 to 300 mg in 24 hours.A1,A3

Nifedipine, 10 mg oral initial dose. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after 30 minutes, administer an additional 20 mg orally. If above threshold BP 30 minutes after second dose, administer additional 20 mg. May then administer 10 to 20 mg every 4 to 6 hours.A1


BP = blood pressure; IV = intravenous.

Information from:

A1. Committee on Obstetric Practice. Committee opinion no. 623: emergent therapy for acute-onset, severe hypertension during pregnancy and the postpartum period. Obstet Gynecol. 2015;125(2):521–525.

A2. American College of Obstetricians and Gynecologists; Task Force on Hypertension in Pregnancy. Hypertension in pregnancy. Obstet Gynecol. 2013;122(5):1122–1131.

A3. Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. Am J Obstet Gynecol. 2000;183(1):S1–S22.

A4. Sibai BM. Diagnosis and management of gestational hypertension and pre-eclampsia. Obstet Gynecol. 2003;102(1):181–192.

eTable B.

Dosing of Hydralazine, Labetalol, and Nifedipine for Severe Preeclampsia

Hydralazine, 5 to 10 mg IV over 2 minutes. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after 20 minutes, administer an additional 10 mg IV. If above threshold BP after an additional 20 minutes, switch to IV labetalol.A1 May use constant IV infusion at rate of 0.5 to 10 mg per hour.A2

Labetalol, 20 mg IV initial dose. If the initial dose is not effective, double to 40 mg and then again to 80 mg at 10-minute intervals until target BP is reached. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after the 80-mg dose, switch to IV hydralazine.A3,A4 The maximal dosage of IV labetalol is 220 to 300 mg in 24 hours.A1,A3

Nifedipine, 10 mg oral initial dose. If systolic BP ≥ 160 mm Hg or diastolic BP ≥ 110 mm Hg after 30 minutes, administer an additional 20 mg orally. If above threshold BP 30 minutes after second dose, administer additional 20 mg. May then administer 10 to 20 mg every 4 to 6 hours.A1


BP = blood pressure; IV = intravenous.

Information from:

A1. Committee on Obstetric Practice. Committee opinion no. 623: emergent therapy for acute-onset, severe hypertension during pregnancy and the postpartum period. Obstet Gynecol. 2015;125(2):521–525.

A2. American College of Obstetricians and Gynecologists; Task Force on Hypertension in Pregnancy. Hypertension in pregnancy. Obstet Gynecol. 2013;122(5):1122–1131.

A3. Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. Am J Obstet Gynecol. 2000;183(1):S1–S22.

A4. Sibai BM. Diagnosis and management of gestational hypertension and pre-eclampsia. Obstet Gynecol. 2003;102(1):181–192.

Expectant Management. Antenatal testing in women who have preeclampsia with severe features may include daily nonstress tests, amniotic fluid assessment, and periodic ultrasonography to assess fetal growth. Between 24 and 34 weeks' gestation, fetal lung maturity may be accelerated by the use of betamethasone (two 12-mg intramuscular doses given 24 hours apart) or dexamethasone (four 6-mg intramuscular doses given 12 hours apart).37

Delivery route and timing are based on maternal factors (e.g., disease progression, parity, cervical examination findings) and fetal considerations (e.g., gestational age, antenatal testing).38,39 Data are limited about expectant management of women who have preeclampsia with severe features between 24 and 34 weeks' gestation.40 Expectant management in a hospital with perinatal and neonatology services decreases neonatal morbidity and intensive care unit stay. However, many women are not candidates for expectant management and require urgent delivery.40 Delivery is indicated after maternal stabilization without waiting 48 hours after corticosteroid administration in women with resistant severe hypertension, eclampsia, pulmonary edema, abruption, or other maternal or fetal deterioration. Delivery should occur after 48 hours of antenatal corticosteroid administration in women with thrombocytopenia (platelet count less than 100 × 103 per μL [100 × 109 per L]), transaminase levels two times the upper limit of normal, intrauterine growth restriction (less than 5th percentile), severe oligohydramnios, umbilical artery reversed end-diastolic flow, or new or worsening renal dysfunction. If maternal and fetal conditions allow, corticosteroids should be administered to women with preeclampsia and preterm labor or rupture of membranes before 34 weeks' estimated gestational age.1

Attempted vaginal delivery is recommended in women who have preeclampsia with severe features if it is not otherwise contraindicated.6 Indications for cesarean delivery include recurrent seizures refractory to medical management, severely elevated BP that is resistant to antihypertensive medications, and maternal or fetal deterioration remote from delivery. Some experts recommend cesarean delivery in preeclamptic patients with severe features and an unfavorable cervix who require delivery before 30 weeks' gestation.37

HELLP Syndrome

HELLP syndrome occurs in less than 1% of all pregnancies, but in 20% of pregnancies complicated by pre-eclampsia with severe features.1,41,42 HELLP syndrome may present at term (18%), preterm (53%, including 11% before 27 weeks' gestation), or postpartum (30%).41 Diagnosis is challenging because symptoms can mimic those of other illnesses.38,43 Clinicians must consider HELLP syndrome in patients who do not have classic preeclampsia symptoms because 12% to 18% of women with the condition are normotensive and 13% do not have proteinuria.39 Although HELLP syndrome may be considered a subtype of preeclampsia, atypical HELLP syndrome can be diagnosed without meeting the BP criteria for the diagnosis of preeclampsia.1,39 Evaluation includes a complete blood count and liver transaminase testing38  (eTable C). A disseminated intravascular coagulation workup (fibrinogen, prothrombin time, partial thromboplastin time) should be ordered for women with abnormal bleeding or a platelet count less than 50 × 103 per μL (50 × 109 per L).

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eTable C.

Diagnostic Criteria for HELLP Syndrome

Alanine or aspartate transaminase levels ≥ 2 times upper limit of normal

Hemolysis

Lactate dehydrogenase > 600 U per L (10.0 μkat per L)

Peripheral blood smear shows evidence of damaged erythrocytes (e.g., schistocytes, burr cells, helmet cells)

Serum bilirubin ≥ 1.2 mg per dL (20.5 μmol per L)

Platelet count < 100 × 103 per μL (100 × 109 per L)


HELLP = hemolysis, elevated liver enzymes, and low platelet count.

Information from American College of Obstetricians and Gynecologists. Hypertension in pregnancy. http://www.acog.org/Resources-And-Publications/Task-Force-and-Work-Group-Reports/Hypertension-in-Pregnancy. Accessed November 23, 2015.

eTable C.

Diagnostic Criteria for HELLP Syndrome

Alanine or aspartate transaminase levels ≥ 2 times upper limit of normal

Hemolysis

Lactate dehydrogenase > 600 U per L (10.0 μkat per L)

Peripheral blood smear shows evidence of damaged erythrocytes (e.g., schistocytes, burr cells, helmet cells)

Serum bilirubin ≥ 1.2 mg per dL (20.5 μmol per L)

Platelet count < 100 × 103 per μL (100 × 109 per L)


HELLP = hemolysis, elevated liver enzymes, and low platelet count.

Information from American College of Obstetricians and Gynecologists. Hypertension in pregnancy. http://www.acog.org/Resources-And-Publications/Task-Force-and-Work-Group-Reports/Hypertension-in-Pregnancy. Accessed November 23, 2015.

Women with HELLP syndrome should receive MgSO4 from admission until 24 to 48 hours postpartum.39 Platelets are indicated for those with counts less than 20 × 103 per μL (20 × 109 per L) before vaginal delivery or less than 50 × 103 per μL before cesarean delivery or in women with abnormal bleeding. Regional anesthesia is safe when the platelet count is greater than 100 × 103 per μL, but should be avoided if the count is less than 50 × 103 per μL. Corticosteroids increase platelet counts in women with HELLP syndrome,44,45 but they have not been shown to improve fetal or maternal outcomes except for the proven benefit on fetal lung maturation before 34 weeks' gestation.

Eclampsia

Eclamptic seizures are a life-threatening emergency and can occur antepartum (53%), intrapartum (19%), or postpartum (28%).46 Eclampsia before 20 weeks' gestation is rare in the absence of gestational trophoblastic disease. Eclampsia may be preceded by central nervous system symptoms such as headache (80%) and visual changes (45%).47 However, seizures can occur without other severe features of preeclampsia and with a normal BP; 15% of women with eclampsia have a diastolic BP less than 90 mm Hg.46  Eclamptic seizures are usually generalized 60- to 90-second seizures. Postictal confusion, agitation, or combativeness may follow. During an eclamptic seizure, the fetus often manifests hypoxia-related bradycardia, but usually recovers. Table 4 presents principles for management of eclamptic seizures.33

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Table 4.

Principles of Management of Eclamptic Seizures

Maintain situational awareness. An eclamptic seizure is dramatic and disturbing. The attending clinician is challenged to maintain a purposeful calm and to avoid unnecessary interventions that can result in iatrogenic complications.33

Avoid polypharmacy. Do not attempt to shorten or abolish the initial convulsion by using drugs such as diazepam (Valium) or phenytoin (Dilantin). Magnesium sulfate is the drug of choice for initial and recurrent convulsions. Polypharmacy can lead to maternal or neonatal respiratory depression, aspiration, or other adverse effects.

Protect the airway, and minimize the risk of aspiration. Place the patient on her left side and suction her mouth. Call for someone skilled in intubation to be immediately available.

Prevent maternal injury. Falls from the bed can result in contusions or fractures, and head injury may result from violent seizure activity. Close observation and use of soft padding and side rails on the bed may help prevent injuries.

Administer magnesium sulfate to control convulsions. If the patient has already received a prophylactic loading dose and is receiving a continuous infusion when the seizure occurs, an additional 2 g should be given intravenously. Otherwise, a 4- to 6-g loading dose should be given intravenously over 15 to 20 minutes, followed by a continuous infusion of 2 g per hour. The loading dose and subsequent bolus should not total more than 8 g for a recurrent seizure.33

Follow delivery plan. Avoid the temptation to perform immediate cesarean delivery for a self-limited seizure episode.


Information from reference 33.

Table 4.

Principles of Management of Eclamptic Seizures

Maintain situational awareness. An eclamptic seizure is dramatic and disturbing. The attending clinician is challenged to maintain a purposeful calm and to avoid unnecessary interventions that can result in iatrogenic complications.33

Avoid polypharmacy. Do not attempt to shorten or abolish the initial convulsion by using drugs such as diazepam (Valium) or phenytoin (Dilantin). Magnesium sulfate is the drug of choice for initial and recurrent convulsions. Polypharmacy can lead to maternal or neonatal respiratory depression, aspiration, or other adverse effects.

Protect the airway, and minimize the risk of aspiration. Place the patient on her left side and suction her mouth. Call for someone skilled in intubation to be immediately available.

Prevent maternal injury. Falls from the bed can result in contusions or fractures, and head injury may result from violent seizure activity. Close observation and use of soft padding and side rails on the bed may help prevent injuries.

Administer magnesium sulfate to control convulsions. If the patient has already received a prophylactic loading dose and is receiving a continuous infusion when the seizure occurs, an additional 2 g should be given intravenously. Otherwise, a 4- to 6-g loading dose should be given intravenously over 15 to 20 minutes, followed by a continuous infusion of 2 g per hour. The loading dose and subsequent bolus should not total more than 8 g for a recurrent seizure.33

Follow delivery plan. Avoid the temptation to perform immediate cesarean delivery for a self-limited seizure episode.


Information from reference 33.

Postpartum Management of Preeclampsia

After delivery, most women with preeclampsia experience diuresis, a decrease in BP, and general improvement. The greatest risk of post-partum eclampsia is in the first 48 hours33; hypertension may worsen after delivery as third space fluid returns to the vasculature. MgSO4 should be continued for 12 to 24 hours after delivery.33,37,48 Inpatient observation or close home monitoring is recommended for 72 hours postpartum in women with gestational hypertension or preeclampsia.1 The postpartumtreatment threshold is a systolic BP of 150 mm Hg or greater, or a diastolic BP of 100 mm Hg or greater on two occasions at least four hours apart. Women with a systolic BP of 160 mm Hg or greater or diastolic BP of 110 mm Hg or greater should be rechecked within 15 minutes, and antihypertensive treatment should be started within 60 minutes if BP is still elevated.9

Women with hypertension that persists for more than 24 hours after delivery should not take nonsteroidal anti-inflammatory drugs because they may worsen BP.1 Although data on postpartum hypertensive management are lacking,49 oral nifedipine or labetalol and intravenous labetalol or hydralazine are commonly used.9,37 Patients should be rechecked seven to 10 days after discharge, or earlier if symptomatic.1 Preeclampsia may begin postpartum, so all women should receive information about symptoms before discharge. Preeclampsia is a risk factor for future cardiovascular disease, especially if it occurs in multiple pregnancies or is associated with intrauterine growth restriction or required delivery before 37 weeks' gestation.1 Prevention or treatment of comorbidities for cardiovascular disease is recommended.

Prevention

The use of low-dose aspirin (80 mg) has a small to moderate effect on the prevention of preeclampsia (NNT = 72); the effect is greatest (NNT = 19) in women at highest risk of developing preeclampsia.50 The American College of Obstetricians and Gynecologists (ACOG) recommends low-dose aspirin starting in the late first trimester for women with a previous delivery before 37 weeks' gestation due to preeclampsia or in more than one previous pregnancy.1 The U.S. Preventive Services Task Force (USPSTF) expands the recommendation to include women with multifetal pregnancies, chronic hypertension, type 1 or 2 diabetes mellitus, renal disease, autoimmune diseases, or several moderate risk factors.51 Calcium supplementation may prevent hypertension, preeclampsia, and maternal death in high-risk women with low calcium intake, which is rare in developed countries.1,52 A decision model analysis demonstrated that using the broader USPSTF criteria would decrease the rate of preeclampsia from 4.18% to 3.83% through treatment of 23.5% of women compared with a decrease to 4.17% through the treatment of 0.35% of women with the ACOG criteria.53

Data Sources: A PubMed search was completed in Clinical Queries using key terms including preeclampsia, eclampsia, and gestational hypertension. The search included meta-analyses, randomized controlled trials, clinical trials, and reviews. Also searched were the Cochrane database, UpToDate, Essential Evidence Plus, the National Guideline Clearing-house, and clinical guidelines and evidence reports from the Agency for Healthcare Research and Quality. Search date: November 15, 2014, and November 15, 2015.

This article is one in a series on “Advanced Life Support in Obstetrics (ALSO),” initially established by Mark Deutchman, MD, Denver, Colo. The coordinator of this series is Larry Leeman, MD, MPH, ALSO Managing Editor, Albuquerque, N.M.

This review updates a previous article on this topic by Leeman and Fontaine.54

The Authors

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LAWRENCE LEEMAN, MD, MPH, is a professor of family and community medicine and of obstetrics and gynecology at the University of New Mexico School of Medicine in Albuquerque. He is the director of Family Medicine Maternal and Child Health Service and co-medical director of the mother-baby unit at the University of New Mexico Hospital. Dr. Leeman is managing editor of the Advanced Life Support in Obstetrics (ALSO) program....

LEE T. DRESANG, MD, is a professor and maternity care clinical coordinator in the Department of Family Medicine and Community Health at the University of Wisconsin School of Medicine and Public Health, Madison. He is a member of the ALSO Editorial Board and the Family Physicians Inquiry Network Board.

PATRICIA FONTAINE, MD, MS, is a senior clinical research investigator at the HealthPartners Institute for Education and Research in Bloomington, Minn. She is a member of the ALSO Advisory Board.

Address correspondence to Lawrence Leeman, MD, MPH, University of New Mexico, 2400 Tucker NE, 3rd Floor, Albuquerque, NM 87131 (e-mail: lleeman@salud.unm.edu). Reprints are not available from the authors.

Author disclosure: No relevant financial affiliations.

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