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Basics

Description
Epidemiology

Prevalence

  • Hypertension complicates ~20% of pregnancies
  • GH is encountered in ~5% of pregnancies.
  • Chronic hypertension is present in 1–2% of pregnancies.
  • Preeclampsia–eclampsia develops in ~5% of pregnancies in the US; nearly 20% of women with chronic hypertension develop preeclampsia.

Morbidity

  • Sustained hypertension can result in end-organ damage such as renal failure, left ventricular hypertrophy, and/or cerebrovascular accident.
  • Maternal morbidity associated with preeclampsia–eclampsia includes pulmonary edema, disseminated intravascular coagulation, hepatic rupture, HELLP syndrome (hemolysis, elevated liver enzymes, low platelets), and seizures.
  • Fetal morbidity is due to increased incidence of placental abruption, intrauterine growth restriction, and preterm delivery.

Mortality

  • PIH is the third leading cause of maternal mortality in the US behind pulmonary embolus and hemorrhage. It accounts for ~10% of all deaths, with intracranial hemorrhage as the primary cause.
  • Approximately 10% of neonatal deaths occur in the presence of PIH.
Etiology/Risk Factors
Physiology/Pathophysiology
Anesthetic GOALS/GUIDING Principles

Diagnosis

Symptoms

History

  • Prenatal history: Nulliparity, multiple gestations, molar pregnancy
  • PIH risk factors
  • Fetal anomalies/intrauterine growth restriction
  • Fasting status if urgent/emergent Cesarean delivery becomes necessary.

Signs/Physical Exam

  • Airway: Pharyngolaryngeal edema
  • Pulmonary: Pulmonary edema, hypoxemia.
  • Cardiovascular: Hypertension, LV hypertrophy, and/or decreased CVP.
  • Hematologic: Anemia, thrombocytopenia, and/or disseminated intravascular coagulation (DIC).
  • Renal: Decreased GFR, increased proteinuria, increased uric acid, increased urine protein:creatinine ratio, and/or oliguria.
  • Hepatic: Increased serum transaminases, hepatic edema, hepatic hematoma, periportal hepatic necrosis, rupture of Glisson's capsule with hepatic hemorrhage
  • Neurologic: Cerebral edema, cerebral hemorrhage.
  • Placental: Intrauterine growth restriction, non-reassuring fetal heart tracing, and/or placental abruption.
Medications
Diagnostic Tests & Interpretation

Labs/Studies

  • Labs: Urinalysis for proteinuria, CBC (especially platelets and Hct), CMP (magnesium), coagulation studies, type and cross.
  • Imaging studies (if indicated): Chest x-ray (pulmonary edema), head CT (useful in identifying cerebral edema, loss of cortical sulci, and/or cerebral hemorrhage), abdominal ultrasound, CT, or MRI (if hepatic infarction, hematoma or rupture suspected), echocardiogram (if cardiac dysfunction is suspected).
Circumstances to delay/Conditions
Classifications

Treatment

PREOPERATIVE PREPARATION

Premedications

  • Aspiration prophylaxis in the setting of GETA (nonparticulate antacids, metoclopramide, H2 blockers)
  • BP control
  • Seizure prophylaxis for preeclampsia–eclampsia.
INTRAOPERATIVE CARE

Choice of Anesthesia

  • Neuraxial anesthesia (spinal or epidural) preferred. Contraindications for neuraxial anesthesia include patient refusal, elevated intracranial pressure (ICP), inability to cooperate, evidence of coagulopathy, signs of local infection.
  • General anesthesia may be necessary in emergent deliveries (fetal distress, placental abruption, hepatic rupture, severe pulmonary edema, seizure, and/or end-organ dysfunction).
    • Associated with increased risk of aspiration, transient neonatal depression, severe hypertension, and cerebral hemorrhage.
    • Maternal mortality is 7-fold greater with GETA compared with neuraxial anesthesia. Failed intubations are 10 times more likely in obstetric patients compared with general population.

Monitors

  • Pulse oximetry: Decrease in SpO2 in the setting of pulmonary edema, respiratory depression, and/or pulmonary aspiration.
  • BP monitoring: Consider invasive BP monitoring in the setting of refractory hypertension (BP >180/120) or for frequent blood sampling.
  • Central venous pressure: May be useful in determining volume status and for infusion of vasodilators.
  • Pulmonary arterial catheter rarely indicated but may be useful in the setting of severe cardiac disease and/or pulmonary hypertension.
  • Urinary output: Useful in evaluation of volume resuscitation and renal function.
  • Fetal heart tracing

Induction/Airway Management

  • Limit use of benzodiazepines and opioids prior to delivery; use is associated with neonatal depression.
  • General anesthesia for emergent deliveries.
    • Rapid sequence intubation with cricoid pressure to minimized risk of aspiration.
    • Avoid hypertensive response to laryngoscopy with deepening of anesthetic, remifentanil, and/or esmolol.

Maintenance

General anesthesia may be maintained with a combination of volatile anesthetic and nitrous oxide. Volatile anesthetic at <0.5 MAC minimizes a decrease in the uterine tone. IV opioids and benzodiazepines can be given following clamping of the cord. Magnesium sulfate prolongs duration of non-depolarizing neuromuscular blockade.

Extubation/Emergence

  • Airway edema may necessitate reintubation.
  • Severe hypertension and cerebral hemorrhage may accompany emergence and extubation.

Follow-Up

Bed Acuity
Medications/Lab Studies/Consults
Complications

References

  1. Turner JA. Diagnosis and management of preeclampsia, an update. Int J Womens Health. 2010;2:327337.
  2. American College of Obstetricians and Gynecologists (ACOG) Practice bulletin. Diagnosis and management of preeclampsia and eclampsia. Obstet Gynecol. 2002;99(1):159167.
  3. Practice guidelines for obstetric anesthesia: An updated report by the American Society of Anesthesiologists Task force on Obstetric Anesthesia. Available at: http://www.asahq.org/publicationsandServices/OBguide.pdf. Accessed on Jan 08, 2011.

Additional Reading

See Also (Topic, Algorithm, Electronic Media Element)

Codes

ICD9

642.90 Unspecified hypertension complicating pregnancy, childbirth, or the puerperium, unspecified as to episode of care or not applicable

ICD10

Clinical Pearls

Author(s)

Richard C. Jensen , MD

Judith A. Turner , MD, PhD