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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;2:327–337.
  2. American College of Obstetricians and Gynecologists (ACOG) Practice bulletin. Diagnosis and management of preeclampsia and eclampsia. Obstet Gynecol. 2002;99(1):159–167.
  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