Abstract

Critical illness is an uncommon but potentially devastating complication of pregnancy. The majority of pregnancy-related critical care admissions occur postpartum. Antenatally, the pregnant patient is more likely to be admitted with diseases non-specific to pregnancy, such as pneumonia. Pregnancy-specific diseases resulting in ICU admission include obstetric hemorrhage, pre-eclampsia/eclampsia, HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome, amniotic fluid embolus syndrome, acute fatty liver of pregnancy, and peripartum cardiomyopathy. Alternatively, critical illness may result from pregnancy-induced worsening of pre-existing diseases (for example, valvular heart disease, myasthenia gravis, and kidney disease). Pregnancy can also predispose women to diseases seen in the non-pregnant population, such as acute respiratory distress syndrome (for example, pneumonia and aspiration), sepsis (for example, chorioamnionitis and pyelonephritis) or pulmonary embolism. The pregnant patient may also develop conditions co-incidental to pregnancy such as trauma or appendicitis. Hemorrhage, particularly postpartum, and hypertensive disorders of pregnancy remain the most frequent indications for ICU admission. This review focuses on pregnancy-specific causes of critical illness. Management of the critically ill mother poses special challenges. The physiologic changes in pregnancy and the presence of a second, dependent, patient may necessitate adjustments to therapeutic and supportive strategies. The fetus is generally robust despite maternal illness, and therapeutically what is good for the mother is generally good for the fetus. For pregnancy-induced critical illnesses, delivery of the fetus helps resolve the disease process. Prognosis following pregnancy-related critical illness is generally better than for age-matched non-pregnant critically ill patients.

Highlights

  • Pregnancy is a normal physiologic process that is defined by the presence of the utero-placental complex

  • Physiologic changes associated with pregnancy may result in strain on organ systems with limited reserve and result in deterioration of pre-existing medical conditions (Table 1)

  • The pregnant patient may be admitted to intensive care because of diseases that occur only in pregnancy (Table 2), diseases that are worsened by pregnancy resulting in critical illness, diseases for which the pregnant patient is at elevated risk, and diseases co-incidental to pregnancy

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Summary

Introduction

Pregnancy is a normal physiologic process that is defined by the presence of the utero-placental complex. HELLP syndrome complicates up to 3 per 1,000 pregnancies, may present as a severe manifestation of PET, and occurs in up to 20% of patients. Amniotic fluid embolus syndrome AFE syndrome is a devastating complication that usually occurs within 24 hours of delivery It manifests with acute severe hypoxic respiratory failure, associated with shock, disseminated intravascular coagulopathy (DIC), confusion, and seizures (Table 3 and Figure 2). Considering current data and the specific exclusion of pregnant (but not postpartum) patients from the PROWESS (Recombinant Human Activated Protein C Worldwide Evaluation in Severe Sepsis) trial and other trials, we cannot recommend the use of activated protein C during pregnancy This agent may be of value in the postpartum period and clinicians should weigh up its value as a potent anti-inflammatory/anticoagulant agent versus the risk of bleeding complications. It may appear expensive to sustain the vegetative state of the brain-dead mother, this cost may be significantly less than the long-term cost of care of a severely premature neonate, which would require neonatal ICU and a variety of health-care interventions

Conclusions
Findings
17. Clark SL

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