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Congenital High Airway Obstruction Syndrome / CHAOS

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Read about EXIT to Airway procedure for Congenital High Airway Obstructions Syndrome / CHAOS at the Fetal Care Center of Cincinnati.
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Overview of Congenital High Airway Obstruction Syndrome

Definition | Cause(s) | Incidence of CHAOS | Diagnosis | Management of Pregnancy | Fetal Surgery and Intervention

What is a Congenital High Airway Obstruction Syndrome / CHAOS?

Congenital High Airway Obstruction Syndrome / CHAOS is a condition in which the fetus has:

  • Massively enlarged lungs
  • A flattened diaphragm
  • A dilated tracheobronchial tree
  • Fluid in the abdomen
  • Other signs of in utero heart failure (non-immune hydrops) due to complete or nearly complete obstruction of the fetal airway

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What Causes Congenital High Airway Obstruction Syndrome / CHAOS?

The airway obstruction in Congenital High Airway Obstruction Syndrome / CHAOS may be due to:

  • The absence of or blockage of the larynx
  • The absence of or blockage of the trachea
  • A cyst which blocks the airway

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What is the Incidence of Congenital High Airway Obstruction Syndrome / CHAOS?

Congenital High Airway Obstruction Syndrome / CHAOS is a rare condition with fewer than 50 cases reported since 1989.

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How is Congenital High Airway Obstruction Syndrome / CHAOS Diagnosed?

Congenital High Airway Obstruction Syndrome / CHAOS is detected by ultrasound as a complete or nearly complete obstruction of the upper airway.

The lungs appear extremely large. The diaphragm may be inverted and the heart compressed.

The heart may appear elongated with its chambers compressed by the enlarged large lungs.

The tracheobronchial tubes may be dilated and the fetus may have abnormal breathing movements.

Although a fetus diagnosed with Congenital High Airway Obstruction Syndrome (associated with hydrops) is unlikely to survive without fetal intervention, in some cases the hydrops resolves and the fetus can survive.

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How is Pregnancy Managed When Congenital High Airway Obstruction Syndrome / CHAOS is Suspected?

The mother should have a detailed ultrasound to detect associated abnormalities. A fetal echocardiogram will detect structural heart disease. A prenatal karyotype (the study of the chromosomes of cells) will confirm chromosomal abnormalities.

The fetus should be followed closely for early signs of hydrops (in uteru heart failure). The parents will want to consult with a medical geneticist and a pediatric surgeon to plan for delivery at a tertiary-care hospital that has expertise and experience in the EXIT (ex utero intrapartum treatment) procedure.

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What are the Fetal Interventions for Congenital High Airway Obstruction Syndrome / CHAOS?

Fetal intervention for Congenital High Airway Obstruction Syndrome / CHAOS depends upon the gestational age at diagnosis and the presence or absence of hydrops. In rare cases, less than 30 weeks gestation, where it is known that the fetus is at significant risk for intrauterine death, open fetal surgery may be attempted. After 30 weeks gestation, an EXIT procedure may also be performed in order to obtain an airway at the time of delivery.

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Revised 1/05

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