Congenital diaphragmatic hernia allows abdominal organs to enter the fetal chest and can restrict lung development. Prognosis varies widely. FETO—fetoscopic endoluminal tracheal occlusion—places a detachable balloon in the fetal trachea for a defined period to retain lung fluid and stimulate lung growth.

Severity assessment comes first

Evaluation usually includes detailed anatomy, side of the defect, observed-to-expected lung-to-head ratio, liver position, gestational age, fetal echocardiography, genetic testing, and review for additional abnormalities. Measurements must be obtained and interpreted by teams familiar with CDH because technique and reference standards affect classification.

Evidence is severity-specific

Randomised evidence in isolated severe left-sided CDH found improved survival to hospital discharge with FETO, accompanied by increased risks of preterm prelabour rupture of membranes and preterm birth. A separate trial in moderate left-sided disease did not show a significant improvement in its primary survival outcomes. These findings are why “CDH” alone is not an indication for FETO.

Balloon removal is part of the treatment

FETO requires a plan for balloon removal, usually by a later fetoscopic procedure or another established retrieval pathway. Families must know what to do if labour, membrane rupture, bleeding, or maternal illness occurs while the balloon is in place. Emergency access to a team capable of securing the fetal or neonatal airway is essential.

The neonatal pathway remains critical

FETO does not repair the diaphragm. After birth, the baby may require advanced ventilation, pulmonary-hypertension management, intensive care, and postnatal surgical repair. Counselling should cover survival, respiratory morbidity, feeding, neurodevelopment, recurrence, and long-term multidisciplinary follow-up.

The dated programme-status panel classifies the FETO pathway and its qualification. Assessment remains subject to strict case-specific eligibility, programme criteria, a confirmed balloon-removal pathway, governance, and informed consent.

The evidence room / TOTAL trials, 2021

Same procedure.
Different evidence.

Severity changes the conversation about FETO for isolated left-sided congenital diaphragmatic hernia. Compare the findings within each randomized trial—not between the two patient populations.

Severe left-sided CDH80 pregnanciesFETO 27–29 weeks

Survival to NICU discharge

Percent of the relevant trial group

FETO16 / 4040%
Expectant care6 / 4015%

Birth before 37 weeks

Percent of the relevant trial group

FETO30 / 4075%
Expectant care11 / 3829%

How to read this result

A survival benefit, with more preterm birth.

The severe trial found improved survival to neonatal intensive care discharge. It stopped early for benefit. The confidence interval was wide, and the increase in preterm birth remains important.

Relative risk of survival
2.67
95% confidence interval
1.22–6.11

Research results—not Mediclinic outcomes or an individual prediction. Both groups received standardized postnatal care. Birth-outcome denominators differ in the severe trial; moderate-trial birth percentages are reported as published.

Open the original trial referenceDeprest et al. · NEJM 2021 · DOI: 10.1056/NEJMoa2027030
Moderate left-sided CDH196 pregnanciesFETO 30–32 weeks

Survival to NICU discharge

Percent of the relevant trial group

FETO62 / 9863%
Expectant care49 / 9850%

Birth before 37 weeks

Percent of the relevant trial group

FETO64%
Expectant care22%

How to read this result

The survival difference was not statistically significant.

In the moderate trial, the survival confidence interval included 1 (P=0.06). Preterm birth was more frequent with FETO. A higher percentage alone does not establish a proven benefit.

Relative risk of survival
1.27
95% confidence interval
0.99–1.63

Research results—not Mediclinic outcomes or an individual prediction. Both groups received standardized postnatal care. Birth-outcome denominators differ in the severe trial; moderate-trial birth percentages are reported as published.

Open the original trial referenceDeprest et al. · NEJM 2021 · DOI: 10.1056/NEJMoa2026983

What the balloon does—and does not do.

FETO temporarily occludes the fetal trachea to retain lung fluid and encourage lung growth. It does not close the hole in the diaphragm. Balloon removal, a planned delivery pathway, neonatal intensive care, and postnatal repair remain essential parts of care.

Read the complete FETO guide

The essential distinctions

FETO supports lung growth; it does not repair the diaphragm.

Eligibility depends on detailed CDH severity assessment, maternal factors, and the complete care pathway.

  1. Temporary balloon

    A balloon blocks the fetal trachea for a planned period, retaining lung fluid.

  2. Lung development

    Retained fluid can stimulate lung growth in carefully selected severe cases.

  3. Removal and newborn care

    Balloon removal is essential. Delivery planning, neonatal intensive care, and postnatal surgery remain necessary.

Read the supporting source ↗

Sources and further reading

  1. NEJM — Randomized Trial of Fetal Surgery for Severe Left Diaphragmatic Hernia
  2. NEJM — Randomized Trial for Moderate Left Diaphragmatic Hernia