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Follow-up of fetuses with congenital diaphragmatic hernia: The quantitative lung index
Carlota Rodó1, Tamara Illescas1, Silvia Arévalo1
1Maternal-fetal Medicine Unit, Department of Obstetrics, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Spain.
Insights
The Quantitative Lung Index (QLI) remained stable during pregnancy for fetuses with congenital diaphragmatic hernia. Lower QLI values were observed in fetuses undergoing tracheal occlusion, indicating its utility in monitoring this condition.
Area of Science:
- Perinatal medicine
- Fetal surgery
- Medical imaging
Background:
- Congenital diaphragmatic hernia (CDH) is a severe condition requiring careful fetal monitoring.
- The Quantitative Lung Index (QLI) is a potential metric for assessing lung development in fetuses with CDH.
Purpose of the Study:
- To evaluate the longitudinal behavior of the Quantitative Lung Index (QLI) in fetuses diagnosed with congenital diaphragmatic hernia (CDH).
- To compare QLI performance between fetuses managed with expectant care versus those undergoing tracheal occlusion (TO).
Main Methods:
- Retrospective analysis of 58 fetuses with isolated left CDH.
- QLI was calculated from prior lung-to-head ratio (LHR) measurements.
- A repeated measures mixed-effects model was employed to analyze QLI trends throughout gestation.
Main Results:
- QLI remained constant throughout pregnancy in both expectant (n=38) and tracheal occlusion (n=20) groups.
- Fetuses undergoing TO, characterized by LHR <1, o/eLHR ≤45%, and intrathoracic liver, exhibited lower QLI values compared to the non-TO group (p<0.03).
- Survival rates were 87% for non-TO and 60% for TO groups (p=0.02).
Conclusions:
- The Quantitative Lung Index (QLI) demonstrates a stable longitudinal behavior during pregnancy in fetuses with CDH.
- QLI is lower in fetuses selected for tracheal occlusion, suggesting its potential role in risk stratification and management decisions for CDH.
Objective:
To assess the longitudinal behavior of Quantitative Lung Index (QLI) for the follow-up of fetuses with congenital diaphragmatic hernia.
Study Design:
Retrospective study of fetuses with isolated left congenital diaphragmatic hernia. The fetuses were assessed by ultrasound at different gestational ages and QLI was retrospectively calculated by means of previous lung-to-head ratio measurements. We used a random effects model (mixed model with repeated measurements) to compare the performance of the QLI in operated and non-operated fetuses throughout pregnancy.
Results:
Fifty-eight cases of isolated left diaphragmatic hernia with complete follow-up were assessed in Hospital Universitari Vall d'Hebron in Barcelona (2003-2015). Thirty-eight of them were managed expectantly (non-TO) and the other 20 underwent tracheal occlusion (TO). All fetuses undergoing tracheal occlusion had lung-to-head ratio (LHR) <1, observed-to-expected LHR (o/eLHR) ≤45%, QLI <0.6 and liver up inside the thorax. The survival rate was 87% for the non-TO group and 60% for the TO group (p = 0.02). The QLI remained constant throughout pregnancy in both groups. The QLI in the TO group had lower values than the non-TO group (p < 0.03).
Conclusion:
The quantitative lung index was constant during pregnancy. This index was lower in fetuses undergoing tracheal occlusion but no significant changes were seen in its performance during pregnancy.
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