# Key ultrasound predictors in the prenatal assessment of congenital pulmonary airway malformation: a single-center experience

**Authors:** Isabella Fabietti, Alice Novak, Laura Valfrè, Chiara Vassallo, Domenico Umberto De Rose, Milena Viggiano, Andrea Conforti, Chiara Iacusso, Marco Bonito, Pietro Bagolan, Leonardo Caforio

PMC · DOI: 10.3389/fped.2025.1555539 · Frontiers in Pediatrics · 2025-05-16

## TL;DR

This study identifies key ultrasound measurements that help predict whether fetal therapy is needed for a lung condition called congenital pulmonary airway malformation.

## Contribution

The study evaluates the effectiveness of combining ultrasound indicators to improve prediction of fetal therapy in CPAM cases.

## Key findings

- CVR above 1.25 reliably predicts the need for fetal therapy with high sensitivity and specificity.
- MSA greater than 13.3° also shows high sensitivity and specificity for predicting fetal therapy.
- Combining CVR and MSA may improve prediction accuracy and guide clinical decision-making.

## Abstract

This study assesses the sensitivity and specificity of congenital pulmonary airway malformation (CPAM) Volume Ratio (CVR) in predicting the need for fetal therapy (FT) and explores the role of additional ultrasound indicators, including the Observed/Expected Lung to Head Ratio (O/E LHR) and Mediastinal Angle Shift (MSA), in improving FT prediction.

We retrospectively studied all CPAM cases referred to our Center from 2018 to 2022. FT was provided at any CVR value in cases of hydrops, rapid lesion growth, or polyhydramnios. The worst CVR, O/E LHR, and MSA values between 20 and 28 weeks of gestation were analyzed.

Among 62 CPAM cases, 56.4% right-sided and 43.5% left-sided. Hydrops occurred in 5 cases, all right-sided. FT was required in 14 cases (11 receiving steroids and 3 thoraco-amniotic shunt). CVR was significantly higher in the FT group compared to the non-FT group (p < 0.0001), with an optimal cut-off of 1.25 (Sn 100%; Sp 89.6%) for predicting FT. The O/E LHR was significantly lower in the FT group (mean 44.8 vs. 58.3; p = 0.0046, AUC 0.75), with a Sn of 84% and Sp of 62%. MSA was significantly higher in the FT compared to the non-FT group (p < 0.0001), with a threshold of 13.3° providing high Sn (92.8%) and Sp (89.3%) for predicting FT.

CVR is the most reliable predictor of the need for FT, even at lower thresholds. MSA can effectively complement CVR in predicting FT, and using multiple parameters may improve parental counseling and identify cases needing closer monitoring.

## Linked entities

- **Diseases:** congenital pulmonary airway malformation (MONDO:0016580), polyhydramnios (MONDO:0004585)

## Full-text entities

- **Diseases:** CPAM (MESH:D056151), Hydrops (MESH:D004487), polyhydramnios (MESH:D006831)
- **Chemicals:** steroids (MESH:D013256)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12122531/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12122531/full.md

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Source: https://tomesphere.com/paper/PMC12122531