Evidence map›Paper›PMID 41491054›Full record

ArticleScientific reports2026

Prenatal characteristics and prognosis of congenital pulmonary airway malformation: a retrospective multicenter cohort study.

Yutian Miao, Sheng Wang, Jiyuan Li, Sisi Peng, Hui Cao, Yingchun Luo, Haiyan Kuang

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yutian MiaoUltrasound Medical Center, Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, 410008, Hunan, China.
Sheng WangDepartment of Radiology, Hunan Children's Hospital, No. 86 Ziyuan Road, Changsha, 410007, Hunan, China.
Jiyuan LiDepartment of Ultrasonography, Liuyang Maternal and Child Health Care Hospital, No. 53, Beizheng North Road, Liuyang, 410300, Hunan, China.
Sisi PengUltrasound Medical Center, Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, 410008, Hunan, China.
Hui CaoUltrasound Medical Center, Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, 410008, Hunan, China.
Yingchun LuoUltrasound Medical Center, Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, 410008, Hunan, China.
Haiyan KuangUltrasound Medical Center, Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, 410008, Hunan, China. 15343689@qq.com.

Funding

Hunan Provincial Hospital of Maternal and Child Health Care's High-Level Talent Development Scheme 20240130 - 1004the Natural Science Foundation Project of Hunan Province 2024JJ9330the Scientific Research Fund Project of Hunan Provincial Health Commission W20243133
6 · The paper itself

Abstract

objectiveThis study evaluated the impact of prenatal characteristics of congenital pulmonary airway malformation (CPAM) on postnatal outcomes, and investigated management strategies and outcomes in surgical versus non-surgical cases. This retrospective multicenter cohort study included 145 cases of CPAM diagnosed by prenatal ultrasound between January 2019 and May 2024. The cohort was stratified into two groups based on prenatal cystic volume ratio (CVR): CVR < 1.6 (n = 131) and CVR ≥ 1.6 (n = 14) for comparative analysis. Live-born infants were further categorized into surgical (n = 40) and non-surgical (n = 89) groups according to treatment methods. Statistical analyses included chi-square tests, t-tests, logistic regression, and Cox proportional hazards models. Univariate analysis revealed that the prevalence of prenatal large cystic lesions (macrocystic ≥ 0.5 cm), prenatal mediastinal shift, and prenatal pleural effusion/ascites were significantly higher in the CVR ≥ 1.6 group compared to the CVR < 1.6 group (all P < 0.05). The proportion of cases with prenatal CVR ≥ 1.6 combined with prenatal mediastinal shift was significantly greater in the surgical group than in the non-surgical group (P < 0.05). However, multivariate regression analysis demonstrated that after incorporating postnatal variables, prenatal variables (including CVR) were not independent factors influencing surgical intervention. Only postnatal respiratory symptoms were independently associated with the decision for surgical intervention (P < 0.05). Additionally, 95% of surgical procedures were performed within 20 months of birth. Postnatal respiratory symptoms are the primary clinical determinant guiding surgical intervention in infants with CPAM. Prenatal ultrasound parameters may indirectly aid in assessing the risk of surgical intervention through their potential association with postnatal symptoms. Conservative observation is safe and feasible for asymptomatic infants, whereas the onset of respiratory symptoms warrants active consideration of surgical intervention.

Indexed as

Cystic Adenomatoid Malformation of Lung, CongenitalLungUltrasonography, PrenatalAdultFemaleHumansInfantInfant, NewbornMalePregnancyPrognosisRetrospective StudiesCongenital pulmonary airway malformationCVROperativePrenatalSurgical proceduresTreatment outcomeUltrasonography

Identifiers

PMID41491054
PMCPMC12868729

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.