Evidence map›Paper›PMID 29046943›Full record

ReviewEuropean journal of pediatrics2017

Congenital pulmonary airway malformations: state-of-the-art review for pediatrician's use.

Claire Leblanc, Marguerite Baron, Emilie Desselas, Minh Hanh Phan, Alexis Rybak, Guillaume Thouvenin, Clara Lauby, Sabine Irtan

Abstract readReview
PubMed Publisher
In one paragraph

Review in European journal of pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% of its field
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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 200 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Article
  9. Genetic Disorders Detectable by Fetal MRI: A Review.Diagnostics (Basel, Switzerland) · 2026
    Review
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8 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Claire LeblancDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.ORCID http://orcid.org/0000-0003-1666-7945
Marguerite BaronDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Emilie DesselasDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Minh Hanh PhanDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Alexis RybakDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Guillaume ThouveninDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Clara LaubyDepartment of Pediatric Pulmonology, APHP Hôpital Armand Trousseau, Paris, France.
Sabine IrtanUPMC Univ Paris 06, Centre de Recherche St Antoine Inserm UMRS.938, Sorbonne Universités, Paris, France. sabine.irtan@gmail.com.
Sorbonne Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital pulmonary airway malformations or CPAM are rare developmental lung malformations, leading to cystic and/or adenomatous pulmonary areas. Nowadays, CPAM are diagnosed prenatally, improving the prenatal and immediate postnatal care and ultimately the knowledge on CPAM pathophysiology. CPAM natural evolution can lead to infections or malignancies, whose exact prevalence is still difficult to assess. The aim of this "state-of-the-art" review is to cover the recently published literature on CPAM management whether the pulmonary lesion was detected during pregnancy or after birth, the current indications of surgery or surveillance and finally its potential evolution to pleuro-pulmonary blastoma.

conclusionSurgery remains the cornerstone treatment of symptomatic lesions but the postnatal management of asymptomatic CPAM remains controversial. There are pros and cons of surgical resection, as increasing rate of infections over time renders the surgery more difficult after months or years of evolution, as well as risk of malignancy, though exact incidence is still unknown. What is known: • Congenital pulmonary airway malformations (CPAM) are rare developmental lung malformations mainly antenatally diagnosed. • While the neonatal management of symptomatic CPAM is clear and includes prompt surgery, controversies remain for asymptomatic CPAM due to risk of infections and malignancies. What is new: • Increased rate of infection over time renders the surgery more difficult after months or years of evolution and pushes for recommendation of early elective surgery. • New molecular or pathological pathways may help in the distinction of type 4 CPAM from type I pleuropulmonary blastoma.

Indexed as

Cystic Adenomatoid Malformation of Lung, CongenitalDisease ProgressionFemaleGenetic Predisposition to DiseaseHumansLungLung NeoplasmsPediatricsPregnancyPrenatal DiagnosisPulmonary BlastomaCPAMPleuropulmonary blastomaState of the art

Identifiers

PMID29046943
OpenAlexW2765302553

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.