Evidence map›Paper›PMID 31477056›Full record

SynthesisBMC pediatrics2019

Congenital bronchopulmonary foregut malformation: systematic review of the literature.

Gang Yang, Lina Chen, Chang Xu, Miao Yuan, Yuan Li

Open access · goldAbstract readCase ReportsSystematic Review
In one paragraph

Synthesis in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Unclassified bronchopulmonary foregut malformation in a 2-year-old girl.General thoracic and cardiovascular surgery cases · 2023
    Article
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Esophageal Lung in a Preterm Boy-Report on a Multidisciplinary Treatment.European journal of pediatric surgery reports · 2019
    Article
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

5 authors at 3 institutions in 1 country.

Gang YangDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Guoxue Xiang No.37, Chengdu, 610041, China.
Lina ChenDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Chang XuDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Guoxue Xiang No.37, Chengdu, 610041, China.
Miao YuanDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Guoxue Xiang No.37, Chengdu, 610041, China.
Yuan LiDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Guoxue Xiang No.37, Chengdu, 610041, China. liyuanletters@163.com.
Sichuan University · CNWest China Hospital of Sichuan University · CNWest China Second University Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital bronchopulmonary foregut malformation (CBPFM) is a rare congenital malformation involving both the digestive and respiratory system. Early diagnosis is difficult, and delayed recognition may result in considerable complications. The aim of the study was to identify and analyze the clinical characteristics and radiological features of CBPFMs.

methodsA systematic review was conducted in accordance with PRISMA guidelines. PubMed, Ovid database, EMBASE were searched for relevant publications to identify all published case-reports of CBPFM since 1992. Data about the demography, clinical presentation, pathology, imaging features, treatment and prognosis were collected.

resultsSixty-one cases were included in our study. Cases were aged from 1 day to 59 years with the majority aged 3 years or younger. The most common type was group III (37.7%), followed by group II (29.5%)group I (27.9%) and group IV (4.9%). The presentations included respiratory distress (32.8%), cough/choking following food intake and other presentations associated respiratory infection. Thirty-eight cases (62.3%) were diagnosed by upper gastrointestinal series (UGI). Misdiagnosis was common. Eight cases (13.1%) of the included cases died.

conclusionsEarly recognition and extensive delineation of the anatomy of CBPFM are important to correct these anomalies successfully. UGI is the first choice to confirm the abnormal bronchus communicating with the esophagus. Resection of abnormal pulmonary tissue, lobe or even unilateral lung is preferred. Reconstruction procedures are feasible in selected patients.

Indexed as

AdolescentAdultBronchiChildChild, PreschoolDextrocardiaEsophageal AtresiaEsophagusFemaleHumansInfantInfant, NewbornLungMaleMiddle AgedPulmonary ArteryCongenital bronchopulmonary foregut malformationEsophageal bronchusEsophageal lungSystematic review

Identifiers

PMID31477056
PMCPMC6721191
OpenAlexW2970366019

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.