Evidence map›Paper›PMID 32429981›Full record

ArticleJournal of cardiothoracic surgery2020

Clinical and surgical aspects of congenital lobar over-inflation: a single center retrospective study.

Mohamed Abdel-Bary, Mohamed Abdel-Naser, Ahmed Okasha, Mohammed Zaki, Khaled Abdel-Baseer

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiothoracic surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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  5. Congenital lobar emphysema in monozygotic twins.Respiratory medicine case reports · 2023
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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

5 authors at 3 institutions in 1 country.

Mohamed Abdel-BaryDepartment of Cardiothoracic Surgery, Qena Faculty of Medicine, South Valley University, Safaga Road, Qena, 83523, Egypt. Dr_abdelbary@med.svu.edu.eg.ORCID https://orcid.org/0000-0002-7734-9089
Mohamed Abdel-NaserDepartment of Anaesthesia and ICU, Assiut Faculty of Medicine, Assiut University, Assiut, Egypt.ORCID https://orcid.org/0000-0002-3798-2322
Ahmed OkashaDepartment of Radiology, Qena Faculty of Medicine, South Valley University, Qena, Egypt.
Mohammed ZakiDepartment of Radiology, Sohag Faculty of Medicine, Sohag University, Sohag, Egypt.
Khaled Abdel-BaseerDepartment of Pediatrics, Qena Faculty of Medicine, South Valley University, Qena, Egypt.ORCID https://orcid.org/0000-0002-5761-0614
South Valley University · EGAssiut University · EGSohag University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital lobar overinflation (CLOI) is one of the most important causes of infantile respiratory distress (RD). We aim to evaluate our experience in CLOI management emphasizing on clinical features, diagnostic modalities, surgery and outcomes.

methodsThis is a retrospective study for all CLOI cases undergoing surgical management at Qena University Hospital. Demographic data, clinical data, radiographic findings, surgery and postoperative follow-up were reviewed.

resultsA total of 37 neonates and infants with CLOI were presented to our center between January 2015 and January 2019; their mean age was 111.43 ± 65.19 days and 22 were males. All cases presented with RD; and cyanosis in 19 cases. 15 cases presented with recurrent pneumonia and fever. Diminished breath sounds on the affected side and wheezes were the main clinical findings in 30 and 22 cases respectively. On CXR, emphysema was detected in all cases. A confirmatory CT chest was done for all cases. Left upper lobe was affected in 23 cases, right middle lobe in 7 and right upper lobe in 7 cases. Lobectomy was done in thirty-one cases; their mean age at surgery was 147.58 ± 81.49 days and 19 were males. Postoperative complications were noted in 5 cases and postoperative ventilation was required for 2 of them. No morbidity or mortality was reported. The follow-up duration ranged from 3 months to 1 year and all patients were doing well except one case that lost follow up after 3 months.

conclusionCLOI is a rare bronchopulmonary malformation that requires a high index of clinical suspicion, especially in persistent and recurrent infantile RD. CT chest is the most useful diagnostic modality. Early management of CLOI improves outcome and avoid life-threatening complications. Surgical management is the treatment of choice in our center without recorded mortality.

Indexed as

BronchiFemaleFollow-Up StudiesHospitals, UniversityHumansInfantInfant, NewbornLungMalePostoperative ComplicationsPostoperative PeriodPulmonary EmphysemaRespirationRespiratory Distress Syndrome, NewbornRespiratory InsufficiencyRespiratory SoundsCongenital lobar overinflationLobectomyNeonatal respiratory distress

Identifiers

PMID32429981
PMCPMC7236189
OpenAlexW3027271616

What OpenQuestion holds

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LicenceCC BY
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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.