Evidence map›Paper›PMID 40698238›Full record

ArticleCureus2025

Radiological Patterns of Pediatric Non-cystic Fibrosis Bronchiectasis: A Retrospective Study From Oman.

Majid Al Jabri, Ons Al Humaimi, Fatma Al Yousufi, Abdullah Al Farsi, Tabinda Qureshi, Hussein Al Kindy

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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Majid Al JabriChild Health Department, Sultan Qaboos University Hospital, Muscat, OMN.
Ons Al HumaimiChild Health Department, Sultan Qaboos University Hospital, College of Medicine and Health Sciences, Muscat, OMN.
Fatma Al YousufiChild Health Department, Sultan Qaboos University Hospital, College of Medicine and Health Sciences, Muscat, OMN.
Abdullah Al FarsiChild Health Department, Sultan Qaboos University Hospital, College of Medicine and Health Sciences, Muscat, OMN.
Tabinda QureshiChild Health Department, Sultan Qaboos University Hospital, Muscat, OMN.
Hussein Al KindyChild Health Department, Sultan Qaboos University Hospital, College of Medicine and Health Sciences, Muscat, OMN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-cystic fibrosis bronchiectasis (NCFB) remains underdiagnosed in pediatric populations, particularly in the Middle East.

objectiveTo characterize the high-resolution computed tomography (HRCT) features of NCFB in pediatric patients, including extent, morphological subtype, and lobar distribution, and to evaluate their associations with underlying clinical diagnoses at a tertiary care center in Oman.

methodsWe conducted a retrospective cross-sectional study at Sultan Qaboos University Hospital (SQUH), a tertiary center in Oman, reviewing pediatric patients ≤18 years diagnosed with NCFB between January 2000 and December 2022. High-resolution computed tomography (HRCT) reports prepared by pediatric radiologists were reviewed. Data on clinical features, radiological patterns, lobar involvement, and etiologies were analyzed descriptively using IBM SPSS Statistics for Macintosh, Version 19.0 (IBM Corp., Armonk, NY).

resultsOf the 150 patients reviewed, 61 met the inclusion criteria. The mean age at diagnosis was 7.3 years, with 35 (57.4%) being male. Diffuse bronchiectasis was predominant, observed in 48 patients (78.7%), and involved more than two lobes in 40 cases (65.6%). The left lower lobe was the most frequently affected, seen in 13 patients (21.6%). Cylindrical bronchiectasis was present in all patients, while cystic in 25 patients (41.0%) and varicose in 19 patients (31.1%) forms were more common in those with systemic disorders, such as primary immunodeficiency (PID, 18 patients; 37.5%) and primary ciliary dyskinesia (PCD, 8 patients; 16.7%). Patients diagnosed at age ≥5 years had a significantly higher prevalence of diffuse disease.

conclusionHRCT is a crucial diagnostic tool for pediatric NCFB, particularly in children with recurrent infections or systemic comorbidities, such as PID or PCD. Early imaging may prevent irreversible damage and guide targeted treatment. Establishing national guidelines for pediatric chest CT utilization and incorporating multidisciplinary assessments may improve diagnostic timeliness and outcomes.

Indexed as

ct imagingnon-cystic fibrosis bronchiectasisprimary ciliary dyskinesiaprimary immunodeficiencyradiological featuressultan qaboos university hospital

Identifiers

PMID40698238
PMCPMC12281239

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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.