ArticleJournal of cardiothoracic surgery2020
Clinical and surgical aspects of congenital lobar over-inflation: a single center retrospective study.
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.
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7 citing papers in PubMed, 15 citations in OpenAlex.
- Endovascular Repair of a Subclavian Artery Aneurysm With Re-purposed Aorto-Iliac Stent Graft Components.EJVES vascular forum · 2025Article
- High comorbidity rates in congenital lobar emphysema and the effect on clinical presentation.European journal of pediatrics · 2024Article
- Congenital Lobar Emphysema in Children: Case Series.Cureus · 2023Article
- Article
- Congenital lobar emphysema in monozygotic twins.Respiratory medicine case reports · 2023Article
- Surgery versus conservative management in congenital lobar emphysema: follow up and indicators for surgery.Pediatric surgery international · 2022Article
- Convex and Concave Model 3D Printing for Designing Right-side Bronchial Blocker for Infants.International journal of bioprinting · 2022Article
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
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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.
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