Non-Cystic Fibrosis Bronchiectasis in Children: Clinical Profile, Etiology and Outcome.

dc.contributor.authorKumar, Ajay
dc.contributor.authorLodha, Rakesh
dc.contributor.authorKumar, Prawin
dc.contributor.authorKabra, S K
dc.date.accessioned2016-01-27T11:28:43Z
dc.date.available2016-01-27T11:28:43Z
dc.date.issued2015-01
dc.description.abstractObjective: To describe clinical profile, etiology and outcome in children with non-cystic fibrosis bronchiectasis. Methods: A chart review of children diagnosed with non-cystic fibrosis bronchiectasis, attending pediatric chest clinic of tertiary care hospital. Results: The underlying cause was identified in 51 (63.8%) out of 80 children (mean age, 9.6 y). Common causes were post-infectious in 19 (23.8%), suspected primary ciliary dyskinesia in 12 (15%), and allergic bronchopulmonary aspergillosis in 6 (7.5%). One or more complications were observed in 76 (95%) patients; 14 (17.5%) children required surgery and 5 (11.1%) children died. Conclusions: Common causes of non-cystic fibrosis bronchiectasis are post infectious and primary ciliary dyskinesia. There is a need to create awareness about early diagnosis of bronchiectasis as it is often delayed.en_US
dc.identifier.citationKumar Ajay, Lodha Rakesh, Kumar Prawin, Kabra S K. Non-Cystic Fibrosis Bronchiectasis in Children: Clinical Profile, Etiology and Outcome. Indian Pediatrics. 2015 Jan; 52(1): 35-37.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/171006
dc.language.isoenen_US
dc.source.urihttps://www.indianpediatrics.net/jan2015/jan-35-37.htmen_US
dc.subjectAllergic bronchopulmonary aspergillosisen_US
dc.subjectChronic coughen_US
dc.subjectPneumoniaen_US
dc.subjectSuppurative lung diseaseen_US
dc.titleNon-Cystic Fibrosis Bronchiectasis in Children: Clinical Profile, Etiology and Outcome.en_US
dc.typeArticleen_US
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