Publication: Long-term respiratory outcomes of post-op congenital lung malformations
| dc.contributor.author | KARADAĞ, BÜLENT TANER | |
| dc.contributor.authors | Dincel, Alican; Yilmaz Yegit, Cansu; Ergenekon, Almala Pinar; Erdem Eralp, Ela; Gokdemir, Yasemin; Kiyan, Gursu; Karadag, Bulent | |
| dc.date.accessioned | 2022-03-12T22:55:36Z | |
| dc.date.available | 2022-03-12T22:55:36Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Background Congenital lung malformations (CLM) are rare disorders and surgical intervention is the definitive treatment. Our aim is to evaluate the long-term lung function of patients with CLM after surgery compared to healthy children. Methods Sixteen children with CLM (M/F: 9/7) and 30 age-matched, healthy controls (M/F: 13/17) were included in the study. Demographic data were recorded and both groups were compared by spirometry and the nitrogen-based Lung Clearance Index (LCI). Results Mean +/- SD age of the patients was 12.0 +/- 5.4 years. The mean forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), FEV1/FVC, and forced expiratory flow between 25% and 75% of force expiration (FEF25-75) predicted was, 86.68 +/- 16.65, 88.00 +/- 14.58, 97.44 +/- 9.89, and 79.00 +/- 26.41, respectively in the patient group. Patients with CLM had significantly lower values in FEV1, FVC, FEF25-75 than healthy controls (P = 0.002, P 0.007, P 0.045). While the mean LCI2,5% value in patients' group was 8.33 +/- 1.52, it was 7.28 +/- 0.80 in healthy controls (P = 0.023). Strong inverse correlation between LCI and FEV1, FEV1/FVC was detected in the patient group (P = 0.023; r: -0.581, P 0.017; r: -0.606 respectively). Conclusion This study revealed that, in long-term follow-up, patients who had surgery because of CLM have impairment in the pulmonary function compared to healthy children and LCI may be more accurate in detecting airway diseases early than spirometry. | |
| dc.identifier.doi | 10.1111/ped.14488 | |
| dc.identifier.eissn | 1442-200X | |
| dc.identifier.issn | 1328-8067 | |
| dc.identifier.pubmed | 32991002 | |
| dc.identifier.uri | https://hdl.handle.net/11424/236787 | |
| dc.identifier.wos | WOS:000654380100001 | |
| dc.language.iso | eng | |
| dc.publisher | WILEY | |
| dc.relation.ispartof | PEDIATRICS INTERNATIONAL | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | congenital lung malformations | |
| dc.subject | lung clearance index | |
| dc.subject | pulmonary function test | |
| dc.subject | spirometry | |
| dc.subject | INERT-GAS WASHOUT | |
| dc.subject | MULTIPLE-BREATH WASHOUT | |
| dc.subject | PULMONARY-FUNCTION | |
| dc.subject | CLEARANCE INDEX | |
| dc.subject | CHILDREN | |
| dc.subject | LOBECTOMY | |
| dc.subject | DISEASE | |
| dc.subject | STATEMENT | |
| dc.subject | CHILDHOOD | |
| dc.subject | RESECTION | |
| dc.title | Long-term respiratory outcomes of post-op congenital lung malformations | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| local.avesis.id | 4e444ff5-aa2b-46fd-bc8a-a367b3c36a3a | |
| local.import.package | SS17 | |
| local.indexed.at | WOS | |
| local.indexed.at | SCOPUS | |
| local.indexed.at | PUBMED | |
| local.journal.numberofpages | 6 | |
| oaire.citation.endPage | 709 | |
| oaire.citation.issue | 6 | |
| oaire.citation.startPage | 704 | |
| oaire.citation.title | PEDIATRICS INTERNATIONAL | |
| oaire.citation.volume | 63 | |
| relation.isAuthorOfPublication | 218b489d-97ab-49dd-9db6-0c2a732f1999 | |
| relation.isAuthorOfPublication.latestForDiscovery | 218b489d-97ab-49dd-9db6-0c2a732f1999 |