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Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation
Pulmonary complications are major causes of morbidity and mortality after haematopoietic stem cell transplantation (HSCT). We hypothesise that elevated exhaled nitric oxide (FeNO) levels early after HSCT in children are predictive for pulmonary complications. The present prospective study included 3...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102378/ https://www.ncbi.nlm.nih.gov/pubmed/22350283 http://dx.doi.org/10.1007/s00431-012-1692-x |
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author | Fazekas, T. Eickhoff, P. Lawitschka, A. Knotek, B. Pötschger, U. Peters, C. |
author_facet | Fazekas, T. Eickhoff, P. Lawitschka, A. Knotek, B. Pötschger, U. Peters, C. |
author_sort | Fazekas, T. |
collection | PubMed |
description | Pulmonary complications are major causes of morbidity and mortality after haematopoietic stem cell transplantation (HSCT). We hypothesise that elevated exhaled nitric oxide (FeNO) levels early after HSCT in children are predictive for pulmonary complications. The present prospective study included 30 children (age, 4–18 years) before HSCT. FeNO levels were evaluated 10 days before transplant, at day 0, day +28 and day +60 after HSCT. During the follow-up period until day +100, pulmonary complications and lung function were assessed. Before HSCT, the mean FeNO levels were comparable in children with or without post-transplant pulmonary complications. However, they differed at day 0 and day +28 with a mean of 7 (±1.95) and 13 (±3.44) ppb at day 0 and a mean of 13 (±3.44) and 14 (±3.57) ppb at day +28, respectively. Conclusion: Children with pulmonary complications after day +28 have higher mean FeNO levels 28 days after HSCT than children without later pulmonary complications. Therefore, FeNO could be an important diagnostic tool for hyperinflammatory response in bronchial epithelium after paediatric HSCT. |
format | Online Article Text |
id | pubmed-7102378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-71023782020-03-31 Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation Fazekas, T. Eickhoff, P. Lawitschka, A. Knotek, B. Pötschger, U. Peters, C. Eur J Pediatr Original Article Pulmonary complications are major causes of morbidity and mortality after haematopoietic stem cell transplantation (HSCT). We hypothesise that elevated exhaled nitric oxide (FeNO) levels early after HSCT in children are predictive for pulmonary complications. The present prospective study included 30 children (age, 4–18 years) before HSCT. FeNO levels were evaluated 10 days before transplant, at day 0, day +28 and day +60 after HSCT. During the follow-up period until day +100, pulmonary complications and lung function were assessed. Before HSCT, the mean FeNO levels were comparable in children with or without post-transplant pulmonary complications. However, they differed at day 0 and day +28 with a mean of 7 (±1.95) and 13 (±3.44) ppb at day 0 and a mean of 13 (±3.44) and 14 (±3.57) ppb at day +28, respectively. Conclusion: Children with pulmonary complications after day +28 have higher mean FeNO levels 28 days after HSCT than children without later pulmonary complications. Therefore, FeNO could be an important diagnostic tool for hyperinflammatory response in bronchial epithelium after paediatric HSCT. Springer-Verlag 2012-02-16 2012 /pmc/articles/PMC7102378/ /pubmed/22350283 http://dx.doi.org/10.1007/s00431-012-1692-x Text en © Springer-Verlag 2012 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Fazekas, T. Eickhoff, P. Lawitschka, A. Knotek, B. Pötschger, U. Peters, C. Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title | Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title_full | Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title_fullStr | Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title_full_unstemmed | Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title_short | Exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
title_sort | exhaled nitric oxide and pulmonary complications after paediatric stem cell transplantation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102378/ https://www.ncbi.nlm.nih.gov/pubmed/22350283 http://dx.doi.org/10.1007/s00431-012-1692-x |
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