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The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study

BACKGROUND: No studies have investigated the immediate impact of receiving an allogeneic hematopoietic stem cell transplant (HSCT) on pulmonary inflammation or lung function. METHODS: Using a prospective study design, we quantified the changes in these outcome measures in eligible adult individuals...

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Autores principales: Enocson, Alexandra, Hubbard, Richard, McKeever, Tricia, Russell, Nigel, Byrne, Jennifer, Das-Gupta, Emma, Watson, Lynne, Fogarty, Andrew W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584947/
https://www.ncbi.nlm.nih.gov/pubmed/23311727
http://dx.doi.org/10.1186/1471-2466-13-2
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author Enocson, Alexandra
Hubbard, Richard
McKeever, Tricia
Russell, Nigel
Byrne, Jennifer
Das-Gupta, Emma
Watson, Lynne
Fogarty, Andrew W
author_facet Enocson, Alexandra
Hubbard, Richard
McKeever, Tricia
Russell, Nigel
Byrne, Jennifer
Das-Gupta, Emma
Watson, Lynne
Fogarty, Andrew W
author_sort Enocson, Alexandra
collection PubMed
description BACKGROUND: No studies have investigated the immediate impact of receiving an allogeneic hematopoietic stem cell transplant (HSCT) on pulmonary inflammation or lung function. METHODS: Using a prospective study design, we quantified the changes in these outcome measures in eligible adult individuals in the first six months after receiving an allogeneic hematopoietic stem cell transplant. RESULTS: Between January 2007 and December 2008, 72 patients were eligible to participate in the cohort, and of these 68 (94%) were included in the study. Compared to baseline, pulmonary inflammation as measured by exhaled nitric oxide increased after receiving a HSCT with the largest increment seen at three months (+6.0ppb, 95%CI: +0.4 to +11.5), and this was sustained at six months. Percent predicted forced expiratory volume in one second decreased over the same period, with the largest decrease observed at six weeks (−5.9%, 95% CI: -8.9 to −2.9), and this was also sustained over a six month period. Similar associations were observed for FVC. A larger increase in exhaled nitric oxide from baseline at six weeks and three months may be associated with decreased mortality (p=0.06, p=0.04 respectively). CONCLUSION: Our data demonstrate that recipients of an allogeneic HSCT experience an increase in biomarkers of pulmonary inflammation and a decrease in lung function in the first six months after the procedure. If independently validated in other study populations, these observations could have potential as a prognostic biomarker for this patient group.
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spelling pubmed-35849472013-03-02 The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study Enocson, Alexandra Hubbard, Richard McKeever, Tricia Russell, Nigel Byrne, Jennifer Das-Gupta, Emma Watson, Lynne Fogarty, Andrew W BMC Pulm Med Research Article BACKGROUND: No studies have investigated the immediate impact of receiving an allogeneic hematopoietic stem cell transplant (HSCT) on pulmonary inflammation or lung function. METHODS: Using a prospective study design, we quantified the changes in these outcome measures in eligible adult individuals in the first six months after receiving an allogeneic hematopoietic stem cell transplant. RESULTS: Between January 2007 and December 2008, 72 patients were eligible to participate in the cohort, and of these 68 (94%) were included in the study. Compared to baseline, pulmonary inflammation as measured by exhaled nitric oxide increased after receiving a HSCT with the largest increment seen at three months (+6.0ppb, 95%CI: +0.4 to +11.5), and this was sustained at six months. Percent predicted forced expiratory volume in one second decreased over the same period, with the largest decrease observed at six weeks (−5.9%, 95% CI: -8.9 to −2.9), and this was also sustained over a six month period. Similar associations were observed for FVC. A larger increase in exhaled nitric oxide from baseline at six weeks and three months may be associated with decreased mortality (p=0.06, p=0.04 respectively). CONCLUSION: Our data demonstrate that recipients of an allogeneic HSCT experience an increase in biomarkers of pulmonary inflammation and a decrease in lung function in the first six months after the procedure. If independently validated in other study populations, these observations could have potential as a prognostic biomarker for this patient group. BioMed Central 2013-01-11 /pmc/articles/PMC3584947/ /pubmed/23311727 http://dx.doi.org/10.1186/1471-2466-13-2 Text en Copyright ©2013 Enocson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Enocson, Alexandra
Hubbard, Richard
McKeever, Tricia
Russell, Nigel
Byrne, Jennifer
Das-Gupta, Emma
Watson, Lynne
Fogarty, Andrew W
The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title_full The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title_fullStr The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title_full_unstemmed The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title_short The acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
title_sort acute impact of a hematopoietic allograft on lung function and inflammation: a prospective observational study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584947/
https://www.ncbi.nlm.nih.gov/pubmed/23311727
http://dx.doi.org/10.1186/1471-2466-13-2
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