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

被引:3
|
作者
Enocson, Alexandra [1 ]
Hubbard, Richard [1 ]
McKeever, Tricia [1 ]
Russell, Nigel [2 ]
Byrne, Jennifer [2 ]
Das-Gupta, Emma [2 ]
Watson, Lynne [2 ]
Fogarty, Andrew W. [1 ]
机构
[1] Univ Nottingham, Nottingham Biomed Res Unit, Div Epidemiol & Publ Hlth, City Hosp, Nottingham NG5 1PB, England
[2] Univ Nottingham Hosp, Dept Haematol, Bone Marrow Transplant Unit, Nottingham NG5 1PB, England
来源
BMC PULMONARY MEDICINE | 2013年 / 13卷
关键词
Lung function; Inflammation; Haematopoietic transplant; STEM-CELL TRANSPLANTATION; PULMONARY COMPLICATIONS; NITRIC-OXIDE; AIRWAYS; ROLES;
D O I
10.1186/1471-2466-13-2
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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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页数:6
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