Hematology Department, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
Microbiology Service, Hospital Clínico Universitario, Institute for Research INCLIVA, Valencia, Spain.
J Infect. 2019 May;78(5):393-401. doi: 10.1016/j.jinf.2019.02.009. Epub 2019 Feb 21.
To date no definitive cut-off value for cytomegalovirus (CMV) DNA load in bronchoalveolar lavage (BAL) fluid specimens has been established to discriminate between CMV pneumonia and pulmonary CMV DNA shedding in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients.
The current retrospective study is aimed at assessing the range of CMV DNA loads quantified in BAL fluid specimens from allo-HSCT patients with pneumonia in which different microorganisms were causally involved.
A total of 144 BAL specimens from 123 patients were included. CMV DNA was detected in 56 out of 144 BAL fluid specimens and the median CMV DNA load from patients in whom CMV pneumonia was unlikely or could be tentatively ruled out was 1210 (31-68, 920) IU/ml. The frequency of CMV DNA detection and median CMV DNA loads were comparable, irrespective of the attributable cause of pneumonia. Detection of CMV DNA loads in BAL fluid specimens >500 IU/ml was independently associated with pneumonia-attributable mortality.
The current study highlights the difficulty in establishing universal CMV DNA load thresholds in BAL fluid specimens for distinguishing between CMV pneumonia and pulmonary CMV DNA shedding, and suggests that the presence of CMV DNA in BAL fluid specimens beyond a certain level may have a deleterious impact on patient outcome.
迄今为止,尚无明确的支气管肺泡灌洗液(BAL)标本中巨细胞病毒(CMV)DNA 载量的临界值可用于区分异基因造血干细胞移植(allo-HSCT)受者中的 CMV 肺炎和肺部 CMV DNA 脱落。
本回顾性研究旨在评估与不同微生物因果相关的肺炎 allo-HSCT 患者 BAL 液标本中 CMV DNA 载量的范围。
共纳入 123 例患者的 144 份 BAL 标本。144 份 BAL 液标本中有 56 份检测到 CMV DNA,CMV 肺炎可能性较小或可暂排除的患者的 CMV DNA 中位载量为 1210(31-68,920)IU/ml。无论肺炎的归因原因如何,CMV DNA 的检出频率和中位 CMV DNA 载量均相似。BAL 液标本中 CMV DNA 载量>500 IU/ml 的检测与肺炎归因性死亡率独立相关。
本研究强调了在 BAL 液标本中建立用于区分 CMV 肺炎和肺部 CMV DNA 脱落的通用 CMV DNA 载量阈值的困难,并提示 BAL 液标本中 CMV DNA 的存在超过一定水平可能对患者预后产生有害影响。