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下呼吸道呼吸道病毒感染会增加异基因造血干细胞移植后低强度治疗患者侵袭性曲霉病的风险。

Lower respiratory tract respiratory virus infections increase the risk of invasive aspergillosis after a reduced-intensity allogeneic hematopoietic SCT.

机构信息

Division of Clinical Hematology, Hospital de la Sant Creu i Sant Pau, Autonomous University of Barcelona, Sant Antoni Maria Claret 167, Barcelona, Catalunya, Spain.

出版信息

Bone Marrow Transplant. 2009 Dec;44(11):749-56. doi: 10.1038/bmt.2009.78. Epub 2009 Apr 27.

DOI:10.1038/bmt.2009.78
PMID:19398963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7091792/
Abstract

We have analyzed the incidence and risk factors for the occurrence of invasive aspergillosis (IA) among 219 consecutive recipients of an allogeneic hematopoietic SCT after a reduced-intensity conditioning regimen (Allo-RIC). Twenty-seven patients developed an IA at a median of 218 days (range 24-2051) post-Allo-RIC, for a 4-year incidence of 13% (95% confidence interval 4-24%). In multivariate analysis, risk factors for developing IA were steroid therapy for moderate-to-severe graft vs host disease (GVHD) (Hazard Ratio (HR) 2.9, P=0.03), occurrence of a lower respiratory tract infection (LRTI) by a respiratory virus (RV) (HR 4.3, P<0.01) and CMV disease (HR 2.8, P=0.03). Variables that decreased survival after Allo-RIC were advanced disease phase (HR 1.9, P=0.02), steroid therapy for moderate-to-severe GVHD (HR 2.2, P<0.01), not developing chronic GVHD (HR 4.3, P<0.01), occurrence of LRTI by an RV (HR 3.4, P<0.01) and CMV disease (HR 2, P=0.01), whereas occurrence of IA had no effect on survival (P=0.5). Our results show that IA is a common infectious complication after an Allo-RIC, which occurs late post-transplant and may not have a strong effect on survival. An important observation is the possible role of LRTI by conventional RVs as risk factors for IA.

摘要

我们分析了 219 例接受低强度预处理异基因造血干细胞移植(Allo-RIC)患者侵袭性曲霉菌病(IA)的发生率和危险因素。27 例患者在 Allo-RIC 后中位时间 218 天(范围 24-2051)发生 IA,4 年发生率为 13%(95%置信区间 4-24%)。多变量分析显示,发生 IA 的危险因素为中重度移植物抗宿主病(GVHD)的类固醇治疗(危险比(HR)2.9,P=0.03)、呼吸道病毒(RV)下呼吸道感染(LRTI)(HR 4.3,P<0.01)和 CMV 疾病(HR 2.8,P=0.03)。降低 Allo-RIC 后生存率的变量为晚期疾病阶段(HR 1.9,P=0.02)、中重度 GVHD 的类固醇治疗(HR 2.2,P<0.01)、未发生慢性 GVHD(HR 4.3,P<0.01)、RV 引起的 LRTI(HR 3.4,P<0.01)和 CMV 疾病(HR 2,P=0.01),而 IA 的发生对生存率没有影响(P=0.5)。我们的结果表明,IA 是 Allo-RIC 后的常见感染并发症,发生在移植后晚期,可能对生存率没有强烈影响。一个重要的观察结果是,常规 RV 引起的 LRTI 可能是 IA 的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/b099f43b9afd/41409_2009_Article_BFbmt200978_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/d172b7d808bb/41409_2009_Article_BFbmt200978_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/9b70597f8dd1/41409_2009_Article_BFbmt200978_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/b099f43b9afd/41409_2009_Article_BFbmt200978_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/d172b7d808bb/41409_2009_Article_BFbmt200978_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/9b70597f8dd1/41409_2009_Article_BFbmt200978_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8c/7091792/b099f43b9afd/41409_2009_Article_BFbmt200978_Fig3_HTML.jpg

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