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Initially fewer bloodstream infections for allogeneic vs. autologous stem-cell transplants in neutropenic patients.中性粒细胞减少的患者中,异体与自体干细胞移植相比,血流感染更少。
Epidemiol Infect. 2013 Jan;141(1):158-64. doi: 10.1017/S0950268812000283. Epub 2012 Mar 7.
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Support Care Cancer. 2015 Jan;23(1):13-9. doi: 10.1007/s00520-014-2297-x. Epub 2014 Jun 8.

本文引用的文献

1
Immune reconstitution after allogeneic transplantation and expanding options for immunomodulation: an update.异基因移植后的免疫重建和免疫调节选择的扩展:最新进展。
Blood. 2010 May 13;115(19):3861-8. doi: 10.1182/blood-2009-12-234096. Epub 2010 Mar 9.
2
Pseudomonas aeruginosa bacteremia over a 10-year period: multidrug resistance and outcomes in transplant recipients.10年期间铜绿假单胞菌血症:移植受者的多重耐药性及预后
Transpl Infect Dis. 2009 Jun;11(3):227-34. doi: 10.1111/j.1399-3062.2009.00380.x. Epub 2009 Mar 2.
3
Bloodstream infections in haematology: risks and new challenges for prevention.血液学中的血流感染:预防的风险与新挑战
Blood Rev. 2009 May;23(3):113-22. doi: 10.1016/j.blre.2008.10.003. Epub 2008 Nov 28.
4
Meta-analyses of chronic disease trials with competing causes of death may yield biased odds ratios.对存在多种死亡原因的慢性病试验进行的荟萃分析可能会产生有偏差的比值比。
J Clin Epidemiol. 2008 Apr;61(4):365-72. doi: 10.1016/j.jclinepi.2007.05.009. Epub 2007 Oct 15.
5
Sample size calculations in the presence of competing risks.存在竞争风险时的样本量计算。
Stat Med. 2007 Dec 30;26(30):5370-80. doi: 10.1002/sim.3114.
6
Bloodstream infections among transplant recipients: results of a nationwide surveillance in Spain.移植受者的血流感染:西班牙全国性监测结果
Am J Transplant. 2007 Nov;7(11):2579-86. doi: 10.1111/j.1600-6143.2007.01964.x. Epub 2007 Sep 14.
7
A competing risks analysis of bloodstream infection after stem-cell transplantation using subdistribution hazards and cause-specific hazards.使用亚分布风险和特定病因风险对干细胞移植后血流感染进行的竞争风险分析。
Stat Med. 2007 Dec 30;26(30):5360-9. doi: 10.1002/sim.3006.
8
Risk factor analysis of blood stream infection and pneumonia in neutropenic patients after peripheral blood stem-cell transplantation.外周血干细胞移植后中性粒细胞减少患者血流感染和肺炎的危险因素分析
Bone Marrow Transplant. 2007 Feb;39(3):173-8. doi: 10.1038/sj.bmt.1705561.
9
Tutorial in biostatistics: competing risks and multi-state models.生物统计学教程:竞争风险与多状态模型
Stat Med. 2007 May 20;26(11):2389-430. doi: 10.1002/sim.2712.
10
Time-to-event analyses for long-term treatments--the APPROVe trial.长期治疗的事件发生时间分析——APPROVe试验。
N Engl J Med. 2006 Jul 13;355(2):113-7. doi: 10.1056/NEJMp068137. Epub 2006 Jun 26.

中性粒细胞减少的患者中,异体与自体干细胞移植相比,血流感染更少。

Initially fewer bloodstream infections for allogeneic vs. autologous stem-cell transplants in neutropenic patients.

机构信息

Freiburg Centre for Data Analysis and Modelling, Freiburg University, Freiburg, Germany.

出版信息

Epidemiol Infect. 2013 Jan;141(1):158-64. doi: 10.1017/S0950268812000283. Epub 2012 Mar 7.

DOI:10.1017/S0950268812000283
PMID:22394546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9170586/
Abstract

Chemotherapy and/or radiotherapy used as conditioning regimens before autologous or allogeneic haematopoietic cell transplantations (HCTs) cause neutropenia, which is the main reason for bloodstream infections. Autologous HCTs are considered to be superior to allogeneic HCTs in terms of infection outcome. A previous analysis suggested that patients with allogeneic HCTs are exposed to a reduced infection hazard and that an unfavourable infection outcome of allogeneic HCTs may be mediated through prolonged neutropenia. Therefore, we investigated whether allogeneic HCTs initially lead to fewer infections. We evaluated data from a prospective non-randomized multi-centre cohort study, with a total of 1616 patients. Of these, 703 patients received autologous and 913 patients received allogeneic HCTs from January 2000 to June 2004. The retrospective analysis used simultaneous confidence bands for the cumulative infection probability in the presence of competing risks. Patients with allogeneic HCTs experienced fewer infections during the early phase of neutropenia. As patients with autologous HCTs are not necessarily subject to antibiotic prophylaxis, a future study should investigate this policy. A limitation of the analysis is that it did not find the effect of crossing cumulative infection probabilities to be significant.

摘要

在自体或异体造血细胞移植(HCT)之前,使用化疗和/或放疗作为预处理方案会导致中性粒细胞减少症,这是血流感染的主要原因。与异体 HCT 相比,自体 HCT 在感染结果方面被认为更具优势。先前的分析表明,异体 HCT 患者的感染风险降低,而异体 HCT 感染结果不佳可能是通过中性粒细胞减少持续时间延长介导的。因此,我们研究了异体 HCT 是否最初会导致更少的感染。我们评估了一项前瞻性非随机多中心队列研究的数据,共纳入 1616 例患者。其中,703 例患者接受自体 HCT,913 例患者在 2000 年 1 月至 2004 年 6 月期间接受异体 HCT。回顾性分析采用同时置信区间来评估存在竞争风险时的累积感染概率。异体 HCT 患者在中性粒细胞减少的早期阶段感染较少。由于自体 HCT 患者不一定需要接受抗生素预防,因此未来的研究应该调查这一政策。该分析的局限性在于它没有发现交叉累积感染概率的效果具有统计学意义。