首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Defining incidence, risk factors, and impact on survival of central line-associated blood stream infections following hematopoietic cell transplantation in acute myeloid leukemia and myelodysplastic syndrome
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Defining incidence, risk factors, and impact on survival of central line-associated blood stream infections following hematopoietic cell transplantation in acute myeloid leukemia and myelodysplastic syndrome

机译:定义急性髓细胞白血病和骨髓增生异常综合症造血细胞移植后中枢相关血流感染的发生率,危险因素及其对存活率的影响

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Central line-associated blood stream infections (CLABSI) commonly complicate the care of patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) after allogeneic stem cell transplantation (HCT). We developed a modified CLABSI (MCLABSI) definition that attempts to exclude pathogens usually acquired because of disruption of mucosal barriers during the vulnerable neutropenic period following HCT that are generally included under the original definition (OCLABSI). We conducted a retrospective study of all AML and MDS patients undergoing HCT between August 2009 and December 2011 at the Cleveland Clinic (N = 73), identifying both OCLABSI and MCLABSI incidence. The median age at transplantation was 52 years (range, 16 to 70); 34 had a high (≥3) HCT comorbidity index (HCT-CI); 34 received bone marrow (BM), 24 received peripheral stem cells (PSC), and 15 received umbilical cord blood cells (UCB). Among these 73 patients, 23 (31.5%) developed OCLABSI, of whom 16 (69.6%) died, and 8 (11%) developed MCLABSI, of whom 7 (87.5%) died. OCLABSI was diagnosed a median of 9 days from HCT: 5 days (range, 2 to 12) for UCB and 78 days (range, 7 to 211) for BM/PSC (P .001). MCLABSI occurred a median of 12 days from HCT, with similar earlier UCB and later BM/PSC diagnosis (P = .030). Risk factors for OCLABSI in univariate analysis included CBC (P .001), human leukocyte antigen (HLA)-mismatch (P = .005), low CD34+ count (P = .007), low total nucleated cell dose (P = .016), and non-Caucasian race (P = .017). Risk factors for OCLABSI in multivariable analysis were UCB (P .001) and high HCT-CI (P = .002). There was a significant increase in mortality for both OCLABSI (hazard ratio, 7.14; CI, 3.31 to 15.37; P .001) and MCLABSI (hazard ratio, 6.44; CI, 2.28 to 18.18; P .001). CLABSI is common and associated with high mortality in AML and MDS patients undergoing HCT, especially in UCB recipients and those with high HCT-CI. We propose the MCLABSI definition to replace the OCLABSI definition, given its greater precision for identifying preventable infection in HCT patients.
机译:异基因干细胞移植(HCT)后,与中枢线相关的血流感染(CLABSI)通常会使急性髓细胞性白血病(AML)和骨髓增生异常综合症(MDS)患者的护理复杂化。我们制定了修改后的CLABSI(MCLABSI)定义,试图排除通常在原始定义(OCLABSI)下包括的因HCT后易感性中性粒细胞减少期间粘膜屏障破坏而通常获得的病原体。我们对2009年8月至2011年12月在克利夫兰诊所(N = 73)接受HCT的所有AML和MDS患者进行了回顾性研究,确定了OCLABSI和MCLABSI的发病率。移植时的中位年龄为52岁(范围为16到70)。 34岁的HCT合并症指数(HCT-CI)高(≥3); 34例接受骨髓(BM),24例接受外周干细胞(PSC),而15例接受脐血细胞(UCB)。在这73名患者中,有23名(31.5%)患OCLABSI,其中16名(69.6%)死亡,8名(11%)患有MCLABSI,其中7名(87.5%)死亡。 OCLABSI被诊断出距HCT为9天的中位数:UCB为5天(范围为2至12),而BM / PSC为78天(范围为7至211)(P <.001)。 MCLABSI从HCT开始发生的中位数为12天,早期UCB和晚期BM / PSC诊断相似(P = .030)。单因素分析中OCLABSI的危险因素包括CBC(P <.001),人白细胞抗原(HLA)不匹配(P = .005),CD34 +计数低(P = .007),总核细胞剂量低(P =。 016)和非高加索人种(P = .017)。多变量分析中OCLABSI的危险因素是UCB(P <.001)和高HCT-CI(P = .002)。 OCLABSI(危险比,7.14; CI,3.31至15.37; P <0.001)和MCLABSI(危险比,6.44; CI,2.28至18.18; P <.001)的死亡率均显着增加。在接受HCT的AML和MDS患者中,尤其是在UCB接受者和HCT-CI高的患者中,CLABSI很常见并与高死亡率相关。考虑到HCT患者识别可预防感染的准确性更高,我们建议用MCLABSI定义代替OCLABSI定义。

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