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本文引用的文献

1
MBI-LCBI and CLABSI: more than scrubbing the line.多腔导管相关血流感染和中心静脉导管相关血流感染:不仅仅是擦拭导管。
Bone Marrow Transplant. 2019 Dec;54(12):1932-1939. doi: 10.1038/s41409-019-0489-1. Epub 2019 Feb 26.
2
Bloodstream Infection Due to Vancomycin-resistant Enterococcus Is Associated With Increased Mortality After Hematopoietic Cell Transplantation for Acute Leukemia and Myelodysplastic Syndrome: A Multicenter, Retrospective Cohort Study.血流感染性耐万古霉素肠球菌与急性白血病和骨髓增生异常综合征造血细胞移植后死亡率增加相关:一项多中心回顾性队列研究。
Clin Infect Dis. 2019 Oct 30;69(10):1771-1779. doi: 10.1093/cid/ciz031.
3
Bacterial blood stream infections (BSIs), particularly post-engraftment BSIs, are associated with increased mortality after allogeneic hematopoietic cell transplantation.细菌血流感染(BSI),特别是移植后 BSI,与异基因造血细胞移植后死亡率增加相关。
Bone Marrow Transplant. 2019 Aug;54(8):1254-1265. doi: 10.1038/s41409-018-0401-4. Epub 2018 Dec 13.
4
Effect of Levofloxacin Prophylaxis on Bacteremia in Children With Acute Leukemia or Undergoing Hematopoietic Stem Cell Transplantation: A Randomized Clinical Trial.左氧氟沙星预防急性白血病或造血干细胞移植患儿菌血症的随机临床试验。
JAMA. 2018 Sep 11;320(10):995-1004. doi: 10.1001/jama.2018.12512.
5
Multiple bloodstream infections in pediatric stem cell transplant recipients: A case series.儿童干细胞移植受者的多次血流感染:病例系列。
Pediatr Blood Cancer. 2018 Dec;65(12):e27388. doi: 10.1002/pbc.27388. Epub 2018 Aug 9.
6
Antibiotic Exposure and Reduced Short Chain Fatty Acid Production after Hematopoietic Stem Cell Transplant.造血干细胞移植后抗生素暴露与短链脂肪酸生成减少。
Biol Blood Marrow Transplant. 2018 Dec;24(12):2418-2424. doi: 10.1016/j.bbmt.2018.07.030. Epub 2018 Jul 26.
7
Incidence and risk factors of bacterial and fungal infection during induction chemotherapy for high-risk neuroblastoma.高危神经母细胞瘤诱导化疗期间细菌和真菌感染的发生率及危险因素
Pediatr Hematol Oncol. 2017 Aug;34(5):331-342. doi: 10.1080/08880018.2017.1396386. Epub 2017 Dec 4.
8
A Prospective, Holistic, Multicenter Approach to Tracking and Understanding Bloodstream Infections in Pediatric Hematology-Oncology Patients.一种用于追踪和了解儿科血液肿瘤患者血流感染情况的前瞻性、整体、多中心研究方法。
Infect Control Hosp Epidemiol. 2017 Jun;38(6):690-696. doi: 10.1017/ice.2017.57. Epub 2017 Apr 12.
9
Bacterial bloodstream infections in the allogeneic hematopoietic cell transplant patient: new considerations for a persistent nemesis.异基因造血细胞移植患者的血流细菌感染:持续宿敌的新考虑因素。
Bone Marrow Transplant. 2017 Aug;52(8):1091-1106. doi: 10.1038/bmt.2017.14. Epub 2017 Mar 27.
10
Health care institutional charges associated with ambulatory bloodstream infections in pediatric oncology and stem cell transplant patients.儿科肿瘤学和干细胞移植患者门诊血流感染相关的医疗保健机构费用。
Pediatr Blood Cancer. 2017 Feb;64(2):324-329. doi: 10.1002/pbc.26194. Epub 2016 Aug 24.

住院儿科血液科/肿瘤科和干细胞移植患者血流感染的结局。

Outcomes after bloodstream infection in hospitalized pediatric hematology/oncology and stem cell transplant patients.

机构信息

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

University of Cincinnati College of Medicine, Cincinnati, Ohio.

出版信息

Pediatr Blood Cancer. 2019 Dec;66(12):e27978. doi: 10.1002/pbc.27978. Epub 2019 Sep 5.

DOI:10.1002/pbc.27978
PMID:31486593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11150005/
Abstract

BACKGROUND

Pediatric hematology/oncology (PHO) patients receiving therapy or undergoing hematopoietic stem cell transplantation (HSCT) often require a central line and are at risk for bloodstream infections (BSI). There are limited data describing outcomes of BSI in PHO and HSCT patients.

METHODS

This is a multicenter (n = 17) retrospective analysis of outcomes of patients who developed a BSI. Centers involved participated in a quality improvement collaborative referred to as the Childhood Cancer and Blood Disorder Network within the Children's Hospital Association. The main outcome measures were all-cause mortality at 3, 10, and 30 days after positive culture date; transfer to the intensive care unit (ICU) within 48 hours of positive culture; and central line removal within seven days of the positive blood culture.

RESULTS

Nine hundred fifty-seven BSI were included in the analysis. Three hundred fifty-four BSI (37%) were associated with at least one adverse outcome. All-cause mortality was 1% (n = 9), 3% (n = 26), and 6% (n = 57) at 3, 10, and 30 days after BSI, respectively. In the 165 BSI (17%) associated with admission to the ICU, the median ICU stay was four days (IQR 2-10). Twenty-one percent of all infections (n = 203) were associated with central line removal within seven days of positive blood culture.

CONCLUSIONS

BSI in PHO and HSCT patients are associated with adverse outcomes. These data will assist in defining the impact of BSI in this population and demonstrate the need for quality improvement and research efforts to decrease them.

摘要

背景

接受治疗或接受造血干细胞移植 (HSCT) 的儿科血液学/肿瘤学 (PHO) 患者通常需要中央导管,并存在血流感染 (BSI) 的风险。目前关于 PHO 和 HSCT 患者 BSI 结局的数据有限。

方法

这是一项多中心(n=17)回顾性分析,研究对象为发生 BSI 的患者。参与的中心参与了一个名为儿童癌症和血液疾病网络的质量改进合作,该网络是儿童医院协会的一部分。主要结局指标是阳性培养后 3、10 和 30 天的全因死亡率;阳性培养后 48 小时内转入重症监护病房(ICU);以及阳性血培养后 7 天内拔除中央导管。

结果

共纳入 957 例 BSI。354 例 BSI(37%)与至少 1 个不良结局相关。BSI 后 3、10 和 30 天的全因死亡率分别为 1%(n=9)、3%(n=26)和 6%(n=57)。在 165 例与 ICU 入院相关的 BSI 中,ICU 中位住院时间为 4 天(IQR 2-10)。21%的所有感染(n=203)在阳性血培养后 7 天内拔除中央导管。

结论

PHO 和 HSCT 患者的 BSI 与不良结局相关。这些数据将有助于确定 BSI 在该人群中的影响,并表明需要进行质量改进和研究工作以减少 BSI。