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本文引用的文献

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Prospective validation of a risk prediction model for severe sepsis in children with cancer and high-risk febrile neutropenia.癌症患儿和高危发热性中性粒细胞减少症患儿严重脓毒症风险预测模型的前瞻性验证
Pediatr Infect Dis J. 2013 Dec;32(12):1318-23. doi: 10.1097/01.inf.0000436128.49972.16.
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Antimicrobial prophylaxis and outpatient management of fever and neutropenia in adults treated for malignancy: American Society of Clinical Oncology clinical practice guideline.恶性肿瘤成人患者发热与中性粒细胞减少的抗菌预防和门诊管理:美国临床肿瘤学会临床实践指南。
J Clin Oncol. 2013 Feb 20;31(6):794-810. doi: 10.1200/JCO.2012.45.8661. Epub 2013 Jan 14.
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Prediction of bacteremia in children with febrile episodes during chemotherapy for acute lymphoblastic leukemia.急性淋巴细胞白血病化疗期间发热儿童菌血症的预测
Pediatr Hematol Oncol. 2013 Mar;30(2):131-40. doi: 10.3109/08880018.2012.748111. Epub 2013 Jan 2.
4
Guideline for the management of fever and neutropenia in children with cancer and/or undergoing hematopoietic stem-cell transplantation.儿童癌症患者和/或接受造血干细胞移植后发热与中性粒细胞减少的管理指南。
J Clin Oncol. 2012 Dec 10;30(35):4427-38. doi: 10.1200/JCO.2012.42.7161. Epub 2012 Sep 17.
5
Fluoroquinolones in children with fever and neutropenia: a systematic review of prospective trials.氟喹诺酮类药物在发热伴中性粒细胞减少症儿童中的应用:前瞻性试验的系统评价。
Pediatr Infect Dis J. 2012 May;31(5):431-5. doi: 10.1097/INF.0b013e318245ab48.
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Predicting bacteremia in children with cancer and fever in chemotherapy-induced neutropenia: results of the prospective multicenter SPOG 2003 FN study.在化疗诱导性中性粒细胞减少症伴发热的癌症患儿中预测菌血症:前瞻性多中心 SPOG 2003 FN 研究的结果。
Pediatr Infect Dis J. 2011 Jul;30(7):e114-9. doi: 10.1097/INF.0b013e318215a290.
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Validation of a new risk assessment model for predicting adverse events in children with fever and chemotherapy-induced neutropenia.一种用于预测发热且化疗引起中性粒细胞减少症儿童不良事件的新风险评估模型的验证
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Predicting the risk of severe bacterial infection in children with chemotherapy-induced febrile neutropenia.预测化疗引起的发热性中性粒细胞减少症儿童发生严重细菌感染的风险。
Pediatr Blood Cancer. 2010 Oct;55(4):662-7. doi: 10.1002/pbc.22586.
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Risk prediction in pediatric cancer patients with fever and neutropenia.儿童癌症患者发热伴中性粒细胞减少的风险预测。
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Bacteremia in febrile nonneutropenic pediatric oncology patients.发热性非中性粒细胞减少的儿科肿瘤患者的菌血症
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用于诊断发热性、非中性粒细胞减少性癌症患儿血流感染的预测模型的开发与验证

Development and validation of a prediction model for diagnosing blood stream infections in febrile, non-neutropenic children with cancer.

作者信息

Esbenshade Adam J, Pentima M Cecilia Di, Zhao Zhiguo, Shintani Ayumi, Esbenshade Jennifer C, Simpson Monique E, Montgomery Kathleen C, Lindell Robert B, Lee Haerin, Wallace Ato, Garcia Kelly L, Moons Karel G M, Friedman Debra L

机构信息

Department of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee.

Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.

出版信息

Pediatr Blood Cancer. 2015 Feb;62(2):262-268. doi: 10.1002/pbc.25275. Epub 2014 Oct 18.

DOI:10.1002/pbc.25275
PMID:25327666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4402108/
Abstract

BACKGROUND

Pediatric oncology patients are at increased risk for blood stream infections (BSI). Risk in the absence of severe neutropenia (absolute neutrophil count [ANC] ≥500/µl) is not well defined.

PROCEDURE

In a retrospective cohort of febrile (temperature ≥38.0° for >1 hr or ≥38.3°) pediatric oncology patients with ANC ≥500/µl, a diagnostic prediction model for BSI was constructed using logistic regression modeling and the following candidate predictors: age, ANC, absolute monocyte count, body temperature, inpatient/outpatient presentation, sex, central venous catheter type, hypotension, chills, cancer diagnosis, stem cell transplant, upper respiratory symptoms, and exposure to cytarabine, anti-thymocyte globulin, or anti-GD2 antibody. The model was internally validated with bootstrapping methods.

RESULTS

Among 932 febrile episodes in 463 patients, we identified 91 cases of BSI. Independently significant predictors for BSI were higher body temperature (Odds ratio [OR] 2.36 P < 0.001), tunneled external catheter (OR 13.79 P < 0.001), peripherally inserted central catheter (OR 3.95 P = 0.005), elevated ANC (OR 1.19 P = 0.024), chills (OR 2.09 P = 0.031), and hypotension (OR 3.08 P = 0.004). Acute lymphoblastic leukemia diagnosis (OR 0.34 P = 0.026), increased age (OR 0.70 P = 0.049), and drug exposure (OR 0.08 P < 0.001) were associated with decreased risk for BSI. The risk prediction model had a C-index of 0.898; after bootstrapping adjustment for optimism, corrected C-index 0.885.

CONCLUSIONS

We developed a diagnostic prediction model for BSI in febrile pediatric oncology patients without severe neutropenia. External validation is warranted before use in clinical practice. Pediatr Blood Cancer 2015;62:262-268. © 2014 Wiley Periodicals, Inc.

摘要

背景

儿科肿瘤患者发生血流感染(BSI)的风险增加。在无严重中性粒细胞减少(绝对中性粒细胞计数[ANC]≥500/µl)的情况下,其风险尚不明确。

方法

在一组ANC≥500/µl的发热(体温≥38.0°持续>1小时或≥38.3°)儿科肿瘤患者的回顾性队列研究中,使用逻辑回归模型和以下候选预测因素构建了BSI的诊断预测模型:年龄、ANC、绝对单核细胞计数、体温、住院/门诊情况、性别、中心静脉导管类型、低血压、寒战、癌症诊断、干细胞移植、上呼吸道症状以及接触阿糖胞苷、抗胸腺细胞球蛋白或抗GD2抗体。该模型采用自抽样法进行内部验证。

结果

在463例患者的932次发热发作中,我们确定了91例BSI病例。BSI的独立显著预测因素为体温较高(比值比[OR]2.36,P<0.001)、隧道式外置导管(OR 13.79,P<0.001)、外周静脉穿刺中心静脉导管(OR 3.95,P = 0.005)、ANC升高(OR 1.19,P = 0.024)、寒战(OR 2.09,P = 0.031)和低血压(OR 3.08,P = 0.004)。急性淋巴细胞白血病诊断(OR 0.34,P = 0.026)、年龄增加(OR 0.70,P = 0.049)和药物暴露(OR 0.08,P<0.001)与BSI风险降低相关。风险预测模型的C指数为0.898;经自抽样法校正乐观偏倚后,校正C指数为0.885。

结论

我们为无严重中性粒细胞减少的发热儿科肿瘤患者开发了一种BSI诊断预测模型。在临床实践中使用前需进行外部验证。《儿科血液与癌症》2015年;62:262 - 268。©2014威利期刊公司。