Predicting bacterial infections among pediatric cancer patients with febrile neutropenia: External validation of the PICNICC model

医学 发热性中性粒细胞减少症 中性粒细胞减少症 小儿癌症 接收机工作特性 小儿肿瘤学 抗生素管理 置信区间 抗生素 癌症 内科学 重症监护医学 儿科 化疗 抗生素耐药性 微生物学 生物
作者
Rohit P. Ojha,Peter H. Asdahl,Ewout W. Steyerberg,Henrik Schrøeder
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:65 (4) 被引量:12
标识
DOI:10.1002/pbc.26935
摘要

Abstract Introduction The Predicting Infectious Complications in Neutropenic Children and Young People with Cancer (PICNICC) model was recently developed for antibiotic stewardship among pediatric cancer patients, but limited information is available about its clinical usefulness. We aimed to assess the performance of the PICNICC model for predicting microbiologically documented bacterial infections among pediatric cancer patients with febrile neutropenia. Materials and methods We used data for febrile neutropenia episodes at a pediatric cancer center in Aarhus, Denmark between 2000 and 2016. We assessed the area under the receiver operating characteristic curve (AUC), calibration, and clinical usefulness (i.e., net benefit). We also recalibrated the model using statistical updating methods. Results We observed 306 microbiologically documented bacterial infections among 1,892 episodes of febrile neutropenia. The AUC of the model was 0.73 (95% confidence limits [CL]: 0.71–0.75). The calibration intercept (calibration‐in‐the‐large) was −0.69 (95% CL: −0.86 to −0.51) and the slope was 0.77 (95% CL: 0.65–0.89). Modest net benefit was observed at a decision threshold of 5%. Recalibration improved calibration but did not improve net benefit. Conclusions The PICNICC model has potential for reducing unnecessary antibiotic exposure for pediatric cancer patients with febrile neutropenia, but continued validation and refinement is necessary to optimize clinical usefulness.

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