Departments of Pediatrics.
Center for Health and the Social Sciences, University of Chicago, Chicago, IL.
J Pediatr Hematol Oncol. 2022 Mar 1;44(2):e334-e342. doi: 10.1097/MPH.0000000000002242.
Invasive fungal diseases (IFDs) are opportunistic infections that result in significant morbidity and mortality in pediatric oncology patients. Predictive risk tools for IFD in pediatric cancer are not available.
We conducted a 7-year retrospective study of pediatric oncology patients with a diagnosis of febrile neutropenia at UCM Comer Children's Hospitals. Fourteen clinical, laboratory, and treatment-related risk factors for IFD were analyzed. Stepwise variable selection for multiple logistic regression was used to develop a risk prediction model for IFD. Two comparative analyses have been conducted: (i) all suspected IFD cases and (ii) all proven and probable IFD cases.
A total of 667 febrile neutropenia episodes were identified in 265 patients. IFD was diagnosed in 62 episodes: 13 proven, 27 probable, and 22 possible. In the final multiple logistic regression models, 5 variables were independently significant for both analyses: fever days, neutropenia days, hypotension, and absolute lymphocyte count <250 at the time of diagnosis. The odds ratio and a relative weight for each factor were then calculated and summed to calculate a predictive score. A risk score of ≤4 and ≤5 (10/11 maximum) for each model signifies low risk, respectively (<1.2% incidence). Model discrimination was evaluated by the area under the receiver operator characteristics curve with an area under the curve of 0.95/0.94 for each model.
Our prediction IFD risk models perform well, are easy-to-use, and are based on readily available clinical data. Profound lymphopenia absolute lymphocyte count <250 mm3 could serve as a new important prognostic marker for the development of IFD in pediatric cancer and hematopoietic stem cell transplant patients.
侵袭性真菌病(IFD)是机会性感染,可导致儿科肿瘤患者发病率和死亡率显著增加。目前尚无儿科癌症患者 IFD 的预测风险工具。
我们对 UCM Comer 儿童医院患有发热性中性粒细胞减少症的儿科肿瘤患者进行了一项为期 7 年的回顾性研究。分析了 14 个与 IFD 相关的临床、实验室和治疗相关的危险因素。采用逐步变量选择多因素逻辑回归方法建立 IFD 风险预测模型。进行了两项比较分析:(i)所有疑似 IFD 病例和(ii)所有确诊和可能 IFD 病例。
共确定了 265 例患者的 667 例发热性中性粒细胞减少症发作。62 例诊断为 IFD:13 例确诊,27 例可能,22 例可能。在最终的多因素逻辑回归模型中,2 个分析均有 5 个变量独立显著:发热天数、中性粒细胞减少天数、低血压和诊断时绝对淋巴细胞计数<250。然后计算每个因素的比值比和相对权重,并将其相加以计算预测评分。每个模型的预测评分≤4 和≤5(各 11 分中的 10 分)分别表示低风险(<1.2%的发生率)。通过接收者操作特征曲线下面积评估模型的区分度,每个模型的曲线下面积分别为 0.95/0.94。
我们的预测 IFD 风险模型性能良好,易于使用,且基于易于获得的临床数据。绝对淋巴细胞计数<250mm3 的严重淋巴细胞减少症可作为儿科癌症和造血干细胞移植患者发生 IFD 的新的重要预后标志物。