Division/Center of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, PR China; The Pediatric Leukemia Diagnostic and Therapeutic Technology Research Center of Zhejiang Province, National Clinical Research Center for Child Health, #57 Zhuganxiang Road, Yan-an Street, Hangzhou 310003, PR China.
Division/Center of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, PR China; The Pediatric Leukemia Diagnostic and Therapeutic Technology Research Center of Zhejiang Province, National Clinical Research Center for Child Health, #57 Zhuganxiang Road, Yan-an Street, Hangzhou 310003, PR China.
Clin Chim Acta. 2022 Dec 1;537:133-139. doi: 10.1016/j.cca.2022.10.008. Epub 2022 Oct 22.
The aim of this study was to evaluate the performance of metagenomic next-generation sequencing (mNGS) in identifying microbiological etiologies in pediatric patients with hematological malignancies undergoing fever of unknown origin (FUO).
A total of 147 children with hematological malignancy suffering febrile diseases without definite microbiological etiologies under conventional tests were enrolled. The clinical record, serum inflammatory biomarkers and mNGS results were analyzed.
At least one microorganism was identified by mNGS in 112 of 147 patients (76.2 %). Two or more types of organisms were detected simultaneously in 35.7 % (40/112) of samples. Of the 112 cases with positive mNGS results, the reported microorganisms were considered as etiologies of fever in 50 (44.6 %) cases. The initial antimicrobial regimens were adjusted according to the mNGS results in 48 cases, with 41 patients' febrile diseases resolved. Totally, 27.9 % (41/147) of patients benefit from mNGS. High IL-6 (>390 pg/mL) level was associated with bacterial infection and could help to interpret the results of mNGS.
mNGS is a novel approach to determine the microbiological etiology of FUO in hematological malignancy patients, which benefits about a quarter of all patients tested. Integration of IL-6 can improve the diagnostic precision of bacterial infection.
本研究旨在评估宏基因组下一代测序(mNGS)在识别接受不明原因发热(FUO)治疗的血液系统恶性肿瘤儿科患者的微生物病因方面的性能。
共纳入 147 例血液系统恶性肿瘤且常规检查未能明确发热病因的患儿。分析了临床记录、血清炎症生物标志物和 mNGS 结果。
mNGS 在 147 例患者中的 112 例(76.2%)中至少鉴定出一种微生物。35.7%(40/112)的样本同时检测到两种或两种以上类型的病原体。在 112 例 mNGS 阳性结果的病例中,报告的微生物被认为是 50 例(44.6%)发热的病因。根据 mNGS 结果调整了 48 例初始抗菌治疗方案,41 例患者发热缓解。总共有 27.9%(41/147)的患者受益于 mNGS。高 IL-6(>390pg/mL)水平与细菌感染有关,有助于解释 mNGS 的结果。
mNGS 是一种确定血液系统恶性肿瘤患者 FUO 微生物病因的新方法,约四分之一的受检患者受益。整合 IL-6 可以提高细菌感染的诊断精度。