An Updated Systematic Review and Meta-analysis of the Predictive Value of Serum Biomarkers in the Assessment of Fever During Neutropenia in Children With Cancer

被引:39
|
作者
Haeusler, Gabrielle M. [1 ,2 ]
Carlesse, Fabianne [3 ]
Phillips, Robert S. [4 ,5 ]
机构
[1] Royal Childrens Hosp Melbourne, Childrens Canc Ctr, Parkville, Vic, Australia
[2] Peter MacCallum Canc Ctr, Dept Infect Dis & Infect Control, East Melbourne, Australia
[3] Univ Fed Sao Paulo, Dept Pediat, Pediat Oncol Inst IOP GRACC, Sao Paulo, Brazil
[4] Univ York, Alcuin Coll, Ctr Reviews & Disseminat, York YO10 5DD, N Yorkshire, England
[5] Leeds Teaching Hosp Trust, Reg Dept Paediat Haematol Oncol, Leeds, W Yorkshire, England
关键词
febrile neutropenia; child; biomarker; risk; review; C-REACTIVE PROTEIN; CHEMOTHERAPY-INDUCED NEUTROPENIA; PEDIATRIC ONCOLOGY PATIENTS; FEBRILE NEUTROPENIA; SEVERE INFECTION; DIAGNOSTIC-VALUE; YOUNG-PEOPLE; RISK-FACTORS; PROCALCITONIN; INTERLEUKIN-6;
D O I
10.1097/INF.0b013e31829ae38d
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Fever during neutropenia (FN) is a frequent and potentially life-threatening complication of the treatment of childhood cancer. The role of biomarkers in predicting morbidity and mortality associated with FN in children has been explored with varying results. This systematic review identified, critically appraised and synthesized information on the use of biomarkers for the prediction of outcome of FN in children/young adults, updating a review of initial assessment and adding further analysis of their value at reassessment. Methods: This review was conducted in accordance with the Centre for Reviews and Dissemination Methods, using 3 different random effects meta-analysis models. Results: Thirty-seven studies involving over 4689 episodes of FN in children were assessed, including an additional 13 studies investigating 18 biomarkers in 1670 FN episodes since the original review. Meta-analysis was possible for admission C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 and interleukin-8 in their ability to detect significant infection. Marked heterogeneity exists, precluding clear clinical interpretation of the results. Qualitative synthesis of the role of serial biomarkers suggests their predictive ability may be more pronounced at 24 to 48 hours compared with admission. Direct comparisons of the discriminatory power of admission values of PCT and CRP showed PCT generally had a better discriminatory estimate of serious infection than CRP. Conclusions: There remains a paucity of robust and reproducible data on the use of biomarkers in prediction of serious infection in children with FN. Available evidence suggests PCT has better discriminatory ability than CRP and that the role of serial biomarkers warrants further study.
引用
收藏
页码:E390 / E396
页数:7
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