Life-threatening infections during treatment for acute lymphoblastic leukemia on the Malaysia-Singapore 2003 and 2010 clinical trials: A risk prediction model

被引:1
|
作者
Oh, Bernice L. Z. [1 ,2 ]
Fan, Lijia [3 ,4 ]
Lee, Shawn H. R. [1 ,2 ]
Foo, Koon Mian [5 ]
Chiew, Kean Hui [1 ,2 ]
Seeto, Zelia Z. L. [2 ]
Chen, Zhi Wei [1 ,2 ]
Neoh, Cheryl C. C. [1 ]
Liew, Germaine S. M. [5 ]
Eng, Jing Jia [5 ]
Lam, Joyce C. M. [5 ]
Thuan Chong Quah [1 ,2 ]
Tan, Ah Moy [5 ]
Chan, Yiong Huak [6 ]
Yeoh, Allen E. J. [1 ,2 ]
机构
[1] Natl Univ Hlth Syst, Natl Univ Hosp, Khoo Teck Puat Natl Univ Childrens Med Inst, Viva Univ Childrens Canc Ctr, Singapore, Singapore
[2] Natl Univ Singapore, Dept Paediat, Yong Loo Lin Sch Med, Singapore, Singapore
[3] Natl Univ Singapore Hosp, Khoo Teck Puat Natl Univ Childrens Med Inst, Div Crit Care, Singapore, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore, Singapore
[5] KK Womens & Childrens Hosp, Dept Paediat Subspecialties Haematol Oncol Serv, Singapore, Singapore
[6] Natl Univ Singapore, Yong Loo Lin Sch Med, Bios Tatist Unit, Singapore, Singapore
基金
英国医学研究理事会;
关键词
acute lymphoblastic leukemia; children; intensive care; risk score; sepsis; CANCER-PATIENTS; ADVERSE EVENTS; GUT-ORIGIN; CHILDREN; SEPSIS; NEUTROPENIA; FEBRILE; FEVER;
D O I
10.1111/ajco.13756
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim Life-threatening infections significantly impact the care of children undergoing therapy for acute lymphoblastic leukemia (ALL) who are at risk of severe sepsis due to both host and treatment factors. Our aim was to develop a life-threatening infection risk prediction model that would allow remote rapid triage of patients to reduce time to first dose of antibiotics and sepsis-related mortality. Methods A retrospective analysis of 2068 fever episodes during ALL therapy was used for model building and subsequent internal validation. Results Three hundred and seventy-seven patients were treated for ALL in two institutions with comparable critical and supportive care resources. A total of 55 patients accounted for 71 admissions to the critical care unit for sepsis that led to eight septic deaths during a 16-year study period. A retrospective analysis of risk factors for sepsis enabled us to build a model focused on 13 variables that discriminated admissions requiring critical care well: area under the receiver operating characteristic curve of .82; 95% CI .76-.87, p<.001, and Brier score of .033. Significant univariate predictors included neutropenia, presence of symptoms of abdominal pain, diarrhea, fever during induction or steroid-based phases, and the lack of any localizing source of infection at time of presentation. Conclusion We have developed a risk prediction model that can reliably identify ALL patients undergoing treatment who are at a higher risk of life-threatening sepsis. Clinical applicability can potentially be extended to low-middle income settings, and its utility should be further studied in real-world settings.
引用
收藏
页码:E456 / E468
页数:13
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