Volume 69, Issue 12 e29931
PSYCHOSOCIAL AND SUPPORTIVE CARE: RESEARCH ARTICLE

Non-neutropenic fever in children with cancer: Management, outcomes and clinical decision rule validation

Hannah Walker

Corresponding Author

Hannah Walker

The Children's Cancer Centre, The Royal Children's Hospital Parkville, Parkville, Victoria, Australia

Correspondence

Hannah Walker, Children's Cancer Centre, The Royal Children's Hospital, 50 Flemington Rd, Parkville, VIC 3052, Australia.

Email: [email protected]

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Adam J. Esbenshade

Adam J. Esbenshade

Department of Pediatrics, Vanderbilt University Medical Centre, Nashville, Tennessee, USA

Vanderbilt Ingram Cancer Centre, Nashville, Tennessee, USA

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Stephanie Dale

Stephanie Dale

The Children's Cancer Centre, The Royal Children's Hospital Parkville, Parkville, Victoria, Australia

The Children's Cancer Centre, Monash Children's Hospital, Clayton, Victoria, Australia

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Kanika Bhatia

Kanika Bhatia

The Children's Cancer Centre, The Royal Children's Hospital Parkville, Parkville, Victoria, Australia

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Zhiguo Zhao

Zhiguo Zhao

Vanderbilt Ingram Cancer Centre, Nashville, Tennessee, USA

Department of Biostatistics, Vanderbilt University Medical Centre, Nashville, Tennessee, USA

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Franz E. Babl

Franz E. Babl

Emergency Department, The Royal Children's Hospital Parkville, Parkville, Victoria, Australia

Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australia

Department of Paediatrics and Critical Care, University of Melbourne, Parkville, Victoria, Australia

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Rachel Conyers

Rachel Conyers

The Children's Cancer Centre, The Royal Children's Hospital Parkville, Parkville, Victoria, Australia

Department of Paediatrics and Critical Care, University of Melbourne, Parkville, Victoria, Australia

Cardiac Regeneration, Murdoch Children's Research Institute, Parkville, Victoria, Australia

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Gabrielle M. Haeusler

Gabrielle M. Haeusler

Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australia

Department of Paediatrics and Critical Care, University of Melbourne, Parkville, Victoria, Australia

The Paediatric Integrated Cancer Service, Parkville, Victoria, Australia

Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

Department of Infectious Diseases, Royal Children's Hospital, Parkville, Victoria, Australia

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First published: 28 August 2022
Citations: 1

Abstract

Introduction

Fever and infection are an important complication of childhood cancer therapy. Most research and guideline development has focussed on febrile neutropenia, with a paucity directed at non-neutropenic fever (NNF). We describe the clinical presentation, management and outcomes of NNF in children with cancer, and externally validate the Esbenshade Vanderbilt (EsVan) clinical decision rules (CDR) to predict bacteraemia.

Method

Using a prospective database, retrospective data were collected on consecutive NNF episodes (fever ≥38.0°C and absolute neutrophil count >1.0 cells/mm3). Sensitivity, specificity and area under the receiver operator characteristic curve (AUC-ROC) of the CDR were compared to derivation study.

Results

There were 203 NNF episodes occurring in 125 patients. Severe sepsis was uncommon (n = 2, 1%) and bacteraemia occurred in 10 (4.9%, 95% confidence interval [CI]: 2.7%–8.8%) episodes. A confirmed or presumed bacterial infection requiring antibiotics occurred in 31 (15%) patients. Total 202 (99%) episodes received at least one dose of intravenous broad-spectrum antibiotic and 141 (70%) episodes were admitted to hospital. Six (3%) episodes required intensive care unit (ICU)-level care and there were no infection-related deaths. The EsVan 1 rule had an AUC-ROC of 0.67, 80% were identified as low risk, and sensitivity and specificity were 50% and 81.5%, respectively, for a risk threshold of 10%.

Conclusions

Serious infection and adverse outcome are uncommon in children with NNF. Many children did not have a bacterial cause of infection identified, but were still treated with broad-spectrum antibiotics and admitted to hospital. National clinical practice guidelines should be developed for this important cohort to enable risk stratification and optimise antibiotic management. Further research is required to determine appropriateness of EsVan CDR in our cohort.

CONFLICT OF INTEREST

The authors have no conflicts of interest to declare.

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