Guideline for the Management of Fever and Neutropenia in Pediatric Patients With Cancer and Hematopoietic Cell Transplantation Recipients: 2023 Update

Author:

Lehrnbecher Thomas1ORCID,Robinson Paula D.2,Ammann Roland A.34ORCID,Fisher Brian5ORCID,Patel Priya26ORCID,Phillips Robert7,Beauchemin Melissa P.8ORCID,Carlesse Fabianne9,Castagnola Elio10ORCID,Davis Bonnie L.11,Elgarten Caitlin W.12ORCID,Groll Andreas H.13ORCID,Haeusler Gabrielle M.141516ORCID,Koenig Christa34ORCID,Santolaya Maria E.17ORCID,Tissing Wim J.E.1819,Wolf Joshua2021ORCID,Alexander Sarah22ORCID,Hu Helen223,Dupuis L. Lee62324ORCID,Sung Lillian2224ORCID

Affiliation:

1. Pediatric Hematology and Oncology, Hospital for Children and Adolescents, Johann Wolfgang Goethe University, Frankfurt, Germany

2. Pediatric Oncology Group of Ontario, Toronto, Canada

3. Division of Pediatric Hematology/Oncology, Department of Pediatrics, Inselspital, Bern University Hospital, Bern, Switzerland

4. Kinderaerzte KurWerk, Burgdorf, Switzerland

5. Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA

6. Department of Pharmacy, The Hospital for Sick Children, Toronto, Canada

7. Department of Haematology and Oncology, Leeds Teaching Hospital, NHS Trust, Leeds, United Kingdom

8. Columbia University/Herbert Irving Cancer Center, Columbia University School of Nursing, New York, NY

9. Pediatric Oncology Institute, GRAACC/Federal University of Sao Paulo, Sao Paulo, Brazil

10. Infectious Diseases Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, Genova, Italy

11. Not applicable (patient representative)

12. Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA

13. Infectious Disease Research Program, Center for Bone Marrow Transplantation, Department of Pediatric Hematology/Oncology, University Children's Hospital, Muenster, Germany

14. Department of Infectious Diseases, Royal Children's Hospital, Melbourne, Australia

15. Department of Infectious Diseases, Peter MacCallum Cancer Center, Melbourne, Australia

16. NHMRC National Center for Infections in Cancer, Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Australia

17. Department of Pediatrics, Hospital Dr Luis Calvo Mackenna, Faculty of Medicine, Universidad de Chile, Santiago, Chile

18. Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands

19. Department of Pediatric Oncology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands

20. Division of Infectious Disease, St Jude Children's Research Hospital, Memphis, TN

21. Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN

22. Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Canada

23. Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada

24. Child Health Evaluative Sciences, Research Institute, The Hospital for Sick Children, Toronto, Canada

Abstract

PURPOSE To update a clinical practice guideline (CPG) for the empiric management of fever and neutropenia (FN) in pediatric patients with cancer and hematopoietic cell transplantation recipients. METHODS The International Pediatric Fever and Neutropenia Guideline Panel reconvened to conduct the second update of this CPG. We updated the previous systematic review to identify new randomized controlled trials (RCTs) evaluating any strategy for the management of FN in pediatric patients. Using the Grading of Recommendations Assessment, Development and Evaluation framework, evidence quality was classified as high, moderate, low, or very low. The panel updated recommendations related to initial management, ongoing management, and empiric antifungal therapy. Changes from the 2017 CPG were articulated, and good practice statements were considered. RESULTS We identified 10 new RCTs in addition to the 69 RCTs identified in previous FN CPGs to inform the 2023 FN CPG. Changes from the 2017 CPG included two conditional recommendations regarding (1) discontinuation of empiric antibacterial therapy in clinically well and afebrile patients with low-risk FN if blood cultures remain negative at 48 hours despite no evidence of marrow recovery and (2) pre-emptive antifungal therapy for invasive fungal disease in high-risk patients not receiving antimold prophylaxis. The panel created a good practice statement to initiate FN CPG-consistent empiric antibacterial therapy as soon as possible in clinically unstable febrile patients. CONCLUSION The updated FN CPG incorporates important modifications on the basis of recently published trials. Future work should focus on addressing knowledge gaps, improving CPG implementation, and measuring the impact of CPG-consistent care.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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