8th European Conference on Infections in Leukaemia: 2020 guidelines for the use of antibiotics in paediatric patients with cancer or post-haematopoietic cell transplantation
- PMID: 33811814
- DOI: 10.1016/S1470-2045(20)30725-7
8th European Conference on Infections in Leukaemia: 2020 guidelines for the use of antibiotics in paediatric patients with cancer or post-haematopoietic cell transplantation
Abstract
Paediatric patients with cancer and those undergoing haematopoietic cell transplantation are at high risk of bacterial infections. The 8th European Conference on Infections in Leukaemia (ECIL-8) convened a Paediatric Group to review the literature and to formulate recommendations for the use of antibiotics according to the European Society of Clinical Microbiology and Infectious Diseases grading system. The evaluation of antibacterial prophylaxis included mortality, bloodstream infection, febrile neutropenia, emergence of resistance, and adverse effects as endpoints. Initial antibacterial therapy and antibiotic de-escalation or discontinuation focused on patients with a clinically stable condition and without previous infection or colonisation by resistant bacteria, and on patients with a clinically unstable condition or with previous infection or colonisation by resistant bacteria. The final considerations and recommendations of the ECIL-8 Paediatric Group on antibacterial prophylaxis, initial therapy, and de-escalation strategies are summarised in this Policy Review.
Copyright © 2021 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests TL reports unrestricted research support from Gilead Sciences; is a consultant for Gilead Sciences, Merck Sharp and Dohme, Pfizer, Astellas, and Roche; and serves at the speakers' bureau of Gilead Sciences, Merck Sharp and Dohme, Astellas, Pfizer, and GlaxoSmithKline. DA reports research support from Merck Sharp and Dohme; was a consultant for Pfizer; and served at the speakers' bureau of GlaxoSmithKline. EC is a consultant for Angelini and Ferrer. CG-V reports research grants from Gilead Sciences and Merck Sharp and Dohme; research grants from the Spanish Ministerio de Sanidad, Consumo y Bienestar Social, the Instituto de Salud Carlos III in Madrid, Spain, the European Regional Development Fund, and the European Institute of Innovation and Technology; and served at the speakers' bureau of Gilead Sciences, Merck Sharp and Dohme, Novartis, Pfizer, Janssen, and Lilly. JK is a consultant for Bayer. FL served at the speakers' bureau of Gilead Sciences and Basilea. MM is a consultant for and served at the speakers' bureau of Pfizer, Gilead Sciences, Merck Sharp and Dohme, Janssen, and Biotest. MS reports research support from Gilead Sciences, Merck Sharp and Dohme, and F2G; and served on the speakers' bureau of Merck Sharp and Dohme and Gilead Sciences. JS reports support from Gilead Sciences, Merck Sharp and Dohme, Astellas, Roche, Jazz Pharmaceuticals, and Pfizer; is a consultant for Gilead Sciences, Novartis, Pfizer, Merck Sharp and Dohme; and served at the speakers' bureau of Gilead Sciences, Merck Sharp and Dohme, Fresenius, and Astellas. AW is supported by the MRC Centre for Medical Mycology at the University of Exeter (grant MR/N006364/2); reports research support from Gilead Sciences; and served at the speakers' bureau of Gilead Sciences. AHG reports research support from Gilead Sciences, Merck Sharp and Dohme, and Pfizer; is a consultant for Amplyx, Astellas, Basilea, F2G, Gilead Sciences, Merck Sharp and Dohme, and Pfizer; and served at the speakers' bureau of Astellas, Basilea, F2G, Gilead Sciences, Merck Sharp and Dohme, and Pfizer. All other authors declare no competing interests.
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