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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Intravenous colistin use for infections due to MDR Gram-negative bacilli in critically ill paediatric patients: A systematic review and meta-analysis

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Auteur
Karageorgos S.A., Bassiri H., Siakallis G., Miligkos M., Tsioutis C.
Date
2019
Language
en
DOI
10.1093/jac/dkz165
Sujet
colistin
creatinine
antiinfective agent
colistin
Acinetobacter infection
antibiotic therapy
bacterial clearance
child
clinical effectiveness
clinical outcome
colistin resistance
creatinine blood level
critically ill patient
disseminated intravascular clotting
drug safety
Gram negative infection
hematuria
human
loading drug dose
lower respiratory tract infection
meta analysis
mortality
multidrug resistance
nephrotoxicity
neurotoxicity
pediatric intensive care unit
Review
systematic review
tonic clonic seizure
Acinetobacter baumannii
adolescent
critical illness
drug effect
female
Gram negative bacterium
Gram negative infection
intravenous drug administration
male
microbiology
multidrug resistance
preschool child
Acinetobacter baumannii
Acinetobacter Infections
Administration, Intravenous
Adolescent
Anti-Bacterial Agents
Child
Child, Preschool
Colistin
Critical Illness
Drug Resistance, Multiple, Bacterial
Female
Gram-Negative Bacteria
Gram-Negative Bacterial Infections
Humans
Intensive Care Units, Pediatric
Male
Oxford University Press
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Résumé
Background: Data are limited regarding the clinical effectiveness and safety of intravenous colistin for treatment of infections due to MDR Gram-negative bacilli (GNB) in paediatric ICUs (PICUs). Methods: Systematic review of intravenous colistin use in critically ill paediatric patients with MDR-GNB infection in PubMed, Scopus and EMBASE (up to 31 January 2018). Results: Out of 1181 citations, 7 studies were included on the use of intravenous colistin for 405 patients in PICUs. The majority of patients were diagnosed with lower respiratory tract infections, Acinetobacter baumannii being the predominant pathogen. Colistin dosages ranged between 2.6 and 18 mg/kg/day, with only one case reporting a loading dose. Emergence of colistin resistance during treatment was reported in two cases. Nephrotoxicity and neurotoxicity were reported in 6.1% and 0.5%, respectively, but concomitant medications and severe underlying illness limited our ability to definitively associate use of colistin with nephrotoxicity. Crude mortality was 29.5% (95% CI=21.7%-38.1%), whereas infection-related mortality was 16.6% (95% CI=12.2%-21.5%). Conclusions: While the reported incidence of adverse events related to colistin was low, reported mortality rates for infections due to MDR-GNB in PICUs were notable. In addition to severity of disease and comorbidities, inadequate daily dosage and the absence of a loading dose may have contributed to mortality. As the use of colistin for treatment of MDR-GNB infections increases, it is imperative to understand whether optimal dosing of colistin in paediatric patients differs across different age groups. Thus, future studies to establish the pharmacokinetic properties of colistin in different paediatric settings are warranted. © 2019 The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
URI
http://hdl.handle.net/11615/74334
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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