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Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting

BACKGROUND: Colistin use is increasing with the rise in MDR Gram-negative infections globally. Effective antibiotic stewardship is essential to preserve this antibiotic of last resort. OBJECTIVES: This study investigated stewardship and safety errors related to colistin use to identify opportunities...

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Autores principales: Moolla, Muhammad S, Whitelaw, Andrew, Decloedt, Eric H, Koegelenberg, Coenraad F N, Parker, Arifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599735/
https://www.ncbi.nlm.nih.gov/pubmed/34806008
http://dx.doi.org/10.1093/jacamr/dlab169
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author Moolla, Muhammad S
Whitelaw, Andrew
Decloedt, Eric H
Koegelenberg, Coenraad F N
Parker, Arifa
author_facet Moolla, Muhammad S
Whitelaw, Andrew
Decloedt, Eric H
Koegelenberg, Coenraad F N
Parker, Arifa
author_sort Moolla, Muhammad S
collection PubMed
description BACKGROUND: Colistin use is increasing with the rise in MDR Gram-negative infections globally. Effective antibiotic stewardship is essential to preserve this antibiotic of last resort. OBJECTIVES: This study investigated stewardship and safety errors related to colistin use to identify opportunities for improvement. PATIENTS AND METHODS: A prospective descriptive study involving all patients 13 years and older treated with colistin at a tertiary hospital in Cape Town, South Africa, between August 2018 and June 2019. We collected clinical, laboratory and outcome data and assessed provided treatment for stewardship and safety errors. RESULTS: We included 44 patients. Treatment errors were identified for 34 (77%) patients (median = 1), most commonly inadequate monitoring of renal function (N = 16, 32%). We also identified no rational indication for colistin (N = 9, 20%), loading dose error (N = 12, 27%); maintenance dose error (N = 10, 23%); no prior culture (N = 11, 25%); and failure to de-escalate (2 of 9) or adjust dose to changes in renal function (6 of 15). All cause in-hospital mortality was 47%. Amongst survivors, median ICU stay was 6 days and hospital stay more than 30 days. Eight (18%) patients developed renal injury or failure during treatment. Three (7%) patients in this study were found to have colistin-resistant organisms including two prior to colistin exposure. CONCLUSIONS: This study has identified opportunities to enhance colistin stewardship and improve efficacy and safety of prescription. The appearance of colistin-resistant organisms reinforces the urgent need to ensure effective and appropriate use of colistin.
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spelling pubmed-85997352021-11-18 Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting Moolla, Muhammad S Whitelaw, Andrew Decloedt, Eric H Koegelenberg, Coenraad F N Parker, Arifa JAC Antimicrob Resist Original Article BACKGROUND: Colistin use is increasing with the rise in MDR Gram-negative infections globally. Effective antibiotic stewardship is essential to preserve this antibiotic of last resort. OBJECTIVES: This study investigated stewardship and safety errors related to colistin use to identify opportunities for improvement. PATIENTS AND METHODS: A prospective descriptive study involving all patients 13 years and older treated with colistin at a tertiary hospital in Cape Town, South Africa, between August 2018 and June 2019. We collected clinical, laboratory and outcome data and assessed provided treatment for stewardship and safety errors. RESULTS: We included 44 patients. Treatment errors were identified for 34 (77%) patients (median = 1), most commonly inadequate monitoring of renal function (N = 16, 32%). We also identified no rational indication for colistin (N = 9, 20%), loading dose error (N = 12, 27%); maintenance dose error (N = 10, 23%); no prior culture (N = 11, 25%); and failure to de-escalate (2 of 9) or adjust dose to changes in renal function (6 of 15). All cause in-hospital mortality was 47%. Amongst survivors, median ICU stay was 6 days and hospital stay more than 30 days. Eight (18%) patients developed renal injury or failure during treatment. Three (7%) patients in this study were found to have colistin-resistant organisms including two prior to colistin exposure. CONCLUSIONS: This study has identified opportunities to enhance colistin stewardship and improve efficacy and safety of prescription. The appearance of colistin-resistant organisms reinforces the urgent need to ensure effective and appropriate use of colistin. Oxford University Press 2021-11-17 /pmc/articles/PMC8599735/ /pubmed/34806008 http://dx.doi.org/10.1093/jacamr/dlab169 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Moolla, Muhammad S
Whitelaw, Andrew
Decloedt, Eric H
Koegelenberg, Coenraad F N
Parker, Arifa
Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title_full Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title_fullStr Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title_full_unstemmed Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title_short Opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
title_sort opportunities to enhance antibiotic stewardship: colistin use and outcomes in a low-resource setting
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599735/
https://www.ncbi.nlm.nih.gov/pubmed/34806008
http://dx.doi.org/10.1093/jacamr/dlab169
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