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Low self-reported penicillin allergy in South Africa—implications for global public health response

OBJECTIVES: In high-income countries, up to 25% of inpatients have a self-reported penicillin allergy (PA). After testing, 95% of these self-reported PAs are incorrect. These incorrectly labelled PAs increase the use of broad-spectrum antibiotics, and drive bacterial resistance. The epidemiology of...

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Autores principales: Day, Cascia, Mendelson, Marc, Peter, Jonny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942546/
https://www.ncbi.nlm.nih.gov/pubmed/36824225
http://dx.doi.org/10.1093/jacamr/dlad015
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author Day, Cascia
Mendelson, Marc
Peter, Jonny
author_facet Day, Cascia
Mendelson, Marc
Peter, Jonny
author_sort Day, Cascia
collection PubMed
description OBJECTIVES: In high-income countries, up to 25% of inpatients have a self-reported penicillin allergy (PA). After testing, 95% of these self-reported PAs are incorrect. These incorrectly labelled PAs increase the use of broad-spectrum antibiotics, and drive bacterial resistance. The epidemiology of PA in low- and middle-income countries is unknown. We aimed to describe the epidemiology and delabelling outcomes of self-reported PA in South African (SA) inpatients. METHODS: We conducted point prevalence surveys between April 2019 and June 2021 at seven hospitals in Cape Town, South Africa. A team trained in the PEN-FAST allergy decision tool conducted in-person interviews, and reviewed patient notes to identify and risk stratify inpatients with a self-reported PA. These patients were referred to the Groote Schuur Hospital (GSH) allergy clinic for delabelling. RESULTS: A total of 1486 hospital inpatients were surveyed and 3.2% (n = 48) carried a PA label. Importantly, 64.6% (n = 31) were classified by PEN-FAST as low risk for true penicillin hypersensitivity. Overall, 25% of the self-reported PAs received a β-lactam antibiotic in hospital and were directly delabelled. Delabelling attrition was very high, with 6.3% (3/48) of the self-reported PAs attending the GSH allergy clinic, and only one patient proceeding to a negative oral penicillin challenge. CONCLUSIONS: Inpatient self-reported PA was lower in South Africa hospitals compared with other upper-middle-income countries, and the majority of patients carried a low-risk PA label. Linkage for delabelling with the allergy clinic was very poor, and thus strategies to improve access and delivery of delabelling remains an urgent public health issue.
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spelling pubmed-99425462023-02-22 Low self-reported penicillin allergy in South Africa—implications for global public health response Day, Cascia Mendelson, Marc Peter, Jonny JAC Antimicrob Resist Original Article OBJECTIVES: In high-income countries, up to 25% of inpatients have a self-reported penicillin allergy (PA). After testing, 95% of these self-reported PAs are incorrect. These incorrectly labelled PAs increase the use of broad-spectrum antibiotics, and drive bacterial resistance. The epidemiology of PA in low- and middle-income countries is unknown. We aimed to describe the epidemiology and delabelling outcomes of self-reported PA in South African (SA) inpatients. METHODS: We conducted point prevalence surveys between April 2019 and June 2021 at seven hospitals in Cape Town, South Africa. A team trained in the PEN-FAST allergy decision tool conducted in-person interviews, and reviewed patient notes to identify and risk stratify inpatients with a self-reported PA. These patients were referred to the Groote Schuur Hospital (GSH) allergy clinic for delabelling. RESULTS: A total of 1486 hospital inpatients were surveyed and 3.2% (n = 48) carried a PA label. Importantly, 64.6% (n = 31) were classified by PEN-FAST as low risk for true penicillin hypersensitivity. Overall, 25% of the self-reported PAs received a β-lactam antibiotic in hospital and were directly delabelled. Delabelling attrition was very high, with 6.3% (3/48) of the self-reported PAs attending the GSH allergy clinic, and only one patient proceeding to a negative oral penicillin challenge. CONCLUSIONS: Inpatient self-reported PA was lower in South Africa hospitals compared with other upper-middle-income countries, and the majority of patients carried a low-risk PA label. Linkage for delabelling with the allergy clinic was very poor, and thus strategies to improve access and delivery of delabelling remains an urgent public health issue. Oxford University Press 2023-02-21 /pmc/articles/PMC9942546/ /pubmed/36824225 http://dx.doi.org/10.1093/jacamr/dlad015 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Day, Cascia
Mendelson, Marc
Peter, Jonny
Low self-reported penicillin allergy in South Africa—implications for global public health response
title Low self-reported penicillin allergy in South Africa—implications for global public health response
title_full Low self-reported penicillin allergy in South Africa—implications for global public health response
title_fullStr Low self-reported penicillin allergy in South Africa—implications for global public health response
title_full_unstemmed Low self-reported penicillin allergy in South Africa—implications for global public health response
title_short Low self-reported penicillin allergy in South Africa—implications for global public health response
title_sort low self-reported penicillin allergy in south africa—implications for global public health response
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942546/
https://www.ncbi.nlm.nih.gov/pubmed/36824225
http://dx.doi.org/10.1093/jacamr/dlad015
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