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Impact of Extended and Restricted Antibiotic Deescalation on Mortality

Background: More data are needed about the safety of antibiotic de-escalation in specific clinical situations as a strategy to reduce exposure to broad-spectrum antibiotics. This study aims to compare the survival curve of patient de-escalated (early or late) against those not de-escalated on antibi...

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Autores principales: Teh, Hwei Lin, Abdullah, Sarimah, Ghazali, Anis Kausar, Khan, Rahela Ambaras, Ramadas, Anitha, Leong, Chee Loon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772729/
https://www.ncbi.nlm.nih.gov/pubmed/35052899
http://dx.doi.org/10.3390/antibiotics11010022
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author Teh, Hwei Lin
Abdullah, Sarimah
Ghazali, Anis Kausar
Khan, Rahela Ambaras
Ramadas, Anitha
Leong, Chee Loon
author_facet Teh, Hwei Lin
Abdullah, Sarimah
Ghazali, Anis Kausar
Khan, Rahela Ambaras
Ramadas, Anitha
Leong, Chee Loon
author_sort Teh, Hwei Lin
collection PubMed
description Background: More data are needed about the safety of antibiotic de-escalation in specific clinical situations as a strategy to reduce exposure to broad-spectrum antibiotics. This study aims to compare the survival curve of patient de-escalated (early or late) against those not de-escalated on antibiotics, to determine the association of patient related, clinical related, and pressure sore/device related characteristics on all-cause 30-day mortality and determine the impact of early and late antibiotic de-escalation on 30-day all-cause mortality. Methods: This is a retrospective cohort study on patients in medical ward Hospital Kuala Lumpur, admitted between January 2016 and June 2019. A Kaplan–Meier survival curve and Fleming–Harrington test were used to compare the overall survival rates between early, late, and those not de-escalated on antibiotics while multivariable Cox proportional hazards regression was used to determine prognostic factors associated with mortality and the impact of de-escalation on 30-day all-cause mortality. Results: Overall mortality rates were not significantly different when patients were not de-escalated on extended or restricted antibiotics, compared to those de-escalated early or later (p = 0.760). Variables associated with 30-day all-cause mortality were a Sequential Organ Function Assessment (SOFA) score on the day of antimicrobial stewardship (AMS) intervention and Charlson’s comorbidity score (CCS). After controlling for confounders, early and late antibiotics were not associated with an increased risk of mortality. Conclusion: The results of this study reinforce that restricted or extended antibiotic de-escalation in patients does not significantly affect 30-day all-cause mortality compared to continuation with extended and restricted antibiotics.
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spelling pubmed-87727292022-01-21 Impact of Extended and Restricted Antibiotic Deescalation on Mortality Teh, Hwei Lin Abdullah, Sarimah Ghazali, Anis Kausar Khan, Rahela Ambaras Ramadas, Anitha Leong, Chee Loon Antibiotics (Basel) Article Background: More data are needed about the safety of antibiotic de-escalation in specific clinical situations as a strategy to reduce exposure to broad-spectrum antibiotics. This study aims to compare the survival curve of patient de-escalated (early or late) against those not de-escalated on antibiotics, to determine the association of patient related, clinical related, and pressure sore/device related characteristics on all-cause 30-day mortality and determine the impact of early and late antibiotic de-escalation on 30-day all-cause mortality. Methods: This is a retrospective cohort study on patients in medical ward Hospital Kuala Lumpur, admitted between January 2016 and June 2019. A Kaplan–Meier survival curve and Fleming–Harrington test were used to compare the overall survival rates between early, late, and those not de-escalated on antibiotics while multivariable Cox proportional hazards regression was used to determine prognostic factors associated with mortality and the impact of de-escalation on 30-day all-cause mortality. Results: Overall mortality rates were not significantly different when patients were not de-escalated on extended or restricted antibiotics, compared to those de-escalated early or later (p = 0.760). Variables associated with 30-day all-cause mortality were a Sequential Organ Function Assessment (SOFA) score on the day of antimicrobial stewardship (AMS) intervention and Charlson’s comorbidity score (CCS). After controlling for confounders, early and late antibiotics were not associated with an increased risk of mortality. Conclusion: The results of this study reinforce that restricted or extended antibiotic de-escalation in patients does not significantly affect 30-day all-cause mortality compared to continuation with extended and restricted antibiotics. MDPI 2021-12-27 /pmc/articles/PMC8772729/ /pubmed/35052899 http://dx.doi.org/10.3390/antibiotics11010022 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Teh, Hwei Lin
Abdullah, Sarimah
Ghazali, Anis Kausar
Khan, Rahela Ambaras
Ramadas, Anitha
Leong, Chee Loon
Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title_full Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title_fullStr Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title_full_unstemmed Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title_short Impact of Extended and Restricted Antibiotic Deescalation on Mortality
title_sort impact of extended and restricted antibiotic deescalation on mortality
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772729/
https://www.ncbi.nlm.nih.gov/pubmed/35052899
http://dx.doi.org/10.3390/antibiotics11010022
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