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The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients

Purpose: Antimicrobial resistant infections are common in patients on haemodialysis, often needing long courses of carbapenems. This results in a longer hospital stay and risk of iatrogenic complications. However, carbapenems can be given intermittently to allow for earlier discharge. We aim to desc...

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Autores principales: Ho, Vanda, Tay, Felecia, Wu, Jia En, Lum, Lionel, Tambyah, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696023/
https://www.ncbi.nlm.nih.gov/pubmed/33207584
http://dx.doi.org/10.3390/antibiotics9110815
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author Ho, Vanda
Tay, Felecia
Wu, Jia En
Lum, Lionel
Tambyah, Paul
author_facet Ho, Vanda
Tay, Felecia
Wu, Jia En
Lum, Lionel
Tambyah, Paul
author_sort Ho, Vanda
collection PubMed
description Purpose: Antimicrobial resistant infections are common in patients on haemodialysis, often needing long courses of carbapenems. This results in a longer hospital stay and risk of iatrogenic complications. However, carbapenems can be given intermittently to allow for earlier discharge. We aim to describe the clinical outcomes of intermittent versus daily meropenem in stable, intermittently haemodialysed patients. Methods: In total, 103 records were examined retrospectively. Data collected include demographics, clinical interventions and outcomes such as hospital length of stay (LOS), 30-day readmission rates and adverse events. Findings: Mean age 61.6 ± 14.2 years, 57.3% male. Most common bacteria cultured were Klebsiella pneumoniae (16.5%). The most common indication was pneumonia (27.2%). Mean duration of therapy on meropenem was 12.4 ± 14.4 days; eight patients needed more than 30 days of meropenem. In total, 55.3% did not have intervention for source control; 86.4% received daily dosing of meropenem; 7.8% patients received intermittent dosing of meropenem only, and 5.8 patients received both types of dosing regimens. LOS of the index admission was shorter for the intermittent arm (15.5 ± 7.6 days versus daily: 30.2 ± 24.5 days), though 30-day readmission was higher (50% versus daily: 38.2%). Implications: We recommend further rigorous randomised controlled trials to investigate the clinical utility of intermittent meropenem dosing in patients on stable haemodialysis.
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spelling pubmed-76960232020-11-29 The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients Ho, Vanda Tay, Felecia Wu, Jia En Lum, Lionel Tambyah, Paul Antibiotics (Basel) Brief Report Purpose: Antimicrobial resistant infections are common in patients on haemodialysis, often needing long courses of carbapenems. This results in a longer hospital stay and risk of iatrogenic complications. However, carbapenems can be given intermittently to allow for earlier discharge. We aim to describe the clinical outcomes of intermittent versus daily meropenem in stable, intermittently haemodialysed patients. Methods: In total, 103 records were examined retrospectively. Data collected include demographics, clinical interventions and outcomes such as hospital length of stay (LOS), 30-day readmission rates and adverse events. Findings: Mean age 61.6 ± 14.2 years, 57.3% male. Most common bacteria cultured were Klebsiella pneumoniae (16.5%). The most common indication was pneumonia (27.2%). Mean duration of therapy on meropenem was 12.4 ± 14.4 days; eight patients needed more than 30 days of meropenem. In total, 55.3% did not have intervention for source control; 86.4% received daily dosing of meropenem; 7.8% patients received intermittent dosing of meropenem only, and 5.8 patients received both types of dosing regimens. LOS of the index admission was shorter for the intermittent arm (15.5 ± 7.6 days versus daily: 30.2 ± 24.5 days), though 30-day readmission was higher (50% versus daily: 38.2%). Implications: We recommend further rigorous randomised controlled trials to investigate the clinical utility of intermittent meropenem dosing in patients on stable haemodialysis. MDPI 2020-11-16 /pmc/articles/PMC7696023/ /pubmed/33207584 http://dx.doi.org/10.3390/antibiotics9110815 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Ho, Vanda
Tay, Felecia
Wu, Jia En
Lum, Lionel
Tambyah, Paul
The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title_full The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title_fullStr The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title_full_unstemmed The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title_short The Case for Intermittent Carbapenem Dosing in Stable Haemodialysis Patients
title_sort case for intermittent carbapenem dosing in stable haemodialysis patients
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696023/
https://www.ncbi.nlm.nih.gov/pubmed/33207584
http://dx.doi.org/10.3390/antibiotics9110815
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