Cargando…

Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis

BACKGROUND: Diabetic Foot Infection (DFI) guidelines recommend empiric methicillin-resistant Staphylococcus aureus (MRSA)-targeted therapy in settings where there is high prevalence of MRSA infections or in cases of severe infection; however, they do not provide recommendations for de-escalation. Th...

Descripción completa

Detalles Bibliográficos
Autores principales: Harb, Gaielle, Hopkins, Teri, Yang, Linda, Morneau, Kathleen, Cadena-Zuluaga, Jose, Walter, Elizabeth, Frei, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163799/
https://www.ncbi.nlm.nih.gov/pubmed/37147579
http://dx.doi.org/10.1186/s12879-023-08248-2
_version_ 1785037959115833344
author Harb, Gaielle
Hopkins, Teri
Yang, Linda
Morneau, Kathleen
Cadena-Zuluaga, Jose
Walter, Elizabeth
Frei, Christopher
author_facet Harb, Gaielle
Hopkins, Teri
Yang, Linda
Morneau, Kathleen
Cadena-Zuluaga, Jose
Walter, Elizabeth
Frei, Christopher
author_sort Harb, Gaielle
collection PubMed
description BACKGROUND: Diabetic Foot Infection (DFI) guidelines recommend empiric methicillin-resistant Staphylococcus aureus (MRSA)-targeted therapy in settings where there is high prevalence of MRSA infections or in cases of severe infection; however, they do not provide recommendations for de-escalation. This approach has the potential to increase unnecessary use of broad-spectrum antibiotics; therefore, additional strategies are needed to optimize appropriate antibiotic use. This study evaluates the effect of MRSA nasal PCR testing on MRSA-targeted antibiotic use and clinical outcomes in patients with DFI. METHODS: This was a retrospective quasi-experimental study of patients admitted to South Texas Veterans Health Care System for DFI, with or without osteomyelitis (OM), who had an MRSA nasal PCR and culture data. Eligible patients were identified from the Corporate Data Warehouse and reviewed via electronic health record. Patients were allocated into two groups: PRE (5/1/2019-4/30/2020) and POST (12/1/2020-11/30/2021) protocol implementation for de-escalation or avoidance of MRSA-targeted antibiotics. The primary outcome was median (interquartile range [IQR]) hours of empiric inpatient MRSA-targeted antibiotic therapy. A Wilcoxon Rank Sum test was used to assess the difference between the groups for the primary outcome. Secondary outcomes included the proportion of patients needing MRSA coverage added back for MRSA after de-escalation, hospital readmission, length of hospital stay (LOS), patient mortality, and acute kidney injury. RESULTS: A total of 151 patients were included (83 PRE; 68 POST). Most patients were male (98% PRE; 97% POST) with a median age of 64 (IQR, 56–72) years. Incidence of MRSA in DFI in the cohort was 14.7% overall (12% PRE and 17.6% POST). MRSA was detected via nasal PCR in 12% of patients 15.7% PRE and 7.4% POST). After protocol implementation, there was a significant decrease in empiric MRSA-targeted antibiotic therapy use, from a median of 72 (IQR, 27–120) hours in the PRE group, to 24 (IQR, 12–72) hours in the POST group (p < 0.01). No significant differences were found for other secondary outcomes. CONCLUSION: This study of patients presenting to a Veterans Affairs (VA) hospital with DFI identified a statistically significant decrease in median duration of MRSA-targeted antibiotic use post-protocol implementation. This suggests a favorable effect of MRSA nasal PCR for de-escalation or avoidance of MRSA-targeted antibiotics in DFI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08248-2.
format Online
Article
Text
id pubmed-10163799
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-101637992023-05-07 Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis Harb, Gaielle Hopkins, Teri Yang, Linda Morneau, Kathleen Cadena-Zuluaga, Jose Walter, Elizabeth Frei, Christopher BMC Infect Dis Research BACKGROUND: Diabetic Foot Infection (DFI) guidelines recommend empiric methicillin-resistant Staphylococcus aureus (MRSA)-targeted therapy in settings where there is high prevalence of MRSA infections or in cases of severe infection; however, they do not provide recommendations for de-escalation. This approach has the potential to increase unnecessary use of broad-spectrum antibiotics; therefore, additional strategies are needed to optimize appropriate antibiotic use. This study evaluates the effect of MRSA nasal PCR testing on MRSA-targeted antibiotic use and clinical outcomes in patients with DFI. METHODS: This was a retrospective quasi-experimental study of patients admitted to South Texas Veterans Health Care System for DFI, with or without osteomyelitis (OM), who had an MRSA nasal PCR and culture data. Eligible patients were identified from the Corporate Data Warehouse and reviewed via electronic health record. Patients were allocated into two groups: PRE (5/1/2019-4/30/2020) and POST (12/1/2020-11/30/2021) protocol implementation for de-escalation or avoidance of MRSA-targeted antibiotics. The primary outcome was median (interquartile range [IQR]) hours of empiric inpatient MRSA-targeted antibiotic therapy. A Wilcoxon Rank Sum test was used to assess the difference between the groups for the primary outcome. Secondary outcomes included the proportion of patients needing MRSA coverage added back for MRSA after de-escalation, hospital readmission, length of hospital stay (LOS), patient mortality, and acute kidney injury. RESULTS: A total of 151 patients were included (83 PRE; 68 POST). Most patients were male (98% PRE; 97% POST) with a median age of 64 (IQR, 56–72) years. Incidence of MRSA in DFI in the cohort was 14.7% overall (12% PRE and 17.6% POST). MRSA was detected via nasal PCR in 12% of patients 15.7% PRE and 7.4% POST). After protocol implementation, there was a significant decrease in empiric MRSA-targeted antibiotic therapy use, from a median of 72 (IQR, 27–120) hours in the PRE group, to 24 (IQR, 12–72) hours in the POST group (p < 0.01). No significant differences were found for other secondary outcomes. CONCLUSION: This study of patients presenting to a Veterans Affairs (VA) hospital with DFI identified a statistically significant decrease in median duration of MRSA-targeted antibiotic use post-protocol implementation. This suggests a favorable effect of MRSA nasal PCR for de-escalation or avoidance of MRSA-targeted antibiotics in DFI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08248-2. BioMed Central 2023-05-05 /pmc/articles/PMC10163799/ /pubmed/37147579 http://dx.doi.org/10.1186/s12879-023-08248-2 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Harb, Gaielle
Hopkins, Teri
Yang, Linda
Morneau, Kathleen
Cadena-Zuluaga, Jose
Walter, Elizabeth
Frei, Christopher
Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title_full Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title_fullStr Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title_full_unstemmed Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title_short Clinical utility of methicillin-resistant Staphylococcus aureus nasal PCR to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
title_sort clinical utility of methicillin-resistant staphylococcus aureus nasal pcr to streamline antimicrobial use in treatment of diabetic foot infection with or without osteomyelitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163799/
https://www.ncbi.nlm.nih.gov/pubmed/37147579
http://dx.doi.org/10.1186/s12879-023-08248-2
work_keys_str_mv AT harbgaielle clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT hopkinsteri clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT yanglinda clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT morneaukathleen clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT cadenazuluagajose clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT walterelizabeth clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis
AT freichristopher clinicalutilityofmethicillinresistantstaphylococcusaureusnasalpcrtostreamlineantimicrobialuseintreatmentofdiabeticfootinfectionwithorwithoutosteomyelitis