Cited 0 times in
Clinical outcome of ampicillin or ampicillin/sulbactam versus glycopeptides in ampicillin-susceptible Enterococcus faecalis/faecium bacteremia: a 10-year retrospective cohort study
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seong, YJ | - |
dc.contributor.author | Song, JE | - |
dc.contributor.author | Lee, E | - |
dc.contributor.author | Kim, EJ | - |
dc.contributor.author | Heo, JY | - |
dc.contributor.author | Choi, YH | - |
dc.contributor.author | Kim, YC | - |
dc.date.accessioned | 2024-10-11T07:49:47Z | - |
dc.date.available | 2024-10-11T07:49:47Z | - |
dc.date.issued | 2024 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/32908 | - |
dc.description.abstract | Background: Glycopeptides for ampicillin-susceptible Enterococcus faecalis/faecium bacteremia are readily prescribed depending on the severity of the condition. However, there is limited data on the outcomes of glycopeptide use compared to ampicillin-containing regimens for ampicillin-susceptible E. faecalis/faecium bacteremia. From an antibiotic stewardship perspective, it is important to determine whether the use of glycopeptides is associated with improved clinical outcomes in patients with ampicillin-susceptible E. faecalis/faecium bacteremia. Methods: This retrospective cohort study was conducted at a university-affiliated hospital between January 2010 and September 2019. We collected data from patients with positive blood cultures for Enterococcus species isolates. The clinical data of patients who received ampicillin-containing regimens or glycopeptides as definitive therapy for ampicillin-susceptible E. faecalis/faecium bacteremia were reviewed. Multivariate logistic regression analysis was performed to identify risk factors for 28-day mortality. Results: Ampicillin-susceptible E. faecalis/faecium accounted for 41.2% (557/1,353) of enterococcal bacteremia cases during the study period. A total of 127 patients who received ampicillin-containing regimens (N = 56) or glycopeptides (N = 71) as definitive therapy were included in the analysis. The 28-day mortality rate was higher in patients treated with glycopeptides (19.7%) than in those treated with ampicillin-containing regimens (3.6%) (p = 0.006). However, in the multivariate model, antibiotic choice was not an independent predictor of 28-day mortality (adjusted OR, 3.7; 95% CI, 0.6–23.6). Conclusions: Glycopeptide use was not associated with improved mortality in patients with ampicillin-susceptible E. faecalis/faecium bacteremia. This study provides insights to reduce the inappropriate use of glycopeptides in ampicillin-susceptible E. faecalis/faecium bacteremia treatment and promote antimicrobial stewardship. | - |
dc.language.iso | en | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Ampicillin | - |
dc.subject.MESH | Anti-Bacterial Agents | - |
dc.subject.MESH | Bacteremia | - |
dc.subject.MESH | Enterococcus faecalis | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Glycopeptides | - |
dc.subject.MESH | Gram-Positive Bacterial Infections | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Microbial Sensitivity Tests | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Sulbactam | - |
dc.subject.MESH | Treatment Outcome | - |
dc.title | Clinical outcome of ampicillin or ampicillin/sulbactam versus glycopeptides in ampicillin-susceptible Enterococcus faecalis/faecium bacteremia: a 10-year retrospective cohort study | - |
dc.type | Article | - |
dc.identifier.pmid | 39223521 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11368023 | - |
dc.subject.keyword | Anti-bacterial agents | - |
dc.subject.keyword | Bacteremia | - |
dc.subject.keyword | Enterococcus faecalis | - |
dc.subject.keyword | Enterococcus faecium | - |
dc.subject.keyword | Mortality | - |
dc.contributor.affiliatedAuthor | Choi, YH | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1186/s12879-024-09824-w | - |
dc.citation.title | BMC infectious diseases | - |
dc.citation.volume | 24 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2024 | - |
dc.citation.startPage | 906 | - |
dc.citation.endPage | 906 | - |
dc.identifier.bibliographicCitation | BMC infectious diseases, 24(1). : 906-906, 2024 | - |
dc.identifier.eissn | 1471-2334 | - |
dc.relation.journalid | J014712334 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.