Daptomycin Plus Oxacillin for Persistent Methicillin-Susceptible

MSSA Staphylococcus aureus bacteremia daptomycin infective endocarditis oxacillin

Journal

The Annals of pharmacotherapy
ISSN: 1542-6270
Titre abrégé: Ann Pharmacother
Pays: United States
ID NLM: 9203131

Informations de publication

Date de publication:
05 Aug 2023
Historique:
medline: 6 8 2023
pubmed: 6 8 2023
entrez: 5 8 2023
Statut: aheadofprint

Résumé

The preferred antibiotic salvage regimen for persistent methicillin-susceptible We sought to evaluate the effectiveness and safety of daptomycin plus oxacillin (D/O) for persistent MSSAB. This was a single-center, retrospective cohort of patients with persistent MSSAB who received D/O between January 1, 2014, and January 1, 2023. Adult patients were included if they had blood cultures positive for MSSA ≥72 hours and received D/O combination for ≥48 hours. Patients were excluded if they were pregnant, incarcerated, or received another antibiotic considered to have excellent activity against MSSA. The primary outcome was time to MSSA bacteremia clearance post-daptomycin initiation. Secondary outcomes included microbiological cure, hospital length of stay, 90-day all-cause mortality, MSSA bacteremia-related mortality, 90-day readmission for MSSAB, and incidence of antibiotic-associated adverse effects. Time to MSSAB clearance post-D/O initiation was plotted using Kaplan-Meier estimation. Seven unique patient encounters were identified including 4 with endocarditis. Despite a median MSSA bacteremia duration of 7.8 days, median clearance was 2 days post-daptomycin initiation. All achieved microbiological cure, and no adverse effects were reported. Ninety-day all-cause mortality, MSSAB-related mortality, and 90-day readmission for MSSAB occurred in 28.6%, 14.3%, and 14.3% of patients, respectively. D/O was an effective, well-tolerated salvage regimen in this cohort and may represent a carbapenem-sparing option for persistent MSSAB.

Sections du résumé

BACKGROUND UNASSIGNED
The preferred antibiotic salvage regimen for persistent methicillin-susceptible
OBJECTIVE UNASSIGNED
We sought to evaluate the effectiveness and safety of daptomycin plus oxacillin (D/O) for persistent MSSAB.
METHODS UNASSIGNED
This was a single-center, retrospective cohort of patients with persistent MSSAB who received D/O between January 1, 2014, and January 1, 2023. Adult patients were included if they had blood cultures positive for MSSA ≥72 hours and received D/O combination for ≥48 hours. Patients were excluded if they were pregnant, incarcerated, or received another antibiotic considered to have excellent activity against MSSA. The primary outcome was time to MSSA bacteremia clearance post-daptomycin initiation. Secondary outcomes included microbiological cure, hospital length of stay, 90-day all-cause mortality, MSSA bacteremia-related mortality, 90-day readmission for MSSAB, and incidence of antibiotic-associated adverse effects. Time to MSSAB clearance post-D/O initiation was plotted using Kaplan-Meier estimation.
RESULTS UNASSIGNED
Seven unique patient encounters were identified including 4 with endocarditis. Despite a median MSSA bacteremia duration of 7.8 days, median clearance was 2 days post-daptomycin initiation. All achieved microbiological cure, and no adverse effects were reported. Ninety-day all-cause mortality, MSSAB-related mortality, and 90-day readmission for MSSAB occurred in 28.6%, 14.3%, and 14.3% of patients, respectively.
CONCLUSIONS AND RELEVANCE UNASSIGNED
D/O was an effective, well-tolerated salvage regimen in this cohort and may represent a carbapenem-sparing option for persistent MSSAB.

Identifiants

pubmed: 37542415
doi: 10.1177/10600280231189888
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10600280231189888

Auteurs

Wesley D Kufel (WD)

Binghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY, USA.
State University of New York Upstate Medical University, Syracuse, NY, USA.
State University of New York Upstate University Hospital, Syracuse, NY, USA.

Zoey Zagoria (Z)

Binghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY, USA.

Bruce E Blaine (BE)

Saint John Fisher University, Rochester, NY, USA.

Jeffrey M Steele (JM)

State University of New York Upstate Medical University, Syracuse, NY, USA.
State University of New York Upstate University Hospital, Syracuse, NY, USA.

Rahul Mahapatra (R)

State University of New York Upstate Medical University, Syracuse, NY, USA.
State University of New York Upstate University Hospital, Syracuse, NY, USA.

Kristopher M Paolino (KM)

State University of New York Upstate Medical University, Syracuse, NY, USA.
State University of New York Upstate University Hospital, Syracuse, NY, USA.

Stephen J Thomas (SJ)

State University of New York Upstate Medical University, Syracuse, NY, USA.
State University of New York Upstate University Hospital, Syracuse, NY, USA.

Classifications MeSH