Comparison of Oral and Intravenous Definitive Antibiotic Therapy for Beta-Hemolytic Streptococcus Species Bloodstream Infections from Soft Tissue Sources: a Propensity Score-Matched Analysis.


Journal

Antimicrobial agents and chemotherapy
ISSN: 1098-6596
Titre abrégé: Antimicrob Agents Chemother
Pays: United States
ID NLM: 0315061

Informations de publication

Date de publication:
15 06 2023
Historique:
medline: 19 6 2023
pubmed: 16 5 2023
entrez: 16 5 2023
Statut: ppublish

Résumé

Beta-hemolytic streptococci are common causes of bloodstream infection (BSI). There is emerging data regarding oral antibiotics for BSI but limited for beta-hemolytic streptococcal BSI. We conducted a retrospective study of adults with beta-hemolytic streptococcal BSI from a primary skin/soft tissue source from 2015 to 2020. Patients transitioned to oral antibiotics within 7 days of treatment initiation were compared to those who continued intravenous therapy, after propensity score matching. The primary outcome was 30-day treatment failure (composite of mortality, infection relapse, and hospital readmission). A prespecified 10% noninferiority margin was used for the primary outcome. We identified 66 matched pairs of patients treated with oral and intravenous antibiotics as definitive therapy. Based on an absolute difference in 30-day treatment failure of 13.6% (95% confidence interval 2.4 to 24.8%), the noninferiority of oral therapy was not confirmed (

Identifiants

pubmed: 37191533
doi: 10.1128/aac.00120-23
pmc: PMC10269088
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0012023

Déclaration de conflit d'intérêts

The authors declare a conflict of interest. A.V. reports being an inventor for Mayo Clinic Travel App interaction with Smart Medical Kit and Medical Kit for Pilgrims and receiving funding from Moderna Inc for Advisory Board participation. All other authors have no potential conflicts of interest to report.

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Auteurs

Zachary A Yetmar (ZA)

Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Supavit Chesdachai (S)

Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Brian D Lahr (BD)

Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, Minnesota, USA.

Douglas W Challener (DW)

Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Kellie N Arensman Hannan (KN)

Department of Pharmacy, Mayo Clinic, Mankato, Minnesota, USA.

Kevin Epps (K)

Department of Pharmacy, Mayo Clinic, Jacksonville, Florida, USA.

Ryan W Stevens (RW)

Department of Pharmacy, Mayo Clinic, Rochester, Minnesota, USA.

Maria Teresa Seville (MT)

Divison of Infectious Diseases, Mayo Clinic, Phoenix, Arizona, USA.

Aaron J Tande (AJ)

Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Abinash Virk (A)

Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.

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Classifications MeSH