Potent Activity of Ertapenem Plus Cefazolin Within Staphylococcal Biofilms: A Contributing Factor in the Treatment of Methicillin-Susceptible

Staphylococcus aureus cefazolin endocarditis ertapenem

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
May 2022
Historique:
received: 03 02 2022
accepted: 22 03 2022
entrez: 2 5 2022
pubmed: 3 5 2022
medline: 3 5 2022
Statut: epublish

Résumé

Besides antistaphylococcal beta-lactams and source control, there are limited validated antimicrobial salvage options in patients with prolonged methicillin-susceptible MSSA IE cases treated with ertapenem (ETP) plus cefazolin (CZ) were compared with matched IE cases treated with standard beta-lactam monotherapy. The bactericidal activity of ETP plus CZ was also compared with nafcillin (NAF), CZ, and ETP alone using an in vitro MSSA biofilm model. The median duration of bacteremia experienced by patients (n = 12) while on CZ or NAF was 4 days (range 1-16 days) compared with 1 day (range 1-3 days) for patients (n = 5) treated with ETP + CZ ( Ertapenem reduces CZ concentrations required to eradicate MSSA biofilms to those achievable in vivo by standard dosing, translating into shorter bacteremia duration in patients with MSSA endocarditis. Larger studies are needed to investigate ETP plus CZ therapy in the treatment of biofilm-related MSSA infections such as endocarditis.

Sections du résumé

Background UNASSIGNED
Besides antistaphylococcal beta-lactams and source control, there are limited validated antimicrobial salvage options in patients with prolonged methicillin-susceptible
Methods UNASSIGNED
MSSA IE cases treated with ertapenem (ETP) plus cefazolin (CZ) were compared with matched IE cases treated with standard beta-lactam monotherapy. The bactericidal activity of ETP plus CZ was also compared with nafcillin (NAF), CZ, and ETP alone using an in vitro MSSA biofilm model.
Results UNASSIGNED
The median duration of bacteremia experienced by patients (n = 12) while on CZ or NAF was 4 days (range 1-16 days) compared with 1 day (range 1-3 days) for patients (n = 5) treated with ETP + CZ (
Conclusions UNASSIGNED
Ertapenem reduces CZ concentrations required to eradicate MSSA biofilms to those achievable in vivo by standard dosing, translating into shorter bacteremia duration in patients with MSSA endocarditis. Larger studies are needed to investigate ETP plus CZ therapy in the treatment of biofilm-related MSSA infections such as endocarditis.

Identifiants

pubmed: 35493130
doi: 10.1093/ofid/ofac159
pii: ofac159
pmc: PMC9045957
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofac159

Subventions

Organisme : NIAID NIH HHS
ID : K08 AI151253
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI145310
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI124316
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Jessica Gilbertie (J)

Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.

Erlinda R Ulloa (ER)

Department of Pediatrics, University of California Irvine School of Medicine, Irvine, California, USA.
Division of Infectious Disease, Children's Hospital of Orange County, Orange, California, USA.

Jennifer C Daiker (JC)

Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.

Khanh Nguyen (K)

Sharp Memorial Hospital, San Diego, California, USA.

Dan Smelter (D)

Department and School of Pharmacy, University of Wisconsin Health, Madison, Wisconsin, USA.

Warren Rose (W)

Department and School of Pharmacy, University of Wisconsin Health, Madison, Wisconsin, USA.

Matthew Geriak (M)

Sharp Memorial Hospital, San Diego, California, USA.

Lauren V Schnabel (LV)

Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.

Victor Nizet (V)

Collaborative to Halt Antibiotic-Resistant Microbes (CHARM), Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, California, USA.
Skaggs School of Pharmacy, University of California San Diego, La Jolla, California, USA.

George Sakoulas (G)

Sharp Memorial Hospital, San Diego, California, USA.
Collaborative to Halt Antibiotic-Resistant Microbes (CHARM), Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, California, USA.

Classifications MeSH