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Dalbavancin Sequential Therapy for Gram-Positive Bloodstream Infection: A Multicenter Observational Study.
Rebold, Nicholas; Alosaimy, Sara; Pearson, Jeffrey C; Dionne, Brandon; Taqi, Ahmad; Lagnf, Abdalhamid; Lucas, Kristen; Biagi, Mark; Lombardo, Nicholas; Eudy, Joshua; Anderson, Daniel T; Mahoney, Monica V; Kufel, Wesley D; D'Antonio, Joseph A; Jones, Bruce M; Frens, Jeremy J; Baumeister, Tyler; Geriak, Matthew; Sakoulas, George; Farmakiotis, Dimitrios; Delaportas, Dino; Larew, Jeremy; Veve, Michael P; Rybak, Michael J.
Afiliación
  • Rebold N; Wayne State University, Detroit, MI, USA. nicholas.rebold@howard.edu.
  • Alosaimy S; Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI, 48201, USA. nicholas.rebold@howard.edu.
  • Pearson JC; Department of Clinical and Administrative Pharmacy Sciences, College of Pharmacy, Howard University, 2300 4th St NW, Office 114, Washington, DC, 20059, USA. nicholas.rebold@howard.edu.
  • Dionne B; Wayne State University, Detroit, MI, USA.
  • Taqi A; Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI, 48201, USA.
  • Lagnf A; Department of Pharmacy, Brigham and Women's Hospital, Boston, MA, USA.
  • Lucas K; Department of Pharmacy, Brigham and Women's Hospital, Boston, MA, USA.
  • Biagi M; School of Pharmacy, Northeastern University, Boston, MA, USA.
  • Lombardo N; Department of Pharmacy, Brigham and Women's Hospital, Boston, MA, USA.
  • Eudy J; Wayne State University, Detroit, MI, USA.
  • Anderson DT; Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI, 48201, USA.
  • Mahoney MV; Detroit Medical Center, Detroit Receiving Hospital, Detroit, MI, USA.
  • Kufel WD; Wayne State University, Detroit, MI, USA.
  • D'Antonio JA; Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI, 48201, USA.
  • Jones BM; College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
  • Frens JJ; Department of Pharmacy, Swedish American Health System, Rockford, IL, USA.
  • Baumeister T; Department of Pharmacy, Swedish American Health System, Rockford, IL, USA.
  • Geriak M; Department of Pharmacy, Augusta University Medical Center, Augusta, GA, USA.
  • Sakoulas G; Department of Pharmacy, Augusta University Medical Center, Augusta, GA, USA.
  • Farmakiotis D; Department of Pharmacy, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Delaportas D; Department of Medicine, State University of New York Upstate Medical University, Syracuse, NY, USA.
  • Larew J; Department of Pharmacy Practice, Binghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY, USA.
  • Veve MP; Department of Pharmacy Practice, Binghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, NY, USA.
  • Rybak MJ; Department of Pharmacy, St. Joseph's/Candler Health System, Savannah, GA, USA.
Infect Dis Ther ; 13(3): 565-579, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38427289
ABSTRACT

INTRODUCTION:

Long-acting lipoglycopeptides such as dalbavancin may have utility in patients with Gram-positive bloodstream infections (BSI), particularly in those with barriers to discharge or who require prolonged parenteral antibiotic courses. A retrospective cohort study was performed to provide further multicenter real-world evidence on dalbavancin use as a sequential therapy for Gram-positive BSI.

METHODS:

One hundred fifteen patients received dalbavancin with Gram-positive BSI, defined as any positive blood culture or diagnosed with infective endocarditis, from 13 centers geographically spread across the United States between July 2015 and July 2021.

RESULTS:

Patients had a mean (SD) age of 48.5 (17.5) years, the majority were male (54%), with many who injected drugs (40%). The most common infection sources (non-exclusive) were primary BSI (89%), skin and soft tissue infection (SSTI) (25%), infective endocarditis (19%), and bone and joint infection (17%). Staphylococcus aureus accounted for 72% of index cultures, coagulase-negative Staphylococcus accounted for 18%, and Streptococcus species in 16%. Dalbavancin started a median (Q1-Q3) of 10 (6-19) days after index culture collection. The most common regimen administered was dalbavancin 1500 mg as one dose for 50% of cases. The primary outcome of composite clinical failure occurred at 12.2%, with 90-day mortality at 7.0% and 90-day BSI recurrence at 3.5%.

CONCLUSIONS:

Dalbavancin may serve as a useful tool in facilitating hospital discharge in patients with Gram-positive BSI. Randomized controlled trials are anticipated to validate dalbavancin as a surrogate to current treatment standards.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Infect Dis Ther Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Infect Dis Ther Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Nueva Zelanda