Real-World Dalbavancin Use for Serious Gram-Positive Infections: Comparing Outcomes Between People Who Use and Do Not Use Drugs.

bacteremia dalbavancin endocarditis osteomyelitis people who use drugs

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:
Apr 2024
Historique:
received: 03 01 2024
accepted: 03 04 2024
medline: 23 4 2024
pubmed: 23 4 2024
entrez: 23 4 2024
Statut: epublish

Résumé

Dalbavancin has been used off-label to treat invasive bacterial infections in vulnerable populations like people who use drugs (PWUD) because of its broad gram-positive coverage and unique pharmacological properties. This retrospective, multisite study examined clinical outcomes at 90 days in PWUD versus non-PWUD after secondary treatment with dalbavancin for bacteremia, endocarditis, osteomyelitis, septic arthritis, and epidural abscesses. Patients at 3 teaching hospitals who received dalbavancin for an invasive infection between March 2016 and May 2022 were included. Characteristics of PWUD and non-PWUD, infection highlights, hospital stay and treatment, and outcomes were compared using χ There were a total of 176 patients; 78 were PWUD and 98 were non-PWUD. PWUD were more likely to have a patient-directed discharge (26.9% vs 3.1%; Dalbavancin was an effective treatment option for invasive gram-positive infections in our patient population. Despite higher rates of patient-directed discharge and loss to follow-up, PWUD had similar rates of clinical cure at 90 days compared to non-PWUD.

Sections du résumé

Background UNASSIGNED
Dalbavancin has been used off-label to treat invasive bacterial infections in vulnerable populations like people who use drugs (PWUD) because of its broad gram-positive coverage and unique pharmacological properties. This retrospective, multisite study examined clinical outcomes at 90 days in PWUD versus non-PWUD after secondary treatment with dalbavancin for bacteremia, endocarditis, osteomyelitis, septic arthritis, and epidural abscesses.
Methods UNASSIGNED
Patients at 3 teaching hospitals who received dalbavancin for an invasive infection between March 2016 and May 2022 were included. Characteristics of PWUD and non-PWUD, infection highlights, hospital stay and treatment, and outcomes were compared using χ
Results UNASSIGNED
There were a total of 176 patients; 78 were PWUD and 98 were non-PWUD. PWUD were more likely to have a patient-directed discharge (26.9% vs 3.1%;
Conclusions UNASSIGNED
Dalbavancin was an effective treatment option for invasive gram-positive infections in our patient population. Despite higher rates of patient-directed discharge and loss to follow-up, PWUD had similar rates of clinical cure at 90 days compared to non-PWUD.

Identifiants

pubmed: 38651139
doi: 10.1093/ofid/ofae186
pii: ofae186
pmc: PMC11034951
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofae186

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. All authors: No reported conflicts.

Auteurs

Sarah Zambrano (S)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Molly L Paras (ML)

Massachusetts General Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Joji Suzuki (J)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Jeffrey C Pearson (JC)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Brandon Dionne (B)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Harry Schrager (H)

Newton Wellesley Hospital, Department of Medicine, Boston, Massachusetts, USA.

Jason Mallada (J)

Newton Wellesley Hospital, Department of Medicine, Boston, Massachusetts, USA.

Veronica Szpak (V)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Katie Fairbank-Haynes (K)

Newton Wellesley Hospital, Department of Medicine, Boston, Massachusetts, USA.

Marlene Kalter (M)

Newton Wellesley Hospital, Department of Medicine, Boston, Massachusetts, USA.

Sara Prostko (S)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Daniel A Solomon (DA)

Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Classifications MeSH