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

Author:

Zambrano Sarah1ORCID,Paras Molly L2,Suzuki Joji1ORCID,Pearson Jeffrey C1,Dionne Brandon1,Schrager Harry3,Mallada Jason3,Szpak Veronica1,Fairbank-Haynes Katie3,Kalter Marlene3,Prostko Sara1,Solomon Daniel A1ORCID

Affiliation:

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

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

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

Abstract

Abstract Background 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 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 χ2 for categorical variables, t test for continuous variables, and nonparametric tests where appropriate. Results 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%; P < .001) and be lost to follow-up (20.5% vs 7.14%; P < .01). Assuming loss to follow-up did not achieve clinical cure, 73.1% of PWUD and 74.5% of non-PWUD achieved clinical cure at 90 days (P = .08). Conclusions 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.

Publisher

Oxford University Press (OUP)

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