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Dalbavancin Reduces Hospital Stay and Improves Productivity for Patients with Acute Bacterial Skin and Skin Structure Infections: The ENHANCE Trial.
McCarthy, Matthew W; Keyloun, Katelyn R; Gillard, Patrick; Choi, Justin J; Pickell, Nicholas; Copp, Ronald; Walsh, Thomas J.
Afiliación
  • McCarthy MW; Department of Medicine, Division of General Internal Medicine, Weill Cornell Medicine of Cornell University and New York Presbyterian Hospital, New York, NY, USA. mwm9004@med.cornell.edu.
  • Keyloun KR; Global Health Economics and Outcomes Research, Allergan plc, Irvine, CA, USA.
  • Gillard P; Global Health Economics and Outcomes Research, Allergan plc, Irvine, CA, USA.
  • Choi JJ; Department of Medicine, Division of General Internal Medicine, Weill Cornell Medicine of Cornell University and New York Presbyterian Hospital, New York, NY, USA.
  • Pickell N; Department of Medicine, Infectious Diseases, Weill Cornell Medicine of Cornell University and New York Presbyterian Hospital, New York, NY, USA.
  • Copp R; ICON plc, Dublin, Ireland.
  • Walsh TJ; Departments of Medicine, Pediatrics, and Microbiology and Immunology, Weill Cornell Medicine of Cornell University and New York Presbyterian Hospital, New York, NY, USA.
Infect Dis Ther ; 9(1): 53-67, 2020 Mar.
Article en En | MEDLINE | ID: mdl-31713130
ABSTRACT

INTRODUCTION:

Admissions for acute bacterial skin and skin structure infections (ABSSSI) are often prolonged because of intravenous (IV) antibiotics. Use of a long-acting IV antibiotic may reduce length of stay (LOS) on a hospitalist service. The ENHANCE ABSSSI trial sought to determine the impact on LOS and work productivity in patients treated with a long-acting IV antibiotic, dalbavancin, vs. usual care at an urban tertiary-care center.

METHODS:

A single-center, pre- vs. post-period pragmatic trial at Weill-Cornell Medical Center assessed usual care for consecutively enrolled admitted ABSSSI patients during an observational period (pre-period). Identification and treatment of eligible admitted ABSSSI patients with dalbavancin were implemented in the post-period. Those with life-threatening infections, requiring multiple antibiotics/intensive care, or with unstable comorbidities were excluded. Outcomes were assessed over a 44-day follow-up period.

RESULTS:

Of 48 and 43 patients enrolled, respectively, in the pre- and post-periods, mean infection-related LOS was reduced in the post-period (3.2 days vs. 4.8 days; P = 0.003). Similar results were found in an adjusted LOS analysis. Work productivity and activity impairment outcomes significantly improved in the post-period (P ≤ 0.01). Complete response rates were similar 50% (pre-period) and 57% (post-period). Among AEs identified, 17% (n = 7) were found to have possible causal relation to dalbavancin in the post-period. Few AEs were serious (n = 3; 7% post-period versus n = 1; 2% pre-period).

CONCLUSION:

After implementing the ENHANCE ABSSSI pathway, LOS was significantly reduced by almost 2 days, with potential improvements in work productivity and ability to complete daily activities. TRIAL REGISTRATION ClinicalTrials.gov identifier, NCT03233438.

FUNDING:

Allergan plc.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Infect Dis Ther Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Infect Dis Ther Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
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