Cargando…

1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus

BACKGROUND: Dalbavancin is a lipoglycopeptide antibiotic active against gram-positive organisms. Its extended half-life allows for weekly dosing that can last 4 to 6 weeks with 2 doses. Although approved for treating skin and soft tissue infections, use for more complicated infections is appealing,...

Descripción completa

Detalles Bibliográficos
Autores principales: Streifel, Amber C, Sukerman, Ellie, Sikka, Monica, Makadia, Jina, Lewis, James, Luke, Strnad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777594/
http://dx.doi.org/10.1093/ofid/ofaa439.1452
_version_ 1783630938460127232
author Streifel, Amber C
Sukerman, Ellie
Sikka, Monica
Makadia, Jina
Lewis, James
Luke, Strnad
author_facet Streifel, Amber C
Sukerman, Ellie
Sikka, Monica
Makadia, Jina
Lewis, James
Luke, Strnad
author_sort Streifel, Amber C
collection PubMed
description BACKGROUND: Dalbavancin is a lipoglycopeptide antibiotic active against gram-positive organisms. Its extended half-life allows for weekly dosing that can last 4 to 6 weeks with 2 doses. Although approved for treating skin and soft tissue infections, use for more complicated infections is appealing, particularly when daily intravenous antibiotics are impractical. S aureus is the most common cause of complex infections for which dalbavancin is considered at our institution, so we sought to better understand its use. METHODS: We conducted a retrospective study to describe dalbavancin use at our institution for infections caused by Staphylococcus aureus. We identified all patients ≥18 years who received ≥1 dose of dalbavancin. Infectious disease faculty reviewed charts for clinical characteristics and outcomes of the infections. RESULTS: Fifty-two patients with S. aureus infections (60% MRSA) were treated with at least a partial course of dalbavancin. Twenty-seven (52%) had a history of IV drug use (IDU) and the most common infections were bone and joint infection in 51% and bacteremia in 40% (Table 1). The most common dosing regimen was 1500 mg x 1 in 55% or 1500 mg weekly x 2 in 25% (Table 2). The most common reasons for use of dalbavancin were history of IDU in 48% and lack of a safe home environment in 21%. Suppressive oral antibiotics for the primary infection were prescribed to 3 patients after completing dalbavancin (2 received for other indications). Clinical outcomes include 15% of patients lost to follow-up, readmission due to infection recurrence or dalbavancin adverse effects in 12%, and overall infection recurrence or relapse by day 90 in 31% (Table 3). There were no severe dalbavancin-related adverse drug events. Table 1. Patient and Disease Characteristics [Image: see text] Table 2. Dalbavancin Use Characteristics [Image: see text] Table 3. Clinical Endpoints [Image: see text] CONCLUSION: While our results suggest dalbavancin is well tolerated, questions about relapse rates in the treatment of complicated S. aureus infections remain. Further research is needed to evaluate clinical outcomes for dalbavancin compared to standard of care antibiotics and to better elucidate whether relapses were related to true antibiotic failure versus other complexities of the S. aureus infections. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-7777594
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77775942021-01-07 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus Streifel, Amber C Sukerman, Ellie Sikka, Monica Makadia, Jina Lewis, James Luke, Strnad Open Forum Infect Dis Poster Abstracts BACKGROUND: Dalbavancin is a lipoglycopeptide antibiotic active against gram-positive organisms. Its extended half-life allows for weekly dosing that can last 4 to 6 weeks with 2 doses. Although approved for treating skin and soft tissue infections, use for more complicated infections is appealing, particularly when daily intravenous antibiotics are impractical. S aureus is the most common cause of complex infections for which dalbavancin is considered at our institution, so we sought to better understand its use. METHODS: We conducted a retrospective study to describe dalbavancin use at our institution for infections caused by Staphylococcus aureus. We identified all patients ≥18 years who received ≥1 dose of dalbavancin. Infectious disease faculty reviewed charts for clinical characteristics and outcomes of the infections. RESULTS: Fifty-two patients with S. aureus infections (60% MRSA) were treated with at least a partial course of dalbavancin. Twenty-seven (52%) had a history of IV drug use (IDU) and the most common infections were bone and joint infection in 51% and bacteremia in 40% (Table 1). The most common dosing regimen was 1500 mg x 1 in 55% or 1500 mg weekly x 2 in 25% (Table 2). The most common reasons for use of dalbavancin were history of IDU in 48% and lack of a safe home environment in 21%. Suppressive oral antibiotics for the primary infection were prescribed to 3 patients after completing dalbavancin (2 received for other indications). Clinical outcomes include 15% of patients lost to follow-up, readmission due to infection recurrence or dalbavancin adverse effects in 12%, and overall infection recurrence or relapse by day 90 in 31% (Table 3). There were no severe dalbavancin-related adverse drug events. Table 1. Patient and Disease Characteristics [Image: see text] Table 2. Dalbavancin Use Characteristics [Image: see text] Table 3. Clinical Endpoints [Image: see text] CONCLUSION: While our results suggest dalbavancin is well tolerated, questions about relapse rates in the treatment of complicated S. aureus infections remain. Further research is needed to evaluate clinical outcomes for dalbavancin compared to standard of care antibiotics and to better elucidate whether relapses were related to true antibiotic failure versus other complexities of the S. aureus infections. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7777594/ http://dx.doi.org/10.1093/ofid/ofaa439.1452 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Streifel, Amber C
Sukerman, Ellie
Sikka, Monica
Makadia, Jina
Lewis, James
Luke, Strnad
1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title_full 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title_fullStr 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title_full_unstemmed 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title_short 1268. Dalbavancin for the Treatment of Infections due to Staphylococcus aureus
title_sort 1268. dalbavancin for the treatment of infections due to staphylococcus aureus
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777594/
http://dx.doi.org/10.1093/ofid/ofaa439.1452
work_keys_str_mv AT streifelamberc 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus
AT sukermanellie 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus
AT sikkamonica 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus
AT makadiajina 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus
AT lewisjames 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus
AT lukestrnad 1268dalbavancinforthetreatmentofinfectionsduetostaphylococcusaureus