Evidence map›Paper›PMID 42440168›Full record

ReviewDrugs2026

Long-Acting Lipoglycopeptide Treatment of Invasive Gram-Positive Infections.

Madison E Salam, Daniel B Chastain, Douglas Fish, Andrés F Henao-Martínez, Michal Krsak, Matthew Miller, Taylor Morrisette, Scott Mueller, Martin Krsak

Abstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Madison E SalamDepartment of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, 80045, USA.
Daniel B ChastainDepartment of Clinical & Administrative Pharmacy, University of Georgia College of Pharmacy, Augusta, GA, USA.
Douglas FishDepartment of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, 80045, USA.
Andrés F Henao-MartínezDivision of Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Michal KrsakDolnooravska Nemocnica s Poliklinikou, Dolny Kubin, 02601, Slovakia.
Matthew MillerDepartment of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, 80045, USA.
Taylor MorrisetteDepartment of Clinical Pharmacy & Outcomes Sciences, Medical University of South Carolina College of Pharmacy, Charleston, SC, USA.
Scott MuellerDepartment of Pharmacy, UCHealth University of Colorado Hospital, Aurora, CO, 80045, USA.
Martin KrsakDivision of Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, 80045, USA. martin.krsak@cuanschutz.edu.ORCID http://orcid.org/0000-0002-1746-7462

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gram-positive infections continue to pose a therapeutic challenge owing to their invasive nature (e.g., Staphylococcus aureus and Streptococcus pyogenes) and eradication difficulties (e.g., methicillin-resistant Staphylococcus aureus [MRSA] and vancomycin-resistant enterococci [VRE]). Long-acting lipoglycopeptides (laLGPs) present an effective and conveniently dosed option for the treatment of most invasive Gram-positive pathogens. Improved compliance monitoring associated with their infrequent intravenous dosing, that is not available to such degree with more frequently dosed antimicrobials outside of inpatient settings, is another benefit of laLGPs over more frequently dosed antimicrobials. In this article, we provide a narrative review, including the pharmacological characteristics of dalbavancin (DAL) and oritavancin (ORI), the only currently available laLGPs, as well as their approved and "off-label" use reported in the literature to date. We discuss their respective mechanism of action, caveats in compartments where they do not achieve sufficient concentrations (i.e., central nervous system [CNS]; potentially pneumonias with ORI), as well as their reported efficacy in individual organ systems as reported in literature. Lastly, we summarize insights about laLGP use in special populations and discuss the benefits of therapeutic drug monitoring of these agents, mainly in conditions requiring prolonged therapy (e.g., hardware-associated orthopedic infections).

Indexed as

Anti-Bacterial AgentsGlycopeptidesGram-Positive Bacterial InfectionsLipoglycopeptidesTeicoplaninHumansVancomycinAnti-Bacterial AgentsdalbavancinGlycopeptidesLipoglycopeptidesoritavancinTeicoplaninVancomycin

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.