# TDM-Guided Dalbavancin Treatment for Complex Staphylococcus aureus Osteoarticular Infections in Children

**Authors:** Silvia Garazzino, Giulia Mazzetti, Matteo Sandei, Raffaele Vitale, Camilla Martino, Alice Palermiti, Amedeo De Nicolò, Elisa Funiciello, Alessandro Aprato, Alessia Gerace, Alessandro Bondi, Antonio Curtoni, Antonio D’Avolio, Marco Denina

PMC · DOI: 10.3390/antibiotics15020162 · Antibiotics · 2026-02-03

## TL;DR

Dalbavancin is effective and safe for treating complex staph infections in children, but dosing needs adjustment due to changing drug levels over time.

## Contribution

This study provides the first pediatric evidence on dalbavancin's multi-dose pharmacokinetics and supports TDM for optimized treatment.

## Key findings

- Clinical success rate was 93.8% with no adverse events in 16 pediatric patients.
- Drug concentrations dropped significantly by week 4, with over 50% below 8 mg/L.
- TDM-guided dosing and shorter maintenance intervals are recommended to avoid sub-therapeutic levels.

## Abstract

Background/Objectives: Dalbavancin is approved for pediatric acute bacterial skin and skin structure infections (ABSSSIs), yet real-world practice frequently necessitates off-label use for deep-seated infections requiring prolonged suppression. While adult data support therapeutic drug monitoring (TDM)-guided maintenance, the pediatric evidence for repeated-dose pharmacokinetics (PK) is limited. We evaluated the efficacy, safety, multi-dose PK, and pharmacoeconomic impact of dalbavancin in a complex pediatric cohort. Methods: A retrospective study (2023–2025) of enrolled patients < 18 years treated with dalbavancin. A subgroup receiving ≥3 doses underwent PK analysis to assess concentration decay against conservative efficacy targets (4 and 8 mg/L). A pharmacoeconomic analysis compared resource utilization against the standard of care. Results: Sixteen patients (median age 12) were included, primarily treated for Staphylococcus aureus (S. aureus) osteoarticular infections (75%), and frequently device-associated (66.7%). Clinical success was 93.8% (15/16) with no adverse events. A PK analysis (n = 9; 78 samples) ruled out dangerous accumulation but revealed a significant concentration drop at week 4 (mean 6.06 mg/L; p = 0.005). Logistic regression identified the time since the previous dose as the sole predictor of sub-therapeutic levels, with >50% of the patients dropping below 8 mg/L by the fourth week. An analysis showed median net savings of EUR 3215.84 per patient (p = 0.004). Conclusions: Dalbavancin is effective and cost-saving for complex pediatric infections. However, due to distinct pediatric PK, dosing regimens extrapolated from adults may result in sub-therapeutic concentrations by week 4. We recommend TDM around week 3 to tailor dosing or limiting maintenance intervals to a maximum of 4 weeks.

## Linked entities

- **Chemicals:** dalbavancin (PubChem CID 16134627)
- **Diseases:** osteomyelitis (MONDO:0005246), arthritis (MONDO:0005578)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** bacterial (MESH:D001424), TDM (MESH:D000081015), osteomyelitis (MESH:D010019), Staphylococcus aureus (MESH:D013203), ABSSSIs (MESH:D017192), nosocomial infections (MESH:D003428), Infections (MESH:D007239), drug toxicity (MESH:D064420), ARC (MESH:D006030), OAIs (MESH:D014394), injury to (MESH:D014947), critically ill (MESH:D016638), skin and skin structure infections (MESH:D012871)
- **Chemicals:** Dalbavancin (MESH:C469289), lipoglycopeptide (MESH:D000077427)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937467/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937467/full.md

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Source: https://tomesphere.com/paper/PMC12937467