TY - JOUR
T1 - Therapeutic Drug Monitoring Versus Fixed-Interval Dosing of Dalbavancin in Implant-Associated Spinal Infections
T2 - Grand Round/A Case Study
AU - Houwen, Jeroen P.A.
AU - Hakkers, Charlotte S.
AU - Schweitzer, Valentijn A.
AU - Bognàr, Tim
AU - Toren-Wielema, Martha L.
AU - Touw, Daniël J.
AU - de Vries Schultink, Aurelia H.M.
N1 - Publisher Copyright:
© 2025
PY - 2025/12/1
Y1 - 2025/12/1
N2 - BACKGROUND: Implant-associated spinal infections (IASI) pose challenges for outpatient management due to the need for frequent intravenous antibiotic administration. Dalbavancin has a prolonged half-life and is a practical alternative. METHODS: Two cases of IASI were treated with dalbavancin in an outpatient setting over 10-12 weeks. One patient received therapeutic drug monitoring (TDM)-guided dosing, while the other was managed with fixed-interval dosing. Dalbavancin plasma concentrations were measured using liquid chromatography-tandem mass spectrometry, and dosing adjustments were guided by pharmacokinetic modeling. RESULTS: In the TDM-guided case, three dalbavancin doses were sufficient to maintain therapeutic plasma concentrations (≥8 mg/L), whereas the fixed-interval approach required four doses. Both patients successfully completed therapy without recurrence of the infection during follow-up. CONCLUSIONS: TDM-guided dalbavancin therapy optimized drug exposure and reduced the number of doses compared with fixed-interval dosing, highlighting its potential to optimize treatment. Further research is required to establish standardized therapeutic drug monitoring protocols for the management of IASI.
AB - BACKGROUND: Implant-associated spinal infections (IASI) pose challenges for outpatient management due to the need for frequent intravenous antibiotic administration. Dalbavancin has a prolonged half-life and is a practical alternative. METHODS: Two cases of IASI were treated with dalbavancin in an outpatient setting over 10-12 weeks. One patient received therapeutic drug monitoring (TDM)-guided dosing, while the other was managed with fixed-interval dosing. Dalbavancin plasma concentrations were measured using liquid chromatography-tandem mass spectrometry, and dosing adjustments were guided by pharmacokinetic modeling. RESULTS: In the TDM-guided case, three dalbavancin doses were sufficient to maintain therapeutic plasma concentrations (≥8 mg/L), whereas the fixed-interval approach required four doses. Both patients successfully completed therapy without recurrence of the infection during follow-up. CONCLUSIONS: TDM-guided dalbavancin therapy optimized drug exposure and reduced the number of doses compared with fixed-interval dosing, highlighting its potential to optimize treatment. Further research is required to establish standardized therapeutic drug monitoring protocols for the management of IASI.
KW - antimicrobial therapy
KW - dalbavancin
KW - implant-associated spinal infection
KW - therapeutic drug monitoring
UR - https://www.scopus.com/pages/publications/105021137195
U2 - 10.1097/FTD.0000000000001386
DO - 10.1097/FTD.0000000000001386
M3 - Article
C2 - 40970606
AN - SCOPUS:105021137195
SN - 0163-4356
VL - 47
SP - 697
EP - 700
JO - Therapeutic drug monitoring
JF - Therapeutic drug monitoring
IS - 6
ER -