Chiara Mariani, Matteo Passerini, Lucia Galli, Alice Covizzi, Marta Colaneri, Martina Offer, Margherita Faenzi, Stefania Merli, Simona Landonio, Marta Fusi, Alberto Dolci, Andrea Gori, Dario Cattaneo
{"title":"主动治疗药物监测指导DALBAvaNcin在骨关节感染(MONTALBANO)中的抑制抗生素治疗(bb10 - 12周)。","authors":"Chiara Mariani, Matteo Passerini, Lucia Galli, Alice Covizzi, Marta Colaneri, Martina Offer, Margherita Faenzi, Stefania Merli, Simona Landonio, Marta Fusi, Alberto Dolci, Andrea Gori, Dario Cattaneo","doi":"10.5194/jbji-10-255-2025","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction</b>: Long-term dalbavancin use is increasingly adopted off-label for osteoarticular infections (OAIs), but data on administration timing and long-term effects beyond 12 weeks are scarce. This study evaluated the pharmacological efficacy of proactive therapeutic drug monitoring (TDM) to optimize dalbavancin administration. <b>Methods</b>: This single-center, retrospective study included adult OAI patients treated with <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> doses of dalbavancin from July 2022 to October 2024. Initial doses were given on days 1, 8, and 43. From the third dose onward, <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> and <math> <mrow><msub><mi>C</mi> <mo>max</mo></msub> </mrow> </math> values informed dosing schedules via log-linear regression models, targeting <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> <mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup>. The primary outcome was the pharmacological efficacy of dalbavancin, assessed by the proportion of patients with <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> <mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup> and <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> mg L<sup>-1</sup> after the third dose. Clinical outcomes and safety data were collected as descriptive data. <b>Results</b>: A total of 33 patients provided 118 <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> determinations. Pharmacological efficacy was achieved in 93 <math><mo>/</mo></math> 118 (78.8 %) and 114 <math><mo>/</mo></math> 118 (96.6 %) determinations for <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> thresholds of <math><mrow><mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup> and <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> mg L<sup>-1</sup>, respectively. Efficacy improved when considering only determinations at the correct timing. A total of 18 (54.5 %) patients are still in treatment, while 11 (33.3 %) completed therapy with clinical success. Three patients experienced a relapse after the end of the treatment, while one patient experienced failure, and no adverse events were reported. <b>Conclusions</b>: Dalbavancin is a viable option for prolonged OAI management when other therapies are unavailable or high-risk. Proactive TDM effectively supports this approach by ensuring adequate drug exposure while preventing accumulation.</p>","PeriodicalId":15271,"journal":{"name":"Journal of Bone and Joint Infection","volume":"10 4","pages":"255-263"},"PeriodicalIF":2.8000,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12311387/pdf/","citationCount":"0","resultStr":"{\"title\":\"Proactive Therapeutic Drug MONiToring to Guide Suppressive Antibiotic Therapy with DALBAvaNcin ( > 12 weeks) in Osteoarticular Infections (MONTALBANO).\",\"authors\":\"Chiara Mariani, Matteo Passerini, Lucia Galli, Alice Covizzi, Marta Colaneri, Martina Offer, Margherita Faenzi, Stefania Merli, Simona Landonio, Marta Fusi, Alberto Dolci, Andrea Gori, Dario Cattaneo\",\"doi\":\"10.5194/jbji-10-255-2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction</b>: Long-term dalbavancin use is increasingly adopted off-label for osteoarticular infections (OAIs), but data on administration timing and long-term effects beyond 12 weeks are scarce. This study evaluated the pharmacological efficacy of proactive therapeutic drug monitoring (TDM) to optimize dalbavancin administration. <b>Methods</b>: This single-center, retrospective study included adult OAI patients treated with <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> doses of dalbavancin from July 2022 to October 2024. Initial doses were given on days 1, 8, and 43. From the third dose onward, <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> and <math> <mrow><msub><mi>C</mi> <mo>max</mo></msub> </mrow> </math> values informed dosing schedules via log-linear regression models, targeting <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> <mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup>. The primary outcome was the pharmacological efficacy of dalbavancin, assessed by the proportion of patients with <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> <mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup> and <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> mg L<sup>-1</sup> after the third dose. Clinical outcomes and safety data were collected as descriptive data. <b>Results</b>: A total of 33 patients provided 118 <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> determinations. Pharmacological efficacy was achieved in 93 <math><mo>/</mo></math> 118 (78.8 %) and 114 <math><mo>/</mo></math> 118 (96.6 %) determinations for <math> <mrow><msub><mi>C</mi> <mo>min</mo></msub> </mrow> </math> thresholds of <math><mrow><mo>≥</mo> <mn>8</mn></mrow> </math> mg L<sup>-1</sup> and <math><mrow><mo>≥</mo> <mn>4</mn></mrow> </math> mg L<sup>-1</sup>, respectively. Efficacy improved when considering only determinations at the correct timing. A total of 18 (54.5 %) patients are still in treatment, while 11 (33.3 %) completed therapy with clinical success. Three patients experienced a relapse after the end of the treatment, while one patient experienced failure, and no adverse events were reported. <b>Conclusions</b>: Dalbavancin is a viable option for prolonged OAI management when other therapies are unavailable or high-risk. Proactive TDM effectively supports this approach by ensuring adequate drug exposure while preventing accumulation.</p>\",\"PeriodicalId\":15271,\"journal\":{\"name\":\"Journal of Bone and Joint Infection\",\"volume\":\"10 4\",\"pages\":\"255-263\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12311387/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bone and Joint Infection\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5194/jbji-10-255-2025\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bone and Joint Infection","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5194/jbji-10-255-2025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Proactive Therapeutic Drug MONiToring to Guide Suppressive Antibiotic Therapy with DALBAvaNcin ( > 12 weeks) in Osteoarticular Infections (MONTALBANO).
Introduction: Long-term dalbavancin use is increasingly adopted off-label for osteoarticular infections (OAIs), but data on administration timing and long-term effects beyond 12 weeks are scarce. This study evaluated the pharmacological efficacy of proactive therapeutic drug monitoring (TDM) to optimize dalbavancin administration. Methods: This single-center, retrospective study included adult OAI patients treated with doses of dalbavancin from July 2022 to October 2024. Initial doses were given on days 1, 8, and 43. From the third dose onward, and values informed dosing schedules via log-linear regression models, targeting mg L-1. The primary outcome was the pharmacological efficacy of dalbavancin, assessed by the proportion of patients with mg L-1 and mg L-1 after the third dose. Clinical outcomes and safety data were collected as descriptive data. Results: A total of 33 patients provided 118 determinations. Pharmacological efficacy was achieved in 93 118 (78.8 %) and 114 118 (96.6 %) determinations for thresholds of mg L-1 and mg L-1, respectively. Efficacy improved when considering only determinations at the correct timing. A total of 18 (54.5 %) patients are still in treatment, while 11 (33.3 %) completed therapy with clinical success. Three patients experienced a relapse after the end of the treatment, while one patient experienced failure, and no adverse events were reported. Conclusions: Dalbavancin is a viable option for prolonged OAI management when other therapies are unavailable or high-risk. Proactive TDM effectively supports this approach by ensuring adequate drug exposure while preventing accumulation.