Bork Jacqueline T, Heil Emily L, Berry Shanna, Lopes Eurides, Davé Rohini, Gilliam Bruce L, Amoroso Anthony
Division of Infectious Disease, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Department of Medicine, VA Maryland Health Care System, Baltimore, MD, USA.
Infect Dis Ther. 2019 Jun;8(2):171-184. doi: 10.1007/s40121-019-0247-0. Epub 2019 May 3.
Dalbavancin is approved for acute bacterial skin and skin structure infections (ABSSSIs) but offers a potential treatment option for complicated invasive gram-positive infections. Importantly, dalbavancin's real benefits may be in treating complicated infections in vulnerable patient populations, such as persons who inject drugs (PWID).
A multicenter retrospective analysis was performed from March 2014 to April 2017 to assess 30- and 90-day clinical cure and adverse drug events (ADEs) in adult patients who received ≥ 1 dose of dalbavancin for a non-ABSSSI indication.
During the study period, 45 patients received dalbavancin, 28 for a non-ABSSSI indication. The predominant infections treated included osteomyelitis (46%), endovascular infection (25%) and uncomplicated bacteremia (14%). Half of the patients had positive Staphylococcus aureus in cultures, 29% methicillin resistant and 21% methicillin susceptible. Most patients were prescribed dalbavancin as sequential treatment with a median of 13.5 days of prior antibiotic therapy. The most common reason for choosing dalbavancin over standard therapy use was PWID (54%). Seven patients were lost to follow-up at day 30. Of the remaining evaluable patients, 30-day clinical cure was achieved in 15/21 (71%) patients. The most common reason for failure was lack of source control (4/6, 67%). At day 90, relapse occurred in two patients. Three patients had a potential dalbavancin-associated ADE: two patients with renal dysfunction and one patient with pruritus.
This study demonstrates a possible role for dalbavancin in the treatment of non-ABSSSI invasive gram-positive infections in select vulnerable OPAT patients.
达巴万星已被批准用于治疗急性细菌性皮肤及皮肤结构感染(ABSSSI),但它为复杂的侵袭性革兰氏阳性菌感染提供了一种潜在的治疗选择。重要的是,达巴万星的实际益处可能在于治疗弱势群体中的复杂感染,例如注射吸毒者(PWID)。
进行了一项多中心回顾性分析,时间跨度为2014年3月至2017年4月,以评估接受≥1剂达巴万星用于非ABSSSI适应症的成年患者的30天和90天临床治愈率及药物不良事件(ADE)。
在研究期间,45例患者接受了达巴万星治疗,其中28例用于非ABSSSI适应症。接受治疗的主要感染包括骨髓炎(46%)、血管内感染(25%)和非复杂性菌血症(14%)。一半的患者培养出金黄色葡萄球菌阳性,其中29%对甲氧西林耐药,21%对甲氧西林敏感。大多数患者接受达巴万星作为序贯治疗,之前抗生素治疗的中位时间为13.5天。相较于标准治疗,选择达巴万星的最常见原因是患者为注射吸毒者(54%)。7例患者在30天时失访。在其余可评估的患者中,15/21(71%)例患者实现了30天临床治愈。治疗失败的最常见原因是缺乏源头控制(4/6,67%)。在90天时,2例患者复发。3例患者出现了可能与达巴万星相关的ADE:2例肾功能不全患者和1例瘙痒患者。
本研究证明了达巴万星在治疗特定弱势门诊患者非ABSSSI侵袭性革兰氏阳性菌感染中可能发挥的作用。