614. Long-Acting Lipoglycopeptides for the Treatment of Bone and Joint Infections and Bacteremia in Infectious Disease Outpatient Infusion Clinics

IF 3.8 4区 医学 Q2 IMMUNOLOGY Open Forum Infectious Diseases Pub Date : 2020-12-31 DOI:10.1093/ofid/ofaa439.808
B. Metzger, R. Prokesch, J. Bernett, R. Mandel, Ramesh V Nathan, K. Stock, T. Hardin, Claudia P Schroeder, L. V. Anglen
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Abstract

Long-acting lipoglycopeptides (LGPs) are approved for the treatment of acute bacterial skin and skin-structure infections. Broad Gram-positive coverage and weekly dosing regimens are useful for other diagnoses, but real-world data supporting such use are sparse. We review our experience of dalbavancin and oritavancin for the treatment of bone and joint infection (BJI) and bacteremia (BAC) in outpatient infusion clinics (OICs). We conducted a multicenter, retrospective, observational cohort study of patients (pts) receiving long-acting LGPs in OICs over 2 yrs from 2018-2019 for BJI and BAC. Data collected included demographics, diagnosis, dosing regimen, microbiology, clinical outcomes, and adverse events (AEs). Clinical success, defined as resolution of infection with continued oral antibiotics allowed, was assessed at the next follow-up visit. Worsening infection, the need for additional intravenous therapy, and discontinuations during therapy were deemed non-successful. We identified 70 pts (mean age: 64±16 years, 53% male) from 25 OICs, who received dalbavancin (n=50), oritavancin (n=19) and both (n=1). BJI accounted for 55 (79%) with 31 osteomyelitis, 9 bursitis, 7 prosthetic joint, 7 septic arthritis and 1 tenosynovitis. BAC was the primary diagnosis in 15 (21%) and sources were 6 device, 2 lower respiratory tract, 2 urinary tract and 5 unknown. 46% of pts were treated in the OIC without prior hospitalization. 72 Gram-positive isolates were obtained from 67 pts, with Staphylococcus aureus predominant (42/72, 58%), including methicillin-resistant (26/72, 36%) and methicillin-susceptible isolates (16/72, 22%). Median number of doses administered were 2 [IQR 1-2] in BJI and 1 in BAC [IQR 1-2]. Overall clinical success was 86% (57/66), with 4 non-evaluable. BJI had 85% success (44/52), with 90% in osteomyelitis (28/31), 50% in prosthetic joint (3/6) and 87% (13/15) in the others. Clinical success was 93% (13/14) in BAC. Three pts (4%) on dalbavancin experienced mild AEs, none resulting in discontinuation of therapy. This multicenter real-world study of long-acting LGPs demonstrates safety and high clinical success rates in BJI and BAC. Our experience suggests a role for use of these agents in treatment of BJI and BAC in the outpatient setting. Brian S. Metzger, MD, MPH, Allergan (Speaker’s Bureau)Cumberland (Speaker’s Bureau)Melinta (Speaker’s Bureau) Ramesh V. Nathan, MD, FIDSA, Merck & Co. (Other Financial or Material Support, Grant Steering Committee Member) Lucinda J. Van Anglen, PharmD, Merck & Co. (Grant/Research Support)
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614.在传染病门诊输液临床中用于治疗骨和关节感染以及细菌血症的长效脂糖肽
长效脂糖肽(LGPs)已被批准用于治疗急性细菌性皮肤和皮肤结构感染。广泛的革兰氏阳性覆盖率和每周给药方案对其他诊断是有用的,但支持这种使用的真实世界数据很少。我们回顾了我们在门诊输液诊所(OICs)使用达尔巴万星和奥他万星治疗骨关节感染(BJI)和菌血症(BAC)的经验。我们进行了一项多中心、回顾性、观察性队列研究,对2018-2019年接受长效LGP的OIC患者(pts)进行了为期2年的BJI和BAC研究。收集的数据包括人口统计学、诊断、给药方案、微生物学、临床结果和不良事件(AE)。在下一次随访中评估临床成功率,定义为在允许继续口服抗生素的情况下解决感染。感染恶化、需要额外的静脉注射治疗以及治疗期间的中断被认为是不成功的。我们从25例OIC中确定了70例患者(平均年龄:64±16岁,53%为男性),他们接受了达尔巴万星(n=50)、奥他万星(n=19)以及两者(n=1)。BJI占55例(79%),其中骨髓炎31例,滑囊炎9例,人工关节7例,感染性关节炎7例,肌腱滑膜炎1例。BAC是15例(21%)的主要诊断,来源为6个装置、2个下呼吸道、2个尿路和5个未知。46%的患者在OIC接受治疗,之前未住院治疗。从67例患者中获得72个革兰氏阳性分离株,以金黄色葡萄球菌为主(42/72,58%),包括耐甲氧西林的分离株(26/72,36%)和对甲氧西林敏感的分离物(16/72,22%)。在BJI中给药的中位剂量为2[IQR1-2],在BAC[IKR1-2]中给药1。总体临床成功率为86%(57/66),其中4例无法评估。BJI成功率85%(44/52),骨髓炎成功率90%(28/31),人工关节成功率50%(3/6),其他关节成功率87%(13/15)。BAC的临床成功率为93%(13/14)。3例(4%)接受达尔巴万星治疗的患者出现轻度AE,无一例导致治疗中断。这项针对长效LGP的多中心真实世界研究证明了BJI和BAC的安全性和高临床成功率。我们的经验表明,这些药物在门诊治疗BJI和BAC中的作用。Brian S.Metzger,医学博士,公共卫生硕士,Allergan(议长局)Cumberland(议长局
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来源期刊
Open Forum Infectious Diseases
Open Forum Infectious Diseases Medicine-Neurology (clinical)
CiteScore
6.70
自引率
4.80%
发文量
630
审稿时长
9 weeks
期刊介绍: Open Forum Infectious Diseases provides a global forum for the publication of clinical, translational, and basic research findings in a fully open access, online journal environment. The journal reflects the broad diversity of the field of infectious diseases, and focuses on the intersection of biomedical science and clinical practice, with a particular emphasis on knowledge that holds the potential to improve patient care in populations around the world. Fully peer-reviewed, OFID supports the international community of infectious diseases experts by providing a venue for articles that further the understanding of all aspects of infectious diseases.
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