Dalbavancin as sequential therapy in infective endocarditis: Real-life experience in elder and comorbid patients.

Eduardo Aparicio-Minguijón, Jorge Boán, Antonio Terrón, Carlos Heredia, Cristina Puente, Asunción Pérez-Jacoiste Asín, M Ángeles Orellana, Laura Domínguez, José Manuel Caro, M Jesús López-Gude, Eva María Aguilar-Blanco, Andrea Eixerés-Esteve, Francisco López-Medrano
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Abstract

Objectives: This study aimed to evaluate the effectiveness of dalbavancin as sequential therapy in patients with infective endocarditis (IE) due to gram positive bacteria (GPB) in a real-life heterogenous cohort with comorbid patients.

Methods: A single center retrospective cohort study including all patients with definite IE treated with dalbavancin between January 2017 and February 2022 was developed. A 6-month follow-up was performed. The main outcomes were clinical cure rate, clinical and microbiological relapse, 6-month mortality, and adverse effects (AEs) rate.

Results: The study included 61 IE episodes. The median age was 78.5 years (interquartile range [IQR] 63.2-85.2), 78.7% were male, with a median Charlson comorbidity index of 7 (IQR 4-9) points. Overall, 49.2% suffered native valve IE. The most common microorganism was Staphylococcus aureus (26.3%) followed by Enterococcus faecalis (21.3%). The median duration of initial antimicrobial therapy and dalbavancin therapy were 27 (IQR 20-34) and 14 days (IQR 14-28) respectively. The total reduction of hospitalization was 1090 days. The most frequent dosage was 1500mg of dalbavancin every 14 days (96.7%). An AE was detected in 8.2% of patients, only one (1.6%) was attributed to dalbavancin (infusion reaction). Clinical cure was achieved in 86.9% of patients. One patient (1.6%) with Enterococcus faecalis IE suffered relapse. The 6-month mortality was 11.5%, with only one IE-related death (1.6%).

Conclusion: This study shows a high efficacy of dalbavancin in a heterogeneous real-world cohort of IE patients, with an excellent safety profile. Dalbavancin allowed a substantial reduction of in-hospital length of stay.

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达巴万星作为感染性心内膜炎的序贯疗法:老年患者和合并症患者的实际经验。
研究目的本研究旨在评估达巴万星作为序贯疗法在革兰阳性菌(GPB)所致感染性心内膜炎(IE)患者中的有效性:单中心回顾性队列研究包括2017年1月至2022年2月期间接受达巴万星治疗的所有确诊IE患者。进行了 6 个月的随访。主要结果为临床治愈率、临床和微生物学复发率、6个月死亡率和不良反应(AEs)率:研究包括 61 例 IE 病例。中位年龄为 78.5 岁(四分位距[IQR] 63.2-85.2),78.7% 为男性,中位 Charlson 合并症指数为 7(IQR 4-9)分。49.2%的患者患有原发性瓣膜IE。最常见的微生物是金黄色葡萄球菌(26.3%),其次是粪肠球菌(21.3%)。初始抗菌治疗和达巴万星治疗的中位持续时间分别为 27 天(IQR 20-34)和 14 天(IQR 14-28)。住院总天数减少了 1090 天。最常用的剂量是每 14 天服用 1500 毫克达巴万星(96.7%)。8.2%的患者出现了不良反应,只有1例(1.6%)是达巴万星引起的(输液反应)。86.9%的患者实现了临床治愈。一名粪肠球菌 IE 患者(1.6%)复发。6 个月的死亡率为 11.5%,只有一名患者(1.6%)死于肠球菌感染:这项研究表明,达巴万星对不同类型的 IE 患者具有很高的疗效,而且安全性极佳。达巴万星可大幅缩短住院时间。
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