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Eosinophilic pneumonia in patients treated with daptomycin: Review of the literature and US FDA adverse event reporting system reports

机译:达托霉素治疗的患者的嗜酸性粒细胞性肺炎:文献复习和美国FDA不良事件报告系统报告

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Background: Eosinophilic pneumonia (EP) has been noted in association with daptomycin use. The product labelling was recently updated to include EP in the Warnings and Precautions and Post-Marketing Experience sections. Objective: The objective of this study was to analyse adverse event (AE) reports submitted to the US FDA as well as published cases to characterize the clinical features and course of EP in daptomycin-treated patients. Methods: We searched for EP cases associated with daptomycin administration in the FDA Adverse Event Reporting System (AERS) submitted from 2004 to 2010, and the published literature. Cases were defined as definite, probable, possible and unlikely in terms of the diagnosis of EP and the potential association with daptomycin exposure. Definite cases had concurrent exposure to daptomycin, fever, dyspnoea with increased oxygen requirement or required mechanical ventilation, new infiltrates on chest imaging, bronchoalveolar lavage with >25% eosinophils and clinical improvement following daptomycin withdrawal. Additionally, we assessed inpatient daptomycin utilization. Results: We identified 7 definite, 13 probable, 38 possible cases of daptomycin-induced EP, and 23 unlikely cases. The seven definite EP cases had resolution after daptomycin was stopped, including two with EP recurrence following daptomycin rechallenge. Regarding the definite cases: (i) ages ranged from 60 to 87 years; (ii) dosing ranged from 4.4 to 8.0 mg/kg/day; and (iii) EP developed 10 days to 4 weeks after starting daptomycin. There was a gradual increase in the number of patients with an inpatient hospital discharge billing for daptomycin from the year 2004 to 2010. Conclusions: We report 7 definite, 13 probable and 38 possible EP cases associated with daptomycin administration. As AERS is based on voluntary reporting, the incidence of EP cannot be assessed. Healthcare providers should have heightened awareness of this serious AE associated with daptomycin use.
机译:背景:嗜酸性肺炎(EP)与达托霉素的使用有关。产品标签最近进行了更新,在“警告和注意事项”以及“上市后经验”部分中添加了EP。目的:本研究的目的是分析提交给美国FDA的不良事件(AE)报告以及已发表的病例,以表征达托霉素治疗患者的临床特征和EP病程。方法:我们在2004年至2010年提交的FDA不良事件报告系统(AERS)中搜索了与达托霉素给药相关的EP病例,以及已发表的文献。根据EP的诊断以及与达托霉素接触的潜在关联,将病例定义为确定,可能,可能和不可能的病例。明确的病例同时发生达托霉素暴露,发烧,呼吸困难,需氧量增加或需要机械通气,胸部影像学发现新的浸润,嗜酸性粒细胞> 25%的支气管肺泡灌洗以及达托霉素停用后的临床改善。此外,我们评估了住院达托霉素的利用率。结果:我们确定了7例达托霉素诱导的EP的确切病例,13例可能的38例病例和23例不太可能的病例。停药达托霉素后有7例明确的EP病例得到了解决,其中2例达托霉素再挑战后有EP复发。关于确定的情况:(一)年龄在60至87岁之间; (ii)剂量范围为4.4至8.0 mg / kg /天; (iii)达托霉素开始10天至4周后,EP出现。从2004年到2010年,住院患者出院达托霉素计费的患者数量逐渐增加。结论:我们报告了7例与达托霉素相关的确诊,13例可能和38例可能的EP病例。由于AERS基于自愿报告,因此无法评估EP的发生率。医疗保健提供者应提高对与达托霉素使用相关的严重AE的认识。

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