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首页> 外文期刊>BMC Cardiovascular Disorders >The FReedom from Ischemic Events - New Dimensions for Survival (FRIENDS) registry: design of a prospective cohort study of patients with advanced peripheral artery disease
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The FReedom from Ischemic Events - New Dimensions for Survival (FRIENDS) registry: design of a prospective cohort study of patients with advanced peripheral artery disease

机译:来自缺血性事件的FReedom-生存新维度(FRIENDS)注册表:针对晚期外周动脉疾病患者的前瞻性队列研究设计

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Background Advanced lower extremity peripheral artery disease (PAD), whether presenting as acute limb ischemia (ALI) or chronic critical limb ischemia (CLI), is associated with high rates of cardiovascular ischemic events, amputation, and death. Past research has focused on strategies of revascularization, but few data are available that prospectively evaluate the impact of key process of care factors (spanning pre-admission, acute hospitalization, and post-discharge) that might contribute to improving short and long-term health outcomes. Methods/Design The FRIENDS registry is designed to prospectively evaluate a range of patient and health system care delivery factors that might serve as future targets for efforts to improve limb and systemic outcomes for patients with ALI or CLI. This hypothesis-driven registry was designed to evaluate the contributions of: (i) pre-hospital limb ischemia symptom duration, (ii) use of leg revascularization strategies, and (iii) use of risk-reduction pharmacotherapies, as pre-specified factors that may affect amputation-free survival. Sequential patients would be included at an index “vascular specialist-defined” ALI or CLI episode, and patients excluded only for non-vascular etiologies of limb threat. Data including baseline demographics, functional status, co-morbidities, pre-hospital time segments, and use of medical therapies; hospital-based use of revascularization strategies, time segments, and pharmacotherapies; and rates of systemic ischemic events (e.g., myocardial infarction, stroke, hospitalization, and death) and limb ischemic events (e.g., hospitalization for revascularization or amputation) will be recorded during a minimum of one year follow-up. Discussion The FRIENDS registry is designed to evaluate the potential impact of key factors that may contribute to adverse outcomes for patients with ALI or CLI. Definition of new “health system-based” therapeutic targets could then become the focus of future interventional clinical trials for individuals with advanced PAD.
机译:背景晚期下肢周围动脉疾病(PAD),无论是急性肢体缺血(ALI)还是慢性重症肢体缺血(CLI),都与心血管缺血事件,截肢和死亡的发生率高相关。过去的研究集中在血运重建策略上,但是很少有数据可用来评估关键护理过程(包括入院前,急性住院和出院后)的关键过程的影响,这些因素可能有助于改善短期和长期健康结果。方法/设计FRIENDS注册中心旨在前瞻性评估一系列患者和卫生系统护理提供因素,这些因素可能会成为将来为改善ALI或CLI患者的肢体和全身结局做出努力的目标。该假设驱动的注册表旨在评估以下方面的贡献:(i)院前肢体缺血症状持续时间,(ii)使用腿部血运重建策略,以及(iii)使用降低风险的药物疗法作为预先指定的因素,可能会影响无截肢生存。序贯的患者将被纳入“血管专家定义的” ALI或CLI发作指数,而这些患者仅因肢体威胁的非血管病因而被排除在外。数据包括基线人口统计,功能状态,合并症,院前时间段以及药物治疗的使用;基于医院的血运重建策略,时间段和药物治疗的使用;并在至少一年的随访期间记录全身缺血事件(例如,心肌梗塞,中风,住院和死亡)和肢体缺血事件(例如,因血运重建或截肢而住院)的发生率。讨论FRIENDS注册表旨在评估可能导致ALI或CLI患者不良结局的关键因素的潜在影响。新的“基于健康系统的”治疗目标的定义可能会成为未来患有PAD的个体的介入性临床试验的重点。

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