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In-vivo-validation of a cardiovascular risk prediction tool: the arriba-pro study

机译:心血管风险预测工具的体内验证:arriba-pro研究

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Background Calculation of individual risk is the cornerstone of effective cardiovascular prevention. arriba is a software to estimate the individual risk to suffer a cardiovascular event in 10 years. Prognosis and the absolute effects of pharmacological and lifestyle interventions help the patient make a well-informed decision. The risk calculation algorithm currently used in arriba is based on the Framingham risk algorithm calibrated to the German setting. The objective of this study is to evaluate and adapt the algorithm for the target population in primary care in Germany. Methods/design arriba -pro will be conducted within the primary care scheme provided by a large health care insurer in Baden-Württemberg, Germany. Patients who are counseled with arriba by their general practitioners (GPs) will be included in the arriba -pro cohort. Exposure data from the consultation with arriba such as demographic data and risk factors will be recorded automatically by the practice software and transferred to the study centre. Information on relevant prescription drugs (effect modifiers) and cardiovascular events (outcomes) will be derived from administrative sources. Discussion The study is unique in simulating a therapy na?ve cohort, matching exactly research and application setting, using a robust administrative data base, and, finally, including patients with known cardiovascular disease who have been excluded from previous studies. Trial registration The study is registered with Deutsches Register Klinischer Studien (DRKS00004633).
机译:背景个人风险的计算是有效预防心血管疾病的基础。 arriba是一种软件,用于估计10年内罹患心血管事件的个人风险。药理和生活方式干预的预后以及绝对效果可帮助患者做出明智的决定。当前在arriba中使用的风险计算算法基于已校准为德国设置的Framingham风险算法。这项研究的目的是评估和适应德国初级保健目标人群的算法。方法/设计arriba-pro将在德国巴登-符腾堡州的一家大型医疗保险公司提供的初级医疗计划内进行。由其全科医生(GPs)咨询过arriba的患者将包括在arriba -pro队列中。练习软件会自动记录与arriba进行磋商后得到的暴露数据,例如人口统计数据和危险因素,并将其传输到研究中心。有关处方药(效果调节剂)和心血管事件(结果)的信息将来自行政来源。讨论本研究的独特之处在于,它使用一个强大的管理数据库模拟了一个幼稚的队列,精确地匹配了研究和应用环境,最后包括了先前研究未包括的已知心血管疾病患者。试用注册该研究已在Deutsches Register Klinischer Studien(DRKS00004633)中注册。

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