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Centralised Biological Therapy Registry for Moderate to Severe Plaque Psoriasis – Overview and Methodology

机译:中度至重度斑块状牛皮癣的集中式生物疗法注册中心–概述和方法

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The introduction of new pharmacotherapy entities in the last decade accentuate the necessity to set up treatment guidelines based on real life evidence. Randomized controlled trials remain golden standard of a research. Data derived from studies aiming on daily clinical practice should bring needed, added value. Disease prevalence growth, due to increased life expectancy, better diagnostic procedures and earlier medical intervention, as well as ever growing demand for highly priced, sophistically produced drugs put stress on healthcare budgets even in developed countries. Large databases commonly called - therapy registries are implemented to collect data on therapy effectivity in terms of effectiveness, safety and patient long-term on therapy survival. Registries importance rose together with biological therapies introduction. New in class molecules entered the market conditionally being obliged to provide additional e.g. safety data. Such procedures require involvement of many different professionals, e.g. physicians, professional medical bodies, IT experts, database administrators, statisticians and government institutions. Paper based, followed by computer based forms were distributed among physicians to collect these data. eHealth technologies provide physicians with centralized, more intuitive applications. The particularities of different diagnosis caused great variations within each specific registry launched. Important information was missing since they were pointed out as optional and many were redundant causing frustration among physicians due to inadequate administrative workload. The main objective of this work was to set up the therapy registry standards and procedures. Methodology of ?ideal“ moderate to severe plaque psoriasis biology therapy registry development, introduction, administration and evaluation was prepared to assist any government institution or professional body when planning registry deployment. Electronic application based on widely used MS Excel platform was developed and installed in the biological therapy centers as a standalone application for the pilot use.
机译:在过去的十年中,新的药物治疗实体的引入突显了根据现实生活证据制定治疗指南的必要性。随机对照试验仍然是研究的黄金标准。从针对日常临床实践的研究得出的数据应带来所需的附加价值。由于预期寿命的延长,更好的诊断程序和更早的医疗干预,以及对高价,精巧生产的药物的需求不断增长,疾病患病率的增长也给发达国家的医疗保健预算带来了压力。大型数据库通常被称为“治疗注册表”,用于收集有关有效性,安全性和患者长期治疗存活率的治疗有效性数据。随着生物疗法的引入,注册管理机构的重要性也随之提高。新型分子有条件地进入市场,必须提供额外的,例如安全数据。这样的程序需要许多不同的专业人员的参与,例如医生,专业医疗机构,IT专家,数据库管理员,统计学家和政府机构。在医生之间分发基于纸张的表格,然后是基于计算机的表格,以收集这些数据。 eHealth技术为医生提供了集中的,更直观的应用程序。不同诊断的特殊性在启动的每个特定注册表中引起了很大差异。缺少重要信息,因为它们被指出是可选的,并且许多信息是多余的,由于管理工作量不足而使医生感到沮丧。这项工作的主要目的是建立治疗注册标准和程序。制定,引入,管理和评估“理想的”中度至重度斑块状牛皮癣生物疗法注册表的方法,旨在协助任何政府机构或专业机构规划注册表的部署。开发了基于广泛使用的MS Excel平台的电子应用程序,并将其安装在生物治疗中心中,作为独立的应用程序进行试点使用。

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