首页> 外文期刊>JMIR Research Protocols >Multiple Sclerosis Therapy With Disease-Modifying Treatments in Germany: The PEARL (ProspEctive phArmacoeconomic cohoRt evaluation) Noninterventional Study Protocol
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Multiple Sclerosis Therapy With Disease-Modifying Treatments in Germany: The PEARL (ProspEctive phArmacoeconomic cohoRt evaluation) Noninterventional Study Protocol

机译:德国采用疾病改善疗法的多发性硬化症疗法:PEARL(预测性药物经济学评估)非干预性研究方案

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Background Patients with multiple sclerosis (MS) require long-term therapy and have a wide variety of needs for health-related support. The efficacy and safety of MS therapy, as assessed by both clinicians and patients, are important parameters that need to be considered. However, few studies combine data on efficacy and safety outcomes with pharmacoeconomic data. Objective Here, we present the study design of the ProspEctive phArmacoeconomic cohoRt evaluation (PEARL), a prospective, multicenter, noninterventional cohort study on patients with relapsing-remitting MS (RRMS) treated with disease-modifying treatments (DMTs). Methods During a prospective observational phase of 24 months per patient, PEARL evaluated clinical and patient-perceived efficacy and safety measures, as well as pharmacoeconomic data on RRMS patients treated with DMTs—interferon beta and glatiramer acetate. Measurements of the patients' perceptions included the assessment of patient-reported quality of life, treatment satisfaction, and compliance. The study was planned to include 1800 outpatients from 180 German neurological practices who had continuously been treated with an approved DMT for at least 30 days. The primary statistical analyses of the PEARL study will be descriptive. Particular focus will be on specific subgroups, such as patients who switched DMTs during therapy and patients with disease worsening or disease activity. Subgroups will be compared using stratified analyses. Results Data collection for PEARL started in September 2010 and ended in July 2013. As of July 2015, the study is completed and is currently being analyzed and written up. Conclusions PEARL is evaluating both the health status and resource utilization of RRMS patients treated with DMTs in Germany. The combination of pharmacoeconomic data with clinical and patients' self-perceived efficacy and safety outcomes will add useful information to the currently incomplete picture of the overall RRMS burden in Germany.
机译:背景多发性硬化症(MS)患者需要长期治疗,并且对健康相关支持的需求多种多样。由临床医生和患者评估的MS治疗的有效性和安全性是需要考虑的重要参数。但是,很少有研究将功效和安全性结果数据与药物经济学数据相结合。目的在这里,我们提出对预期的药物经济学评估(PEARL)的研究设计,这是一项对前瞻性,多中心,非干预性队列研究,研究对象是采用疾病缓解疗法(DMT)治疗的复发缓解型MS(RRMS)患者。方法在每位患者24个月的前瞻性观察阶段中,PEARL评估了接受DMT干扰素-干扰素β和醋酸格拉替雷治疗的RRMS患者的临床和患者感知的疗效和安全性措施以及药物经济学数据。对患者知觉的测量包括对患者报告的生活质量,治疗满意度和依从性的评估。该研究计划包括来自180个德国神经病学实践部门的1800名门诊患者,他们接受了批准的DMT连续治疗至少30天。 PEARL研究的主要统计分析将具有描述性。特别要关注的是特定的亚组,例如在治疗期间更换DMT的患者以及疾病恶化或疾病活动的患者。将使用分层分析比较亚组。结果PEARL的数据收集于2010年9月开始,至2013年7月结束。截至2015年7月,研究已完成,目前正在分析和编写中。结论PEARL正在德国评估DMT治疗的RRMS患者的健康状况和资源利用。药物经济学数据与临床和患者自我感觉到的疗效和安全性结果的结合将为目前不完整的德国RRMS总体负担状况提供有用的信息。

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