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首页> 外文期刊>Lancet Neurology >Effectiveness and cost-effectiveness of interferon beta and glatiramer acetate in the UK Multiple Sclerosis Risk Sharing Scheme at 6 years: a clinical cohort study with natural history comparator
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Effectiveness and cost-effectiveness of interferon beta and glatiramer acetate in the UK Multiple Sclerosis Risk Sharing Scheme at 6 years: a clinical cohort study with natural history comparator

机译:β-干扰素和醋酸格拉替雷在6年英国多发性硬化风险分担计划中的有效性和成本效益:与自然史比较者的一项临床队列研究

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Background In 2002, the UK's National Institute for Clinical Excellence (NICE) concluded that interferon beta and glatiramer acetate would be cost effective as disease-modifying therapies (DMTs) for multiple sclerosis only if the short-term disability benefits reported in clinical trials were maintained. The UK Multiple Sclerosis Risk Sharing Scheme (RSS) was established to assess whether disability progression was consistent with a cost-effectiveness target of 36000 pound per quality-adjusted life-year projected over 20 years. We aimed to evaluate the long-term effectiveness and cost-effectiveness of these DMTs by comparing a cohort of patients with relapsing-remitting multiple sclerosis enrolled in the UK RSS with a natural history cohort from British Columbia, Canada.
机译:背景2002年,英国国家临床卓越研究所(NICE)得出结论,只有在临床试验中报告的短期残疾益处得以维持的情况下,β-干扰素和醋酸格拉替雷才可作为治疗多发性硬化症的疾病改良疗法(DMT)具有成本效益。 。建立了英国多发性硬化症风险分担计划(RSS),以评估残疾进展是否符合20年来每质量调整生命年36000磅的成本效益目标。我们旨在通过比较英国RSS中纳入的复发缓解型多发性硬化症患者队列与加拿大不列颠哥伦比亚省的自然史队列来评估这些DMT的长期有效性和成本效益。

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