首页> 外文期刊>Trials >Clinical and cost-effectiveness analysis of an open label, single-centre, randomised trial of spinal cord stimulation (SCS) versus percutaneous myocardial laser revascularisation (PMR) in patients with refractory angina pectoris: The SPiRiT trial
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Clinical and cost-effectiveness analysis of an open label, single-centre, randomised trial of spinal cord stimulation (SCS) versus percutaneous myocardial laser revascularisation (PMR) in patients with refractory angina pectoris: The SPiRiT trial

机译:对难治性心绞痛患者进行的开放标签,单中心,脊髓刺激(SCS)与经皮心肌激光血运重建(PMR)随机对照试验的临床和成本效益分析:SPiRiT试验

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Background Patients with refractory angina have significant morbidity. This study aimed to compare two of the treatment options, Spinal Cord Stimulation (SCS) and Percutaneous Myocardial Laser Revascularisation (PMR) in terms of clinical outcomes and cost-effectiveness. Methods Eligible patients were randomised to PMR or SCS and followed up for exercise tolerance time (ETT), Canadian Cardiovascular Society (CCS) classification and the quality of life measures SF-36, Seattle Angina Questionnaire and the EuroQoL at 3, 12 and 24 months. Utilities were calculated using the EQ-5D and these and costs were compared between groups. The incremental cost-effectiveness ratio (ICER) per QALY for SCS compared to PMR was also calculated. Results At 24 months post-randomisation, patients that had SCS and PMR had similar ETT (mean difference 0.05, 95% CI -2.08, 2.18, p = 0.96) and there was no difference in CCS classification or quality of life outcomes. The difference in overall mean costs when comparing SCS to PMR was GBP5,520 (95% CI GBP1,966 to GBP8,613; p Conclusion Outcomes after SCS did not differ appreciably from those after PMR, with the former procedure being less cost-effective as currently applied. Larger studies could clarify which patients would most benefit from SCS, potentially increasing cost-effectiveness. Trial registration Current Controlled Trials ISRCTN09648950
机译:背景难治性心绞痛患者的发病率很高。这项研究旨在比较两种治疗选择,即脊髓刺激(SCS)和经皮心肌激光血管重建术(PMR)的临床效果和成本效益。方法将符合条件的患者随机分为3个月,12个月和24个月,分别接受PMR或SCS并进行运动耐力时间(ETT),加拿大心血管协会(CCS)分类和生活质量测量指标SF-36,西雅图心绞痛问卷和EuroQoL随访。使用EQ-5D计算公用事业,并比较各组之间的成本。还计算了与PMR相比,SCS每QALY的增量成本效益比(ICER)。结果随机分组后24个月,患有SCS和PMR的患者的ETT相似(平均差异0.05,95%CI -2.08,2.18,p = 0.96),CCS分类或生活质量无差异。将SCS与PMR进行比较时,总体平均成本差异为5,520英镑(95%CI 1,966英镑至8,613英镑; p结论)SCS后的结果与PMR后的结果没有显着差异,前一种方法的成本效益较低如目前应用,更大的研究可以阐明哪些患者将从SCS中获益最大,从而可能提高成本效益。试验注册当前对照试验ISRCTN09648950

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