Institute for Medical Technology Assessment, Erasmus University Medical Center, DR Rotterdam, The Netherlands.
Adv Ther. 2009 Sep;26(9):872-85. doi: 10.1007/s12325-009-0063-0. Epub 2009 Sep 19.
In budesonide/formoterol (Symbicort(R) Turbuhaler(R), AstraZeneca, Lund, Sweden) maintenance and reliever therapy (SMART), patients with asthma take a daily maintenance dose of budesonide/formoterol, with the option of taking additional doses for symptom relief instead of a short-acting beta(2)-agonist (SABA). This study assesses the cost-effectiveness of SMART compared with usual care in patients with mild-to-moderate persistent asthma treated by general practitioners in the Netherlands from a societal perspective.
The study was linked to a randomized, active-controlled, open-label, multicenter, 12-month clinical trial, with a prospective collection of resource use. One hundred and two patients > or =18 years with mild-to-moderate persistent asthma and daily inhaled corticosteroids (ICS) prior to the trial were included. SMART was given as two inhalations of budesonide/formoterol (100/6 microg) once daily, plus additional doses as needed. The control group was treated according to guidelines, which prescribe medium daily doses of ICS plus an SABA if needed. A long-acting beta(2)-agonist (LABA) is added if necessary. Effectiveness was measured as the proportion of asthma-control days, Asthma Control Questionnaire (ACQ) scores, the net proportion of patients with relevant ACQ improvement, and the proportion of well-controlled patients. Costs included asthma medication, physician contacts, and absence from work.
Mean total costs for SMART were
Treating primary care patients with mild-to-moderate persistent asthma with SMART instead of ICS plus bronchodilators does not affect health outcomes and does not increase costs; therefore, is likely to be an alternative for guideline-directed treatment, from a health and economic perspective.
在布地奈德/福莫特罗(Symbicort(R)Turbuhaler(R),阿斯利康,瑞典隆德)维持和缓解治疗(SMART)中,哮喘患者每天使用布地奈德/福莫特罗维持剂量,并有选择地使用额外剂量缓解症状,而不是使用短效β(2)-激动剂(SABA)。本研究从社会角度评估了轻度至中度持续性哮喘患者在荷兰的全科医生治疗中,与常规护理相比,SMART 的成本效益。
该研究与一项随机、活性对照、开放标签、多中心、为期 12 个月的临床试验相关联,并前瞻性地收集资源利用情况。102 名年龄>或=18 岁的轻度至中度持续性哮喘患者,在试验前每天使用吸入皮质激素(ICS),并纳入该研究。SMART 作为每日一次两次吸入布地奈德/福莫特罗(100/6 微克),根据需要额外剂量。对照组根据指南进行治疗,规定如果需要,中剂量每日 ICS 加 SABA。如果需要,则添加长效β(2)-激动剂(LABA)。有效性以哮喘控制天数、哮喘控制问卷(ACQ)评分、相关 ACQ 改善患者的净比例以及控制良好患者的比例来衡量。成本包括哮喘药物、医生接触和旷工。
SMART 的平均总成本降低了<欧元>134.81(95%CI:-<欧元>439.48;<欧元>44.85)。SMART 减少了<欧元>94.10(95%CI:-<欧元>300.60;<欧元>0.29)的生产损失(<欧元>10.77 与<欧元>104.87)。两组患者的健康结果没有显著差异,SMART 患者的哮喘控制天数减少了 3.81 天/患者年(95%CI:-36.8;30.8),ACQ 评分提高了 0.049(95%CI:-0.21;0.29),改善患者的净比例增加了 5.8%(95%CI:t15.6%;27.3%),控制良好患者的比例增加了 2.1%(95%CI:-25.5;20.8%)。
在初级保健患者中,使用 SMART 替代 ICS 加支气管扩张剂治疗轻度至中度持续性哮喘不会影响健康结果,也不会增加成本;因此,从健康和经济角度来看,它可能是指南导向治疗的替代方法。