Sullivan Sean D, Buxton Martin, Andersson L Fredrik, Lamm Carl Johan, Liljas Bengt, Chen Yu Zhi, Pauwels Romain A, Weiss Kevin B
Department of Pharmacy and Health Services, University of Washington, Seattle, Washington 98195-7630, USA.
J Allergy Clin Immunol. 2003 Dec;112(6):1229-36. doi: 10.1016/j.jaci.2003.09.025.
The Inhaled Steroid as Regular Therapy in Early Asthma (START) study reported that early intervention with budesonide in mild persistent asthma reduces severe asthmatic events and improves symptom outcomes and lung function in adults and children.
We sought to estimate the incremental cost-effectiveness of early intervention with budesonide, as observed within the START study.
START was a randomized, 3-year controlled trial of budesonide in early onset mild asthma among 7165 subjects ages 5 to 66 years. Three age groups (5-10, 11-17, and >or=18 years) were studied separately and overall. Differences in the probability of emergency treatments, symptom-free days (SFDs), and costs of health care were determined. Incremental cost-effectiveness ratios were estimated from the health care payer and societal perspectives.
Compared with usual therapy, patients receiving budesonide experienced an average of 14.1 (SE, 1.3) more SFDs per year (P <.001), fewer hospital days (69%, P <.001), and fewer emergency department visits (67%, P <.05). From the health care payer perspective, the net cost of early use of budesonide was an additional US dollars 0.42 (SE, dollars 0.04) per day, and the resultant cost-effectiveness ratio was US dollars 11.30 (95% CI, US dollars 8.60-US dollars 14.90) per SFD gained. From the societal perspective, the cost offsets of lower absence from school or work reduced the net cost of early budesonide to US dollars 0.14 (SE, US dollars 0.07) per day and decreased the cost-effectiveness ratio to US dollars 3.70 (95% CI, US dollars 0.10-US dollars 8.00). Early intervention was more effective and cost saving in the youngest age group.
Long-term treatment with budesonide appears to be cost-effective in patients with mild persistent asthma of recent onset.
吸入性糖皮质激素作为早期哮喘的常规治疗(START)研究报告称,在轻度持续性哮喘中,早期使用布地奈德进行干预可减少严重哮喘事件,并改善成人和儿童的症状结局及肺功能。
我们试图评估在START研究中观察到的布地奈德早期干预的增量成本效益。
START是一项针对7165名年龄在5至66岁的早发性轻度哮喘患者进行的布地奈德随机、为期3年的对照试验。对三个年龄组(5 - 10岁、11 - 17岁和≥18岁)分别进行研究,并进行总体研究。确定了紧急治疗概率、无症状天数(SFDs)和医疗保健成本的差异。从医疗保健支付方和社会角度估计了增量成本效益比。
与常规治疗相比,接受布地奈德治疗的患者每年平均多14.1(标准误,1.3)个无症状天数(P <.001),住院天数更少(69%,P <.001),急诊科就诊次数更少(67%,P <.05)。从医疗保健支付方的角度来看,早期使用布地奈德的净成本为每天额外增加0.42美元(标准误,0.04美元),每获得一个无症状天数的成本效益比为11.30美元(95%可信区间,8.60美元 - 14.90美元)。从社会角度来看,因上学或工作缺勤减少带来的成本抵消将早期布地奈德的净成本降至每天0.14美元(标准误,0.07美元),并将成本效益比降至3.70美元(95%可信区间,0.10美元 - 8.00美元)。早期干预在最年轻的年龄组中更有效且节省成本。
布地奈德长期治疗对于近期发病的轻度持续性哮喘患者似乎具有成本效益。