Thomas K, Peter J V, Cherian A M, Guyatt G
Department of Medicine and Clinical Epidemiology, Christian Medical College, Vellore, Tamil Nadu, India.
Natl Med J India. 1996 Jul-Aug;9(4):159-62.
Oral beta-stimulants are widely used in the management of chronic asthma in India, in spite of evidence suggesting the superiority of inhaled medication in achieving maximum bronchodilatation. An economic evaluation was performed in a randomized double-blind cross-over trial to evaluate the role of adjuvant oral beta-stimulants in the treatment of asthma.
Patients who had seasonal or perennial asthma and were using metered dose inhalers for control of symptoms were randomly selected for the study. They received either 4 mg of oral salbutamol or placebo as adjuvant treatment. During the study they controlled their symptoms by adjusting the dose of the inhaler medication. A cost minimization technique was used to assess the economic impact of this intervention in the treatment and control periods. A sensitivity analysis was performed to assess the robustness of the conclusions.
The mean cost was significantly greater in the treatment period and a patient lost approximately Rs 20 per month (CI: 13 to 27; p = 0.001) as a result of the adjuvant treatment. There was no significant difference in the quality of life or peak expiratory flow rate during the two periods. The patients also noted mild but significantly increased tremors (p = 0.01) and palpitations (p = 0.001) during the treatment period. There was no treatment-to-period interaction.
Adjuvant oral beta-agonists do not improve the quality of life or bronchodilatation in asthmatics using an inhaled beta-agonist for control of symptoms.
在印度,口服β受体激动剂广泛用于慢性哮喘的治疗,尽管有证据表明吸入药物在实现最大程度支气管扩张方面更具优势。在一项随机双盲交叉试验中进行了一项经济学评估,以评价辅助性口服β受体激动剂在哮喘治疗中的作用。
随机选取患有季节性或常年性哮喘且使用定量吸入器控制症状的患者进行研究。他们接受4毫克口服沙丁胺醇或安慰剂作为辅助治疗。在研究期间,他们通过调整吸入器药物剂量来控制症状。采用成本最小化技术评估该干预措施在治疗期和对照期的经济影响。进行敏感性分析以评估结论的稳健性。
治疗期的平均成本显著更高,辅助治疗使患者每月损失约20卢比(置信区间:13至27;p = 0.001)。两个时期的生活质量或呼气峰值流速无显著差异。患者在治疗期还注意到轻微但显著增加的震颤(p = 0.01)和心悸(p = 0.001)。不存在治疗与时期的交互作用。
对于使用吸入β受体激动剂控制症状的哮喘患者,辅助性口服β受体激动剂并不能改善生活质量或支气管扩张情况。