Research Group in Pharmacology and Toxicology "INFARTO". Department of Pharmacology and Toxicology, Facultad de Medicina, University of Antioquia, Carrera 51D #62-29, Medellin, Colombia.
Hospital Infantil Concejo de Medellin, Medellin, Colombia.
BMC Pulm Med. 2021 Dec 5;21(1):397. doi: 10.1186/s12890-021-01775-1.
Recent asthma guidelines, such as the Global Initiative for Asthma (GINA), recommend in adult patients as-needed inhaled corticosteroids (ICS)-formoterol as an alternative to maintenance ICS in mild to moderate persistent asthma. The introduction of these recommendations concerns whether using as-needed budesonide-formoterol would be more cost-effective than to maintenance ICS. This study aimed to evaluate the cost-effectiveness of as-needed combination low-dose budesonide-formoterol compared to short-acting β2-agonist (SABA) reliever therapy in patients with mild asthma.
A probabilistic Markov model was created to estimate the cost and quality-adjusted life-years (QALYs) of patients with mild asthma in Colombia. Total costs and QALYs of low-dose budesonide-formoterol compared to short-acting β2-agonist (SABA) were calculated over a lifetime horizon. Multiple sensitivity analyses were conducted. Cost-effectiveness was evaluated at a willingness-to-pay value of $19,000.
The model suggests a potential gain of 0.37 QALYs and per patient per year on as-needed ICS-formoterol and a reduction in the discounted cost per person-year, of as-needed ICS-formoterol to maintenance ICS, of US$40. This position of dominance of as-needed ICS-formoterol negates the need to calculate an incremental cost-effectiveness ratio. In the deterministic and probabilistic sensitivity analysis, our base-case results were robust to variations in all assumptions and parameters.
Low-dose budesonide-formoterol as a reliever was cost-effective when added to usual care in patients with mild asthma. Our study provides evidence that should be used by decision-makers to improve clinical practice guidelines and should be replicated to validate their results in other middle-income countries.
最近的哮喘指南,如全球哮喘倡议(GINA),建议在成年患者中按需使用吸入皮质类固醇(ICS)-福莫特罗作为轻度至中度持续性哮喘维持 ICS 的替代方案。这些建议的引入引发了一个问题,即按需使用布地奈德-福莫特罗是否比维持 ICS 更具成本效益。本研究旨在评估按需使用低剂量布地奈德-福莫特罗与短效 β2-激动剂(SABA)缓解治疗在轻度哮喘患者中的成本效益。
创建了一个概率马尔可夫模型,以评估哥伦比亚轻度哮喘患者的成本和质量调整生命年(QALYs)。在终生范围内计算了低剂量布地奈德-福莫特罗与短效 β2-激动剂(SABA)相比的总成本和 QALYs。进行了多次敏感性分析。以 19000 美元的意愿支付价值评估成本效益。
该模型表明,按需使用 ICS-福莫特罗可能会获得 0.37 个 QALYs 和每个患者每年的收益,并且降低了按需使用 ICS-福莫特罗相对于维持 ICS 的患者每年的折扣成本,为 40 美元。这种按需 ICS-福莫特罗的优势地位否定了计算增量成本效益比的必要性。在确定性和概率敏感性分析中,我们的基本情况结果对所有假设和参数的变化都具有稳健性。
在轻度哮喘患者中,将低剂量布地奈德-福莫特罗作为缓解药物添加到常规护理中是具有成本效益的。我们的研究提供了证据,决策者应该利用这些证据来改善临床实践指南,并在其他中等收入国家进行复制以验证其结果。