Payet Stéphanie, Denis Philippe, Berdeaux Gilles, Launois Robert
Réseau d'Evaluation en Economie de la Santé, Paris, France.
Clin Drug Investig. 2008;28(3):183-98. doi: 10.2165/00044011-200828030-00005.
Control of intraocular pressure (IOP) is a major factor in avoiding visual impairment related to glaucoma. Both the cost and the effectiveness of therapy should be considered when initiating this lifelong treatment. The aim of this study was to assess the cost effectiveness of travoprost versus latanoprost as single agents for the treatment of glaucoma in France.
Two surveys, one documenting efficacy and the other costs, were used to provide data for a Markov model. The model reproduced the 5-year course of patients receiving a prostaglandin analogue, travoprost or latanoprost, as monotherapy. The effectiveness criterion was fitted with a Weibull distribution from a national study. Transition probabilities and costs per treatment line were extracted from two French observational databases. Bootstrap techniques were implemented to drive the probabilistic sensitivity analyses. The study compared both treatments given once daily as monotherapy to ambulatory patients with primary open-angle glaucoma or ocular hypertension. The main outcome measure was mean time to treatment change (MTTC). Possible treatment changes were the addition of adjunctive medication, treatment substitution, laser therapy or surgery. After laser therapy or surgery, patients could continue with no treatment or proceed to prostaglandin analogue as monotherapy or treatment substitution. IOP was stratified at treatment onset as < or =20, 21-23 and > or =24 mmHg, respectively. All costs were expressed in 2005 euros.
MTTC was 44.3 months for travoprost and 37.8 for latanoprost. Additional 5-year costs for travoprost were euro51, resulting in an incremental cost-effectiveness ratio without treatment change of euro95 per year. Of patients treated with latanoprost, 1.9% underwent laser therapy or surgery, compared with 1.2% of patients treated with travoprost. The results differed with baseline IOP values, such that 55.6%, 53.9% and 50.4% of patients with pretreatment IOP values of < or =20, 21-23 and > or =24 mmHg, respectively, continued to receive travoprost treatment at 5 years, compared with 32.3%, 26.1% and 26.1% of patients, respectively, receiving latanoprost. Thus, incremental cost-effectiveness ratios (ICERs) without treatment change were euro140, euro45 and euro123 per year, respectively.
Travoprost demonstrated a longer effectiveness profile than latanoprost and minimized early treatment changes. The smaller proportion of patients needing a new treatment, laser therapy or surgery virtually compensated for the higher travoprost acquisition cost. Overall, travoprost is cost effective compared with latanoprost, and is most cost effective in patients with pretreatment IOPs between 21 and 23 mmHg.
控制眼压(IOP)是避免青光眼相关视力损害的主要因素。在开始这种终身治疗时,应同时考虑治疗的成本和效果。本研究的目的是评估在法国,曲伏前列素与拉坦前列素作为单药治疗青光眼的成本效益。
两项调查,一项记录疗效,另一项记录成本,用于为马尔可夫模型提供数据。该模型再现了接受前列腺素类似物曲伏前列素或拉坦前列素单药治疗的患者的5年病程。有效性标准根据一项全国性研究采用威布尔分布进行拟合。从两个法国观察性数据库中提取每个治疗方案的转移概率和成本。采用自助法进行概率敏感性分析。该研究比较了两种药物作为单药每日一次给药,用于治疗原发性开角型青光眼或高眼压症门诊患者的情况。主要结局指标是治疗改变的平均时间(MTTC)。可能的治疗改变包括加用辅助药物、更换治疗药物、激光治疗或手术。激光治疗或手术后,患者可以继续不进行治疗,或继续使用前列腺素类似物单药治疗或更换治疗药物。治疗开始时眼压分别分层为≤20、21 - 23和≥24 mmHg。所有成本均以2005年欧元表示。
曲伏前列素的MTTC为44.3个月,拉坦前列素为37.8个月。曲伏前列素额外的5年成本为51欧元,导致无治疗改变情况下的增量成本效益比为每年95欧元。接受拉坦前列素治疗的患者中,1.9%接受了激光治疗或手术,而接受曲伏前列素治疗的患者为1.2%。结果因基线眼压值而异,治疗前眼压值≤20、21 - 23和≥24 mmHg的患者中,分别有55.6%、53.9%和50.4%在5年后继续接受曲伏前列素治疗,而接受拉坦前列素治疗的患者分别为32.3%、26.1%和26.1%。因此,无治疗改变情况下的增量成本效益比(ICER)分别为每年140欧元、45欧元和123欧元。
曲伏前列素比拉坦前列素具有更长的有效时间,且早期治疗改变最少。需要新治疗、激光治疗或手术的患者比例较小,几乎弥补了曲伏前列素较高的购置成本。总体而言,与拉坦前列素相比,曲伏前列素具有成本效益,并且在治疗前眼压为21至23 mmHg的患者中成本效益最高。