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Assessment of the Cost Effectiveness of Travoprost versus Latanoprost as Single Agents for Treatment of Glaucoma in France

机译:在法国评估特拉沃前列素与拉坦前列素作为单药治疗青光眼的成本效益

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Background and objective: 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. Methods: 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 mono-therapy. 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 < =20, 21-23 and >=24 mmHg, respectively. All costs were expressed in 2005 euros. Results: MTTC was 44.3 months for travoprost and 37.8 for latanoprost. Additional 5-year costs for travoprost were euvopean dollow51, resulting in an incremental cost-effectiveness ratio without treatment change of euvopean dollow95 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 < =20, 21-23 and >=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 euvopean dollow140, euvopean dollow45 and euvopean dollow123 per year, respectively. Conclusion: 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.
机译:背景与目的:控制眼内压(IOP)是避免与青光眼有关的视力障碍的主要因素。开始这种终生治疗时,应同时考虑治疗的费用和有效性。这项研究的目的是评估在法国,travoprost与latanoprost作为单一药物治疗青光眼的成本效益。方法:使用两项调查,一项记录疗效,另一项成本,为Markov模型提供数据。该模型重现了接受前列腺素类似物,travoprost或latanoprost作为单一疗法的患者的5年病程。有效性标准符合国家研究的威布尔分布。从两个法国观测数据库中提取了转移概率和每个治疗线的成本。采用自举技术来驱动概率敏感性分析。该研究比较了每日两次单药治疗原发性开角型青光眼或高眼压的非卧床患者的两种治疗方法。主要结局指标是平均治疗时间(MTTC)。可能的治疗变化是添加辅助药物,治疗替代,激光治疗或手术。在进行激光治疗或手术后,患者可以不进行任何治疗,也可以继续进行前列腺素类似物的单一治疗或替代治疗。在治疗开始时,眼压分别为<= 20、21-23和> = 24 mmHg。所有费用均以2005欧元表示。结果:travoprost的MTTC为44.3个月,拉坦前列素的MTTC为37.8个月。 travoprost的5年额外费用为戊uv 51,从而导致成本效益比增加,而每年不更改戊change 95的治疗方法。在接受拉坦前列素治疗的患者中,有1.9%接受了激光治疗或外科手术,而接受travoprost治疗的患者为1.2%。结果与基线IOP值不同,治疗前IOP值分别为<= 20、21-23和> = 24 mmHg的患者中,分别有55.6%,53.9%和50.4%的患者在5年时继续接受travoprost治疗分别有32.3%,26.1%和26.1%的患者接受拉坦前列素治疗。因此,在不改变治疗的情况下,每年的成本效益比(ICER)分别为euvopean dollow140,euvopean dollow45和euvopean dollow123。结论:Travoprost与拉坦前列素相比,具有更长的疗效,并能将早期治疗改变降至最低。需要新疗法,激光疗法或手术的患者比例较小,实际上抵消了travoprost的较高获取成本。总体而言,与拉坦前列素相比,travoprost具有更高的成本效益,并且对于IOP在21至23 mmHg之间的患者,其最具有成本效益。

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