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比较青光眼和高眼压症中前列腺素类似物治疗模式。

Comparison of Prostaglandin Analog Treatment Patterns in Glaucoma and Ocular Hypertension.

机构信息

Health Outcomes Division, College of Pharmacy, The University of Texas at Austin, and Genesis Research, Hoboken, New Jersey.

Health Outcomes Division, College of Pharmacy, The University of Texas at Austin.

出版信息

J Manag Care Spec Pharm. 2019 Sep;25(9):1001-1010. doi: 10.18553/jmcp.2019.25.9.1001.

Abstract

BACKGROUND

Prostaglandin analogs (PGAs) are considered an initial therapy to manage increased intraocular pressure (IOP) for patients with glaucoma. When the initial PGA treatment fails to lower IOP adequately, the patient may add or change medications or have surgery/laser treatment.

OBJECTIVE

To compare medication adherence, duration of therapy, and treatment patterns among 3 PGAs-latanoprost, travoprost, and bimatoprost-as initial therapies for patients with glaucoma or ocular hypertension.

METHODS

This was a retrospective cohort study using administrative claims data. The cohort consisted of patients newly diagnosed with glaucoma or ocular hypertension with at least 1 prescription claim for latanoprost, travoprost, or bimatoprost and enrolled in a Medicare Advantage plan between 2007 and 2012. The 24-month medication possession ratio (MPR) was used to measure medication adherence. Discontinuation of first-line PGA therapy was defined as nonpersistence (90-day gap allowance) of the index PGA or a change in therapy during the 24-month follow-up period. Types of second-line therapy (i.e., switch, addition, and surgery) were identified. The 1:1:1 propensity score matching was used.

RESULTS

Patients who met the inclusion criteria were propensity score matched, resulting in 1,296 patients per PGA group. Latanoprost users showed higher adherence (50.1%) than travoprost (48.8%) and bimatoprost (43.0%) users. The latanoprost and travoprost groups had significantly higher MPRs than bimatoprost ( < 0.0001). The latanoprost group showed significantly longer duration of first-line therapy (372 days) than the bimatoprost group (343 days; = 0.003) but not the travoprost group (361 days). After controlling for demographic and clinical characteristics, a Cox proportional hazards model showed that the travoprost and bimatoprost groups had a higher risk of discontinuation of first-line therapy than the latanoprost group ( < 0.0001). The percentage of patients continuing on the index PGA without treatment pattern change (i.e., switches, additions, and surgery) was higher for latanoprost users (52.9%) compared with travoprost (39.0%) or bimatoprost users (42.1%; < 0.001).

CONCLUSIONS

Patients who used latanoprost as their initial therapy were more likely to adhere and persist to the index PGA compared with bimatoprost users. The latanoprost group demonstrated a lower risk of discontinuing first-line therapy than the travoprost and bimatoprost groups. The results may assist ophthalmologists in determining the optimal management of this patient population with respect to treatment patterns.

DISCLOSURES

No outside funding supported this study. All authors except Heo and Nair are employed by The University of Texas at Austin College of Pharmacy. Heo was with the Health Outcomes Division, The University of Texas at Austin College of Pharmacy during a portion of this study and is employed by Genesis Research. Nair is employed by Humana. The authors have no financial relationships relevant to this article to disclose. This study was presented as a poster at the 2016 International Society for Pharmacoeconomics and Outcomes Research Annual Meeting, May 2016, Washington, DC.

摘要

背景

前列腺素类似物(PGAs)被认为是治疗青光眼患者眼压升高的初始疗法。当最初的 PGA 治疗不能充分降低 IOP 时,患者可能会添加或改变药物治疗,或进行手术/激光治疗。

目的

比较三种 PGA(拉坦前列素、曲伏前列素和贝美前列素)作为青光眼或高眼压症初始治疗的药物依从性、治疗持续时间和治疗模式。

方法

这是一项使用行政索赔数据的回顾性队列研究。该队列包括在 2007 年至 2012 年间至少有一次拉坦前列素、曲伏前列素或贝美前列素处方的新诊断为青光眼或高眼压症的患者,并参加了 Medicare Advantage 计划。使用药物占有比例(MPR)24 个月来衡量药物依从性。一线 PGA 治疗的停药定义为指数 PGA 出现 90 天的用药空白期或在 24 个月的随访期间改变治疗方案。确定了二线治疗(即转换、添加和手术)的类型。采用 1:1:1 倾向评分匹配。

结果

符合纳入标准的患者进行了倾向评分匹配,每个 PGA 组匹配了 1296 名患者。拉坦前列素使用者的依从性(50.1%)高于曲伏前列素(48.8%)和贝美前列素(43.0%)使用者。拉坦前列素和曲伏前列素组的 MPR 明显高于贝美前列素(<0.0001)。拉坦前列素组的一线治疗持续时间明显长于贝美前列素组(372 天;=0.003),但与曲伏前列素组无显著差异(361 天)。在控制人口统计学和临床特征后,Cox 比例风险模型显示,曲伏前列素和贝美前列素组比拉坦前列素组停药的风险更高(<0.0001)。继续使用指数 PGA 而不改变治疗模式(即转换、添加和手术)的患者比例,拉坦前列素使用者(52.9%)高于曲伏前列素(39.0%)或贝美前列素(42.1%;<0.001)使用者。

结论

与贝美前列素使用者相比,使用拉坦前列素作为初始治疗的患者更有可能坚持并持续使用指数 PGA。拉坦前列素组与曲伏前列素和贝美前列素组相比,停药的风险较低。研究结果可能有助于眼科医生确定针对这一患者群体的最佳治疗管理模式。

披露

本研究无外部资金支持。除 Heo 和 Nair 外,所有作者均就职于德克萨斯大学奥斯汀分校药学院。Heo 在本研究的一部分时间内就职于德克萨斯大学奥斯汀分校药学院卫生成果司,并受雇于 Genesis Research。Nair 受雇于 Humana。作者与本研究无关的财务关系不相关,本研究以海报形式提交给 2016 年国际药物经济学与结果研究学会年会,2016 年 5 月,华盛顿特区。

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