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从共付额改为 coinsurance 对药物使用和支出的影响

Effect on drug utilization and expenditures of a cost-share change from copayment to coinsurance.

作者信息

Klepser Donald G, Huether Jeffrey R, Handke Lee J, Williams Clint E

机构信息

Department of Pharmacy Practice, University of Nebraska Medical Center College of Pharmacy, Omaha 68198-6045, USA.

出版信息

J Manag Care Pharm. 2007 Nov-Dec;13(9):765-77. doi: 10.18553/jmcp.2007.13.9.765.

Abstract

BACKGROUND

While increases in prescription drug spending have moderated in recent years, drug spending is still a concern among managed care organizations and health plan administrators. In order to minimize cost increases from year to year, many health care plans have shifted more of the cost of medications to the member-consumer. Coinsurance, a benefit design in which the patient pays a percentage of the cost of the medication, is garnering more attention as a type of cost-sharing that differs from the traditional copayment model.

OBJECTIVE

To estimate the impact on medication expenditures and utilization of a pharmacy benefit design change from 3-tier copayment to coinsurance.

METHODS

Drug expenditures and utilization of beneficiaries aged >or =18 years and continuously enrolled in 2 privately insured groups were compared before and after a benefit design change in 1 of the groups. For the 12 months before the benefit design change, both groups had a 3-tier, fixed-dollar copayment structure with identical cost-sharing per 30-day supply: $10 tier-1 copayment for generic drugs, $25 tier-2 copayment for preferred brand drugs, and $40 tier-3 copayment for non-preferred brand drugs. On September 1, 2005, a 4-tier coinsurance benefit design (25% for all tiers except tier-3 [non-preferred] drugs at 50%, with minimum and maximum patient out-of-pocket [OOP] cost applied to each tier) was implemented in the intervention group (N = 46,311). The 3-tier copayment design was maintained in the comparison group (N = 7,916). A difference-in-difference analysis was used to estimate the effect of the benefit design change on expenditures and utilization, overall (for all prescription drugs), and for 3 classes of essential medications: antihypertensives, antidepressants, and statins. Analyses measured changes in outcomes from 6 months pre-change (October 1, 2004, through March 31, 2005) through 6 months post-change (October 1, 2005, through March 31, 2006). In the overall (all drug) analyses, per member per month (PMPM) outcome measures were total pharmacy claims and cost, beneficiary (patient OOP) cost, and employer (plan sponsor) cost. Analyses of the 3 essential drug classes were limited to members with at least 1 claim in the drug class in both the pre-change and post-change periods (N = 11,917, intervention group; 1,792, comparison group), and assessed per patient per month (PPPM) days supply, beneficiary cost, employer cost, and total cost.

RESULTS

Beneficiaries in the intervention group paid 31.8% of total pharmacy benefit cost at the point of care versus 31.5% in the comparison group in the post-change period. The increases in beneficiary cost from the pre-change period to the post-change period were not significantly different for the intervention (7.5%) and comparison (3.0%) groups (P = 0.983). From the pre-change period to the post-change period, total spending per member increased $4.57 PMPM (6.3%), from $72.29 to $76.87 in the intervention group versus a $5.87 PMPM increase (9.5%), from $61.54 to $67.41, in the comparison group, a relative difference of $1.30 PMPM (P = 0.013). The increases in utilization from the pre-change period to the post-change period were not significantly different in the intervention group (2.4%) versus the comparison group (4.6%, P = 0.189). Utilization per patient in the 3 essential drug classes increased 4.1% (1.59 days PPPM) in the intervention group versus 9.0% (3.23 days PPPM) in the comparison group (P = 0.004). Total expenditures in the 3 classes for the intervention and comparison groups increased 8.2% ($5.07 PPPM) and 13.3% ($7.80 PPPM), respectively, a difference of $2.73 PPPM (P = 0.003). Beneficiary cost for all 3 drug classes increased $2.20 PPPM (9.2%) in the intervention group versus $2.12 PPPM (9.1%) in the comparison group (P = 0.032). The increases in employer cost for the 3 essential drug classes in the intervention group (7.5%, $2.86 PPPM) and comparison group (16.1%, $5.67 PPPM) did not significantly differ (P = 0.057).

CONCLUSIONS

A pharmacy benefit design change from tiered copayment to tiered coinsurance, without a significant increase in beneficiary OOP costs, was associated with a lower rate of increase in total pharmacy benefit cost and no significant reduction in utilization. For utilizers in 3 essential drug classes, drug utilization and total spending increased in the coinsurance group but at a lower rate of increase compared with the copayment group. The coinsurance design provides another approach for controlling prescription utilization and spending for certain medication classes.

摘要

背景

尽管近年来处方药支出的增长有所缓和,但药品支出仍是管理式医疗组织和健康计划管理者关注的问题。为了尽量减少逐年的成本增加,许多医疗保健计划已将更多的药品成本转嫁给会员消费者。共付保险是一种福利设计,患者需支付一定比例的药费,作为一种不同于传统自付费用模式的成本分摊方式,正受到越来越多的关注。

目的

评估药房福利设计从三级自付费用改为共付保险对药物支出和使用的影响。

方法

比较了年龄≥18岁且持续参保于两个私人保险组的受益人的药物支出和使用情况,其中一组进行了福利设计变更。在福利设计变更前的12个月里,两组都采用三级固定金额自付费用结构,每30天供应量的费用分摊相同:一级仿制药自付10美元,二级优选品牌药自付25美元,三级非优选品牌药自付40美元。2005年9月1日,干预组(N = 46,311)实施了四级共付保险福利设计(除三级[非优选]药物为50%外,其他各级均为25%,且对各级设定了患者自付费用的最低和最高限额)。对照组(N = 7,916)维持三级自付费用设计。采用差异分析来估计福利设计变更对支出和使用的影响,总体上(针对所有处方药)以及三类基本药物:抗高血压药、抗抑郁药和他汀类药物。分析测量了从变更前6个月(2004年10月1日至2005年3月31日)到变更后6个月(2005年10月1日至2006年3月31日)的结果变化。在总体(所有药物)分析中,每月每位成员(PMPM)的结果指标包括药房总索赔和成本、受益人(患者自付)成本以及雇主(计划赞助商)成本。对三类基本药物的分析仅限于在变更前和变更后期间至少有一次该类药物索赔的成员(干预组N = 11,917;对照组1,792),并评估每月每位患者(PPPM)的供应天数、受益人成本、雇主成本和总成本。

结果

变更后期间,干预组受益人在就医时支付了药房福利总成本 的31.8%,而对照组为31.5%。干预组(7.5%)和对照组(3.0%)从变更前到变更后期间受益人的成本增加无显著差异(P = 0.983)。从变更前到变更后期间,干预组每位成员的总支出每月增加4.57美元(6.3%),从72.29美元增至76.87美元,而对照组每月增加5.87美元(9.5%),从61.54美元增至67.41美元,相对差异为每月1.30美元(P = 0.013)。从变更前到变更后期间,干预组(2.4%)与对照组(4.6%)的使用增加无显著差异(P = 0.189)。干预组三类基本药物的每位患者使用量增加了4.1%(每月1.59天PPPM),而对照组增加了9.0%(每月3.23天PPPM)(P = 0.004)。干预组和对照组三类药物的总支出分别增加了8.2%(每月5.07美元PPPM)和13.3%(每月7.80美元PPPM),差异为每月2.73美元(P = 0.003)。干预组所有三类药物的受益人成本每月增加2.20美元(9.2%),而对照组增加2.12美元(9.1%)(P = 0.032)。干预组(7.5%,每月2.86美元PPPM)和对照组(16.1%,每月5.67美元PPPM)三类基本药物的雇主成本增加无显著差异(P = 0.057)。

结论

药房福利设计从分级自付费用改为分级共付保险,在受益人自付成本无显著增加的情况下,与药房福利总成本较低的增长率相关,且使用量无显著减少。对于三类基本药物的使用者,共付保险组的药物使用和总支出增加,但与自付费用组相比增长率较低。共付保险设计为控制某些药物类别的处方使用和支出提供了另一种方法。

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