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首页> 外文期刊>Neuromodulation: journal of the International Neuromodulation Society >The Effect of Sacral Neuromodulation on Anticholinergic Use and Expenditures in a Privately Insured Population
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The Effect of Sacral Neuromodulation on Anticholinergic Use and Expenditures in a Privately Insured Population

机译:of神经调节对私人参保人群抗胆碱能使用和支出的影响

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Objectives: Sacral neuromodulation is Food and Drug Administration approved for many types of voiding dysfunction. Goals of treatment often include cessation of anticholinergic therapy. With the goal of understanding the impact of sacral neuromodulation on anticholinergic use, we analyzed patterns of care using a national claims-based dataset. Materials and Methods: The Ingenix (i3) data base contains insurance claims, including utilization and cost data, for 75 large employers. De-identified patients who underwent sacral neuromodulation between 2002 and 2007 were identified by the unique current procedural terminology-4 procedure code for pulse generator implantation, code 64590. The number and costs of anticholinergic prescriptions were compared before and after treatment. Results: There were 266 percutaneous and 794 two-staged procedures performed from 2002 to 2007 in the i3 dataset. A total of 484 pulse generator implantations were performed, representing 46% of the test procedures. During the year prior to pulse generator placement, each patient purchased an average of 2.1 prescriptions for an anticholinergic agent (SD 3.5). During the year after neuromodulation, each patient purchased an average of 1.0 prescription (SD 2.3, p < 0.0001 by f-test). Prescription charges were $241.31 per patient before and $103.52 after neuromodulation, a statistically significant cost difference (p < 0.0001 by f-test). During the year before the procedure, 50% of patients filled anticholinergic prescriptions. This decreased to 23% after the procedure (p < 0.0001 by chi-square test). Conclusions Sacral neuromodulation was associated with a significant decrease in the use of anticholinergic medication. Cost-effectiveness analyses that take into account patient quality-adjusted life years are needed to determine the true cost-benefit ratio of sacra! neuromodulation.
机译:目的:S神经调节已被美国食品药品监督管理局批准用于多种类型的排尿障碍。治疗的目标通常包括停止抗胆碱能治疗。为了了解of神经调节对抗胆碱能药物使用的影响,我们使用了基于国家索赔的数据集来分析护理模式。资料和方法:Ingenix(i3)数据库包含针对75个大型雇主的保险索赔,包括使用率和成本数据。身份不明的患者在2002年至2007年之间接受神经调节,并通过当前唯一的脉冲发生器植入程序术语4程序代码(代码64590)进行识别。比较了治疗前后的抗胆碱能药物处方的数量和费用。结果:从2002年到2007年,i3数据集中进行了266例经皮和794例两阶段手术。总共进行了484次脉冲发生器植入,占测试程序的46%。在放置脉冲发生器之前的一年中,每位患者平均购买了2.1份抗胆碱能药物处方(SD 3.5)。在神经调节后的一年中,每位患者平均购买了1.0处方(SD 2.3,通过f检验p <0.0001)。处方费用在神经调节之前为每位患者241.31美元,在神经调节后为103.52美元,这是统计学上显着的费用差异(通过f检验,p <0.0001)。在手术前一年中,有50%的患者使用了抗胆碱药处方。手术后降低到23%(卡方检验p <0.0001)。结论S神经调节与抗胆碱能药物的使用显着减少有关。需要进行成本效益分析,并考虑患者质量调整的生命年限,以确定sacra!的真正成本效益比!神经调节。

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