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系统阿片类药物处方模式与脊髓刺激疗法起始患者的总医疗费用:一项回顾性分析。

Systemic Opioid Prescribing Patterns and Total Cost of Care in Patients Initiating Spinal Cord Stimulation Therapy: A Retrospective Analysis.

机构信息

Spectrum Medical, Danville, Virginia.

Northwest Pain Care, Inc. Spokane, Washington.

出版信息

Pain Med. 2021 Apr 20;22(4):784-799. doi: 10.1093/pm/pnab033.

Abstract

BACKGROUND

Few studies have evaluated patterns of systemic opioid use among patients initiating spinal cord stimulation therapy for chronic pain. This study evaluated systemic opioid discontinuation and/or dose reduction and total health care cost after the start of spinal cord stimulation therapy.

METHODS

Using a commercial insurance claims database (2008-2017), we analyzed opioid utilization patterns in patients initiating spinal cord stimulation therapy over a 1-year baseline and 2-year follow-up. The primary end point was defined as either discontinuation (≥365-day gap between prescription fills or total days' supply in follow-up ≤30 days) or ≥50% reduction in average daily morphine milligram equivalent dose. "Costs" were defined as total payer plus patient out-of-pocket payments.

RESULTS

A total of 5,878 patients met the selection criteria. Of these, 152 (2.6%) showed no opioid prescription data at any point in the study period. Among patients with one or more prescriptions, 42.0% met the primary end point (22.0% discontinued, and 20.0% reduced their dose by 50% or more). Mean total adjusted costs were significantly reduced in years 1 and 2 of follow-up relative to baseline (excluding device insertion costs). The average time to breakeven when accounting for device trial and permanent insertion cost was 3.1 years among those who met the composite end point and 4.2 years among those who did not.

CONCLUSIONS

This analysis shows that among patients who continued spinal cord stimulation therapy for at least 2 years, a significant proportion were able to reduce and/or discontinue systemic opioid use, with costs after the start of therapy significantly reduced relative to baseline.

摘要

背景

很少有研究评估慢性疼痛患者开始脊髓刺激治疗后全身阿片类药物使用的模式。本研究评估了开始脊髓刺激治疗后阿片类药物停药和/或剂量减少以及总医疗保健费用。

方法

使用商业保险索赔数据库(2008-2017 年),我们分析了在 1 年基线和 2 年随访期间开始脊髓刺激治疗的患者的阿片类药物使用模式。主要终点定义为停药(处方之间的间隔≥365 天或随访期间的总天供应量≤30 天)或平均每日吗啡毫克当量剂量减少≥50%。“成本”定义为总付款加患者自付费用。

结果

共有 5878 名患者符合入选标准。其中,152 名(2.6%)在研究期间的任何时候都没有阿片类药物处方数据。在有一个或多个处方的患者中,42.0%达到主要终点(22.0%停药,20.0%剂量减少 50%或更多)。与基线相比,随访第 1 年和第 2 年的总调整后成本显著降低(不包括设备插入成本)。考虑设备试验和永久插入成本时,达到复合终点的患者的盈亏平衡平均时间为 3.1 年,而未达到复合终点的患者的盈亏平衡平均时间为 4.2 年。

结论

这项分析表明,在至少继续接受脊髓刺激治疗 2 年的患者中,相当一部分患者能够减少和/或停止使用全身阿片类药物,治疗开始后的成本与基线相比显著降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d25/8058769/882ce5fdffed/pnab033f1.jpg

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