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美国摇头丸辅助疗法治疗创伤后应激障碍的最新成本效益:一项3期试验的结果

Updated cost-effectiveness of MDMA-assisted therapy for the treatment of posttraumatic stress disorder in the United States: Findings from a phase 3 trial.

作者信息

Marseille Elliot, Mitchell Jennifer M, Kahn James G

机构信息

Global Initiative for Psychedelic Science Economics, University of California, Berkeley, CA, United States of America.

Department of Neurology, University of California, San Francisco, San Francisco, CA, United States of America.

出版信息

PLoS One. 2022 Feb 25;17(2):e0263252. doi: 10.1371/journal.pone.0263252. eCollection 2022.

Abstract

BACKGROUND

Severe posttraumatic stress disorder (PTSD) is a prevalent and debilitating condition in the United States. and globally. Using pooled efficacy data from six phase 2 trials, therapy using 3,4-methylenedioxymethamphetamine (MDMA) appeared cost-saving from a payer's perspective. This study updates the cost-effectiveness analysis of this novel therapy using data from a new phase 3 trial, including the incremental cost-effectiveness of the more intensive phase 3 regimen compared with the shorter phase 2 regimen.

METHODS

We adapted a previously-published Markov model to portray the costs and health benefits of providing MDMA-assisted therapy (MDMA-AT) to patients with chronic, severe, or extreme PTSD in a recent phase 3 trial, compared with standard care. Inputs were based on trial results and published literature. The trial treated 90 patients with a clinician administered PTSD scale (CAPS-5) total severity score of 35 or greater at baseline, and duration of PTSD symptoms of 6 months or longer. The primary outcome was assessed 8 weeks after the final experimental session. Patients received three 90-minute preparatory psychotherapy sessions, three 8-hour active MDMA or placebo sessions, and nine 90-minute integrative psychotherapy sessions. Our model calculates the per-patient cost of MDMA-AT, net all-cause medical costs, mortality, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratios (ICERs). We reported results from the U.S. health care payer's perspective for multiple analytic time horizons, (base-case is 30 years), and conducted extensive sensitivity analyses. Costs and QALYs were discounted by 3% annually. Costs were adjusted to 2020 U.S. dollars according to the medical component of the U.S. Bureau of Labor Statistics' Consumer Price Index (CPI).

RESULTS

MDMA-AT as conducted in the phase 3 trial costs $11,537 per patient. Compared to standard of care for 1,000 patients, MDMA-AT generates discounted net health care savings of $132.9 million over 30 years, accruing 4,856 QALYs, and averting 61.4 premature deaths. MDMA-AT breaks even on cost at 3.8 years while delivering 887 QALYs. A third MDMA session generates additional medical savings and health benefits compared with a two-session regimen. Hypothetically assuming no savings in health care costs, MDMA-AT has an ICER of $2,384 per QALY gained.

CONCLUSIONS

MDMA-AT provided to patients with severe or extreme chronic PTSD is cost-saving from a payer's perspective, while delivering substantial clinical benefit.

摘要

背景

严重创伤后应激障碍(PTSD)在美国乃至全球都是一种普遍且使人衰弱的病症。利用六项2期试验的汇总疗效数据,从支付方的角度来看,使用3,4-亚甲基二氧甲基苯丙胺(摇头丸)进行治疗似乎具有成本效益。本研究使用一项新的3期试验的数据更新了这种新型疗法的成本效益分析,包括与较短的2期治疗方案相比,更强化的3期治疗方案的增量成本效益。

方法

我们采用了先前发表的马尔可夫模型,来描绘在最近一项3期试验中为慢性、严重或极端PTSD患者提供摇头丸辅助治疗(MDMA-AT)与标准治疗相比的成本和健康效益。输入数据基于试验结果和已发表的文献。该试验治疗了90名患者,这些患者在基线时临床医生评定的PTSD量表(CAPS-5)总严重程度评分达到35或更高,且PTSD症状持续时间为6个月或更长。主要结局在最后一次实验疗程后8周进行评估。患者接受了三次90分钟的预备心理治疗疗程、三次8小时的活性摇头丸或安慰剂疗程,以及九次90分钟的综合心理治疗疗程。我们的模型计算了MDMA-AT的人均成本、全因医疗成本净额、死亡率、质量调整生命年(QALY)以及增量成本效益比(ICER)。我们从美国医疗保健支付方的角度报告了多个分析时间范围(基本情况为30年)的结果,并进行了广泛的敏感性分析。成本和QALY每年按3%进行贴现。根据美国劳工统计局消费者价格指数(CPI)的医疗组成部分,将成本调整为2020年的美元价值。

结果

3期试验中实施的MDMA-AT每位患者成本为11,537美元。与1000名患者的标准治疗相比,MDMA-AT在30年内产生贴现后的医疗保健净节省1.329亿美元,获得4856个QALY,并避免61.4例过早死亡。MDMA-AT在3.8年时成本收支平衡,同时产生887个QALY。与两疗程方案相比,第三个摇头丸疗程可带来额外的医疗节省和健康效益。假设医疗保健成本没有节省,MDMA-AT每获得一个QALY的ICER为2384美元。

结论

从支付方的角度来看,为严重或极端慢性PTSD患者提供MDMA-AT具有成本效益,同时带来显著的临床益处。

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