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5-羟色胺再摄取抑制剂的直接成本、成本效益及相关药物不良反应比较

A comparison of the direct costs and cost effectiveness of serotonin reuptake inhibitors and associated adverse drug reactions.

作者信息

Sullivan Patrick W, Valuck Robert, Saseen Joseph, MacFall Holly M

机构信息

Pharmaceutical Outcomes Research Program, Department of Clinical Pharmacy, School of Pharmacy, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.

出版信息

CNS Drugs. 2004;18(13):911-32. doi: 10.2165/00023210-200418130-00006.

Abstract

BACKGROUND

The economic burden of depression is known to be high and was estimated to be USD 83.1 billion in 2000. Serotonin reuptake inhibitors (SRIs), including both selective serotonin reuptake inhibitors (SSRIs) and serotonin norepinephrine reuptake inhibitors (SNRIs), have a superior adverse effect and safety profile relative to traditional agents (e.g. TCAs), and as a result have demonstrated superior cost effectiveness. Although efficacy across the SRIs is similar, the incidence of adverse drug reactions (ADRs) within SRIs remains significant and varies by agent. Patients who experience ADRs from SRIs may seek medical care, require additional treatment, and even discontinue treatment altogether, leading to increased utilisation and cost of therapy.

OBJECTIVE

This study estimates the direct cost and cost effectiveness, taking into account the impact of treatment-related ADRs, of eight currently marketed SRIs (citalopram, escitalopram, generic fluoxetine, paroxetine, paroxetine controlled release [CR], sertraline, venlafaxine and venlafaxine extended release [XR]) used as initial treatment for depression.

METHODS

A decision analytic model with a 6-month treatment goal was used to estimate the direct cost and cost effectiveness of treatment from the managed care/payer perspective. Estimates of SRI-related ADRs, associated treatments and costs were derived from the US FDA-approved prescribing information and published literature. Efficacy was assumed to be similar across all SRIs. Effectiveness was measured using quality-adjusted life years (QALY) based on EuroQol EQ-5D scores derived from the 2000 Medical Expenditure Panel Survey (MEPS). Censored least absolute deviations (CLAD) regression analysis was used to derive age-adjusted estimates of utility for all health states. Univariate and Bayesian second-order multivariate probabilistic sensitivity analyses were conducted to examine the impact of uncertainty in the parameter estimates.

RESULTS

The expected direct cost and cost effectiveness of treatment from least to most expensive were: escitalopram (USD 3891; 0.341), citalopram (USD 3938; 0.340), generic fluoxetine (USD 4034; 0.335), venlafaxine XR (USD 4226; 0.336), sertraline (USD 4250; 0.335), generic paroxetine (USD 4385; 0.332), paroxetine CR (USD 4440; 0.332) and venlafaxine (USD 4613; 0.326). Monte Carlo simulation results suggested that escitalopram was the most likely (77%) to be cost effective for a willingness to pay < or = USD 50,000 per QALY, followed by citalopram (22%), generic fluoxetine (0.3%) and all other SRIs (0%). Sensitivity analyses indicated that the results of the study were robust to the assumptions underpinning the model.

CONCLUSIONS

SRI-related ADRs have a significant impact on the direct cost and cost effectiveness of treatment. Escitalopram, with the lowest ADR rate of the SRIs, had the lowest expected treatment cost and greatest effectiveness when compared with citalopram, generic fluoxetine, generic paroxetine, paroxetine CR, sertraline, venlafaxine and venlafaxine XR.

摘要

背景

抑郁症的经济负担已知很高,2000年估计为831亿美元。血清素再摄取抑制剂(SRI),包括选择性血清素再摄取抑制剂(SSRI)和血清素去甲肾上腺素再摄取抑制剂(SNRI),相对于传统药物(如三环类抗抑郁药)具有更好的不良反应和安全性,因此已证明具有更高的成本效益。尽管所有SRI的疗效相似,但SRI内部药物不良反应(ADR)的发生率仍然很高,并且因药物而异。经历SRI相关ADR的患者可能会寻求医疗护理、需要额外治疗,甚至完全停止治疗,从而导致治疗利用率和成本增加。

目的

本研究估计了目前上市的八种SRI(西酞普兰、艾司西酞普兰、通用型氟西汀、帕罗西汀、帕罗西汀控释片[CR]、舍曲林、文拉法辛和文拉法辛缓释片[XR])作为抑郁症初始治疗的直接成本和成本效益,同时考虑了治疗相关ADR的影响。

方法

使用一个设定6个月治疗目标的决策分析模型,从管理式医疗/付款人的角度估计治疗的直接成本和成本效益。SRI相关ADR、相关治疗和成本的估计值来自美国食品药品监督管理局(FDA)批准的处方信息和已发表的文献。假设所有SRI的疗效相似。使用基于2000年医疗支出面板调查(MEPS)得出的欧洲五维健康量表(EuroQol EQ-5D)评分的质量调整生命年(QALY)来衡量有效性。使用删失最小绝对偏差(CLAD)回归分析得出所有健康状态的年龄调整效用估计值。进行单变量和贝叶斯二阶多变量概率敏感性分析,以检验参数估计中不确定性的影响。

结果

从最便宜到最昂贵的治疗预期直接成本和成本效益依次为:艾司西酞普兰(3891美元;0.341)、西酞普兰(3938美元;0.340)、通用型氟西汀(4034美元;0.335)、文拉法辛缓释片(4226美元;0.336)、舍曲林(4250美元;0.335)、通用型帕罗西汀(4385美元;0.33)、帕罗西汀控释片(4440美元;0.332)和文拉法辛(4613美元;0.326)。蒙特卡罗模拟结果表明,对于每QALY支付意愿≤50000美元的情况,艾司西酞普兰最有可能具有成本效益(77%),其次是西酞普兰(22%)、通用型氟西汀(0.3%)和所有其他SRI(0%)。敏感性分析表明,该研究结果对模型所依据的假设具有稳健性。

结论

SRI相关ADR对治疗的直接成本和成本效益有重大影响。与西酞普兰、通用型氟西汀、通用型帕罗西汀、帕罗西汀控释片、舍曲林、文拉法辛和文拉法辛缓释片相比,艾司西酞普兰的ADR发生率最低,预期治疗成本最低,有效性最高。

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