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文拉法辛缓释胶囊与度洛西汀治疗首发抑郁症患者的对照研究

Cost-effectiveness of vortioxetine compared with levomilnacipran and vilazodone in patients with major depressive disorder switching from an initial antidepressant.

机构信息

Lundbeck SAS, Issy-les-Moulineaux , Paris, France.

Follow the Molecule: CNS Consulting LLC , Marina del Rey, CA, USA.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2021 Feb;21(1):29-42. doi: 10.1080/14737167.2021.1855979. Epub 2021 Jan 17.

Abstract

Many patients with major depressive disorder (MDD) do not achieve remission with their first antidepressant (AD), resulting in a high burden due to treatment failure. Vortioxetine is a valid treatment option for patients with MDD only partially responding to their first AD. Characterization of vortioxetine's potential benefits versus other approved treatments is important. The cost-effectiveness of vortioxetine, including cognitive outcomes, was modeled in comparison with levomilnacipran and vilazodone for patients switched to these medications after inadequate responses to a first AD. Vortioxetine was associated with incremental quality-adjusted life-year (QALY) gains versus levomilnacipran (0.008) or vilazodone (0.009). Vortioxetine was dominant versus levomilnacipran and cost-effective versus vilazodone (incremental cost-effectiveness ratio [ICER],33,829 USD/QALY). In sensitivity analyses using residual cognitive dysfunction rates (vortioxetine, 49%; levomilnacipran, 58%, and vilazodone, 64%), incremental QALY gains for vortioxetine versus levomilnacipran (0.0085) or vilazodone (0.0109) were found. Vortioxetine remained dominant versus levomilnacipran and cost-effective versus vilazodone (ICER, 27,633 USD/QALY). ICER reduction was found with cognition outcomes inclusion. This model provides additional support for considering vortioxetine for patients requiring a switch of MDD treatments, although its conclusions are limited by the data available for inclusion. Additional research and real-world trials are needed to confirm the findings.

摘要

许多患有重度抑郁症(MDD)的患者首次使用抗抑郁药(AD)后并未达到缓解,导致因治疗失败而负担沉重。文拉法辛只有部分应答的 MDD 患者,维拉唑酮是一种有效的治疗选择。与其他已批准的治疗方法相比,文拉法辛的潜在益处的特征很重要。对于因首次 AD 治疗反应不足而改用这些药物的患者,文拉法辛的成本效益(包括认知结果)与左米那普仑和维拉佐酮进行了建模比较。与左米那普仑(0.008)或维拉佐酮(0.009)相比,文拉法辛与增量质量调整生命年(QALY)获益相关。与左米那普仑相比,文拉法辛具有优势,且比维拉佐酮具有成本效益(增量成本效益比[ICER],33829 美元/QALY)。在使用残余认知功能障碍率(文拉法辛 49%;左米那普仑 58%和维拉佐酮 64%)进行敏感性分析时,文拉法辛与左米那普仑(0.0085)或维拉佐酮(0.0109)相比,增量 QALY 获益。与左米那普仑相比,文拉法辛具有优势,且比维拉佐酮具有成本效益(ICER,27633 美元/QALY)。纳入认知结果可降低 ICER。该模型为需要转换 MDD 治疗的患者考虑文拉法辛提供了额外的支持,尽管其结论受到纳入数据的限制。需要进一步的研究和真实世界的试验来证实这些发现。

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