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米氮平相关的运动障碍:文献综述

Mirtazapine-associated movement disorders: A literature review.

作者信息

Rissardo Jamir Pitton, Caprara Ana Leticia Fornari

机构信息

Department of Medicine, Federal University of Santa Maria, Santa Maria, Brazil.

出版信息

Tzu Chi Med J. 2020 Jul 13;32(4):318-330. doi: 10.4103/tcmj.tcmj_13_20. eCollection 2020 Oct-Dec.

DOI:10.4103/tcmj.tcmj_13_20
PMID:33163376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7605300/
Abstract

Mirtazapine (MTZ) is an atypical antidepressant approved by the FDA, which mechanism of action involves the antagonism of alpha-2, H1, 5-HT2A, 5-HT2C, and 5-HT3 receptors. In this context, the aim of this literature review is to evaluate the clinical epidemiological profile, pathological mechanisms, and management of MTZ-associated movement disorders (MDs). Relevant reports of six databases were identified and assessed by two reviewers without language restriction. Fifty-two reports containing 179 cases from 20 countries were assessed. The mean age was 57 year (range, 17-85). The majority of the individuals were female (60%) and of European origin. The mean time from MTZ start to symptom onset was 7.54 days; the time from management to MD improvement was within one week in 82.60% of the individuals. The MDs associated with MTZ were 69 restless legs syndrome (RLS), 35 tremors, 10 akathisia (AKT), 9 periodic limb MD, 6 dystonia, 4 rapid eye movement sleep behavior disorders, 3 dyskinesia, 2 parkinsonism, and 1 tic, and in the group not clearly identified, 18 restlessness, 15 hyperkinesis, and 1 extrapyramidal symptom. In the literature, the majority of the reports lack important information about the neurological examination. The management should be the MTZ withdrawal, except in RLS that other options are possible. In AKT, the MTZ should not be rechallenge, and if available, the prescription of a benzodiazepine may reduce recovery time.

摘要

米氮平(MTZ)是一种经美国食品药品监督管理局(FDA)批准的非典型抗抑郁药,其作用机制涉及对α-2、H1、5-羟色胺2A(5-HT2A)、5-羟色胺2C(5-HT2C)和5-羟色胺3(5-HT3)受体的拮抗作用。在此背景下,本综述的目的是评估米氮平相关运动障碍(MDs)的临床流行病学特征、病理机制及管理。两名评审员对六个数据库的相关报告进行了识别和评估,无语言限制。共评估了来自20个国家的52份报告,包含179例病例。平均年龄为57岁(范围17 - 85岁)。大多数个体为女性(60%),且来自欧洲。从开始服用米氮平到症状出现的平均时间为7.54天;82.60%的个体从开始处理到MD改善的时间在一周内。与米氮平相关的MDs包括69例不安腿综合征(RLS)、35例震颤、10例静坐不能(AKT)、9例周期性肢体运动障碍、6例肌张力障碍、4例快速眼动睡眠行为障碍、3例运动障碍、2例帕金森综合征和1例抽搐,在未明确分类的组中,有18例烦躁不安、15例运动亢进和1例锥体外系症状。在文献中,大多数报告缺乏关于神经学检查的重要信息。处理方法应为停用米氮平,但RLS除外,后者有其他处理选择。对于AKT,不应再次使用米氮平,如有可能,开具苯二氮䓬类药物可缩短恢复时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/e84a89a16bba/TCMJ-32-318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/5c5aa17bb067/TCMJ-32-318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/9b5deb045217/TCMJ-32-318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/178c498867ee/TCMJ-32-318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/e84a89a16bba/TCMJ-32-318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/5c5aa17bb067/TCMJ-32-318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/9b5deb045217/TCMJ-32-318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/178c498867ee/TCMJ-32-318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448f/7605300/e84a89a16bba/TCMJ-32-318-g004.jpg

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