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一种可能降低复发风险的抗精神病药物逐渐减量方法。

A Method for Tapering Antipsychotic Treatment That May Minimize the Risk of Relapse.

机构信息

Division of Psychiatry, University College London, Maple House, 149 Tottenham Court Road, Fitzrovia, London W1T 7BN, UK.

North East London Foundation Trust. Goodmayes Hospital, 157 Barley Lane, Goodmayes, Ilford IG3 8XJ, UK.

出版信息

Schizophr Bull. 2021 Jul 8;47(4):1116-1129. doi: 10.1093/schbul/sbab017.

Abstract

The process of stopping antipsychotics may be causally related to relapse, potentially linked to neuroadaptations that persist after cessation, including dopaminergic hypersensitivity. Therefore, the risk of relapse on cessation of antipsychotics may be minimized by more gradual tapering. There is converging evidence that suggests that adaptations to antipsychotic exposure can persist for months or years after stopping the medication-from animal studies, observation of tardive dyskinesia in patients, and the clustering of relapses in this time period after the cessation of antipsychotics. Furthermore, PET imaging demonstrates a hyperbolic relationship between doses of antipsychotic and D2 receptor blockade. We, therefore, suggest that when antipsychotics are reduced, it should be done gradually (over months or years) and in a hyperbolic manner (to reduce D2 blockade "evenly"): ie, reducing by one quarter (or one half) of the most recent dose of antipsychotic, equivalent approximately to a reduction of 5 (or 10) percentage points of its D2 blockade, sequentially (so that reductions become smaller and smaller in size as total dose decreases), at intervals of 3-6 months, titrated to individual tolerance. Some patients may prefer to taper at 10% or less of their most recent dose each month. This process might allow underlying adaptations time to resolve, possibly reducing the risk of relapse on discontinuation. Final doses before complete cessation may need to be as small as 1/40th a therapeutic dose to prevent a large decrease in D2 blockade when stopped. This proposal should be tested in randomized controlled trials.

摘要

抗精神病药物停药过程可能与复发有关,这可能与停药后持续存在的神经适应有关,包括多巴胺能超敏。因此,通过更缓慢地逐渐减少剂量,可以最大限度地降低抗精神病药物停药后复发的风险。越来越多的证据表明,抗精神病药物暴露后的适应可以在停药后数月或数年持续存在——从动物研究、观察患者迟发性运动障碍以及停药后这段时间复发的聚集情况中可以看出。此外,正电子发射断层扫描(PET)成像显示抗精神病药物剂量与 D2 受体阻断之间呈双曲线关系。因此,我们建议在减少抗精神病药物时,应逐渐进行(数月或数年),且呈双曲线方式(以“均匀”减少 D2 阻断):即,将最近一次抗精神病药物剂量减少四分之一(或一半),相当于其 D2 阻断减少约 5(或 10)个百分点,依次进行(因此随着总剂量的减少,减少量会越来越小),间隔 3-6 个月,根据个体耐受情况进行滴定。一些患者可能更喜欢每月以最近剂量的 10%或更少的速度逐渐减少。这一过程可能使潜在的适应有时间得到解决,从而可能降低停药后复发的风险。在完全停药之前,最终剂量可能需要低至治疗剂量的 1/40,以防止停药时 D2 阻断发生较大下降。这一建议应在随机对照试验中进行检验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2dd/8266572/01c4d6227409/sbab017f0001.jpg

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