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精神药物治疗参考范围:系统评价方案

Therapeutic Reference Ranges for Psychotropic Drugs: A Protocol for Systematic Reviews.

作者信息

Hart Xenia M, Eichentopf Luzie, Lense Xenija, Riemer Thomas, Wesner Katja, Hiemke Christoph, Gründer Gerhard

机构信息

Department of Molecular Neuroimaging, Medical Faculty Mannheim, Central Institute of Mental Health, Heidelberg University, Mannheim, Germany.

Berlin Institute of Health, Institute of Clinical Pharmacology and Toxicology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.

出版信息

Front Psychiatry. 2021 Nov 24;12:787043. doi: 10.3389/fpsyt.2021.787043. eCollection 2021.

Abstract

For many psychotropic drugs, monitoring of drug concentrations in the blood (Therapeutic Drug Monitoring; TDM) has been proven useful to individualize treatments and optimize drug effects. Clinicians hereby compare individual drug concentrations to population-based reference ranges for a titration of prescribed doses. Thus, established reference ranges are pre-requisite for TDM. For psychotropic drugs, guideline-based ranges are mostly expert recommendations derived from a conglomerate of cohort and cross-sectional studies. A systematic approach for identifying therapeutic reference ranges has not been published yet. This paper describes how to search, evaluate and grade the available literature and validate published therapeutic reference ranges for psychotropic drugs. Following PRISMA guidelines, relevant databases have to be systematically searched using search terms for the specific psychotropic drug, blood concentrations, drug monitoring, positron emission tomography (PET) and single photon emission computed tomography (SPECT). The search should be restricted to humans, and diagnoses should be pre-specified. Therapeutic references ranges will not only base upon studies that report blood concentrations in relation to clinical effects, but will also include implications from neuroimaging studies on target engagement. Furthermore, studies reporting concentrations in representative patient populations are used to support identified ranges. Each range will be assigned a level of underlying evidence according to a systematic grading system. Following this protocol allows a comprehensive overview of TDM literature that supports a certain reference range for a psychotropic drug. The assigned level of evidence reflects the validity of a reported range rather than experts' opinions.

摘要

对于许多精神药物而言,监测血液中的药物浓度(治疗药物监测;TDM)已被证明有助于实现个体化治疗并优化药物疗效。临床医生据此将个体药物浓度与基于人群的参考范围进行比较,以滴定规定剂量。因此,既定的参考范围是TDM的先决条件。对于精神药物,基于指南的范围大多是来自队列研究和横断面研究汇总的专家建议。尚未发表一种确定治疗参考范围的系统方法。本文描述了如何搜索、评估和分级现有文献,并验证已发表的精神药物治疗参考范围。遵循PRISMA指南,必须使用针对特定精神药物、血药浓度、药物监测、正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)的搜索词,系统地搜索相关数据库。搜索应限于人类,并预先指定诊断。治疗参考范围不仅将基于报告血药浓度与临床疗效关系的研究,还将包括神经影像学研究对靶点结合的影响。此外,报告代表性患者群体中浓度的研究用于支持确定的范围。每个范围将根据系统分级系统被赋予一定水平的基础证据。遵循该方案可以全面概述支持某种精神药物参考范围的TDM文献。所赋予的证据水平反映的是报告范围的有效性,而非专家意见。

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