Smessaert Sarah, Detraux Johan, Desplenter Franciska, De Hert Marc
University Psychiatric Center Katholieke Universiteit Leuven, Leuvensesteenweg 517, 3070, Kortenberg, Belgium.
Department of Biomedical Sciences, Research Group Psychiatry, University Psychiatric Center KU Leuven, Leuvensesteenweg 517, 3070, Kortenberg, Belgium.
CNS Drugs. 2024 Feb;38(2):105-123. doi: 10.1007/s40263-023-01054-z. Epub 2024 Jan 18.
Despite the evidence that no other antipsychotic is effective as clozapine for the treatment of resistant schizophrenia, it is associated with various metabolic, neuroendocrine, cardiovascular, and gastrointestinal adverse effects. Guidelines aiming to address the monitoring of clozapine's (serious) adverse effects can be helpful to prevent and treat these effects. However, many of these guidelines seem to lack one or more important monitoring recommendations. We aimed to systematically review the content and quality of existing monitoring guidelines/recommendations for clozapine-induced adverse effects.
A comprehensive and systematic literature search, using the MEDLINE, Embase, Web of Science, and Cochrane databases, was conducted for guidelines/recommendations on the monitoring of clozapine-induced adverse events, published between January 2004 and April 2023 (last search 16 April 2023). Only peer-reviewed published guidelines reporting on the comprehensive monitoring of all major clozapine-induced adverse effects and including evidence-based recommendations, developed after the year 2004, were included. Studies reporting on the monitoring of adverse effects of clozapine without being a formal guideline, guidelines reporting on the monitoring of one or a limited number of adverse effects of clozapine, guidelines that were not peer reviewed or published, expert opinion papers without formal consensus guideline development, or guidelines developed before the year 2004, were excluded. The Appraisal of Guidelines for Research and Evaluation II (AGREE-II) tool was used to evaluate the guidelines/recommendations' quality.
Only one guideline met the inclusion criteria. This consensus statement made recommendations for hematological monitoring, and the monitoring of metabolic, cardiac, and three other adverse effects. Highest scores for the qualitative assessment were found for the domains "scope and purpose" (66.7%), "clarity of presentation" (44.4%), and "editorial independence" (66.7%). Lowest scores were found for "rigor of development" (14.6%) and "applicability" (0%).
Future guidelines should develop more comprehensive recommendations about specific clozapine-induced adverse effects, including constipation, myocarditis, tachycardia, and seizures, as well as include a rechallenge policy. There is an urgent need for well-developed, methodologically stringent, guidelines.
PROSPERO registration number, CRD42023402480.
尽管有证据表明,在治疗难治性精神分裂症方面,没有其他抗精神病药物能像氯氮平那样有效,但它会引发各种代谢、神经内分泌、心血管和胃肠道不良反应。旨在解决氯氮平(严重)不良反应监测问题的指南,可能有助于预防和治疗这些不良反应。然而,许多此类指南似乎缺少一项或多项重要的监测建议。我们旨在系统地回顾现有氯氮平所致不良反应监测指南/建议的内容和质量。
利用MEDLINE、Embase、科学引文索引和考克兰数据库,对2004年1月至2023年4月(最后一次检索时间为2023年4月16日)发表的关于氯氮平所致不良事件监测的指南/建议进行全面系统的文献检索。仅纳入2004年后发表的、经同行评审的、报告对氯氮平所有主要不良反应进行全面监测并包含循证建议的指南。排除那些报告氯氮平不良反应监测情况但并非正式指南的研究、报告氯氮平一种或有限几种不良反应监测情况的指南、未经同行评审或发表的指南、没有正式达成共识的指南制定过程的专家意见论文,以及2004年前制定的指南。使用《研究与评价指南评估II》(AGREE-II)工具评估指南/建议的质量。
只有一项指南符合纳入标准。该共识声明就血液学监测以及代谢、心脏和其他三种不良反应的监测提出了建议。在定性评估中,“范围与目的”领域(66.7%)、“表述清晰度”领域(44.4%)和“编辑独立性”领域(66.7%)得分最高。“制定严谨性”领域(14.6%)和“适用性”领域(0%)得分最低。
未来的指南应就氯氮平所致特定不良反应,包括便秘、心肌炎、心动过速和癫痫发作,制定更全面的建议,并纳入重新用药策略。迫切需要制定完善、方法严谨的指南。
国际前瞻性系统评价注册库登记号,CRD42023402480。