The time has come for revising the rules of clozapine blood monitoring in Europe. A joint expert statement from the European Clozapine Task Force.

IF 6.7 2区 医学 Q1 PSYCHIATRY European Psychiatry Pub Date : 2025-01-10 DOI:10.1192/j.eurpsy.2024.1816
Hélène Verdoux, Robert A Bittner, Alkomiet Hasan, Mishal Qubad, Elias Wagner, Alexis Lepetit, Manuel Arrojo-Romero, Christian Bachmann, Marieke Beex-Oosterhuis, Jan Bogers, Andreja Celofiga, Dan Cohen, Domenico de Berardis, Marc de Hert, Carlos de Las Cuevas, Bjørn H Ebdrup, Konstantinos N Fountoulakis, Daniel Guinart, Dolores Keating, Miloslav Kopeček, John Lally, Judit Lazáry, Jurjen J Luykx, Olalla Maronas Amigo, Espen Molden, Jimmi Nielsen, Brian O'Donoghue, Pierre Oswald, Flavian S Radulescu, Christopher Rohde, Marina Sagud, Emilio J Sanz, Ivona Šimunović Filipčić, Iris E Sommer, Heidi Taipale, Jari Tiihonen, Heli Tuppurainen, Selene Veerman, Alina Wilkowska, Edoardo Spina, Peter Schulte
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Abstract

The European Clozapine Task Force is a group of psychiatrists and pharmacologists practicing in 18 countries under European Medicines Agency (EMA) regulation, who are deeply concerned about the underuse of clozapine in European countries. Although clozapine is the most effective antipsychotic for people with treatment-resistant schizophrenia, a large proportion of them do not have access to this treatment. Concerns about clozapine-induced agranulocytosis and stringent blood monitoring rules are major barriers to clozapine prescribing and use. There is a growing body of evidence that the incidence of clozapine-induced agranulocytosis is very low after the first year of treatment. Maintaining lifelong monthly blood monitoring after this period contributes to unjustified discontinuation of clozapine. We leverage recent and replicated evidence on the long-term safety of clozapine to call for the revision and updating of the EMA's blood monitoring rules, thus aiming to overcome this major barrier to clozapine prescribing and use. We believe the time has come for relaxing the rules without increasing the risks for people using clozapine in Europe.

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是时候修改欧洲氯氮平血液监测规则了。欧洲氯氮平特别工作组的联合专家声明。
欧洲氯氮平工作组是一个由精神病学家和药理学家组成的小组,在欧洲药品管理局(EMA)的监管下,在18个国家执业,他们对欧洲国家氯氮平的使用不足深感担忧。虽然氯氮平是治疗难治性精神分裂症患者最有效的抗精神病药物,但他们中的很大一部分人无法获得这种治疗。对氯氮平引起的粒细胞缺乏症的担忧和严格的血液监测规则是氯氮平处方和使用的主要障碍。越来越多的证据表明,氯氮平引起的粒细胞缺乏症在治疗的第一年后发病率非常低。在此期间后维持终身每月血液监测有助于不合理地停用氯氮平。我们利用氯氮平长期安全性的最新和重复证据,呼吁修订和更新EMA的血液监测规则,从而旨在克服氯氮平处方和使用的这一主要障碍。我们认为,现在是时候放松规定,同时不增加欧洲人使用氯氮平的风险。
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来源期刊
European Psychiatry
European Psychiatry 医学-精神病学
CiteScore
8.50
自引率
3.80%
发文量
2338
审稿时长
4.5 weeks
期刊介绍: European Psychiatry, the official journal of the European Psychiatric Association, is dedicated to sharing cutting-edge research, policy updates, and fostering dialogue among clinicians, researchers, and patient advocates in the fields of psychiatry, mental health, behavioral science, and neuroscience. This peer-reviewed, Open Access journal strives to publish the latest advancements across various mental health issues, including diagnostic and treatment breakthroughs, as well as advancements in understanding the biological foundations of mental, behavioral, and cognitive functions in both clinical and general population studies.
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