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在南澳大利亚地方卫生网络中对氯氮平相关性心肌炎进行的为期 12 个月的审计:筛查和个体化滴定的重要性。

A 12-month audit of clozapine associated myocarditis in a South Australian Local Health Network: The importance of screening and personalised titration.

机构信息

School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, South Australia, Australia.

Office of the Chief Psychiatrist, Adelaide, South Australia, Australia.

出版信息

Schizophr Res. 2024 Jun;268:88-93. doi: 10.1016/j.schres.2023.09.019. Epub 2023 Sep 16.

Abstract

Clozapine is effective in up to 50 % of patients resistant to other antipsychotics. Its use is restricted to third-line due to adverse effects which include myocarditis. Australia reports the highest incidence of clozapine-associated myocarditis (CAM) in the context of pharmacovigilance and relatively rapid titration. An audit of patients commenced on clozapine within the Central Adelaide Local Health Network (CALHN) between 2012 and 2015 found an incidence of 8.6 %. We present here a case series from a follow up audit considering titration relevant risk factors for CAM. We reviewed anecdotal cases and data from all hospital-based commencements of clozapine across CALHN for the period July 2021 to June 2022 using pharmacy and medical record databases. We identified 5 cases of CAM and all had risk factors impacting on clozapine metabolism, including rapid titration, elevated baseline CRP, Asian ethnicity and concomitant treatment with inhibitors of clozapine metabolism. While personalisation of clozapine treatment needs further investigation in prospective trials, slower titration to lower targets for risk groups may not impact on hospital length of stay and has the potential to significantly reduce the burden of adverse events. Australian manufacturer approved titration rates exceed those recommended for personalised dosing and may not be safe for patients with risk factors. Early clozapine levels at week two could identify slow metabolisers for dose adjustment. Closer ties between psychiatrists and cardiologists are critical for the development of protocols for safely maintaining clozapine treatment during low level cardiac inflammation and to support safe rechallenge.

摘要

氯氮平对其他抗精神病药物耐药的患者有效率高达 50%。由于包括心肌炎在内的不良反应,其仅被限制用于三线治疗。澳大利亚报告了在药物警戒和相对快速滴定的背景下,氯氮平相关心肌炎(CAM)发病率最高。在 2012 年至 2015 年期间,对中央阿德莱德当地卫生网络(CALHN)内开始使用氯氮平的患者进行的一项审计发现,发病率为 8.6%。在这里,我们呈现了一项后续审计的病例系列,该审计考虑了与 CAM 相关的滴定相关危险因素。我们使用药房和医疗记录数据库,回顾了 CALHN 期间所有基于医院的氯氮平起始的轶事病例和数据,时间为 2021 年 7 月至 2022 年 6 月。我们确定了 5 例 CAM,所有病例都有影响氯氮平代谢的危险因素,包括快速滴定、基线 CRP 升高、亚洲种族和同时使用氯氮平代谢抑制剂。虽然个性化氯氮平治疗需要进一步在前瞻性试验中进行研究,但对于风险群体,将滴定速度降低到较低目标可能不会影响住院时间,并且有可能显著降低不良事件的负担。澳大利亚制造商批准的滴定率超过了个性化剂量推荐的滴定率,对于有危险因素的患者可能不安全。在第 2 周时进行早期氯氮平水平检测,可能可以识别出代谢较慢的患者,从而进行剂量调整。精神科医生和心脏病专家之间建立更紧密的联系对于制定安全维持低水平心脏炎症期间氯氮平治疗的方案以及支持安全重新挑战至关重要。

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