精神分裂症和急性精神病的抗精神病药物延长QT间期-一项前瞻性研究。

Industrial Psychiatry Journal Pub Date : 2025-05-01 Epub Date: 2025-07-18 DOI:10.4103/ipj.ipj_495_24
Anirban Saha, Ajay Kumar, Satyajit Singh, Aditya Somani
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引用次数: 0

摘要

背景:抗精神病药物有可能导致qt间期延长(QTIP),这可能导致点扭转和心源性猝死。因此,了解QTIP的发生率和危险因素是很重要的。目的:本研究的主要目的是了解精神分裂症合并急性精神病患者使用抗精神病药物两周后QTIP的发生率。次要目的是寻找QTIP的危险因素。材料和方法:研究纳入了160例年龄≥18岁,男女均可,诊断为精神分裂症或急性精神病,在过去15天内未服用口服/水基注射抗精神病药物或在过去6个月内未服用任何长效抗精神病药物的患者。排除其他精神障碍、尼古丁/咖啡因以外的物质使用、低血清钾/钙/镁水平、先天性长QT间期综合征、心脏病史或服用QTIP高风险药物的患者。在开始治疗前和抗精神病药物治疗至少2周后记录心电图。校正QT间期(QTc)采用Fridericia's和Bazett's公式计算。QTc >450 ms为雄性,>460 ms为雌性。结果:研究参与者的平均年龄为35.88岁(SD: 13.32),男性88人(55%);138人(86.3%)患有精神分裂症。71例(44.4%)接受利培酮治疗,74例(46.3%)接受奥氮平治疗。12人(7.5%)发展出QTIP(使用Fridericia公式计算QTc)。25例(15.6%)出现QTIP(使用Bazett公式计算QTc)。在研究样本中无法确定QTIP的其他危险因素。结论:QTIP存在于合理数量的受试者中。在服用抗精神病药物的患者中,必须定期仔细筛选和评估可能增加QTIP发生几率的风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

QT interval prolongation from antipsychotics in schizophrenia and acute psychosis - A prospective study.

QT interval prolongation from antipsychotics in schizophrenia and acute psychosis - A prospective study.

Background: Antipsychotic drugs have the potential to cause QT-interval prolongation (QTIP), which may lead to Torsades de Pointes and sudden cardiac death. Thus, it is important to know about the incidence and risk factors for QTIP.

Aim: The primary objective of the study was to find out the incidence of QTIP due to the use of antipsychotic drugs in patients with schizophrenia and acute psychosis after two weeks of drug use. The secondary objective was to find the risk factors for QTIP.

Materials and methods: The study included 160 consenting patients, aged ≥18 years, either sex, diagnosed with schizophrenia or acute psychosis, who had not taken oral/water-based injectable antipsychotics during the last 15 days or any long-acting antipsychotic injectable during the previous 6 months. Patients with other psychiatric disorders, substance use other than nicotine/caffeine, low serum levels of potassium/calcium/magnesium, congenital long QT syndrome, history of cardiac conditions, or those taking drugs with high risk to cause QTIP were excluded. ECG was recorded before starting treatment and after at least 2 weeks of treatment with antipsychotic drugs. Corrected QT interval (QTc) was calculated using Fridericia's and Bazett's formulae. QTc >450 ms in males and >460 ms in females was considered prolonged.

Results: The mean age of study participants was 35.88 years (SD: 13.32), and 88 (55%) were males; 138 (86.3%) suffered from schizophrenia. Seventy-one (44.4%) and 74 (46.3%) received risperidone and olanzapine, respectively. Twelve (7.5%) developed QTIP (QTc calculated using Fridericia's formula). Twenty-five (15.6%) were seen to develop QTIP (QTc calculated using Bazett's formula). Additional risk factors for QTIP could not be identified in the study sample.

Conclusion: QTIP is present in a reasonable number of participants. Careful screening and assessment for risk factors that could increase the chances of QTIP must be done regularly in patients getting antipsychotic drugs.

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