Prescrire Int. 2002 Oct;11(61):146-50.
(1) Neuroleptics prolong the QT interval, with a risk of torsades de pointes, ventricular tachycardia, syncope and sudden death. This adverse reaction is dose-dependent. (2) Most published cases have involved phenothiazines, and especially thioridazine. Most other neuroleptics have also been involved, including recent drugs such as risperidone and olanzapine. 'Hidden neuroleptics' such as cisapride and injectable domperidone carry the same risk. (3) While this effect has been known for several decades, the degree of risk associated with the various neuroleptics is still poorly known, and few epidemiological data are available. (4) The cornerstones of prevention of cardiac arrhythmia in patients treated with neuroleptics are to weigh up carefully the indications, prescribe the lowest effective dose, and monitor the ECG. All patients should also be screened for precipitating factors, such as other risk factors for torsades de pointes and combination with other drugs that favour torsades de pointes or provoke pharmacokinetic interactions.
(1) 抗精神病药物会延长QT间期,存在发生尖端扭转型室性心动过速、室性心动过速、晕厥和猝死的风险。这种不良反应具有剂量依赖性。(2) 大多数已发表的病例涉及吩噻嗪类药物,尤其是硫利达嗪。大多数其他抗精神病药物也有相关报道,包括最近的药物如利培酮和奥氮平。“隐性抗精神病药物”如西沙必利和注射用多潘立酮也有同样的风险。(3) 虽然这种效应已为人所知数十年,但与各种抗精神病药物相关的风险程度仍知之甚少,且几乎没有流行病学数据。(4) 接受抗精神病药物治疗的患者预防心律失常的关键在于仔细权衡用药指征,开具最低有效剂量,并监测心电图。所有患者还应筛查诱发因素,如其他尖端扭转型室性心动过速的风险因素以及与其他易引发尖端扭转型室性心动过速或引起药代动力学相互作用的药物联用情况。