Mesquita A, Almeida M, Adragão P, Neves J, Morgado F, Parreira L, Nascimento R, Araújo J J, Mendes M, Bonhorst D, Martins M, Seabra-Gomes R
Interno do Internato Complementar de Cardiologia, Serviço de Cardiologia do Hospital de Santa Cruz.
Rev Port Cardiol. 1996 Jan;15(1):45-55.
The cases of two young patients with repetitive syncopal attacks due to idiopathic long QT syndrome (ILQTS) are reported. Both had been primarily misdiagnosed for seizures. In one of the cases the QT interval in the ECG at rest was normal. The same patient had a previous episode of cardiac arrest with ventricular fibrillation. The treadmill stress test was of great value, revealing polymorphic ventricular tachycardia induced by exercise, and evaluating the efficacy of beta-blocking therapy in the follow-up. The ILQTS should be considered a possible etiology in any patient presenting with new onset seizures, especially in the young. The treatments were different in both cases. In the first one, the treatment with nadolol (100 mg od) revealed to be very effective with total remission of symptoms. The treadmill stress test performed 15 days after the beginning of treatment did not show any ventricular arrhythmias, and it was assumed that the patient was effectively protected against ventricular arrhythmias. After 4.5 months of follow up, no syncopal episodes occurred. In the second case due to young age, the frequency, and the severity of the attacks (cardiac arrest with ventricular fibrillation), and the inefficacy of beta-adrenergic-blocking agents, the implantable cardioversor-defibrillator was the treatment chosen, although the beta blocking therapy was maintained to reduce the number of arrhythmic events. The ILQTS is a rare anomaly related to sudden cardiac death. The ILQTS is characterised by the association of several distinctive electrocardiographic features, among which prolongation of the QT interval is the best known. Life-threatening arrhythmia occurs usually under conditions of physical or psychological stress. Relatively effective therapies do exist and are represented by antiadrenergic interventions: beta-adrenergic-blocking agents are the treatment of choice. When they fail, left sympathetic denervation or the automatic implantable cardioversor-defibrillator have also proved to be effective.
报告了两例因特发性长QT综合征(ILQTS)导致反复晕厥发作的年轻患者病例。两人最初均被误诊为癫痫。其中一例患者静息心电图QT间期正常。该患者曾有过一次心脏骤停伴室颤发作。平板运动试验具有重要价值,可揭示运动诱发的多形性室性心动过速,并在随访中评估β受体阻滞剂治疗的疗效。对于任何新发癫痫的患者,尤其是年轻人,都应考虑ILQTS可能是病因。两例患者的治疗方法不同。第一例患者,使用纳多洛尔(每日100毫克)治疗显示非常有效,症状完全缓解。治疗开始15天后进行的平板运动试验未显示任何室性心律失常,且认为该患者得到了有效的室性心律失常防护。随访4.5个月后,未发生晕厥发作。第二例患者由于年龄小、发作频率和严重程度(心脏骤停伴室颤)以及β肾上腺素能阻滞剂治疗无效,尽管维持β受体阻滞剂治疗以减少心律失常事件的发生,但仍选择植入式心脏复律除颤器作为治疗方法。ILQTS是一种与心源性猝死相关的罕见异常。ILQTS的特征是几种独特的心电图特征相关联,其中QT间期延长最为人所知。危及生命的心律失常通常在身体或心理应激条件下发生。确实存在相对有效的治疗方法,以抗肾上腺素能干预为代表:β肾上腺素能阻滞剂是首选治疗方法。当它们无效时,左颈胸交感神经节切除术或自动植入式心脏复律除颤器也已证明是有效的。