低钾血症伴QT间期正常的点扭转1例。

K. Kusano, Y. Hata, A. Yumoto, T. Emori, T. Sato, T. Ohe
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引用次数: 21

摘要

患者男,46岁,腹泻后有晕厥发作史。采用动态心电图检测短偶联早心室复合体诱发的非持续性多态性室性心动过速(PVT)。无器质性心脏病,窦性心律QT间期正常。我们认为PVT可能与低钾血症有关,因此在低钾血症(K=3.4mmol/L)、钾负荷(K=4.2mmol/L)和口服胺碘酮治疗后进行电生理研究。低钾状态下,非持续性PVT自发发生,右心尖90%复极单相动作电位持续时间(MAPD90)极短(175 ms)。加载钾(230ms)和口服胺碘酮(240ms)后,MAPD90恢复正常,PVT不再发生。在持续口服胺碘酮和螺内酯治疗的情况下,患者在5年的随访期间没有晕厥发作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Torsade de pointes with a normal QT interval associated with hypokalemia: a case report.
The patient was a 46-year-old man with a history of syncope attack after diarrhea. Nonsustained polymorphic ventricular tachycardia (PVT) initiated by short-coupled premature ventricular complex was detected by Holter monitoring. No organic heart disease was found, and the QT interval during sinus rhythm was normal. It was thought that the PVT might be related to hypokalemia, so electrophysiological studies were performed under the condition of hypokalemia (K=3.4mmol/L), after potassium loading (K=4.2mmol/L) and after oral amiodarone therapy. Under the condition of hypokalemia, nonsustained PVT occurred spontaneously, and the monophasic action potential duration at 90% repolarization (MAPD90) at the right ventricular apex was very short (175 ms). The MAPD90 returned to normal after loading potassium (230ms) and after oral amiodarone therapy (240ms), and PVT no longer occurred. With continued oral amiodarone and spironolactone therapy, the patient has been free of syncope attack over a follow-up period of 5 years.
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