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哇巴因对预激综合征和折返性心动过速患者的电生理效应。

Electrophysiologic effects of ouabain in patients with preexcitation and circus movement tachycardia.

作者信息

Dhingra R C, Palileo E V, Strasberg B, Swiryn S, Bauernfeind R, Wyndham C, Rosen K M

出版信息

Am J Cardiol. 1981 Jan;47(1):139-44. doi: 10.1016/0002-9149(81)90302-7.

Abstract

Effects of intravenous ouabain were evaluated in 19 patients with an anomalous conduction pathway (14 with manifest and 5 with concealed preexcitation (utilizing intracardiac stimulation and recording. Anterograde conduction through the anomalous pathway was present in all 14 patients with manifest preexcitation at a maximal atrial paced rate of 140 to 250 beats/min (mean +/- standard error of the mean 214 +/- 7.2) before and at 150 to 240 beats/min (mean 206 +/- 7.1) after ouabain (difference not significant [NS]). The anterograde effective refractory period of the anomalous pathway, measured at an equivalent atrial paced rate in 10 patients, was 250 to 450 ms (mean 309 +/- 19.7) before and 260 to 450 ms (mean 300 +/- 17.2) after ouabain (NS). Retrograde conduction through the anomalous pathway was possible at maximal ventricular paced rates (17 patients) of 160 to 250 beats/min (mean 222 +/- 6.6) before and 190 to 250 beats/min (mean 221 +/- 4.4) after ouabain (NS). Sustained atrioventricular (A-V) reentrant paroxysmal supraventricular tachycardia was inducible in all 19 patients before and in 17 patients (89 percent) after ouabain (tachycardia could not be induced in two patients because of increased A-V nodal refractoriness). The mean cycle length of tachycardia in the 17 patients was 320 +/- 6.7 ms before and 340 +/- 8.1 ms after ouabain (p < 0.01). In conclusion, ouabain has no significant effect on either anterograde or retrograde anomalous pathway refractoriness. Although ouabain slightly increases the cycle length of tachycardia, it does not interfere with induction of tachycardia in most patients with preexcitation. Oral cardiac glycosides alone would appear to be of limited value in patients with preexcitation and recurrent supraventricular tachycardia.

摘要

对19例有异常传导通路的患者(14例显性预激和5例隐匿性预激,采用心内刺激和记录)进行了静脉注射哇巴因的效应评估。在所有14例显性预激患者中,在最大心房起搏频率为140至250次/分钟(平均值±平均标准误差214±7.2)时,以及在静脉注射哇巴因后150至240次/分钟(平均值206±7.1)时,均存在经异常通路的前向传导(差异无统计学意义[NS])。在10例患者中,以等效心房起搏频率测量的异常通路前向有效不应期,在静脉注射哇巴因前为250至450毫秒(平均值309±19.7),注射后为260至450毫秒(平均值300±17.2)(差异无统计学意义)。在最大心室起搏频率(17例患者)为160至250次/分钟(平均值222±6.6)时,静脉注射哇巴因前可发生经异常通路的逆向传导,注射后为190至250次/分钟(平均值221±4.4)(差异无统计学意义)。在所有19例患者中,静脉注射哇巴因前均可诱发持续性房室(A-V)折返性阵发性室上性心动过速,注射后17例患者(89%)可诱发(2例患者因房室结不应期增加而无法诱发心动过速)。17例患者心动过速的平均周期长度在静脉注射哇巴因前为320±6.7毫秒,注射后为340±8.1毫秒(p<0.01)。总之,哇巴因对前向或逆向异常通路不应期均无显著影响。虽然哇巴因会轻微增加心动过速的周期长度,但在大多数预激患者中并不干扰心动过速的诱发。单独使用口服强心苷对预激和复发性室上性心动过速患者似乎价值有限。

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