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首页> 外文期刊>British journal of clinical pharmacology >Small doses of droperidol do not present relevant torsadogenic actions: a double‐blind, ondansetron‐controlled study
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Small doses of droperidol do not present relevant torsadogenic actions: a double‐blind, ondansetron‐controlled study

机译:小剂量氟哌利多没有相关的致畸作用:一项双盲,恩丹西酮对照研究

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Aim Drugs used for postoperative nausea and vomiting prophylaxis are believed to provoke torsadogenic changes in cardiac repolarization. The aim of this study was to assess the effect of small doses of droperidol on the parameters of cardiac repolarization, including the QTc interval and transmural dispersion of repolarization. Methods A total of 75 patients were randomly allocated to receive 0.625 or 1.25?mg droperidol or 8?mg ondansetron. The QTc interval was calculated using Bazett's formula and the Framingham correction. The transmural dispersion of repolarization was determined as Tpeak–Tend time. Results Transient QT prolongation, corrected with both formulae, followed 1.25?mg of droperidol 10?min after administration. No change in the QTc value was observed in the other groups. When corrected with Bazett's formula, QTc was prolonged above 480 ms in two patients receiving 1.25?mg droperidol (at the 10th and 20th minute of the study) and in one receiving ondansetron. No patients developed a QTcB prolongation over 500 ms. No increase above 480 ms was observed relative to the Framingham correction method. There were no significant differences in the Tpeak–Tend time either between or within the groups. Conclusion In men without cardiovascular disorders small doses (1.25?mg) of droperidol prophylaxis induced transient QTc prolongation without changes in transmural dispersion of repolarization. The apparently low risk of the drug applies only in low risk male patients with a low pro-QTc score.
机译:目的据信用于术后恶心和呕吐预防的药物可引起心脏复极的致畸变化。这项研究的目的是评估小剂量氟哌啶对心脏复极参数的影响,包括QT c 间隔和复极的透壁分散。方法共有75例患者被随机分配接受0.625或1.25mg氟哌利多或8mg恩丹西酮。使用Bazett公式和Framingham校正计算QT c 间隔。复极的透壁分散度确定为T peak –T end 时间。结果两种制剂均纠正了短暂的QT延长,给药后10min服用1.25μmg的氟哌啶。在其他组中,未观察到QT 值的变化。用巴泽特公式校正后,两名接受1.25?mg氟哌利多的患者(分别在10 sups和20 sups )的QT c 延长至480 ms以上分钟的学习时间)和一个接受恩丹西酮的患者。没有患者在500 ms内出现QT c B延长。相对于Framingham校正方法,未观察到超过480 ms的增加。组之间或组内的T peak –T end 时间没有显着差异。结论在无心血管疾病的男性中,小剂量氟哌啶醇预防(1.25?mg)可导致短暂的QT c 延长,而复极的透壁分散性无变化。该药物的明显低风险仅适用于Q-pro c 得分低的低风险男性患者。

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