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首页> 外文期刊>Pharmacoepidemiology and drug safety >Magnitude of QT prolongation associated with a higher risk of Torsades de Pointes.
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Magnitude of QT prolongation associated with a higher risk of Torsades de Pointes.

机译:QT延长的幅度与较高的Torsades de Pointes风险相关。

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PURPOSE: Drug induced Torsades de Pointes (TdP) is a major concern for new drugs seeking regulatory approval. Prolongation of QT intervals greater than 60 millisecond or to longer than 500 millisecond in an individual patient has been considered to be associated with a higher risk. The purpose of this study is to identify values inferred from a population that predict a stronger potential for TdP. METHODS: Prolongation data of 30 non-antiarrhythmic QT prolonging drugs were analysed. Depending on how strong the drugs were associated with TdP, they were categorized as strong or borderline torsadogens. The differences in mean QTc increases between the two groups were compared and cut-off values that distinguished strong from borderline drugs were searched for. RESULTS: The average QTc increase of 19.3 millisecond of strong torsadogens was significantly greater than the 8.0 millisecond of borderline torsadogens. Prolongation greater than 12 millisecond in the context of monotherapy or 25 millisecond in the presence of metabolic inhibition and an upper bound of 95% confidence interval (CI) for the mean QTc increase greater than 14 millisecond in monotherapy or 30.1 millisecond in combination therapy with metabolic inhibitors favoured a stronger association with TdP. CONCLUSIONS: Drugs strongly associated with TdP have greater QTc increases than those with less concern. Several cut-off values have been noted to distinguish between them. These values may be helpful for evaluation of TdP risk for future QT prolonging drugs.
机译:用途:药物诱发的扭转性扭转性肥胖症(TdP)是寻求监管部门批准的新药的主要关注点。个体患者的QT间隔延长大于60毫秒或大于500毫秒被认为与更高的风险有关。这项研究的目的是确定从人群中推断出的预测TdP潜力更大的价值。方法:分析30种非抗心律失常性QT延长药物的延长数据。根据药物与TdP结合的强度,将其归类为强力或边缘性Torsadogens。比较了两组之间平均QTc升高的差异,并搜索了区分临界药物和临界药物的临界值。结果:强的torsadogens的平均QTc增加19.3毫秒,明显大于临界torsadogens的8.0毫秒。在单一疗法中,延长时间大于12毫秒,在存在代谢抑制作用的情况下,延长时间大于25毫秒,平均QTc上限的95%置信区间(CI)上限在单一疗法中大于14毫秒,在代谢疗法中大于30.1毫秒抑制剂倾向于与TdP建立更强的联系。结论:与TdP密切相关的药物的QTc增加比那些关注较少的药物更大。已经注意到几个临界值以区分它们。这些值可能有助于评估未来延长QT药物的TdP风险。

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