de Vonderweid U, Benettoni A, Piovan D, Padrini R
Int J Cardiol. 1984 Nov;6(5):581-6. doi: 10.1016/0167-5273(84)90002-0.
Efficacy and pharmacokinetics of verapamil were studied in two neonates affected by supraventricular paroxysmal tachycardia, under maintenance treatment with the drug. Verapamil proved to be fully effective in suppressing arrhythmic episodes at the daily doses of 1.5 mg/kg four times a day in case 1 and of 2 mg/kg in case 2. The results of plasma half-life of the drug, calculated in a dose interval, were 3.14 hr and 2.10 hr, respectively. In patient 2, doses less than 0.95 mg/kg four times a day did not produce detectable drug plasma levels, while a further stepwise increase of dose up to 2 mg/kg four times a day produced a steep rise in trough concentration. So, in view of this dose-concentration relationship, caution is recommended in adjusting verapamil oral dosage.
在两名接受维拉帕米维持治疗的室上性阵发性心动过速新生儿中研究了维拉帕米的疗效和药代动力学。在病例1中,维拉帕米以每日剂量1.5mg/kg、每日4次给药时,被证明对抑制心律失常发作完全有效;在病例2中,每日剂量为2mg/kg时有效。在一个剂量间隔内计算得出的药物血浆半衰期结果分别为3.14小时和2.10小时。在患者2中,每日4次剂量低于0.95mg/kg时未产生可检测到的药物血浆水平,而进一步逐步增加剂量至每日4次2mg/kg时,谷浓度急剧上升。因此,鉴于这种剂量-浓度关系,建议在调整维拉帕米口服剂量时谨慎行事。