首页> 外文期刊>Therapeutic Drug Monitoring >Effects of aging, renal dysfunction, left ventricular systolic impairment, and weight on steady state pharmacokinetics of perhexiline.
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Effects of aging, renal dysfunction, left ventricular systolic impairment, and weight on steady state pharmacokinetics of perhexiline.

机译:衰老,肾功能不全,左心室收缩功能障碍和体重对哌克西林稳态药代动力学的影响。

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MATERIALS AND METHODS: Two hundred patients at steady-state on long-term perhexiline were identified retrospectively. The ratio of maintenance dose to steady-state plasma concentration (dose:[Px]) was correlated with the following putative determinants via simple and multiple linear regression analyses: age, weight, left ventricular ejection fraction (LVEF), and creatinine clearance (CrCl, Cockroft-Gault formula). A Mann-Whitney U test was performed to determine if severe left ventricular systolic impairment affected maintenance dose. RESULTS: Advanced age, left ventricular systolic impairment, and renal impairment were frequently encountered. Using simple linear regression, age was a negative correlate of dose:[P] (R = 0.23, P = 0.001), whereas weight (R = 0.27, P = 0.0001) and CrCl (R = 0.30, P < 0.0001) were positive correlates. Mann-Whitney U analysis showed no difference between dose: [Px] among patients with LVEF of less than 30% versus 30% or greater. Advancing age was strongly associated with decreasing weight (R = -0.45, P < 0.00001) and calculated CrCl varied directly with weight, as expected (R = 0.66, P < 0.0001). Stepwise multiple linear regression using age, LVEF, CrCl, and weight as potential predictors of dose:[P] yielded only weight as a significant determinant. DISCUSSION: Perhexiline has become a "last-line" agent for refractory angina as a result of complex pharmacokinetics and potential toxicity. Use has increased predictably in the aged and infirm who have exhausted standard medical and surgical therapeutic options. Beyond genotype, the effect of patient characteristics on maintenance dose has not been explored in detail. In this study, dose requirement declined with age in a frail and wasting population as a result of weight-related pharmacokinetic factors. LVEF had no apparent effect on maintenance dose and should not be considered a contraindication to use. CONCLUSION: A weight-adjusted starting dose may facilitate the safe and effective prescription of perhexiline and is calculated by 50 + 2 x weight (kg) mg/d, rounded to the closest 50 mg/day.
机译:材料与方法:回顾性分析200例长期服用他昔林的患者。通过简单和多重线性回归分析,维持剂量与稳态血浆浓度之比(剂量:[Px])与以下推定的决定因素相关:年龄,体重,左心室射血分数(LVEF)和肌酐清除率(CrCl) ,Cockroft-Gault公式)。进行了Mann-Whitney U测试,以确定严重的左心室收缩损伤是否影响维持剂量。结果:高龄,左心室收缩功能障碍和肾功能损害经常遇到。通过简单的线性回归,年龄与剂量呈负相关:[P](R = 0.23,P = 0.001),而体重(R = 0.27,P = 0.0001)和CrCl(R = 0.30,P <0.0001)是正相关。相关。 Mann-Whitney U分析显示,LVEF小于30%与30%或更大的患者之间的剂量之间无差异[Px]。年龄的增长与体重的减少密切相关(R = -0.45,P <0.00001),计算出的CrCl随重量的变化直接变化,正如预期的那样(R = 0.66,P <0.0001)。使用年龄,LVEF,CrCl和体重作为剂量的潜在预测因子的逐步多元线性回归:[P]仅产生体重作为重要的决定因素。讨论:由于复杂的药代动力学和潜在的毒性,哌克西林已成为难治性心绞痛的“最后一线”药物。可以预见的是,已经用尽标准医学和外科治疗选择的年老体弱者的使用量有所增加。除基因型外,尚未详细探讨患者特征对维持剂量的影响。在这项研究中,由于体重相关的药代动力学因素,体弱和浪费人群的剂量需求随着年龄的增长而下降。 LVEF对维持剂量无明显影响,不应视为使用禁忌症。结论:体重调整后的起始剂量可能有助于安全有效地处方哌克昔林,其剂量为50 + 2 x体重(kg)mg / d,四舍五入至最接近的50 mg / day。

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