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维持性血液透析期间大量普萘洛尔代谢物潴留

Massive propranolol metabolite retention during maintenance hemodialysis.

作者信息

Stone W J, Walle T

出版信息

Clin Pharmacol Ther. 1980 Oct;28(4):449-55. doi: 10.1038/clpt.1980.187.

Abstract

Eight outpatients on long-term hemodialysis receiving propranolol therapy were studied on a nondialysis day, 11 +/- 1 hr after the last dose. Steady-state daily dosage of propranolol averaged 225 +/- 36 mg (range, 80 to 400). Plasma concentrations of propranolol and three of its metabolites were measured by gas chromatography--mass spectrometry (x +/- SEM): propranolol, 47 +/0 17 ng/ml; propranolol glucuronide, 2.119 +/0 597 ng/ml; 4-hydroxypropranolol glucuronide, 789 +/- 149 ng/ml; and naphthoxylactic acid, 4,357 +/- 727 ng/ml. The plasma levels of these metabolites were 18, 20, and 29 times, respectively, as high as in patients with normal renal function and correlated well with the dose of propranolol. The total concentration of these metabolites exceeded the concentration of propranolol to 239 times (range 74 to 476). Four long-term hemodialysis patients on propranolol were hospitalized to ensure compliance. Plasma levels of propranolol and of the three metatolites were followed during a dosage interval. Plasma propranolol correlated well with dose (r = 0.94) and declined with approximately normal half-lifes of 3.2 to 5.4 hr. There was little variation in the extremely high plasma levels of the three metabolites during a dosage interval. The total metabolite to propranolol plasma concentration ratio in these four patients ranged from 109 to 705. The correlation between total metabolite concentrations and propranolol dose was striking (r = 0.997). Massive retention of propranolol metabolites occurs uniformly in uremia, is highly predictable from the dose, and could have important clinical implications.

摘要

对8名接受普萘洛尔治疗的长期血液透析门诊患者在非透析日、最后一剂药物后11±1小时进行了研究。普萘洛尔的稳态日剂量平均为225±36毫克(范围为80至400毫克)。通过气相色谱-质谱法测量普萘洛尔及其三种代谢物的血浆浓度(x±SEM):普萘洛尔,47±17纳克/毫升;普萘洛尔葡萄糖醛酸苷,2.119±0.597纳克/毫升;4-羟基普萘洛尔葡萄糖醛酸苷,789±149纳克/毫升;萘氧乳酸,4357±727纳克/毫升。这些代谢物的血浆水平分别比肾功能正常的患者高18倍、20倍和29倍,并且与普萘洛尔的剂量密切相关。这些代谢物的总浓度超过普萘洛尔浓度达239倍(范围为74至476倍)。4名接受普萘洛尔治疗的长期血液透析患者住院以确保依从性。在一个给药间隔期间监测普萘洛尔和三种代谢物的血浆水平。血浆普萘洛尔与剂量密切相关(r = 0.94),并以约3.2至5.4小时的正常半衰期下降。在一个给药间隔期间,三种代谢物极高的血浆水平几乎没有变化。这4名患者中代谢物与普萘洛尔血浆浓度的总比值范围为109至705。代谢物总浓度与普萘洛尔剂量之间的相关性非常显著(r = 0.997)。普萘洛尔代谢物在尿毒症中普遍大量潴留,从剂量上可高度预测,并且可能具有重要的临床意义。

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