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通过唾液样本监测小儿苯巴比妥和苯妥英治疗情况。

Monitoring of phenobarbitone and phenytoin therapy in small children by salivary samples.

作者信息

Mucklow J C, Bacon C J, Hierons A M, Webb J K, Rawlins M D

出版信息

Ther Drug Monit. 1981;3(3):275-7. doi: 10.1097/00007691-198103000-00008.

Abstract

Concentrations of phenytoin or phenobarbitone have been measured serially using saliva samples in 75 very young children receiving one of these drugs for prevention of recurrent febrile convulsions. Saliva samples were easily obtained and the measured concentrations were a valuable guide to drug dosage during the treatment period. Mean (+/- SD) saliva concentrations were, for phenytoin, 1.0 +/- 0.8 mg/litre (3.8 +/- 3.0 mumol/litre) and, for phenobarbitone, 7.9 +/- 2.6 mg/litre (24.0 +/- 11.3 mumol/litre) and did not alter significantly during the period of observation. Despite frequent review with assessment of compliance, it proved difficult to achieve and maintain target drug concentrations. Paired samples of saliva and plasma were obtained from 36 children before treatment was terminated. Drug concentrations in saliva correlated well with those in plasma and mean plasma: saliva ratios (phenytoin, 8.4; phenobarbitone, 2.2) were comparable to results obtained previously in adults.

摘要

在75名接受苯妥英或苯巴比妥预防复发性热性惊厥的幼儿中,连续使用唾液样本测量了苯妥英或苯巴比妥的浓度。唾液样本易于获取,所测浓度对治疗期间的药物剂量是一个有价值的指导。苯妥英的平均(±标准差)唾液浓度为1.0±0.8毫克/升(3.8±3.0微摩尔/升),苯巴比妥为7.9±2.6毫克/升(24.0±11.3微摩尔/升),在观察期间没有显著变化。尽管经常进行复查并评估依从性,但事实证明难以达到并维持目标药物浓度。在治疗结束前,从36名儿童中获取了配对的唾液和血浆样本。唾液中的药物浓度与血浆中的浓度相关性良好,平均血浆:唾液比率(苯妥英为8.4;苯巴比妥为2.2)与先前在成人中获得的结果相当。

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