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1
The accuracy of a pharmacokinetic theophylline predictor using once daily dosing.使用每日一次给药的茶碱药代动力学预测指标的准确性。
Br J Clin Pharmacol. 1987 Sep;24(3):301-7. doi: 10.1111/j.1365-2125.1987.tb03173.x.
2
Bayesian derived predictions for twice daily theophylline under outpatient conditions and an assessment of optimal sampling times.门诊条件下每日两次茶碱的贝叶斯推导预测及最佳采样时间评估。
Br J Clin Pharmacol. 1989 Feb;27(2):215-21. doi: 10.1111/j.1365-2125.1989.tb05353.x.
3
Evaluation of a novel Bayesian method for individualizing theophylline dosage.一种用于个体化茶碱剂量的新型贝叶斯方法的评估。
J Clin Chem Clin Biochem. 1988 Jun;26(6):405-14. doi: 10.1515/cclm.1988.26.6.405.
4
Individualization of theophylline dosage: a Bayesian method evaluated in patients with once-daily dosing.茶碱剂量个体化:一种在每日一次给药患者中评估的贝叶斯方法。
Ther Drug Monit. 1991 Sep;13(5):420-4.
5
The accuracy and stability of Bayesian theophylline predictions.贝叶斯茶碱预测的准确性和稳定性。
Ther Drug Monit. 1988;10(3):299-305. doi: 10.1097/00007691-198803000-00011.
6
The design of oral sustained-release theophylline dosing after conversion from intravenous to oral therapy.从静脉给药转换为口服治疗后口服缓释茶碱的给药设计。
Int J Clin Pharmacol Ther. 1994 Nov;32(11):625-31.
7
Abbott PKS system: a new version for applied pharmacokinetics including Bayesian estimation.
Int J Biomed Comput. 1994 Jun;36(1-2):127-30. doi: 10.1016/0020-7101(94)90103-1.
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Evaluation of three theophylline dosing methods in pediatric patients.评估三种小儿患者茶碱给药方法。
DICP. 1991 Feb;25(2):179-85. doi: 10.1177/106002809102500213.
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A comparison of the accuracy of a least squares regression, a Bayesian, Chiou's and the steady-state clearance method of individualising theophylline dosage.比较最小二乘回归法、贝叶斯法、邱氏法和稳态清除率法个体化茶碱剂量的准确性。
Clin Pharmacokinet. 1988 May;14(5):311-20. doi: 10.2165/00003088-198814050-00003.
10
Theophylline levels after single daily and divided dosing of a once-a-day theophylline preparation in asthmatic children.
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引用本文的文献

1
Use of low-dose oral theophylline as an adjunct to inhaled corticosteroids in preventing exacerbations of chronic obstructive pulmonary disease: study protocol for a randomised controlled trial.低剂量口服茶碱作为吸入性糖皮质激素辅助药物预防慢性阻塞性肺疾病急性加重的应用:一项随机对照试验的研究方案
Trials. 2015 Jun 10;16:267. doi: 10.1186/s13063-015-0782-2.
2
Dose response relation to oral theophylline in severe chronic obstructive airways disease.重度慢性阻塞性气道疾病中口服氨茶碱的剂量反应关系。
BMJ. 1988 Dec 10;297(6662):1506-10. doi: 10.1136/bmj.297.6662.1506.
3
Bayesian derived predictions for twice daily theophylline under outpatient conditions and an assessment of optimal sampling times.门诊条件下每日两次茶碱的贝叶斯推导预测及最佳采样时间评估。
Br J Clin Pharmacol. 1989 Feb;27(2):215-21. doi: 10.1111/j.1365-2125.1989.tb05353.x.
4
An updated comparison of drug dosing methods. Part II: Theophylline.药物给药方法的最新比较。第二部分:茶碱
Clin Pharmacokinet. 1991 Apr;20(4):280-92. doi: 10.2165/00003088-199120040-00003.
5
Bayesian parameter estimation and population pharmacokinetics.
Clin Pharmacokinet. 1992 Jun;22(6):447-67. doi: 10.2165/00003088-199222060-00004.

本文引用的文献

1
Some suggestions for measuring predictive performance.一些关于衡量预测性能的建议。
J Pharmacokinet Biopharm. 1981 Aug;9(4):503-12. doi: 10.1007/BF01060893.
2
Bayesian individualization of pharmacokinetics: simple implementation and comparison with non-Bayesian methods.药代动力学的贝叶斯个体化:简单实现及与非贝叶斯方法的比较。
J Pharm Sci. 1982 Dec;71(12):1344-8. doi: 10.1002/jps.2600711209.
3
Comparison of orally administered metaproterenol and theophylline in the control of chronic asthma.
J Pediatr. 1982 Aug;101(2):281-7. doi: 10.1016/s0022-3476(82)80142-x.
4
Current concepts. Slow-release theophylline rationale and basis for product selection.当前概念。缓释型茶碱的原理及产品选择依据。
N Engl J Med. 1983 Mar 31;308(13):760-4. doi: 10.1056/NEJM198303313081306.
5
Comparison of three methods for estimating theophylline pharmacokinetics.三种估算茶碱药代动力学方法的比较
Clin Pharm. 1983 Mar-Apr;2(2):148-52.
6
Clinical pharmacokinetics: a comprehensive system for therapeutic drug monitoring and prescribing.临床药代动力学:治疗药物监测与处方的综合系统。
Br Med J (Clin Res Ed). 1984 Feb 18;288(6416):541-5. doi: 10.1136/bmj.288.6416.541.
7
Single-dose slow-release aminophylline at night prevents nocturnal asthma.夜间单剂量缓释氨茶碱可预防夜间哮喘。
Lancet. 1982 Feb 6;1(8267):299-301. doi: 10.1016/s0140-6736(82)91566-5.
8
Pharmacokinetics of theophylline. Application to adjustment of the clinical dose of aminophylline.茶碱的药代动力学。在氨茶碱临床剂量调整中的应用。
Clin Pharmacol Ther. 1972 May-Jun;13(3):349-60. doi: 10.1002/cpt1972133349.
9
A comparison of graphical nomogram methods with a computerized Bayesian analysis method in the interpretation of serum phenytoin concentrations.在血清苯妥英浓度解读中图形列线图方法与计算机化贝叶斯分析方法的比较。
J Clin Hosp Pharm. 1986 Dec;11(6):443-8. doi: 10.1111/j.1365-2710.1986.tb00871.x.
10
The pharmacokinetics of uniphyllin in nocturnal asthma.单硝酸异山梨酯在夜间哮喘中的药代动力学。
Br J Dis Chest. 1986 Jul;80(3):235-41. doi: 10.1016/0007-0971(86)90058-6.

使用每日一次给药的茶碱药代动力学预测指标的准确性。

The accuracy of a pharmacokinetic theophylline predictor using once daily dosing.

作者信息

Chrystyn H, Mulley B A, Peake M D

机构信息

Pontefract General Infirmary, West Yorkshire.

出版信息

Br J Clin Pharmacol. 1987 Sep;24(3):301-7. doi: 10.1111/j.1365-2125.1987.tb03173.x.

DOI:10.1111/j.1365-2125.1987.tb03173.x
PMID:3663446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1386250/
Abstract
  1. The accuracy of a computer based pharmacokinetic prediction method based on Bayesian analysis has been evaluated for an oral show release form of theophylline. 2. In 83 patients from seven centres 24 h serum theophylline concentration-time profiles were measured under a variety of circumstances. 3. Revised predictions of 24 h serum theophylline concentration profiles were generated by Bayesian analysis using single serum drug concentrations taken before, during and after the study days in different subgroups of those patients. Comparing the predicted and measured profiles the mean prediction error (bias) was 0.05 mg l-1 for peak concentrations and 0.04 mg l-1 for trough concentrations during once daily dosing. The corresponding root mean squared prediction errors (precision) were 2.59 and 1.17 mg l-1, respectively. 4. This accuracy is considered more than adequate for clinical purposes. 5. The technique can be used with a variety of other drugs and can form a valuable part of a routine therapeutic drug monitoring service.
摘要
  1. 基于贝叶斯分析的计算机药代动力学预测方法对茶碱口服缓释制剂的准确性进行了评估。2. 在来自七个中心的83名患者中,在多种情况下测量了24小时血清茶碱浓度-时间曲线。3. 通过贝叶斯分析,使用这些患者不同亚组在研究日之前、期间和之后采集的单次血清药物浓度,生成了24小时血清茶碱浓度曲线的修正预测值。比较预测曲线和实测曲线,每日一次给药时,峰浓度的平均预测误差(偏差)为0.05 mg/L,谷浓度的平均预测误差为0.04 mg/L。相应的均方根预测误差(精密度)分别为2.59和1.17 mg/L。4. 这种准确性被认为对于临床目的而言绰绰有余。5. 该技术可用于多种其他药物,并可成为常规治疗药物监测服务的重要组成部分。