Schulz M, Schmoldt A
Drug Information Center, ABDA-Federal Union of German Associations of Pharmacists, Eschborn, Germany.
Pharmazie. 1997 Dec;52(12):895-911.
In order to assess the significance of drug levels measured in clinical and forensic toxicology as well as for Therapeutic Drug Monitoring (TDM) it is essential that good collections of data are readily available. For more than 500 frequently used drugs therapeutic and, if data was available, toxic, and fatal plasma concentrations as well as elimination half-lives were compiled in a table. The compilation includes data for hypnotics like barbiturates and benzodiazepines, diphenhydramine, neuroleptics, antidepressants, sedatives, analgesics, antiinflammatory agents (e.g., NSAIDs), antihistamines, antiepileptics, betaadrenergic antagonists, antibiotics (penicillins, cephalosporins, aminoglycosides, gyrase inhibitors), diuretics, calcium-channel blockers, cardiac glycosides, antiarrhythmics, antiasthmatics, ACE-inhibitors, opiate agonists, and local anesthetics, among others. In addition, some toxicological relevant xenobiotics were listed. Data have been abstracted from published information, both compilations and primary sources and have been completed with data collected in our own forensic and clinical toxicology laboratories. Wherever possible, ranges for therapeutic plasma concentrations are expressed as trough concentration at steady state. The half-life values given for each drug are chosen to represent the terminal log-linear phase at most. It is the purpose to rapidly assess the significance of drug levels for the therapeutic monitoring of patients, and to facilitate the diagnostic assessment in case of intoxications.
为了评估临床和法医毒理学以及治疗药物监测(TDM)中所测药物浓度的意义,必须要有现成的良好数据集。针对500多种常用药物,将治疗浓度(若有数据,还包括毒性和致死性血浆浓度)以及消除半衰期整理成了表格。该整理包括以下各类药物的数据:催眠药(如巴比妥类和苯二氮䓬类)、苯海拉明、抗精神病药、抗抑郁药、镇静剂、镇痛药、抗炎药(如非甾体抗炎药)、抗组胺药、抗癫痫药、β肾上腺素能拮抗剂、抗生素(青霉素类、头孢菌素类、氨基糖苷类、回旋酶抑制剂)、利尿剂、钙通道阻滞剂、强心苷、抗心律失常药、抗哮喘药、血管紧张素转换酶抑制剂、阿片类激动剂以及局部麻醉药等。此外,还列出了一些与毒理学相关的外源化学物。数据摘自已发表的资料,包括汇编资料和原始资料,并补充了我们自己的法医和临床毒理学实验室收集的数据。只要有可能,治疗性血浆浓度范围均表示为稳态时的谷浓度。每种药物给出的半衰期值尽量代表终末对数线性期。目的是快速评估药物浓度对患者治疗监测的意义,并便于在中毒情况下进行诊断评估。