Hanus P M
Am J Hosp Pharm. 1980 Apr;37(4):510-3.
The pharmacology, side effects, and possible drug interactions of metrizamide, a water-solulbe contrast medium for myelography, are reviewed. Metrizamide concentration in the brain reaches maximal levels two to six hour after lumbar injection, depending on dose and patient positioning, and is largely (55-96%) excreted from the body after 24 hours. Its lower neurotoxicity, compared with other water-soluble contrast agents, can be attributed in part to its undissociated, non-ionic nature. Common side effects, which include headache, nausea, and vomiting, occur to the same degree as with other myelographic contrast media. Reported data suggest that convulsions, which have occurred in a very small percentage of patients, are related to the amount of contrast medium reaching the brain which, in turn, is largely a factor of dose and examination technique. Although the risk of seizures is small, it is recommended that drugs that lower the seizure threshold (phenothiazine derivatives, butyrophenones, tricyclic antidepressants, and MAO-inhibitors) should be avoided 48 hours before metrizamide administration (if possible), should not be used to control nausea, and should not be resumed for 24 to 48 hours after the myelographic procedure. The value of premedication (e.g., with diazepam) to prevent seizures has not been established and is not recommended.
本文综述了用于脊髓造影的水溶性造影剂甲泛葡胺的药理作用、副作用及可能的药物相互作用。腰椎注射后,甲泛葡胺在脑中的浓度在2至6小时达到最高水平,这取决于剂量和患者体位,24小时后大部分(55 - 96%)从体内排出。与其他水溶性造影剂相比,其神经毒性较低,部分原因可归因于其未离解的非离子性质。常见副作用包括头痛、恶心和呕吐,其发生率与其他脊髓造影剂相同。报告数据表明,在极少数患者中发生的惊厥与进入脑内的造影剂剂量有关,而这又主要取决于剂量和检查技术。尽管癫痫发作的风险较小,但建议在甲泛葡胺给药前48小时(如果可能)避免使用降低癫痫阈值的药物(吩噻嗪衍生物、丁酰苯类、三环类抗抑郁药和单胺氧化酶抑制剂),这些药物不应被用于控制恶心,并且在脊髓造影术后24至48小时内不应恢复使用。预防癫痫发作的预处理药物(如地西泮)的价值尚未确立,不建议使用。