Kowalsky S F, Andritz M B, Hamilton R A, Platek T E
Hosp Pharm. 1989 Feb;24(2):105-8.
A drug utilization evaluation (DUE) of cimetidine surveyed use, dose, route of administration, indications, and safety in five New York hospitals. Drug use and patient information were recorded on cimetidine data collection forms; data on indications were noted on physician response forms. In addition to FDA-approved indications, cimetidine was frequently used for non-approved indications substantiated by the H2-antagonist literature. Prophylaxis accounted for 42.5% of total use, followed by nonulcer (25.5%), ulcer (18.8%), and other indications (13.1%). Appropriateness of dosage could not be determined in 42 (16.1%) patients with insufficient creatinine clearance data. One hundred and thirty patients (49.8%) whose renal function could be estimated were within dosage guidelines; 89 (34.1%) were above or below dosage recommendations. The incidence of adverse effects was low (3.83%), although many patients were "at risk" of untoward events or drug-drug interactions.
一项关于西咪替丁的药物利用评估(DUE)调查了纽约五家医院中该药的使用情况、剂量、给药途径、适应症及安全性。西咪替丁的数据收集表记录了用药情况和患者信息;医生答复表记录了适应症数据。除了美国食品药品监督管理局(FDA)批准的适应症外,西咪替丁还经常用于H2拮抗剂文献证实的未获批适应症。预防性用药占总用药量的42.5%,其次是非溃疡性疾病(25.5%)、溃疡(18.8%)和其他适应症(13.1%)。42名(16.1%)肌酐清除率数据不足的患者无法确定用药剂量是否合适。130名(49.8%)肾功能可评估的患者用药剂量符合指导原则;89名(34.1%)患者的用药剂量高于或低于推荐剂量。不良反应发生率较低(3.83%),尽管许多患者有发生不良事件或药物相互作用的“风险”。