Asplund K, Wiholm B E, Lithner F
Diabetologia. 1983 Jun;24(6):412-7. doi: 10.1007/BF00257338.
In the largest series of patients with glibenclamide-associated hypoglycaemia reported so far, 51 cases reported to the Swedish Adverse Drug Reactions Advisory Committee and six additional cases are reviewed and related to sales and prescription data of glibenclamide. Median age of the patients with hypoglycaemia was 75 years and 21% were 85 years or above. For comparison, the median age of a random sample (1 in 288 of all patients prescribed glibenclamide) was 70 years and only 5% were 85 years or older. In eight out of 40 cases where duration of glibenclamide treatment was recorded, the hypoglycaemic event occurred during the first month of treatment. The median daily dose of glibenclamide prescribed was 10 mg both in the hypoglycaemic cases and in the prescription sample. Coma or disturbed consciousness was the most common clinical presentation in this series and the minimum blood glucose value was 1.3 mmol/l (median). Twenty-two patients responded immediately to treatment, 24 had protracted hypoglycaemia of 12-72 h duration and 10 died. Fatal outcome was observed even with small doses of glibenclamide (2.5-5 mg/day). Previous strokes and cardiac disorders were isolated as two independent determinants of a serious course of the hypoglycaemia. Other contributing factors included impaired renal function, low food intake, diarrhoea, alcohol intake and interaction with other drugs. Thus, it is not uncommon for glibenclamide, like the first-generation sulphonylureas, to cause serious, protracted and even fatal hypoglycaemic events.
在迄今为止报告的关于格列本脲相关性低血糖的最大系列患者中,有51例向瑞典药物不良反应咨询委员会报告,另外6例进行了回顾,并与格列本脲的销售和处方数据相关。低血糖患者的年龄中位数为75岁,21%的患者年龄在85岁及以上。作为对比,一个随机样本(所有开具格列本脲处方患者中的1/288)的年龄中位数为70岁,只有5%的患者年龄在85岁及以上。在记录了格列本脲治疗时长的40例患者中,有8例低血糖事件发生在治疗的第一个月。低血糖病例和处方样本中开具的格列本脲每日剂量中位数均为10 mg。昏迷或意识障碍是该系列中最常见的临床表现,最低血糖值为1.3 mmol/L(中位数)。22例患者治疗后立即恢复,24例出现持续12 - 72小时的低血糖,10例死亡。即使使用小剂量格列本脲(2.5 - 5 mg/天)也观察到了致命结局。既往中风和心脏疾病被确定为低血糖严重病程的两个独立决定因素。其他促成因素包括肾功能损害、食物摄入量低、腹泻、酒精摄入以及与其他药物的相互作用。因此,与第一代磺酰脲类药物一样,格列本脲引起严重、持续性甚至致命的低血糖事件并不罕见。