Vlakhov V, Bakracheva N, Popova L
Vutr Boles. 1988;27(2):80-5.
The risk of agranulocytosis following the use of metamizole was studied by the method of controlled cases. All cases of agranulocytosis and their control cases in Sofia for the period 1982-1986 were included in the study. The mean agranulocytosis morbidity for this period was 3.16 cases for one million population for one year. The etiologic fraction was 7.1%. The relative risk of agranulocytosis following the use of metamizole is 1.25, the maximal risk is 0.03 cases for one million persons using metamizole for one year and the maximal lethal risk is 0.007 cases for one million persons using metamizole for one year. The use of metamizole in Bulgaria for the same period was studied, too. The data presented as a number of defined daily doses used by 1000 population for one day show that the use of metamizole in this country is high. A tendency toward an increase of 7.3% per year was found during the investigation. At the same time the agranulocytosis morbidity remained constant during the period of investigation. The results of the study lead to the conclusion that the use of metamizole is not related to a higher risk of agranulocytosis.
采用对照病例法对使用安乃近后发生粒细胞缺乏症的风险进行了研究。该研究纳入了1982年至1986年期间索非亚所有粒细胞缺乏症病例及其对照病例。该时期粒细胞缺乏症的年平均发病率为每百万人口3.16例。病因分数为7.1%。使用安乃近后发生粒细胞缺乏症的相对风险为1.25,最大风险为每百万使用安乃近一年的人群中有0.03例,最大致死风险为每百万使用安乃近一年的人群中有0.007例。同时,对保加利亚同期安乃近的使用情况也进行了研究。以每1000人口每天使用的限定日剂量数表示的数据表明,该国安乃近的使用量很高。调查期间发现每年有7.3%的增长趋势。与此同时,在调查期间粒细胞缺乏症的发病率保持不变。研究结果得出结论,使用安乃近与粒细胞缺乏症的较高风险无关。