Colin-Jones D G, Langman M J, Lawson D H, Logan R F, Paterson K R, Vessey M P
Queen Alexandra Hospital, Portsmouth.
Gut. 1992 Sep;33(9):1280-4. doi: 10.1136/gut.33.9.1280.
A total of 9928 cimetidine users were identified from prescriptions in four centres and followed for 10 years. The 'all-cause' mortality ratio fell from 1.9 in year 1 to 1.0 in years 8 to 10. Most of the early excess in mortality was attributable to cimetidine being given in the late stages of many diseases, often to counter adverse gastric effects of other drugs. Specific causes of mortality during years 5-10 of the study, were generally unremarkable. Significant increases in mortality ratios were apparent, however, for oesophageal cancer (years 5-7, 2.3; years 8-10, 1.9); lung cancer (years 5-7, 1.1; years 8-10, 1.7); diseases of the oesophagus, stomach, and duodenum (years 5-7, 3.3; years 8-10, 2.3); and chronic liver disease (years 5-7, 2.4; years 8-10, 3.3). None of these increases in mortality seems to be attributable to an adverse effect of cimetidine use. Data are also presented for mortality from diseases of the nervous system. Eight deaths (of which one was miscoded) were certified as being from motor neurone disease, representing a mortality ratio of 2.6 for years 2-10 of the study which is of borderline statistical significance. This study confirms that cimetidine is safe. Mortality from some diseases increased over the study period, but selection rather than any adverse effect of the drug is likely to be the explanation.
从四个中心的处方中识别出总共9928名使用西咪替丁的患者,并对其进行了10年的随访。“全因”死亡率从第1年的1.9降至第8至10年的1.0。早期死亡率过高主要是因为在许多疾病的晚期使用西咪替丁,通常是为了对抗其他药物的不良胃部影响。在研究的第5至10年期间,具体的死亡原因一般并不显著。然而,食管癌(第5至7年,2.3;第8至10年,1.9)、肺癌(第5至7年,1.1;第8至10年,1.7)、食管、胃和十二指肠疾病(第5至7年,3.3;第8至10年,2.3)以及慢性肝病(第5至7年,2.4;第8至10年,3.3)的死亡率有显著上升。这些死亡率的上升似乎都不能归因于使用西咪替丁的不良反应。还给出了神经系统疾病的死亡率数据。有8例死亡(其中1例编码错误)被证明是运动神经元病导致的,在研究的第2至10年,死亡率为2.6,具有边缘统计学意义。这项研究证实西咪替丁是安全的。在研究期间,某些疾病的死亡率有所上升,但可能的解释是选择因素而非药物的任何不良反应。