Bardhan K D, Hunter J O, Miller J P, Thomson A B, Graham D Y, Russell R I, Sontag S, Hines C, Martin T, Gaussen L
District General Hospital, Rotherham.
Gut. 1988 Dec;29(12):1748-54. doi: 10.1136/gut.29.12.1748.
The effectiveness of antacid maintenance therapy in preventing duodenal ulcer (DU) relapse was investigated. Two hundred and fifty one asymptomatic patients with healed DU were stratified into smokers and non-smokers and randomised to receive for one year either placebo, or Maalox TC three tablets (81 mmol) at bedtime (hs), or Maalox TC three tablets in the morning plus three tablets at bedtime (bd) (162 mmol), or cimetidine 400 mg at bedtime. A double dummy technique was used to render the study double blind. In 176 patients evaluable for efficacy, the cumulative relapse at one year was: placebo 57%; Maalox TC hs 39%; Maalox TC bd 23%; cimetidine 25%. Maalox TC bd and cimetidine were equally effective and superior to placebo (p less than 0.01) and bedtime Maalox TC (p less than 0.04). The benefit of treatment was significant for the overall sample and for the subgroup of smokers. The results for the non-smokers also supported efficacy for these two treatments but, perhaps because of small sample sizes, these comparisons were not significant. All 251 patients were assessed for safety. Approximately half the patients in each treatment group had adverse events, leading to withdrawal in three, seven, 12, and four patients on placebo, Maalox hs, Maalox bd, and cimetidine respectively. Diarrhoea occurred in 12 patients in Maalox TC bd and eight in each other group. Serum magnesium concentrations were unchanged; aluminium concentrations were higher than baseline at six and 12 months in both antacid groups and at 12 months in the cimetidine group but the differences were not significant. Maalox TC three tablets bd are as effective as cimetidine 400 mg at bedtime in reducing DU relapse and both are superior to placebo.
研究了抗酸维持疗法预防十二指肠溃疡(DU)复发的有效性。251例无症状的DU愈合患者被分为吸烟者和非吸烟者,并随机接受为期一年的治疗,治疗方案分别为:安慰剂;睡前服用3片麦滋林TC(81毫摩尔);早上服用3片麦滋林TC加睡前服用3片(每日两次,162毫摩尔);睡前服用400毫克西咪替丁。采用双模拟技术使研究保持双盲。在176例可评估疗效的患者中,一年时的累积复发率分别为:安慰剂组57%;睡前服用麦滋林TC组39%;每日两次服用麦滋林TC组23%;西咪替丁组25%。每日两次服用麦滋林TC组和西咪替丁组疗效相当,且均优于安慰剂组(p<0.01)和睡前服用麦滋林TC组(p<0.04)。治疗对总体样本和吸烟者亚组均有显著益处。非吸烟者的结果也支持这两种治疗方法的疗效,但可能由于样本量较小,这些比较无统计学意义。对所有251例患者进行了安全性评估。每个治疗组中约一半的患者出现不良事件,导致安慰剂组、睡前服用麦滋林TC组、每日两次服用麦滋林TC组和西咪替丁组分别有3例、7例、12例和4例患者退出研究。每日两次服用麦滋林TC组有12例患者出现腹泻,其他组各有8例。血清镁浓度无变化;抗酸剂组在6个月和12个月时以及西咪替丁组在12个月时血清铝浓度高于基线水平,但差异无统计学意义。每日两次服用3片麦滋林TC在降低DU复发方面与睡前服用400毫克西咪替丁同样有效,且两者均优于安慰剂。