Sood A, Midha V, Sood N, Kaushal V
Department of Medicine, Dayanand Medical College and Hospital, Ludhiana, Punjab.
Indian J Gastroenterol. 2000 Jan-Mar;19(1):14-6.
To investigate the efficacy of azathioprine in treating patients with severe ulcerative colitis.
One-year, randomized, placebo-controlled trial.
83 patients with severe ulcerative colitis were enrolled. Fifty patients who relapsed within two months on corticosteroid withdrawal were randomized into two groups. The azathioprine group received oral sulfasalazine (6-8 g/day), oral prednisolone (1 mg/Kg/day) and oral azathioprine (2 mg/Kg/day). The placebo group received oral sulfasalazine (6-8 g/day), oral prednisolone (1 mg/Kg/day) and placebo. Corticosteroids were tapered over 12-16 weeks.
Five patients (2 in azathioprine group, 3 in placebo group) dropped out of the study. Three patients in the azathioprine group had side effects. The number of patients going into complete remission and partial remission was not significantly different in the two groups. The proportion of relapses in the azathioprine group was lower than in the placebo group (p < 0.05).
In patients with ulcerative colitis, azathioprine had no effect in achieving remission, when given in combination with prednisolone; however, it lowers the proportion of relapses. Side effects like pancreatitis and hepatitis are mild and respond promptly to drug withdrawal.
研究硫唑嘌呤治疗重度溃疡性结肠炎患者的疗效。
为期一年的随机、安慰剂对照试验。
纳入83例重度溃疡性结肠炎患者。50例在停用皮质类固醇激素后两个月内复发的患者被随机分为两组。硫唑嘌呤组接受口服柳氮磺胺吡啶(6 - 8克/天)、口服泼尼松龙(1毫克/千克/天)和口服硫唑嘌呤(2毫克/千克/天)。安慰剂组接受口服柳氮磺胺吡啶(6 - 8克/天)、口服泼尼松龙(1毫克/千克/天)和安慰剂。皮质类固醇激素在12 - 16周内逐渐减量。
5例患者(硫唑嘌呤组2例,安慰剂组3例)退出研究。硫唑嘌呤组有3例患者出现副作用。两组进入完全缓解和部分缓解的患者数量无显著差异。硫唑嘌呤组的复发率低于安慰剂组(p < 0.05)。
在溃疡性结肠炎患者中,硫唑嘌呤与泼尼松龙联合使用时对实现缓解无作用;然而,它可降低复发率。胰腺炎和肝炎等副作用较轻,停药后反应迅速。