Zeng Jian, Lv Lin, Mei Zhe-Chuan
Department of Gastroenterology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
J Gastroenterol Hepatol. 2017 Mar;32(3):558-566. doi: 10.1111/jgh.13604.
Budesonide is a second-generation steroid with prominent topical effects and minimal systemic activity for patients with ulcerative colitis (UC). We perform a systematic review and meta-analysis of randomized placebo-controlled trials to assess the efficacy and safety of budesonide foam in mild-to-moderate distal UC.
Comprehensive searches were performed to identify all eligible studies. Outcome measures were clinical remission, endoscopic improvement, elimination of rectal bleeding, and adverse events. The risk ratio (RR) with 95% confidence interval (CI) was estimated for each outcome. All statistical analyses were performed in STATA 12.0.
Three randomized placebo-controlled trials recruiting 711 patients with mild-to-moderate distal UC were included in this study. No significant bias and heterogeneity was identified. Pooled analyses showed that budesonide foam was significantly superior to placebo for induction of clinical remission (RR = 1.83, 95%CI: 1.41, 2.37; P < 0.001) and endoscopic improvement (RR = 1.44, 95%CI: 1.23, 1.68; P < 0.001), and eliminating rectal bleeding at week 2 (RR = 2.00, 95%CI: 1.50, 2.66; P < 0.001), week 4 (RR = 1.73, 95%CI: 1.42, 2.12; P < 0.001), and week 6 (RR = 1.76, 95%CI: 1.45, 2.14; P < 0.001). No statistically significant difference was observed in the incidence of treatment-related adverse events and therapeutic discontinuation because of adverse events between budesonide foam and placebo.
Budesonide foam is well tolerated and superior to placebo in inducing clinical remission and endoscopic improvement, and eliminating rectal bleeding for mild-to-moderate distal UC.
布地奈德是一种第二代类固醇药物,对溃疡性结肠炎(UC)患者具有显著的局部作用且全身活性极小。我们对随机安慰剂对照试验进行系统评价和荟萃分析,以评估布地奈德泡沫剂治疗轻至中度远端UC的疗效和安全性。
进行全面检索以识别所有符合条件的研究。结局指标为临床缓解、内镜改善、直肠出血消失及不良事件。对每个结局估计风险比(RR)及95%置信区间(CI)。所有统计分析均在STATA 12.0中进行。
本研究纳入了3项随机安慰剂对照试验,共711例轻至中度远端UC患者。未发现显著偏倚和异质性。汇总分析显示,布地奈德泡沫剂在诱导临床缓解(RR = 1.83,95%CI:1.41,2.37;P < 0.001)、内镜改善(RR = 1.44,95%CI:1.23,1.68;P < 0.001)以及在第2周(RR = 2.00,95%CI:1.50,2.66;P < 0.001)、第4周(RR = 1.73,95%CI:1.42,2.12;P < 0.001)和第6周(RR = 1.76,95%CI:1.45,2.14;P < 0.001)消除直肠出血方面显著优于安慰剂。在布地奈德泡沫剂与安慰剂之间,治疗相关不良事件的发生率以及因不良事件导致的治疗中断方面未观察到统计学显著差异。
布地奈德泡沫剂耐受性良好,在诱导轻至中度远端UC临床缓解、内镜改善以及消除直肠出血方面优于安慰剂。