Cézard J P, Duhamel J F, Meyer M, Pharaon I, Bellaiche M, Maurage C, Ginies J L, Vaillant J M, Girardet J P, Lamireau T, Poujol A, Morali A, Sarles J, Olives J P, Whately-Smith C, Audrain S, Lecomte J M
Pediatric Gastroenterology Unit, Paris, France.
Gastroenterology. 2001 Mar;120(4):799-805. doi: 10.1053/gast.2001.22544.
BACKGROUND & AIMS: Oral rehydration therapy is the only treatment recommended by the World Health Organization in acute diarrhea in children. Antisecretory drugs available could not be used because of their side effects, except for racecadotril, which is efficient in acute diarrhea in adults.
The efficacy and tolerability of racecadotril (1.5 mg/kg administered orally 3 times daily) as adjuvant therapy to oral rehydration were compared with those of placebo in 172 infants aged 3 months to 4 years (mean age, 12.8 months) who had acute diarrhea. The treatment groups were comparable in terms of age, duration of diarrhea, number of stools, and causative microorganism at inclusion.
During the first 48 hours of treatment, patients receiving racecadotril had a significantly lower stool output (grams per hour) than those receiving placebo. The 95% confidence interval was 43%-88% for the full data set (n = 166; P = 0.009) and 33%-75% for the per-protocol population (n = 116; P = 0.001). There was no difference between treatments depending on rotavirus status. Significant differences between treatment groups were also found after 24 hours of treatment: full data set (n = 167; P = 0.026) and per-protocol population (n = 121; P = 0.015). Tolerability was good in both groups of patients.
This study demonstrates the efficacy (up to 50% reduction in stool output) and tolerability of racecadotril as adjuvant therapy to oral rehydration solution in the treatment of severe diarrhea in infants and children.
口服补液疗法是世界卫生组织推荐的治疗儿童急性腹泻的唯一方法。除消旋卡多曲外,现有的抗分泌药物因副作用而无法使用,消旋卡多曲对成人急性腹泻有效。
将消旋卡多曲(1.5毫克/千克,每日口服3次)作为口服补液辅助疗法的疗效和耐受性,与安慰剂在172名3个月至4岁(平均年龄12.8个月)患急性腹泻的婴儿中进行比较。治疗组在纳入时的年龄、腹泻持续时间、大便次数和致病微生物方面具有可比性。
在治疗的前48小时内,接受消旋卡多曲治疗的患者每小时的粪便排出量明显低于接受安慰剂治疗的患者。完整数据集(n = 166;P = 0.009)的95%置信区间为43%-88%,符合方案人群(n = 116;P = 0.001)的95%置信区间为33%-75%。根据轮状病毒感染情况,治疗之间没有差异。在治疗24小时后,治疗组之间也发现了显著差异:完整数据集(n = 167;P = 0.026)和符合方案人群(n = 121;P = 0.015)。两组患者的耐受性都很好。
本研究证明了消旋卡多曲作为口服补液溶液辅助疗法治疗婴幼儿严重腹泻的疗效(粪便排出量最多可减少50%)和耐受性。