Effectiveness of Polyethylene Glycol 3350 versus Lactulose in Management of Functional Constipation in Children

Mansour Hanin Ahmed, I. Ali, M. Ali
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Abstract

Introduction: Constipation is one of the common problems in childhood. Recently, Polyethylene Glycol (PEG 3350) has been suggested as a good alternative laxative to Lactulose as a treatment option in pediatric constipation. The current study aimed to compare the efficacy of two laxatives (PEG 3350 and Lactulose) in the management of functional constipation and evaluate the side effects. Methods and materials: In an open-label clinical trial, 1-13 year-old children with functional constipation according to ROME IV criteria and the presence of RAIR based on anorectal manometry were studied. The patients were randomized to receive either PEG3350 (0.8 g/kg/d) or Lactulose (2 ml/kg/d). Both groups received the medication orally in two divided doses for 12 weeks. They were evaluated clinically at the end of 4, 8, and 12 weeks of therapy, and the end of 16 and 20 weeks from enrolment. At the end of the 12th week, Success was defined as a defecation frequency ≥ 3/week and improvement in stool consistency without painful defecation, as well as encopresis ≤ 1 every two weeks. Results: We enrolled 43 patients (M20, F23) aged 4.16 ± 2.3 years. At the end of the 12th week, good clinical outcomes were achieved in 95% (PEG) and 77.3% (Lactulose). The PEG group had a significant increase in defecations in a week compared with the Lactulose group (6.26 ± 0.5 vs. 4.94 ± 0.8, p = 0.0001) and a significant decrease in encopresis (35% vs. 10, p = 0.01). PEG achieved defecation without pain (0% vs. 22.7%) and less hard stools (5% vs. 18.2%, p = 0.1). Patients reported less abdominal pain and bloating than children using Lactulose (25% and 0% vs. 68.2% and 27.3%, respectively). We reported a significant relapse because of sudden ceasession of treatment in the Lactulose group (13.6% vs. 5%, p = 0.04) compared with the PEG group. Conclusion: PEG3350 compared with Lactulose provided a higher success rate, less relapse rate, and fewer side effects in the treatment of constipated children.
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聚乙二醇3350与乳果糖治疗儿童功能性便秘的疗效
导读:便秘是儿童时期常见的问题之一。最近,聚乙二醇(PEG 3350)被认为是一种很好的替代乳果糖的泻药,作为儿童便秘的治疗选择。本研究旨在比较两种泻药(PEG 3350和乳果糖)治疗功能性便秘的疗效并评估其副作用。方法和材料:在一项开放标签临床试验中,研究了1-13岁的功能性便秘儿童,根据ROME IV标准和基于肛门直肠测压法的RAIR存在。患者随机接受PEG3350 (0.8 g/kg/d)或乳果糖(2 ml/kg/d)治疗。两组均口服两剂,疗程12周。在治疗4周、8周和12周结束时,以及入组后16周和20周结束时,对患者进行临床评估。在第12周结束时,成功定义为排便频率≥3次/周,大便一致性改善,无排便疼痛,每两周小便≤1次。结果:纳入患者43例(M20例,F23例),年龄4.16±2.3岁。在第12周结束时,95% (PEG)和77.3%(乳果糖)的临床结果良好。与乳果糖组相比,聚乙二醇组一周内排便量显著增加(6.26±0.5比4.94±0.8,p = 0.0001),粪尿率显著降低(35%比10,p = 0.01)。PEG实现了无痛排便(0%比22.7%)和较少的硬便(5%比18.2%,p = 0.1)。与使用乳果糖的儿童相比,患者报告的腹痛和腹胀较少(分别为25%和0% vs. 68.2%和27.3%)。我们报道,与PEG组相比,乳果糖组因突然停止治疗而显著复发(13.6% vs. 5%, p = 0.04)。结论:与乳果糖相比,PEG3350治疗便秘患儿的成功率更高,复发率更低,副作用更小。
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