首页> 外文期刊>Iranian red crescent medical journal >Comparison Between the Cassia Fistula`s Emulsion With Polyethylene Glycol (PEG4000) in the Pediatric Functional Constipation: A Randomized Clinical Trial
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Comparison Between the Cassia Fistula`s Emulsion With Polyethylene Glycol (PEG4000) in the Pediatric Functional Constipation: A Randomized Clinical Trial

机译:决明子瘘乳剂与聚乙二醇(PEG4000)在儿科功能性便秘中的比较:一项随机临床试验

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There are few effective drugs for pediatric functional constipation (FC). Objectives: Comparing the effectiveness of Cassia fistula’s emulsion (CFE) with Polyethylene glycol (PEG4000) in FC; and evaluation of safety of both drugs in the treatment of FC. Materials and Methods: A randomized open label, prospective, controlled, parallel-group clinical trial was carried on 109 children (M/F: 63/46; mean age ± SD: 59.7 ± 28.8 months) in Amirkola children’s hospital, Babol, Iran. The inclusion criteria were based on diagnosis of FC according to the Rome III criteria and age range between 2 - 15 years. They received CFE or PEG randomly for 4 weeks. Frequencies of defecation, severity of pain, consistency of stool, fecal incontinence and retentive posturing were compared between the two groups and with baselines. Children were counted as improved when they exited from Rome III criteria of FC. Results: Fifty seven patients were assigned to receive PEG and 52 patients received CFE. After 4weeks of medication, 86.5% of children in CFE group and 77.1% in PEG group (RR = 1.121, CI95%:0.939 - 1.338) exited from the criteria of FC. All measurable criteria improved in both groups without any significant difference, except in the frequency of defecation that in CFE group (10.96 ± 5.7) was significantly more than PEG group (6.9 ± 3.5) (P < 0.0001). Compliances of PEG were significantly better in the 2 first weeks (P = 0.002, 0.008) but not in third and fourth week (P = 0.061, 0.062). None of these two drugs cause clinically significant side effects. Conclusions: CFE can be as effective as PEG in the 4-weeks treatment of children with FC.
机译:儿科功能性便秘(FC)的有效药物很少。目的:比较决明子瘘乳剂(CFE)和聚乙二醇(PEG4000)在FC中的有效性;和两种药物在FC治疗中的安全性评估。材料和方法:在伊朗巴博尔的阿米尔科拉儿童医院对109名儿童(男/女:63/46;平均年龄±SD:59.7±28.8个月)进行了一项随机,开放,前瞻性,对照,平行分组的临床试验。 。纳入标准基于根据罗马三世标准进行的FC诊断,年龄范围在2至15岁之间。他们随机接受CFE或PEG治疗4周。比较了两组的排便频率,疼痛严重程度,大便的一致性,大便失禁和保持姿势,并与基线进行了比较。当儿童退出FC的罗马三世标准时,被视为有进步。结果:57位患者被分配接受PEG,52位患者接受CFE。服药4周后,CFE组的儿童中有86.5%,PEG组的儿童中有77.1%(RR = 1.121,CI95%:0.939-1.338)退出了FC标准。两组的所有可测量标准均有改善,除排便频率外,CFE组(10.96±5.7)明显大于PEG组(6.9±3.5)(P <0.0001)。头两个星期的PEG依从性明显更好(P = 0.002,0.008),而在第三和第四个星期则没有(P = 0.061,0.062)。这两种药物均未引起临床上显着的副作用。结论:在FC儿童的4周治疗中,CFE与PEG一样有效。

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