Pediatric Department, University of Messina, Messina 98100, Italy.
World J Gastroenterol. 2013 Jan 14;19(2):235-40. doi: 10.3748/wjg.v19.i2.235.
To assess the effects of partially hydrolyzed guar gum (PHGG) diet supplement in pediatric chronic abdominal pain (CAP) and irritable bowel syndrome (IBS).
A randomized, double-blind pilot study was performed in sixty children (8-16 years) with functional bowel disorders, such as CAP or IBS, diagnosed according to Rome III criteria. All patients underwent ultrasound, blood and stool examinations to rule out any organic disease. Patients were allocated to receive PHGG at dosage of 5 g/d (n = 30) or placebo (fruit-juice n = 30) for 4 wk. The evaluation of the efficacy of fiber supplement included IBS symptom severity score (Birmingham IBS Questionnaire), severity of abdominal pain (Wong-Baker Face Pain Rating Score) and bowel habit (Bristol Stool Scale). Symptom scores were completed at 2, 4, and 8 wk. The change from baseline in the symptom severity scale at the end of treatment and at 4 wk follow-up after treatment was the primary endpoint. The secondary endpoint was to evaluate compliance to supplementation with the PHGG in the pediatric population. Differences within groups during the treatment period and follow-up were evaluated by the Wilcoxon signed-rank test.
The results of the study were assessed considering some variables, such as frequency and intensity of symptoms with modifications of the bowel habit. Both groups were balanced for baseline characteristics and all patients completed the study. Group A (PHGG group) presented a higher level of efficacy compared to group B (control group), (43% vs 5%, P = 0.025) in reducing clinical symptoms with modification of Birmingham IBS score (median 0 ± 1 vs 4 ± 1, P = 0.025), in intensity of CAP assessed with the Wong-Baker Face Pain Rating Score and in normalization of bowel habit evaluated with the Bristol Stool Scale (40% vs 13.3%, P = 0.025). In IBS subgroups, statistical analysis shown a tendency toward normalization of bowel movements, but there was no difference in the prevalence of improvement in two bowel habit subsets. PHGG was therefore better tolerated without any adverse effects.
Although the cause of pediatric functional gastrointestinal disorders is not known, the results show that complementary therapy with PHGG may have beneficial effects on symptom control.
评估部分水解瓜尔胶(PHGG)饮食补充剂对儿科慢性腹痛(CAP)和肠易激综合征(IBS)的影响。
对 60 例功能性肠病患儿(8-16 岁)进行了一项随机、双盲的初步研究,这些患儿根据罗马 III 标准被诊断为 CAP 或 IBS 等疾病。所有患者均接受了超声、血液和粪便检查以排除任何器质性疾病。患者被随机分配接受 PHGG 剂量为 5 g/d(n=30)或安慰剂(果汁 n=30)治疗 4 周。纤维补充的疗效评估包括 IBS 症状严重程度评分(Birmingham IBS 问卷)、腹痛严重程度(Wong-Baker 面部疼痛评分量表)和排便习惯(布里斯托粪便量表)。症状评分在 2、4 和 8 周时完成。治疗结束时和治疗结束后 4 周时症状严重程度量表的基线变化是主要终点。次要终点是评估 PHGG 在儿科人群中的依从性。治疗期间和随访期间组内的差异采用 Wilcoxon 符号秩检验进行评估。
考虑到一些变量,如症状的频率和强度以及排便习惯的改变,对研究结果进行了评估。两组在基线特征和所有患者均完成研究方面均平衡。A 组(PHGG 组)在降低临床症状(Birmingham IBS 评分中位数 0±1 对 4±1,P=0.025)、改善 CAP 严重程度(Wong-Baker 面部疼痛评分量表)以及改善排便习惯(Bristol 粪便量表)方面的疗效高于 B 组(对照组)(43%对 5%,P=0.025)。在 IBS 亚组中,统计分析显示排便正常的趋势,但在两个排便习惯亚组的改善发生率方面无差异。PHGG 因此具有更好的耐受性,没有任何不良反应。
尽管儿科功能性胃肠疾病的病因尚不清楚,但结果表明 PHGG 补充治疗可能对症状控制有益。