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丙氨酸基口服补液溶液:儿童急性非霍乱性腹泻疗效评估

Alanine-based oral rehydration solution: assessment of efficacy in acute noncholera diarrhea among children.

作者信息

Sazawal S, Bhatnagar S, Bhan M K, Saxena S K, Arora N K, Aggarwal S K, Kashyap D K

机构信息

Department of Pediatrics, All India Institute of Medical Sciences, New Delhi.

出版信息

J Pediatr Gastroenterol Nutr. 1991 May;12(4):461-8.

PMID:1865280
Abstract

This randomized, double-blind trial determined whether adding 90 mmol/L of alanine with a reduction in glucose to 90 mmol/L (alanine ORS) improves the efficacy of the standard oral rehydration solution (WHO-ORS). One hundred twenty-nine males aged 3-48 months with weight for length greater than or equal to 70% of NCHS, diarrheal duration less than or equal to 96 h, and clinical signs of mild to moderate dehydration were randomly allocated to either treatment group. During 0-6 h of treatment, ORS was offered at 120 ml/kg for rehydration without food or water. Beyond 6 h, ORS was offered as a volume-to-volume replacement for stool losses and a mixed diet of uniform composition was offered in amounts standardized for body weight. The most frequently isolated pathogens in alanine ORS and WHO-ORS groups were rotavirus (42 and 48%, respectively) and enterotoxigenic Escherichia coli (15 and 12%, respectively). In the 0-6 h period when food was withheld, median urine output in ml/kg (8;5, p less than 0.05) and percentage decrease in total serum solids (9:7%, p = 0.06) was significantly greater in alanine ORS than in WHO-ORS; median ORS intake and stool output were marginally lower in the alanine group but the differences were statistically not significant. Between 0 h and recovery, although the median values for duration of diarrhea (56.5 and 65.0 h), ORS consumption (260 and 323 ml/kg), and stool output (188.4 and 216.3 g/kg) were lower in the alanine ORS group, these differences with the WHO-ORS group were not statistically significant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

这项随机双盲试验旨在确定添加90毫摩尔/升丙氨酸并将葡萄糖浓度降至90毫摩尔/升(丙氨酸口服补液盐)是否能提高标准口服补液盐(世界卫生组织口服补液盐)的疗效。129名年龄在3至48个月、身长体重比大于或等于美国国家卫生统计中心标准70%、腹泻持续时间小于或等于96小时且有轻至中度脱水临床体征的男性被随机分配至治疗组。在治疗的0至6小时期间,口服补液盐按120毫升/千克给予以进行补液,期间不进食或饮水。6小时后,口服补液盐按等量补充粪便丢失量给予,同时提供成分均匀的混合饮食,其数量按体重标准化。丙氨酸口服补液盐组和世界卫生组织口服补液盐组中最常分离出的病原体分别是轮状病毒(分别为42%和48%)和产肠毒素大肠杆菌(分别为15%和12%)。在禁食的0至6小时期间,丙氨酸口服补液盐组每千克体重的尿量中位数(8;5,P<0.05)和总血清固体减少百分比(9:7%,P = 0.06)显著高于世界卫生组织口服补液盐组;丙氨酸组口服补液盐摄入量和粪便排出量中位数略低,但差异无统计学意义。在0小时至恢复期间,虽然丙氨酸口服补液盐组腹泻持续时间(56.5和65.0小时)、口服补液盐消耗量(260和323毫升/千克)和粪便排出量(188.4和216.3克/千克)的中位数较低,但与世界卫生组织口服补液盐组的这些差异无统计学意义。(摘要截短至250字)

相似文献

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Alanine-based oral rehydration solution: assessment of efficacy in acute noncholera diarrhea among children.丙氨酸基口服补液溶液:儿童急性非霍乱性腹泻疗效评估
J Pediatr Gastroenterol Nutr. 1991 May;12(4):461-8.
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Amylase-resistant starch as adjunct to oral rehydration therapy in children with diarrhea.抗淀粉酶淀粉作为腹泻儿童口服补液疗法的辅助手段。
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A randomised, double-blind clinical trial of a maltodextrin containing oral rehydration solution in acute infantile diarrhoea.一项关于含麦芽糊精口服补液溶液治疗急性婴幼儿腹泻的随机双盲临床试验。
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引用本文的文献

1
The effect of oral rehydration solution and recommended home fluids on diarrhoea mortality.口服补液盐和推荐的家庭补液对腹泻死亡率的影响。
Int J Epidemiol. 2010 Apr;39 Suppl 1(Suppl 1):i75-87. doi: 10.1093/ije/dyq025.
2
Improving the ORS: does glutamine have a role?改良口服补液盐:谷氨酰胺有作用吗?
J Health Popul Nutr. 2007 Sep;25(3):263-6.
3
Clinical trials of improved oral rehydration salt formulations: a review.改良口服补液盐配方的临床试验:综述
Bull World Health Organ. 1994;72(6):945-55.
4
Development of an improved oral rehydration solution.
Indian J Pediatr. 1991 Nov-Dec;58(6):757-61. doi: 10.1007/BF02825431.
5
Fluid therapy in acute diarrhea.
Indian J Pediatr. 1991 Nov-Dec;58(6):733-43. doi: 10.1007/BF02825429.