机构地区:[1]南京医科大学附属南京医院(南京市第一医院)儿科,江苏省南京市210006
出 处:《世界华人消化杂志》2014年第31期4853-4857,共5页World Chinese Journal of Digestology
摘 要:目的:探讨无乳糖奶粉佐治轮状病毒(rotavirus,RV)性肠炎合并乳糖不耐受(lactose intolerance,LI)的临床疗效.方法:选取2010-10/2012-12门诊病例90例RV性肠炎合并LI患者作为研究对象,按照随机数字表法将患儿分为葡萄糖酸锌组、无乳糖奶粉组及联合组,每组各30例.3组患儿均进行常规口服补液,口服乳糖酶、双歧三联活菌等.在此基础上,葡萄糖酸锌组患儿给予葡萄糖酸锌口服液治疗,无乳糖奶粉组患儿给予无乳糖奶粉治疗,联合组患儿给予葡萄糖酸锌口服液联合无乳糖奶粉治疗.比较3组患儿临床疗效、总病程、临床症状缓解时间以及治疗前后心肌酶谱[天门冬氨酸氨基转移酶(aspartate aminotransferase,AST)、乳酸脱氢酶(lactic dehydrogenase,LDH)、肌酸激酶(creatine kinase,CK)及同工酶(creatine kinase-MB,CK-MB)]变化情况.结果:葡萄糖酸锌组和无乳糖奶粉组患儿总有效率均显著低于联合组,(83.33%vs96.67%),(80.00%vs 96.67%),差异具有统计学意义(P<0.05);葡萄糖酸锌组和无乳糖奶粉组患儿总病程和临床症状缓解时间均显著长于联合组,(7.32 d±2.14 d)vs(5.52 d±1.81 d)、(5.15 d±0.46 d)vs(3.18 d±0.77d),(7.41 d±2.03 d)vs(5.52 d±1.81 d)、(5.23 d±0.44 d)vs(3.18 d±0.77 d)(P<0.05),差异具有统计学意义(P<0.05);3组患儿治疗后AST、LDH、CK及CK-MB水平均显著下降,与治疗前比较,(39.66 U/L±3.28 U/L)vs(64.02 U/L±5.75 U/L)、(108.25 U/L±10.18U/L)vs(161.08 U/L±12.17 U/L)、(117.27U/L±9.86 U/L)vs(153.59 U/L±12.85 U/L)、(32.55 U/L±3.50 U/L)vs(57.45 U/L±6.77 U/L),(40.17 U/L±3.31 U/L)vs(63.89U/L±5.63 U/L)、(112.27 U/L±11.08 U/L)vs(160.12 U/L±12.49 U/L)、(120.07 U/L±9.92 U/L)vs(153.62 U/L±12.80 U/L)、(33.06 U/L±3.52 U/L)vs(57.68 U/L±6.73U/L),(26.75 U/L±2.68 U/L)vs(64.11 U/L±5.88 U/L)、(86.88 U/L±6.30 U/L)vs(159.62U/L±12.30 U/L)、(87.20 U/L±6.34 U/L)vs(154.10 U/L±12.97 U/L)、(24.11 U/L±2.62U/L)vs(57.56 U/L±6.39 U/L),差异具有统计学意义(P<0.05);葡萄糖�AIM: To explore the effects of lactose-free milk in adjunctive treatment of infants with rotavirus enteritis and lactose intolerance(RV-SLI).METHODS: Ninety patients with RV-SLI were randomly divided into three groups: a zinc gluconate group(n = 30), a lactose-free milk group(n = 30) and a combination group(n = 30). All the patients were treated with conventional oral rehydration solution, oral lactase, and bifid triple viable. On the basis of this treatment, the zinc gluconate group was treated with zinc gluconate, the lactose-free milk group was treated with lactose-free milk powder, and the combination group was treated with zinc gluconate and lactose-free milk powder. The clinical effects, total course, time to relief of clinical symptoms, and myocardial enzyme spectrum [aspartate aminotransferase(AST), lactic dehydrogenase(LDH), creatine kinase(CK), creatine kinase-MB(CK-MB)] were compared before and after treatment for the two groups.RESULTS: The effective rates rate for the two monotherapy groups were significantly lower than that for the combination group(83.33%, 80.00% vs 96.67%, P 0.05). The total course and time to relief of clinical symptoms were significantly longer in the two monotherapy groups than in the combination group(7.32 d ± 2.14 d, 7.41 d ± 2.03 d vs 5.52 d ± 1.81 d; 5.15 d ± 0.46 d, 5.23 d ± 0.44 d vs 3.18 d ± 0.77 d; P 0.05). AST, LDH, CK and CK-MB levels were significantly lower after treatment than prior treatment in all the three groups(39.66 U/L ± 3.28 U/L vs 64.02 U/L ± 5.75 U/L, 108.25 U/L ± 10.18 U/L vs 161.08 U/L ± 12.17 U/L, 117.27 U/L ± 9.86 U/L vs 153.59 U/L ± 12.85 U/L, 32.55 U/L ± 3.50 U/L vs 57.45 U/L ± 6.77 U/L, 40.17 U/L ± 3.31 U/L vs 63.89 U/L ± 5.63 U/L, 112.27 U/L ± 11.08 U/L vs 160.12 U/L ± 12.49 U/L, 120.07 U/L ± 9.92 U/L vs 153.62 U/L ± 12.80 U/L, 33.06 U/L ± 3.52 U/L vs 57.68 U/L ± 6.73 U/L, 26.75 U/L ± 2.68 U/L vs 64.11 U/L ± 5.88 U/L, 86.88 U/L ± 6.30 U/L vs 159.62 U/L ± 12.30 U/L, 87.20 U
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