奥美拉唑联合益生菌对小儿幽门螺杆菌阳性慢性胃炎的疗效及对炎症反应和胃肠道功能的影响

乔婕, 杨新军, 彭亮, 等. 奥美拉唑联合益生菌对小儿幽门螺杆菌阳性慢性胃炎的疗效及对炎症反应和胃肠道功能的影响[J]. 中国中西医结合消化杂志, 2023, 31(10): 793-797. doi: 10.3969/j.issn.1671-038X.2023.10.12
引用本文: 乔婕, 杨新军, 彭亮, 等. 奥美拉唑联合益生菌对小儿幽门螺杆菌阳性慢性胃炎的疗效及对炎症反应和胃肠道功能的影响[J]. 中国中西医结合消化杂志, 2023, 31(10): 793-797. doi: 10.3969/j.issn.1671-038X.2023.10.12
QIAO Jie, YANG Xinjun, PENG Liang, et al. Effect of omeprazole combined with probiotics on Helicobacter pylori-positive chronic gastritis in children and its influence on inflammatory response and gastrointestinal function[J]. Chin J Integr Tradit West Med Dig, 2023, 31(10): 793-797. doi: 10.3969/j.issn.1671-038X.2023.10.12
Citation: QIAO Jie, YANG Xinjun, PENG Liang, et al. Effect of omeprazole combined with probiotics on Helicobacter pylori-positive chronic gastritis in children and its influence on inflammatory response and gastrointestinal function[J]. Chin J Integr Tradit West Med Dig, 2023, 31(10): 793-797. doi: 10.3969/j.issn.1671-038X.2023.10.12

奥美拉唑联合益生菌对小儿幽门螺杆菌阳性慢性胃炎的疗效及对炎症反应和胃肠道功能的影响

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Effect of omeprazole combined with probiotics on Helicobacter pylori-positive chronic gastritis in children and its influence on inflammatory response and gastrointestinal function

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  • 目的 研究奥美拉唑联合益生菌对小儿幽门螺杆菌阳性慢性胃炎的疗效及对炎症反应和胃肠道功能的影响。方法 选取2020年5月—2022年5月收治的幽门螺杆菌阳性慢性胃炎患儿120例,按照随机数字表法分为对照组(n=60)和研究组(n=60)。对照组给予克拉霉素+阿莫西林+奥美拉唑治疗,研究组在对照组基础上给予益生菌治疗。比较治疗前后2组的炎性因子[肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、C反应蛋白(CRP)]水平、胃肠道功能[胃肠道功能症状评定量表(GSRS)]、胃蛋白酶原比值(PGR)、胃蛋白酶原Ⅰ(PGⅠ)及胃泌素17(G-17)水平,并比较治疗后2组的临床疗效(总有效率)、幽门螺杆菌根治率及治疗后3个月的复发率,同时统计2组不良反应发生率。结果 治疗后,研究组总有效率、幽门螺杆菌根治率均显著高于对照组,复发率、TNF-α、IL-6及CRP水平、GSRS评分、PGR、PGⅠ及G-17水平均显著低于对照组(P<0.05),2组不良反应发生率差异无统计学意义(P>0.05)。结论 奥美拉唑联合益生菌治疗幽门螺杆菌阳性慢性胃炎可改善患儿临床症状,降低炎症反应及调节黏膜分泌,恢复胃肠道功能,安全有效。
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  • 表 1  2组临床疗效比较 例(%)

    组别 例数 治愈 显效 有效 无效 总有效
    对照组 60 16(26.67) 20(33.33) 14(23.33) 10(16.67) 50(83.33)
    研究组 60 25(41.67) 17(28.33) 16(26.67) 2(3.33) 58(96.67)
    χ2 5.926
    P 0.015
    下载: 导出CSV

    表 2  2组炎性因子水平比较 X±S

    组别 例数 TNF-α/(pg/mL) IL-6/(pg/mL) CRP/(mg/L)
    治疗前 治疗后 治疗前 治疗后 治疗前 治疗后
    对照组 60 58.26±9.62 36.92±6.451) 42.99±7.26 25.23±4.861) 25.27±4.63 14.83±2.421)
    研究组 60 59.27±9.29 23.43±4.161) 43.07±7.34 15.24±2.281) 26.24±4.11 8.17±1.731)
    t 0.585 13.614 0.060 14.415 1.214 17.342
    P 0.560 < 0.001 0.952 < 0.001 0.227 < 0.001
    与本组治疗前比较,1)P<0.05。
    下载: 导出CSV

    表 3  2组GSRS评分比较 分,X±S

    组别 例数 治疗前 治疗后
    对照组 60 74.53±8.64 39.55±5.261)
    研究组 60 75.65±8.33 25.36±4.741)
    t 0.723 15.523
    P 0.471 < 0.001
    与本组治疗前比较,1)P<0.05。
    下载: 导出CSV

    表 4  2组PGR、PGⅠ及G-17水平比较 X±S

    组别 例数 PGR PGⅠ/(μg/L) G-17/(pmol/L)
    治疗前 治疗后 治疗前 治疗后 治疗前 治疗后
    对照组 60 7.86±1.54 6.46±1.221) 126.67±25.37 115.74±18.371) 7.46±1.58 6.45±0.861)
    研究组 60 7.91±1.62 5.31±0.851) 127.11±26.16 102.28±16.631) 7.51±1.66 5.13±0.481)
    t 0.173 5.991 0.094 4.208 0.169 10.382
    P 0.863 < 0.001 0.926 < 0.001 0.866 < 0.001
    与本组治疗前比较,1)P<0.05。
    下载: 导出CSV
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出版历程
收稿日期:  2023-01-05
刊出日期:  2023-10-15

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