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首页> 外文期刊>Journal of Traditional and Complementary Medicine >Clinical efficacy and tolerability of Gosha-jinki-gan, a?Japanese traditional herbal medicine, for nocturia
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Clinical efficacy and tolerability of Gosha-jinki-gan, a?Japanese traditional herbal medicine, for nocturia

机译:日本传统草药Gosha-Jinki-gan对夜尿症的临床疗效和耐受性

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We evaluated the efficacy and tolerability of Gosha-jinki-gan (GJG; 濟生腎氣丸 jì shēng shèn qì wán) in 30 cases of nocturia (夜尿 yè niào) unresponsive to α1-blockers or antimuscarinic drugs. All patients received GJG extract powder (2.5 g) three times a day for 12 weeks as an add-on therapy to α1-blockers or antimuscarinic drugs. Subjective outcomes assessed by the International Prostate Symptom Score—quality of life, and the benign prostatic hyperplasia impact index and objective outcomes assessed by urinary frequency and the urine production rate at night showed significant improvement after treatment. Moreover, other objective outcomes assessed by maximum flow rates, postvoid residual, serum human atrial natriuretic peptide levels, and urinary 8-hydroxy-2′-deoxyguanosine levels did not change. Adverse events were observed in 10% of cases; however, these events were mild. GJG appears to be a safe and effective potential therapeutic alternative for patients with nocturia unresponsive to α1-blockers or antimuscarinic drugs. Further clinical investigations are required to elucidate the precise pathophysiologic mechanisms of GJG in nocturia. Graphical abstract Display Omitted.
机译:我们评估了Gosha-jinki-gan(GJG;济生肾气丸)对30例对α1-受体阻滞剂或抗毒蕈碱药物无反应的夜尿症(夜尿yèniào)的疗效和耐受性。所有患者每天接受3次GJG提取物粉末(2.5克)治疗12周,作为α1受体阻滞剂或抗毒蕈碱药物的补充疗法。通过国际前列腺症状评分评估的主观结果-生活质量,良性前列腺增生影响指数以及通过尿频和夜间尿液产生率评估的客观结果显示治疗后明显改善。此外,通过最大流速,无后遗症,血清人心钠素水平和尿中的8-羟基-2'-脱氧鸟苷水平评估的其他客观结果没有改变。在10%的病例中观察到不良事件;但是,这些事件是轻微的。对于对α1受体阻滞剂或抗毒蕈碱药物无反应的夜尿症患者,GJG似乎是一种安全有效的潜在治疗选择。需要进一步的临床研究以阐明夜尿症中GJG的确切病理生理机制。图形抽象显示被忽略。

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