Shim Soo Bo, Ahn Hye Li, Lee Hyun Hee, Lee Ju Ah, Lee Hye Lim
Department of Paediatrics, College of Korean Medicine, Daejeon University, Daejeon, Republic of Korea.
Hwa-pyeong Institute of Integrative Medicine, Incheon, Republic of Korea.
Evid Based Complement Alternat Med. 2022 Aug 9;2022:5725258. doi: 10.1155/2022/5725258. eCollection 2022.
Herbal medicines (HM) and growth hormones (GH) are widely used to treat short stature (SS) in children. This systematic review aimed to evaluate the effectiveness and safety of combination therapy with HM and GH (CHG) compared to those of GH monotherapy (GHM) in children with SS.
We searched 17 electronic databases from inception to 1 April 2021. Only randomized controlled trials (RCTs) were included. Two authors independently performed the selection and quality assessment of the included studies using Cochrane Handbook criteria. Relative risk (RR) was used to measure dichotomous outcomes with a 95% confidence interval (CI). Mean difference (MD) or standard MD (SMD) was used to measure continuous outcomes with a 95% CI.
Seven RCTs involving 455 participants with SS were included. Standard deviations in height (MD = 0.31, 95% CI: 0.24-0.38, < 0.00001), and insulin-like growth factor binding protein-3 (MD = 1.39, 95% CI: 0.93-1.85, < 0.00001) were significantly higher in the CHG group than in the GHM group. Growth velocity (MD = 1.82, 95% CI: 1.34-2.31, < 0.00001) and insulin-like growth factor-1 (MD = 61.85, 95% CI: 55.80-67.90, < 0.00001) were significantly higher in the CHG group. Adverse events were significantly lower in the CHG group (risk ratio: 0.10, 95% CI: 0.02-0.54, = 0.007). However, the level of evidence was low.
CHG demonstrated significantly better efficacy than GHM for treating SS, with a low incidence of adverse events. However, since the level of evidence is low, methodologically standardized RCTs are required to verify these results.
草药(HM)和生长激素(GH)被广泛用于治疗儿童身材矮小(SS)。本系统评价旨在评估与生长激素单一疗法(GHM)相比,草药与生长激素联合疗法(CHG)治疗SS患儿的有效性和安全性。
我们检索了从建库至2021年4月1日的17个电子数据库。仅纳入随机对照试验(RCT)。两位作者根据Cochrane手册标准独立对纳入研究进行筛选和质量评估。相对危险度(RR)用于衡量二分结局,95%置信区间(CI)。均差(MD)或标准化均差(SMD)用于衡量连续性结局,95%CI。
纳入7项涉及455例SS患儿的RCT。CHG组的身高标准差(MD = 0.31,95%CI:0.24 - 0.38,P < 0.00001)和胰岛素样生长因子结合蛋白-3(MD = 1.39,95%CI:0.93 - 1.85,P < 0.00001)显著高于GHM组。CHG组的生长速度(MD = 1.82,95%CI:1.34 - 2.31,P < 0.00001)和胰岛素样生长因子-1(MD = 61.85,95%CI:55.80 - 67.90,P < 0.00001)显著更高。CHG组的不良事件显著更低(风险比:0.10,95%CI:0.02 - 0.54,P = 0.0(此处原文有误,应为0.007))。然而,证据水平较低。
CHG治疗SS的疗效显著优于GHM,不良事件发生率低。然而,由于证据水平较低,需要方法学标准化的RCT来验证这些结果。