Su Pei-Yu, Lee Ya-Han, Kuo Li-Na, Chen Yen-Cheng, Chen Chiehfeng, Kang Yi-No, Chang Elizabeth H
Department of Pharmacy, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Department of Clinical Pharmacy, School of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Front Pharmacol. 2021 Jul 26;12:676345. doi: 10.3389/fphar.2021.676345. eCollection 2021.
AST-120, an oral spherical activated carbon, may delay the need for kidney dialysis and improve uremia symptoms because it can adsorb acidic and basic organic compounds, especially small-molecule uremic toxins. However, previous studies produced no conclusive evidence regarding the benefits of AST-120 in delaying the progression of chronic kidney disease (CKD). Therefore, this systematic review and network meta-analysis evaluated the effects of AST-120 in patients with CKD. Related keywords of CKD and AST-120 were used to search four databases to obtain potential evidence on this topic, and two authors individually completed evidence selection, data extraction, and quality assessment. Network meta-analysis was performed for mortality, end-stage renal disease, composite renal outcomes, and laboratory outcomes based on a frequentist approach. In total, 15 randomized controlled trials ( = 3,763) were included in the present synthesis, and the pooled results revealed non-significant differences in mortality among the treatment strategies. Low- and high-dose AST-120 were not superior to no AST-120 treatment regarding renal outcomes. However, the event rates of end-stage renal disease (risk ratio [RR] = 0.78, 95% confidence interval [CI] = 0.62-0.99) and composite renal outcomes (RR = 0.78, 95% CI: 0.63-0.97) were significantly lower in the tailored-dose AST-120 group than in no AST-120 group. The results did not reveal a small-study effect on the outcomes. Tailored dosing of AST-120 appeared to represent an optimal treatment strategy because it resulted in lower rates of composite renal outcomes and end-stage renal disease.
AST-120是一种口服球形活性炭,它可以吸附酸性和碱性有机化合物,尤其是小分子尿毒症毒素,因此可能会延迟肾脏透析的需求并改善尿毒症症状。然而,先前的研究并未得出关于AST-120在延缓慢性肾脏病(CKD)进展方面益处的确凿证据。因此,本系统评价和网状荟萃分析评估了AST-120对CKD患者的影响。使用CKD和AST-120的相关关键词检索四个数据库,以获取关于该主题的潜在证据,两位作者分别完成证据筛选、数据提取和质量评估。基于频率学派方法,对死亡率、终末期肾病、综合肾脏结局和实验室结局进行网状荟萃分析。本综述共纳入15项随机对照试验( = 3763),汇总结果显示各治疗策略之间的死亡率无显著差异。低剂量和高剂量AST-120在肾脏结局方面并不优于未使用AST-120治疗。然而,量身定制剂量的AST-120组终末期肾病的事件发生率(风险比[RR] = 0.78,95%置信区间[CI] = 0.62 - 0.99)和综合肾脏结局的事件发生率(RR = 0.78,95% CI:0.63 - 0.97)显著低于未使用AST-120组。结果未显示出对结局有小研究效应。AST-120的量身定制剂量似乎是一种最佳治疗策略,因为它导致综合肾脏结局和终末期肾病的发生率较低。