Yu-Huan Song, AiBing Ning, Na Guo, Ying Yang, Fei Tang, Na Zhao, Jun Hu, Hong Wu, Ting Peng, Yue-Fei Xiao, Guang-Yan Cai
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The primary outcome was coronary artery calcification scores (CACS) or abdominal aortic calcification scores (AACS) or Kauppila index. The secondary outcome was pulse-wave velocity (PWV). Laboratory data were shown in safety data. A random-effect model was used to provide the summary measures of effect [standardised mean difference (SMD) and 95% confidence interval (CI)].</p><p><strong>Results: </strong>Seven randomised, controlled trials and one nonrandomised, controlled trial involving 370 patients were included. Six studies reported that the progression of CACS or AACS was slower in the intravenous STS group compared with the control group (SMD -3.24, 95% CI: -5.29, -1.18, <i>p</i> = 0.002). Two studies showed the increase in PWV was less in the STS group compared with the control group (SMD -0.52, 95% CI: -0.92, -0.13, <i>p</i> = 0.009). During the trial period, a lower high-sensitivity C-reactive protein level (SMD 1.61, 95% CI: 0.19, 3.04, <i>p</i> = 0.03), a decrease in serum bicarbonate level (SMD 0.67, 95% CI: 0.22, 1.11, <i>p</i> = 0.003) and an increase in serum phosphate level (SMD -0.32, 95% CI: -0.62, -0.03, <i>p</i> = 0.03) were noted in the intravenous STS group compared with the control group. However, serum calcium and parathyroid hormone levels showed no difference between the two groups after the trials. The most common adverse events were temporary nausea and vomiting, which occurred in 12.5 to 75% of patients.</p><p><strong>Conclusions: </strong>Intravenous STS may slow down the progression of vascular calcification and ameliorate arterial stiffness in dialysis patients. Reliably defining the efficacy and safety of intravenous STS in attenuating the progression of vascular calcification requires a high-quality trial with a large sample size.</p>","PeriodicalId":9434,"journal":{"name":"Cardiovascular Journal of Africa","volume":"34 ","pages":"1-10"},"PeriodicalIF":0.7000,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of intravenous sodium thiosulfate on vascular calcification in dialysis patients with end-stage renal disease: a systematic review and meta-analysis.\",\"authors\":\"Yu-Huan Song, AiBing Ning, Na Guo, Ying Yang, Fei Tang, Na Zhao, Jun Hu, Hong Wu, Ting Peng, Yue-Fei Xiao, Guang-Yan Cai\",\"doi\":\"10.5830/CVJA-2023-020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>In dialysis patients, vascular calcification is a common complication and is closely related to the morbidity and mortality of cardiovascular disease. We performed a systematic review to determine the efficacy and safety of sodium thiosulfate (STS) in the progression of vascular calcification in dialysis patients with end-stage renal disease.</p><p><strong>Methods: </strong>The PubMed, Web of Science, Embase, Cochrane Library, Wanfang, CNKI, China Biology Medicine disc and Weipu databases were searched up to 9 March 2022 for clinical trials to synthesise findings on the efficacy and safety of STS in the progression of vascular calcification in dialysis patients. The primary outcome was coronary artery calcification scores (CACS) or abdominal aortic calcification scores (AACS) or Kauppila index. The secondary outcome was pulse-wave velocity (PWV). Laboratory data were shown in safety data. A random-effect model was used to provide the summary measures of effect [standardised mean difference (SMD) and 95% confidence interval (CI)].</p><p><strong>Results: </strong>Seven randomised, controlled trials and one nonrandomised, controlled trial involving 370 patients were included. Six studies reported that the progression of CACS or AACS was slower in the intravenous STS group compared with the control group (SMD -3.24, 95% CI: -5.29, -1.18, <i>p</i> = 0.002). Two studies showed the increase in PWV was less in the STS group compared with the control group (SMD -0.52, 95% CI: -0.92, -0.13, <i>p</i> = 0.009). During the trial period, a lower high-sensitivity C-reactive protein level (SMD 1.61, 95% CI: 0.19, 3.04, <i>p</i> = 0.03), a decrease in serum bicarbonate level (SMD 0.67, 95% CI: 0.22, 1.11, <i>p</i> = 0.003) and an increase in serum phosphate level (SMD -0.32, 95% CI: -0.62, -0.03, <i>p</i> = 0.03) were noted in the intravenous STS group compared with the control group. 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引用次数: 0
摘要
背景:在透析患者中,血管钙化是一种常见的并发症,与心血管疾病的发病率和死亡率密切相关。我们进行了一项系统综述,以确定硫代硫酸钠(STS)在终末期肾病透析患者血管钙化进展中的有效性和安全性。方法:检索截至2022年3月9日的PubMed、Web of Science、Embase、Cochrane Library、万方、中国知网、中国生物医学磁盘和卫普数据库,进行临床试验,综合研究STS对透析患者血管钙化进展的疗效和安全性。主要转归为冠状动脉钙化评分(CACS)或腹主动脉钙化评分(AACS)或Kauppila指数。次要指标为脉搏波速度(PWV)。实验室数据显示在安全数据中。随机效应模型用于提供效应的汇总度量[标准化平均差(SMD)和95%置信区间(CI)]。结果:纳入7项随机对照试验和1项非随机对照试验,共纳入370例患者。6项研究报道,静脉注射STS组CACS或AACS的进展较对照组慢(SMD -3.24, 95% CI: -5.29, -1.18, p = 0.002)。两项研究显示,与对照组相比,STS组PWV的增加较少(SMD: -0.52, 95% CI: -0.92, -0.13, p = 0.009)。在试验期间,与对照组相比,静脉注射STS组高敏c反应蛋白水平较低(SMD 1.61, 95% CI: 0.19, 3.04, p = 0.03),血清碳酸氢盐水平降低(SMD 0.67, 95% CI: 0.22, 1.11, p = 0.003),血清磷酸盐水平升高(SMD -0.32, 95% CI: -0.62, -0.03, p = 0.03)。然而,血清钙和甲状旁腺激素水平在试验后两组之间没有差异。最常见的不良事件是暂时性恶心和呕吐,发生在12.5 - 75%的患者中。结论:静脉注射STS可减缓透析患者血管钙化的进展,改善动脉僵硬。可靠地确定静脉注射STS减轻血管钙化进展的有效性和安全性需要高质量的大样本量试验。
Effects of intravenous sodium thiosulfate on vascular calcification in dialysis patients with end-stage renal disease: a systematic review and meta-analysis.
Background: In dialysis patients, vascular calcification is a common complication and is closely related to the morbidity and mortality of cardiovascular disease. We performed a systematic review to determine the efficacy and safety of sodium thiosulfate (STS) in the progression of vascular calcification in dialysis patients with end-stage renal disease.
Methods: The PubMed, Web of Science, Embase, Cochrane Library, Wanfang, CNKI, China Biology Medicine disc and Weipu databases were searched up to 9 March 2022 for clinical trials to synthesise findings on the efficacy and safety of STS in the progression of vascular calcification in dialysis patients. The primary outcome was coronary artery calcification scores (CACS) or abdominal aortic calcification scores (AACS) or Kauppila index. The secondary outcome was pulse-wave velocity (PWV). Laboratory data were shown in safety data. A random-effect model was used to provide the summary measures of effect [standardised mean difference (SMD) and 95% confidence interval (CI)].
Results: Seven randomised, controlled trials and one nonrandomised, controlled trial involving 370 patients were included. Six studies reported that the progression of CACS or AACS was slower in the intravenous STS group compared with the control group (SMD -3.24, 95% CI: -5.29, -1.18, p = 0.002). Two studies showed the increase in PWV was less in the STS group compared with the control group (SMD -0.52, 95% CI: -0.92, -0.13, p = 0.009). During the trial period, a lower high-sensitivity C-reactive protein level (SMD 1.61, 95% CI: 0.19, 3.04, p = 0.03), a decrease in serum bicarbonate level (SMD 0.67, 95% CI: 0.22, 1.11, p = 0.003) and an increase in serum phosphate level (SMD -0.32, 95% CI: -0.62, -0.03, p = 0.03) were noted in the intravenous STS group compared with the control group. However, serum calcium and parathyroid hormone levels showed no difference between the two groups after the trials. The most common adverse events were temporary nausea and vomiting, which occurred in 12.5 to 75% of patients.
Conclusions: Intravenous STS may slow down the progression of vascular calcification and ameliorate arterial stiffness in dialysis patients. Reliably defining the efficacy and safety of intravenous STS in attenuating the progression of vascular calcification requires a high-quality trial with a large sample size.
期刊介绍:
The Cardiovascular Journal of Africa (CVJA) is an international peer-reviewed journal that keeps cardiologists up to date with advances in the diagnosis and treatment of cardiovascular disease. Topics covered include coronary disease, electrophysiology, valve disease, imaging techniques, congenital heart disease (fetal, paediatric and adult), heart failure, surgery, and basic science.