Article(id=1291404878618808963, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291404791758975909, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.11.001, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1735488000000, receivedDateStr=2024-12-30, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785824516204, onlineDateStr=2026-08-04, pubDate=1750089600000, pubDateStr=2025-06-17, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785824516204, onlineIssueDateStr=2026-08-04, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785824516204, creator=13701087609, updateTime=1785824516204, updator=13701087609, issue=Issue{id=1291404791758975909, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='11', pageStart='1501', pageEnd='1650', issueExtLink='null', onlineDate='null', pubDate='1750089600000', pubDateStr='2025-06-17', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785824495496, creator='13701087609', updateTime=1785824495496, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=1501, endPage=1505, ext={EN=ArticleExt(id=1291404878878855812, articleId=1291404878618808963, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Clinical trial of piperazine ferulate combined with continuous renal replacement therapy in the treatment of children with acute renal failure, columnId=1246531407326105792, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Clinical and Basic Bridging Research, runingTitle=null, highlight=null, articleAbstract=
Objective To observe the clinical efficacy and safety of ferulic acid piperazine tablets combined with continuous renal replacement therapy in the treatment of children with acute renal failure.
Methods Children with acute renal failure were randomly divided into control group and treatment group. Both groups were given basic treatment, based on which, the control group was given continuous renal replacement therapy; the treatment group was given piperazine ferulate tablets 100 mg per time, orally, tid, on the basis of control group. Two groups were treated for 2 weeks. The clinical efficacy, renal function, levels of renal injury markers and safety were compared between the two groups.
Results Treatment group was enrolled 85 cases, 2 cases dropped out, and 83 cases were finally included in the statistical analysis. Control group was enrolled 84 cases, 3 cases dropped out, and 81 cases were finally included in the statistical analysis. After treatment, the total effective rates of treatment and control groups were 92.77% (77 cases/83 cases) and 81.48% (66 cases / 81 cases) with statistically significant difference (P<0.05). After treatment, the serum creatinine levels of treatment and control groups were (120.35±17.12) and (148.12±20.03) μmoL·L-1; the blood urea nitrogen levels were (12.29±2.14) and (15.64±3.01) μmoL·L-1; the β2-microglobulin levels were (1.87±0.25) and (2.14±0.39) mg·L-1; the 24-h urinary protein quantification were (0.94±0.31) and (1.24±0.47) g·24 h-1; N-acetyl-β-D-glucosidase contents were (17.03±2.98) and (20.36±3.51) U·L-1; the renal injury molecule 1 contents were (1.62±0.27) and (2.09±0.32) μg·L-1; the neutrophil gelatinase-associated lipid transport protein contents were (50.36±8.13) and (59.23±10.14) μg·L-1, respectively, and the differences were all statistically significant (all P<0.05). The adverse drug reactions of treatment group were nausea, vomiting and abdominal distension, while those in the control group were dizziness, nausea and vomiting. The total incidences of adverse drug reactions in the treatment and control groups were 7.23% and 4.94% without significant difference (P>0.05).
Conclusion Ferulic acid piperazine tablets combined with continuous renal replacement therapy have definitive clinical efficacy in the treatment of children with acute renal failure, which can significantly improve the renal function of children, reduce renal injury, without increasing the incidence of adverse drug reactions.
, authors=Yan-yan CHAI
1a, 2, Yao SHENG
1a, Dan-qun JIN
1a, Wen-jia TONG
1a, Yun WANG
1a, Fang DENG
1b, 2, authorsList=Yan-yan CHAI, Yao SHENG, Dan-qun JIN, Wen-jia TONG, Yun WANG, Fang DENG, authorCompany=null, correspAuthors=Fang DENG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1291404879218594437, articleId=1291404878618808963, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=阿魏酸哌嗪联合连续性肾替代疗法治疗急性肾衰竭患儿的临床研究, columnId=1246531407485489349, journalTitle=中国临床药理学杂志, columnName=临床与基础桥接研究, runingTitle=null, highlight=null, articleAbstract=
目的 观察阿魏酸哌嗪片联合连续性肾替代疗法治疗急性肾衰竭患儿的临床疗效及安全性。
方法 将急性肾衰竭患儿随机分为对照组和试验组。2组患儿均给予基础治疗,在此基础上,对照组给予连续性肾替代疗法;试验组在对照组治疗的基础上,联合阿魏酸哌嗪片每次100 mg,口服,tid。2组患儿均治疗2周。比较2组患儿的临床疗效、肾功能、肾损伤标志物水平,以及安全性。
结果 试验组入组85例,脱落2例,最终有83例纳入统计分析;对照组入组84例,脱落3例,最终有81例纳入统计分析。治疗后,试验组和对照组的总有效率分别为92.77%(77例/83例)和81.48%(66例/81例),在统计学上差异有统计学意义(P<0.05)。治疗后,试验组和对照组的血清肌酸酐水平分别为(120.35±17.12)和(148.12±20.03)μmoL·L-1,血尿素氮水平分别为(12.29±2.14)和(15.64±3.01)μmoL·L-1,β2-微球蛋白含量分别为(1.87±0.25)和(2.14±0.39)mg·L-1,24 h尿蛋白定量分别为(0.94±0.31)和(1.24±0.47)g·24 h-1,N-乙酰-β-D-葡萄糖苷酶含量分别为(17.03±2.98)和(20.36±3.51)U·L-1,肾损伤分子1含量分别为(1.62±0.27)和(2.09±0.32)μg·L-1,中性粒细胞明胶酶相关脂质运载蛋白含量分别为(50.36±8.13)和(59.23±10.14)μg·L-1,在统计学上差异均有统计学意义(均P<0.05)。试验组的药物不良反应主要有恶心、呕吐、腹胀,对照组的药物不良反应主要有头晕、恶心、呕吐。试验组和对照组的总药物不良反应发生率分别为7.23%和4.94%,在统计学上差异无统计学意义(P>0.05)。
结论 阿魏酸哌嗪片联合连续性肾替代疗法治疗急性肾衰竭患儿的临床疗效显著,其能够显著改善患儿的肾功能,减轻肾损伤,且不增加药物不良反应的发生率。
, authors=柴彦艳
1a, 2, 盛瑶
1a, 金丹群
1a, 童文佳
1a, 王云
1a, 邓芳
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柴彦艳(1979-),女,硕士研究生,副主任医师,主要从事儿童重症医学方向的临床诊疗工作
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