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Curative efficacy and safety of traditional Chinese medicine xuebijing injections combined with ulinastatin for treating sepsis in the Chinese population: A meta-analysis

机译:血必净注射液联合乌司他丁治疗中国人败血症的疗效和安全性的Meta分析

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Background: Sepsis is a clinically critical disease. However, it is still controversial whether the combined use of traditional Chinese medicine Xuebijing injections (XBJI) and western medicine can enhance curative efficacy and ensure safety compared with western medicine alone. Thus, this research consisted of a systematic review of the curative efficacy and safety of traditional Chinese medicine XBJI combined with ulinastatin for treating sepsis in the Chinese population. Methods: A total of 8 databases were retrieved: 4 foreign databases, namely, PubMed, The Cochrane Library, Embase, and Web of Science; and 4 Chinese databases, namely, Sino Med, China National Knowledge Infrastructure (CNKI), VIP, and Wangfang Data. The time span of retrieval began from the establishment of each database and ended on August 1, 2017. Published randomized controlled trials about the combined use of traditional Chinese medicine XBJI and western medicine were included, regardless of language. Stata12.0 software was used for statistical analysis. Results: Finally, 16 papers involving 1335 cases were included. The result of meta-analysis showed that compared with the single use of ulinastatin , traditional Chinese medicine XBJI combined with ulinastatin could reduce the time of mechanical ventilation, shorten the length of intensive care unit (ICU) stay, improve the 28-day survival rate, and decrease the occurrence rate of multiple organ dysfunction syndrome, case fatality rate, procalcitonin (PCT) content, APACKEII score, tumor necrosis factor (TNF)-α level, and interleukin (IL)-6 level. Conclusion: On the basis of the common basic therapeutic regimen, the combined use of traditional Chinese medicine XBJI and ulinastatin was compared with the use of ulinastatin alone for treating sepsis in the Chinese population. It was found that the number of adverse events of combination therapy is not significantly increased, and its clinical safety is well within the permitted range. However, considering the limitations of this conclusion due to the low-quality articles included in the present research, it is necessary to conduct high-quality randomized controlled trials.
机译:背景:败血症是一种临床上的关键疾病。然而,与单纯的西药相比,中药血必净注射液(XBJI)与西药的结合使用能否提高疗效并确保安全性仍存在争议。因此,本研究包括对中药XBJI联合乌司他丁治疗中国人群脓毒症的疗效和安全性的系统评价。方法:共检索到8个数据库:4个国外数据库,分别是PubMed,Cochrane图书馆,Embase和Web of Science。还有4个中文数据库,分别是Sino Med,中国国家知识基础设施(CNKI),VIP和Wangfang Data。检索的时间跨度从每个数据库的建立开始,至2017年8月1日结束。无论语言如何,均包括已发表的有关中药XBJI和西药联合使用的随机对照试验。使用Stata12.0软件进行统计分析。结果:最后纳入16篇论文,涉及1335例。荟萃分析结果表明,与单用乌司他丁相比,中药XBJI联合乌司他丁可以减少机械通气时间,缩短重症监护病房(ICU)停留时间,提高28天生存率,并降低多器官功能障碍综合征的发生率,病死率,降钙素原(PCT)含量,APACKEII评分,肿瘤坏死因子(TNF)-α水平和白介素(IL)-6水平。结论:在普遍的基本治疗方案的基础上,比较了中药XBJI和乌司他丁的联合使用与单独使用乌司他丁治疗中国人群脓毒症的比较。发现联合疗法的不良事件数量没有显着增加,并且其临床安全性完全在允许范围内。但是,考虑到由于本研究中的文章质量低而导致该结论的局限性,因此有必要进行高质量的随机对照试验。

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