Martí-Carvajal Arturo J, Solà Ivan, Martí-Carvajal Pedro I
Facultad de Ciencias de la Salud Eugenio Espejo, Universidad Tecnológica Equinoccial, Quito, Ecuador.
Cochrane Database Syst Rev. 2012 Sep 12(9):CD006007. doi: 10.1002/14651858.CD006007.pub3.
Upper gastrointestinal bleeding is one of the most frequent causes of morbidity and mortality in the course of liver cirrhosis. Patients with liver disease frequently have haemostatic abnormalities like hyperfibrinolysis. Therefore, antifibrinolytic amino acids have been proposed to be used as supplementary interventions alongside any of the primary treatments for upper gastrointestinal bleeding in patients with liver diseases.
To assess the beneficial and harmful effects of antifibrinolytic amino acids for upper gastrointestinal bleeding in patients with acute or chronic liver disease.
We searched the Cochrane Hepato-Biliary Group Controlled Trials Register (11 June 2012), Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library (2012, Issue 5 of 12), MEDLINE (Ovid SP) (1946 to June 2012), EMBASE (Ovid SP) (1974 to June 2012), Science Citation Index EXPANDED (1900 to June 2012), LILACS (1982 to June 2012), Clinical Trials Search Portal of the WHO (accessed June 18, 2012), and the Metaregister of Controlled Trials (accessed June 18, 2012). We scrutinised the reference lists of the retrieved publications.
Randomised clinical trials irrespective of blinding, language, or publication status for assessment of benefits and harms. Observational studies for assessment of harms.
Data from randomised clinical trials were to be summarised by standard Cochrane Collaboration methodologies.
We could not find any randomised clinical trials assessing antifibrinolytic amino acids for treating upper gastrointestinal bleeding in patients with acute or chronic liver disease. We could not identify quasi-randomised, historically controlled, or observational studies in which we could assess harms.
AUTHORS' CONCLUSIONS: No randomised clinical trials assessing the benefits and harms of antifibrinolytic amino acids for upper gastrointestinal bleeding in patients with acute or chronic liver disease were identified. The benefits and harms of antifibrinolytic amino acids need to be tested in randomised clinical trials. Unless randomised clinical trials are conducted to assess the trade off between benefits and harms, we cannot recommend nor refute antifibrinolytic amino acids for upper gastrointestinal bleeding in patients with acute or chronic liver diseases.
上消化道出血是肝硬化病程中最常见的发病和死亡原因之一。肝病患者常有止血异常,如纤维蛋白溶解亢进。因此,抗纤维蛋白溶解氨基酸已被提议作为肝病患者上消化道出血的主要治疗方法之外的辅助干预措施。
评估抗纤维蛋白溶解氨基酸对急慢性肝病患者上消化道出血的有益和有害影响。
我们检索了Cochrane肝胆组对照试验注册库(2012年6月11日)、Cochrane图书馆中Cochrane对照试验中心注册库(CENTRAL)(2012年第5期,共12期)、MEDLINE(Ovid SP)(1946年至2012年6月)、EMBASE(Ovid SP)(1974年至2012年6月)、科学引文索引扩展版(1900年至2012年6月)、LILACS(1982年至2012年6月)、世界卫生组织临床试验搜索门户(2012年6月18日访问)以及对照试验元注册库(2012年6月18日访问)。我们仔细审查了检索到的出版物的参考文献列表。
用于评估益处和危害的随机临床试验,不考虑盲法、语言或发表状态。用于评估危害的观察性研究。
来自随机临床试验的数据将采用Cochrane协作网的标准方法进行汇总。
我们未找到任何评估抗纤维蛋白溶解氨基酸治疗急慢性肝病患者上消化道出血的随机临床试验。我们也未找到可用于评估危害的半随机、历史对照或观察性研究。
未发现评估抗纤维蛋白溶解氨基酸对急慢性肝病患者上消化道出血的益处和危害的随机临床试验。抗纤维蛋白溶解氨基酸的益处和危害需要在随机临床试验中进行检验。除非进行随机临床试验来评估利弊权衡,否则我们既不能推荐也不能反驳抗纤维蛋白溶解氨基酸用于急慢性肝病患者的上消化道出血。