Mekky Mohamed A, Riad Ahmad R, Gaber Marwa A, Abdel-Malek Mohamed O, Swifee Yosef M
Department of Tropical Medicine and Gastroenterology, Assiut University Hospital, Assiut 71515 Egypt.
Department of Tropical Medicine and Gastroenterology, Assiut University Hospital, Assiut 71515 Egypt.
Arab J Gastroenterol. 2018 Jun;19(2):76-79. doi: 10.1016/j.ajg.2018.06.001. Epub 2018 Jun 20.
Many regimens are tried in managing overt hepatic encephalopathy (HE). We investigated the efficacy of rifaximin versus metronidazole in management of an acute episode of HE on top of cirrhosis.
An open label prospective controlled trial was conducted on patients with an acute episode of HE on top of cirrhosis who were randomly divided into metronidazole-group (M-group) and rifaximin-group (R-group) with 60 patients in each. The main outcome measure was the clinical improvement of HE, duration of hospital stay and the changes in the level of serum ammonia after 3 days of starting therapy.
Both M-group and R-group were comparable as regards age and sex (mean age 51 ± 11 years and 49 ± 12; male/female ratio 45:15 and 50:10, respectively). Forty-six patients (76.7%) in M-group compared with forty-five (75%) in R-group showed clinical improvement (p = 0.412). Hospital stays were comparable between both group; 4.2 ± 2.1 and 3.9 ± 1.7 for M-group and R-group; respectively (p = 0.435). There was no significant difference of venous ammonia levels (Mean of delta 160.77 ± 185.34 µg/dL and 207.95 ± 218.43 µg/dL with p 0.664 and 0.974 in M-group and R-group, respectively). No adverse events were reported throughout the whole study.
Rifaximin and metronidazole are equally effective in management of acute episode of overt HE, therefore, re-auditing of treatment protocols of HE are warranted especially in limited resource settings.
在治疗显性肝性脑病(HE)时尝试了多种方案。我们研究了利福昔明与甲硝唑在肝硬化基础上治疗急性HE发作的疗效。
对肝硬化基础上发生急性HE发作的患者进行了一项开放标签前瞻性对照试验,将患者随机分为甲硝唑组(M组)和利福昔明组(R组),每组60例。主要观察指标为HE的临床改善情况、住院时间以及开始治疗3天后血清氨水平的变化。
M组和R组在年龄和性别方面具有可比性(平均年龄分别为51±11岁和49±12岁;男女比例分别为45:15和50:10)。M组46例患者(76.7%)与R组45例患者(75%)显示临床改善(p = 0.412)。两组住院时间相当;M组和R组分别为4.2±2.1天和3.9±1.7天(p = 0.435)。两组静脉血氨水平无显著差异(M组和R组的平均差值分别为160.77±185.34μg/dL和207.95±218.43μg/dL,p分别为0.664和0.974)。在整个研究过程中未报告不良事件。
利福昔明和甲硝唑在治疗显性HE急性发作方面同样有效,因此,有必要对HE的治疗方案进行重新审核,尤其是在资源有限的环境中。