Ahire Kiran, Sonawale Archana
Assistant Professor.
Associate Professor, Seth G.S. Medical College, KEM Hospital, Mumbai, Maharashtra.
J Assoc Physicians India. 2017 Aug;65(8):42-46.
Hepatic encephalopathy is challenging complication of liver dysfunction. Therapeutic treatment options for hepatic encephalopathy are currently limited and have appreciable risks and benefits associated with their use. Rifaximin is a novel anti microbiological agent with wide spectrum of activity that has shown promise as an alternative option for hepatic encephalopathy.
The present study was undertaken to compare the effectiveness of Rifaximin and Lactulose as a combination vs Lactulose alone, to compare the adverse effects and to study the rapidity of therapeutic effects of Rifaximin and Lactulose.
It was a prospective observational study. 60 patients suffering from hepatic encephalopathy (HE) were studied. Patients were investigated and treated as per treating physician's decision. At the time of analysis, patients were divided into 2 groups, Rifaximin group who received Rifaximin+Lactulose (R+L) and Lactulose group(L), who received Lactulose only. Parameters such as mental status grade, Asterixis grade, Serum Ammonia grade, Number Connection Test grade (NCT grade), Hepatic Encephalopathy Index (HE index) were evaluated and compared in both groups. Clinical efficacy was determined using HE index improvement. Primary end points were decrease in HE index and reversal of HE grades. Secondary end points were mortality from HE or any other cause, decrease in mental status grade, asterixis grade, serum Ammonia grade, NCT grade.
Out of 60 patients, 32 received Rifaximin+Lactulose combination and 28 patients received Lactulose alone. Mean Child-Turcotte-Pugh score (CTP score) was 10.6 in R+L group and 10.32 in L group. There was statistically significant improvement in mental status grade, Asterixis grade, Serum Ammonia grade, NCT grade, Hepatic encephalopathy index in both groups, p value <0.05 but no statistically significant difference between improvement in mental status grade, Asterixis grade, Serum Ammonia grade, NCT grade, HE index between the two groups. Rifaximin + Lactulose combination was effective in 31 out of 32 i.e.96.87% and Lactulose alone in 24 out of 28 patients, i.e. in 85.71%, which is not statistically different, p=0.3251.
Rifaximin+ Lactulose combination is not superior to Lactulose alone in treatment of refractory hepatic encephalopathy. Addition of Rifaximin may help in the treatment of refractory hepatic encephalopathy.
Rifaximin + Lactulose combination is effective, but not superior to Lactulose alone in treatment of hepatic encephalopathy.
肝性脑病是肝功能障碍具有挑战性的并发症。目前,肝性脑病的治疗选择有限,且使用这些治疗方法存在明显的风险和益处。利福昔明是一种新型抗菌药物,具有广泛的活性谱,已显示出有望成为肝性脑病的替代治疗选择。
本研究旨在比较利福昔明和乳果糖联合使用与单独使用乳果糖的有效性,比较不良反应,并研究利福昔明和乳果糖治疗效果的快速性。
这是一项前瞻性观察性研究。对60例肝性脑病(HE)患者进行了研究。根据主治医生的决定对患者进行检查和治疗。在分析时,将患者分为两组,利福昔明组接受利福昔明+乳果糖(R+L),乳果糖组(L)仅接受乳果糖。评估并比较两组的精神状态分级、扑翼样震颤分级、血清氨分级、数字连接试验分级(NCT分级)、肝性脑病指数(HE指数)等参数。使用HE指数改善情况确定临床疗效。主要终点是HE指数降低和HE分级逆转。次要终点是HE或任何其他原因导致的死亡率、精神状态分级降低、扑翼样震颤分级降低、血清氨分级降低、NCT分级降低。
60例患者中,32例接受利福昔明+乳果糖联合治疗,28例仅接受乳果糖治疗。R+L组的平均Child-Turcotte-Pugh评分(CTP评分)为10.6,L组为10.32。两组的精神状态分级、扑翼样震颤分级、血清氨分级、NCT分级、肝性脑病指数均有统计学显著改善,p值<0.05,但两组在精神状态分级、扑翼样震颤分级、血清氨分级、NCT分级、HE指数改善方面无统计学显著差异。利福昔明+乳果糖联合治疗在32例中有31例有效,即96.87%,单独使用乳果糖在28例中有24例有效,即85.71%,差异无统计学意义,p=0.3251。
在难治性肝性脑病的治疗中,利福昔明+乳果糖联合治疗并不优于单独使用乳果糖。添加利福昔明可能有助于难治性肝性脑病的治疗。
利福昔明+乳果糖联合治疗有效,但在肝性脑病治疗中并不优于单独使用乳果糖。