Mantry P S, Mehta A, Graydon R
Hepatobiliary Tumor Program, The Liver Institute at Methodist Dallas Medical Center, Dallas, Texas.
Hepatobiliary Tumor Program, The Liver Institute at Methodist Dallas Medical Center, Dallas, Texas.
Transplant Proc. 2014 Dec;46(10):3481-6. doi: 10.1016/j.transproceed.2014.10.021.
Rifaximin is a non-absorbable antibiotic which is approved for the treatment of hepatic encephalopathy (HE) in the United States. Our goal was to retrospectively assess this in patients with very advanced liver disease with our center data.
Between 2003 and 2010, we examined a total of 286 consecutive patients from our center who were on a combination of rifaximin and lactulose, who had been evaluated or listed as eligible for a liver transplant. Patients who received less than 3 months of rifaximin and lactulose were excluded. Patients who had incomplete data; specifically, a lack of MELD score upon hospital admission were excluded from this analysis. The retrospective chart review was approved by the institutional review board.
We observed a total of 723 hospitalizations among the patients. Of the 723 hospitalizations, 218 were due to portosystemic encephalopathy (PSE), whereas 505 were due to other causes. We observed that patients with a MELD < 20 had an average of 2.5 hospitalizations per 6 month period, and that those with a MELD > 20 had an average of 1.6 hospitalizations per 6 month period for HE. At the same time, patients who had a MELD score < 20 had 3.29 hospitalizations for HE unrelated causes and those whose MELD was >20 had 3.73 hospitalizations for causes not related to HE. In this cohort 65% of all hospitalizations from HE were in patients whose MELD was < 20, and 35% of all hospitalizations were for patients with a MELD > 20.
In our experience, HE related hospitalizations were lower in patients whose MELD > 20 who were on a combination of rifaximin and lactulose compared to patients with MELD < 20. In contrast, patients whose MELD > 20 had greater hospitalizations for non HE events which may be an expected result owing to the overall increased severity of their liver disease. The limitation of this study is its retrospective nature and single center experience. In conclusion, administration of rifaximin appears to significantly reduce hospitalizations from HE in patients with MELD > 20 and therefore is advocated in maintenance of remission of HE in patients with very advanced liver disease.
利福昔明是一种不被吸收的抗生素,在美国已被批准用于治疗肝性脑病(HE)。我们的目标是利用我们中心的数据对患有非常晚期肝病的患者进行回顾性评估。
在2003年至2010年期间,我们检查了来自我们中心的总共286例连续患者,这些患者同时使用利福昔明和乳果糖,他们已被评估或列为符合肝移植条件。接受利福昔明和乳果糖治疗少于3个月的患者被排除。数据不完整的患者;具体而言,入院时缺乏终末期肝病模型(MELD)评分的患者被排除在本分析之外。回顾性病历审查获得了机构审查委员会的批准。
我们观察到患者共有723次住院。在这723次住院中,218次是由于门体分流性脑病(PSE),而505次是由于其他原因。我们观察到,MELD<20的患者每6个月平均住院2.5次,而MELD>20的患者因HE每6个月平均住院1.6次。同时,MELD评分<20的患者因与HE无关的原因住院3.29次,而MELD>20的患者因与HE无关的原因住院3.73次。在这个队列中,所有因HE住院的患者中有65%的MELD<20,所有住院患者中有35%的MELD>20。
根据我们的经验,与MELD<20的患者相比,MELD>20且同时使用利福昔明和乳果糖的患者因HE相关的住院次数较少。相比之下,MELD>20的患者因非HE事件的住院次数更多,这可能是由于其肝病总体严重程度增加所致。本研究局限性在于其回顾性性质和单中心经验。总之,使用利福昔明似乎能显著减少MELD>20患者因HE的住院次数,因此主张用于维持非常晚期肝病患者HE的缓解。