Sidhu Sandeep S, Goyal Omesh, Parker Richard A, Kishore Harsh, Sood Ajit
Department of Gastroenterology, Dayanand Medical College and Hospital, Ludhiana, Punjab, India.
Edinburgh Health Services Research Unit, University of Edinburgh, Edinburgh, UK.
Liver Int. 2016 Mar;36(3):378-85. doi: 10.1111/liv.12921. Epub 2015 Aug 17.
BACKGROUND & AIMS: Lactulose and rifaximin have already been shown to improve both cognitive functions and health related quality of life (HRQOL) in MHE patients. We aimed to compare the efficacy of rifaximin with lactulose in reversal of MHE and improvement in HRQOL in cirrhotic patients with MHE.
This prospective, randomized, open label, non-inferiority trial, was conducted at the Gastroenterology department of a tertiary care institute in Northern India. MHE was diagnosed if any two of the five neuro-psychometric (NP) tests were positive. HRQOL was assessed using the sickness impact profile (SIP) questionnaire (John Hopkins University, USA).
Of 527 cirrhotics screened, 351 were found eligible and tested for MHE. A total of 112 (31.9%) patients were found to have MHE and then randomized into two groups group A (lactulose; 30-120 ml/day) and B (Tablet. rifaximin; 400 mg thrice a day). Based on the intention-to-treat population, the proportion of patients with MHE reversal at 3 months was 73.7% (42/57) in the rifaximin arm and 69.1% (38/55) in the lactulose arm [4.6% difference (90% CI -9.3% to 18.4%)]. However, non-inferiority of rifaximin over lactulose could not be established as the pre-specified non-inferiority margin (-5%) lies within the two-sided 90% confidence interval of the difference. HRQOL was significantly improved in both groups (P = 0.20). However, the proportion of patients with flatulence (P = 0.004) and diarrhoea (P = 0.0002) was significantly higher in patients who took lactulose.
Non-inferiority of rifaximin over lactulose for MHE reversal was not established.
乳果糖和利福昔明已被证明可改善轻微肝性脑病(MHE)患者的认知功能和健康相关生活质量(HRQOL)。我们旨在比较利福昔明与乳果糖在逆转肝硬化合并MHE患者的MHE及改善HRQOL方面的疗效。
这项前瞻性、随机、开放标签、非劣效性试验在印度北部一家三级医疗机构的胃肠病科进行。如果五项神经心理测量(NP)测试中的任意两项呈阳性,则诊断为MHE。使用疾病影响概况(SIP)问卷(美国约翰霍普金斯大学)评估HRQOL。
在527名接受筛查的肝硬化患者中,351名被认为符合条件并接受了MHE检测。共有112名(31.9%)患者被发现患有MHE,然后随机分为两组:A组(乳果糖;30 - 120毫升/天)和B组(利福昔明片;400毫克,每日三次)。基于意向性治疗人群,利福昔明组在3个月时MHE逆转的患者比例为73.7%(42/57),乳果糖组为69.1%(38/55)[差异为4.6%(90%CI -9.3%至18.4%)]。然而,由于预先设定的非劣效性界值(-5%)处于差异的双侧90%置信区间内,因此无法确定利福昔明相对于乳果糖的非劣效性。两组的HRQOL均有显著改善(P = 0.20)。然而,服用乳果糖的患者出现肠胃胀气(P = 0.004)和腹泻(P = 0.0002)的比例显著更高。
未证实利福昔明在逆转MHE方面相对于乳果糖具有非劣效性。