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Randomized controlled trial comparing lactulose plus albumin versus lactulose alone for treatment of hepatic encephalopathy

Background Hepatic encephalopathy (HE) is associated with poor prognosis and treatment of HE is primarily directed at the reduction of the blood ammonia levels. The study evaluated the efficacy and safety of albumin plus lactulose versus lactulose alone for treatment of overt HE. Methods In prospect...

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Published in:Journal of gastroenterology and hepatology 2017-06, Vol.32 (6), p.1234-1239
Main Authors: Sharma, Barjesh Chander, Singh, Jatinderpal, Srivastava, Siddharth, Sangam, Alok, Mantri, Alok Kumar, Trehanpati, Nirupma, Sarin, Shiv Kumar
Format: Article
Language:English
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Summary:Background Hepatic encephalopathy (HE) is associated with poor prognosis and treatment of HE is primarily directed at the reduction of the blood ammonia levels. The study evaluated the efficacy and safety of albumin plus lactulose versus lactulose alone for treatment of overt HE. Methods In prospective randomized controlled trial, 120 patients with overt HE were randomized in two groups: group A lactulose plus albumin (n = 60) and group B lactulose alone (n = 60). Primary end point was complete reversal of HE, and secondary end points were mortality and hospital stay. Results A total of 120 patients (mean age 40.4 ± 9.3 years) were included in this study. Thirty‐six (30%) patients were in Child–Turcotte–Pugh (CTP) class B, and 84 (70%) were in CTP Class C. Mean CTP score was 9.8 ± 2.1, and model for end‐stage liver disease score was 26.1 ± 5.3. Twenty seven (22.5%) had grade 2, 57 (47.5%) had grade 3, and 36 (30%) had grade 4 HE at the time of admission. Forty‐five (75%) patients in group A compared with 32 (53.3%) patients in group B had complete reversal of HE (P = 0.03). Mortality was significantly lower in lactulose plus albumin group (11[18.3%]) versus lactulose alone (19 [31.6%], [P 
ISSN:0815-9319
1440-1746
DOI:10.1111/jgh.13666