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A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
Published on: September 20, 2019
A double-blind randomized placebo-controlled trial of albumin in outpatients with hepatic encephalopathy: HEAL study
Andrew Fagan1, Edith A Gavis1, Mary Leslie Gallagher1
1Division of Gastroenterology, Hepatology and Nutrition, Richmond, Virginia, USA.
Background & Aims:
Even after recovery from overt hepatic encephalopathy (HE), minimal HE (MHE), which impairs quality of life (QoL), can persist. A double-blind, placebo-controlled randomized clinical trial was performed to determine the impact of albumin vs. saline on MHE and QoL in individuals with prior HE already on standard of care.
Methods:
Outpatients with cirrhosis and prior HE, MHE and hypoalbuminemia already on treatment for HE were included. Patients on regular IV albumin infusions were excluded. Participants were randomized 1:1 to receive either weekly infusions of 25% IV albumin 1.5 g/kg or saline over 5 weeks. MHE was defined using either psychometric hepatic encephalopathy score (PHES), Stroop or critical clicker frequency. MHE, QoL (based on sickness impact profile [SIP] total, physical, psychosocial domain) and serum markers (inflammation, endothelial dysfunction, and ischemia-modified albumin) were compared between baseline, the final infusion visit (end-of-drug [EOD]) and 1-week post final infusion (end-of-study [EOS]).
Results:
Forty-eight (24/group) participants were randomized and balanced (including by HE medication use) at baseline. Adverse events were similar, with MELD and ammonia remaining stable between/within groups. Albumin levels increased and ischemia-modified albumin decreased only in the albumin group at EOD and EOS vs. baseline. PHES and Stroop MHE reversal and improvement were greater in the albumin group at EOD and persisted at EOS. SIP total and psychosocial, but not physical, domain improved only in the albumin group at EOD and EOS vs. baseline. A significant reduction in IL-1β and endothelial dysfunction markers was also observed in the albumin group.
Conclusion:
In a double-blind, placebo-controlled trial of outpatients with cirrhosis, prior HE and current MHE, albumin infusions were associated with improved cognitive function and psychosocial QoL, likely due to amelioration of endothelial dysfunction.
Clinical Trials Registration:
www.
Clinicaltrials:
gov NCT03585257.
Impact And Implications:
Even after recovery from overt hepatic encephalopathy (HE), minimal HE (MHE), which impairs quality of life, can persist. We found that intravenous albumin infusions were associated with improved cognitive function and psychosocial quality of life, likely owing to amelioration of endothelial dysfunction, compared to placebo in outpatients with prior HE and current MHE. In patients who continue to demonstrate cognitive dysfunction and impaired quality of life despite standard of care therapy for HE, albumin infusions could be considered if these results are validated.
Insights
Intravenous albumin infusions improved cognitive function and quality of life in patients with minimal hepatic encephalopathy (MHE) after prior overt HE. This suggests albumin may help address persistent MHE symptoms and improve patient well-being.
Area of Science:
- Hepatology
- Clinical Trials
- Neuroscience
Background:
- Minimal hepatic encephalopathy (MHE) can persist after overt hepatic encephalopathy (HE), impairing quality of life (QoL).
- Standard care may not fully resolve MHE and its associated QoL deficits.
Purpose of the Study:
- To evaluate the efficacy of intravenous albumin versus placebo in improving MHE and QoL in outpatients with cirrhosis and prior HE.
- To assess the impact of albumin on cognitive function, psychosocial well-being, and specific serum markers.
Main Methods:
- A double-blind, placebo-controlled randomized clinical trial involving outpatients with cirrhosis, prior HE, and current MHE.
- Participants received weekly infusions of 25% IV albumin (1.5 g/kg) or saline for 5 weeks.
- MHE, QoL (SIP), and serum markers were assessed at baseline, end-of-drug, and end-of-study.
Main Results:
- Albumin infusions significantly improved MHE reversal and cognitive function (PHES, Stroop) compared to placebo.
- Patients receiving albumin showed significant improvements in overall and psychosocial QoL (SIP), but not physical QoL.
- Albumin treatment led to increased albumin levels, decreased ischemia-modified albumin, and reduced IL-1β and endothelial dysfunction markers.
Conclusions:
- Intravenous albumin infusions effectively improved cognitive function and psychosocial QoL in patients with MHE despite standard HE therapy.
- The benefits of albumin may be linked to the amelioration of endothelial dysfunction.
- Albumin infusions represent a potential therapeutic option for persistent MHE and associated QoL impairments in cirrhotic patients.
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