Evidence map›Paper›PMID 41930749›Full record

Trial reportClinical transplantation2026

Feasibility of Early Oral Nutritional Supplementation After Liver Transplantation: A Randomized Pilot Study.

Amal Trigui, Crystèle Hogue, Mélanie Tremblay, Geneviève Huard, An Tang, Justine Racette, Christopher F Rose, Chantal Bémeur

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical transplantation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Amal TriguiDepartment of Nutrition, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Crystèle HogueCentre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
Mélanie TremblayCentre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
Geneviève HuardDepartment of Hepatology and Liver Transplantation, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada.
An TangCentre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
Justine RacetteCentre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
Christopher F RoseCentre de recherche du Centre hospitalier de l'Université de Montréal (CRCHUM), Montreal, Quebec, Canada.
Chantal BémeurDepartment of Nutrition, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.

Funding

Canadian Donation and Transplantation Research Program (CDTRP)Fonds de recherche du Québec-Santé (FRQS) Merit #298509Fonds de recherche du Québec-Santé (FRQS) Merit FRQS #34939Mission Universitaire de Tunisie en Amérique du Nord (MUTAN)
6 · The paper itself

Abstract

Catabolic and inflammatory changes after liver transplantation (LT) increase energy and protein requirements. This study assessed the feasibility of a 12-week high-energy/high-protein oral nutrition supplementation (ONS) initiated after resumption of solid oral intake post-LT. Secondary objectives were 1) to describe changes in nutritional risk, muscle strength, and quality of life during the pre-transplant period, and 2) to explore the potential impact of ONS after LT on these outcomes and muscle mass.

methodsIn this randomized feasibility study, patients awaiting LT were assessed for nutritional risk (Liver Disease Under nutrition Screening Tool), muscle strength (Chair Stand Test, CST), and quality of life (SF-36) before LT, every three months until surgery, at discharge, and again at 12 weeks post-LT. Muscle mass was assessed by CT scan at LT admission and 12 weeks later. After LT, participants were randomized to a control group or an intervention group receiving ONS for 12 weeks. Feasibility outcomes included eligibility, recruitment and target sample size, adherence to the protocol and intervention, attrition, and safety.

resultsOf the seven predefined feasibility criteria, four were met, two were partially met (eligibility and recruitment rates), and one was not met (target sample size rate). Fifty-five patients were followed before LT, 17 underwent LT, and 14 were analyzed. Six patients developed new-onset diabetes after LT, limiting randomization to three patients in the intervention group and five in the control group. Before LT, 85.5% (47/55) of included patients were at risk of malnutrition, which remained stable during waiting time (p = 0.418), while muscle strength declined (p = 0.039). At 12 weeks post-LT, the intervention group had 0% malnutrition risk and a median CST time of 11.5 s, compared with 60% and 15.1 s, respectively, in the control group. The prevalence of sarcopenia did not change before and after the intervention.

conclusionEarly post-LT ONS was feasible regarding adherence, retention, and safety; however, recruitment and achieving the targeted transplanted sample size were major barriers. The study highlights the high prevalence of malnutrition and sarcopenia before and after LT. PRACTITIONER POINTS: Early post-transplant nutritional supplementation showed feasibility for 4 of the 7 evaluated criteria. Most patients (85.5%) awaiting liver transplantation are at risk of malnutrition, with low and declining muscle strength during the waiting period. Challenges in participant recruitment suggest that refined recruitment approaches are needed for larger-scale studies.

Indexed as

Dietary SupplementsLiver TransplantationMalnutritionNutritional StatusPostoperative ComplicationsQuality of LifeAdultFeasibility StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedMuscle StrengthPilot ProjectsPrognosisfeasibility studyliver transplantationmalnutritionmuscle massmuscle strengthnutritional interventionquality of lifesarcopenia

Identifiers

PMID41930749
PMCPMC13047882

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.