# Impact of quantitative dietary guidance on postoperative outcomes in patients undergoing transjugular intrahepatic portosystemic shunt surgery: a retrospective cohort study

**Authors:** Yue Xu, Qin Yin, Jiangqiang Xiao, Qing Zhao, Xiaotian Chen, Ming Zhang, Bo Gao

PMC · DOI: 10.3389/fnut.2026.1671392 · Frontiers in Nutrition · 2026-02-11

## TL;DR

A structured diet after TIPS surgery in cirrhotic patients reduces mortality and hepatic encephalopathy, showing the benefits of targeted nutritional management.

## Contribution

This study introduces a quantitative dietary intervention for post-TIPS patients and demonstrates its clinical benefits.

## Key findings

- Quantitative dietary guidance reduced mortality and overt hepatic encephalopathy compared to usual care.
- Liver-related mortality was significantly lower in the dietary guidance group.
- Dietary intervention was independently associated with reduced risks of hepatic encephalopathy and liver-related death.

## Abstract

The optimal nutritional management strategy after transjugular intrahepatic portosystemic shunt (TIPS) procedure in cirrhotic patients remained controversial. A quantitative dietary intervention approach was developed for patients in the post-TIPS period, and its impact on clinical outcomes was evaluated in this study.

This study was a retrospective, non-randomized controlled cohort study. A total of 92 cirrhotic patients who underwent TIPS were enrolled. Following TIPS, patients were categorized into two groups according to whether they received TIPS-oriented quantitative dietary intervention during hospitalization. The quantitative dietary guidance group received individualized and quantitative dietary instructions after TIPS, and the usual care group served as control. The primary endpoint was death, and the secondary endpoint was overt hepatic encephalopathy (OHE) occurrence. Kaplan–Meier survival analysis and Cox proportional hazards regression models were used to evaluate the association between quantitative dietary intervention and outcomes.

The quantitative dietary guidance group (n=54) showed significantly lower mortality rates (5.56% vs. 21.05%, p=0.05) and OHE occurrence (12.96% vs. 36.84%, p=0.01) during follow-up than the usual care group (n=38). Liver-related mortality was also significantly lower in the quantitative dietary guidance group (1.85% vs. 15.79%, p=0.04). Multivariate Cox regression analysis demonstrated that the dietary intervention was independently associated with lower liver-related mortality risk (HR 0.09, 95% CI 0.01–0.75, p=0.03) and OHE risk (HR 0.34, 95% CI 0.14–0.85, p=0.02). Survival analysis demonstrated that the OHE probability was significantly lower in the quantitative dietary guidance group compared to the usual care group (HR 0.32, 95% CI 0.13–0.77, p=0.01), as was liver-related survival (HR 0.13, 95% CI 0.02–0.66, p=0.03).

A structured quantitative dietary intake protocol following the TIPS procedure could improve survival rates and reduce the incidence of HE. These findings highlighted the importance of TIPS-oriented nutritional management for cirrhotic patients.

## Linked entities

- **Diseases:** cirrhosis (MONDO:0005155), hepatic encephalopathy (MONDO:0001711)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** edema (MESH:D004487), Liver cirrhosis (MESH:D008103), tumor (MESH:D009369), renal insufficiency (MESH:D051437), non-alcoholic fatty liver disease (MESH:D065626), neurotoxic effects (MESH:D020258), cirrhotic (MESH:D000094724), cirrhosis (MESH:D005355), hepatic insufficiency (MESH:D048550), metabolic disturbance (MESH:D024821), esophagogastric variceal bleeding (MESH:D014648), muscle wasting (MESH:D009133), chronic liver disease (MESH:D008107), sarcopenia (MESH:D055948), stupor (MESH:D053608), confusional (MESH:D003221), obese (MESH:D009765), insulin resistance (MESH:D007333), hyperammonemia (MESH:D022124), Protein (MESH:D011488), Malnutrition (MESH:D044342), death (MESH:D003643), MELD (MESH:D058625), ascites (MESH:D001201), portal hypertension (MESH:D006975), coma (MESH:D003128), HE (MESH:D006501), cardiac dysfunction (MESH:D006331), Liver-related death (MESH:D017093), hepatic necroinflammation (MESH:D056486), muscle loss (MESH:D009135)
- **Chemicals:** triacylglycerol (MESH:D014280), Ammonia (MESH:D000641), polytetrafluoroethylene (MESH:D011138), branched-chain amino acids (MESH:D000597), carbohydrates (MESH:D002241), RUPS (-), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932184/full.md

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Source: https://tomesphere.com/paper/PMC12932184