{"title":"Continuous versus intermittent tube feeding after feeding jejunostomy, a pilot randomized controlled trial","authors":"Peticha Tanprasert , Phanuwat Tharathipphayakun , Wasana Ko-iam , Sirikan Limpakan , Bandhuphat Chakrabandhu","doi":"10.1016/j.clnesp.2025.05.018","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Feeding jejunostomy is employed in cases of upper gastrointestinal tract disorders; nonetheless, there are limited guidelines about post-procedural feeding approaches. This study aims to examine the effects of continuous and intermittent feeding strategies on time to achieve full feeding, gastrointestinal adverse events, and metabolic alterations following jejunostomy surgery.</div></div><div><h3>Method</h3><div>This randomized controlled pilot non-inferiority trial included 40 people with diseases of the upper GI tract who had a feeding jejunostomy at Chiang Mai University Hospital. The patients were not blinded and were randomly split into two groups using the block-of-four method. After completion of recruitment, 18 patients in the continuous feeding group and 20 patients in the intermittent feeding group (5 separated meals in 15 min each) were included in the final analysis. The primary outcome was determined based on the time to achieve complete feeding (30 ml/kg/day). The secondary outcome includes the presence of adverse gastrointestinal symptoms and any metabolic alterations.</div></div><div><h3>Results</h3><div>There were no statistically significant differences in the time taken to achieve a full feed in continuous and intermittent (48 ± 0 h. vs. 50.4 ± 5.6 h, p = 0.080) or as regards gastrointestinal adverse events, abdominal discomfort (27.8 vs. 30.0 %) and diarrhea (5.6 vs. 10 %) (p = 1.000). The metabolic outcome also showed no difference between the two groups.</div></div><div><h3>Conclusion</h3><div>There was no significant difference between continuous and intermittent feeding in terms of the time required to achieve a full feed, gastrointestinal adverse events such as abdominal discomfort and diarrhea, or metabolic changes.</div></div><div><h3>Trial registration</h3><div>TCTR20241008004; Thai Clinical Trials Registry.</div></div>","PeriodicalId":10352,"journal":{"name":"Clinical nutrition ESPEN","volume":"68 ","pages":"Pages 292-299"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical nutrition ESPEN","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405457725003158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NUTRITION & DIETETICS","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Feeding jejunostomy is employed in cases of upper gastrointestinal tract disorders; nonetheless, there are limited guidelines about post-procedural feeding approaches. This study aims to examine the effects of continuous and intermittent feeding strategies on time to achieve full feeding, gastrointestinal adverse events, and metabolic alterations following jejunostomy surgery.
Method
This randomized controlled pilot non-inferiority trial included 40 people with diseases of the upper GI tract who had a feeding jejunostomy at Chiang Mai University Hospital. The patients were not blinded and were randomly split into two groups using the block-of-four method. After completion of recruitment, 18 patients in the continuous feeding group and 20 patients in the intermittent feeding group (5 separated meals in 15 min each) were included in the final analysis. The primary outcome was determined based on the time to achieve complete feeding (30 ml/kg/day). The secondary outcome includes the presence of adverse gastrointestinal symptoms and any metabolic alterations.
Results
There were no statistically significant differences in the time taken to achieve a full feed in continuous and intermittent (48 ± 0 h. vs. 50.4 ± 5.6 h, p = 0.080) or as regards gastrointestinal adverse events, abdominal discomfort (27.8 vs. 30.0 %) and diarrhea (5.6 vs. 10 %) (p = 1.000). The metabolic outcome also showed no difference between the two groups.
Conclusion
There was no significant difference between continuous and intermittent feeding in terms of the time required to achieve a full feed, gastrointestinal adverse events such as abdominal discomfort and diarrhea, or metabolic changes.
期刊介绍:
Clinical Nutrition ESPEN is an electronic-only journal and is an official publication of the European Society for Clinical Nutrition and Metabolism (ESPEN). Nutrition and nutritional care have gained wide clinical and scientific interest during the past decades. The increasing knowledge of metabolic disturbances and nutritional assessment in chronic and acute diseases has stimulated rapid advances in design, development and clinical application of nutritional support. The aims of ESPEN are to encourage the rapid diffusion of knowledge and its application in the field of clinical nutrition and metabolism. Published bimonthly, Clinical Nutrition ESPEN focuses on publishing articles on the relationship between nutrition and disease in the setting of basic science and clinical practice. Clinical Nutrition ESPEN is available to all members of ESPEN and to all subscribers of Clinical Nutrition.