AI Article Synopsis

  • This systematic review evaluates the feasibility and safety of early oral feeding (EOF) after radical gastrectomy in gastric cancer patients, analyzing eight studies from 2011 to 2020.
  • Most patients began oral feeding within 72 hours post-surgery with high adherence rates, showing EOF to be generally well-tolerated and associated with comparable or lower postoperative complications than traditional feeding methods.
  • Despite potential benefits like shorter hospital stays and improved nutritional status, results varied, highlighting the need for individualized patient approaches and calling for larger trials to develop standardized EOF protocols.

Article Abstract

This systematic review examines the feasibility and safety of early oral feeding (EOF) after radical gastrectomy in patients with gastric cancer. A comprehensive literature search identified eight eligible studies, including both clinical trials and cohort studies, conducted between 2011 and 2020. The review analyzed outcomes such as postoperative complications, length of hospital stay, time to first flatus/bowel movement, and changes in nutritional markers. The findings suggest that EOF is generally feasible and well-tolerated, with high adherence rates reported across studies. Most patients successfully initiated oral intake within 72 hours post-surgery without significant protocol deviations. Regarding safety, the studies reported comparable or lower rates of postoperative complications in EOF groups compared to traditional feeding protocols, though some noted non-significant increases in complications with EOF. Several studies observed potential benefits of EOF, including shorter hospital stays, earlier return of gastrointestinal function, and improved nutritional status. However, the results were mixed, with some studies finding no significant differences in these outcomes. While the review suggests EOF is a viable option for postoperative management after radical gastrectomy, it emphasizes the importance of patient-specific factors and close monitoring during implementation. The heterogeneity in study designs, EOF protocols, and outcome measures limits direct comparisons. Future large-scale randomized controlled trials are warranted to establish standardized EOF protocols and provide more robust evidence for this patient population.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11380650PMC
http://dx.doi.org/10.7759/cureus.66463DOI Listing

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