AI Article Synopsis

  • * A study compared 261 patients treated under ERAS protocols to 166 who were not, focusing on hospital stay duration, early discharge rates, post-operative complications, and rehospitalization.
  • * Results showed ERAS patients had a significantly shorter hospital stay (3.18 days vs. 4.87 days) and a higher early discharge rate (47.5% vs. 14.5%), indicating ERAS is beneficial, especially for older patients.

Article Abstract

Endometrial cancer is the fifth most common cancer among French women and occurs most frequently in the over-70-year-old population. Recent years have seen a significant shift towards minimally invasive surgery and Enhanced Recovery After Surgery (ERAS) protocols in endometrial cancer management. However, the impact of ERAS on endometrial cancer has not been well-established. We conducted a prospective observational study in a comprehensive cancer center, comparing the outcomes between endometrial cancer patients who received care in an ERAS pathway (261) and those who did not (166) between 2006 and 2020. We performed univariate and multivariate analysis. Our primary objective was to evaluate the impact of ERAS on length of hospital stay (LOS), with the secondary objectives being the determination of the rates of early discharge, post-operative morbidity, and rehospitalization. We found that patients in the ERAS group had a significantly shorter length of stay, with an average of 3.18 days compared to 4.87 days for the non-ERAS group (estimated decrease -1.69, < 0.0001). This effect was particularly pronounced among patients over 70 years old (estimated decrease -2.06, < 0.0001). The patients in the ERAS group also had a higher chance of early discharge (47.5% vs. 14.5% in the non-ERAS group, < 0.0001), for which there was not a significant increase in post-operative complications. Our study suggests that ERAS protocols are beneficial for the management of endometrial cancer, particularly for older patients, and could lead to the development of ambulatory pathways.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296872PMC
http://dx.doi.org/10.3390/cancers15123244DOI Listing

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