Finetuning and optimizing an enhanced recovery protocol for liver surgery in the era of minimally invasive liver surgery: a single centre experience with 630 liver resections.
{"title":"Finetuning and optimizing an enhanced recovery protocol for liver surgery in the era of minimally invasive liver surgery: a single centre experience with 630 liver resections.","authors":"Julie Vercauteren, Celine De Meyere, Isabelle Parmentier, Pieter J Steelant, Mathieu D'Hondt","doi":"10.1016/j.hpb.2025.06.008","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Enhanced recovery after surgery (ERAS) principles are increasingly applied in liver surgery. The aim of this retrospective cohort study was to evaluate the effectiveness of optimized clinical pathways in liver surgery in conjunction with patient adherence to the ERAS-protocol.</p><p><strong>Methods: </strong>Our centre implemented a first liver clinical pathway in 2015(CP1), followed by an optimized version in 2019(CP2). New ERAS-elements were introduced, such as no routine use of epidural analgesia and avoidance of surgical drains. More attention was paid to patient mobilization and resumption of a normal diet intake. Outcome measures included length of hospital stay, readmission rate, complications, and mortality. Adherence was measured by the percentage of patients who were discharged on or before the scheduled day.</p><p><strong>Results: </strong>630 patients were included in the study, of which 329 (52.2 %) followed CP2 and 301 (47.8 %) followed CP1. The length of hospital stay after surgery significantly reduced in CP2(2[1-4]days vs 4[3-6]days; P < 0.001), without an increase in readmission rate (5.5 % vs 4.0% p:0.38), postoperative morbidity (12.5 % vs 14.3 %; P = 0.50) and 90-day mortality (0.91 % vs 1.00 %; P = 0.58). Adherence improved significantly in CP2(67.8 % vs 55.8 %; P = 0.002).</p><p><strong>Conclusion: </strong>The implementation of an optimized CP in liver surgery resulted in a shorter hospital stay and higher adherence rate to the ERAS-protocol.</p>","PeriodicalId":13229,"journal":{"name":"Hpb","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hpb","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.hpb.2025.06.008","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Enhanced recovery after surgery (ERAS) principles are increasingly applied in liver surgery. The aim of this retrospective cohort study was to evaluate the effectiveness of optimized clinical pathways in liver surgery in conjunction with patient adherence to the ERAS-protocol.
Methods: Our centre implemented a first liver clinical pathway in 2015(CP1), followed by an optimized version in 2019(CP2). New ERAS-elements were introduced, such as no routine use of epidural analgesia and avoidance of surgical drains. More attention was paid to patient mobilization and resumption of a normal diet intake. Outcome measures included length of hospital stay, readmission rate, complications, and mortality. Adherence was measured by the percentage of patients who were discharged on or before the scheduled day.
Results: 630 patients were included in the study, of which 329 (52.2 %) followed CP2 and 301 (47.8 %) followed CP1. The length of hospital stay after surgery significantly reduced in CP2(2[1-4]days vs 4[3-6]days; P < 0.001), without an increase in readmission rate (5.5 % vs 4.0% p:0.38), postoperative morbidity (12.5 % vs 14.3 %; P = 0.50) and 90-day mortality (0.91 % vs 1.00 %; P = 0.58). Adherence improved significantly in CP2(67.8 % vs 55.8 %; P = 0.002).
Conclusion: The implementation of an optimized CP in liver surgery resulted in a shorter hospital stay and higher adherence rate to the ERAS-protocol.
期刊介绍:
HPB is an international forum for clinical, scientific and educational communication.
Twelve issues a year bring the reader leading articles, expert reviews, original articles, images, editorials, and reader correspondence encompassing all aspects of benign and malignant hepatobiliary disease and its management. HPB features relevant aspects of clinical and translational research and practice.
Specific areas of interest include HPB diseases encountered globally by clinical practitioners in this specialist field of gastrointestinal surgery. The journal addresses the challenges faced in the management of cancer involving the liver, biliary system and pancreas. While surgical oncology represents a large part of HPB practice, submission of manuscripts relating to liver and pancreas transplantation, the treatment of benign conditions such as acute and chronic pancreatitis, and those relating to hepatobiliary infection and inflammation are also welcomed. There will be a focus on developing a multidisciplinary approach to diagnosis and treatment with endoscopic and laparoscopic approaches, radiological interventions and surgical techniques being strongly represented. HPB welcomes submission of manuscripts in all these areas and in scientific focused research that has clear clinical relevance to HPB surgical practice.
HPB aims to help its readers - surgeons, physicians, radiologists and basic scientists - to develop their knowledge and practice. HPB will be of interest to specialists involved in the management of hepatobiliary and pancreatic disease however will also inform those working in related fields.
Abstracted and Indexed in:
MEDLINE®
EMBASE
PubMed
Science Citation Index Expanded
Academic Search (EBSCO)
HPB is owned by the International Hepato-Pancreato-Biliary Association (IHPBA) and is also the official Journal of the American Hepato-Pancreato-Biliary Association (AHPBA), the Asian-Pacific Hepato Pancreatic Biliary Association (A-PHPBA) and the European-African Hepato-Pancreatic Biliary Association (E-AHPBA).