Compliance With ERAS Protocol in Pancreatic Surgery, Stress Response and Outcomes

Overview

The purpose of this study is to evaluate the impact of compliance with enhanced recovery after surgery (ERAS) program on patient reported outcomes (PROs), surgery-specific outcomes and stress response after pancreatic surgery. This prospective observational study will include all consecutive patients undergoing pancreatic surgery over a period of three years (2022 - 2025) at two sites, namely University General Hospital of Larissa and IASO Thessalias, in Greece. Patients will be prospectively enrolled after written informed consent. Data will be collected on patient characteristics, surgical and anaesthetic techniques, complications, and length of stay. Quality of life questionnaires will be administered to patients preoperatively, on the fith postoperative day, first follow-up after discharge, one month and six months after the operation. The stress response will be assessed by measuring the Neutrophil-Lymphocyte Ratio and Platelet-Lymphocyte Ratio (NLR and PLR) preoperatively, and on the first five postoperative days. Data will be collected on pancreatic surgery-specific complications such as delayed gastric emptying (DGE), post-pancreatectomy haemorrhage (PPH) and postoperative pancreatic fistula (POPF) formation. Anonymised data will be uploaded by the principal investigator on a protected excel spreadsheet for analysis.

In this study the ERAS program is applied to patients undergoing pancreatic surgery.This is a prospective observational cohort study.The study will take place in two hospitals, the University General Hospital of Larissa (academic center), and IASO Thessalias (largest private general hospital in Thessaly). The study period is three years between May 2022 and April 2025. All patients undergoing pancreatic surgery during this period will be invited to participate in the study. Recruitment will take place at the first appointment with the surgeon when the patient is listed for surgery. The patient will be provided with detailed information about the program which also includes an information leaflet. A written consent form will be signed by patients willing to participate in the study. Enrolled patients will follow the ERAS pathway for pancreatic surgery during the preoperative, intraoperative, and postoperative period. The ERAS protocol is based on ERAS society recommendations for enhanced recovery after pancreatoduodenectomy. The ERAS protocol consists of the following items: First appointment preoperative: * Patient education about the program * Prehabilitation with advice on physical exercise and nutritional support * Advice to stop smoking and alcohol consumption * Plan for optimisation of comorbidities * Completion of quality of life questionnaire Day before surgery: * Discussion about the program to address any patient concerns and anxieties * Light meal and carbohydrate drink before bedtime * Anti-clotting injection 12 hours before surgery Day of surgery: * Carbohydrate drink and painkillers 3 hours before surgery * Clear fluids allowed up to 3 hours before surgery * Antibiotics within 1 hour before surgical incision Intraoperative * Epidural catheter is sited before general anaesthesia * Multimodal and opioid-sparing analgesia * Nausea and vomiting prophylaxis * Goal directed fluid therapy * Active warming to avoid hypothermia * Monitoring of blood glucose to maintain normoglycaemia * Bile culture * Repeat antibiotics if surgery lasts more than 4 hours Postoperative: * Removal of nasogastric tube by postoperative day 1 * Removal of drains by postoperative day 3 * Multimodal analgesia, epidural catheter for 3 days, minimisation of opioids * Early and scheduled mobilisation and respiratory physiotherapy protocol * Diet protocol with nutritional drinks and gradual progression from light to solid diet by postoperative day 5 * Removal of urinary catheter when patients able to mobilise on their own, by postoperative day 5 * Cessation of intravenous fluids when patients able to drink 1.5 liters of water, by postoperative day 5 * Regular gastrokinetic medication and gum chewing * Glycaemic control protocol * Cessation of antibiotics if bile culture negative and no other indication to continue The study group will use a checklist with ERAS criteria to follow for each patient and data will be collected on adherence rates to these criteria. Data will be collected on patient demographics such as sex, age, Body Mass Index (BMI), American Society of Anaesthesiologists (ASA) physical status, and co-morbidities. Data will also be collected on surgical approach and technique, and tumour stage (pTNM). Data will be collected on complications including cardiovascular and respiratory complications, infectious complications (surgical site infection, chest infection, urinary tract infection, intra-abdominal abscess, sepsis), anaesthetic complications (severe pain, delirium, cognitive decline), functional complications (functional decline, new mobility aid use, pressure ulcer, discharge to nursing or rehabilitation facility), renal failure, ileus, return to theatre, readmission, and death. Data will be collected on length of stay and pancreatic surgery-specific complications such as DGE, PPH and POPF formation. International consensus guidelines will be used for definition and grading of these complications. Quality of life will be assessed by Patient Reported Outcome Measures (PROMS). The stress response will be assessed by measuring NLR and PLR. After anonymization, all data will be prospectively uploaded by local investigators on a protected database and incorporated into a spreadsheet for data analysis. The data will be analyzed using PROMs, NLR and PLR ratios, postoperative complications, length of hospital stay and cancer recurrence rates as the main outcome variables.The influence of the following factors will be assessed: age, BMI, sex, surgical technique, pTNM stage, preoperative comorbidity, ASA classification, previous SARS-CoV-2 infection, and compliance to the ERAS protocol (\<50%, 50-70%, 70-90%, \>90%). Adherence will be calculated as the number of interventions fulfilled/20 (total number of preoperative and perioperative interventions). The statistical model will be multivariate regression analysis. Sample size guidelines for observational studies with regression analysis are based on simulation studies and suggest that the minimum number of events per variable (EPV) should be 10. According to these guidelines the minimum sample size is calculated at 90. To account for 25% loss to follow-up the investigators aim for a total enrollment goal of 120 participants. IBM® SPSS 26 software will be used for statistical analysis. Continuous variables will be compared with One-Way ANOVA or Student's t test for parametric data and with a non-parametric test (Mann-Whitney U test or Kruskal-Wallis test), as indicated. Categorical data will be analysed by using the chi squared or Fisher's exact test where indicated. Quantitative values will be expressed as mean ± standard deviation (SD), median and range, categorical data with percentage frequencies. The odds ratio (OR) will be presented followed by 95% confidence interval (95% CI). Differences in survival and complications between different degrees of compliance will be assessed by the application of log rank test. P \< 0.05 will be considered statistically significant.