Perioperative oral nutritional support for patients diagnosed with primary colon adenocarcinoma undergoing radical surgical procedures -Peri-Nutri Trial: study protocol for a randomized controlled trial

• Published in: BMC nutrition Vol. 8; no. 1; pp. 1 - 89
• Main Authors: Aro, Raila, Ohtonen, Pasi, Rautio, Tero, Saarnio, Juha, Mäkäräinen, Elisa, Häivälä, Reetta, Mäkinen, Markus J., Tuomisto, Anne, Schwab, Ursula, Meriläinen, Sanna
• Format: Journal Article
• Language: English
• Published: London BioMed Central 02.09.2022; BMC
• Subjects: Cancer therapies; Chemotherapy; Clinical trials; Cohort analysis; Colon cancer; Colorectal cancer; Dietary supplements; Disease; Gastrointestinal surgery; Hospitals; Informed consent; Malnutrition; Medical diagnosis; Mortality; NRS-2002; Nutrition; Nutritional status; Parenteral nutrition; Patients; Perioperative oral nutritional support; Quality of life; Randomized controlled trial; Study Protocol; Finland
• ISSN: 2055-0928; 2055-0928
• DOI: 10.1186/s40795-022-00591-y

Abstract Background Colon cancer is one of the most common cancers in Finland and worldwide. Cancer-related malnutrition is a well-known risk factor for increased morbidity and mortality after surgery, and it is associated with complications and longer hospitalizations. There are no established recommendations on how to improve the nutritional status of colon cancer patients´ during the perioperative phase. Administration of simple oral nutritional supplements has been suggested to reduce complication rates, but evidence to support this practice is scarce. Methods The Peri-Nutri trial is a prospective, multicenter, randomized, controlled trial. Its primary endpoint is to evaluate whether perioperative oral nutritional support (ONS) decreases the number of complications during the 30-day follow-up after surgery. Secondary endpoints are to study the effect of ONS on quality of life after surgery, length of stay in institutional care, 90-day mortality rate, five-year disease-free survival and overall survival. The patients with a Nutritional risk screening 2002 (NRS-2002) questionnaire result between 2 and 5 (≥ 3 are classified at risk of malnutrition) will be randomized (1:1 ratio) into either the intervention or control group. The intervention group will receive preoperative ONS two weeks before the operation, and nutritional support will continue 10 days after the operation. The control group will not receive ONS. A total of 318 patients will be randomized into two groups and patients are followed five years. Discussion Peri-Nutri study evaluate the impact of ONS to short-term and long-term postoperative morbidity and mortality rates of colon cancer patients undergoing curative surgery. If ONS will decrease patients´ morbidity and mortality, that has a huge impact on patients´ quality of life and also to financial cost. Trial registration ClinicalTrials.gov, NCT03863236 , Registered 25 February 2019.