The goal of this clinical trial is to evaluate nutrition administration in the time around the tracheostomy in patients with breathing tubes. The main questions it aims to answer are: * Will continuing nutrition up to the time of surgery (tracheostomy) decrease nutrition interruptions, thereby increasing food intake? * Does continuing nutrition up to the time of surgery increase instances of food going into the lungs or lung infections? Researchers will compare patients who have nutrition withheld 6 hours prior to surgery versus those who receive nutrition up until the time of surgery to see if there are differences in food intake, instances of food entering the lungs or lung infections.
Malnutrition is a significant problem in the critically ill, however with busy operating room schedules, we often find that feeds are interrupted repetitively prior to elective surgery. These interruptions are practiced based on the American Society of Anesthesiologist guidelines for fasting intervals for elective surgery. These guidelines, however, were not created for critically ill, intubated patients. The theoretical concern for an increased risk of aspiration with continuation of enteral feeds up to the time of surgery persists without supporting evidence. Thus, there is a need for a universal evidence-based guideline on perioperative enteral feeding to benefit critical care patients. To this end, the goal of the present study is to implement a protocol designed to decrease the interruption of enteral feeds in critical care patients undergoing tracheostomy and prospectively evaluate whether this leads to a quantitative increase in nutritional intake without increasing the risk of aspiration. Additionally, we hope that increasing quantitative nutrition may decrease morbidity especially in the small subset of patients where feed interruptions occur repetitively. If the aims of the project are achieved, the data obtained from this study will be used to create an evidence-based platform from which physicians can practice. This will end the anecdotal controversy regarding perioperative tube feed management for tracheostomy; thereby increasing quantitative nutrition and hopefully improving the care of critically ill patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
200
Enteral feeds are continued up until time of surgery
Enteral feeds are stopped 6 or more hours before surgery
Nuvance Health - Danbury Hospital
Danbury, Connecticut, United States
RECRUITINGSt. Mary's Medical Center
West Palm Beach, Florida, United States
RECRUITINGHCA Research Medical Center
Kansas City, Missouri, United States
RECRUITINGErie County Medical Center (University at Buffalo)
Buffalo, New York, United States
RECRUITINGLehigh Valley Health Network
Allentown, Pennsylvania, United States
RECRUITINGUniversity of South Carolina Sch of Medicine /Prisma Health Richland
Columbia, South Carolina, United States
RECRUITINGRate of aspiration pneumonia
To assess differences in rates of aspiration events, a log-rank test for differences in survival curves model will be used. Assuming proportional hazards and non-informative censoring, a cox-model will be used to estimate follow-up hazard ratios for development of aspiration pneumonia between the two groups of interest.
Time frame: Over 7 days from the time of tracheostomy
Volume of tube feed delivery
We will compare the volume of tube feeds delivered daily between the two groups for the duration of the study.
Time frame: From day of consent to completion of study which is 7 days from the time of tracheostomy.
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