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Assessing Gastric Motility and Distention in Postoperative Gastrointestinal Surgery Using Bedside Gastric Ultrasound: Predicting Risk of Aspiration Pneumonia, Ileus, Return of Bowel Function

Postoperative Complications Clinical Trial

Official title:
Assessing Gastric Motility and Distention in Postoperative Gastrointestinal Surgery Using Bedside Gastric Ultrasound: Predicting Risk of Aspiration Pneumonia, Ileus, Return of Bowel Function

Clinical Trial Summary

Point-of-care gastric ultrasound will be used to measure stomach contents postoperative in patients who underwent colorectal surgery. Stomach volume and status (empty or full) will be compared retrospectively to the standard clinical criteria for diet advancement to determine if stomach volume via ultrasound is associated with successful diet advancement, nausea/vomiting, nasogastric tube replacement, length of stay, and other clinical outcomes. Clinicians performing clinical care will be blinded to the ultrasound exam results.

Clinical Trial Description

Patient population: Patients undergoing colorectal surgery will be enrolled prospectively (both cancer and non-cancer patients). Inclusion Criteria: - Patients aged > 18 years of age - Patients undergoing colorectal surgery (both cancer and non-cancer) Exclusion Criteria: - Patients < 18 years of age - Patients with previous gastric surgery - Patients with inadequate or difficult baseline gastric ultrasound images - Any other patient deemed a poor study candidate by the treating physicians Research Design/Protocol: We will perform postoperative point-of-care ultrasound examinations in colorectal surgery patients and will record gastric volumes at set time points, including preoperative and the morning of postoperative day 1. The surgical team, who will be blinded to the results of the ultrasound exam, will make decisions to advance diet, remove nasogastric tube, and begin oral medications based on standard clinical criteria. At the completion of the study we will determine if there is any association between gastric volume on ultrasound and patient complications, such as nausea/vomiting, replacement of nasogastric tube, aspiration of gastric contents, inability to tolerate solid diet, prolonged admission/length of stay, and other clinical outcomes. Outcomes: Our exploratory outcome measures will be tolerance of diet, replacement of NG tube, nausea/vomiting, time to flatus, aspiration pneumonia/pneumonitis, and length of stay. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04747691
Study type Observational [Patient Registry]
Source Thomas Jefferson University
Contact
Status Completed
Phase
Start date February 12, 2021
Completion date July 1, 2021
View Details
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