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

Eric Schwenk

Status: Completed

Conditions: Postoperative Complications; Postoperative Nausea and Vomiting; Postoperative Ileus; Aspiration Vomitus; Postoperative Vomiting; Postoperative Nausea

Treatments: Diagnostic Test: Bedside gastric ultrasound

Study type: Observational

Funder types: Other

Identifiers

NCT04747691

20D.1009

Details and patient eligibility

About

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.

Full 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.

Enrollment: 22 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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 difficult or poor ultrasound images at baseline
  • Any patient deemed a poor candidate by the treating physicians

Trial design

22 participants in 1 patient group

Patients assessed with postoperative bedside gastric ultrasound

Description:

This patient population will include postoperative patients who received a gastrointestinal surgery and are being assessed with the bedside gastric ultrasound.

Treatment:

Diagnostic Test: Bedside gastric ultrasound