Summary
The goal of this pilot prospective cohort study is to examine the reproducibility of gastric volume and emptying as measured by gastric ultrasound and its correlation to a gold-standard test for gastric emptying in the perioperative period in pediatric patients. The main questions it aims to answer are: What is the reliability (inter-rater variability between expert and novice assessors, and intra-rater variability) of a) the gastric antral cross-sectional area (CSA) and b) gastric volume using the Perlas US qualitative grading assessment, measured by using an ultrasound device in pediatric patients undergoing general anesthesia for elective surgery? What is the correlation between ultrasound assessment of gastric emptying by the antral-CSA and gastric emptying determined by the acetaminophen absorption test (AAT), the gold standard? The study will include two cohorts. Cohort assignment will be based on age and anesthesia induction plan. Subjects >7yrs of age and expected to get an IV induction will be assigned to Cohort #1. Subjects <7yrs of age and not expected to get an IV induction will be assigned to Cohort #2. Cohort 1 will include abdominal ultrasound for gastric assessment AND the acetaminophen absorption test which includes administering enteral acetaminophen (tylenol) with 6 oz of water and drawing of blood samples through a peripheral intravenous line. Cohort 2 will include subjects for whom a peripheral intravenous line placement is not part of routine pre-operative care. Procedures for Cohort 2 will include abdominal ultrasound only in the pre-op area (no tylenol). This cohort is included to examine the reliability of measurements across age groups.
Conditions
Fasting, Delayed Gastric Emptying, Aspiration Pneumonia, Respiratory Aspiration of Gastric Content
Recruitment Status
Recruiting
Eligibility Criteria
Inclusion Criteria:
Perioperative patients with ASA classification 1-2
Ages: 2 years- less than 18 years
Locations: Longwood and Waltham campuses of Boston Childrens Hospital
Exclusion Criteria:
History of gastrointestinal surgery
Gastrostomy
Known GI dysmotility (cohort 1 only)
Acetaminophen allergy (cohort 1 only)
Liver or renal dysfunction- pre-diagnosed or, if available, when serum biomarkers are 2 standard deviations above the highest value considered normal for age. (cohort 1 only)
Consumption of acetaminophen in the 4 hours prior (cohort 1 only)
Intervention
Intervention Type
Intervention Name
Diagnostic Test
Gastric Ultrasound Baseline Scans
Diagnostic Test
Acetaminophen Absorption Test (AAT)
Diagnostic Test
Gastric Ultrasound Serial Scans
Gender
All
Min Age
2 Years
Max Age
18 Years
Download Date
January 19, 2024
Principal Investigator
Principal Investigator: Walid Alrayashi, MD
Sub-Investigator: Enid Martinez, MD
This field has been modified from ClinicalTrials.gov to show a contact specific to Boston Children's.
Primary Contact Information
jocelyn.booth@childrens.harvard.edu
Rachel Bernier, MPH
rachel.bernier@childrens.harvard.edu
This field has been modified from ClinicalTrials.gov to show a contact specific to Boston Children's.
For more information on this trial, visit clinicaltrials.gov.
Contact
For more information and to contact the study team: