- Hypothesis
The study will be based on two working hypotheses:
Gastric ultrasonography performed by trained anesthesiologists is a useful tool for
assessing gastric content and making clinical decisions regarding airway management.
- Methodology
The reference population will consist of patients undergoing scheduled surgery with a
conventional preoperative fasting period (at least 6 hours).
Inclusion criteria for the study will be:
Patients taking GLP-1 analog medications. Adults over 18 years of age. Patients
undergoing scheduled surgery after a fasting period greater than 6 hours and less than 8
hours (first patient of the morning surgical schedule).
Patients who have been properly informed and have signed the informed consent form,
expressing their agreement to participate in the study.
ASA I-III classification. Sufficient intellectual capacity to understand the procedure
and the equipment used.
Exclusion criteria will include:
Not meeting the previously stated criteria. History of esophagogastric pathology or
previous abdominal surgery. Hiatal hernia/gastroesophageal reflux disease. Autonomic
nervous system disorders. Neurological or neuromuscular diseases. Use of
medications/drugs that affect autonomic regulation and delay gastric emptying (opioids)
or potentiate it (prokinetics).
Pregnancy. Presence of arrhythmias.
- Description of the Intervention
Immediately prior to surgery, a gastric ultrasound will be performed on the patient in
both supine and right lateral decubitus positions. A qualitative, semi-quantitative, and
quantitative measurement of gastric content and volumes will be conducted according to
the algorithm designed by Perlas et al. Data will be recorded in the researcher's data
collection notebook. Following this, the anesthetic and surgical procedures will proceed
as planned.
- Ethical, Legal, and Economic Considerations
Patients who choose to participate in the study will be asked for both verbal and written
consent (see patient information sheet and informed consent form). Since the study is
purely observational and will involve no interventions, there will be no legal liability
arising from the study that necessitates insurance coverage. Any ultrasound machine
available in the anesthesia department will be used for the study, meaning that
conducting the study will not incur any additional costs for the hospital.
- Results
The results will be analyzed by the study investigators, with the ultimate goal of
publication in a relevant specialty journal. If any results are applicable for improving
standard clinical practice in our hospital, they will be communicated to the Department
of Anesthesiology and Resuscitation and to any other interested parties through a
clinical session.