Ontology highlight
ABSTRACT: Methods:
We systematically searched Embase, PubMed, Cochrane Central Register of Controlled Trials, CINAHL (via EBSCO), China National Knowledge Infrastructure, and Web of Science (1946–April 2020) databases for randomized controlled trials of gastrointestinal endoscopy (upper gastrointestinal endoscopy, colonoscopy, and advanced endoscopy) using etomidate or propofol as sedatives. We pooled odds ratios (ORs) for the safety profile and patient and anesthesiologist satisfaction using mixed-effects conditional logistic models and standardized mean differences for efficiency outcomes using random-effects models. Results:
Twenty-four studies involving 3875 patients were included. Compared with propofol, etomidate resulted in significantly reduced apnea (OR: 0.22; 95% confidence interval [CI]: 0.13–0.37; P < .001), hypoxemia (OR: 0.43; 95% CI: 0.35–0.54; P < .001), hypotension (OR: 0.20; 95% CI: 0.11–0.36; P < .001), and bradycardia (OR: 0.52; 95% CI: 0.30–0.91; P = .02) but led to increased myoclonus (OR: 8.54; 95% CI: 5.20–14.01; P < .001) and lowered anesthesiologist satisfaction (OR: 0.60; 95% CI: 0.39–0.91; P = .02). Conclusion:
Etomidate may be a good alternative to propofol for gastrointestinal endoscopy, especially advanced endoscopy. Etomidate appears to be safe as an inducer for hemodynamically unstable patients or older adult patients undergoing gastrointestinal endoscopy.
SUBMITTER: Hong J
PROVIDER: S-EPMC9907930 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature