Effect of ciprofol with etomidate on the occurrence of hypotension in elderly patients undergoing upper gastrointestinal endoscopy: a prospective randomized controlled study

环丙酚联合依托咪酯对老年患者上消化道内镜检查中低血压发生率的影响:一项前瞻性随机对照研究

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Abstract

BACKGROUND: Ciprofol is increasingly used for endoscopic sedation due to its reduced injection pain, but evidence regarding its safety when combined with etomidate in elderly patients remains limited. This study evaluated the efficacy and safety of ciprofol–etomidate compared with ciprofol alone and propofol–etomidate in elderly patients undergoing upper gastrointestinal endoscopy. METHODS: In this randomized controlled trial, 402 patients aged ≥ 60 years scheduled for upper gastrointestinal endoscopy were assigned to one of three groups: ciprofol–etomidate (EC: 0.3 mg/kg ciprofol + 0.12 mg/kg etomidate), ciprofol (C: 0.4 mg/kg) alone, or propofol–etomidate (EP: 1.2 mg/kg propofol + 0.12 mg/kg etomidate). All patients received remifentanil 0.3 µg/kg before sedation. The primary outcome was hypotension incidence. Secondary outcomes included sedation success, vital signs, and other adverse events. RESULTS: Hypotension incidence differed significantly among groups (EC: 64.5%, C: 80.9%, EP: 75.2%; p = 0.008), with a lower rate in the EC group versus the C group (p = 0.003). Injection pain was rare in both EC (0.7%) and C (1.5%) groups compared with EP (9.0%; p < 0.001). Induction time was longer in EC and C groups than in EP. Recovery and discharge times were prolonged in the C group compared with EP. Other adverse events, including bradycardia, hypoxemia, nausea, vomiting, dizziness, and tremors, did not differ significantly among groups. CONCLUSIONS: The combination of ciprofol and etomidate offers effective sedation, reducing hypotension compared with ciprofol alone and injection pain compared with propofol–etomidate, and may therefore represent a safer alternative for elderly patients undergoing upper gastrointestinal endoscopy. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR2300077770 (date: 20/11/2023). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-026-03767-2.

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