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Additive Effects of Clonidine Used in Propofol Sedation in Colonoscopy
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Background: Propofol is commonly used for sedation during colonoscopy but often requires high doses. Objectives: This study aimed to compare the outcomes of propofol alone versus propofol combined with clonidine for colonoscopy sedation. Methods: In this randomized, double-blind controlled trial, 60 adult patients scheduled for elective colonoscopy were enrolled. Patients were divided into two groups: Group 1 (G1) received propofol alone, while group 2 (G2) received propofol plus 2 μg/kg clonidine intravenously over 10 minutes. Propofol infusion was initiated at 25 - 75 μg/kg/min IV for the first 10 - 15 minutes, then titrated to 25 - 50 μg/kg/min based on clinical response. Results: Sedation onset was significantly faster in G2 than in G1 (P = 0.001). The total propofol requirement was 22% lower in G2 (P = 0.001). Heart rate (HR) and mean arterial pressure (MAP) were significantly lower in G2 at induction and at the end of the procedure (P < 0.05). Patient satisfaction scores were higher in G2 (P = 0.042). The observer's assessment of alertness/sedation (OAA/S) score after induction was lower in G2 (P = 0.015), indicating deeper sedation. However, Aldrete scores in the post-anesthesia care unit (PACU) were lower in G2 (P = 0.001), suggesting a slower recovery. Conclusions: The addition of clonidine to propofol for colonoscopy sedation led to faster sedation onset, reduced propofol requirements, improved patient satisfaction, and deeper sedation, but with potentially prolonged recovery times.
Title: Additive Effects of Clonidine Used in Propofol Sedation in Colonoscopy
Description:
Background: Propofol is commonly used for sedation during colonoscopy but often requires high doses.
Objectives: This study aimed to compare the outcomes of propofol alone versus propofol combined with clonidine for colonoscopy sedation.
Methods: In this randomized, double-blind controlled trial, 60 adult patients scheduled for elective colonoscopy were enrolled.
Patients were divided into two groups: Group 1 (G1) received propofol alone, while group 2 (G2) received propofol plus 2 μg/kg clonidine intravenously over 10 minutes.
Propofol infusion was initiated at 25 - 75 μg/kg/min IV for the first 10 - 15 minutes, then titrated to 25 - 50 μg/kg/min based on clinical response.
Results: Sedation onset was significantly faster in G2 than in G1 (P = 0.
001).
The total propofol requirement was 22% lower in G2 (P = 0.
001).
Heart rate (HR) and mean arterial pressure (MAP) were significantly lower in G2 at induction and at the end of the procedure (P < 0.
05).
Patient satisfaction scores were higher in G2 (P = 0.
042).
The observer's assessment of alertness/sedation (OAA/S) score after induction was lower in G2 (P = 0.
015), indicating deeper sedation.
However, Aldrete scores in the post-anesthesia care unit (PACU) were lower in G2 (P = 0.
001), suggesting a slower recovery.
Conclusions: The addition of clonidine to propofol for colonoscopy sedation led to faster sedation onset, reduced propofol requirements, improved patient satisfaction, and deeper sedation, but with potentially prolonged recovery times.
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