Comparison of the efficacy and safety of sedation between dexmedetomidine-remifentanil and propofol-remifentanil during endoscopic submucosal dissection

doi:10.3748/wjg.v21.i12.3671

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Mar 28, 2015 (publication date) through Aug 25, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Randomized Controlled Trial

World J Gastroenterol. Mar 28, 2015; 21(12): 3671-3678
Published online Mar 28, 2015. doi: 10.3748/wjg.v21.i12.3671

Table 4 Patient characteristics

	DR group(n = 29)	PR group(n = 30)	P value
Age (yr)	62.1 ± 10.3	62.9 ± 12.3	0.763
Male	19 (65.5)	22 (73.3)	0.514
Height (cm)	162.2 ± 7.7	164.8 ± 5.8	0.274
Weight (kg)	62.8 ± 8.5	65.1 ± 10.2	0.276
ASA classification n (%)			0.390
I	19 (65.5)	15 (50.0)
II	9 (31.0)	12 (40.0)
III	1 (3.4)	3 (10.0)
Snoring history	9 (31.0)	7 (23.3)	0.506

Values are presented as the mean ± SD or frequency (percentage). DR group: Indicates dexmedetomidine-remifentanil group; PR group: Propofol-remifentanil group; ASA: American society of anesthesiologists.

Citation: Kim N, Yoo YC, Lee SK, Kim H, Ju HM, Min KT. Comparison of the efficacy and safety of sedation between dexmedetomidine-remifentanil and propofol-remifentanil during endoscopic submucosal dissection. World J Gastroenterol 2015; 21(12): 3671-3678
URL: https://www.wjgnet.com/1007-9327/full/v21/i12/3671.htm
DOI: https://dx.doi.org/10.3748/wjg.v21.i12.3671