1. Comparison of propofol with midazolam in endoscopic submucosal dissection for esophageal squamous cell carcinoma: a randomized controlled trial
- Author
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Taishi Sakai, Tetsuo Arakawa, Toshio Watanabe, Masaki Ominami, Shusei Fukunaga, Noriko Kamata, Satoshi Sugimori, Yasuaki Nagami, Hirohisa Machida, Hirotsugu Maruyama, Kunihiro Kato, Hirokazu Yamagami, Hiroaki Minamino, Fumio Tanaka, Tetsuya Tanigawa, Masatsugu Shiba, Yasuhiro Fujiwara, and Kazunari Tominaga
- Subjects
Male ,Alcohol Drinking ,Endoscopic Mucosal Resection ,Esophageal Neoplasms ,medicine.drug_class ,Sedation ,Midazolam ,law.invention ,Hospitals, University ,03 medical and health sciences ,0302 clinical medicine ,Randomized controlled trial ,Japan ,law ,medicine ,Humans ,Single-Blind Method ,Propofol ,Aged ,business.industry ,Gastroenterology ,Esophageal cancer ,Middle Aged ,medicine.disease ,Discontinuation ,Logistic Models ,Treatment Outcome ,030220 oncology & carcinogenesis ,Sedative ,Anesthesia ,Multivariate Analysis ,030211 gastroenterology & hepatology ,Female ,Esophageal Squamous Cell Carcinoma ,medicine.symptom ,business ,Anesthetics, Intravenous ,Abdominal surgery ,medicine.drug - Abstract
Interruption of sedation due to a poor response to modified neuroleptanalgesia (m-NLA) with midazolam often occurs during endoscopic submucosal dissection (ESD) for esophageal squamous cell carcinoma (ESCC) because most patients have a history of heavy alcohol intake. Recently, propofol has been used feasibly and safely during endoscopic procedures. The aim of this study was to clarify the efficacy and safety of propofol compared with that of midazolam during ESD for ESCC. This was a single-blind, randomized controlled trial in a single center. Patients with ESCC scheduled for ESD were included in the study. Patients were randomly assigned to one of two groups: the propofol group and the midazolam group. The main outcome was the incidence of discontinuation of the procedure due to a poor response to sedation. Secondary outcomes included risk factors for a poor response to sedation. Between April 2014 and October 2015, 132 patients (n = 66 per group) who underwent ESD for ESCC were enrolled in this study. The incidence of discontinuation due to a poor response to sedation in the propofol and midazolam groups was 0% (0/66) and 37.9% (25/66), respectively (p
- Published
- 2017