首页> 外文期刊>BMC Anesthesiology >Propofol and sufentanil may affect the patients’ sleep quality independently of the surgical stress response: a prospective nonrandomized controlled trial in 1033 patients’ undergone diagnostic upper gastrointestinal endoscopy
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Propofol and sufentanil may affect the patients’ sleep quality independently of the surgical stress response: a prospective nonrandomized controlled trial in 1033 patients’ undergone diagnostic upper gastrointestinal endoscopy

机译:异丙酚和舒芬太尼可能独立于手术应激反应而影响患者的睡眠质量:一项针对1033例接受诊断性上消化道内镜检查的患者的前瞻性非随机对照试验

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Background It is unknown whether sedative per se contributes to the postoperative sleep disturbance. Diagnostic upper gastrointestinal endoscopy (UGE) is a minimally invasive procedure which is not likely to cause tissue trauma and pain. The purpose of this study was to evaluate the sleep quality of patients undergoing routine (without sedative) diagnostic UGE or UGE with sedative, before, 1?week, and 1?month after the procedure. Methods One thousand and thirty-three patients undergoing UGE were enrolled. Patients chose sedative or without sedative. Propofol and sufentanil were administered to the sedative group, not allowed for the routine group. The Pittsburgh Sleep Quality Index (PSQI) was measured before, 1?week and 1?month after the procedure. Results Five hundred and ten patients were enrolled in the sedative group and 523 in the routine group. One week after the procedure, patients in the sedative group showed significantly higher PSQI scores (worse sleep quality) than the baseline PSQI scores ( p Conclusions The sedative group showed impaired sleep quality 1?week after diagnostic UGE. Propofol and sufentanil may independently affect the sleep quality of patients after sedative of diagnostic UGE for only one week. Trial registration This study is registered on Chinese Clinical Trial Registry ( IDChiCTR-OCH-13003128 ). Registered 2 April 2013.
机译:背景技术镇静剂本身是否会导致术后睡眠障碍尚不清楚。诊断性上消化道内窥镜检查(UGE)是一种微创手术,不太可能引起组织创伤和疼痛。这项研究的目的是评估在手术前,手术后1周和1个月内接受常规(无镇静剂)诊断性UGE或具有镇静剂的UGE的患者的睡眠质量。方法纳入133例行UGE的患者。患者选择使用镇静剂或不使用镇静剂。丙泊酚和舒芬太尼用于镇静组,常规组不允许。匹兹堡睡眠质量指数(PSQI)在手术前,手术后1周和1个月进行测量。结果镇静组510例,常规组523例。手术后一周,镇静组患者的PSQI评分(糟糕的睡眠质量)明显高于基线PSQI评分(p结论)镇静组在诊断UGE 1周后显示睡眠质量受损,丙泊酚和舒芬太尼可能独立影响诊断性UGE镇静后患者的睡眠质量仅一周,试验注册该研究在中国临床试验注册中心(IDChiCTR-OCH-13003128)进行注册,于2013年4月2日注册。

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