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Development and validation of a clinical prediction score (the SCOPE score) to predict sedation outcomes in patients undergoing endoscopic procedures

机译:制定和验证临床预测评分(SCOPE评分)以预测接受内窥镜手术患者的镇静效果

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Background Use of anaesthesia services during endoscopy has increased, increasing cost of endoscopy. Aim To identify risk factors for and develop a clinical prediction score to predict difficult conscious sedation. Methods We performed a retrospective cross-sectional study of all patients who underwent oesophagogastroduodenoscopy (OGD) and colonoscopy with endoscopist-administered conscious sedation. The endpoint of difficult sedation was a composite of receipt of high doses (top quintile) of benzodiazepines and opioids, or the documentation of agitation or discomfort. Univariate and multivariate analyses were performed to measure association of the outcome with: age, sex, body mass index (BMI), procedure indication, tobacco use, self-reported psychiatric history, chronic use of benzodiazepines, opioids or other psychoactive medications, admission status and participation of a trainee. A clinical prediction score was constructed using statistically significant variables. Results We identified 13 711 OGDs and 21 763 colonoscopies, 1704 (12.4%) and 2299 (10.6%) of which met the primary endpoint, respectively. On multivariate analysis, factors associated with difficulty during OGD were younger age, procedure indication, male sex, presence of a trainee, psychiatric history and benzodiazepine and opioid use. Factors associated with difficulty during colonoscopy were younger age, female sex, BMI <25, procedure indication, tobacco, benzodiazepine, opioid and other psychoactive medication use. A clinical prediction score was developed and validated that may be used to risk-stratify patients undergoing OGD and colonoscopy across five risk classes. Conclusions Using the Stratifying Clinical Outcomes Prior to Endoscopy (SCOPE) score, patients may be risk stratified for difficult sedation/high sedation requirement during OGD and colonoscopy.
机译:背景技术在内窥镜检查期间麻醉服务的使用增加了,增加了内窥镜检查的成本。目的确定危险因素并制定临床预测评分,以预测难于清醒的镇静作用。方法我们对所有经食管胃十二指肠镜检查(OGD)和结肠镜检查并接受内镜医师镇静镇静的患者进行了回顾性横断面研究。镇静困难的终点是接受高剂量(最高五分之一)的苯二氮卓类药物和阿片类药物,或出现躁动或不适的证据。进行单因素和多因素分析,以衡量结局与以下因素的关联:年龄,性别,体重指数(BMI),手术适应症,吸烟,自我报告的精神病史,长期使用苯二氮卓类药物,阿片类药物或其他精神药物,入院状态和学员的参与。使用统计学上显着的变量构建临床预测分数。结果我们确定了13 711个OGD和21 763个结肠镜检查,分别达到主要终点的1704个(12.4%)和2299个(10.6%)。在多变量分析中,与OGD期间困难相关的因素是年龄较小,手术适应症,男性,受训人员的存在,精神病史以及苯二氮卓和阿片类药物的使用。结肠镜检查中与困难相关的因素是年龄,女性,BMI <25,手术适应症,烟草,苯二氮卓,阿片类药物和其他精神药物的使用。制定并验证了临床预测评分,该评分可用于对五种风险类别中接受OGD和结肠镜检查的患者进行风险分层。结论使用内镜检查前的分层临床结果评分(SCOPE),在OGD和结肠镜检查过程中,患者可能因镇静困难/镇静要求高而分层。

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