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首页> 外文期刊>Scandinavian journal of gastroenterology. >Validation of a brief inventory for diagnosis and monitoring of symptomatic gastro-oesophageal reflux.
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Validation of a brief inventory for diagnosis and monitoring of symptomatic gastro-oesophageal reflux.

机译:确认用于诊断和监测有症状胃食管反流的简要清单的有效性。

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BACKGROUND: This article presents a brief inventory for the diagnosis and monitoring of GORD symptoms. METHODS: The inventory consists of five items pertaining to different aspects of GORD to be graded for frequency on a 5-point Likert scale. It was validated on a consecutive group of GORD patients diagnosed either by endoscopy (n = 25) or by 24-h ambulatory pH monitoring (acid exposure time > or = 5%; n = 233) and control subjects (n = 300). RESULTS: Each of the inventory items was significantly associated with GORD (P < 0.001). Factor analysis indicated that all items loaded on a single scale with a high reliability (Cronbach alpha 0.88). Each item was weighted by its respective odds ratio in favour of GORD and a total score for the scale was then calculated as the sum of weighted scores on the five individual items. Receiver-operator (ROC) curve analysis implemented on a random sample comprising 67% of the group indicated that a total weighted score of 31.6 (percentage of the maximal possible weighted score) was 91% sensitive and 92% specific in the diagnosis of GORD. This score was then validated on the rest of the sample, where it correctly classified patients and controls with a sensitivity of 89% and specificity of 94%. The score proved stable on repeated administration in controls and in patients with stable symptoms, and decreased by 66% (P < 0.001) after 1 month of treatment with omeprazole in patients who reported symptom relief. CONCLUSIONS: The scale described in this article is a brief, simple and accurate measure, for the diagnosis of GORD as well as for monitoring its symptoms.
机译:背景:本文提供了用于诊断和监测GORD症状的简要清单。方法:清单由与GORD不同方面有关的五个项目组成,这些项目将按5点李克特量表进行频率分级。通过内窥镜检查(n = 25)或通过24小时动态pH监测(酸暴露时间>或= 5%; n = 233)和对照组(n = 300)诊断出的连续GORD患者组中已验证了这一点。结果:每个清单项目与GORD显着相关(P <0.001)。因子分析表明,所有物品均以高可靠性装载在单个秤上(Cronbach alpha 0.88)。通过有利于GORD的各个项目的比值比对每个项目进行加权,然后将量表的总分计算为五个单独项目的加权分之和。对包括67%的人群的随机样本进行的接收者-操作者(ROC)曲线分析表明,在GORD诊断中,总加权分数31.6(最大可能加权分数的百分比)为91%敏感性和92%特异性。然后在其余样品上对该分数进行验证,在该样本中,其对患者和对照进行了正确分类,敏感性为89%,特异性为94%。证明在对照组和症状稳定的患者中重复给药后该评分稳定,在报告症状缓解的患者中,用奥美拉唑治疗1个月后该评分降低了66%(P <0.001)。结论:本文描述的量表是一种简短,简单,准确的量度,用于诊断GORD以及监测其症状。

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