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22 项鼻-鼻窦结局测试的心理测量效度。

Psychometric validity of the 22-item Sinonasal Outcome Test.

机构信息

Guy' and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Clin Otolaryngol. 2009 Oct;34(5):447-54. doi: 10.1111/j.1749-4486.2009.01995.x.

Abstract

OBJECTIVES

We set out to determine the psychometric validation of a disease-specific health related quality of life instrument for use in chronic rhinosinusitis, the 22 item Sinonasal Outcome Test (SNOT-22), a modification of a pre-existing instrument, the SNOT-20.

DESIGN, SETTING AND PARTICIPANTS: The National Comparative Audit of Surgery for Nasal Polyposis and Chronic Rhinosinusitis was a prospective cohort study collecting data on 3128 adult patients undergoing sinonasal surgery in 87 NHS hospitals in England and Wales. Data were collected preoperatively and at 3 months after surgery, and analysed to determine validity of the SNOT-22. Test-retest reliability was assessed in a separate cohort of patients in a single centre.

MAIN OUTCOME MEASURES

The SNOT-22, a derivative of the SNOT-20 was the main outcome measure. Patients were also asked to report whether they felt better, the same or worse following surgery. To evaluate the SNOT-22, the internal consistency, responsiveness, known group differences and validity were analysed.

RESULTS

Preoperative SNOT-22 scores were completed by 2803 patients. 3-month postoperative SNOT-22 scores were available for 2284 patients of all patients who completed a preoperative form (81.5% response rate). The Cronbach's alpha scores for the SNOT-22 were 0.91 indicating high internal consistency. The test-retest reliability coefficient was 0.93, indicating high reliability of repeated measures. The SNOT-22 was able to discriminate between patients known to suffer with chronic rhinosinusitis and a group of healthy controls (P < 0.0001, t = 85.3). It was also able to identify statistically significant differences in sub-groups of patients with chronic rhinosinusitis. There was a statistically significant (P < 0.0001, t = 39.94) decrease in patient reported SNOT-22 scores at 3 months. At 3 months the overall effect size in all patients was 0.81, which is considered large. We found the minimally important difference that is the smallest change in SNOT-22 score that can be detected by a patient, to be 8.9 points.

CONCLUSIONS

We have found the SNOT-22 to be valid and easy to use. It can be used to facilitate routine clinical practice to highlight the impact of chronic rhinosinusitis on the patient's quality of life, and may also be used to measure the outcome of surgical intervention. The minimally important difference allows us to interpret scores in a clinical context, and may help to improve patient selection for surgery.

摘要

目的

我们旨在确定一种特定于疾病的健康相关生活质量工具的心理测量验证,该工具用于慢性鼻-鼻窦炎,即 22 项鼻-鼻窦结局测试(SNOT-22),这是对现有工具 SNOT-20 的修改。

设计、设置和参与者:全国鼻息肉和慢性鼻-鼻窦炎手术比较审计是一项前瞻性队列研究,在英格兰和威尔士的 87 家 NHS 医院对 3128 名成年接受鼻-鼻窦手术的患者进行了数据收集。数据在术前和术后 3 个月收集,并进行分析以确定 SNOT-22 的有效性。在单个中心的另一组患者中评估了测试-再测试的可靠性。

主要观察指标

SNOT-22 是 SNOT-20 的衍生工具,是主要的观察指标。患者还被要求报告手术后感觉更好、相同或更差。为了评估 SNOT-22,分析了内部一致性、反应性、已知群体差异和有效性。

结果

2803 名患者完成了术前 SNOT-22 评分。2284 名患者完成了所有完成术前表格的患者的术后 3 个月 SNOT-22 评分(81.5%的应答率)。SNOT-22 的 Cronbach's alpha 评分为 0.91,表明内部一致性很高。测试-再测试可靠性系数为 0.93,表明重复测量的可靠性很高。SNOT-22 能够区分患有慢性鼻-鼻窦炎的患者和一组健康对照组(P < 0.0001,t = 85.3)。它还能够识别慢性鼻-鼻窦炎患者的亚组之间的统计学显著差异。在所有患者中,患者报告的 SNOT-22 评分在 3 个月时具有统计学显著(P < 0.0001,t = 39.94)下降。3 个月时,所有患者的总体效应大小为 0.81,这被认为是较大的。我们发现最小的重要差异是患者可以检测到的 SNOT-22 评分的最小变化,为 8.9 分。

结论

我们发现 SNOT-22 是有效的且易于使用的。它可以用于促进常规临床实践,以突出慢性鼻-鼻窦炎对患者生活质量的影响,也可用于测量手术干预的结果。最小的重要差异使我们能够在临床环境中解释分数,并可能有助于改善患者对手术的选择。

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