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《COVID-19 症状指数的有效性和可靠性:一种评估一般和耳鼻喉症状严重程度的工具》。

Validity and reliability of the COVID-19 symptom index, an instrument evaluating severity of general and otolaryngological symptoms.

机构信息

COVID-19 Task Force of the Young-Otolaryngologists of the International Federations of Oto-Rhino-Laryngological Societies (YO-IFOS), Paris, France.

Department of Otolaryngology-Head and Neck Surgery, Foch Hospital, School of Medicine, UFR Simone Veil, Université Versailles Saint-Quentin-en-Yvelines (Paris Saclay University), Paris, France.

出版信息

Acta Otolaryngol. 2021 Jun;141(6):615-620. doi: 10.1080/00016489.2021.1899282. Epub 2021 Mar 18.

Abstract

BACKGROUND

There is no clinical instrument evaluating symptoms of COVID-19.

OBJECTIVE

To develop a clinical instrument for evaluating symptoms of COVID-19 mild-to-moderate forms.

METHODS

COVID-19 patients were recruited from EpiCURA Hospital (Belgium). They completed the COVID-19 Symptom Index (CSI) twice to assess the test-retest reliability. The internal consistency was evaluated with Cronbach's alpha. CSI was completed by healthy subjects to assess the internal validity. Patients completed CSI 6 weeks after the COVID-19 resolution to evaluate the responsiveness to change.

RESULTS

Ninety-four COVID-19 patients and 55 healthy individuals completed the evaluations. Symptoms associated with the higher severity score were fatigue, headache and myalgia. The Cronbach's alpha value was 0.801, indicating high internal consistency. The test-retest reliability was adequate (r = 0.535,  = .001). The correlation between CSI total score and SNOT-22 was high (r = 0.782;  < .001), supporting a high external validity. COVID-19 patients reported significant higher CSI score than healthy individuals, suggesting an adequate internal validity. The mean CSI significantly decreased after the COVID-19 resolution, supporting a high responsiveness to change property.

CONCLUSION AND SIGNIFICANCE

The CSI is a reliable and valid patient reported outcome questionnaire for the evaluation of symptom severity of COVID-19 patients.

摘要

背景

目前尚无评估 COVID-19 症状的临床仪器。

目的

开发一种用于评估 COVID-19 轻症至中度患者症状的临床仪器。

方法

从 EpiCURA 医院(比利时)招募 COVID-19 患者。他们两次完成 COVID-19 症状指数(CSI)以评估测试-重测信度。采用 Cronbach's alpha 评估内部一致性。健康受试者完成 CSI 以评估内部有效性。患者在 COVID-19 痊愈后 6 周完成 CSI 以评估对变化的反应能力。

结果

94 名 COVID-19 患者和 55 名健康个体完成了评估。与较高严重程度评分相关的症状是疲劳、头痛和肌痛。Cronbach's alpha 值为 0.801,表明具有较高的内部一致性。测试-重测信度良好(r=0.535,P=.001)。CSI 总分与 SNOT-22 的相关性较高(r=0.782;P<.001),支持具有较高的外部有效性。COVID-19 患者报告的 CSI 评分明显高于健康个体,表明具有较高的内部有效性。COVID-19 痊愈后,CSI 均值显著下降,支持具有较高的变化反应能力。

结论和意义

CSI 是一种可靠且有效的患者报告结局问卷,可用于评估 COVID-19 患者的症状严重程度。

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