4.1 Article

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

Journal

ACTA OTO-LARYNGOLOGICA
Volume 141, Issue 6, Pages 615-620

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/00016489.2021.1899282

Keywords

COVID-19; symptom; patient-reported outcome questionnaire; questionnaire; SARS-CoV-2; coronavirus; follow-up; clinical; instrument; validity

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A clinical instrument, the CSI, was developed to evaluate symptoms of COVID-19 patients, showing high internal consistency, validity, and responsiveness to change.
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(s) = 0.535, p = .001). The correlation between CSI total score and SNOT-22 was high (r(s) = 0.782; p < .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.

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