Validity and reliability of the reflux symptom score

Jérôme R. Lechien(University of Mons), François Bobin(International Federation of Red Cross and Red Crescent Societies), Vinciane Muls(Université Libre de Bruxelles), Marie‐Paule Thill(Centre Hospitalier Universitaire de Saint-Pierre), Mihaéla Horoi(Centre Hospitalier Universitaire de Saint-Pierre), Katharina Ostermann(Centre Hospitalier Universitaire de Saint-Pierre), Kathy Huet(University of Mons), Bernard Harmegnies(University of Mons), Didier Dequanter(International Federation of Red Cross and Red Crescent Societies), Giovanni Dapri(Université Libre de Bruxelles), Marie-Thérèse Maréchal(Université Libre de Bruxelles), Camille Finck(International Federation of Red Cross and Red Crescent Societies), Alexandra Rodriguez Ruiz(International Federation of Red Cross and Red Crescent Societies), Sven Saussez(University of Mons)
The Laryngoscope
April 14, 2019
Cited by 178Open Access
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Abstract

OBJECTIVES/HYPOTHESIS: To develop and validate the Reflux Symptom Score (RSS), a self-administered patient-reported outcome questionnaire for patients with laryngopharyngeal reflux (LPR). STUDY DESIGN: Prospective controlled study. METHODS: A total of 113 patients with LPR were enrolled and treated with diet and 3 months of pantoprazole, alginate, and/or magaldrate depending on the LPR characteristics (acid, nonacid, or mixed). Eighty asymptomatic individuals completed the study. Patients and controls completed the RSS twice within a 7-day period to assess test-retest reliability. Internal consistency was measured using Cronbach's α for the RSS items in patients and controls. Validity was assessed by comparing the baseline RSS with the Reflux Symptom Index (RSI) and Voice Handicap Index (VHI). Seventy-seven patients completed the RSS at baseline and after 6 and 12 weeks of treatment to assess responsiveness to change. The RSS cutoff for determining the presence and absence of LPR was examined by receiver operating characteristic analysis. RESULTS: = 0.831). Internal validity was excellent based on the higher RSS in patients compared with controls (P = .001). RSS, RSI, and VHI scores significantly improved from pre- to posttreatment, indicating a high responsiveness to change. RSS >13 can be considered suggestive of LPR-related symptoms. RSS was not influenced by the occurrence of gastroesophageal reflux disease, LPR subtypes, or patient characteristics. CONCLUSIONS: RSS is a self-administered patient-reported outcome questionnaire that demonstrates high reliability and excellent criterion-based validity. RSS can be used in diagnosing and monitoring LPR disease. LEVEL OF EVIDENCE: 3b Laryngoscope, 130:E98-E107, 2020.


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