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Content validation of a daily patient-reported outcome measure for assessing symptoms in patients with Small Intestinal Bacterial Overgrowth.
Durgam, Neha; Dashputre, Ankur A; Moshkovich, Olga; Rezaie, Ali; Martinez, Nicholas; Enayati, Pedram; Stansbury, James; Joseph, George.
Afiliación
  • Durgam N; ICON plc, 4130 Parklake Ave Suite 400, Raleigh, NC, 27612, USA.
  • Dashputre AA; Bausch Pharma US, LLC, Bridgewater, NJ, USA. Ankur.Dashputre@bauschhealth.com.
  • Moshkovich O; ICON plc, 4130 Parklake Ave Suite 400, Raleigh, NC, 27612, USA.
  • Rezaie A; Cedars-Sinai Medical Center, Los Angeles, CA, USA.
  • Martinez N; Gastroenterology Clinic, San Antonio, TX, USA.
  • Enayati P; Cedars-Sinai Medical Center, Los Angeles, CA, USA.
  • Stansbury J; ICON plc, 4130 Parklake Ave Suite 400, Raleigh, NC, 27612, USA.
  • Joseph G; Bausch Pharma US, LLC, Bridgewater, NJ, USA.
Qual Life Res ; 32(9): 2573-2585, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37212941
PURPOSE: The aim of this study was to generate evidence supporting the development and content validity of a new PRO instrument, the Small Intestinal Bacterial Overgrowth (SIBO) Symptom Measure (SSM) daily diary. The SSM assesses symptom severity in SIBO patients, with the ultimate goal of providing a fit for purpose PRO for endpoint measurement. METHODS: Qualitative research included 35 SIBO patients in three study stages, using a hybrid concept elicitation (CE)/cognitive interview (CI) method with US patients, ≥ 18 years. Stage 1 included a literature review, clinician interviews, and initial CE interviews with SIBO patients to identify symptoms important to patients for inclusion in the SSM. Stage 2 included hybrid CE/CI to learn more about patients' SIBO experience and test the draft SSM. Finally, stage 3 used CIs to refine the instrument and test its content validity. RESULTS: In stage 1 (n = 8), 15 relevant concepts were identified, with items drafted based on the literature review/clinician interviews and elicitation work. Within stage 2 (n = 15), the SSM was refined to include 11 items; with wording revised for three items. Stage 3 (n = 12) confirmed the comprehensiveness of the SSM, as well as appropriateness of the item wording, recall period, and response scale. The resulting 11-item SSM assesses the severity of bloating, abdominal distention, abdominal discomfort, abdominal pain, flatulence, physical tiredness, nausea, diarrhea, constipation, appetite loss, and belching. CONCLUSIONS: This study provides evidence supporting the content validity of the new PRO. Comprehensive patient input ensures that the SSM is a well-defined measure of SIBO, ready for psychometric validation studies.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Calidad de Vida / Medición de Resultados Informados por el Paciente Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Qual Life Res Asunto de la revista: REABILITACAO / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Calidad de Vida / Medición de Resultados Informados por el Paciente Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Qual Life Res Asunto de la revista: REABILITACAO / TERAPEUTICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos