Cargando…

Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia

BACKGROUND: Due to important biases, conventional end‐of‐day and end‐of‐week assessment methods of gastrointestinal symptoms in functional dyspepsia (FD) are considered suboptimal. Real‐time symptom assessment based on the experience sampling method (ESM) could be a more accurate measurement method....

Descripción completa

Detalles Bibliográficos
Autores principales: Klaassen, Tim, Smeets, Fabienne G. M., Vork, Lisa, Tack, Jan, Talley, Nicholas J., Simrén, Magnus, Aziz, Qasim, Ford, Alexander C., Kruimel, Joanna W., Conchillo, José M., Leue, Carsten, Masclee, Adrian A. M., Keszthelyi, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519073/
https://www.ncbi.nlm.nih.gov/pubmed/33934444
http://dx.doi.org/10.1111/nmo.14136
_version_ 1784584374094659584
author Klaassen, Tim
Smeets, Fabienne G. M.
Vork, Lisa
Tack, Jan
Talley, Nicholas J.
Simrén, Magnus
Aziz, Qasim
Ford, Alexander C.
Kruimel, Joanna W.
Conchillo, José M.
Leue, Carsten
Masclee, Adrian A. M.
Keszthelyi, Daniel
author_facet Klaassen, Tim
Smeets, Fabienne G. M.
Vork, Lisa
Tack, Jan
Talley, Nicholas J.
Simrén, Magnus
Aziz, Qasim
Ford, Alexander C.
Kruimel, Joanna W.
Conchillo, José M.
Leue, Carsten
Masclee, Adrian A. M.
Keszthelyi, Daniel
author_sort Klaassen, Tim
collection PubMed
description BACKGROUND: Due to important biases, conventional end‐of‐day and end‐of‐week assessment methods of gastrointestinal symptoms in functional dyspepsia (FD) are considered suboptimal. Real‐time symptom assessment based on the experience sampling method (ESM) could be a more accurate measurement method. This study aimed to evaluate validity and reliability of an ESM‐based patient‐reported outcome measure (PROM) for symptom assessment in FD. METHODS: Thirty‐five patients with FD (25 female, mean age 44.7 years) completed the ESM‐based PROM (a maximum of 10 random moments per day) and an end‐of‐day symptom diary for 7 consecutive days. On day 7, end‐of‐week questionnaires were completed including the Nepean Dyspepsia Index (NDI) and Patient Assessment of Gastrointestinal Symptom Severity Index (PAGI‐SYM). KEY RESULTS: Experience sampling method and corresponding end‐of‐day scores for gastrointestinal symptoms were significantly associated (ICCs range 0.770–0.917). However, end‐of‐day scores were significantly higher (Δ0.329–1.031) than mean ESM scores (p < 0.05). Comparing ESM with NDI and PAGI‐SYM scores, correlations were weaker (Pearson's r range 0.467–0.846). Cronbach's α coefficient was good for upper gastrointestinal symptoms (α = 0.842). First half‐week and second half‐week scores showed very good consistency (ICCs range 0.913–0.975). CONCLUSION AND INFERENCES: Good validity and reliability of a novel ESM‐based PROM for assessing gastrointestinal symptoms in FD patients was demonstrated. Moreover, this novel PROM allows to evaluate individual symptom patterns and can evaluate interactions between symptoms and environmental/contextual factors. ESM has the potential to increase patients' disease insight, provide tools for self‐management, and improve shared decision making. Hence, this novel tool may aid in the transition toward personalized health care for FD patients.
format Online
Article
Text
id pubmed-8519073
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-85190732021-10-22 Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia Klaassen, Tim Smeets, Fabienne G. M. Vork, Lisa Tack, Jan Talley, Nicholas J. Simrén, Magnus Aziz, Qasim Ford, Alexander C. Kruimel, Joanna W. Conchillo, José M. Leue, Carsten Masclee, Adrian A. M. Keszthelyi, Daniel Neurogastroenterol Motil Original Articles BACKGROUND: Due to important biases, conventional end‐of‐day and end‐of‐week assessment methods of gastrointestinal symptoms in functional dyspepsia (FD) are considered suboptimal. Real‐time symptom assessment based on the experience sampling method (ESM) could be a more accurate measurement method. This study aimed to evaluate validity and reliability of an ESM‐based patient‐reported outcome measure (PROM) for symptom assessment in FD. METHODS: Thirty‐five patients with FD (25 female, mean age 44.7 years) completed the ESM‐based PROM (a maximum of 10 random moments per day) and an end‐of‐day symptom diary for 7 consecutive days. On day 7, end‐of‐week questionnaires were completed including the Nepean Dyspepsia Index (NDI) and Patient Assessment of Gastrointestinal Symptom Severity Index (PAGI‐SYM). KEY RESULTS: Experience sampling method and corresponding end‐of‐day scores for gastrointestinal symptoms were significantly associated (ICCs range 0.770–0.917). However, end‐of‐day scores were significantly higher (Δ0.329–1.031) than mean ESM scores (p < 0.05). Comparing ESM with NDI and PAGI‐SYM scores, correlations were weaker (Pearson's r range 0.467–0.846). Cronbach's α coefficient was good for upper gastrointestinal symptoms (α = 0.842). First half‐week and second half‐week scores showed very good consistency (ICCs range 0.913–0.975). CONCLUSION AND INFERENCES: Good validity and reliability of a novel ESM‐based PROM for assessing gastrointestinal symptoms in FD patients was demonstrated. Moreover, this novel PROM allows to evaluate individual symptom patterns and can evaluate interactions between symptoms and environmental/contextual factors. ESM has the potential to increase patients' disease insight, provide tools for self‐management, and improve shared decision making. Hence, this novel tool may aid in the transition toward personalized health care for FD patients. John Wiley and Sons Inc. 2021-05-02 2021-09 /pmc/articles/PMC8519073/ /pubmed/33934444 http://dx.doi.org/10.1111/nmo.14136 Text en © 2021 The Authors. Neurogastroenterology & Motility published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Klaassen, Tim
Smeets, Fabienne G. M.
Vork, Lisa
Tack, Jan
Talley, Nicholas J.
Simrén, Magnus
Aziz, Qasim
Ford, Alexander C.
Kruimel, Joanna W.
Conchillo, José M.
Leue, Carsten
Masclee, Adrian A. M.
Keszthelyi, Daniel
Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title_full Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title_fullStr Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title_full_unstemmed Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title_short Psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
title_sort psychometric evaluation of an experience sampling method–based patient‐reported outcome measure in functional dyspepsia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519073/
https://www.ncbi.nlm.nih.gov/pubmed/33934444
http://dx.doi.org/10.1111/nmo.14136
work_keys_str_mv AT klaassentim psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT smeetsfabiennegm psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT vorklisa psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT tackjan psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT talleynicholasj psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT simrenmagnus psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT azizqasim psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT fordalexanderc psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT kruimeljoannaw psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT conchillojosem psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT leuecarsten psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT mascleeadrianam psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia
AT keszthelyidaniel psychometricevaluationofanexperiencesamplingmethodbasedpatientreportedoutcomemeasureinfunctionaldyspepsia