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Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)

BACKGROUND: The Pica, ARFID, and Rumination Disorder Interview (PARDI) is a structured interview that can be used to determine diagnosis, presenting characteristics, and severity across three disorders, including avoidant/restrictive food intake disorder (ARFID). The purpose of this study was to eva...

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Autores principales: Bryant-Waugh, Rachel, Stern, Casey M., Dreier, Melissa J., Micali, Nadia, Cooke, Lucy J., Kuhnle, Megan C., Burton Murray, Helen, Wang, Shirley B., Breithaupt, Lauren, Becker, Kendra R., Misra, Madhusmita, Lawson, Elizabeth A., Eddy, Kamryn T., Thomas, Jennifer J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682666/
https://www.ncbi.nlm.nih.gov/pubmed/36419081
http://dx.doi.org/10.1186/s40337-022-00706-7
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author Bryant-Waugh, Rachel
Stern, Casey M.
Dreier, Melissa J.
Micali, Nadia
Cooke, Lucy J.
Kuhnle, Megan C.
Burton Murray, Helen
Wang, Shirley B.
Breithaupt, Lauren
Becker, Kendra R.
Misra, Madhusmita
Lawson, Elizabeth A.
Eddy, Kamryn T.
Thomas, Jennifer J.
author_facet Bryant-Waugh, Rachel
Stern, Casey M.
Dreier, Melissa J.
Micali, Nadia
Cooke, Lucy J.
Kuhnle, Megan C.
Burton Murray, Helen
Wang, Shirley B.
Breithaupt, Lauren
Becker, Kendra R.
Misra, Madhusmita
Lawson, Elizabeth A.
Eddy, Kamryn T.
Thomas, Jennifer J.
author_sort Bryant-Waugh, Rachel
collection PubMed
description BACKGROUND: The Pica, ARFID, and Rumination Disorder Interview (PARDI) is a structured interview that can be used to determine diagnosis, presenting characteristics, and severity across three disorders, including avoidant/restrictive food intake disorder (ARFID). The purpose of this study was to evaluate the psychometric properties of a questionnaire focused specifically on ARFID (PARDI-AR-Q), which has the potential to provide related information with less participant burden. METHODS: Adolescents and adults (n = 71, ages 14–40 years) with ARFID (n = 42) and healthy control participants (HC, n = 29) completed the PARDI-AR-Q and other measures. A subset of the ARFID group (n = 27) also completed the PARDI interview. RESULTS: An exploratory factor analysis of proposed subscale items identified three factors corresponding to the ARFID phenotypes of avoidance based on the sensory characteristics of food, lack of interest in eating or food, and concern about aversive consequences of eating. Further analyses supported the internal consistency and convergent validity of the PARDI-AR-Q subscales, and subscale ratings on the questionnaire showed large and significant correlations (all p-values < 0.001; r’s ranging from 0.48 to 0.77) with the corresponding subscales on the interview. The ARFID group scored significantly higher than HC on all subscales. Furthermore, 90% of the ARFID group scored positive on the PARDI-AR-Q diagnostic algorithm while 93% of the HC scored negative. CONCLUSIONS: Though replication in larger and more diverse samples is needed, findings provide early support for the validity of the PARDI-AR-Q as a self-report measure for possible ARFID in clinical or research settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40337-022-00706-7.
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spelling pubmed-96826662022-11-24 Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q) Bryant-Waugh, Rachel Stern, Casey M. Dreier, Melissa J. Micali, Nadia Cooke, Lucy J. Kuhnle, Megan C. Burton Murray, Helen Wang, Shirley B. Breithaupt, Lauren Becker, Kendra R. Misra, Madhusmita Lawson, Elizabeth A. Eddy, Kamryn T. Thomas, Jennifer J. J Eat Disord Research BACKGROUND: The Pica, ARFID, and Rumination Disorder Interview (PARDI) is a structured interview that can be used to determine diagnosis, presenting characteristics, and severity across three disorders, including avoidant/restrictive food intake disorder (ARFID). The purpose of this study was to evaluate the psychometric properties of a questionnaire focused specifically on ARFID (PARDI-AR-Q), which has the potential to provide related information with less participant burden. METHODS: Adolescents and adults (n = 71, ages 14–40 years) with ARFID (n = 42) and healthy control participants (HC, n = 29) completed the PARDI-AR-Q and other measures. A subset of the ARFID group (n = 27) also completed the PARDI interview. RESULTS: An exploratory factor analysis of proposed subscale items identified three factors corresponding to the ARFID phenotypes of avoidance based on the sensory characteristics of food, lack of interest in eating or food, and concern about aversive consequences of eating. Further analyses supported the internal consistency and convergent validity of the PARDI-AR-Q subscales, and subscale ratings on the questionnaire showed large and significant correlations (all p-values < 0.001; r’s ranging from 0.48 to 0.77) with the corresponding subscales on the interview. The ARFID group scored significantly higher than HC on all subscales. Furthermore, 90% of the ARFID group scored positive on the PARDI-AR-Q diagnostic algorithm while 93% of the HC scored negative. CONCLUSIONS: Though replication in larger and more diverse samples is needed, findings provide early support for the validity of the PARDI-AR-Q as a self-report measure for possible ARFID in clinical or research settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40337-022-00706-7. BioMed Central 2022-11-22 /pmc/articles/PMC9682666/ /pubmed/36419081 http://dx.doi.org/10.1186/s40337-022-00706-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bryant-Waugh, Rachel
Stern, Casey M.
Dreier, Melissa J.
Micali, Nadia
Cooke, Lucy J.
Kuhnle, Megan C.
Burton Murray, Helen
Wang, Shirley B.
Breithaupt, Lauren
Becker, Kendra R.
Misra, Madhusmita
Lawson, Elizabeth A.
Eddy, Kamryn T.
Thomas, Jennifer J.
Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title_full Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title_fullStr Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title_full_unstemmed Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title_short Preliminary validation of the pica, ARFID and rumination disorder interview ARFID questionnaire (PARDI-AR-Q)
title_sort preliminary validation of the pica, arfid and rumination disorder interview arfid questionnaire (pardi-ar-q)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682666/
https://www.ncbi.nlm.nih.gov/pubmed/36419081
http://dx.doi.org/10.1186/s40337-022-00706-7
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