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


Journal

Journal of eating disorders
ISSN: 2050-2974
Titre abrégé: J Eat Disord
Pays: England
ID NLM: 101610672

Informations de publication

Date de publication:
22 Nov 2022
Historique:
received: 19 07 2022
accepted: 15 11 2022
entrez: 24 11 2022
pubmed: 25 11 2022
medline: 25 11 2022
Statut: epublish

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 36419081
doi: 10.1186/s40337-022-00706-7
pii: 10.1186/s40337-022-00706-7
pmc: PMC9682666
doi:

Types de publication

Journal Article

Langues

eng

Pagination

179

Subventions

Organisme : NIMH NIH HHS
ID : F31 MH125495
Pays : United States
Organisme : NIMH NIH HHS
ID : K23 MH125143
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH108595
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Rachel Bryant-Waugh (R)

South London and Maudsley NHS Foundation Trust, London, UK.
Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK.

Casey M Stern (CM)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.

Melissa J Dreier (MJ)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Department of Psychology, Rutgers University, Piscataway, USA.

Nadia Micali (N)

Department of Psychiatry, University of Geneva, Geneva, Switzerland.
Department of Pediatrics, Gynecology and Obstetrics, University of Geneva, Geneva, Switzerland.
Eating Disorders Research Unit, Mental Health Center Ballerup, Mental Health Services of the Capital Region of Denmark, Ballerup, Denmark.

Lucy J Cooke (LJ)

Great Ormond Street Hospital for Children NHS Trust, London, UK.

Megan C Kuhnle (MC)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Department of Epidemiology, Boston University, Boston, USA.

Helen Burton Murray (H)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Center for Neurointestinal Health, Massachusetts General Hospital, Boston, USA.
Harvard Medical School, Boston, USA.

Shirley B Wang (SB)

Department of Psychology, Harvard University, Cambridge, USA.

Lauren Breithaupt (L)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Harvard Medical School, Boston, USA.
Department of Psychiatry, Athinoula A. Martinos Center for Biomedical Imaging, Boston, USA.

Kendra R Becker (KR)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Harvard Medical School, Boston, USA.

Madhusmita Misra (M)

Harvard Medical School, Boston, USA.
Neuroendocrine Unit, Massachusetts General Hospital, Boston, USA.

Elizabeth A Lawson (EA)

Harvard Medical School, Boston, USA.
Neuroendocrine Unit, Massachusetts General Hospital, Boston, USA.

Kamryn T Eddy (KT)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA.
Harvard Medical School, Boston, USA.

Jennifer J Thomas (JJ)

Eating Disorders Clinical and Research Program, Massachusetts General Hospital, 2 Longfellow Place, Suite 200, Boston, MA, 02114, USA. jjthomas@mgh.harvard.edu.
Harvard Medical School, Boston, USA. jjthomas@mgh.harvard.edu.

Classifications MeSH