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Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms

PURPOSE: Evaluate the psychometric properties of the 5-item Very Quick Inventory of Depressive Symptomatology self-report and clinician-rated versions (VQIDS-SR(5)/VQIDS-C(5)), compare their relative performance, create crosswalks between their total scores and other accepted depressive symptom rati...

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Autores principales: Rush, A John, Madia, Nancy D, Carmody, Thomas, Trivedi, Madhukar H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860726/
https://www.ncbi.nlm.nih.gov/pubmed/35210776
http://dx.doi.org/10.2147/NDT.S342457
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author Rush, A John
Madia, Nancy D
Carmody, Thomas
Trivedi, Madhukar H
author_facet Rush, A John
Madia, Nancy D
Carmody, Thomas
Trivedi, Madhukar H
author_sort Rush, A John
collection PubMed
description PURPOSE: Evaluate the psychometric properties of the 5-item Very Quick Inventory of Depressive Symptomatology self-report and clinician-rated versions (VQIDS-SR(5)/VQIDS-C(5)), compare their relative performance, create crosswalks between their total scores and other accepted depressive symptom ratings, and define clinically relevant depressive symptom severity thresholds and categorical outcomes for both versions. PATIENTS AND METHODS: The Sequenced Treatment Alternatives to Relieve Depression trial obtained baseline and exit 17-item Hamilton Rating Scale for Depression (HRSD(17)) and 30-item Inventory of Depressive Symptomatology – Clinician-rated scores, and baseline and visit-wise QIDS-SR(16) and QIDS-C(16) ratings from the first treatment step (citalopram). The VQIDS-C(5) and the VQIDS-SR(5) items (sad mood, self-outlook, involvement, fatigue, psychomotor slowing) (each rated 0–3), extracted from the corresponding 16-item ratings, were selected to best reflect the 6-item HRSD (HRSD(6)) (exclusive of anxiety). Classical Test Theory (CTT) and Item-Response Theory (IRT) analyses assessed psychometric features. IRT analyses produced total score crosswalks between the VQIDS(5), QIDS-C(16), QIDS-SR(16) and HRSD(6). Clinically relevant VQIDS symptom severity thresholds and treatment outcomes were estimated based on cross-walks from the parent QIDS(16) ratings. RESULTS: Both VQIDS versions were unifactorial with acceptable internal consistencies (Cronbach’s alphas >0.80), item-total correlations (0.57–0.74) by CCT, and strong IRT item performance. Based on QIDS(16) severity thresholds (none 0–5; mild 6–10; moderate 11–15; severe 16–20; and very severe 21–27), comparable thresholds were 0–2; 3–5; 6–9; 9–12; and >12 for VQIDS-C(5), and 0–2; 2–5; 6–8; 9–12; and >12 for VQIDS-SR(5). Kappa values were acceptable in comparing categories of outcomes (eg, no benefit, remission, etc) based on VQIDS and corresponding QIDS categories. CONCLUSION: The VQIDS-C(5) and VQIDS-SR(5) assess selected core depressive symptoms with psychometrically acceptable properties. Theelf-report and clinician-rated versions provide virtually identical information, symptom severity thresholds and symptom change categories. Both are as sensitive to change as the corresponding QIDS(16), making them suitable for use in busy practices.
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spelling pubmed-88607262022-02-23 Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms Rush, A John Madia, Nancy D Carmody, Thomas Trivedi, Madhukar H Neuropsychiatr Dis Treat Original Research PURPOSE: Evaluate the psychometric properties of the 5-item Very Quick Inventory of Depressive Symptomatology self-report and clinician-rated versions (VQIDS-SR(5)/VQIDS-C(5)), compare their relative performance, create crosswalks between their total scores and other accepted depressive symptom ratings, and define clinically relevant depressive symptom severity thresholds and categorical outcomes for both versions. PATIENTS AND METHODS: The Sequenced Treatment Alternatives to Relieve Depression trial obtained baseline and exit 17-item Hamilton Rating Scale for Depression (HRSD(17)) and 30-item Inventory of Depressive Symptomatology – Clinician-rated scores, and baseline and visit-wise QIDS-SR(16) and QIDS-C(16) ratings from the first treatment step (citalopram). The VQIDS-C(5) and the VQIDS-SR(5) items (sad mood, self-outlook, involvement, fatigue, psychomotor slowing) (each rated 0–3), extracted from the corresponding 16-item ratings, were selected to best reflect the 6-item HRSD (HRSD(6)) (exclusive of anxiety). Classical Test Theory (CTT) and Item-Response Theory (IRT) analyses assessed psychometric features. IRT analyses produced total score crosswalks between the VQIDS(5), QIDS-C(16), QIDS-SR(16) and HRSD(6). Clinically relevant VQIDS symptom severity thresholds and treatment outcomes were estimated based on cross-walks from the parent QIDS(16) ratings. RESULTS: Both VQIDS versions were unifactorial with acceptable internal consistencies (Cronbach’s alphas >0.80), item-total correlations (0.57–0.74) by CCT, and strong IRT item performance. Based on QIDS(16) severity thresholds (none 0–5; mild 6–10; moderate 11–15; severe 16–20; and very severe 21–27), comparable thresholds were 0–2; 3–5; 6–9; 9–12; and >12 for VQIDS-C(5), and 0–2; 2–5; 6–8; 9–12; and >12 for VQIDS-SR(5). Kappa values were acceptable in comparing categories of outcomes (eg, no benefit, remission, etc) based on VQIDS and corresponding QIDS categories. CONCLUSION: The VQIDS-C(5) and VQIDS-SR(5) assess selected core depressive symptoms with psychometrically acceptable properties. Theelf-report and clinician-rated versions provide virtually identical information, symptom severity thresholds and symptom change categories. Both are as sensitive to change as the corresponding QIDS(16), making them suitable for use in busy practices. Dove 2022-02-17 /pmc/articles/PMC8860726/ /pubmed/35210776 http://dx.doi.org/10.2147/NDT.S342457 Text en © 2022 Rush et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Rush, A John
Madia, Nancy D
Carmody, Thomas
Trivedi, Madhukar H
Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title_full Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title_fullStr Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title_full_unstemmed Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title_short Psychometric and Clinical Evaluation of the Clinician (VQIDS-C(5)) and Self-Report (VQIDS-SR(5)) Versions of the Very Quick Inventory of Depressive Symptoms
title_sort psychometric and clinical evaluation of the clinician (vqids-c(5)) and self-report (vqids-sr(5)) versions of the very quick inventory of depressive symptoms
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860726/
https://www.ncbi.nlm.nih.gov/pubmed/35210776
http://dx.doi.org/10.2147/NDT.S342457
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