The Inventory of Depressive Symptomatology (IDS): Clinician (IDS‐C) and Self‐Report (IDS‐SR) ratings of depressive symptoms

Rush, A. John; Carmody, Thomas; Reimitz, Paul-Egbert

doi:10.1002/mpr.79

Cited by 372 publications

(266 citation statements)

References 32 publications

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“…At baseline and exit visits in the TMAP project, both the self-report and clinician-rated versions of the 30-item Inventory of Depressive Symptomatology (Rush et al 1986(Rush et al , 1996(Rush et al , 2000Trivedi et al 2004a) Each domain is scored from 0 to 3 reflecting increasing amounts of pathology, so the total test score can range from 0 to 27 (Rush et al 2000).…”

Section: Methodsmentioning

confidence: 99%

“…At baseline and exit visits in the TMAP project, both the self-report and clinician-rated versions of the 30-item Inventory of Depressive Symptomatology (Rush et al 1986(Rush et al , 1996(Rush et al , 2000Trivedi et al 2004a) were obtained (in English or Spanish) by a Research Coordinator not involved in the treatment of patients. The order of test administration was not strictly randomized, but the IDS-C 30 was completed without knowledge of the IDS-SR 30 responses.…”

Section: Methodsmentioning

confidence: 99%

“…The remaining domains are each rated by a single item. Each domain is scored from 0 to 3 reflecting increasing amounts of pathology, so the total test score can range from 0 to 27 (Rush et al 2000).…”

Section: Methodsmentioning

confidence: 99%

“…A recent study (Rush et al in press) compared three versions of QIDS (Rush et al 2000(Rush et al , 2003bTrivedi et al 2004a): the QIDS-SR 16 , QIDS-C 16 , and a version provided by a telephonebased system ). Both classical test theory (CTT), which defines depression in terms of an observable test score, and item response theory (IRT) (see Embretson & Reise 2000), which defines depression as a latent trait, were employed.…”

Section: Objectivesmentioning

confidence: 99%

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Clinical vs. self-report versions of the quick inventory of depressive symptomatology in a public sector sample

Bernstein

Rush

Carmody

et al. 2007

Journal of Psychiatric Research

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Objectives-Recent work using classical test theory (CTT) and item response theory (IRT) has found that the self-report ) and clinician-rated (QIDS-C 16 ) versions of the 16-item Quick Inventory of Depressive Symptomatology were generally comparable in outpatients with nonpsychotic major depressive disorder (MDD). This report extends this comparison to a less welleducated, more treatment-resistant sample that included more ethnic/racial minorities using IRT and selected classical test analyses. 16 and QIDS-C 16 were obtained in a sample of 441 outpatients with nonpsychotic MDD seen in the public sector in the Texas Medication Algorithm Project (TMAP). The Samejima graded response IRT model was used to compare the QIDS-SR 16 and QIDS-C 16 . 16 and QIDS-C 16 related well to overall depression. The slopes of the item response functions a), which index the strength of relationship between overall depression and each symptom, were extremely similar with the two measures. Likewise, the CTT and IRT indices of symptom frequency (item means and locations of the item response functions, b i ) were also similar with these two measures. For example, sad mood and difficulty with concentration/decision making were highly related to the overall depression severity with both the QIDS-C 16 and QIDS-SR 16 . Likewise, sleeping difficulties were commonly reported, even though they were not as strongly related to overall magnitude of depression. Methods-The QIDS-SR Results-The nine symptom domains in the QIDS-SR Conclusion-In this less educated, socially disadvantaged sample, differences between the QIDS-C 16 and QIDS-SR 16 were minor. The QIDS-SR 16 is a satisfactory substitute for the more timeconsuming QIDS-C 16 in a broad range of adult, nonpsychotic, depressed outpatients. KeywordsQuick Inventory of Depressive Symptomatology; Inventory of Depressive Symptomatology; Item response theory; Samejima graded response model; depressive symptoms OBJECTIVESThe accurate, rapid, and cost-efficient measurement of depressive symptoms serves both clinical and research purposes. Clinicians can gauge the benefit of treatment and make timely adjustments in the treatment plan. Research, on the other hand, can be made less costly if such measures are available. The Quick Inventory of Depressive Symptomatology (QIDS) is a 16-item scale that measures each of the nine symptom domains that define a major depressive , which defines depression as a latent trait, were employed. The particular IRT model we employed was developed by Samejima (1969Samejima ( , 1997 to examine graded responses. The recent study (Rush et al. in press) focused on a subset of patients with nonpsychotic major depressive disorder (MDD) derived from the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial (Fava et al. 2003;Rush et al. 2004a). These patients were reasonably well educated as a group and were drawn from both primary and psychiatric care settings. They were selected to not be treatment resistant. Results were generally comparable between...

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Section: Methodsmentioning

confidence: 99%

“…At baseline and exit visits in the TMAP project, both the self-report and clinician-rated versions of the 30-item Inventory of Depressive Symptomatology (Rush et al 1986(Rush et al , 1996(Rush et al , 2000Trivedi et al 2004a) were obtained (in English or Spanish) by a Research Coordinator not involved in the treatment of patients. The order of test administration was not strictly randomized, but the IDS-C 30 was completed without knowledge of the IDS-SR 30 responses.…”

Section: Methodsmentioning

confidence: 99%

Section: Methodsmentioning

confidence: 99%

Section: Objectivesmentioning

confidence: 99%

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Clinical vs. self-report versions of the quick inventory of depressive symptomatology in a public sector sample

Bernstein

Rush

Carmody

et al. 2007

Journal of Psychiatric Research

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“…The ROAs used a telephone interview to collect the HRSD 17 , as well as the 30-item Inventory of Depressive Symptomatology (IDS-C 30 ) (Rush et al, 1996;Rush et al, 2000) which uses unconfounded items to measure both core criterion diagnostic symptoms and associated symptoms of depression. The IDS-C 30 was used to determine the presence of the atypical (Novic et al, 2005) and melancholic (Kahn et al, 2006) features of depression, and the HRSD17 was used to define the presence of the anxious features of depression .…”

Section: Assessmentsmentioning

confidence: 99%

Influences of hormone-based contraception on depressive symptoms in premenopausal women with major depression

Young

Kornstein

Harvey³

et al. 2007

Psychoneuroendocrinology

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SummaryObjective-Hormone-based contraceptives affect mood in healthy women or in women with Premenstrual Dysphoric Disorder. No study has yet examined their association with mood in women with major depressive disorder (MDD). The purpose of this study was to determine whether estrogenprogestin combination or progestin-only contraceptives are associated with depression severity, function and quality of life, or general medical or psychiatric comorbidity in women with MDD.Methods-This analysis focused on a large population of female outpatients less than 40 years of age with non-psychotic MDD who were treated in 18 primary and 23 psychiatric care settings across the United States, using data from the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study. Baseline demographic and clinical information was gathered and compared Corresponding Author: Elizabeth A Young, MBNI, 205 Zina Pitcher place, Ann Arbor MI, 48109-0720, 1-734-936-2087 (Phone), 1-734-647-4130 (fax), eayoung@umich.edu. Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. NIH Public Access Author ManuscriptPsychoneuroendocrinology. Author manuscript; available in PMC 2008 August 1. Published in final edited form as:Psychoneuroendocrinology. 2007 August ; 32(7): 843-853. NIH-PA Author ManuscriptNIH-PA Author Manuscript NIH-PA Author Manuscript between three groups based on hormonal use: combination (estrogen-progestin)(N=232), progestinonly (N=58), and no hormone treatment (N=948).Results-Caucasians were significantly more likely to use combined hormone contraception. Women on progestin-only had significantly more general medical comorbidities; greater hypersomnia, weight gain and gastrointestinal symptoms; and worse physical functioning than women in either of the other groups. Those on combined hormone contraception were significantly less depressed than those with no hormone treatment by the 16-item Quick Inventory of Depressive Symptomatology -Self-Rated. The combined hormone group also demonstrated better physical functioning and less obsessive-compulsive disorder comorbidity than either of the other groups.Conclusions-Synthetic estrogen and progestins may influence depressive and physical symptoms in depressed women.

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Prevalence and Distribution of Major Depressive Disorder in African Americans, Caribbean Blacks, and Non-Hispanic Whites

Williams¹,

González²,

Neighbors³

et al. 2007

Arch Gen Psychiatry

1,124

925

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The Inventory of Depressive Symptomatology (IDS): Clinician (IDS‐C) and Self‐Report (IDS‐SR) ratings of depressive symptoms

Cited by 372 publications

References 32 publications

Clinical vs. self-report versions of the quick inventory of depressive symptomatology in a public sector sample

Clinical vs. self-report versions of the quick inventory of depressive symptomatology in a public sector sample

Influences of hormone-based contraception on depressive symptoms in premenopausal women with major depression

Prevalence and Distribution of Major Depressive Disorder in African Americans, Caribbean Blacks, and Non-Hispanic Whites

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