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Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients
Depression in oncology patients is under-recognised and associated with poor outcomes. Screening can increase case recognition. The Brief Case-Find for Depression (BCD) is a four-question, interviewer-administered instrument that has been previously validated in a general medical setting. The primar...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409870/ https://www.ncbi.nlm.nih.gov/pubmed/15305199 http://dx.doi.org/10.1038/sj.bjc.6602057 |
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author | Jefford, M Mileshkin, L Richards, K Thomson, J Matthews, J P Zalcberg, J Jennens, R McLachlan, S-A Wein, S Antill, Y Clarke, D M |
author_facet | Jefford, M Mileshkin, L Richards, K Thomson, J Matthews, J P Zalcberg, J Jennens, R McLachlan, S-A Wein, S Antill, Y Clarke, D M |
author_sort | Jefford, M |
collection | PubMed |
description | Depression in oncology patients is under-recognised and associated with poor outcomes. Screening can increase case recognition. The Brief Case-Find for Depression (BCD) is a four-question, interviewer-administered instrument that has been previously validated in a general medical setting. The primary aim of this study was to validate the BCD in a medical oncology/palliative care setting, primarily by comparing its association with physical illness measures and with the Primary Care Evaluation of Mental Disorders (PRIME-MD), the Beck Depression Inventory (BDI) and the Hospital Anxiety and Depression Scale (HADS). Eligible adult oncology patients gave informed consent and completed the above measures and a pain scale. Agreement between the BCD and other instruments was assessed. Construct validity was determined by comparing depressed/nondepressed patients with respect to performance status, symptoms, pain score and functional impairment. A total of 100 patients had a median age of 58 (range 21–90) and ECOG performance status (PS) 2 (0–4). In all, 60% had metastatic disease. The therapeutic goal was curative/adjuvant in 39% and palliative in 61%. Prevalence of depression according to the various measures was: BCD 34%, PRIME-MD 12%, BDI 19% and HADS 14%. In total, 45% of patients responded positively to a single-item screening question. The BCD showed fair agreement with the PRIME-MD (kappa=0.21), moderate agreement with the BDI (kappa=0.43) and fair agreement with the HADS (kappa=0.27). Against the PRIME-MD diagnosis of depression, the BCD had greater sensitivity, but lesser specificity and overall agreement, compared with the BDI and depression scale of the HADS. Patients with probable depression (according to BCD) had inferior PS (P=0.0064), increased pain (P=0.045) and greater impairment of functioning (PRIME-MD: P=0.0003). There was no association with gender, age, disease status or therapeutic goal. Depression is common in oncology patients. The BCD is a quick, easy-to-administer screen for depression, which has reasonable psychometric properties in this population. |
format | Text |
id | pubmed-2409870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24098702009-09-10 Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients Jefford, M Mileshkin, L Richards, K Thomson, J Matthews, J P Zalcberg, J Jennens, R McLachlan, S-A Wein, S Antill, Y Clarke, D M Br J Cancer Clinical Depression in oncology patients is under-recognised and associated with poor outcomes. Screening can increase case recognition. The Brief Case-Find for Depression (BCD) is a four-question, interviewer-administered instrument that has been previously validated in a general medical setting. The primary aim of this study was to validate the BCD in a medical oncology/palliative care setting, primarily by comparing its association with physical illness measures and with the Primary Care Evaluation of Mental Disorders (PRIME-MD), the Beck Depression Inventory (BDI) and the Hospital Anxiety and Depression Scale (HADS). Eligible adult oncology patients gave informed consent and completed the above measures and a pain scale. Agreement between the BCD and other instruments was assessed. Construct validity was determined by comparing depressed/nondepressed patients with respect to performance status, symptoms, pain score and functional impairment. A total of 100 patients had a median age of 58 (range 21–90) and ECOG performance status (PS) 2 (0–4). In all, 60% had metastatic disease. The therapeutic goal was curative/adjuvant in 39% and palliative in 61%. Prevalence of depression according to the various measures was: BCD 34%, PRIME-MD 12%, BDI 19% and HADS 14%. In total, 45% of patients responded positively to a single-item screening question. The BCD showed fair agreement with the PRIME-MD (kappa=0.21), moderate agreement with the BDI (kappa=0.43) and fair agreement with the HADS (kappa=0.27). Against the PRIME-MD diagnosis of depression, the BCD had greater sensitivity, but lesser specificity and overall agreement, compared with the BDI and depression scale of the HADS. Patients with probable depression (according to BCD) had inferior PS (P=0.0064), increased pain (P=0.045) and greater impairment of functioning (PRIME-MD: P=0.0003). There was no association with gender, age, disease status or therapeutic goal. Depression is common in oncology patients. The BCD is a quick, easy-to-administer screen for depression, which has reasonable psychometric properties in this population. Nature Publishing Group 2004-08-31 2004-08-10 /pmc/articles/PMC2409870/ /pubmed/15305199 http://dx.doi.org/10.1038/sj.bjc.6602057 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Jefford, M Mileshkin, L Richards, K Thomson, J Matthews, J P Zalcberg, J Jennens, R McLachlan, S-A Wein, S Antill, Y Clarke, D M Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title | Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title_full | Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title_fullStr | Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title_full_unstemmed | Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title_short | Rapid screening for depression – validation of the Brief Case-Find for Depression (BCD) in medical oncology and palliative care patients |
title_sort | rapid screening for depression – validation of the brief case-find for depression (bcd) in medical oncology and palliative care patients |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409870/ https://www.ncbi.nlm.nih.gov/pubmed/15305199 http://dx.doi.org/10.1038/sj.bjc.6602057 |
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