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Prevalence and detection of psychosocial problems in cancer genetic counseling

Only a minority of individuals who undergo cancer genetic counseling experience heightened levels of psychological distress, but many more experience a range of cancer genetic-specific psychosocial problems. The aim of this study was to estimate the prevalence of such psychosocial problems, and to i...

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Autores principales: Eijzenga, W., Bleiker, E. M. A., Hahn, D. E. E., Van der Kolk, L. E., Sidharta, G. N., Aaronson, N. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630247/
https://www.ncbi.nlm.nih.gov/pubmed/25968807
http://dx.doi.org/10.1007/s10689-015-9809-9
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author Eijzenga, W.
Bleiker, E. M. A.
Hahn, D. E. E.
Van der Kolk, L. E.
Sidharta, G. N.
Aaronson, N. K.
author_facet Eijzenga, W.
Bleiker, E. M. A.
Hahn, D. E. E.
Van der Kolk, L. E.
Sidharta, G. N.
Aaronson, N. K.
author_sort Eijzenga, W.
collection PubMed
description Only a minority of individuals who undergo cancer genetic counseling experience heightened levels of psychological distress, but many more experience a range of cancer genetic-specific psychosocial problems. The aim of this study was to estimate the prevalence of such psychosocial problems, and to identify possible demographic and clinical variables associated significantly with them. Consenting individuals scheduled to undergo cancer genetic counseling completed the Psychosocial Aspects of Hereditary Cancer (PAHC) questionnaire, the Hospital Anxiety and Depression Scale (HADS) and the Distress Thermometer (DT) prior to or immediately following their counseling session. More than half of the 137 participants reported problems on three or more domains of the PAHC, most often in the domains ‘living with cancer’ (84 %), ‘family issues’ (46 %), ‘hereditary predisposition’ (45 %), and ‘child-related issues’ (42 %). Correlations between the PAHC, the HADS and the DT were low. Previous contact with a psychosocial worker, and having a personal history of cancer were associated significantly with HADS scores, but explained little variance (9 %). No background variables were associated significantly with the DT. Previous contact with a psychosocial worker, and having children were significantly associated with several PAHC domains, again explaining only a small percentage of the variance (2–14 %). The majority of counselees experience specific cancer genetic counseling-related psychosocial problems. Only a few background variables are associated significantly with distress or psychosocial problems. Thus we recommend using the PAHC or a similar problem-oriented questionnaire routinely in cancer genetic counseling to identify individuals with such problems.
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spelling pubmed-46302472015-11-06 Prevalence and detection of psychosocial problems in cancer genetic counseling Eijzenga, W. Bleiker, E. M. A. Hahn, D. E. E. Van der Kolk, L. E. Sidharta, G. N. Aaronson, N. K. Fam Cancer Original Article Only a minority of individuals who undergo cancer genetic counseling experience heightened levels of psychological distress, but many more experience a range of cancer genetic-specific psychosocial problems. The aim of this study was to estimate the prevalence of such psychosocial problems, and to identify possible demographic and clinical variables associated significantly with them. Consenting individuals scheduled to undergo cancer genetic counseling completed the Psychosocial Aspects of Hereditary Cancer (PAHC) questionnaire, the Hospital Anxiety and Depression Scale (HADS) and the Distress Thermometer (DT) prior to or immediately following their counseling session. More than half of the 137 participants reported problems on three or more domains of the PAHC, most often in the domains ‘living with cancer’ (84 %), ‘family issues’ (46 %), ‘hereditary predisposition’ (45 %), and ‘child-related issues’ (42 %). Correlations between the PAHC, the HADS and the DT were low. Previous contact with a psychosocial worker, and having a personal history of cancer were associated significantly with HADS scores, but explained little variance (9 %). No background variables were associated significantly with the DT. Previous contact with a psychosocial worker, and having children were significantly associated with several PAHC domains, again explaining only a small percentage of the variance (2–14 %). The majority of counselees experience specific cancer genetic counseling-related psychosocial problems. Only a few background variables are associated significantly with distress or psychosocial problems. Thus we recommend using the PAHC or a similar problem-oriented questionnaire routinely in cancer genetic counseling to identify individuals with such problems. Springer Netherlands 2015-05-13 2015 /pmc/articles/PMC4630247/ /pubmed/25968807 http://dx.doi.org/10.1007/s10689-015-9809-9 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Eijzenga, W.
Bleiker, E. M. A.
Hahn, D. E. E.
Van der Kolk, L. E.
Sidharta, G. N.
Aaronson, N. K.
Prevalence and detection of psychosocial problems in cancer genetic counseling
title Prevalence and detection of psychosocial problems in cancer genetic counseling
title_full Prevalence and detection of psychosocial problems in cancer genetic counseling
title_fullStr Prevalence and detection of psychosocial problems in cancer genetic counseling
title_full_unstemmed Prevalence and detection of psychosocial problems in cancer genetic counseling
title_short Prevalence and detection of psychosocial problems in cancer genetic counseling
title_sort prevalence and detection of psychosocial problems in cancer genetic counseling
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630247/
https://www.ncbi.nlm.nih.gov/pubmed/25968807
http://dx.doi.org/10.1007/s10689-015-9809-9
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