Client-centred clinical genetic diagnostics
| Autor: | Maarten Otter, Therese van Amelsvoort, Constance T. R. M. Stumpel |
|---|---|
| Přispěvatelé: | RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, RS: GROW - R4 - Reproductive and Perinatal Medicine, Klinische Genetica, MUMC+: DA KG Polikliniek (9), MUMC+: MA Med Staf Spec Psychiatrie (9) |
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Value (ethics) Quality of life Destigmatization INTELLECTUAL DISABILITY Referral Clinical genetic diagnostics CHROMOSOME DISORDERS media_common.quotation_subject CHILDREN 030105 genetics & heredity 03 medical and health sciences 0302 clinical medicine Quality of life (healthcare) Originality XXY Intellectual disability 47 XXY medicine Physical examination in developmental delay Shared decision-making media_common Medical model Medical education IDENTIFICATION DEVELOPMENTAL-DISABILITIES TRIPLE X SYNDROME Behavioural phenotype of genetic syndromes medicine.disease Psychiatry and Mental health Identification (information) INDIVIDUALS PEDIATRIC NEUROLOGY Psychology Psychosocial 030217 neurology & neurosurgery |
| Zdroj: | Advances in Mental Health and Intellectual Disabilities, 12(1), 1-10. Emerald Group Publishing Ltd. |
| ISSN: | 2044-1282 |
| Popis: | Purpose The purpose of this paper is to establish the value of clinical genetic diagnostics in the lives of people with an intellectual disability (ID), their families, and their primary and professional caregivers. It has been shown that psychologists are more likely to make use of the opportunities offered by clinical genetic diagnostics if they have seen the psychological benefits in their own practice. Moreover, this paper aims to promote the practice of informing people with ID, their families, and other caregivers regarding the current technological advances in genetic diagnostics, thereby allowing these patients to decide for themselves whether to utilise these opportunities. Design/methodology/approach The authors report four case studies in which the psychosocial value to each patient is pivotal. Findings In these four cases, it is clear the medical model can augment the social model by providing an interpretation of its meaningfulness in the lives of the people concerned. Research limitations/implications Case studies alone can have limited scientific significance. This approach examining the significance of clinical genetic diagnosis should be studied further in larger groups. Practical implications It is hoped that psychologists and other professional caregivers will become enthused about the value of clinical genetic diagnostics and will choose to discuss the option of referral for clinical genetic diagnostics with their patients more often. Social implications People with an ID who are seeking mental health care, and their caregivers, should be given the opportunity to take part in the decision regarding whether to use clinical genetic diagnostics, which may even have a destigmatising effect. Originality/value Quality of life may improve for people with an ID seeking mental healthcare and for their caregivers as well by opening up discussion regarding the opportunities presented by clinical genetic diagnostics. The fact that people are able to make their own choices based on their own considerations can have a destigmatising effect. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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