AutomedicationFrancoV1, Main, Exploration, bibRecord, 000D85

Suicidality in Huntington's Disease: A Qualitative Study on Coping Styles and Support Strategies.

Identifieur interne : 000D85 ( Main/Exploration ); précédent : 000D84; suivant : 000D86

Suicidality in Huntington's Disease: A Qualitative Study on Coping Styles and Support Strategies.

Auteurs : Anna A M. Hubers [Pays-Bas] ; Annette Hamming [Pays-Bas] ; Erik J. Giltay [Pays-Bas] ; Margaret Von Faber [Pays-Bas] ; Raymund A C. Roos [Pays-Bas] ; Rose C. Van Der Mast [Pays-Bas, Belgique] ; Erik Van Duijn [Pays-Bas]

Source :

Journal of Huntington's disease [ 1879-6400 ] ; 2016.

RBID : pubmed:27258585

Descripteurs français

KwdFr :
- Adaptation psychologique (physiologie), Adulte (MeSH), Adulte d'âge moyen (MeSH), Expression faciale (MeSH), Facteurs de risque (MeSH), Femelle (MeSH), Humains (MeSH), Maladie de Huntington (complications), Maladie de Huntington (génétique), Maladie de Huntington (psychologie), Mâle (MeSH), Protéine huntingtine (génétique), Répétitions de trinucléotides (génétique), Suicide (psychologie), Sujet âgé (MeSH), Troubles de la cognition (étiologie).
MESH :
- génétique : Maladie de Huntington, Protéine huntingtine, Répétitions de trinucléotides.
- physiologie : Adaptation psychologique.
- psychologie : Maladie de Huntington, Suicide.
- étiologie : Troubles de la cognition.
- Adulte, Adulte d'âge moyen, Expression faciale, Facteurs de risque, Femelle, Humains, Mâle, Sujet âgé.

English descriptors

KwdEn :
- Adaptation, Psychological (physiology), Adult (MeSH), Aged (MeSH), Cognition Disorders (etiology), Discrimination, Psychological (MeSH), Facial Expression (MeSH), Female (MeSH), Humans (MeSH), Huntingtin Protein (genetics), Huntington Disease (complications), Huntington Disease (genetics), Huntington Disease (psychology), Male (MeSH), Middle Aged (MeSH), Risk Factors (MeSH), Suicide (psychology), Trinucleotide Repeats (genetics).
MESH :
- chemical , genetics : Huntingtin Protein.
- complications : Huntington Disease.
- etiology : Cognition Disorders.
- genetics : Huntington Disease, Trinucleotide Repeats.
- physiology : Adaptation, Psychological.
- psychology : Huntington Disease, Suicide.
- Adult, Aged, Discrimination, Psychological, Facial Expression, Female, Humans, Male, Middle Aged, Risk Factors.

Abstract

BACKGROUND

Huntington's disease (HD) mutation carriers are at increased risk of suicidal ideation, suicide attempts, and completed suicide. However, research is lacking on coping strategies and treatment options that can be offered to suicidal HD mutation carriers.

OBJECTIVE

This study explores how individuals with pre-motor or motor symptomatic HD cope with suicidality, how their partners support them, and their ideas and wishes regarding how relatives and healthcare professionals can help them in coping with suicidality.

METHODS

This qualitative study included 11 HD mutation carriers who experienced suicidal ideation or attempted suicide and 3 of their partners. They participated in a focus group discussion or an individual in-depth interview. Two independent researchers fragmented the transcribed interviews, coded these fragments, grouped them under themes, and structured the data.

RESULTS

HD study participants used four main strategies to cope with suicidality, including talking about suicidality, employing self-management activities, using medication, and discussing end-of-life wishes. Partners, relatives, and healthcare professionals can support suicidal HD mutation carriers in each of those four strategies.

CONCLUSIONS

Despite the absence of a turnkey solution for suicidality in HD, healthcare professionals can play an important role in supporting suicidal HD mutation carriers by providing an opportunity to talk about suicidality, providing psychoeducation on self-management, prescribing medication, and discussing end-of-life wishes. Future HD-specific intervention studies could investigate the effect of combining these treatment strategies into one holistic approach.

DOI: 10.3233/JHD-160188
PubMed: 27258585

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<series><title level="j">Journal of Huntington's disease</title>
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<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Cognition Disorders (etiology)</term>
<term>Discrimination, Psychological (MeSH)</term>
<term>Facial Expression (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Huntingtin Protein (genetics)</term>
<term>Huntington Disease (complications)</term>
<term>Huntington Disease (genetics)</term>
<term>Huntington Disease (psychology)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Risk Factors (MeSH)</term>
<term>Suicide (psychology)</term>
<term>Trinucleotide Repeats (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adaptation psychologique (physiologie)</term>
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Expression faciale (MeSH)</term>
<term>Facteurs de risque (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Maladie de Huntington (complications)</term>
<term>Maladie de Huntington (génétique)</term>
<term>Maladie de Huntington (psychologie)</term>
<term>Mâle (MeSH)</term>
<term>Protéine huntingtine (génétique)</term>
<term>Répétitions de trinucléotides (génétique)</term>
<term>Suicide (psychologie)</term>
<term>Sujet âgé (MeSH)</term>
<term>Troubles de la cognition (étiologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Huntingtin Protein</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Huntington Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Cognition Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Huntington Disease</term>
<term>Trinucleotide Repeats</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Maladie de Huntington</term>
<term>Protéine huntingtine</term>
<term>Répétitions de trinucléotides</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Adaptation psychologique</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Adaptation, Psychological</term>
</keywords>
<keywords scheme="MESH" qualifier="psychologie" xml:lang="fr"><term>Maladie de Huntington</term>
<term>Suicide</term>
</keywords>
<keywords scheme="MESH" qualifier="psychology" xml:lang="en"><term>Huntington Disease</term>
<term>Suicide</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Troubles de la cognition</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Discrimination, Psychological</term>
<term>Facial Expression</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Risk Factors</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Expression faciale</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
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<front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b>
</p>
<p>Huntington's disease (HD) mutation carriers are at increased risk of suicidal ideation, suicide attempts, and completed suicide. However, research is lacking on coping strategies and treatment options that can be offered to suicidal HD mutation carriers.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>OBJECTIVE</b>
</p>
<p>This study explores how individuals with pre-motor or motor symptomatic HD cope with suicidality, how their partners support them, and their ideas and wishes regarding how relatives and healthcare professionals can help them in coping with suicidality.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>METHODS</b>
</p>
<p>This qualitative study included 11 HD mutation carriers who experienced suicidal ideation or attempted suicide and 3 of their partners. They participated in a focus group discussion or an individual in-depth interview. Two independent researchers fragmented the transcribed interviews, coded these fragments, grouped them under themes, and structured the data.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>RESULTS</b>
</p>
<p>HD study participants used four main strategies to cope with suicidality, including talking about suicidality, employing self-management activities, using medication, and discussing end-of-life wishes. Partners, relatives, and healthcare professionals can support suicidal HD mutation carriers in each of those four strategies.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>CONCLUSIONS</b>
</p>
<p>Despite the absence of a turnkey solution for suicidality in HD, healthcare professionals can play an important role in supporting suicidal HD mutation carriers by providing an opportunity to talk about suicidality, providing psychoeducation on self-management, prescribing medication, and discussing end-of-life wishes. Future HD-specific intervention studies could investigate the effect of combining these treatment strategies into one holistic approach.</p>
</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27258585</PMID>
<DateCompleted><Year>2017</Year>
<Month>10</Month>
<Day>23</Day>
</DateCompleted>
<DateRevised><Year>2019</Year>
<Month>12</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1879-6400</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>5</Volume>
<Issue>2</Issue>
<PubDate><Year>2016</Year>
<Month>05</Month>
<Day>31</Day>
</PubDate>
</JournalIssue>
<Title>Journal of Huntington's disease</Title>
<ISOAbbreviation>J Huntingtons Dis</ISOAbbreviation>
</Journal>
<ArticleTitle>Suicidality in Huntington's Disease: A Qualitative Study on Coping Styles and Support Strategies.</ArticleTitle>
<Pagination><MedlinePgn>185-98</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.3233/JHD-160188</ELocationID>
<Abstract><AbstractText Label="BACKGROUND">Huntington's disease (HD) mutation carriers are at increased risk of suicidal ideation, suicide attempts, and completed suicide. However, research is lacking on coping strategies and treatment options that can be offered to suicidal HD mutation carriers.</AbstractText>
<AbstractText Label="OBJECTIVE">This study explores how individuals with pre-motor or motor symptomatic HD cope with suicidality, how their partners support them, and their ideas and wishes regarding how relatives and healthcare professionals can help them in coping with suicidality.</AbstractText>
<AbstractText Label="METHODS">This qualitative study included 11 HD mutation carriers who experienced suicidal ideation or attempted suicide and 3 of their partners. They participated in a focus group discussion or an individual in-depth interview. Two independent researchers fragmented the transcribed interviews, coded these fragments, grouped them under themes, and structured the data.</AbstractText>
<AbstractText Label="RESULTS">HD study participants used four main strategies to cope with suicidality, including talking about suicidality, employing self-management activities, using medication, and discussing end-of-life wishes. Partners, relatives, and healthcare professionals can support suicidal HD mutation carriers in each of those four strategies.</AbstractText>
<AbstractText Label="CONCLUSIONS">Despite the absence of a turnkey solution for suicidality in HD, healthcare professionals can play an important role in supporting suicidal HD mutation carriers by providing an opportunity to talk about suicidality, providing psychoeducation on self-management, prescribing medication, and discussing end-of-life wishes. Future HD-specific intervention studies could investigate the effect of combining these treatment strategies into one holistic approach.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hubers</LastName>
<ForeName>Anna A M</ForeName>
<Initials>AA</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hamming</LastName>
<ForeName>Annette</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Giltay</LastName>
<ForeName>Erik J</ForeName>
<Initials>EJ</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>von Faber</LastName>
<ForeName>Margaret</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Roos</LastName>
<ForeName>Raymund A C</ForeName>
<Initials>RA</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>van der Mast</LastName>
<ForeName>Rose C</ForeName>
<Initials>RC</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Collaborative Antwerp Psychiatric Research Institute (CAPRI), Faculty of Medicine, University of Antwerp, Antwerp, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>van Duijn</LastName>
<ForeName>Erik</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Department of Psychiatry, Leiden University Medical Center, Leiden, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Center for Mental Health Care Delfland, Delft, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>Netherlands</Country>
<MedlineTA>J Huntingtons Dis</MedlineTA>
<NlmUniqueID>101589965</NlmUniqueID>
<ISSNLinking>1879-6397</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C086055">HTT protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000071058">Huntingtin Protein</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000223" MajorTopicYN="N">Adaptation, Psychological</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003072" MajorTopicYN="N">Cognition Disorders</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004192" MajorTopicYN="Y">Discrimination, Psychological</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005149" MajorTopicYN="N">Facial Expression</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000071058" MajorTopicYN="N">Huntingtin Protein</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006816" MajorTopicYN="N">Huntington Disease</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000523" MajorTopicYN="Y">psychology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012307" MajorTopicYN="N">Risk Factors</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013405" MajorTopicYN="N">Suicide</DescriptorName>
<QualifierName UI="Q000523" MajorTopicYN="Y">psychology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018911" MajorTopicYN="N">Trinucleotide Repeats</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Neurodegenerative diseases</Keyword>
<Keyword MajorTopicYN="Y">coping behaviour</Keyword>
<Keyword MajorTopicYN="Y">psychopathology</Keyword>
<Keyword MajorTopicYN="Y">qualitative research</Keyword>
<Keyword MajorTopicYN="Y">suicide</Keyword>
<Keyword MajorTopicYN="Y">therapy</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2016</Year>
<Month>6</Month>
<Day>4</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2016</Year>
<Month>6</Month>
<Day>4</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2017</Year>
<Month>10</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">27258585</ArticleId>
<ArticleId IdType="pii">JHD160188</ArticleId>
<ArticleId IdType="doi">10.3233/JHD-160188</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>Belgique</li>
<li>Pays-Bas</li>
</country>
<region><li>Hollande-Méridionale</li>
<li>Province d'Anvers</li>
<li>Région flamande</li>
</region>
<settlement><li>Anvers</li>
<li>Leyde</li>
</settlement>
<orgName><li>Université d'Anvers</li>
</orgName>
</list>
<tree><country name="Pays-Bas"><region name="Hollande-Méridionale"><name sortKey="Hubers, Anna A M" sort="Hubers, Anna A M" uniqKey="Hubers A" first="Anna A M" last="Hubers">Anna A M. Hubers</name>
</region>
<name sortKey="Giltay, Erik J" sort="Giltay, Erik J" uniqKey="Giltay E" first="Erik J" last="Giltay">Erik J. Giltay</name>
<name sortKey="Hamming, Annette" sort="Hamming, Annette" uniqKey="Hamming A" first="Annette" last="Hamming">Annette Hamming</name>
<name sortKey="Roos, Raymund A C" sort="Roos, Raymund A C" uniqKey="Roos R" first="Raymund A C" last="Roos">Raymund A C. Roos</name>
<name sortKey="Van Der Mast, Rose C" sort="Van Der Mast, Rose C" uniqKey="Van Der Mast R" first="Rose C" last="Van Der Mast">Rose C. Van Der Mast</name>
<name sortKey="Van Duijn, Erik" sort="Van Duijn, Erik" uniqKey="Van Duijn E" first="Erik" last="Van Duijn">Erik Van Duijn</name>
<name sortKey="Van Duijn, Erik" sort="Van Duijn, Erik" uniqKey="Van Duijn E" first="Erik" last="Van Duijn">Erik Van Duijn</name>
<name sortKey="Von Faber, Margaret" sort="Von Faber, Margaret" uniqKey="Von Faber M" first="Margaret" last="Von Faber">Margaret Von Faber</name>
</country>
<country name="Belgique"><region name="Région flamande"><name sortKey="Van Der Mast, Rose C" sort="Van Der Mast, Rose C" uniqKey="Van Der Mast R" first="Rose C" last="Van Der Mast">Rose C. Van Der Mast</name>
</region>
</country>
</tree>
</affiliations>
</record>

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Suicidality in Huntington's Disease: A Qualitative Study on Coping Styles and Support Strategies.

Suicidality in Huntington's Disease: A Qualitative Study on Coping Styles and Support Strategies.

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