Walking Alongside: Views of Family Members on Medical Assistance in Dying for Mental Illness as the Sole Underlying Medical Condition
Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life,...
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Veröffentlicht in: | Qualitative health research 2023-11, Vol.33 (13), p.1140-1153 |
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creator | Bastidas-Bilbao, Hamer Stergiopoulos, Vicky Cappe, Vivien van Kesteren, Mary Rose Stewart, Donna E. Gupta, Mona Simpson, Alexander I. F. Dawthorne, Michael Rajji, Tarek K. Castle, David Hawke, Lisa D. |
description | Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life, autonomy, family involvement, and healthcare system constraints have been debated intensively. Recent studies have not explored the views of family members of persons with mental illness on MAiD MI-SUMC. This study aimed to fill this knowledge gap. Twenty-five Ontario residents who had a loved one with mental illness participated. A persona–scenario exercise was designed to explore participants’ views on MAiD MI-SUMC in hypothetical situations. Reflexive thematic analysis was used to analyze the data. A lived experience-advisory panel was engaged throughout the study. Seven themes were developed: Witnessing suffering; A road with barriers and limitations; Societal barriers; The unknowns of mental illness; Individual choices: the life or death that a person wants; MAiD MI-SUMC as an acceptable choice when suffering cannot be relieved with available treatments and supports; and The emotional outcome. Participants constructed their views based on their experience of supporting a loved one with mental illness. MAiD MI-SUMC was perceived as a multifaceted issue, whose acceptability and potential introduction required a concurrent exploration and discussion of the challenges arising due to limitations of the healthcare system, the opportunities and limits to family involvement, and the value of patient autonomy. |
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A persona–scenario exercise was designed to explore participants’ views on MAiD MI-SUMC in hypothetical situations. Reflexive thematic analysis was used to analyze the data. A lived experience-advisory panel was engaged throughout the study. Seven themes were developed: Witnessing suffering; A road with barriers and limitations; Societal barriers; The unknowns of mental illness; Individual choices: the life or death that a person wants; MAiD MI-SUMC as an acceptable choice when suffering cannot be relieved with available treatments and supports; and The emotional outcome. Participants constructed their views based on their experience of supporting a loved one with mental illness. MAiD MI-SUMC was perceived as a multifaceted issue, whose acceptability and potential introduction required a concurrent exploration and discussion of the challenges arising due to limitations of the healthcare system, the opportunities and limits to family involvement, and the value of patient autonomy.</description><identifier>ISSN: 1049-7323</identifier><identifier>EISSN: 1552-7557</identifier><identifier>DOI: 10.1177/10497323231197365</identifier><identifier>PMID: 37773095</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Assisted suicide ; Autonomy ; Death & dying ; Health care ; Illnesses ; Legislation ; Mental disorders ; Parent participation ; Quality of life ; Relatives ; Suffering ; Walking</subject><ispartof>Qualitative health research, 2023-11, Vol.33 (13), p.1140-1153</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023 2023 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-b00d2aafd84cdf6d4c234cd2b9647f919749d316060973f3e098e82f1bcdd1e53</citedby><cites>FETCH-LOGICAL-c444t-b00d2aafd84cdf6d4c234cd2b9647f919749d316060973f3e098e82f1bcdd1e53</cites><orcidid>0000-0002-1103-6530</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/10497323231197365$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/10497323231197365$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,30999,43621,43622</link.rule.ids></links><search><creatorcontrib>Bastidas-Bilbao, Hamer</creatorcontrib><creatorcontrib>Stergiopoulos, Vicky</creatorcontrib><creatorcontrib>Cappe, Vivien</creatorcontrib><creatorcontrib>van Kesteren, Mary Rose</creatorcontrib><creatorcontrib>Stewart, Donna E.</creatorcontrib><creatorcontrib>Gupta, Mona</creatorcontrib><creatorcontrib>Simpson, Alexander I. F.</creatorcontrib><creatorcontrib>Dawthorne, Michael</creatorcontrib><creatorcontrib>Rajji, Tarek K.</creatorcontrib><creatorcontrib>Castle, David</creatorcontrib><creatorcontrib>Hawke, Lisa D.</creatorcontrib><title>Walking Alongside: Views of Family Members on Medical Assistance in Dying for Mental Illness as the Sole Underlying Medical Condition</title><title>Qualitative health research</title><addtitle>Qual Health Res</addtitle><description>Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life, autonomy, family involvement, and healthcare system constraints have been debated intensively. Recent studies have not explored the views of family members of persons with mental illness on MAiD MI-SUMC. This study aimed to fill this knowledge gap. Twenty-five Ontario residents who had a loved one with mental illness participated. A persona–scenario exercise was designed to explore participants’ views on MAiD MI-SUMC in hypothetical situations. Reflexive thematic analysis was used to analyze the data. A lived experience-advisory panel was engaged throughout the study. Seven themes were developed: Witnessing suffering; A road with barriers and limitations; Societal barriers; The unknowns of mental illness; Individual choices: the life or death that a person wants; MAiD MI-SUMC as an acceptable choice when suffering cannot be relieved with available treatments and supports; and The emotional outcome. Participants constructed their views based on their experience of supporting a loved one with mental illness. MAiD MI-SUMC was perceived as a multifaceted issue, whose acceptability and potential introduction required a concurrent exploration and discussion of the challenges arising due to limitations of the healthcare system, the opportunities and limits to family involvement, and the value of patient autonomy.</description><subject>Assisted suicide</subject><subject>Autonomy</subject><subject>Death & dying</subject><subject>Health care</subject><subject>Illnesses</subject><subject>Legislation</subject><subject>Mental disorders</subject><subject>Parent participation</subject><subject>Quality of life</subject><subject>Relatives</subject><subject>Suffering</subject><subject>Walking</subject><issn>1049-7323</issn><issn>1552-7557</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>7QJ</sourceid><recordid>eNp1kctuFDEQRVuIiDzgA9hZYsOmg1_dbrNBo4FApEQsILC03HZ54uC2E7sHNB-Q_8aTSUCAkBe-8r11VK5qmucEHxMixCuCuRSM1kNIFX33qDkgXUdb0XXicdXVb7eB_eawlCuMscCMPWn2mRCCYdkdNLdfdfjm4wotQoqr4i28Rl88_CgoOXSiJx826BymEXJ9iVVab3RAi1J8mXU0gHxEbzdbgku5-nGu9mkIEUpBuqD5EtCnFABdRAs53CUfKMsUrZ99ik-bPadDgWf391FzcfLu8_JDe_bx_elycdYazvncjhhbqrWzAzfW9ZYbyqqio-y5cLLOgEvLSI97XMfhGGA5wEAdGY21BDp21LzZca_X4wTW1G6zDuo6-0nnjUraqz-d6C_VKn1XBPe0lwOuhJf3hJxu1lBmNfliIAQdIa2LooPAUjIysBp98Vf0Kq1zrP-rqaGnXAxsCyS7lMmplAzuVzcEq-2W1T9brjXHu5qiV_Cb-v-Cn22GppI</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Bastidas-Bilbao, Hamer</creator><creator>Stergiopoulos, Vicky</creator><creator>Cappe, Vivien</creator><creator>van Kesteren, Mary Rose</creator><creator>Stewart, Donna E.</creator><creator>Gupta, Mona</creator><creator>Simpson, Alexander I. F.</creator><creator>Dawthorne, Michael</creator><creator>Rajji, Tarek K.</creator><creator>Castle, David</creator><creator>Hawke, Lisa D.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1103-6530</orcidid></search><sort><creationdate>20231101</creationdate><title>Walking Alongside: Views of Family Members on Medical Assistance in Dying for Mental Illness as the Sole Underlying Medical Condition</title><author>Bastidas-Bilbao, Hamer ; Stergiopoulos, Vicky ; Cappe, Vivien ; van Kesteren, Mary Rose ; Stewart, Donna E. ; Gupta, Mona ; Simpson, Alexander I. 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F.</au><au>Dawthorne, Michael</au><au>Rajji, Tarek K.</au><au>Castle, David</au><au>Hawke, Lisa D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Walking Alongside: Views of Family Members on Medical Assistance in Dying for Mental Illness as the Sole Underlying Medical Condition</atitle><jtitle>Qualitative health research</jtitle><addtitle>Qual Health Res</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>33</volume><issue>13</issue><spage>1140</spage><epage>1153</epage><pages>1140-1153</pages><issn>1049-7323</issn><eissn>1552-7557</eissn><abstract>Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life, autonomy, family involvement, and healthcare system constraints have been debated intensively. Recent studies have not explored the views of family members of persons with mental illness on MAiD MI-SUMC. This study aimed to fill this knowledge gap. Twenty-five Ontario residents who had a loved one with mental illness participated. A persona–scenario exercise was designed to explore participants’ views on MAiD MI-SUMC in hypothetical situations. Reflexive thematic analysis was used to analyze the data. A lived experience-advisory panel was engaged throughout the study. Seven themes were developed: Witnessing suffering; A road with barriers and limitations; Societal barriers; The unknowns of mental illness; Individual choices: the life or death that a person wants; MAiD MI-SUMC as an acceptable choice when suffering cannot be relieved with available treatments and supports; and The emotional outcome. Participants constructed their views based on their experience of supporting a loved one with mental illness. 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subjects | Assisted suicide Autonomy Death & dying Health care Illnesses Legislation Mental disorders Parent participation Quality of life Relatives Suffering Walking |
title | Walking Alongside: Views of Family Members on Medical Assistance in Dying for Mental Illness as the Sole Underlying Medical Condition |
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