Attitudes towards assisted suicide and euthanasia among care-dependent older adults (50+) in Austria: the role of socio-demographics, religiosity, physical illness, psychological distress, and social isolation.

Abstract:

BACKGROUND:Care-dependency constitutes an important issue with regard to the approval of end-of-life decisions, yet attitudes towards assisted suicide and euthanasia are understudied among care-dependent older adults. We assessed attitudes towards assisted suicide and euthanasia and tested empirical correlates, including socio-demographics, religiosity, physical illness, psychological distress and social isolation. METHODS:A nationwide cross-sectional survey among older care allowance recipients (50+) in private households in Austria was conducted in 2016. In computer-assisted personal interviews, 493 respondents were asked whether or not they approved of the availability of assisted suicide and euthanasia in case of long-term care dependency and whether or not they would consider using assisted suicide or euthanasia for themselves. Multiple logistic regression analysis was used to assess the impact of potential determinants of attitudes towards assisted suicide and euthanasia. RESULTS:About a quarter (24.8-26.0%) of the sampled care-dependent older adults approved of the availability of assisted suicide and euthanasia respectively indicated the will to (hypothetically) make use of assisted suicide or euthanasia. Attitudes towards assisted suicide were most favourable among care-dependent older adults living in urban areas, those who did not trust physicians, those who reported active suicide ideation, and individuals with a strong fear of dying. With regard to euthanasia, living alone, religiosity and fear of dying were the central determinants of acceptance. CONCLUSIONS:Positive attitudes towards and will to (hypothetically) use assisted suicide and euthanasia were expressed by a substantial minority of care-dependent older adults in Austria and are driven by current psychological suffering and fear of the process of dying in the (near) future. Community-based psychosocial care should be expanded to address psychological distress and fears about end-of-life issues among care-dependent older adults.

journal_name

BMC Med Ethics

journal_title

BMC medical ethics

authors

Stolz E,Mayerl H,Gasser-Steiner P,Freidl W

doi

10.1186/s12910-017-0233-6

subject

Has Abstract

pub_date

2017-12-07 00:00:00

pages

71

issue

1

issn

1472-6939

pii

10.1186/s12910-017-0233-6

journal_volume

18

pub_type

杂志文章
  • Clinical Ethics Committees in Africa: lost in the shadow of RECs/IRBs?

    abstract:BACKGROUND:Clinical Ethics Committees (CECs) are well established at healthcare institutions in resource-rich countries. However, there is limited information on established CECs in resource poor countries, especially in Africa. This study aimed to establish baseline data regarding existing formal CECs in Africa to rai...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-00559-2

    authors: Moodley K,Kabanda SM,Soldaat L,Kleinsmidt A,Obasa AE,Kling S

    更新日期:2020-11-18 00:00:00

  • Developing an ethics support tool for dealing with dilemmas around client autonomy based on moral case deliberations.

    abstract:BACKGROUND:Moral Case Deliberations (MCDs) are reflective dialogues with a group of participants on their own moral dilemmas. Although MCD is successful as clinical ethics support (CES), it also has limitations. 1. Lessons learned from individual MCDs are not shared in order to be used in other contexts 2. Moral learni...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-018-0335-9

    authors: Hartman LA,Metselaar S,Molewijk AC,Edelbroek HM,Widdershoven GAM

    更新日期:2018-12-22 00:00:00

  • A biobank management model applicable to biomedical research.

    abstract:BACKGROUND:The work of Research Ethics Boards (REBs), especially when involving genetics research and biobanks, has become more challenging with the growth of biotechnology and biomedical research. Some REBs have even rejected research projects where the use of a biobank with coded samples was an integral part of the s...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-7-4

    authors: Auray-Blais C,Patenaude J

    更新日期:2006-04-06 00:00:00

  • Confidentiality breaches in clinical practice: what happens in hospitals?

    abstract:BACKGROUND:Respect for confidentiality is important to safeguard the well-being of patients and ensure the confidence of society in the doctor-patient relationship. The aim of our study is to examine real situations in which there has been a breach of confidentiality, by means of direct observation in clinical practice...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-016-0136-y

    authors: Beltran-Aroca CM,Girela-Lopez E,Collazo-Chao E,Montero-Pérez-Barquero M,Muñoz-Villanueva MC

    更新日期:2016-09-02 00:00:00

  • Saudi views on consenting for research on medical records and leftover tissue samples.

    abstract:BACKGROUND:Consenting for retrospective medical records-based research (MR) and leftover tissue-based research (TR) continues to be controversial. Our objective was to survey Saudis attending outpatient clinics at a tertiary care hospital on their personal preference and perceptions of norm and current practice in rela...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-11-18

    authors: Al-Qadire MM,Hammami MM,Abdulhameed HM,Al Gaai EA

    更新日期:2010-10-18 00:00:00

  • Between Scylla and Charybdis: reconciling competing data management demands in the life sciences.

    abstract:BACKGROUND:The widespread sharing of biologicaConcluding Comments: Teaching Responsible Datal and biomedical data is recognised as a key element in facilitating translation of scientific discoveries into novel clinical applications and services. At the same time, twenty-first century states are increasingly concerned t...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-016-0112-6

    authors: Bezuidenhout LM,Morrison M

    更新日期:2016-05-17 00:00:00

  • Lessons learned from implementing a responsive quality assessment of clinical ethics support.

    abstract:BACKGROUND:Various forms of Clinical Ethics Support (CES) have been developed in health care organizations. Over the past years, increasing attention has been paid to the question of how to foster the quality of ethics support. In the Netherlands, a CES quality assessment project based on a responsive evaluation design...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-019-0418-2

    authors: Van Baarle EM,Potma MC,van Hoek MEC,Hartman LA,Molewijk BAC,van Gurp JLP

    更新日期:2019-11-01 00:00:00

  • Ethical challenges of integration across primary and secondary care: a qualitative and normative analysis.

    abstract:BACKGROUND:This paper explores ethical concerns arising in healthcare integration. We argue that integration is necessary imperative for meeting contemporary and future healthcare challenges, a far stronger evidence base for the conditions of its effectiveness is required. In particular, given the increasing emphasis a...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-019-0386-6

    authors: McKeown A,Cliffe C,Arora A,Griffin A

    更新日期:2019-07-03 00:00:00

  • Obtaining subjects' consent to publish identifying personal information: current practices and identifying potential issues.

    abstract:BACKGROUND:In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consent forms are managed h...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-14-47

    authors: Yoshida A,Dowa Y,Murakami H,Kosugi S

    更新日期:2013-11-25 00:00:00

  • Viewpoint discrimination and contestation of ideas on its merits, leadership and organizational ethics: expanding the African bioethics agenda.

    abstract::The 3rd Pan-African Ethics Human Rights and Medical Law (3rd EHRML) conference was held in Johannesburg on July 7, 2013, as part of the Africa Health Congress. The conference brought together bioethicists, researchers and scholars from South Africa, Zimbabwe, Kenya and Nigeria working in the field of bioethics as well...

    journal_title:BMC medical ethics

    pub_type:

    doi:10.1186/1472-6939-14-S1-S1

    authors: Chima SC,Mduluza T,Kipkemboi J

    更新日期:2013-01-01 00:00:00

  • Knowledge and attitudes to personal genomics testing for complex diseases among Nigerians.

    abstract:BACKGROUND:The study examined the knowledge and attitudes to personal genomics testing for complex diseases among Nigerians and identified how the knowledge and attitudes vary with gender, age, religion, education and related factors. METHODS:Data were collected using qualitative method in 2 districts of the Federal C...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-15-34

    authors: Fagbemiro L,Adebamowo C

    更新日期:2014-04-27 00:00:00

  • Voluntary participation and comprehension of informed consent in a genetic epidemiological study of breast cancer in Nigeria.

    abstract:BACKGROUND:Studies on informed consent to medical research conducted in low or middle-income settings have increased, including empirical investigations of consent to genetic research. We investigated voluntary participation and comprehension of informed consent among women involved in a genetic epidemiological study o...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-15-38

    authors: Marshall PA,Adebamowo CA,Adeyemo AA,Ogundiran TO,Strenski T,Zhou J,Rotimi CN

    更新日期:2014-05-13 00:00:00

  • Giving samples or "getting checked": measuring conflation of observational biospecimen research and clinical care in Latino communities.

    abstract:BACKGROUND:Expectations of receiving personal health information as a fringe benefit of biospecimen donation-termed diagnostic misconception-are increasingly documented. We developed an instrument measuring conflation of observational biospecimen-based research and clinical care for use with Latino communities, who may...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-015-0041-9

    authors: Knerr S,Ceballos RM

    更新日期:2015-07-17 00:00:00

  • The emergence of ethical issues in the provision of online sexual health outreach for gay, bisexual, two-spirit and other men who have sex with men: perspectives of online outreach workers.

    abstract:BACKGROUND:Mobile applications and socio-sexual networking websites are used by outreach workers to respond synchronously to questions and provide information, resources, and referrals on sexual health and STI/HIV prevention, testing, and care to gay, bisexual and other men who have sex with men (GB2M). This explorator...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-017-0216-7

    authors: Fantus S,Souleymanov R,Lachowsky NJ,Brennan DJ

    更新日期:2017-11-03 00:00:00

  • Legal and ethical framework for global health information and biospecimen exchange - an international perspective.

    abstract:BACKGROUND:The progress of electronic health technologies and biobanks holds enormous promise for efficient research. Evidence shows that studies based on sharing and secondary use of data/samples have the potential to significantly advance medical knowledge. However, sharing of such resources for international collabo...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-0448-9

    authors: Bernasconi L,Şen S,Angerame L,Balyegisawa AP,Hong Yew Hui D,Hotter M,Hsu CY,Ito T,Jörger F,Krassnitzer W,Phillips AT,Li R,Stockley L,Tay F,von Heijne Widlund C,Wan M,Wong C,Yau H,Hiemstra TF,Uresin Y,Senti G

    更新日期:2020-01-21 00:00:00

  • Policy recommendations for addressing privacy challenges associated with cell-based research and interventions.

    abstract:BACKGROUND:The increased use of human biological material for cell-based research and clinical interventions poses risks to the privacy of patients and donors, including the possibility of re-identification of individuals from anonymized cell lines and associated genetic data. These risks will increase as technologies ...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-15-7

    authors: Ogbogu U,Burningham S,Ollenberger A,Calder K,Du L,El Emam K,Hyde-Lay R,Isasi R,Joly Y,Kerr I,Malin B,McDonald M,Penney S,Piat G,Roy DC,Sugarman J,Vercauteren S,Verhenneman G,West L,Caulfield T

    更新日期:2014-02-03 00:00:00

  • Understanding and retention of the informed consent process among parents in rural northern Ghana.

    abstract:BACKGROUND:The individual informed consent model remains critical to the ethical conduct and regulation of research involving human beings. Parental informed consent process in a rural setting of northern Ghana was studied to describe comprehension and retention among parents as part of the evaluation of the existing i...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-9-12

    authors: Oduro AR,Aborigo RA,Amugsi D,Anto F,Anyorigiya T,Atuguba F,Hodgson A,Koram KA

    更新日期:2008-06-19 00:00:00

  • Convergent ethical issues in HIV/AIDS, tuberculosis and malaria vaccine trials in Africa: Report from the WHO/UNAIDS African AIDS Vaccine Programme's Ethics, Law and Human Rights Collaborating Centre consultation, 10-11 February 2009, Durban, South Africa

    abstract:BACKGROUND:Africa continues to bear a disproportionate share of the global HIV/AIDS, tuberculosis (TB) and malaria burden. The development and distribution of safe, effective and affordable vaccines is critical to reduce these epidemics. However, conducting HIV/AIDS, TB, and/or malaria vaccine trials simultaneously in ...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-11-3

    authors: Mamotte N,Wassenaar D,Koen J,Essack Z

    更新日期:2010-03-09 00:00:00

  • Implementing clinical ethics committees as a complex intervention: presentation of a feasibility study in community care.

    abstract:BACKGROUND:How should clinical ethics support services such as clinical ethics committees (CECs) be implemented and evaluated? We argue that both the CEC itself and the implementation of the CEC should be considered as 'complex interventions'. MAIN TEXT:We present a research project involving the implementation of CEC...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-00522-1

    authors: Magelssen M,Karlsen H,Pedersen R,Thoresen L

    更新日期:2020-09-01 00:00:00

  • Partnering with patients in healthcare research: a scoping review of ethical issues, challenges, and recommendations for practice.

    abstract:BACKGROUND:Partnering with patients in healthcare research now benefits from a strong rationale and is encouraged by funding agencies and research institutions. However, this new approach raises ethical issues for patients, researchers, research professionals and administrators. The main objective of this review is to ...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-0460-0

    authors: Martineau JT,Minyaoui A,Boivin A

    更新日期:2020-05-11 00:00:00

  • Effect of written outcome information on attitude of perinatal healthcare professionals at the limit of viability: a randomized study.

    abstract:BACKGROUND:Differences in perception and potential disagreements between parents and professionals regarding the attitude for resuscitation at the limit of viability are common. This study evaluated in healthcare professionals whether the decision to resuscitate at the limit of viability (intensive care versus comfort ...

    journal_title:BMC medical ethics

    pub_type: 杂志文章,随机对照试验

    doi:10.1186/s12910-019-0413-7

    authors: Papadimitriou V,Tosello B,Pfister R

    更新日期:2019-10-22 00:00:00

  • Technology assessment and resource allocation for predictive genetic testing: a study of the perspectives of Canadian genetic health care providers.

    abstract:BACKGROUND:With a growing number of genetic tests becoming available to the health and consumer markets, genetic health care providers in Canada are faced with the challenge of developing robust decision rules or guidelines to allocate a finite number of public resources. The objective of this study was to gain Canadia...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-10-6

    authors: Adair A,Hyde-Lay R,Einsiedel E,Caulfield T

    更新日期:2009-06-18 00:00:00

  • Addressing ethical challenges of disclosure in dementia prediction: limitations of current guidelines and suggestions to proceed.

    abstract:BACKGROUND:Biomarker research is gaining increasing attention focusing on the preclinical stages of the disease. Such interest requires special attention for communication and disclosure in clinical contexts. Many countries give dementia a high health policy priority by developing national strategies and by improving g...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-00476-4

    authors: Alpinar-Sencan Z,Schicktanz S

    更新日期:2020-05-11 00:00:00

  • The involvement of family in the Dutch practice of euthanasia and physician assisted suicide: a systematic mixed studies review.

    abstract:BACKGROUND:Family members do not have an official position in the practice of euthanasia and physician assisted suicide (EAS) in the Netherlands according to statutory regulations and related guidelines. However, recent empirical findings on the influence of family members on EAS decision-making raise practical and eth...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-019-0361-2

    authors: Roest B,Trappenburg M,Leget C

    更新日期:2019-04-05 00:00:00

  • A framework for the ethical assessment of chimeric animal research involving human neural tissue.

    abstract:BACKGROUND:Animal models of human diseases are often used in biomedical research in place of human subjects. However, results obtained by animal models may fail to hold true for humans. One way of addressing this problem is to make animal models more similar to humans by placing human tissue into animal models, renderi...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-019-0345-2

    authors: Porsdam Mann S,Sun R,Hermerén G

    更新日期:2019-01-25 00:00:00

  • An interprofessional cohort analysis of student interest in medical ethics education: a survey-based quantitative study.

    abstract:BACKGROUND:There is continued need for enhanced medical ethics education across the United States. In an effort to guide medical ethics education reform, we report the first interprofessional survey of a cohort of graduate medical, nursing and allied health professional students that examined perceived student need for...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-020-00468-4

    authors: DeFoor MT,Chung Y,Zadinsky JK,Dowling J,Sams RW 2nd

    更新日期:2020-04-08 00:00:00

  • Identification of ethics committees based on authors' disclosures: cross-sectional study of articles published in the European Journal of Anaesthesiology and a survey of ethics committees.

    abstract:BACKGROUND:Since 2010, the European Journal of Anaesthesiology has required the reporting of five items concerning ethical approval in articles describing human research: ethics committee's name and address, chairperson's name, study's protocol number and approval date. We aimed to assess whether this requirement has h...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-018-0289-y

    authors: Zoccatelli D,Tramèr MR,Elia N

    更新日期:2018-06-08 00:00:00

  • The ethical decisions UK doctors make regarding advanced cancer patients at the end of life--the perceived (in) appropriateness of anticoagulation for venous thromboembolism: a qualitative study.

    abstract:BACKGROUND:Cancer patients are at risk of developing blood clots in their veins - venous thromboembolism (VTE) - which often takes the form of a pulmonary embolism or deep vein thrombosis. The risk increases with advanced disease. Evidence based treatment is low molecular weight heparin (LMWH) by daily subcutaneous inj...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-13-22

    authors: Sheard L,Prout H,Dowding D,Noble S,Watt I,Maraveyas A,Johnson M

    更新日期:2012-09-04 00:00:00

  • Generating genius: how an Alzheimer's drug became considered a 'cognitive enhancer' for healthy individuals.

    abstract:BACKGROUND:Donepezil, an acetylcholinesterase inhibitor used in the treatment of Alzheimer's disease, has been widely cited in media and bioethics literature on cognitive enhancement (CE) as having the potential to improve the cognitive ability of healthy individuals. In both literatures, this claim has been repeatedly...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/1472-6939-15-37

    authors: Wade L,Forlini C,Racine E

    更新日期:2014-05-12 00:00:00

  • Actual implementation of sick children's rights in Italian pediatric units: a descriptive study based on nurses' perceptions.

    abstract:BACKGROUND:Several charters of rights have been issued in Europe to solemnly proclaim the rights of children during their hospital stay. However, notwithstanding such general declarations, the actual implementation of hospitalized children's rights is unclear. The purpose of this study was to understand to which extent...

    journal_title:BMC medical ethics

    pub_type: 杂志文章

    doi:10.1186/s12910-015-0021-0

    authors: Bisogni S,Aringhieri C,McGreevy K,Olivini N,Lopez JR,Ciofi D,Merlo AM,Mariotti P,Festini F

    更新日期:2015-05-13 00:00:00