Abstract:BackgroundMedical assistance in dying (MAiD) traverses challenging and emotionally overwhelming territories: healthcare providers (HCPs) across jurisdictions experience myriad of affective responses secondary to possible tensions between normative and interwoven values, such as sanctity of life, dignity in death and dying and duty to care.ObjectiveTo determine the emotional impact on HCPs involved in MAiD.MethodsInclusion restricted to English language qualitative research studies from four databases (OVID Med… Show more
“…However, the consequences of this mindset, that patients' right to autonomy takes precedence over a nurses' personal beliefs and values, was that nurses risked moral distress as a result. This finding is consistent with other research which concluded, nurses' face ethical dilemmas when dealing with AD and moral distress can result (Dholakia et al, 2022;Freeman et al, 2021;Patel et al, 2021).…”
Section: Discussionsupporting
confidence: 92%
“…The findings of this meta‐synthesis were consistent with other research that suggests health practitioners require clear policies and procedural guidelines for AD to feel confident and capable in having key discussions and providing quality service (Dholakia et al., 2022; Fujioka et al., 2018; Oliver et al., 2017). Nurses reported feeling afraid of the legal ramifications that could ensue yet also expressed their desire to be prepared for engaging with patients who expressed a desire for a hastened death.…”
Section: Discussionsupporting
confidence: 85%
“…The personal persuader ‘patient choice and control takes precedence’ described the key aspects that nurses' felt were pivotal in their decision‐making about how they should approach the topic of AD. This demonstrates nurses' often putting the desires or requests of their patients at the forefront of their own moral decision‐making, which can be complex and distressing (Dholakia et al., 2022). In spite of this, nurses described a desire to honour a patient's request for an assisted death as this would offer them control over their own health, irrespective of whether or not the assisted death actually occurred.…”
Section: Discussionmentioning
confidence: 99%
“…The End of Life Choice Act (2019) does not describe the roles and responsibilities of registered nurses as the majority of involvement in AD is carried out by medical practitioners and NPs. Research has shown that nurses are often the health professionals approached by patients to have the early discussions about AD (Dholakia et al., 2022; Wilson et al., 2019). There is a distinct lack of education or training around navigating these challenging situations and engaging in difficult conversations with patients as requests for AD arises.…”
Aims and ObjectivesTo explore nurses' experiences of assisted dying and understand how their perspectives inform their participation decision‐making.BackgroundAssisted dying is a complex and contentious issue with the potential to create moral unrest for nurses. The nursing role in assisted dying varies between jurisdictions.DesignSystematic review. A meta‐synthesis using thematic analysis.MethodsThree electronic databases were searched for primary qualitative studies published in English, from New Zealand, Australia or Canada, up to October 2022. Seven articles were included; themes were analysed and key themes were established. Reporting adhered to PRISMA.ResultsThe findings highlight the complexity of nurses' decision‐making about participation or non‐participation in assisted dying and the moral, philosophical and social influences that impact on their decision‐making. This is presented as a spectrum of influence which persuades or dissuades nurses to participate in assisted dying. The 12 themes have been categorised into four key themes: personal persuaders, personal dissuaders, professional persuaders and professional dissuaders.ConclusionsThe findings suggest that nurses should be involved in policy and procedure guideline development and be offered education and training programmes to ensure safe, confident and informed practice. The need for mentorship programmes was also prevalent in the research.Relevance to Clinical PracticeIt is crucial that nurses be offered education and training in assisted dying. Clear policy and procedure guidelines are essential, and nurses should be involved in the development of these.
“…However, the consequences of this mindset, that patients' right to autonomy takes precedence over a nurses' personal beliefs and values, was that nurses risked moral distress as a result. This finding is consistent with other research which concluded, nurses' face ethical dilemmas when dealing with AD and moral distress can result (Dholakia et al, 2022;Freeman et al, 2021;Patel et al, 2021).…”
Section: Discussionsupporting
confidence: 92%
“…The findings of this meta‐synthesis were consistent with other research that suggests health practitioners require clear policies and procedural guidelines for AD to feel confident and capable in having key discussions and providing quality service (Dholakia et al., 2022; Fujioka et al., 2018; Oliver et al., 2017). Nurses reported feeling afraid of the legal ramifications that could ensue yet also expressed their desire to be prepared for engaging with patients who expressed a desire for a hastened death.…”
Section: Discussionsupporting
confidence: 85%
“…The personal persuader ‘patient choice and control takes precedence’ described the key aspects that nurses' felt were pivotal in their decision‐making about how they should approach the topic of AD. This demonstrates nurses' often putting the desires or requests of their patients at the forefront of their own moral decision‐making, which can be complex and distressing (Dholakia et al., 2022). In spite of this, nurses described a desire to honour a patient's request for an assisted death as this would offer them control over their own health, irrespective of whether or not the assisted death actually occurred.…”
Section: Discussionmentioning
confidence: 99%
“…The End of Life Choice Act (2019) does not describe the roles and responsibilities of registered nurses as the majority of involvement in AD is carried out by medical practitioners and NPs. Research has shown that nurses are often the health professionals approached by patients to have the early discussions about AD (Dholakia et al., 2022; Wilson et al., 2019). There is a distinct lack of education or training around navigating these challenging situations and engaging in difficult conversations with patients as requests for AD arises.…”
Aims and ObjectivesTo explore nurses' experiences of assisted dying and understand how their perspectives inform their participation decision‐making.BackgroundAssisted dying is a complex and contentious issue with the potential to create moral unrest for nurses. The nursing role in assisted dying varies between jurisdictions.DesignSystematic review. A meta‐synthesis using thematic analysis.MethodsThree electronic databases were searched for primary qualitative studies published in English, from New Zealand, Australia or Canada, up to October 2022. Seven articles were included; themes were analysed and key themes were established. Reporting adhered to PRISMA.ResultsThe findings highlight the complexity of nurses' decision‐making about participation or non‐participation in assisted dying and the moral, philosophical and social influences that impact on their decision‐making. This is presented as a spectrum of influence which persuades or dissuades nurses to participate in assisted dying. The 12 themes have been categorised into four key themes: personal persuaders, personal dissuaders, professional persuaders and professional dissuaders.ConclusionsThe findings suggest that nurses should be involved in policy and procedure guideline development and be offered education and training programmes to ensure safe, confident and informed practice. The need for mentorship programmes was also prevalent in the research.Relevance to Clinical PracticeIt is crucial that nurses be offered education and training in assisted dying. Clear policy and procedure guidelines are essential, and nurses should be involved in the development of these.
“…8 An individual’s professional values and level of engagement influence the emotional impact of MAiD. 9 Some of the stressors described by health care professionals include a feeling of isolation, a culture of secrecy, lack of support, few opportunities to talk about experiences, challenging relationships with colleagues who object and witnessing the grief of others. 10,11 Pharmacy students have reported concerns regarding the dispensing aspect of MAiD as well as issues they may encounter when practising in direct patient care.…”
A pharmacist recently participated in a medical assistance in dying (MAiD) provision for the first time. In this instance, their involvement primarily centred on the dispensing of medications. Despite their lack of familiarity with the patient and their family, the pharmacist has struggled to process a gamut of emotions. The pharmacist does not feel comfortable discussing their experience with others and instead expresses a wish to unpack their thoughts and feelings so that they are better able to understand their emotions. What resources are available to support this pharmacist?
Opinion statementIn considering the impact of medically hastened death (MHD) on cancer care, a wide range of variables needs to be considered including demographic factors, diagnoses, local cultural factors, and the legislative frameworks in place. Here, we present a synthesis of recently available published literature and empirical data collected following legislative change to enable MHD in Victoria, Australia to explore in detail the potential impact of MHD on cancer care with a focus on patients/families and professional groups. Our findings reveal that for patients and families, both physical and existential distress frequently underlie MHD requests, with the latter less readily recognised by health professionals. The responses of those around the patient making the request may have a very significant impact on relationships within families and upon the nature of the subsequent bereavement. For palliative care, while differing views may remain, it appears that there has been some accommodation of MHD into or alongside practice over time. The recognition of a shared commitment to relief of suffering of palliative care and MHD appears a helpful means of establishing how these practices may co-exist. In cancer practice more broadly, as individual professionals reflect upon their own roles, new relationships and pathways of patient movement (or referral) must be established in response to patients’ requests. Our findings also highlight many unanswered questions in understanding the impact of MHD, including that upon those dying who choose not to access MHD, First Nations peoples, the participating health professionals’ longer term, and the relief of suffering itself. A systematic approach to the evaluation of MHD legislation must be adopted in order to understand its full impact. Only then could it be determined if the aspirations for such legislative change were being met.
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