Critical Review of Two Qualitative Research Articles on Euthanasia

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Title:  Critical Review of Two Qualitative Research Articles specific to the Study of Euthanasia.

Abstract:  This critique scrutinises the methodology and credibility of rigour used with two articles based on euthanasia.  Two qualitative research studies of ethnographic and grounded-theory origin are explored.  Key results from both studies include the increasing acceptance over time of a euthanasia alternative.  Implications for best practice and recommendations are outlined, including an acknowledgement that palliative care is an important area of study that nurse education needs to pay particular attention to, incorporating the caring focus surrounding palliative care and the euthanasia debate.

 (Article 1):  Kuuppelomäki, M 2000, ‘Attitudes of cancer patients, their family members and health professionals toward active euthanasia’, European Journal of cancer Care, vol. 9, iss. 1, p.16, (on-line Blackwell-Synergy).

(Article 2): Doerclx de Casterle, B & Gastmans, C & Verpoort, C 2004, ‘Palliative care nurses’ views on euthanasia’, Journal of Advanced Nursing, vol. 47, iss. 6, p. 592, (on-line Blackwell-Synergy).

1.        Introduction and objectives of articles.

Article 1: An ethnographic study allows the ‘capture of multiple and different voices’ (Crookes & Davies 2004, p.77).  Kuppelomakis’ qualitative ethnographic study, undertaken in two central hospitals and four Health Centres in Finland, expresses views of patients, family members, nurses and physicians in relation to active euthanasia.  Researchers aimed to discover the attitudes of patients with incurable cancer, family members of these patients, medical and nursing staff towards active euthanasia, and the reasoning behind these attitudes in the different groups.  The researcher defines ‘Active euthanasia’ as the giving of a lethal dose of something to speed death’.  

Article 2:  This qualitative grounded-theory study aimed to report palliative care nurses viewpoints on euthanasia in Belgium where euthanasia was being debated.  Crookes & Davies (2004) explain a grounded-theory study generates knowledge and develops explanations.  The researchers felt that nurses’ voices were not heard during the debates and that their voice was an important one considering their immersion in the caring process surrounding euthanasia.  Researchers felt that nurse’s expertise and daily experience of death, dying and palliative care was an important viewpoint.

2.        Principles of ethical conduct.

Flanagan & Holmes (1999) point out there are four levels of thinking about moral matters which include moral rules and moral principles.  Ethical conduct is about researchers doing what is fair, right, decent and moral and are underpinned by values and beliefs of the community (Crookes & Davies, 2004).  Morals are not tested against reality but against socially acceptable community mores.   The four principles of ethical conduct within research are Autonomy, Beneficence, Non-maleficence, and Justice.  Autonomy is about gaining broad consent and ensuring there is understanding and information disclosure towards the participants.  Relationships must be considered; both between participants and researchers, and the ability to volunteer without fear of reprisal must be ensured.  Beneficence is about maximising benefits to participants, society, medical and nursing staff and directly or indirectly improving care or best practice.   Non-maleficence is about minimising harm to participants, society, medical and nursing staff and directly or indirectly not minimising care towards these groups.  Justice is concerned with the benefits and burdens placed on participants and an equal distribution across the sample. Fairness, degree of vulnerability, manipulation, fear of reprisal, distribution of risk as even, and the needs of participants are primary to the needs of the research model. Fair opportunity to participate and informed consent must be obtained. Vulnerable subjects must not be taken advantage of, deliberate deception must not occur and the study must show a true overall picture of the results for publication purposes. There must be no coercion from researchers for sample participation (adapted from Crookes & Davies, 2004).

Article 1:  Addresses ethical issues with a statement saying that the study plan was evaluated by the ethics board of two central hospitals and that the ethic standards set for scientific research were met.

Article 2:  Addresses ethical issues by clarifying that information was given to participants pertaining to the researchers, the study objectives, significance of participation, rights of participants, and a definition of euthanasia.  Participants gave written consent, anonymity was respected and the data collected was treated with confidentiality.

3.        Benefits and limitations of sampling methods used.

Article 1:  Purposive sampling was used and the study carried out with semi-structured, focused interviews which were pre-tested.  Purposive sampling can add relevant information to meet the aims of the study and the researcher has specific knowledge of the subject to choose appropriate sample population (Funnell, Koutoukidis & Lawrence 2005).  Information gathered is rich in relevance and detail.  Bias may enter due to researcher knowledge of issue studied, but this can be a benefit as the involvement of the interviewer within the data analysis and the effect of his/her own views and experiences on the study can be advantageous to the studies aims (Crookes & Davies, 2004). Knowledge of sample and data collection techniques is important for critiquing rigour (Funnell, Koutoukidis & Lawrence 2005) . Limitations in qualitative research with semi-structured focused interviews include the laborious task of transcribing the data and time taken to transcribe. Barbour (2000) clarifies that representativeness can be important in the qualitative sampling group and and n=1 and upwards is an acceptable sample population.  

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Article 2: This Study was carried out using a convenience sample of 12 palliative care nurses built around social networks (Funnell, Koutoukidis & Lawrence 2005).  It is a useful approach when dealing with a clandestine group (Funnell, Koutoukidis & Lawrence 2005).  Bias may be introduced by not using a sample population with a range of views.  The smaller and more homogenous the sample population the more difficulty there is to generalise the findings.  Sampling methods and data collection are important for critiquing the rigour of the study. Benefits include saturation of themes and synchronized data collection and analysis.

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