Evaluating Marketing Strategies in Organ Donation
Evaluating Marketing Strategies in Organ Donation
Evaluating Marketing Strategies in Organ Donation
10; 2019
ISSN 1916-9736 E-ISSN 1916-9744
Published by Canadian Center of Science and Education
Received: May 28, 2019 Accepted: July 19, 2019 Online Published: August 31, 2019
doi:10.5539/gjhs.v11n10p160 URL: https://doi.org/10.5539/gjhs.v11n10p160
Abstract
Patients suffering from end-stage diseases wait in expectation of life-saving organs that could improve their quality
of life. However, there is widening gap between organ supply and demand. The intention of this study is to explore
and evaluate marketing strategies in organ donation and transplantation. In an attempt to achieve the purpose of
this study, a qualitative approach was employed. Phenomenology was used as the study’s research design. The
study used social marketing and the theory of social constructivism as the theoretical frameworks and data was
collected through in-depths interviews. Qualitative data was analysed through thematic content analysis.
Purposive sampling was used to select 30 organ donation coordinators. The study established that public education
is the main vehicle through which organ donation and transplantation are promoted. Educational talks, distribution
of information, media, social media, expos, awareness events, and corporate and educational talks are amongst the
strategies used to promote organ donation. The study recommends that the Department of Education include the
issue organ donation in school curricula, and that religious organisations, regular worksite campaigns, regular
television advertisements should be used as vehicles through which to promote organ donation and transplantation.
Furthermore, it is recommended that additional public awareness campaigns be held in black communities. It is
respectfully recommended that the Organ Donor Foundation consider opening satellite offices in all nine South
African provinces.
Keywords: evaluation, marketing, organ donation
1. Introduction and Background to the Study
Organ donation is the greatest gift of love, and occurs when organ donors allows their vital body organ to be
removed legally while they are still alive or after their death, with their next of kin’s consent. Vital body organs that
could be removed to save and prolong the lives of patients that are facing death are the heart, lungs, liver, kidneys,
part of the pancreas, bone marrow, the skin, and part of the intestines. The majority of investigations into organ
donation and transplantation reveal that people have positive attitudes regarding organ donation and
transplantation. Nevertheless, there is no correlation between their attitudes and the number of people that are
actually registered as prospective organ donors. The demand for human body organs always supersedes organ
supply due to the lack of committed and registered organ donors. Organ donation is the only efficacious curative
therapy for some end-stage diseases, and therefore it is fundamental to explore strategies that could expand the
donor pool (Stiegler, Bausys, Leber, Strupas, & Schemmer, 2018; Wong & Chow, 2017). It is against this
background that this study seeks to explore and evaluate marketing strategies that are used to expand the donor
pool or raise the awareness about organ donation and transplantation.
1.1 Problem Statement
The acute shortage of human body organs for transplantation is a public health concern both in developed and
developing countries. It is the ambition of health departments to close the widening gap between the demand and
the supply of organs. However, it is widely acknowledged that organ demand is always greater than organ supply,
due to the shortage of organ donors. South Africa has approximately 4,300 patients suffering from end-stage
diseases, and organ donation is their only hope to save them from death and/or to improve and prolong their quality
of life. Li, Garg, Prakash, Grimshaw, Taljaard, Mitchell, Matti, Linklater, Naylor, Dixon, Faulds, Bevan, Getchell,
Knoll, Kim, Sontrop, Bjerre, Tong, and Presseau (2017) report that in 2013 approximately 4,400 patients in
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Canada were on a waiting list and unfortunately 246 died before they could receive a life-saving organ.
Additionally, Queeley and Campbell (2018) also established that 678,000 Americans were suffering from
end-stage renal failure, and it was estimated that patients suffering from end-stage renal disease (ESRD) might
exceed 2,000,000 by 2030. It is important to view the extent of this problem with different lenses and from
different angles in a holistic manner. Good health is an essential aim for people since without good health people
are unable to play their roles in developing their country’s economies. If they are in bad health, they become the
liability of the state, as many of them might not be able to afford the high medical costs that are associated with
ESRD. Furthermore, family life as a system is disrupted by family members facing the reality of their loved one’s
death as a result of the chronic shortage of vital body organs available for transplantation.
The medical transplantation of organs cannot take place without the organ donors’ availability and the commitment.
To add to the difficult circumstances of hopeless patients, the Organ Donation Foundation (2019) reported that
only 0.2% of South Africans are registered as organ donors, and this adds to the situation that both public and
private hospitals cannot guarantee that they will be able to harvest organs from this minute pool of organ donors.
This claim is based on the fact that many countries like South Africa use the opt-in system of organ donation where
family consent is necessary for organs to be harvested from their deceased family members. According to Bhatia
and Tibballs (2017), individuals voluntarily register to donate their vital organs after death. According to Sharif
and Moorlock (2018) it is challenging to obtain consent from the deceased organ donor’s next-of-kin or close
family members. These authors argue that failure to obtain consent is a barrier to organ donation because the
volume of people who decline consent is significantly high and this is an insurmountable obstacle to overcome, as
procurement of organs cannot be made without valid consent. In medical social work organ donation consent is
called the self-determination principle and this is the cornerstone of ethical social work practice. This principle
provides clients with the democratic right to make their own decisions as medical doctors, professional nurses,
social workers, and organ donation coordinators may not coerce them into giving consent. The opt-in system of
organ donation considers organ donation as an act of generosity or an altruistic act because prospective organ
donors are not legally compelled to donate their life-saving organs such as the heart, kidneys, liver, and pancreas.
This kind of system is democratic and it is based on the fundamental human rights as they are enshrined in the
Constitution of the Republic of South Africa, which is regarded as the country’s supreme law.
However, under this opt-in system it is difficult to close the gap between organ supply and demand. There was
mounting pressure to introduce the opt-out system of organ donation in Australia because it is considered to be the
panacea that will remedy the chronic shortage of organs. However, despite these many pleas to introduce the
system, the request was not granted. The acute organ shortage is caused by multifarious factors. Amongst the
factors that hinder people from participating in organ donation are a lack of or insufficient information about organ
donation as well as socio-cultural factors. Sukalla, Wagner, and Rackow (2017) support these views and assert that
people’s reluctance to become organ donors or to consent to organ donation is caused by a lack of knowledge and
misinformation regarding brain death, as well as religious norms. Although a lack of information is considered to
be the main barrier to organ donation, Krupic, Sayed-Noor, and Fatahi (2016) further argue that limited
information from healthcare professionals such as medical social workers, nurses, and doctors is an impediment to
organ donation as they have to shoulder the responsibility of making people aware of organ donation and
transplantation and some of them are not in favour of organ donation. The general public seems to have generally
positive attitudes towards organ donation and transplantation, nevertheless there seems to be no correlation
between people’s attitudes and the supply of organs. The majority of studies on organ donation continue to cite
religion as a deterrent to organ donation and transplantation. These are Williamson, Reynolds-Tylus, Quick, and
Shuck’s (2017) views, and they state that people are concerned about the integrity of the body and life after death
due to their religious beliefs. This is accompanied by factors such as superstition and the fear of donation. This
study seeks to answer this question:
• What are the strategies that are used to promote organ donation?
2. Research Methodology
Research methodology refers to the scientific research procedures and techniques that researchers use to identify,
select, process, and analyse data about the phenomenon under investigation. In this study the research
methodology included the research approach, design, type of research, population, sampling, data collection,
theoretical frameworks, and ethical considerations. Furthermore, this study’s methodology was influenced by the
study’s goal.
2.1 Research Approach
This study’s intention was achieved by using a qualitative approach. This was an appropriate approach because it is
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intense, engaging, challenging, contextualised, and highly variable (Gray, 2018). In addition to this view, Taylor,
Killick, and Mcglade (2015) claim that a qualitative approach is appropriate when the research goal is to explore
the meanings, perceptions, and constructs in real world contexts, particularly where there is extremely limited
information about the subject under investigation. This study’s goal was to engage organ donation coordinators in
analysing existing organ donation marketing strategies and to explore efficacious marketing strategies that can be
used to improve the status of organ donation and transplantation in South Africa. Whittaker (2012) adds that
qualitative studies tend to utilise data in the form of words rather than quantifying the information.
2.2 Research Design
This study adopted phenomenology and a case study as its research design. The majority of researchers describe a
research design as a study’s blueprint, and according De Vos, Strydom, Fouche, and Delport (2011), research
design is seen as those decisions that scientific researchers make when planning their investigations. Babbie and
Mouton (2001) support this definition and state that the purpose of research design is to address the planning of
scientific investigations. Organ donation coordinators currently shoulder the responsibility of raising public
awareness about organ donation and transplantation, recruiting donors, and obtaining informed consent. Therefore,
the phenomenology and case study methods were appropriate. Firstly because this study’s purpose was to explore
and evaluate marketing strategies used to raise the awareness about organ donation and transplantation. Secondly,
the intention was to elicit the organ donation coordinators’ views and experiences in using those strategies.
According to Padgett (2008) phenomenological studies seek to explore the lived experiences of a phenomenon.
This view finds its support in Creswell, Ebersohn, Eloff, Ferreira, Ivankova, Jansen, Nieuwenhuis, Piterson, and
Clark (2016), who maintain that all phenomenological investigations are explorations into the structures of the
human life-world and lived experiences, as experienced in everyday situations and relations.
2.3 Type of Research
Scientific investigations are conducted in order to generate new knowledge and to update available knowledge. In
addition to this purpose, scientific studies are done in order to solve problems that affect individuals, groups, and
communities. This study is classified as basic research because its intention was to evaluate existing organ
donation strategies and to explore and recommend more effective marketing strategies that could be used to
increase awareness in organ donation and transplantation, which will result in a high volume of organ donors.
According to Brynard, Hanekom, and Brynard (2014), basic research is used to increase knowledge in a particular
field.
2.4 Population
A population in scientific investigations refers to a group of people that have specific features that are of interest to
the researcher (Brynard et al., 2014). Brink, Van der Walt, and Van Rensburg (2012) support this view and define a
research population as the entire group of people in a particular geographical location that is of interest to the
researcher. For the purpose of this study, organ donation and transplant coordinators were the unit of analysis. The
study targeted those subjects who had more than three years experience as organ donation and transplant
coordinators
2.5 Sampling
In qualitative studies sampling is done through non-probability sampling techniques. In this study, both the
purposive and snowball techniques were used to select 30 participants who had more than three years’ working
experience in the field of organ donation and transplantation. Shaw and Holland (2014) are of the view that
purposive sampling is used when people, settings, and context are chosen simply because they constitute typical
cases or extreme cases. According to Creswell et al. (2016), purposive sampling is done with a specific purpose in
mind. Furthermore, the researcher should be knowledgeable about the population under investigation.
Snowballing was used to identify inaccessible research participants. De Vos et al. (2011) assert that snowball
sampling is normally used when a researcher has limited access to appropriate participants for the intended
investigation.
2.6 Data Collection
Interviews are a dominant method of collecting data in social work practice. Non-directive interviews were used to
collect data, and all interviews were conducted in an environment conducive to ethical data collection. According
to Gray (2018), non-directive interviews are appropriate to explore issues or topics in depth. An additional
advantage of non-directive interviews is that research questions are not pre-planned.
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depending on Facebook as an instrument of raising the awareness about organ donation and transplantation is that
people might provide misleading information, which could generate fear, mistrust, and result in myths being
transmitted. It is advisable to monitor discussions closely, and all deliberations should be facilitated by experts in
the field of organ donation and transplantation. The major limitation of using Facebook to raise awareness about
organ donation is access to the internet and the financial costs that are associated with it. In comparison to other
countries, data is expensive in South Africa, and the majority of internet users are young people who are
significantly affected by unemployment. The majority of participants also identified expo events as a means of
promoting organ donation and transplantation. Expo events are highly recommended because they are interactive
in nature, and they encourage the general public to raise sensitive questions that bother them about organ donation.
However, according to Symvoulakis, Markaki, Anyfantakis, and Rachiotis (2018), public awareness campaigns
for organ donation and transplantation have yielded mixed results, indicating a growing need for culturally tailored
and issue-targeted media campaigns. Their argument is based on the fact that organ donation and transplantation
perceptions are embedded in socio-cultural factors and it is therefore vital to approach public awareness campaigns
with a culturally tailored approach.
5. Conclusions of the Study
Organ donation and transplantation are one of the major public health concerns confronting South Africa, and as
result, patients suffering from end-stage diseases have little hope of securing an organ due to the acute shortage of
organ donors and thus available organs. There is no correlation between the supply and the demand of vital body
organs. In a quest to close the gap between organ supply and demand, public education, television, social networks
such Facebook, and educational campaigns are used to increase the donor pool. Nevertheless, this study does not
dispute the fact that these strategies do have an impact but they do not result in the expected outcomes necessary to
address the current situation, and this has catastrophic repercussions. South Africa has only 0.2% of registered
organ donors and 4,300 patients are suffering from end-stage diseases.
6. Recommendations of the Study
Based on this study’s findings, which are also mentioned in the study’s conclusion, the following
recommendations are made by the study.
Organ donation and transplantation is an under-researched subject in South Africa. The study recommends further
research should be done. South Africa adopts the opt-in model of organ donation, and as a result is unable to close
the widening gap between the demand and the actual supply of vital body organs. The opt-in model requires
prospective organ donors to register to donate their organs after their deaths. According to the opt-in model, organ
donation is viewed as an altruistic act. The study recommends that the Ministry of Health consider adopting the
opt-out model of organ donation. This is a model that has been successfully adopted by Spain, which has a high
volume of organ donors. However, according to the opt-out model of organ donation the procurement of vital body
organs or tissues is performed routinely after the death of potential organ donors, unless a person has made a
formal request prior to their death that their organs not be harvested. According to Li and Nikolka (2016), the
opt-out model of organ donation reflects a presumed consent policy because all people are classified as potential
organ donors. According to Rodrıguez-Arias and Morgan (2016), the majority of countries that have adopted the
opt-out model of organ donation have higher rates of organ donors.
Public education and awareness campaigns are not out-dated strategies of raising awareness about organ donation
and transplantation, rather they are less costly and they have the potential to reach a higher volume of people.
Nevertheless, the promotion of organ donation should take into consideration the contexts within which organ
donation and transplantation are promoted. Organ donation and transplantation are influenced by socio-cultural
factors and it is therefore essential to design awareness campaigns that are culturally tailored to diverse contexts. It
is further recommended that educational talks, campaigns, and public education be held regularly and that rural
areas are targeted. The subject of organ donation and the transplantation of body organs should take place in as
young audiences as is possible, and organ donation and transplantation should be included in school curricula,
particularly life orientation lessons. The rationale behind this suggestion is that children and young adults are
typically assumed to less prejudicial and it is easier to teach them new concepts. This could enhance the promotion
of organ donation as these learners are likely to discuss organ donation and transplantation with their parents and
peers, and as a result, create a population and communities that are informed about organ donation. It also
recommended that organ donation be promoted regularly through worksite campaigns. Worksite campaigns are
important and useful because they provide a large captive audience that might be difficult to reach through other
channels.
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Rodrıguez-Arias, D., & Morgan, M. (2016). "Nudging" Deceased Donation Through an Opt-Out System: A
Libertarian Approach or Manipulation? The American Journal of Bioethics, 16(11), 25-28.
https://doi.org/10.1080/15265161.2016.1222022
Sharif, A., & Moorlock, G. (2018). Influencing Relatives to Respect Donor Autonomy: Should We Nudge
Families to Consent to Organ Donation? Journal of Bioethics, 2018(32), 155-163.
https://doi.org/10.1111/bioe.12420
Shava, H., & Chinyamurindi, W. T. (2018). Determinants of Social Media Usage among a Sample of Rural South
African Youth. South African Journal of Information Management, 20(1), a827.
https://doi.org/10.4102/sajim.v20i1.827
Shaw, I., & Holland, S. (2014). Doing Qualitative Research in Social Work. London: Sage.
https://doi.org/10.4135/9781473906006
Stiegler, P., Bausys, A., Leber, B., Strupas, K., & Schemmer, P. (2018). Impact of Melatonin in Solid Organ
Transplantation-Is It Time For Clinical Trials? A Comprehensive Review. International Journal of Molecular
Sciences, 2018(19), 1-14. https://doi.org/10.3390/ijms19113509
Sukalla, F., Wagner, A. J. M., & Rackow, I. (2017). Dispelling Fears and Myths of Organ Donation: How
Narratives that Include Information Reduce Ambivalence and Reactance. International Journal of
Communication, 11, 5027-5047.
Symvoulakis, E.K., Markaki, A., Anyfantakis, D. & Rachiotis, G. (2018). Organ Donation Awareness: Rethinking
Media Campaigns. International Journal of Health Policy Management, 7(12), 1165-1166.
https://doi.org/10.15171/ijhpm.2018.85
Taylor, B. J., Killick, C., & Mcglade, A. (2015). Understanding and Using Research in Social Work. London: Sage.
https://doi.org/10.4135/9781473922365
Thomson, D. (2017). Organ donation in South Africa-A Call to Action. South African Journal of Critical Care,
33(2), 36-37. https://doi.org/10.7196/352
Weyers, M. L. (2012). The Theory and Practice of Community Work: A South African Perspective (2nd ed.).
Potchefstroom: Keurkopie.
Whittaker, A. (2012). Research Skills for Social Work (2nd ed.). London: Sage.
Williamson, L. D., Reynolds-Tylus, T., Quick, B. L., & Shuck, M. (2017). African-Americans' Perceptions of
Organ Donation: Simply Boils Down To Mistrust. Journal of Applied Communication, 45(2), 199-217.
https://doi.org/10.1080/00909882.2017.1288293
Wong, S. H., & Chow, A. Y. M. (2017). Perceptions of posthumous organ donation base on the theory of reasoned
action. Journal of Death and Dying, 75(3), 284-299. https://doi.org/10.1177/0030222816633241
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