|Year : 2019 | Volume
| Issue : 3 | Page : 269-276
Toward A Germinal Theory of Knowing-Revealing-Humanizing as Expressions of Caring in Cancer Palliative Care
Chinomso Ugochukwu Nwozichi
Department of Adult Health Nursing, School of Nursing, Babcock University, Ilishan Remo, Ogun State, Nigeria
|Date of Submission||28-Jan-2019|
|Date of Acceptance||04-Mar-2019|
|Date of Web Publication||30-Apr-2019|
Chinomso Ugochukwu Nwozichi
Department of Adult Health Nursing, School of Nursing, Babcock University, Ilishan Remo, Ogun State
Source of Support: None, Conflict of Interest: None
Objective: Survival chances of people with cancer in Nigeria are far worse than those in developed countries. While the chance of finding a lasting solution to cancer in Nigeria is remote, patients living with cancer still need treatment regardless of the terminal outcome, and hence cancer palliative care is necessitated. Caring patterns and expressions differ in diverse contexts. Therefore, this article aimed to present the meanings and expectations of caring and the resulting transformative theory of practice. Methods: A descriptive, qualitative inquiry was conducted with a purposive sample of 12 cancer palliative patients, 9 nurses, 3 physicians, and 5 relatives who were approached for an in-depth interview about their conceived meanings and expectations of caring for or being cared for in the cancer palliative unit. Results: Cancer palliative care in Nigeria is best exemplified through the processes/themes of “knowing,” “revealing,” and “humanizing.” The meaning of care and the expectations of the patients and caregivers were grouped into these three overarching processes which then informed the conceptualization of a germinal theory of knowing-revealing-humanizing (TKRH) as expressions of caring in cancer palliative care. Conclusions: The application of the KRH practice processes is illustrated as a transformative germinal theory of practice. This TKRH as expressions of caring is transformative and can restore positive meanings in the life-world of persons in the cancer palliative care setting.
Keywords: Cancer palliative care, humanizing, knowing, Nigeria, transformative theory
|How to cite this article:|
Nwozichi CU. Toward A Germinal Theory of Knowing-Revealing-Humanizing as Expressions of Caring in Cancer Palliative Care. Asia Pac J Oncol Nurs 2019;6:269-76
|How to cite this URL:|
Nwozichi CU. Toward A Germinal Theory of Knowing-Revealing-Humanizing as Expressions of Caring in Cancer Palliative Care. Asia Pac J Oncol Nurs [serial online] 2019 [cited 2019 Aug 23];6:269-76. Available from: http://www.apjon.org/text.asp?2019/6/3/269/255385
| Introduction|| |
Human care is a universal phenomenon. The capacity to care and the need to be cared for is part of human nature. Fry, a caring scholar, has described caring as a way of being in the world, and tracked her thoughts about caring to the work of Heidegger (1927/2011). Interestingly, Tronto in 2014 shed more light on the meaning of care as those activities “that we do to maintain, continue, and repair our 'world' so we can live in it as well as possible” (p. 33). However, the pattern by which persons express caring and its meanings is diverse across cultures.
Palliative care is the attention and care delivered to persons living with serious or life-threatening health issues, in order to relieve their sufferings and enhance their quality of life. Ferrell et al. and Temel et al. have advocated the integration of palliative care services into standard oncology care. Cancer is an important source of morbidity and death globally and has become a challenge to the health of the public, especially in Nigeria. The dramatic rise in cancer incidence has influenced Nigerian culture in diverse ways.
Cancer patients are victims of progressive disease and daily life struggles that shape their experiences before and during hospitalization. According to reported evidence, there are approximately 102,100 new cases of cancer and a mortality rate of about 71,600 deaths annually in Nigeria, and Nigerians face a 10.4% risk of having cancer before the age of 75 years. This situation is compounded by the evidence that certain cultural beliefs and values make cancer patients approach the health institutions very late when all traditional treatments have failed to cure their illnesses. Moreover, the World Poverty Clock has recently declared that the oil-rich Nigeria outpaced India in May 2018 to emerge as the country with the world's highest number of people (87 million) living in high poverty (living on <$1.90 a day), in comparison with India's 73 million people.
Survival of people with cancer in Nigeria is far worse than that observed in high-income countries, owing to late presentation of cases, a limited number of oncology (medical and nursing) specialists, lack of equipment and other resources, and extreme poverty. Although advocacy for a multidisciplinary approach to the fight against cancer and the care of the afflicted ones is ongoing, the roles of the Nigerian nurses in the fight against cancer have been underreported and underrecognized. While the chances of finding a lasting solution to cancer in Nigeria are remote, patients living with cancer need treatment regardless of the terminal outcome, and hence cancer palliative care is necessitated. However, palliative care for cancer patients in Nigeria is not yet well established; there is limited literature about what constitutes caring and the meanings attributed to caring in the Nigerian cancer palliative care context.
Caring connotes a variety of meanings. Individuals view caring from their own context and therefore, a universal definition may not be possible. Care meanings, expressions, and patterns vary among cultures, but there is a lack of Nigeria-based study about caring in nursing, specifically, in the context of palliative care for cancer patients. The complexity of defining caring in cancer palliative care should be viewed from the perspectives of caregivers and care receivers. By doing so, we can understand the essence of our being that we can formulate our own meanings of caring that are harmonious and congruent within our cultural contexts. Therefore, the purpose of this article was to present the meanings and expectations of caring and the resulting transformative theory of practice for persons living with cancer in Nigeria. This study also aimed to develop an understanding of the concept of caring in the Nigerian cultural context. The analysis of data adopted a humanistic perspective.
The following theoretical assumptions of this article are derived from the theoretical perspectives of caring theorists such as Boykin and Schoenhofer's theory of nursing as caring, Rozzano Locsin's Theory of Technological competency as caring in Nursing, and Jane Watson's theory of transpersonal caring:
- All persons in the palliative care settings are human beings in the first place and only secondly either a caregiver or care receiver
- All persons are caring
- All persons are always whole and do not need to be fixed or measured by mathematical calculations
- Everybody has a perspective of truth and the world; and
- Caring is enabling a person to re-discover, re-value, and re-appreciate self as a human person.
| Methods|| |
The philosophical viewpoint of this inquiry is derived from Heidegger's (1927/2011) concept of the human person, underpinning the understanding of the being of the person as a dynamic, unpredictable, multidimensional, and uniquely whole, and follows the interpretive paradigm. The researcher, being a nurse researcher, co-created the data from the perspectives of the participants. After obtaining approval from the health-care institution in Nigeria, which is a cancer referral center, and informed consent from the participants, a purposive sample comprising 12 cancer palliative patients, nine nurses, three physicians, and five relatives was identified and respondents were approached face to face for an in-depth interview about their experiences of “caring for” or “being cared for” in the cancer palliative unit. The interviews lasted between 40 and 60 min in the participants' preferred location within the unit. Nonparticipants were not present during the interview sessions.
The sample size of this study was dependent on data saturation, as Streubert and Carpenter suggest that sample size in a purely qualitative study is determined when saturation has been reached. The author, a nurse researcher, utilized an interview guide to conduct the interview containing questions such as: what does care mean to you from your experience here? Can you think of any story that portrays your perception of the ideal meaning of caring? Tell me about a time when you felt good about an interaction with a patient (for care providers) or with a health-care provider (for patients). The basic demographic information of the participants was obtained after each interview. The interview was conducted once and was recorded using a digital recorder, and notes were taken simultaneously to summarize nonverbal observations during the interview. Participants were informed that the study is voluntary and that they have the full right to withdraw at any point without any consequences whatsoever. Prior to data collection, the researcher had been trained and is experienced in qualitative nursing research studies.
The recorded interviews were then translated and transcribed verbatim. After data transcription, the researcher listened to the audio recordings separately and compared them with the transcribed texts to ascertain the accuracy, and necessary corrections were made where necessary through participant checking. Data were coded using Nvivo 7 (QSR international, Melbourne, Australia) and were classified as related to the phenomenon of inquiry. Each transcript was read several times, line by line. Descriptors from the words of the participants that describe the phenomenon of interest were identified, to initially generate codes and categories. Data categories were reviewed to discover recurrent patterns of meanings and conceptions of caring. The investigator then identified major themes and constitutive patterns as they emerged. A theoretical framework was formulated to provide a clearer understanding of the phenomenon of inquiry. The four aspects of trustworthiness (credibility, transferability, dependability, and conformability) proposed by Lincoln and Guba were adopted to ensure rigor.
| Results|| |
Data analysis yielded three major themes, 13 categories, and 48 verbal expressions as presented in [Table 1].
Cancer palliative care in Nigeria is best exemplified through the processes of knowing, revealing, and humanizing (KRH). Each care expectation and meaning was grouped into these three overarching KRH processes. The findings of this study reveal that caring was expressed in a broad range of patterns and has a plethora of meanings among cancer palliative care patients, relatives, and health-care professionals.
Knowing [Figure 1] in this model is illustrated as cultural knowing, responsive sensing, silence as an expression of caring, and technological knowing. Majority of the expressions and meanings address the essence of revealing [Table 1]. Revealing in this instance connotes immersing oneself into the life of others in order to reveal concerns that are concealed or not readily expressed by the other. Revealing is achieved through four fundamental processes [Figure 1], namely witnessing the lived experiences, expression of authenticity, engaging in the world of others, and mutual discovery.
The final theme/process is humanizing expressed as intentional caring, re-discovering human persons, liberating self and others, appreciating wholeness of persons, and enabling transcendence.
The conceptualization of this theory was informed by the responses of the participants and viewed from a humanistic perspective. The verbal expressions indicated in [Table 1] are the caring expressions, expectations, and meanings derived from the participants' responses. The analysis of participants' responses was not discriminated. The three cancer palliative care processes are continuous and integrative, with neither a starting point nor an ending [Figure 2]. This model portrays that cancer palliative care is a holistic phenomenon and the focus of care is the wholeness of persons.
| Discussion|| |
The term patient is used in this article to describe a person who is entitled to health care as a human being. It is, however, recognized that the term patient is often used to represent a person receiving medical services with a dehumanizing undercurrent of a passive receptor or an object of care rather than a co-participant. The rudimentary goal of palliative care is the amelioration of pain and suffering. This study attempted to explore what caring means to cancer patients, relatives, and caregivers working on the palliative care units and develop a germinal theory that will have a direct effect on palliative care in Nigeria. The findings of this study revealed that palliative care must also address how patients live, not just how they die. Because a lasting solution for cancer in Nigeria is not yet established, paying attention to palliative care services is hereby justified.
“Knowing” as an expression of caring in palliative care
Knowing was identified as an important theme in this study. Participants described different approaches to knowing that signifies an expression of caring. Patients, relatives, and caregivers pointed out that addressing patients by their names and titles is a way to open more possibilities of caring. As rightly explained by McKenzie, knowing the patient's name and making efforts to pronounce it correctly is essential to building good connection and a trusting relationship between caregivers and the patient and family members. This finding is quite important in the Nigerian context because Nigerians are very proud of titles and they always desire to be addressed with their titles, even when they need health-care services, as a form of respect. Addressing patients with their titles and names, instead of bed number of diagnosis, is an important expression of caring. The role of touch in palliative care has long been explored in the literature. For example, over two decades ago, Sims reported that touch is a powerful way of facilitating communication and enhancing psychological and physical comfort. More recently, Senderovich et al. introduced a therapeutic touch program in palliative care and reported that therapeutic touch yielded relaxation and showed potential value as an adjunct therapy to assist patients in relaxing and coping with prevailing realities. This study found that touch was a means to know patients completely. The touch reported in this study is beyond the touching associated with a procedure or task but a touch that is intentional and often brings about smooth interaction between patients and their caregivers. An interesting mode of knowing in palliative care is silence which was presented as an expression of caring. This corroborates the findings of Back et al. who referred to it as compassionate silence. Other scholars have addressed the role of silence in knowing patients in palliative care. More recently, Sapeta and Simões described silence in palliative care as the “primacy of human presence” (p. 161). Sapeta and Simões further suggested that, although silence is a means of knowing and communicating, it should not be used to shy away from difficult questions. What matters most is the ability to empathize with the silence of the patient, an active presence, to transmit a sincere understanding of what he/she means. Durieux et al. referred to this pattern as “connectional silence” (p. 1). Participants in this study reported that silence is more preferred than empty sets of words; however, silence in this instance goes beyond withholding speech.
In general, the present study identified four modes of knowing [Figure 2] – cultural knowing, responsive sensing, silence as an expression of caring (compassionate silence), and technological knowing. Previous studies have supported these findings. It is only through knowing that providers can render caring that meets the essential and existential needs of the patient, and more truly immerse themselves in the patients' world. Technological knowing is best exemplified by what Locsin described as the co-existence of caring and technology whereby technology is used to know persons more fully as human persons and not objects of care. Responsive sensing as a mode of knowing is described as a position whereby health-care providers advance caring relationships and communication by functioning as a team with patients and relatives in a co-creative process. Bergdahl et al. in their study posited that the co-creative process of responsive sensing could improve the dying patients', the relatives', and the families' possibilities to attain essential goals in palliative care. Cultural knowing or cultural inquiry is an approach that familiarizes health-care professionals with the cultural identity and uniqueness of the persons being cared for. Cultural knowing is the acknowledgment of one's state of mind and presumptions in contrast to others. Therefore, understanding and tolerating the sociocultural, religious, and moral dimensions of a patient's care are important determinants of successful care results. Interestingly, cultural knowing is exemplified as bringing home to the hospital, implying that patients want the hospital environment to have some resemblance of their homes. Unfortunately, the Nigerian public hospital wards, mostly characterized by the famous open multibed wards, are experiencing critical challenges in synchronizing formal and informal activities of the patients within the hospital spaces. The patients mostly accompanied by their families find it difficult to find their daily activities fit into the hospital environment.
“Revealing” as an expression of caring
Oftentimes, palliative patients and their families have needs that are not adequately addressed. For health-care professionals, including nurses, being able to address patients' care needs can be a challenge. Due to certain factors, patients tend to conceal some of their important needs. It is exigent for nurses and other health-care personnel to improve the quality of interaction. According to Barry et al., the most important attribute of patient-centered care is the active engagement of patients. Caregivers need to start out with the right framework which is to incorporate in the person's whole life. Patients' needs have been assessed by clinician researchers, and there is no general consensus about what constitutes the needs of patients. This is compounded especially by patients' needs which do not fall under the health-care domain. Revealing the needs of patients is required to guide their plan of care because palliative care patients and relatives do not freely communicate their concerns to clinicians. Even when patients communicate their concerns, oftentimes, they conceal some important psychosocial concerns that may have a significant impact on their well-being. Others have the impression that clinicians do not want to address such issues. Weighty evidence points to the damaging effects of inadequately meeting patients' total nursing needs. The collaborative relationships are opportunities to attract caring possibilities. Therefore, interactions are directed toward understanding the person as a person, which reveals, defines, or explores other ways of nurturing the person's wholeness, well-being, and more-being.
Findings of the present study identified various modes of revealing as an expression of caring. Such patterns include witnessing the lived experiences, expression of authenticity, engaging in the world of others, and mutual discovery. Witnessing the lived experience involves enabling the patient to recount his or her life before the illness and explore hopes for the future, and expressing interest in the patient's fears. To clarify this, Black et al. opined that engaging with and understanding the perspectives of patients and their family is critical in palliative care. Witnessing the “patient's lived experience” can facilitate the provision of care that is responsive and adaptive to individual palliative patient need. The present study further revealed that caring is characterized by authenticity. Seno identified that patients and family in palliative care have unmet needs because health-care professionals are unprepared to be authentic. Seno further described this attribute as authentic “being-with” (p. 377). The present study found authenticity to be an essential mode of revealing in cancer palliative care. Authenticity is expressed as checking on patients' outside duty hours, expression of interest about patients' expectations after death, and being frank during discussions about death. In a previously mentioned study, each nurse described acceptance of death as part of life; therefore, they were calm and quiet, open, ready, nonjudgmental, and entirely available for the patient and family. The authors further reported that health-care professionals comported themselves toward dying patients and family members in such a way that they cleared the way for people to be themselves, the way they are. These are genuine representations of the characteristics and meanings of caring in the present study. Authenticity is described as a core attitude of health-care professionals and a philosophy in palliative care.
Another pattern of revealing is through engaging in the world of others. Showing genuine concern about family members is considered an act of caring. Engaging in the world of others necessitates accompanying the patient and family in a relational and transformative way. The patient as a person is revealed, and patient–caregiver interactions yield higher possibilities for growth and more-being. The last mode of revealing is mutual discovery, which is otherwise known as caring disclosure. This pattern facilitates the revealing of self to the other in order to strengthen care connectedness. Human beings often hide their inner thoughts and feelings because they are concerned if other people will accept them. Mutual discovery makes the outer world as similar to the inner world as possible. This can be achieved through the presentation of narratives to the familiar other.
“Humanizing” as an expression of caring
Provider–patient interaction magnifies the patient's humanness, thereby helping him or her to re-discover, re-value, and re-appreciate self as a human person. Therefore, when palliative care is humanized, the patient is no longer just a recipient of nursing care but a co-actor and co-participant in the preservation of humanism through caring. The participants in this study expressed that the ultimate goal of caring in palliative care is to preserve human dignity and personhood despite the current limitations of illness. In acknowledging that “dignity enhancing” or “dignity-preserving” care for palliative care patients is essential, interventions such as the dignity model have been magnified as a potent approach to ensuring a human-centered care, thereby advancing patient autonomy and recognizing the person as a human person. Terminal illnesses such as cancer alter the sense of the self of a person, compelling him or her to reach an agreement with the self again in the face of uncertainty. Death necessitates humans to re-appreciate and re-value life and thereby move beyond the apparent nothingness and meaninglessness of life.
The findings of this study revealed five modes of humanizing, namely intentional caring, re-discovering human persons, emancipating self and others, appreciating the wholeness of persons, and enabling transcendence. Intentional caring entails putting human consciousness into action in the preservation of human dignity. Without intentionality, the nurse may be so engrossed in executing tasks and protocols as a matter of necessity that conscious considerations cannot be given to the caring relationship. Participants in this study realized that intentionality is required to overcome this challenge. A previous study conducted among oncology nurses in a Nigerian setting reported that task-oriented nurses are prone to high stress and burnout inherent in cancer care. Intentionality was described by Jane Watson as a framework for transpersonal caring which helps to break any resistance during caregiving. According to Watson, “when one declares intentionality toward an action, whatever resistance may be within tends to mobilize and dissipate, allowing manifestation of intention to be realized (p. 14) …and universal energy-field are posited as the foundation of a caring moment, potentiating healing for both practitioner and patient” (p. 12). There must be a conscious commitment to help the patient to grow in what he or she wishes to become. Elements of intentional caring in the present study include making oneself available and addressing patients by names rather than diagnoses or bed or room numbers, which was identified as a usual practice in Nigeria. The loss of the sense of self during cancer diagnosis and palliative care necessitates caregivers to enable the patient to renegotiate his or her identity within the new context of his/her reality. The goal is to make the person feel like a human person and nothing less. Elements of re-discovering human persons from this study include reinforcing that “we are all human beings regardless of health status” and helping the patient to re-appreciate self as a person. Re-discovering self is directly linked to emancipating self and others. The patient is emancipated when all possibilities are explored to provide total comfort and effective pain relief because everybody deserves to be free from pain regardless of dying status. In the context of appreciating the wholeness of persons, while the biomedical/positivist paradigm considers persons as being made up of parts, humanized caring fosters the wholeness of persons as always complete needing not to be fixed or made whole again. Elements that constitute the wholeness of persons include appreciating nature, re-appreciating self as a person, and acknowledging that patients' preferences are more important than protocols.
The final mode of humanizing is enabling transcendence. Transcendence in this study is associated with one's spirituality and the connectedness between the self and the external world and also the person's ability to think in a creative and transformative way to appreciate art, nature, universal complex, or spiritual entities. The concept of transcendence has attracted so much attention in the literature since the promulgated theoretical framework of Maslow. The development of transcendence among palliative patients was also reported by a similar study. While palliative patients progressively encounter difficulties caused by cancer, they also tend to seek meaning and purpose in their lives. Although Iwamoto, Yamawaki, and Sato reported that palliative patients experience self-transcendence, findings of this study reveal that palliative health-care providers serve to enable patients to find the meaning of their existence, attain high functionality, and explore human possibilities through humanized caring. Elements of enabling transcendence in this study include an appreciation of subjectivity of life, living the meaning of one's own life, appreciation of death, and participating in prayer sessions with patients and family regardless of religion.
| Conclusion|| |
The human experience is a process of expanding consciousness to maximize the power inherent in a person that advances to a higher level of consciousness. The integrality of the KRH processes is represented in [Figure 2] implying that the processes are nonlinear, and therefore have no starting or ending point. This study identified three critical humanistic processes that exemplify caring for cancer patients in palliative settings. The application of KRH practice process is illustrated as a transformative germinal theory of practice. This theory is transformative and can restore positive meanings in the life-worlds of persons in cancer palliative care setting through caring.
The author greatly appreciates the participants of this study for their time and patience.
Financial support and sponsorship
This study was funded by Babcock University, Nigeria, and the Southwest Nigerian Zone of Mandatory Professional Development Program (MCPDP) for Nurses.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Watson J. Human Caring Science: A Theory of Nursing. 2nd
ed. Sudbury, MA: Jones and Bartlett Learning; 2012.
Fry ST. The philosophical foundations of caring. In: Leininger MM, editor. Ethical and Moral Dimensions of Care. Detroit, MI: Wayne State University Press; 1990.
Fry ST. The role of caring in a theory of nursing ethics. Hypatia 1989;4:88-103.
Heidegger M. Being and Time. Translator by Macquarrie J, Robinson E. New York, NY: Harper & Row; 2011.
Tronto JC. Democratic care politics in an age of limits. In: Razavi S, Staab S, editors. Global Variations in the Political and Social Economy of Care: Worlds Apart. New York, NY: Routledge; 2014. p. 29-40.
George J. Nursing Theories: The Base for Professional Nursing Practice. 6th
ed. Upper Saddle River, N.J: Pearson; 2011.
Ferrell BR, Temel JS, Temin S, Alesi ER, Balboni TA, Basch EM, et al.
Integration of palliative care into standard oncology care: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol 2017;35:96-112.
Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, et al.
Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med 2010;363:733-42.
Sylla BS, Wide CP. Cancer burden in Africa in 2030: Invest today and save tomorrow. J Afr Cancer 2012;4:1-2.
Nwozichi CU, Ojewole F, Oluwatosin AO. Understanding the challenges of providing holistic oncology nursing care in Nigeria. Asia Pac J Oncol Nurs 2017;4:18-22.
] [Full text]
Adegoke AA. Factors influencing health beliefs among people in South West Nigeria. Afr Res Rev 2008;2:177-97.
Petri S, Berthelsen CB. Lived experiences of everyday life during curative radiotherapy in patients with non-small-cell lung cancer: A phenomenological study. Int J Qual Stud Health Well-being 2015;10:29397.
International Agency for Research in Cancer. GLOBACAN 2012: Estimated Cancer Incidence, Mortality, and Prevalence Worldwide in 2012. Available from: http://globocan.iarc.fr
. [Last accessed on 2018 Dec 11].
Chukwuneke FN, Ezeonu CT, Onyire BN, Ezeonu PO. Culture and biomedical care in Africa: The influence of culture on biomedical care in a traditional African society, Nigeria, West Africa. Niger J Med 2012;21:331-3.
Soyannwo O, Aikomo O, Maboreje O. Palliative care: Supporting adult cancer patients in Ibadan, Nigeria. J Palliat Care Med 2016;6:1-5.
Eke GK, Ndukwu GU, Chukwuma NS, Diepiri BB. Knowledge and perception of healthcare providers towards palliative care in Rivers State, Nigeria. Port Harcourt Med J 2017;11:156-60. [Full text]
Boykin A, Schoenhofer SO. Nursing as Caring: A Model for Transforming Practice. Boston, MA: Jones and Bartlett; 2001.
Locsin RC. Rozzano Locsin's technological competency as caring and the practice of knowing persons in nursing. In: Parker ME, Smith M, editors. Nursing Theories and Nursing Practice. Philadelphia, PA: F. A. Davis; 2010. p. 460-71.
Watson J. Watson's theory of transpersonal caring. In: Walker PH, Neuman B, editors. Blueprint for Use of Nursing Models: Education, Research, and Administration. New York: National League for Nursing Press; 1996. p. 141-84.
Streubert H, Carpenter D. Qualitative Research in Nursing. Advancing the Humanistic Imperatives. 4th
ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2011.
Lincoln YS, Guba EG. Naturalistic Inquiry. Newbury Park, CA: Sage Publications; 1985.
McKenzie R. Knowing the patient's name. Am J Nurs 2012;112:12.
Falola T. Culture and Customs of Nigeria. Westport, CT: Greenwood Press; 2001.
Sims S. The significance of touch in palliative care. Palliat Med 1988;2:58-61.
Senderovich H, Ip ML, Berall A, Karuza J, Gordon M, Binns M, et al.
Therapeutic touch(®) in a geriatric palliative care unit – A retrospective review. Complement Ther Clin Pract 2016;24:134-8.
Back AL, Bauer-Wu SM, Rushton CH, Halifax J. Compassionate silence in the patient-clinician encounter: A contemplative approach. J Palliat Med 2009;12:1113-7.
Roy DJ. Silence in palliative care? J Palliat Care 2013;29:203-4.
Sapeta A, Simões A. Silences in palliative care-the primacy of human presence. Hosp Palliat Med Int J 2018;2:161-4.
Durieux BN, Gramling CJ, Manukyan V, Eppstein MJ, Rizzo DM, Ross LM, et al.
Identifying connectional silence in palliative care consultations: A tandem machine-learning and human coding method. J Palliat Med 2018; doi: 10.1089/jpm.2018.0270.
Luker KA, Austin L, Caress A, Hallett CE. The importance of 'knowing the patient': Community nurses' constructions of quality in providing palliative care. J Adv Nurs 2000;31:775-82.
Locsin RC. The co-existence of technology and caring in the theory of technological competency as caring in nursing. J Med Invest 2017;64:160-4.
Bergdahl E, Benzein E, Ternestedt BM, Elmberger E, Andershed B. Co-creating possibilities for patients in palliative care to reach vital goals – a multiple case study of home-care nursing encounters. Nurs Inq 2013;20:341-51.
Ariff KM, Beng KS. Cultural health beliefs in a rural family practice: A Malaysian perspective. Aust J Rural Health 2006;14:2-8.
Alkali IA, Ahmad MH, Said I. The challenges of Nigerian hospitals in providing for family participation. Appl Mech Mater 2014;584-586:142-51.
Barry MJ, Edgman-Levitan S. Shared decision making – Pinnacle of patient-centered care. N Engl J Med 2012;366:780-1.
Asadi-Lari M, Packham C, Gray D. Patients' satisfaction and quality of life in coronary artery disease. Health Qual Life Outcomes 2003;1:57.
Wen KY, Gustafson DH. Needs assessment for cancer patients and their families. Health Qual Life Outcomes 2004;2:11.
Epstein RM, Street RL Jr. The values and value of patient-centered care. Ann Fam Med 2011;9:100-3.
Black A, McGlinchey T, Gambles M, Ellershaw J, Mayland CR. The 'lived experience' of palliative care patients in one acute hospital setting – A qualitative study. BMC Palliat Care 2018;17:91.
Seno VL. Being-with dying: Authenticity in end-of-life encounters. Am J Hosp Palliat Med 2010;27:377-86.
Simon ST, Ramsenthaler C, Bausewein C, Krischke N, Geiss G. Core attitudes of professionals in palliative care: A qualitative study. Int J Palliat Nurs 2009;15:405-11.
Genuis QI. Trust, intent, authenticity, and good dying: Beyond the autonomy debates and towards a philosophy of palliative care. Prog Palliat Care 2017;25:286-90.
Shaw CL. Personal narrative revealing self and reflecting other. Hum Commun Res 1997;24:302-19.
Pringle J, Johnston B, Buchanan D. Dignity and patient-centred care for people with palliative care needs in the acute hospital setting: A systematic review. Palliat Med 2015;29:675-94.
Janssens R, Gordijn B. Clinical trials in palliative care: An ethical evaluation. Patient Educ Couns 2000;41:55-62.
Nwozichi CU, Ojewole FU. Potential stressors in cancer care: Perceptions ofoncology nurses in selected teaching hospitals in Southwest Nigeria. Afr J Med Health Sci 2015;14:130-4. [Full text]
Watson J. Intentionality and caring-healing consciousness: A practice of transpersonal nursing. Holist Nurs Pract 2002;16:12-9.
Parse RR. Nursing Science Major Paradigms, Theories and Critiques. Philadelphia: W. B. Saunders; 1987.
Boykin A, Schoenhofer SO. Nursing as Caring: A Model for Transforming Practice. Boston, MA: Jones and Bartlett; 2001.
Maslow AH. Motivation and Personality. New York: Harper and Row; 1954.
Iwamoto R, Yamawaki N, Sato T. Increased self-transcendence in patients with intractable diseases. Psychiatry Clin Neurosci 2011;65:638-47.
Newman MA. Health as Expanding Consciousness. 2nd
ed. New York, NY: National League for Nursing; 1994.
| Authors|| |
Chinomso Ugochukwu Nwozichi
[Figure 1], [Figure 2]