Palliative care for cancer patients in a primary health care setting: Bereaved relatives' experience, a qualitative group interview study
© Neergaard et al; licensee BioMed Central Ltd. 2008
Received: 13 July 2007
Accepted: 15 January 2008
Published: 15 January 2008
Knowledge about the quality and organisation of care to terminally ill cancer patients with a relatives' view in a primary health care setting is limited.
The aim of the study is to analyse experiences and preferences of bereaved relatives to terminally ill cancer patients in a primary care setting to explore barriers and facilitators for delivery of good palliative home care.
Three focus group interviews with fourteen bereaved relatives in Aarhus County, Denmark.
Three main categories of experience were identified: 1) The health professionals' management, where a need to optimize was found. 2) Shared care, which was lacking. 3) The relatives' role, which needs an extra focus.
Relatives experience insufficient palliative care mainly due to organizational and cultural problems among professionals. Palliative care in primary care in general needs improvement and attention should be drawn to the "professionalization" of the relatives and the need to strike a balance between their needs, wishes and resources in end-of-life care and bereavement.
Definition and implications of Shared care
«Shared care is the joint participation of general practitioners and hospital consultants in the planned delivery of care for patients with a chronic condition, informed by an enhanced information exchange over and above routine discharge and referral letters» 
Shared care demands knowledge of the abilities and the qualities of the cooperating partners, but also accept of each others' roles in the delivery of palliative care .
One group of health care professionals often involved is the primary care professionals, e.g. the general practitioners (GPs).
GPs are expected by their patients, policy makers and health organisations to be involved in palliative home care [2, 3]. Many GPs consider palliative care to be typical GP work and one of the best parts of the job . The traditions and values of general medicine corroborate the intentions of palliative care [5, 6], e.g. in seeking a continuing relationship between patient, family and professionals, the continuity of care  and the ability to perform care in co-operation with other health professionals .
GPs' management of palliative care, especially symptom control, has often been a subject of debate. It has been suggested that poor delivery of care in the primary sector may be a major reason why the majority of cancer patients die in hospitals despite their and their relatives' preference for a home-death [9–11]. Hence, there is a profound need for a deeper insight into barriers and facilitators for delivery of good palliative home care.
Evaluation of palliative care has often focused on clinical measures, e.g. the professionals' ability to provide symptom control, at the expense of the cancer patient's and relatives' perception of the total care delivery in the terminal phase. However, the bereaved relatives have invaluable experience of primary health care delivery from the terminal diagnosis until bereavement.
We therefore aimed to analyse experiences and preferences of bereaved relatives to terminally ill cancer patients in a primary care setting to explore barriers and facilitators for delivery of good palliative home care.
We conducted three qualitative, semi-structured group interviews with fourteen relatives of recently deceased cancer patients in Aarhus County (640 000 inhabitants), Denmark (5.5 million inhabitants) from June to October 2005.
The Danish Health care system is financed through taxes and provides free and equal access to health care services. More than 98% of the Danes are registered with a GP and receive free medical care . Danish GPs provide most of the health care themselves and act as gatekeepers for access to specialist treatment.
Specialist palliative teams with consultants, nurses and other healthcare providers are attached to the three major hospitals in the County of Aarhus, and the GPs can refer patients to these teams or ask the specialists for advice. These teams are only available during normal daytime hours.
Palliative home care is divided into a basic and a specialist level . The basic level professionals are the primary care sector, e.g. the GPs, the home care nurses and home care services. The professionals involved in specialist level home care are the primary care sector plus a palliative specialist team, working either as consultants or as active professionals in the patient's home.
At the moment there is no formalised education in palliative care of significance at the pre-graduate level of doctors in Denmark. At the level of specialising toward General Medicine there is a one-day course of theoretical aspects of palliative care. The Danish GPs can participate in non-compulsory courses in palliative care, but these courses are in competition with courses in all other aspects concerning general medicine.
Inclusion criteria for bereaved relatives
Nr of Informants
Group interview number
Relation to deceased
Age of relative
Age of deceased
Type of cancer
Place of death
Months from death to interview
Deceased cancer patients: (14 patients (100%))
7 patients (50%)
7 patients (50%)
Age at time of death, median (range)
64.5 years (44; 83)
Patients in contact with a specialist palliative care team
11 patients (79%)
Place of death:
7 patients (50%)
(14 patients (100%))
3 patients (21%)
2 patients (14%)
Short-term nursing home
2 patients (14%)
Time from patient's death to interview with relative, median (range)
6 months (1; 16)
Relatives interviewed (14 informants (100%))
11 informants (79%)
3 informants (21%)
Family relationship to patient
8 informants (57%)
4 informants (29%)
2 informants (14%)
Age at interview, median (range)
52 years (40; 75)
Place of residence
3 informants (21%)
5 informants (36%)
6 informants (43%)
All group interviews were conducted at The Research Unit for General Practice, The University of Aarhus. The group interviews were conducted by MAN, who was supervised by the co-authors, JS or FO. All three are specialists in general practice and JS and FO are GPs. MAN has completed courses in interview technique and analysis, and JS and FO are experienced in qualitative research methods.
Topic guide themes
Examples of questions
The health professionals' management
The role and management of the GP
How where the management of the GP involved?
What was good/bad?
How could it be improved?
Which role did you wish the GP had played?
(Following aspects were elaborated about the GP: knowledge, resources, availability, continuity, barriers)
Discharge from hospital care to home care
How was the quality of the discharge from the hospital?
How was the co-operation in this situation among the sectors?
What was good/bad?
How could it be improved?
How was the co-operation among the GP and the home care nurses/services?
How was the co-operation among the GP and the hospital/palliative specialist teams during the course of disease at home?
What was good/bad?
How could it be improved?
Organisation of palliative care
How do you think palliative care should be organised?
The role of the relatives
Did you get enough support from the professionals involved as a relative?
What was good/bad?
How could it be improved?
The group interviews were transcribed verbatim by a trained professional secretary. All transcripts were read simultaneously with the sound of the tapes by MAN to ensure correctness of the transcription and were read repeatedly by the authors to get an overall impression of the material before the initial coding . A qualitative description approach was used for the analysis. Following this analytic approach we enhanced rigour by focusing on the following strategies: 1) authenticity, the attention to the voices of participants and the ability to remain true to the phenomena under study, 2) credibility, a reflexion of how believable results are, 3) criticality, the critical appraisal of every decision made throughout the research process and 4) integrity, demonstrated by on-going reflection and self-criticality of the researcher .
All meaningful text units were identified and coded. The codes were subsequently grouped into relevant categories by MAN and at the end seven categories were identified, which again were grouped into three main categories. In this way we allowed the main categories to evolve from the data instead of imposing a framework a priori . No new categories emerged from the analysis of the third group interview.
Agreement was reached in the group of authors after thorough discussion of the initial coding, the categories and the main categories. We used the software package NVivo, ed. 6 (QRS international, Melbourne, Australia) to assist in the coding, sorting and retrieval of data.
The health professionals' management
The analyses revealed that the relatives found three aspects of the professionals' management of palliative home-care to be important: The professionals' knowledge, their behaviour and communication skills and their contact with patient and families.
The health professionals' knowledge
"As soon as we were there, the GP looked things up on the computer and she knew all the time what was going on... she really did." (Informant 10)
"... when the GP cannot manage, he should refer to someone who can. Our GP is the kind of person who thinks he knows best." (Informant 2)
The health professionals' behaviour and communication skills
"... a good thing about my GPs is ... both the female and the male GP in my practice are very competent and have the skills necessary to talk to the patients. They have a way with people." (Informant 1)
"And as I told you before, our own GP actually referred to me as "the widow" already in advance. I think that was a very improper remark." (Informant 2)
"They must have a flair for breaking bad news. Some doctors think you have to know everything, whether you want it or not" (Informant 6)
The professionals' contact with patients and families
"... perhaps the GP could do a little outreach work and phone us asking how we were doing ... the GP did not have the slightest idea of what was going on." (Informant 9)
The relatives described how hard it was always to be the one to take initiative.
"I think it has been very hard work the way we constantly having to keep abreast." (Informant 12)
"The GP spontaneously came to visit us every day until it was over. He came and asked if there was anything he could do. And it was an incredible relief not having to call him first... Then, I really felt that he gave me all the support a doctor could give."(Informant 13)
The informants found it important to know whom to contact during the out-of-hours periods, e.g. evenings, nights, weekends and national holidays. In some cases, the GP gave the family his or her private telephone number for such situations, which was highly appreciated, while others had to use the on-call GPs who were unfamiliar with the patient. The informants also appreciated whenever the health care professionals made an active contact after bereavement, because they often felt left in limbo.
Three categories emerging from the analyses addressed shared care between the different professionals involved: Professional responsibility, inter-professional culture and inter-professional communication
"You see, at first, when we were told by the hospital physician that there was nothing more to do but control the pain, at that time, I felt left alone... ... We were simply left in limbo." (Informant 2)
"Well, I think the GP should have the opportunity to be in charge of the coordination..." (Informant 5)
"... it was not a comforting message we got, that our GP had referred my husband to the hospital too late ... they told us that straight out. A hospital physician told us that they always get the patients too late from that municipality." (Informant 11)
The insinuation of other professionals' incompetence gave the relatives a feeling of insecurity and they did not know whom to trust.
"Honestly, I sometimes think that there is a wide gap between the GPs and the hospitals ... Well, I wish they had closer contact." (Informant 1)
"Our GP asked me to call him, when I got news from the hospital, because it often took too long before he got the information himself..." (Informant 6)
"But I know that the home nurses were very frustrated because they couldn't contact our GP." (Informant 14)
The role of the relatives
All relatives stated that before the patient's death both they and the patients wished that end of life care and death should take place at home. Despite that, only half died at home (Table 4).
"They should be better at explaining people what it actually means to take your loved ones home and care for them there. How much help you can actually get ... And it is not dangerous because the professionals are there for you, all of them."
"My husband's family noticed that when I was with my husband, I did not act as his wife, but as a professional when it came to care and when the GP visited..." (Informant 6)
"I insisted on being allowed to be just a relative. And that was difficult although I told them I had a right to that." (Informant 14)
"... you have to be available twenty-four hours a day. My eighty-year-old dad cried at night when it became too much for him taking care of my terminally ill mother. "I cannot do this anymore", he cried. And then I had to take over..." (Informant 14)
In one case the relative stated that the burden of the role of a "semi-professional" meant that the family gave up on the possibility of home death. This left them with a feeling of inadequacy as relatives since they could not fulfil the patient's wish for a home death.
Since the relatives felt an unspoken pressure from the professionals to be "semi-professionals" themselves and a "professionalization" of the relatives took place, the relatives asked for health professionals who had the necessary knowledge, who were readily available to the patients and their families and more active in establishing personal contact with them. They also described both organizational and cultural problems in the health care system.
Focus group interviews are pertinent, as individual interview to explore the informants' perspectives and experiences concerning a specific topic. The force of group interview is that the interaction in the group can be utilised as a factor of development of views and description among the participants and can make new themes or aspects of the topic emerge . In this way one gets a broad elaboration of the topic. In our study the group setting made new themes emerge but it also gave the relatives a valuable feeling of shared experience and of being able to support each other in the interview situation.
Interviews with terminally ill patients could have added important information to our study, but arranging interviews with terminally ill patients would have entailed ethical and practical difficulties disproportionate to the added value. Choosing close relatives who had participated in the palliative care as informants gave us an insight into the patients experience as well and it gave us the opportunity to explore the role of the relatives.
There was a surprising polarization in the experiences of GPs' management of palliative care. However, most experiences were negative in nature. This may be due to the fact that the relatives who agreed to participate in the group interview were the ones who needed to express their bad experiences which the authors feel that there is a tendency towards in the Danish society or of course might be due to an actual bad performance of the GPs involved. However, this can not be determined in a qualitative study, and will require a follow-up with a quantitative study.
The fact that the interviewers (MAN, JS, and FO) were all specialists in general practice could bias the group interviews and the analyses, but all authors were aware of this potential problem .
In earlier studies of the professionals' management of palliative care some relatives were not satisfied with symptom control in primary care, but they still rated the overall GP care as very good . The overall satisfaction with the GPs was significantly associated with symptom control, time to listen and accessibility . GP home-visits may increase terminally ill cancer patients' possibility of dying at home . In our study, continuity of care and good knowledge of the whole course of disease were among the reasons why the GPs were valued despite their at times poor management of palliative care.
Most studies examining the relatives' role have described that the relatives become emotionally and physically exhausted [11, 23]. We found that an important reason for this could be their "professionalization" and the absence of support from health care professionals, particularly after bereavement. It is important that the professionals help the relatives strike a balance between their needs, wishes and resources [23, 24]. This balance can be difficult to find in end-of-life care situations, where the relatives feel obliged to fulfil the wishes of the dying relative.
The importance of communication between GPs and specialists and the request for shared care have also been found in other palliative studies [25–28]. Also in line with our findings, these studies emphasize that continuous contact with the GP can be maintained by referring the patients back to their GPs after hospitalization, by ensuring good communication between specialists and GPs and by providing a clear definition of the GP's role . However, a fundamental prerequisite for successful shared care is the presence a coordinator . The need for and lack of shared care is well-described, but the reasons for this lack of shared care and ways of improving it are less well-explored. From our study it appears that one of the main barriers to optimizing shared care may be the lack of a shared care culture among health professionals and the lack of a home-care team leader in palliative care.
The issue of "professionalization" of the relatives was an important finding of our study and the extend and significance of this aspect should be further elaborated in future research. It is a challenge to all professionals involved in palliative home care to help relatives to strike a balance between the needs, wishes and resources f the relatives.
Another main challenge to the health care system is to create a shared care culture characterised by cooperation and mutual respect among professionals within the health care system. Further research in this subject is in place, but it seems that the respect and knowledge among different types of professionals are to some extend missing, and maybe shared care is missing as a focus already in the education and training of doctors, nurses and other professionals involved.
Hence, in order to optimize palliative home care, further research is required into how to develop a shared care culture, how to improve communication along the cancer journey, how to delegate professional responsibility and on relatives role.
A questionnaire survey among relatives, home care nurses and GPs is currently being conducted in order to give quantitative estimates of the distributions of opinions and experiences.
Our study indicates that relatives experience insufficient palliative care, mainly due to organizational and cultural problems among professionals. There is a lack of shared care. Palliative care in primary care in general needs improvement, both in terms of professional knowledge, attitude, availability and communication skills. Furthermore, attention should be drawn to the "professionalization" of the relatives and the need to strike a balance between their needs, wishes and resources in end-of-life care and bereavement.
The authors would like to express profound gratitude to all informants for participating.
We thank the home care nurses in Aarhus County and The Palliative Team at the Aarhus University Hospital who helped us identify potential informants.
The study was funded by The County of Aarhus and The Danish National Research Foundation for Primary Care.
The study has been approved by the local ethical committee.
- Bliss J, Cowley S, A W: Interprofessional working in palliative care in the community: a review of the literature. Journal of interprofessional care. 2000, 14: 281-290. 10.1080/713678572.View ArticleGoogle Scholar
- Department of Health: The NHS Cancer Plan. A plan for investment, A plan for reform. 2000, London, Department of HealthGoogle Scholar
- The Danish National Board of Health, Kræftstyregruppen: [National Danish Cancer Action Plan] National kræftplan 2. 2005Google Scholar
- Groot MM, Vernooij-Dassen MJ, Crul BJ, Grol RP: General practitioners (GPs) and palliative care: perceived tasks and barriers in daily practice. Palliat Med. 2005, 19: 111-118. 10.1191/0269216305pm937oa.View ArticlePubMedGoogle Scholar
- Allen J, Gay B, Crebolder H, Heyrman J, Svab I, Ram P: The European Definitions of the Key Features of the Discipline of General Practice: the role of the GP and core competencies. Brit J Gen Pract. 2002, 52: 526-527.Google Scholar
- WHO Technical Report Series. Cancer Pain Relief and Palliative Care. Report of a WHO Expert Committee. 1990, Geneva, World Health Organization, 7-67.Google Scholar
- von B, Eliasson G, Sarvimaki A, Mattsson B, Hjortdahl P: Patients' views on interpersonal continuity in primary care: a sense of security based on four core foundations. Fam Pract. 2006, 23: 210-219.Google Scholar
- Nielsen JD, Palshof T, Mainz J, Jensen AB, Olesen F: Randomised controlled trial of a shared care programme for newly referred cancer patients: bridging the gap between general practice and hospital. Qual Saf Health Care. 2003, 12: 263-272. 10.1136/qhc.12.4.263.View ArticlePubMedPubMed CentralGoogle Scholar
- Thomas C: The place of death of cancer patients: can qualitative data add to known factors?. Soc Sci Med. 2005, 60: 2597-2607. 10.1016/j.socscimed.2004.10.020.View ArticlePubMedGoogle Scholar
- Hanratty B: Palliative care provided by GPs: the carer's viewpoint. Br J Gen Pract. 2000, 50: 653-654.PubMedPubMed CentralGoogle Scholar
- Brazil K, Howell D, Bedard M, Krueger P, Heidebrecht C: Preferences for place of care and place of death among informal caregivers of the terminally ill. Palliat Med. 2005, 19: 492-499. 10.1191/0269216305pm1050oa.View ArticlePubMedGoogle Scholar
- de Fine Olivarius N, Hollnagel H, Krasnik A, Pedersen PA, Thorsen H: The Danish National Health Service Register. Dan Med Bull. 1997, 44: 449-453.Google Scholar
- The National council for palliative care: Palliative care explained. 2007, [http://www.ncpc.org.uk/palliative_care.html]Google Scholar
- Research Methods for Primary Care, Vol.3. Doing qualitative research. Edited by: Crabtree BF and Miller WL. 1992, Newbury Park, Sage PublicationsGoogle Scholar
- Donabedian A: The quality of medical care. Science. 1978, 200: 856-864. 10.1126/science.417400.View ArticlePubMedGoogle Scholar
- Giorgi A: Sketch of a psychological phenomenological method. Phenomenology and psychological research. Edited by: Giorgi A. 1985, Pittsburgh, Duquesne University Press, 2: 23-85. 1Google Scholar
- Sandelowski M: Whatever happened to qualitative description?. Res Nurs Health. 2000, 23: 334-340. 10.1002/1098-240X(200008)23:4<334::AID-NUR9>3.0.CO;2-G.View ArticlePubMedGoogle Scholar
- Milne J, Oberle K: Enhancing rigor in qualitative description: a case study. J Wound Ostomy Continence Nurs. 2005, 32: 413-420.View ArticlePubMedGoogle Scholar
- Pope C, Ziebland S, Mays N: Qualitative research in health care. Analysing qualitative data. BMJ. 320: 114-116. 10.1136/bmj.320.7227.114.Google Scholar
- Kitzinger J: Qualitative research. Introducing focus groups. BMJ. 1995, 311: 299-302.View ArticlePubMedPubMed CentralGoogle Scholar
- Lecouturier J, Jacoby A, Bradshaw C, Lovel T, Eccles M: Lay carers' satisfaction with community palliative care: results of a postal survey. South Tyneside MAAG Palliative Care Study Group. Palliat Med. 1999, 13: 275-283. 10.1191/026921699667368640.View ArticlePubMedGoogle Scholar
- Aabom B, Kragstrup J, Vondeling H, Bakketeig LS, Stovring H: Does persistent involvement by the GP improve palliative care at home for end-stage cancer patients?. Palliat Med. 2006, 20: 507-512. 10.1191/0269216306pm1169oa.View ArticlePubMedGoogle Scholar
- Grbich C, Parker D, Maddocks I: The emotions and coping strategies of caregivers of family members with a terminal cancer. J Palliat Care. 2001, 17: 30-36.PubMedGoogle Scholar
- Proot IM, Abu-Saad HH, Crebolder HF, Goldsteen M, Luker KA, Widdershoven GA: Vulnerability of family caregivers in terminal palliative care at home; balancing between burden and capacity. Scand J Caring Sci. 2003, 17: 113-121. 10.1046/j.1471-6712.2003.00220.x.View ArticlePubMedGoogle Scholar
- Steinhauser KE, Christakis NA, Clipp EC, McNeilly M, McIntyre L, Tulsky JA: Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA. 2000, 284: 2476-2482. 10.1001/jama.284.19.2476.View ArticlePubMedGoogle Scholar
- Norman A, Sisler J, Hack T, Harlos M: Family physicians and cancer care. Palliative care patients' perspectives. Can Fam Physician. 2001, 47: 2009-2012.PubMedPubMed CentralGoogle Scholar
- Evans R, Stone D, Elwyn G: Organizing palliative care for rural populations: a systematic review of the evidence. Fam Pract. 2003, 20: 304-310. 10.1093/fampra/cmg312.View ArticlePubMedGoogle Scholar
- Borgsteede SD, Graafland-Riedstra C, Deliens L, Francke AL, van Eijk JT, Willems DL: Good end-of-life care according to patients and their GPs. Br J Gen Pract. 2006, 56: 20-26.PubMedPubMed CentralGoogle Scholar
- Hickman M, Drummond N, Grimshaw J: A taxonomy of shared care for chronic disease. J Public Health Med. 1994, 16: 447-454.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-684X/7/1/prepub
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