Challenges in supporting lay carers of patients at the end of life: results from focus group discussions with primary healthcare providers
Family caregivers (FCGs) of patients at the end of life (EoL) cared for at home receive support from professional and non-professional care providers. Healthcare providers in general practice play an important role as they coordinate care and establish contacts between the parties concerned. To identify potential intervention targets, this study deals with the challenges healthcare providers in general practice face in EoL care situations including patients, caregivers and networks.
Focus group discussions with general practice teams in Germany were conducted to identify barriers to and enablers of an optimal support for family caregivers. Focus group discussions were analysed using content analysis.
Nineteen providers from 11 general practices took part in 4 focus group discussions. Participants identified challenges in communication with patients, caregivers and within the professional network. Communication with patients and caregivers focused on non-verbal messages, communicating at an appropriate time and perceiving patient and caregiver as a unit of care. Practice teams perceive themselves as an important part of the healthcare network, but also report difficulties in communication and cooperation with other healthcare providers.
Healthcare providers in general practice identified relational challenges in daily primary palliative care with potential implications for EoL care. Communication and collaboration with patients, caregivers and among healthcare providers give opportunities for improving palliative care with a focus on the patient-caregiver dyad. It is insufficient to demand a (professional) support network; existing structures need to be recognized and included into the care.
KeywordsFamily caregivers Focus group discussions Primary care Healthcare provider in general practice End-of-life care Palliative care
End of life
Project Verbesserung der häuslichen Versorgung von Palliativpatienten durch Unterstützung pflegender Angehöriger (Improvement of palliative care at home by supporting family caregivers)
Palliativmedizinische Initiative Nordbaden (palliative care initiative in northern Baden)
Percutaneous endoscopic gastrostomy tube
Spezialisierte ambulante Palliativversorgung (specialized ambulatory palliative care)
Most patients at the end of life (EoL) are at home and receive out-patient care in Germany. They face the challenge to organise their lives and optimize their quality of life . Decisions on the place of EoL care are influenced by available social support networks (involving lay carers such as family members, friends, and neighbours), preferences of patients, and supply of professional healthcare providers . Patients, whose families are involved in their care as family caregivers and whose families are able to cope with the palliative care situation, are less likely to receive hospital care at the EoL  and more likely to die at home . Admission to hospitals during the last days of life [5, 6] are often due to family caregivers feeling overburdened and without adequate professional support .
Lay carers are mostly family caregivers, friends and neighbours. Spouses comprise the largest part of those who support and care (28%), followed by daughters (26%) and parents (14%) . These caregivers often devote a large part of their time (on average 37 h per week) to the care of a single patient  which leads to social isolation and higher perceived caregiver burden . Caregivers are also prone to physical impairments, i.e. sleep deprivation and weight loss . Caregiving is not only physically demanding, lay carers often develop psychological symptoms, i.e. depression and anxiety [9, 10], they experience stress due to caregiving  and may need support themselves. A higher caregiver burden is associated with lower education and living together with the care recipient . Lay carers may receive support from other lay carers as well as professional healthcare providers. Coordination of care across all care givers is regarded a high priority by patients .
In Germany, palliative care has been developed as part of the hospice movement, which cumulated in the foundation of the first palliative care unit in 1983 . For outpatients with life-limiting advanced diseases and complex care needs, a national bill on specialized ambulatory palliative care (SAPV, §37b social security statutes book V) was introduced in 2007. Approximately 10% of outpatients were estimated to be in need of SAPV . For palliative outpatients without complex care needs, general practitioners (GPs) are traditionally in the best position to provide palliative care, including EOL care. A specific qualification program for GPs in palliative care or structured palliative care, comparable to the Gold Standards Framework in the United Kingdom , does not exist nationwide. There are local initiatives available, i.e. a palliative care initiative in northern Baden (PAMINO ). They also provide a platform for networking among general practices.
Networks can be used to share experiences with colleagues, since in Germany, general practices are mainly single-handed with few staff (medical assistants) . Medical assistants take over administrative tasks from physicians and are also increasingly involved in patient care, i.e. disease and care management and home visits . The practice teams should not only take care of the medical problems of patients, but also give social and logistic support. With patients at the EoL, healthcare providers in general practice are confronted with a complex situation involving both patients and caregivers as well as other healthcare providers. This study aims to close the knowledge gap about the challenges healthcare providers in general practice recognize which are posed by patients, lay carers, and professional carers in the care situation at the EoL of a patient and how the providers deal with those challenges.
Questioning guideline (main questions for reported analysis)
What motivated you at first to engage in palliative medicine?
What facilitates or hampers successful palliative care from your point of view?
Thinking of your last palliative care patient:
When did the family caregivers (FCs) get involved?
What was triggering the approach to the FCs?
Who initiates the contact between practice and FCs?
In which situations do you contact FCs directly?
What role does the staff actually play regarding the contact to the FCs?
How do you know if FCs are burdened?
What do you as a practice team do to support FCs?
What offers of assistance do you give?
How do FCs react to offers of assistance?
Can you remember a situation where FCs were especially reluctant or demanding? How did you react?
Do you talk about the possibility to admit the patient to a hospital? In which situations?
What has to change to enable your practice to better support FCs?
What kind of support would you like to have?
To take part in the focus group discussions, healthcare providers in general practice with a special interest in palliative care were approached. This was based on the premise that those practice team members would be more highly motivated to identify and develop a gold standard for palliative care in German general practice than a representative sample. This approach follows purposeful sampling with the aim of a homogeneous sample . The approached recruitment sample consisted of healthcare providers in general practice from the federal state of Baden-Wuerttemberg. It was intended that participants were currently taking care of palliative patients. Contact information for potential participants was sourced from the publicly available register of the Association of Statutory Health Insurance Physicians (Kassenärztliche Vereinigung) Baden-Wuerttemberg. All general practitioners with an additional qualification in palliative medicine were identified and invited to participate in the study. Invitations were mailed to 258 general practices with 275 general practitioners.
Four 90-min focus group discussions were part of 2 recruitment meetings where the study was introduced and some background information on lay carers provided (i.e. facts on how many people take care of a family member underlining the importance of the topic). For the purpose of getting a multi-faceted picture, focus group discussions were mixed (general practitioners (GPs) and medical assistants), but GP and assistants from one practice did not attend the same focus group discussion. The focus group discussions were moderated by one of 3 members of the research team, who all had extensive experience in conducting focus group discussions and had also been involved in developing the questioning guideline (2 medical doctors (PE, FPK) experienced in qualitative research, 1 social scientist (KK)); the moderating medical doctors were also working as GPs and had an additional qualification in palliative medicine. The focus group discussions took place in the Department of General Practice and Health Services Research; GPs interested in the study but not able to attend the focus group discussions were asked to take part in a telephone interview covering the same aspects as the focus group discussions. Before conducting focus group discussions and interviews, all participants provided written informed consent to participating in, audio-recording and analysis of the focus group discussions.
The structured focus group discussions and interviews were audio-recorded and transcribed verbatim. Transcripts were analysed with content analysis  using ATLAS.ti. Two researchers (RAB, KK) reviewed and coded the transcripts independently. First, codes were derived deductively on the basis of the questioning guideline (Table 1); additional topics were derived inductively from the transcripts. During the iterative coding process, the codes were regularly compared, discussed and adapted for further use in the analysis. Finally, consensus was reached with a third researcher (FPK). The whole research team discussed and interpreted the results. While the analysis was performed on the original German data, quotes are translated into English for reporting in this paper.
Description of participants
Focus group discussion 1
practice of GP3
additional palliative care certificate since 2 years
practice of GP4
practice of GP4
since 10 years in the practice
since 22 years in the practice, qualification in palliative medicine since 1 year
since 26 years in the practice, qualification in palliative medicine since 5 years, SAPV
Focus group discussion 2
practice of GP2
since 9 years in the practice, additional palliative care certificate
practice of GP1
since 24 years in the practice, qualification in palliative medicine since 1 year
with S2 and S3
general practitioner since 10 years, since 6 years in the practice
since 27 years in the practice
Focus group discussion 3
since 13 years in the practice, qualification in palliative medicine since 7 years
since 12 years in the practice, qualification in palliative medicine since 3 years, SAPV
since 1 year in practice after neurosurgery for 14 years and general practice for 4 years
same practice as GP11
qualification in palliative medicine since 2 years
Focus group discussion 4
practice of GP7
since 1 year in the practice after completing training in another practice
practice of GP6
since 5 years in the practice after working in hospital
since 10 years in the practice, qualification in palliative medicine since 5 years, care of palliative patients for at least 20 years
same practice as GP9
qualification in palliative medicine since 3 years
since at least 20 years in the practice, qualification in palliative medicine since 1 year
Telephone interview 1
Telephone interview 2
since 3 years in the practice after geriatrics
Challenges with patients
The majority of the participants faced challenges in dealing with patients, especially when they encountered resistance or reactions they did not anticipate: (1) they needed to recognize and accept non-verbal forms of the patient’s volition, (2) they needed to communicate according to the situation, and (3) they needed to realize their own attitudes regarding an “appropriate” death.
With dementia patients […] if someone does not eat or drink anymore, that’s also a form of volition. Then I would absolutely refrain from any infusion or PEG (percutaneous endoscopic gastrostomy tube) or subcutaneous or else. (GP3).
I sometimes notice that if you want to organise things ahead […] but the patient is reasonably well, they decline. (GP6).
For 2 years, I had an old lady, where I asked the relatives to get her into a nursing home, since the couple at home were both heavy alcoholics. And I thought it would be actually awful for this old lady if she had to die at home. (GP12).
Challenges with lay carers
In their contact with caregivers, participants reported a wide range of relations to caregivers: (1) not knowing the relatives of a patient, not knowing if a patient is also a caregiver, but also having a long and close relationship to the caregiver. Healthcare providers were also (2) challenged by either demanding or refusing family caregivers and found individual ways to cope in such situations.
We definitely have people, where we don’t know what’s happening at home. (GP7).
Usually, they are patients we’ve known for years. We’ve known them since we’ve had the practice. And then we know the family structure, too. (GP9).
Of course it happens that the relatives come in a state of absolute exhaustion and then dump everything on the table and say: Now it doesn’t work anymore. And now you (the doctor) best do something immediately. (GP4).
Caregivers, who expect, that others …, that […] everything will be done, and who need to be nudged to become active by themselves. (GP14).
It goes both ways. There are relatives, who [struggle to accept the patient does not] want any therapy anymore, and then try to really convince the patient to do otherwise. (GP6).
A nursing home was not an option for them both. They didn’t want to. The doctor advised to go to a nursing home. No. (S5).
If you offer something in this (early) stage, it will be mostly rejected. [They say:] “No, I don’t need that yet or it is okay or I can do it.” […] would be ideal, to get there at the right time. (GP4).
I try to address diplomatically that they are the most important persons and that their health is enormously important for the patient. Even if the caregiver is not one of my patients, it is the interest of the patient to have a healthy caregiver in all respects. Mentally, and physically. (…) That the quality of the care deteriorates if the exhaustion gets too much. (GP4).
Challenges within the professional network
To provide high-quality palliative care, healthcare providers in general practice need to work together with local professional support. They are involved in a multidisciplinary network which facilitates cooperation and involves nursing services, physiotherapy, spiritual care, volunteers and others.
At the same time, practice team members are faced with challenges within the network: (1) structures are missing, (2) the communication between cooperating partners does not involve all relevant information, and (3) partners who should cooperate in patient care are also competitors on the healthcare market.
We don’t have a hospice, we don’t have a palliative care unit. (GP12).
This gap between hospital and practice. Discharge on Friday afternoon, should get antibiotics and analgesics etc. I see the fax message maybe Saturday morning or Monday morning. (GP5).
An 88-year-old was discharged. I just had her admitted for transfusion, because she was anaemic again and again, and I almost knew there had to be a malignancy behind that. So I had her specifically admitted only for transfusion, and still they did a colonoscopy or tried to do it. Stenosing colorectal carcinoma, and now the clinic offered her an operation. (GP7).
The building of the team was difficult, since the nursing services are firstly competitors and sometimes quarrelling among themselves. But since we physicians took the initiative (…), we brought them all together using really a lot of diplomacy and tact. And so all of a sudden, the structure, the nursing services among themselves, has changed. (GP7).
Healthcare providers in general practice are faced with a multitude of challenges in EoL care in communicating with patients, lay carers and other professional healthcare providers. From their point of view, practice team members have to deal with an appropriate communication with patients, interpreting patients’ non-verbal messages and reacting accordingly. They need to identify lay carers and to find ways to deal with inappropriate demands and unnecessary refusals of support. They perceive themselves as an important part of the healthcare network, but also report difficulties in communication and cooperation with other healthcare providers.
To recognize the appropriate time to communicate with patients and to perceive patients’ behaviour as a non-verbal expression of their wishes are essential communication skills in general practice. In EoL care, not only communication with patients but also with caregivers and within the professional network is of paramount importance. General practice teams need to be aware of the high potential of challenging situations as described in our study.
A systematic review showed that direct support of caregivers can reduce their psychological distress . The interventions described comprise home visits by nurses of up to 1.5 h which are not feasible for German general practices. The topics important for family caregivers , on the other hand, are addressed in general practice, i.e. caregivers learn about symptom management, their health needs are discussed and they receive support provided by social networks and health services providers . The results of the present study additionally stress the importance of communication with patients, caregivers and other health care providers to bring offers and demands of support together.
Another systematic review  summarized facilitators for a good patient-physician communication: the availability of the GP and the initiation of EoL issue discussions. Our participants additionally stressed the point of finding the right moment to initiate discussions with patients and caregivers to lead to effective results. Thus, communicating with and supporting the patient-caregiver dyad needs to be individually targeted . Additionally, it underscores the importance of integrating early palliative care also in the primary care of diseases other than cancer .
Contrary to the situation in several other countries, such as the UK, general practices in Germany are not contractually required to identify (family) caregivers . Still, the challenges for identification are comparable: family caregivers perceive themselves as relatives in the first place before considering themselves as carers . As our participants reported, family caregivers have to be made aware of their need for support, even though they might refuse it. The healthcare providers perceived patients and caregivers as a unit of care and caregivers as potential “hidden patients”  and tried to support them to prevent caregiver collapse.
The perception of patients at the EoL and their caregivers leads to reflections on professional attitude which emerge not only in communication but also in the expression of practice team members’ personal values and the evaluation of cooperation within the professional network.
While working with palliative patients and their family caregivers, healthcare providers in general practice are faced with their own assumptions of a “good” death, which goes further than the biomedical and psychosocial perspective  and might not concur with the views of patients and caregivers . In our study, this topic was not explicitly addressed and thus, is not within the scope of this paper. In addition, to further analyse implicit assumptions of healthcare providers, another methodological approach would be needed.
The communication and cooperation with other healthcare providers needs to be optimized. The statements of the participants demonstrate that the communication has to be improved in both ways: from the practice to other service providers as well as from other service providers to the practice. All partners have to clarify their role and their expectations. This might also strengthen the communication with caregivers, who reported both unmet psychosocial needs and poor coordination of health-care services in a systematic review .
The results of our study show challenges of German healthcare providers in general practice, which were considered challenges in other European countries as well. In the UK, the Gold Standards Framework  addresses those topics and gives practice teams a guideline to deal with i.e. communication, coordination, and carer support. The assessment of burden in family caregivers poses a major challenge for general practitioners. Approaches for assessment have been described by Adelman et al. in a review , but to date in Germany no formal assessment strategies have been implemented. However, recent initiatives in the form of “burden relief programs for family caregivers”, e.g. by the national elderly care insurance fund, have been introduced . Nevertheless, awareness of such initiatives among general practitioners needs to be raised. Promotional information could be shared through GP networks. Recent evidence indicates German GPs actively utilize the German palliative care guidelines . Information on burden relief programs for family caregivers could be included in this resource. Certainly there is room for improvement of palliative care in German primary care to be further improved on policymaking, practical and educational level . Furthermore, our results are in agreement with other studies dealing with organizational challenges , the importance of communication and continuity in patient care as well as to the family caregivers [38, 39].
Strengths and weaknesses of the study
This study is part and the first step of a project to design and develop an intervention that may be implemented and evaluated in primary care to support lay carers. Focus group discussions were conducted with healthcare providers from general practices who were potential participants in the project . They aimed at identifying facilitators and barriers of optimal palliative care in general practice, particularly on supporting lay caregivers. As a result of the focus group discussions, interventions were developed together with participants in the further project process .
The results are based on focus group discussions with a highly selective sample. We purposefully included primary healthcare providers with a special interest in palliative care. Thus, the participants were probably more familiar with the situation of family caregivers of patients at the EoL and could share the strategies they had developed to deal with the specific challenges occurring in such complex situations. We did not countercheck the impressions of the participating healthcare providers with the views of patients, lay carers, and other professional caregivers. Therefore, their views remain highly subjective and might be due to individual perceptions. In spite of this subjectivity, the topics were generally taken up by the participants of the focus group discussions. Reported experiences of general practice teams from our study are in part addressed in findings of studies examining the patient/caregiver end of the EoL care continuum. In particular, communication difficulties with general practitioners, inconsistencies and discontinuity of care have been reported .
Although it is a sample of health care providers, participants could vividly report on the challenges they are faced with in palliative care. However, due to the mixture of GPs and medical assistants in the focus group discussions, statements might be influenced by a possible social status gradient. We sought to minimize this potential bias by assigning members of the same practice team to different focus group discussions that took place in parallel. Additionally, the experienced moderators were conscious to invite reticent participants to share their thoughts and opinions. Nonetheless, there could be other challenges participants were not aware of and therefore did not report. Still, it could be assumed that the challenge for healthcare providers in general practice teams without a special interest in palliative care is even greater.
Healthcare providers in general practice identified many relational challenges in daily primary palliative care. Based on our findings, strategies to resolve these may concern the dimensions knowledge, professional attitude and skills which could be further supported and developed as part mixed interventions with educational and organisational elements. Our results indicate that it is insufficient to demand a support network; existing structures need to be recognized and included into the care in general practices. At the same time, motivations contrary to collaborative care due to a competitive healthcare market need to be considered. Additionally, healthcare providers in general practice should assess the relationship between patients and caregivers as a significant reason for accepting or denying support.
We sincerely thank Sarah Jane Berger (Dept. of General Practice and Health Services Research, University Hospital Heidelberg) for language editing.
The study was supported by the German Ministry for Education and Research (Bundesministerium für Bildung und Forschung, BMBF, Grant Number 01GX1046).
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
KK, RB, PE, JS, and FPK conceived and designed the study. KK, RAB, RB, PE, and FPK acquired the data. KK, RAB, and FPK analysed the data. RB, PE, JS, and MW additionally contributed to the interpretation of the data. KK and RAB drafted the manuscript. All authors revised the manuscript for important intellectual content and gave final approval of the version to be published.
Ethics approval and consent to participate
The study was conducted in accordance with the Medical Professional Codex of the state of Baden-Wuerttemberg (2007) and the Helsinki Declaration as of 2008. The study protocol was approved by the ethics committee of the University of Heidelberg in May 2011 (approval number S-042/2011) with an unrestricted positive vote. All participants provided written informed consent before conducting the focus group discussions. We confirm all patient/personal identifiers have been removed or disguised so the patient/person (s) described are not identifiable and cannot be identified through the details of the story.
Consent for publication
The authors declare that they have no competing interests.
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- 3.Gott M, Frey R, Robinson J, Boyd M, O’Callaghan A, Richards N, Snow B. The nature of, and reasons for, ‘inappropriate’ hospitalisations among patients with palliative care needs: a qualitative exploration of the views of generalist palliative care providers. Palliat Med. 2013;27(8):747–56.CrossRefPubMedGoogle Scholar
- 8.Döhner H, Kofahl C, Lüdecke D, Mnich E. The National Survey Report for Germany. In: EUROFAMCARE Services for Supporting Family Carers of Older Dependent People in Europe: Characteristics, Coverage and Usage; 2007.Google Scholar
- 14.Voltz R. Palliativmedizin: Eine Disziplin für den “ganzen Menschen”. Dtsch Arztebl. 2008;105(1–2):A 20–2.Google Scholar
- 16.Engeser P, Reininghaus W, Zeise-Suess D, Wiesemann A. Palliativmedizin in Nordbaden (PAMINO-Projekt) Welche Einstellungen haben nordbadische Hausärzte zur Palliativmedizin. Z Allg Med. 2003;79:22.Google Scholar
- 21.Mayring P. Qualitative Inhaltsanalyse. In: Flick U, Ev K, Reinbek SI, editors. Qualitative Forschung Ein Handbuch. 5th ed. Reinbek: Rowohlt Taschenbuch; 2007.Google Scholar
- 22.Candy B, Jones L, Drake R, Leurent B, King M. Interventions for supporting informal caregivers of patients in the terminal phase of a disease. Cochrane Database Syst Rev. 2011;(6):CD007617.Google Scholar
- 23.Grande GE, Farquhar MC, Barclay SI, Todd CJ. Valued aspects of primary palliative care: content analysis of bereaved carers’ descriptions. The British journal of general practice : the journal of the Royal College of General Practitioners. 2004;54(507):772–8.Google Scholar
- 24.Krug K, Bölter R, Ballhausen RA, Engeser P, Peters-Klimm F. Burden experienced by family caregivers of patients at the end of life: what do general practice teams offer? Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)). 2016;78(S 01):e128–34.Google Scholar
- 25.Slort W, Schweitzer BP, Blankenstein AH, Abarshi EA, Riphagen II, Echteld MA, Aaronson NK, van der Horst H, Deliens L. Perceived barriers and facilitators for general practitioner-patient communication in palliative care: a systematic review. Palliat Med. 2011;25(6):613–29.CrossRefPubMedGoogle Scholar
- 33.Thomas K. Caring for the dying at home. Oxford: Radcliffe Publishing; 2003.Google Scholar
- 34.Hetzel C, Baumann R, Diekmann J, Frobose I. Description of a multidimensional health program for informal caregivers. Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)). 2016;2018;80:S51-S6.Google Scholar
- 39.Michiels E, Deschepper R, Van Der Kelen G, Bernheim JL, Mortier F, Vander Stichele R, Deliens L. The role of general practitioners in continuity of care at the end of life: a qualitative study of terminally ill patients and their next of kin. Palliat Med. 2007;21(5):409–15.CrossRefPubMedGoogle Scholar
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