Skip to main content

Positive attitudes to advance care planning – a Norwegian general population survey

Abstract

Background

Authorities recommend advance care planning and public acceptance of it is a prerequisite for widespread implementation. Therefore, we did the first study of the Norwegian public with an aim of getting knowledge on their attitudes to issues related to advance care planning.

Methods

An electronic survey to a nationally representative web panel of Norwegian adults.

Results

From 1035 complete responses (response rate 40.7%), we found that more than nine out of ten of the general public wanted to participate in advance care planning, believed it to be useful for many, and wanted to make important healthcare decisions themselves. Almost nine out of ten wanted to be accompanied by next of kin during advance care planning. Most (69%) wanted health care personnel to initiate advance care planning and preferred it to be timed to serious illness with limited lifetime (68%). Only about 9% stated that health care personnel should have the final say in healthcare decisions in serious illness.

Conclusions

Developing and implementing advance care planning as a public health initiative seems warranted based on the results of this study. Patient perspectives should be promoted in decision-making processes. Nevertheless, training of health care personnel should emphasise voluntariness and an individual approach to initiating, timing and conducting advance care planning because of individual variations.

Peer Review reports

Background

Advance care planning (ACP) may prevent decision-making conflicts by involving patients, their next of kin and health care personnel in discussions relevant for decision making before decisions are needed [1]. This is pertinent because end-of-life decision-making is often characterized by ethical problems that can give rise to moral distress for health care personnel [2]. Other potential benefits of ACP implementation range from increasing health care personnel’s comfort in engaging in end-of-life communication [3] to making treatment at the end of life more concordant with patient preferences [4]. ACP is thus recommended by authorities [5] and the European Association for Palliative Care [6].

Importantly, although policy makers endorse ACP and health care personnel recognize it, ACP has little value if patients and the public do not want it. Public opinion may help policymakers develop and implement targeted health care interventions [7] that the public want. While ACP in Norway is seldom (yet increasingly) used [8], it is recommended by the authorities [9]. Meanwhile, in the Norwegian legal framework, ACP is inadequately addressed. Certainly, Norwegian law acknowledges a patient’s right to consent to care and to participate in decision-making. However, Norwegian health laws can be considered quite paternalistic with much power given to physicians and other health care personnel, especially during emergency situations (health personnel act §7) and when patients have reduced/lost competence to consent (patient and user rights act §4–6) [10]. For patients without decision-making competency, the role of next of kin is limited to relaying what the patient has previously expressed about his/her wishes, and does not involve making decisions on the patient’s behalf (patient and user rights act). Information about the patient’s prior wishes shall be obtained by health care personnel and considered when making decisions. Therefore, for these patients to be involved in decision-making processes, it is pressing to talk with them while they are still able. ACP can facilitate this, but Norwegian public opinion about ACP is unknown.

Internationally, there are studies on older people’s attitudes towards ACP [11, 12] and on the public’s attitudes [13,14,15,16]. They indicate that while most people have thought about end-of-life care and decision-making [14] there is a wish for information about prognosis, diagnosis and available treatments when facing life-limiting illness [13, 15]. Furthermore, most seem willing to participate in conversations on end-of-life care [11, 12, 16]. We hypothesized that similar attitudes to ACP prevail in the Norwegian public. If so, it could give the national authorities an incentive to and a warrant for doing more in implementing ACP as a public health initiative. Consequently, we aimed to get knowledge on the Norwegian public’s attitudes on involvement in and preferences for decision-making processes, the usefulness of and willingness to participate in ACP, involvement of next of kin, initiation and timing of ACP, and study demographic determinants of ACP attitudes.

Methods

Design and population

A cross-sectional survey study was conducted. In December 2019, an electronic questionnaire was distributed by the commercial firm Kantar to members of their nationally representative web panel of adults [17], via email. The web panel has 40,000 members who have agreed to answer surveys. As compensation, panel members receive points, which can be spent on gifts, gift cards or donated to charities. Number of points received varies depending on the length of the survey, and panelists are informed about the number of points they will receive when invited to do a survey. Panel members were invited successively until the target number of 1000 responses had been reached. Reporting adheres to the STROBE checklist [18].

Questionnaire

The questionnaire had three sections; this study regards the final section, which was about ACP, while the first two sections explored issues on priority settings in health care and end-of-life decision-making. The questionnaire was in Norwegian, and was designed based on international research on ACP [11, 12], policies, philosophical traditions on autonomy [19], and supported decision-making [20]. It was developed through discussions among the authors. Laypersons pilot tested the electronic version in two stages. Survey questions with corresponding response alternatives are shown in Table 1.

Table. 1 Survey questions and response alternatives

In the questionnaire, ACP was defined and described as “a conversation between patient, health care professional and often also relatives. It is about what is important to the patient, as well as preferences for medical treatment and care. Advance care planning is often offered to elderly patients and patients with chronic and serious illnesses. Through such conversations, it becomes easier to act in accordance with the patient’s wishes and values at a later date, especially if the patient is no longer able to choose for themselves.” The definition and description was inspired by other definitions [21, 22] and our own and others’ research on ACP [3, 23,24,25,26].

Statistical analyses

Statistical analyses were performed with IBM SPSS Statistics version 26. Responses were weighted according to gender, age, and geographical region so that responses from groups underrepresented among the respondents were given increased weight (Table 2). Analyses were performed on weighted data.

Table. 2 Respondent characteristics. N = 1035

We performed multiple logistic regression analyses to calculate odds ratios with 95% confidence intervals for the relationships between decision-making preferences and ACP attitudes (dependent variables), and demographic characteristics (independent variables). Dependent variables were scored on a five-point Likert scale with “fully disagree” (=1) and “fully agree” (=5) as scale anchors.

We dichotomized independent and dependent variables. The dependent variables were dichotomized into “Disagree/neither nor” [1,2,3] and “Agree” [4, 5]. Dichotomized independent variables in the analysis included: religious view of life (“non-religious” indicated “atheist/agnostic” and “non-religious”), highest completed education (“higher education” indicated college/university degree of a length of 3 or more years), and trust in the public health care services (“high trust” indicated response ranging from 7 to 10 on a scale from “no trust” (=1) to “full trust” (=10)). In addition, age, gender and contact with general practitioner (GP) were independent variables. Dichotomized variables excluded ‘do not wish to state’ responses, which led to missing cases in the analysis.

Results

2540 panel members were invited, and 1076 responded. We received 1035 complete responses (response rate 40.7%). Information on the demographic characteristics of the respondents is presented in Table 2.

ACP attitudes and decision-making preferences

A majority of respondents would like to participate in ACP (91.8%) and even more thought ACP could be useful for many patients (93.9%). Many respondents agreed that it was important for them to make important healthcare decisions themselves (92.5%). Interestingly, only 9.2% of respondents wanted health care personnel to have the final say in healthcare decisions, which was fewer than the alternatives ‘myself’ or ‘next of kin’. However, a majority wanted health care personnel to initiate ACP (69%), with most preferring the GP to initiate ACP (33%). Although many were positive to ACP, most seemed to be most inclined to participate at a time of chronic/serious illness and limited lifetime (68.6%; Tables 3 and 4).

Table. 3 Attitudes on decision-making, usefulness of and involvement in advance care planning
Table. 4 Attitudes on final say in decisions, initiation and timing of advance care planning

Factors associated with decision-making preferences and ACP attitudes

The proportion who wanted to participate in ACP was higher for female respondents and for those with a “high trust”; these were statistically significant associations (Table 5). Persons 60 years or older and “non-religious” tended to be more likely to want to participate in ACP, although not statistically significant. Females were (statistically significant) more likely to: want to make important healthcare decisions themselves, think that ACP can be useful, and want to be accompanied by their next of kin during ACP. Persons with “high trust” were more likely to want to make important healthcare decisions themselves and think that ACP can be useful (statistically significant) and want to be accompanied by their next of kin during ACP (approximating statistical significance). In addition, the association between being “non-religious” and thinking ACP can be useful was statistically significant. We found no significant association between attitudes toward ACP and number of contact with GP, income and education.

Table 5 Characteristics of the general population associated with advance care planning attitudea

Discussion

This study indicates that more than nine out of ten in the general Norwegian population want to take part in ACP, want to make important healthcare decisions themselves and believe ACP can be useful for many. Many would participate together with their next of kin. Even though most thought that ACP should occur at the time of serious/chronic illness and limited lifetime and health care personnel should initiate ACP, only a minority thought health care personnel should have the final say in health care decisions. Females and respondents with “high trust” in the public health care services were more likely to be positive about both making important healthcare decisions themselves, viewing ACP beneficial and wanting to participate in ACP.

Public attitudes on ACP participation

Among barriers to doing ACP is a conception among health care personnel that patients do not want to participate in such discussions [27, 28]. Our results indicate that this is a misconception. The general public are mostly willing to participate in ACP according to other surveys in the Netherlands [14], South Korea [16] and in Singapore [29], although our results indicate even higher willingness in Norway. In addition, most respondents in a community intervention study were comfortable discussing their own end-of-life care [30]. In a systematic review, older persons have been found to be willing to discuss their end-of-life care [11]. Some older persons placed low value on ACP because they were comfortable having others decide for them [25]. However, ACP has been well received by patients, next of kin and health care personnel [3].

The overall willingness to and comfort in discussing end-of-life matters should make ACP an intriguing public health initiative – partly because ACP has a potential for contributing to improving end-of-life care [4, 31]. Knowledge of the public’s opinion is prudent when developing health care initiatives and for allocation of scarce resources. If the public is positive to initiatives, such as ACP, authorities and health enterprises may be more inclined to support their implementation. However, ACP is a complex intervention [32, 33], which makes successful implementation more difficult. The complexity of ACP coupled with a lack of implementation support [34], plus lack of public knowledge may contribute to explaining its low uptake [11, 14, 35]. In addition, overcoming barriers is important in achieving widespread use of ACP. Among reported barriers are uncertainty, lack of comfort and lack of knowledge among health care personnel in doing ACP [13, 28, 36,37,38]. Implementation of ACP thus warrants proper education, training and follow-up of health care personnel and leaders.

Patient participation in ACP improves when next of kin participate together with the patient [37, 39]. Furthermore, next of kin may be valuable in supporting patients during ACP, particularly for patients with reduced decision-making capacity. Next of kin support may strengthen the decision-making capacity of patients and is recommended as part of supported decision-making [20]. If the patient is willing, next of kin should be invited to ACP discussions.

Initiation and timing of ACP

The majority view in this study was that health care personnel should initiate ACP, which supports others findings [14, 25, 40]. Health care personnel must therefore recognize their responsibility in initiating the discussions in order to stimulate higher ACP uptake. However, initiation of ACP may be hampered by uncertainty about when such discussions are timely [25, 41].

Most respondents in this study preferred to participate in ACP at a time of chronic/serious illness and limited lifetime, which was higher compared to others [42]. However, that might run contrary to the idea of ACP being held while persons are still able to communicate [22]. In addition, health care personnel have indicated that ACP close to dying is “too close and tense” and a peaceful atmosphere is needed [43]. Health care personnel may worry about causing patients harm by having untimely ACP discussions [44] and this can increase the uncertainties about when ACP is timely. There is little indication that ACP causes distress to patients [25, 45], although it can be experienced as unpleasant and difficult issues should be addressed without “going too far” [39]. In sum, health care personnel need not be overly worried about ACP harming patients. Instead, a patient-centered approach to training, implementation and practice of ACP should be pursued. Identifying an optimal timing of ACP is difficult, because preferred timing is individual [25]. Consequently, optimal timing of ACP is when the patient is ready [39].

ACP has developed from advance directives (living wills) into the communicative process it is today during the past few decades [21, 46]. In Norway, and likely several other countries, ACP has been a tool available for health care services only within the last decade. Most patients accept ACP [47], few experience ACP as distressing [25] and Bhavsar and colleagues declared the “death of outrage over talking about dying” [48]. However, as a public health initiative, it is essential to keep in mind that not all patients want to participate in ACP [11]. Importantly, ACP participation is voluntary. This should be communicated in invitations to participate in order to give patients an opportunity to decline participation. An informative invitation to ACP that recognizes the patient’s right to decline may ease initiation and timing burdens for health care personnel.

Attitudes on decision-making

Fewer than one out of ten respondents wanted health care personnel to have the final say in healthcare decisions, if they get seriously ill. This is another striking result from this study. The survey question did not state that the patient lacked decision-making competence and competent Norwegian patients do have rights in consenting to healthcare decisions. Nevertheless, Norwegian law give physicians vast judicial power in decision-making when patients lack decision-making competence or in emergency care situations (independent of decision-making competence) [10]. However, our results may indicate that the public values patient, next of kin or shared decision-making over leaving decisions to health care personnel.

Respondents wanting next of kin rather than health care personnel to have the final say is supported by other studies [10, 12, 49]. In the Norwegian legal context, opinions of next of kin should not be decisive in end-of-life decision-making. Next of kin should instead contribute by relaying previous statements and values stated by the patient. Contrary to Norwegian law, there are indications that a majority of the Norwegian populace want decision-making authority [10]. Although in practice, next of kin seems to be receiving more responsibility in end-of-life decision-making than they ought to according to the law [50]. In addition, getting end-of-life decision-making responsibilities can be experienced burdensome for next of kin [51, 52].

Factors associated with decision-making preferences and ACP attitudes

Here we discuss factors associated with decision-making preferences and ACP attitudes. Most of the associations we found were in line with others research. Women have been found more likely to discuss ACP with family and friends and to engage in more ACP practices [53] and to think about end-of-life decision-making [14]. Older persons are more likely to being willing to engage in an ACP discussion [29], more likely to being engaged in ACP activities [53] and having thought about end-of-life decision-making [14]. However, contrary to our results, a survey among the Dutch public found that little trust in physicians complying with their wishes about medical care/treatment in the last days of life indicated a preference for making their own decisions [14].

Non-religious persons seem more engaged in ACP [14]. Adding to this is the higher likelihood of “non-religious” persons to refuse life-sustaining treatment at end of life [54]. A possible reason for religious persons more often opting to not participate in ACP and being more likely to accept life-sustaining treatment may be a desire not to interfere with God’s plan [55]. Furthermore, religious persons may be more inclined to view life as sacred – making future planning or life-sustaining treatment less attractive – or finding comfort in being in the care of God.

Differences in ACP attitudes between different sociodemographic groups give knowledge for policy makers and clinicians on developing and targeting ACP interventions. Importantly though, such variations emphasize the importance of a principle relevant to ACP involvement and end-of-life decision-making – voluntariness. If participation in ACP is not voluntary, health care services risk losing the public’s trust and compromising patient beneficence.

Strengths and limitations

This study is population-based founded on a representative sample of the Norwegian population. The moderate response rate might conceivably have contributed to a non-response bias.

As mentioned in the Methods section, the questionnaire consisted of three sections – priority settings, end-of-life decision-making, and ACP. We do not view ACP as end-of-life decision-making, rather a tool to prepare for this end-of-life decision-making in a way that promotes patient autonomy also if the patient is no longer competent to consent. However, the ACP section succeeding end-of-life decision-making may have prompted some respondents to think of ACP as end-of-life decision-making.

Our description of ACP included that “Advance care planning is often offered to elderly patients and patients with chronic and serious illnesses”. When asked about preferred timing of ACP, responses may have been influenced by similarities in the formulation of the most preferred response alternative (“At the time of serious/chronic illness and limited lifetime, independent of age”) and the information we provided on when ACP is usually offered.

ACP is today considered a process consisting of several conversations [21, 22]. Our definition did not sufficiently recognize ACP as a process. A more precise definition might have affected responses. However, we believe this would have led to more responses that are positive rather than negative, because viewing ACP as a process might offset any worries among respondents’ that ACP would not recognize changes to their needs and wishes.

Conclusions

ACP was largely wanted and viewed as useful for many patients, according to this survey of Norwegian adults. Developing and implementing ACP as a public health initiative thus seems warranted. The public responses further implicated that health care services should focus on promoting patient autonomy in decision-making processes. Health care services may want to tailor information about ACP and recruitment strategies to certain groups of society. For instance, men were less likely to want to participate in ACP compared to women in this study and developing ACP to the needs of men might increase the acceptance of ACP among them. Nevertheless, training of health care personnel should emphasize voluntariness and an individual approach to initiating, timing and conducting ACP. That would safeguard variations among patients’ preferences for involvement and could strengthen public trust in the health care services.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ACP:

Advance care planning

GP:

General practitioner

References

  1. 1.

    McMahan RD, Knight SJ, Fried TR, Sudore RL. Advance care planning beyond advance directives: perspectives from patients and surrogates. J Pain Symptom Manag. 2013;46(3):355–65. https://doi.org/10.1016/j.jpainsymman.2012.09.006.

    Article  Google Scholar 

  2. 2.

    Rainer J, Schneider JK, Lorenz RA. Ethical dilemmas in nursing: an integrative review. J Clin Nurs. 2018;27(19–20):3446–61. https://doi.org/10.1111/jocn.14542.

    Article  PubMed  Google Scholar 

  3. 3.

    Sævareid TJL, Førde R, Thoresen L, Lillemoen L, Pedersen R. Significance of advance care planning in nursing homes: views from patients with cognitive impairment, their next of kin, health personnel and managers. Clin Interv Aging. 2019;14:997–1005. https://doi.org/10.2147/CIA.S203298.

    Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Houben CH, Spruit MA, Groenen MT, Wouters EF, Janssen DJ. Efficacy of advance care planning: a systematic review and meta-analysis. J Am Med Dir Assoc. 2014;15(7):477–89. https://doi.org/10.1016/j.jamda.2014.01.008.

    Article  PubMed  Google Scholar 

  5. 5.

    Stein GL, Fineberg IC. Advance care planning in the USA and UK: a comparative analysis of policy, implementation and the social work role. Br J Soc Work. 2013;43(2):233–48. https://doi.org/10.1093/bjsw/bct013.

    Article  Google Scholar 

  6. 6.

    Oliver DJ, Borasio GD, Caraceni A, Visser M, Grisold W, Lorenzl S, et al. A consensus review on the development of palliative care for patients with chronic and progressive neurological disease. Eur J Neurol. 2016;23(1):30–8. https://doi.org/10.1111/ene.12889.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Wight D, Wimbush E, Jepson R, Doi L. Six steps in quality intervention development (6SQuID). J Epidemiol Community Health. 2016;70(5):520–5. https://doi.org/10.1136/jech-2015-205952.

    Article  PubMed  Google Scholar 

  8. 8.

    Gjerberg E, Lillemoen L, Weaver K, Pedersen R, Forde R. Advance care planning in Norwegian nursing homes. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 2017;137(6):447–50. https://doi.org/10.4045/tidsskr.16.0284.

    Article  Google Scholar 

  9. 9.

    Helse- og omsorgsdepartementet. Meld. St. 24. Lindrende behandling og omsorg. Oslo: Helse- og omsorgsdepartementet; 2019–2020.

  10. 10.

    Wikstøl D, Pedersen R, Magelssen M. Public attitudes and health law in conflict: somatic vs. mental care, role of next of kin, and the right to refuse treatment and information. BMC Health Serv Res. 2021;21(1):3.

    Article  Google Scholar 

  11. 11.

    Sharp T, Moran E, Kuhn I, Barclay S. Do the elderly have a voice? Advance care planning discussions with frail and older individuals: a systematic literature review and narrative synthesis. Br J Gen Pract. 2013;63(615):e657–68. https://doi.org/10.3399/bjgp13X673667.

    Article  PubMed  PubMed Central  Google Scholar 

  12. 12.

    Musa I, Seymour J, Narayanasamy MJ, Wada T, Conroy S. A survey of older peoples' attitudes towards advance care planning. Age Ageing. 2015;44(3):371–6. https://doi.org/10.1093/ageing/afv041.

    Article  PubMed  Google Scholar 

  13. 13.

    Cardona M, Lewis E, Shanmugam S, Nicholson M, Williamson M, Hanly L, et al. Dissonance on perceptions of end-of-life needs between health-care providers and members of the public: quantitative cross-sectional surveys. Australasian journal on ageing. 2019;38(3):e75–84. https://doi.org/10.1111/ajag.12630.

    Article  PubMed  Google Scholar 

  14. 14.

    Raijmakers NJ, Rietjens JA, Kouwenhoven PS, Vezzoni C, van Thiel GJ, van Delden JJ, et al. Involvement of the Dutch general population in advance care planning: a cross-sectional survey. J Palliat Med. 2013;16(9):1055–61. https://doi.org/10.1089/jpm.2012.0555.

    Article  PubMed  Google Scholar 

  15. 15.

    De Vleminck A, Pardon K, Roelands M, Houttekier D, Van den Block L, Vander Stichele R, et al. Information preferences of the general population when faced with life-limiting illness. Eur J Pub Health. 2015;25(3):532–8. https://doi.org/10.1093/eurpub/cku158.

    Article  Google Scholar 

  16. 16.

    Park HY, Kim YA, Sim J-A, Lee J, Ryu H, Lee JL, et al. Attitudes of the general public, Cancer patients, family caregivers, and physicians toward advance care planning: a Nationwide survey before the enforcement of the life-sustaining treatment decision-making act. J Pain Symptom Manag. 2019;57(4):774–82. https://doi.org/10.1016/j.jpainsymman.2018.12.332.

    Article  Google Scholar 

  17. 17.

    Norsk Gallup. Om GallupPanelet. 2021. Available from: https://www.galluppanelet.no/About-Us.

  18. 18.

    von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. J Clin Epidemiol. 2008;61(4):344–9. https://doi.org/10.1016/j.jclinepi.2007.11.008.

    Article  Google Scholar 

  19. 19.

    Beauchamp TL, Childress JF. Principles of biomedical ethics. 8th ed. New York: Oxford University Press; 2019.

    Google Scholar 

  20. 20.

    Devi N, Bickenbach J, Stucki G. Moving towards substituted or supported decision-making? Article 12 of the convention on the rights of persons with disabilities. Alter - European Journal of Disability research, Revue européen de recherche sur le handicap. 2011;5(4):249–64.

    Google Scholar 

  21. 21.

    Sudore RL, Lum HD, You JJ, Hanson LC, Meier DE, Pantilat SZ, et al. Defining advance care planning for adults: a consensus definition from a multidisciplinary Delphi panel. J Pain Symptom Manag. 2017;53(5):821–32. https://doi.org/10.1016/j.jpainsymman.2016.12.331.

    Article  Google Scholar 

  22. 22.

    Rietjens JAC, Sudore RL, Connolly M, van Delden JJ, Drickamer MA, Droger M, et al. Definition and recommendations for advance care planning: an international consensus supported by the European Association for Palliative Care. Lancet Oncol. 2017;18(9):e543–e51. https://doi.org/10.1016/S1470-2045(17)30582-X.

    Article  PubMed  Google Scholar 

  23. 23.

    Saevareid TJL, Pedersen R, Thoresen L. Nursing home residents with cognitive impairment can participate in advance care planning: a qualitative study. J Adv Nurs. 2020.

  24. 24.

    Thoresen L, Lillemoen L. I just think that we should be informed a qualitative study of family involvement in advance care planning in nursing homes. BMC medical ethics. 2016;17(1):72.

    Article  Google Scholar 

  25. 25.

    Hall A, Rowland C, Grande G. How should end-of-life advance care planning discussions be conducted according to patients and informal carers? A qualitative review of reviews. J Pain Symptom Manag. 2019;58(2):311–35. https://doi.org/10.1016/j.jpainsymman.2019.04.013.

    Article  Google Scholar 

  26. 26.

    Gilissen J, Pivodic L, Smets T, Gastmans C, Vander Stichele R, Deliens L, et al. Preconditions for successful advance care planning in nursing homes: a systematic review. Int J Nurs Stud. 2017;66:47–59. https://doi.org/10.1016/j.ijnurstu.2016.12.003.

    Article  PubMed  Google Scholar 

  27. 27.

    Daly RL, Bunn F, Goodman C. Shared decision-making for people living with dementia in extended care settings: a systematic review. BMJ Open. 2018;8(6):e018977. https://doi.org/10.1136/bmjopen-2017-018977.

    Article  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Ottoboni G, Chattat R, Camedda C, Galletti M, Macripò S, Mariani E, et al. Nursing home staff members' knowledge, experience and attitudes regarding advance care planning: a cross-sectional study involving 12 Italian nursing homes. Aging Clin Exp Res. 2019;31(11):1675–83. https://doi.org/10.1007/s40520-018-01110-5.

    Article  PubMed  Google Scholar 

  29. 29.

    Ng QX, Kuah TZ, Loo GJ, Ho WH, Wagner NL, Sng JG, et al. Awareness and attitudes of community-dwelling individuals in Singapore towards participating in advance care planning. Ann Acad Med Singap. 2017;46(3):84–90.

    PubMed  Google Scholar 

  30. 30.

    Abba K, Lloyd-Williams M, Horton S. Discussing end of life wishes - the impact of community interventions? BMC Palliat Care. 2019;18(1):26. https://doi.org/10.1186/s12904-019-0407-8.

    Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Brinkman-Stoppelenburg A, Rietjens JA, van der Heide A. The effects of advance care planning on end-of-life care: a systematic review. Palliat Med. 2014;28(8):1000–25. https://doi.org/10.1177/0269216314526272.

    Article  PubMed  Google Scholar 

  32. 32.

    Craig P, Macintyre S, Mitchie S, Nazareth I, Petticrew M. Developing and evaluating complex interventions: the new Medical Research Council guidance. Brit Med J. 2008;337(7676):979.

    Google Scholar 

  33. 33.

    Moore GF, Audrey S, Barker M, Bond L, Bonell C, Hardeman W, Moore L, O'Cathain A, Tinati T, Wight D, Baird J Process evaluation of complex interventions: Medical Research Council guidance. Brit Med J. 2015;350(6). https://doi.org/10.1136/bmj.h1258.

  34. 34.

    Kane RL, Huckfeldt P, Tappen R, Engstrom G, Rojido C, Newman D, et al. Effects of an intervention to reduce hospitalizations from nursing homes: a randomized implementation trial of the INTERACT program. JAMA Intern Med. 2017;177(9):1257–64. https://doi.org/10.1001/jamainternmed.2017.2657.

    Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Sinclair C, Auret KA, Evans SF, Williamson F, Dormer S, Wilkinson A, et al. Advance care planning uptake among patients with severe lung disease: a randomised patient preference trial of a nurse-led, facilitated advance care planning intervention. BMJ Open. 2017;7(2):e013415. https://doi.org/10.1136/bmjopen-2016-013415.

    Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Vanderhaeghen B, Van Beek K, De Pril M, Bossuyt I, Menten J, Rober P. What do hospitalists experience as barriers and helpful factors for having ACP conversations? A systematic qualitative evidence synthesis. Perspectives in Public Health. 2019;139(2):97–105. https://doi.org/10.1177/1757913918786524.

    Article  PubMed  Google Scholar 

  37. 37.

    Tilburgs B, Vernooij-Dassen M, Koopmans R, van Gennip H, Engels Y, Perry M. Barriers and facilitators for GPs in dementia advance care planning: a systematic integrative review. PLoS One. 2018;13(6):e0198535. https://doi.org/10.1371/journal.pone.0198535.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Fosse A, Zuidema S, Boersma F, Malterud K, Schaufel MA, Ruths S. Nursing home physicians’ assessments of barriers and strategies for end-of-life Care in Norway and the Netherlands. J Am Med Dir Assoc. 2017;18(8):713–8. https://doi.org/10.1016/j.jamda.2017.03.005.

    Article  PubMed  Google Scholar 

  39. 39.

    Zwakman M, Jabbarian LJ, van Delden J, van der Heide A, Korfage IJ, Pollock K, et al. Advance care planning: a systematic review about experiences of patients with a life-threatening or life-limiting illness. Palliat Med. 2018;32(8):1305–21. https://doi.org/10.1177/0269216318784474.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Fosse A, Schaufel MA, Ruths S, Malterud K. End-of-life expectations and experiences among nursing home patients and their relatives--a synthesis of qualitative studies. Patient Educ Couns. 2014;97(1):3–9. https://doi.org/10.1016/j.pec.2014.05.025.

    Article  PubMed  Google Scholar 

  41. 41.

    Ryan T, Amen KM, McKeown J. The advance care planning experiences of people with dementia, family caregivers and professionals: a synthesis of the qualitative literature. Annals of palliative medicine. 2017;6(4):380–9. https://doi.org/10.21037/apm.2017.06.15.

    Article  PubMed  Google Scholar 

  42. 42.

    Hickey D, Quinn S. 'I don't want to talk about it.' Raising public awareness of end-of-life care planning in your locality. Int J Palliat Nurs. 2012;18(5):241–7. https://doi.org/10.12968/ijpn.2012.18.5.241.

    Article  PubMed  Google Scholar 

  43. 43.

    Groebe B, Rietz C, Voltz R, Strupp J. How to talk about attitudes toward the end of life: a qualitative study. Am J Hosp Palliat Care. 2019;36(8):697–704. https://doi.org/10.1177/1049909119836238.

    Article  PubMed  Google Scholar 

  44. 44.

    Romoren M, Pedersen R, Forde R. How do nursing home doctors involve patients and next of kin in end-of-life decisions? A qualitative study from Norway. BMC medical ethics. 2016;17(1):5. https://doi.org/10.1186/s12910-016-0088-2.

    Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Skorstengaard MH, Brogaard T, Jensen AB, Andreassen P, Bendstrup E, Løkke A, et al. Advance care planning for patients and their relatives. Int J Palliat Nurs. 2019;25(3):112–27. https://doi.org/10.12968/ijpn.2019.25.3.112.

    Article  PubMed  Google Scholar 

  46. 46.

    Knight K. 50 years of advance care planning: what do we call success? Monash bioethics review; 2021.

    Google Scholar 

  47. 47.

    Burge AT. Advance care planning education in pulmonary rehabilitation: a qualitative study exploring participant perspectives. Palliat Med. 2014;28(8):1069–70. https://doi.org/10.1177/0269216314532702.

    Article  PubMed  Google Scholar 

  48. 48.

    Bhavsar NA, Constand S, Harker M, Taylor DH Jr. Death of outrage over talking about dying. BMJ Support Palliat Care. 2019;9(1):37–9. https://doi.org/10.1136/bmjspcare-2016-001182.

    Article  PubMed  Google Scholar 

  49. 49.

    Bekkema N, de Veer AJE, Wagemans AMA, Hertogh CMPM, Francke AL. Decision making about medical interventions in the end-of-life care of people with intellectual disabilities: a national survey of the considerations and beliefs of GPs, ID physicians and care staff. Patient Educ Couns. 2014;96(2):204–9. https://doi.org/10.1016/j.pec.2014.05.014.

    Article  PubMed  Google Scholar 

  50. 50.

    Dreyer A, Forde R, Nortvedt P. Autonomy at the end of life: life-prolonging treatment in nursing homes - relatives' role in the decision-making process. J Med Ethics. 2009;35(11):672–7. https://doi.org/10.1136/jme.2009.030668.

    CAS  Article  PubMed  Google Scholar 

  51. 51.

    Lord K, Livingston G, Cooper C. A systematic review of barriers and facilitators to and interventions for proxy decision-making by family carers of people with dementia. International psychogeriatrics / IPA. 2015;27(8):1301–12. https://doi.org/10.1017/S1041610215000411.

    Article  Google Scholar 

  52. 52.

    Carter G, McLaughlin D, Kernohan WG, Hudson P, Clarke M, Froggatt K, et al. The experiences and preparedness of family carers for best interest decision-making of a relative living with advanced dementia: a qualitative study. J Adv Nurs. 2018;74(7):1595–604. https://doi.org/10.1111/jan.13576.

    Article  PubMed  Google Scholar 

  53. 53.

    Teixeira AA, Hanvey L, Tayler C, Barwich D, Baxter S, Heyland DK. What do Canadians think of advanced care planning? Findings from an online opinion poll. BMJ Support Palliat Care. 2015;5(1):40–7. https://doi.org/10.1136/bmjspcare-2013-000473.

    Article  PubMed  Google Scholar 

  54. 54.

    van Wijmen MPS, Pasman HRW, Widdershoven GAM, Onwuteaka-Philipsen BD. Continuing or forgoing treatment at the end of life? Preferences of the general public and people with an advance directive. J Med Ethics. 2015;41(8):599–606. https://doi.org/10.1136/medethics-2013-101544.

    Article  PubMed  Google Scholar 

  55. 55.

    de Vries K, Banister E, Dening KH, Ochieng B. Advance care planning for older people: the influence of ethnicity, religiosity, spirituality and health literacy. Nurs Ethics. 2019;969733019833130.

Download references

Acknowledgements

We are grateful to Professor Magne Thoresen at the Department of Biostatistics, University of Oslo, for valuable comments on the statistical analyses.

Author information

Affiliations

Authors

Corresponding author

Correspondence to Trygve Johannes L. Sævareid.

Ethics declarations

Ethics approval and consent to participate

In line with the Norwegian system for research ethics approval the study was evaluated by the Data Protection Official at the Norwegian Centre for Research Data (ref. 589400). Participants were informed about the study in writing, and participation was voluntary. The respondent’s completion of the questionnaire was considered as valid consent to participate (this practice was approved by the Data Protection Official). All methods were carried out in accordance with relevant guidelines and regulations.

Consent for publication

“Not applicable”.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Sævareid, T.J.L., Pedersen, R. & Magelssen, M. Positive attitudes to advance care planning – a Norwegian general population survey. BMC Health Serv Res 21, 762 (2021). https://doi.org/10.1186/s12913-021-06773-x

Download citation

Keywords

  • Advance care planning
  • Attitudes
  • General population
  • Public health care