Skip to main content
  • Research article
  • Open access
  • Published:

Patient reported outcome measures for measuring dignity in palliative and end of life care: a scoping review



Patient reported outcome measures are frequently used standard questionnaires or tools designed to collect information from patients regarding their health status and care. Their use enables accurate and relevant insight into changes in health, quality of life, and symptom severity to be acquired. The purpose of this scoping review was to identify PROMs that had been subject to rigorous development and were suitable for use in palliative and end of life care for clinical practice and/or research purposes. The review had a specific focus on measures which could be used to assess perceptions of dignity in these contexts.


A scoping review of English-language papers published between 2005 and 2015. Searches were devised in conjunction with an information science specialist and were undertaken in Medline; PsycINFO; EMBASE; CINAHL; Social Science Citation Index; ASSIA; CENTRAL; CDSR; DARE; HTA; Oxford PROM Bibliography; PROQOLID, using dignity related terms such as personhood; dignity or dignified; patient-centred care; which were linked (via the Boolean operator “AND”) to care-related terms such as terminal care; hospice care; palliative care; end of life. Papers were assessed against inclusion criteria and appraised for quality.


The search strategy produced an initial 7845 articles. After three rounds of eligibility assessment, eight articles discussing eight patients reported outcome measures were found to meet the inclusion criteria and were included in the final review. These underwent a thorough critical appraisal process. All seven studies were empirical research focused on the development and testing of a PROM.


The eight patient reported outcome measures had all undergone some psychometric testing, and covered dignity aspects suggesting that they could be considered for use for research purposes to assess dignity. There were also indications that some could be implemented into a clinical setting. However, each measure had limitations and scope for further development.

Peer Review reports


Patient reported outcome measures

Patient reported outcome measures (PROMs) are standard questionnaires or tools used to acquire information from patients regarding perceptions of their wellbeing and functional status [1, 2]. They operate by recording changes over time, following an initial baseline measurement being taken [3]. These tools can be used in areas such as palliative care to provide a means of assessing and monitoring care [3]. Measuring outcomes in healthcare require patients to be the primary givers of information, in order to gain accurate and relevant insight into changes in health, quality of life, and symptom severity [3]. PROMs are increasingly encouraged for use in clinical practice, audit and research [3, 4]. In research, PROMs are pivotal for testing the effect of an intervention [4,5,6]. PROMs are advocated for their ability to elicit information directly from the patient, prioritise the perspective of the patient, and when sufficiently validated, they are able to deliver an accurate assessment of the clinical population [1, 3]. PROMs are the ideal strategy to measure patient-centredness by giving patients the opportunity to assess and convey the extent to which they feel that care received meets their values and needs [7]. Furthermore, PROMs can help highlight aspects of care that need to be improved [7]. In addition, assessments allowed through PROMs are crucial to care provision [8].

In palliative and end of life care, the use of PROMs is encouraged to allow palliative care interventions to be assessed, which ultimately provides guidance for teams working in this area. Furthermore, UK supportive and palliative care guidance recommends that systematic assessments are crucial to the provision of supportive care [8, 9]. It has been suggested that the growing landscape of research into experiences of dying have highlighted the importance of focusing on quality improvement in the area of end of life care [10].

The primary goal of palliative care should be to ensure high quality of life for patients who have advanced incurable disease. This involves attending to the person’s psychological, social, and spiritual needs, so ultimately the endeavour of palliative care is to generate the best quality of life for patients and their families [11]. Outcome measures should then strive to assess whether this has been achieved [11]. Hearn and Higginson [12] suggest that PROMs in palliative care should be developed to capture key goals of palliative care philosophies including improving quality of life before death, attending to symptoms, and providing support for loved ones. The information gained from outcome measures is useful since it produces a clinical picture of patients, helps improve symptom assessment, enhances communication between service users and staff, achieves better patient satisfaction, and ultimately supports the delivery of person-centred care [6, 13,14,15]. In turn, this can help improve the quality of the service [6], and supports shared decision making between patients and staff [15]. In addition, data elicited from PROM reporting can also generate key information that may not be otherwise routinely recorded or available in medical and nursing records [14].

Challenges to using PROMs in palliative care

The palliative care environment can pose challenges to the effective use of PROMs [12]. For example, the patient with palliative care needs may be unable to complete PROMs due to advanced illness or cognitive impairment. This potentially leads to situations where PROMs are only used for patients with less problems and therefore excludes those with more severe issues. This also compromises the validity of the PROM, since the use of proxy individuals may not reflect the true perceptions of the patient [16]. Collins et al. [6] propose the use of the term “person-centred outcome measures”, to reflect situations where someone other than the patient (such as a family member of healthcare professional) fills in the measure, but still strives to capture the patient’s priorities. In their systematic review on the use of outcome measures in palliative care, Hearn and Higginson [12] found that no outcome measure in their final included selection was designed to cover more than one relevant domain in palliative care. This is echoed by a more recent review [10] focusing on end of life care, in which they identify a need to take into account “the full spectrum of patients’ and caregivers’ end-of-life experience” (2007:1849). In addition, measuring the diverse outcomes of palliative care requires a holistic approach that includes consideration of what may be seen as obscure domains such as psychosocial and spiritual dimensions [3]. These authors also propose that the realm of palliative care is increasingly complex because of the spectrum of needs and conditions that are present, which then makes measurement difficult. Moreover, certain outcomes, such as quality of life, may be difficult to measure, since this is a multidimensional and subjective concept [7].

There may also be challenges to both the selection of PROMs and implementing them in clinical practice, due to lack of time, resources and training [1]. The unique needs of patients requiring palliative care means that outcome measurement can be challenging [3]. In addition, ethical concerns arise around issues such as whether measuring symptoms might intrude on the patient’s preferred use of time at the end of life; whether it is appropriate to measure symptoms that may be complex and inter-related in presentation; [3]. It is also highlighted that [13] the possible drawbacks of using paper-based outcome measures, suggesting that they may not be flexible; are limited in terms of language and literacy requirement; may not be appropriate for individuals from minority groups; and the inability to generate instant clinical information. Similarly others question the usefulness of questionnaire content, by suggesting that they do not offer clear distinction between statistical and clinical significances [16]. However, in cancer settings, [12] PROMs are useful in helping to distinguish between physical, emotional, and social problems and also providing a means to monitor effects.

The ideal attributes of PROMs

A substantial body of work has been undertaken which provides guidance and recommendations for the development, selection, implementation and use of PROMs in palliative and end of life care, in addition to, addressing some of the identified challenges associated with the use of PROMS. Ideally, PROMs in end of life care should aim to cover the key areas of hope, spirituality, symptom control, self-concept, the therapeutic consultation, and dignity [12]. In order to enhance the evidence base for end of life care, PROMs should capture patient and caregiver experiences and undergo reliability and validity testing [10]. As well as, being selected and implemented from a reliable evidence base [4] Specific projects have prioritised developing and providing guidance for PROMs in palliative and end of life care. These are summarised in Table 1.

Table 1 Recommendations for PROMs from key projects

As part of the Methods of Researching End of life Care (MORECare project) [17] a checklist of components was generated to help researchers in designing and conducting intervention studies in end of life care. This work provides specific recommendations for the design of outcome measures and proposes guidelines for format aspects including short lengths; ease in administering and interpreting; and ensuring that the tool is adaptable to different settings. In addition, this body of work emphasises the importance of the tool being validated and tested for reliability. Similarly, the PRISMA project [18] highlights the importance of validity and reliability and proposes what types of validity and reliability testing should be done. In addition, this work recommends that outcome measures have the ability to be translated into other languages. Both MORECare and PRISMA state that responsiveness to change over time is also a priority for outcome measures to demonstrate [3, 12]. A further key body of work is Witt et al.’s Outcome Assessment and Complexity Collaborative (OACC) Suite of Measures [19], which emphasises the need for outcome measures to capture the domains relevant to palliative care. These recommendations were taken into account when formulating the critical appraisal tool for this current scoping review (Please see section Critical appraisal of PROMs under “Methods”, for further detail).

However, as well as meeting particular quality standards, PROMs also have a responsibility to measure phenomena that are significant for, and prioritised by patients [19]. Dignity is recognised as being integral to human rights and a priority for recipients of palliative and end of life care [20, 21]. Dignity is defined as having a quality that is deemed worthy of receiving respect and, in turn, also promotes self-respect [22]. The tenets of dignity, which revolve around kindness, humanity, and respect, are arguably neglected by professionals working under challenging conditions, including time pressure [23]. Attention to conserving dignity in palliative and end of life care settings is welcomed by patients and the research landscape is increasingly dedicated to developing clinically-appropriate interventions which fulfil this aim [21, 24,25,26]. Nevertheless, dignity is not always made a priority when developing PROMs [27]. Therefore, PROMs which extract dignity-related outcomes are important in order to assess the extent to which patients are satisfied that their dignity is being conserved by care-giving activities and approaches.

Previous reviews

This current review intended to identify key PROMs used in palliative and/or end of life care that related to dignity and were related to and relevant for the nursing context, i.e. care delivered by nurses as part of a multi-professional team caring for people with palliative care needs in the last months of life. In addition, this review, uniquely, seeks to find PROMs which specifically help to measure patient perceptions of dignity, a focus which has not been exclusively attended to by previous reviews. Moreover, as evidence-based practice is central to both medical and nursing care environments [28,29,30,31], it was vital that a review of available evidence was undertaken to ensure that appropriate outcome measures are being used in research and clinical practice.

An early review [3] sought to identify outcome measures which enable palliative care interventions used for patients with advanced cancer to be evaluated. Forty-one measures made it into the final review, including the Edmonton Symptom Assessment Schedule (ESAS), and the McGill Quality of Life Questionnaire (MQQL). These authors proposed key criteria to use when assessing measures, which revolve around validity and reliability considerations, as well as responsiveness to change. The final seven included measures were found to target physical, psychological and spiritual domains to some extent, but no one measure fulfilled all the requirements of an ideal tool. Hearn and Higginson [12] questioned whether such an ideal tool can be achieved, but also stand firm that this endeavour should not be neglected. Mularski et al.’s [10] review had similar aims in seeking to identify appropriate end of life measures, which had undergone good psychometric testing. A larger number of measures were found with 95 being identified from the review; thirty-five from a previous systematic review; and finally 64, which measured end of life experience. The measures varied in the focus, and revolved around quality of life; physical, emotional, spiritual areas; advanced care planning; and caregiver wellbeing. The review highlighted the lack of robust testing for most measures, and a significant gap in appropriate measures to address continuity of care, advanced care planning and spiritual issues. However, the authors acknowledge that amongst the limitations of their review, their broad definition of “end of life” risks being both over-inclusive and possibly not inclusive enough.

Other reviews chose specific measures to focus on; Collins et al. [6], aimed to appraise evidence for use of the Support Team Assessment Schedule (STAS) and the Palliative care/ Patient Outcome Scale (POS). The review highlighted a clear increase in use of both measures in diverse settings and countries, with both being accepted as validated and reliable tools used to assess symptoms and needs. In addition, as well as being part of clinical assessments, the tools were also used in the evaluation of interventions. The POS remained more popular than the STAS, and the authors propose that this may be because the POS is inherently patient-focused by being a PROM. However, the review risks having an element of bias, since their focus on these two measures could arguably have been influenced by the fact that most of the authors had involvement in the development of them.

Finally, Parker and Hodgkinson [3] were interested in determining the reliability, validity, and feasibility of outcome measures used specifically in long term care facilities. Motivated by the lack of work previously addressing the area of long term facilities, the review identified ten outcome measures appropriate for this setting, with the Family Perceptions of end-of-life Care Scale (FPCS) being deemed most appropriate, based on the rigorous development and testing it has undergone. However, the authors found that some validity aspects were difficult to determine, thus compromising this aspect of appraisal.

Development of PROMs research is in line with recent health policy recommendations [9, 32, 33], and acknowledges the importance of prioritising the patient’s perspective, thus supporting patient-centred care. This current scoping review is both relevant and timely, in particular, because no recent reviews focus exclusively on PROMs within the nursing context nor with a focus on dignity. Undertaking a scoping review, as opposed to any other form of knowledge appraisal, allowed us to specifically address an exploratory research question which aimed to map key types of evidence as well as identifying any gaps in that evidence [34]. Moreover, this review intends to identify high quality PROMs that can potentially be used to confidently evaluate palliative and/or end of life interventions, aligning with the MRC’s recommendations [35] for evaluating complex interventions. This will strengthen the evidence-base of these interventions and support their implementation to practice.



To map the evidence and quality of PROMs which assess dignity, and have been used for patients in palliative and/or end of life settings. The key question guiding this scoping review was as follows:

What are the key PROMs available that are used to measure dignity in palliative and end of life care for clinical practice and/or research purposes?

As well as measuring dignity, PROMs were expected to show high standards of development, evidenced by their ability to meet key critical appraisal requirements (see Table 5).

Inclusion criteria were developed early on to guide the narrowing down process of retrieved articles. This conveyed the key criteria that papers were expected to achieve in order to be considered for inclusion. The inclusion criteria are displayed in Table 2 and were used in Stages 1 and 2 of the narrowing down process (please see section Study selection ).

Table 2 Inclusion criteria

Scoping review method

The methods for scoping reviews have come under recent scrutiny [34] and have been developed from the early work of Arksey & O′ Malley [36] with an aim of producing consistent use of methodological guidance and reporting. We followed five of the six methodological steps outlined in the Arksey & O’Malley [36] and Levac et al. [37] framework recommended by Colquhoun et al. [34]. The final stage ‘Consultation’ is optional and involves opportunities for consumer and stakeholder involvement which were beyond the scope of this review:

  1. 1.

    Identifying the research questions

  2. 2.

    Identifying relevant studies

  3. 3.

    Study selection

  4. 4.

    Charting the data

  5. 5.

    Collating summarising and reporting the results

Identifying relevant studies

Figure 1 provides an overview of the key stages of the review process that we undertook.

Fig. 1
figure 1

The stages of narrowing down texts (Prisma diagram)

The search strategy was developed through collaborations between the research team (including a senior clinical academic with expertise in palliative and supportive care; a senior academic with expertise in evidence synthesis; a lecturer in adult nursing with clinical and research experience in community nursing), and an information scientist. In addition to consultations with the expert in evidence synthesis and information scientist, keywords and free text terms were also informed by an early scoping exercise, from which literature was scrutinised for relevant terminology and synonyms. The Medical Subject Headings (MeSH) term browser, provided by the United States’ National Library of Medicine, was also used to identify appropriate index terms. The final search strategy consisted of dignity related terms such as personhood; dignity or dignified; patient-centred care; which were linked (via the Boolean operator “AND”) to care-related terms such as terminal care; hospice care; palliative care; end of life. A sample search strategy from the MEDLINE database is displayed in Table 3.

Table 3 MEDLINE search strategy

Searches were conducted within key nursing, medical, psychological, and social sciences databases to identify papers from the period of 2005–2015. This period was deemed appropriate, since a preliminary exercise and consultation with the research team indicated that relevant papers, featuring the most advanced dignity-related PROMs, were most likely to emerge within this ten-year timescale. The databases that were consulted were ASSIA; CINAHL; Cochrane Central Register of Controlled Trials (CENTRAL); Cochrane Database of Systematic Reviews (CDSR); Database of Abstracts of Reviews of Effects (DARE); EMBASE; Health Technology Assessment Database (HTA); MEDLINE; Oxford PROM Bibliography; PROQOLD; PsycINFO; and Social Science Citation Index.

In addition, grey literature searching was carried out using Google search engine, grey literature databases, and relevant charity and organisation websites. Databases consulted were the Bielefeld Academic Search Engine (BASE) and OpenGrey. Organisation and charity websites, which included Royal College of Nursing, Age UK and Department of Health were consulted. Grey literature searching was supported by consultations with experts in the field. Key terms were adapted from the main search strategy. The grey literature failed to provide any appropriate PROMs which stood up against the criteria outlined in the critical appraisal tool.

Study selection

Database searches retrieved 7845 results which were exported to a referencing management program (Endnote ×6). The numbers of retrieved articles from each database are displayed in Table 4. Thirty-nine duplicate papers were identified and removed, leaving a total of 7806. A narrowing down process was established which consisted of systematic stages. Stage 1 involved members of the research team (MN, BJ, CC) assessing title and abstract against the inclusion criteria. If the titles and abstracts failed to meet the inclusion criteria, the paper was excluded. In Stage 2, the full texts were assessed against the inclusion criteria (BJ; CC; KF; BH; MN). Papers which failed to meet the inclusion criteria were excluded. There were three rounds of eligibility assessments for full texts papers, before the final seven papers were agreed. The narrowing down process is captured in a PRISMA flow diagram as conveyed in Fig. 2.

Table 4 Numbers of articles retrieved from databases
Fig. 2
figure 2

PRISMA flow diagram

Critical appraisal of PROMs

Critical appraisal of the PROMS was undertaken as part of the scoping review as recommended by Daudt et al. [38]. The critical appraisal guidance was developed based on previous work in the field [3, 12, 13, 39] and consisted of key qualities that the patient reported outcome measures being discussed in the papers were expected to have. In line with the recommendations and guidance offered by MORECare, PRISMA, and OACC projects (please see Table 1), the critical appraisal tool of this current review takes into account aspects of formatting; validity and reliability testing; clinical responsiveness; translation expectations; and other issues deemed relevant when appraising PROMs in palliative and end of life care. This tool is displayed in Table 5, and was used in stage 3 of the narrowing down process. This consisted of members of the research team (MN; BJ) assessing the PROMs identified in the papers from stages one and two, against the critical appraisal tool.

Table 5 Critical appraisal tool

The specially developed critical appraisal tool comprises of seven key screening questions, with 17 specific areas to be scored. Where necessary, bullet pointed guidance is given under areas where it was anticipated that further clarification would be needed. The PROMs were scored based on the ability to answer “yes” to the relevant areas. For PROMs where translation was not relevant, there were 15 potential areas to score “yes” on (three under FORMAT; one under DATA COLLECTION TIME POINTS; four under VALIDITY TESTING; four under RELIABILITY TESTING; one under CLINICAL RESPONSIVENESS; and two under ACCEPTABILITY AND APPLICABILITY. Where considerations for translation were relevant, there were 17 areas to score “yes” on (15 as before with the additional two areas that come under TRANSLATION). In addition to using the tool, descriptive summaries of each PROM was produced to ensure that strengths and limitations not captured by the tool were identified.

Charting the data

Table 6 provides a means of charting the data and is an overview of the final included articles. The table headings which assisted the charting process are informed by data extraction techniques employed by previous researchers undertaken similar work [3, 10]. Charting the data around PROMs has allowed useful summaries to be produced, which served to compliment the critical appraisal performed using the tool.

Table 6 measures included in final review

Collating summarising and reporting the results

This next section elaborates on the information provided by the charting process and provides a summary of the strengths and limitations of each PROM – please see Table 6 for a detailed account of the measures.

Relevance to dignity

Five PROMs had explicit dignity foci, as evident in the title of the tool, dignity being directly mentioned in items, and/or dignity being addressed and described in the developmental process. These were the Palliative Nursing Quality Measure [40]; the Patient Dignity Inventory [41] the Jacelon Attributed Dignity Scale [42]; the MIDAM-LTC [43]; and the QCQ-EOL [27]. These PROMs were specifically developed to take into account the need to preserve dignity-conserving care [27]; acknowledge the broad landscape of distress-related concerns of people nearing end of life, and address the physical, psychosocial, existential, and spiritual aspects of the patient’s experience accepted that dignity was an integral theme within palliative care, and that commitment to this is a vital quality of palliative care nurses that enables them to respect humanity [40]; and appreciated the complex and unique nature of dignity [42, 43]. Two PROMs honed in on two particular types of dignity, “attributed dignity” (behaviour with respect to self and to others) [42] and “personal dignity” (individualistic, related to personal circumstances) [43, 44], thus offering a nuanced approach to measuring dignity.

The three other PROMs targeted dignity-related themes, such as kindness, humanity, respect [26]) compassion and person centred care [45]. The short version Problems and Needs in Palliative Care questionnaire [46] contains items that explore the impact of fear and difficulties upon the person’s wellbeing, the extent to which these are problematic, as well as allowing the person to indicate whether they wish for the healthcare professional to attend to this. The term dignity is not mentioned in the development of the questionnaire and does not appear in any items, but it was designed to be patient-centred [45]. Likewise, although The Quality of Communication Questionnaire [47] does not directly reference dignity, communication has been cited as main factor of dignity [48], so the tool can be regarded as relevant for assessing dignity. The Missoula-VITAS Quality of Life Index [49] includes a number of items under five domains, to assess the impact of aspects such as interpersonal and wellbeing factors on quality of life. However, since dignity has been recognised as a potential indicator of quality of life [50], it might have been helpful for the tool to more explicitly include this phenomenon.

Strengths and limitations

The scoping review has successfully identified eight PROMs currently being used in palliative and/or end of life settings to measure dignity amongst people receiving care. The critical appraisal process highlighted some shortcomings in our critical appraisal tool, namely that not all psychometric criteria were covered, for example, ecological validity and factor analysis. This meant that if a study had subjected measures to those types of testing, this could not be acknowledged by our scoring. In addition, the Missoula-VITAS Quality of Life Index- Revised achieved a high score despite the authors suggesting that it was not suitable for use as a research outcome measure [49]. Moreover, the critical appraisal tool did not differentiate between the types of participants used during face validity testing. Therefore claims by researchers to have addressed face validity should be looked at more critically, since this validation is not always attained from the perceptions and responses of patient groups i.e. the end-users; rather it may be that the tool was tested amongst healthcare providers. This may result in a measure consisting of items that do not reflect areas that matter to patients, despite having undergone some form of face validity. However, the critical appraisal tool only partly informed the overall critical appraisal, and the description of measures allowed strengths and limitations to be considered beyond the tool’s criteria.

Implications for research and practice

The eight PROMs identified in this scoping have all been used in and are appropriate for palliative and/ or end of life research. The ones that scored highest on the critical appraisal tool could successfully be used in research studies. Although, some PROMs scored lower, other aspects of the PROMs (beyond the elements covered by the tool) were assessed, such as relevance for measuring dignity-related aspects. In this respect the PROMs performed well, which is why we make the claim that they are all apt for palliative and/or end of life care, since as stated earlier, levels of dignity should be measured since its values are prioritised by recipients of palliative and end of life care. Morever, all the PROMs addressed dignity-related themes, five were recognised as promoting an explicit agenda to assess dignity. All the measures included in the review were appraised to be clinically responsive, administrative manageable, had undergone some element of psychometric testing, and most demonstrated clearly that they could be administered at a baseline and subsequent time points. It would be advisable for further work to be conducted to test for effectiveness in the clinical context, before any of the measures are directly implemented clinically to measure dignity-conserving care. This would enable further development and evaluation of the PROMs to take place and would address some of the limitations that were identified. In particular, face validity should be performed with appropriate participants who represent the intended end-users of the tool.


The review has identified eight PROMs which are designed to measure, at least in part, dignity amongst people with palliative and end of life care needs. All had undergone some level of psychometric testing. For the purposes of this review, a thorough critical appraisal procedure was applied to assess the PROMs in terms of strengths and limitations. Findings suggest that these eight PROMs could be used to help assess patients’ perceptions of dignity in palliative and/or end of life settings. Furthermore, they may also be appropriate for use in palliative and/or end of life intervention studies to capture significant changes in perceived dignity. However, researchers and clinicians should also consider the limitations of these measures, as highlighted in this scoping review, when making decisions around whether to implement them for research and clinical purposes.


Based on the psychometric qualities and critical appraisal the outcome measure of choice from our review is the Patient Dignity Inventory developed by Chochinov et al. [41] which scored 14/15 and the Missoula-VITAS Quality of Life Index Schwartz et al. [49] which scored 12/15. We recommend researchers and clinicians use the measures with the highest scores. We recommend further validity and reliability testing and clinical research for the potentially useful other measures which scored lower regarding psychometric properties and in our critical appraisal. Findings of this review have useful implications for future research and practice. We have identified measures that can be used to measure dignity issues at the end of life. We recommend further PROM developed to improve person centred care at the end of life.


  1. Antunes B, Harding R, Higginson IJ. Implementing patient-reported outcome measures in palliative care clinical practice: a systematic review of facilitators and barriers. Palliat Med. 2014;28(2):158–75.

    Article  PubMed  Google Scholar 

  2. Dawson J, Doll H, Fitzpatrick R, Jenkinson C, Carr AJ. The routine use of patient reported outcome measures in healthcare settings. BMJ. 2010;340:c186.

    Article  PubMed  Google Scholar 

  3. Parker D, Hodgkinson B. A comparison of palliative care outcome measures used to assess the quality of palliative care provided in long-term care facilities: a systematic review. Palliat Med. 2011;25(1):5–20.

    Article  PubMed  Google Scholar 

  4. Oppenheim AN. Questionnaire design, interviewing and attitude measurement. London: Pinter; 1992.

    Google Scholar 

  5. Craig P, Dieppe P, Macintyre S, Michie S, Nazareth I, Petticrew M. Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ. 2008;337:1655.

    Article  Google Scholar 

  6. Collins A. Measuring what really matters. Towards a coherent measurement system to support personcentred care. London: The Health Foundation; 2014. Aviliable at

    Google Scholar 

  7. Aaronson NK, Ahmedzai S, Bergman B, et al. The European Organization for Research and Treatment of cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85:365–76.

    Article  CAS  PubMed  Google Scholar 

  8. Parliament UL. End of Life Care -, House of Commons Health Committee: End of Life Care 5th report of Session. 2015.

  9. Leadership Alliance for the Care of Dying People (LACDP). One chance to get it right- Improving people’s experience of care in the last few days and hours of life. 2014 [cited 2014 December]. Available from:

  10. Mularski RA, Dy SM, Shugarman LR, Wilkinson AM, Lynn J, Shekelle PG, Morton SC, Sun VC, Hughes RG, Hilton LK, Maglione M. A Systematic Review of Measures of End‐of‐Life Care and Its Outcomes. Health Serv Res. 2007;42(5):1848–70.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Crowne D, Marlowe D. A new scale of social desirability independent of 658 psychopathology. J Consult Psychol. 1960;24(4):349–54.

    Article  CAS  PubMed  Google Scholar 

  12. Hearn J, Higginson IJ. Outcome measures in palliative care for advanced cancer patients: a review. J Public Health Med. 1997;19(2):193–9.

    Article  CAS  PubMed  Google Scholar 

  13. Cella D, Hahn EA, Jensen SE, Butt Z, Nowinski CJ, Rothrock N. Lohr KN. Patientreported outcomes in performance measurement. RTI International. 2015. Available at

  14. Oliver K, Innvar S, Lorenc T, Woodman J, Thomas J. A systematic review of barriers to and facilitators of the use of evidence by policymakers. BMC Health Serv Res. 2014;14:2.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Kitson A, Harvey G, McCormack B. Enabling the implementation of evidence based practice: a conceptual framework. Qual Health Care. 1998;7:149–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Aaronson N, Elliott T, Greenhalgh J, Halyard M, Hess R, Miller D, et al. User’s Guide to Implementing Patient-Reported Outcomes Assessment in Clinical Practice. International Society for Quality of Life Research (ISOQOL). 2015.

  17. Higginson IJ, Evans CJ, Grande G, Preston N, Morgan M, McCrone P, et al. Evaluating complex interventions in end of life care: the MORECare statement on good practice generated by a synthesis of transparent expert consultations and systematic reviews. BMC Med. 2013;11:111.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Bausewein C, Daveson BA, Benalia A, Simon ST, Higginson IJ, PRISMA. Outcome measurement in palliative care. The essentials. London: 2011b.

  19. Witt J, Murtagh FEM, de Wolf-Linder S, Higginson IJ, Daveson BA. Introducing the Outcome Assessment and Complexity Collaborative (OACC) Suite of Measures- A Brief Introduction. Kings College London: 2014.

  20. World Health Organization (WHO). Human rights [cited 2016 May]. Available from:

  21. Östlund U, Brown H, Johnston B. Dignity conserving care at end-of-life: A narrative review. European Journal of Oncology Nursing. 2012;16(353–367):353–67.

    Article  PubMed  Google Scholar 

  22. Social Care Institute for Excellence (SCIE). Overview of selected research: What dignity means [cited 2016 May]. Available from:

  23. Chochinov H. Dignity and the essence of medicine: the a, B, C, and D of dignity conserving care. BMJ. 2007;335:184.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Johnston B, Larkin P, Connolly M, Barry C, Narayanasamy M, Östlund U, et al. Dignity-conserving care in palliative care settings: an integrative review. J Clin Nurs. 2015a;24(13–14):1743–72.

    Article  PubMed  Google Scholar 

  25. Johnston B, Pringle J, Gaffney M, Narayanasamy M, McGuire M, Buchanan D. The dignified approach to care: a pilot study using the patient dignity question as an intervention to enhance dignity and person-centred care for people with palliative care needs in the acute hospital setting. BMC Palliat Care. 2015b;14:9.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Chochinov H, McClement S, Hack T, Thompson G, Dufault B, Harlos M. Eliciting personhood within clinical practice: effects on patients, families, and health care providers. J Pain Symptom Manag. 2015;49(6):974–80e2.

    Article  Google Scholar 

  27. Yun YH, Kim S-H, Lee K-M, Park SM, Lee CG, Choi YS, et al. Patient-reported assessment of quality care at end of life: development and validation of quality care questionnaire- end of life (QCQ-EOL). Eur J Cancer. 2006;42:2310–7.

    Article  PubMed  Google Scholar 

  28. Stevens KR. Delivering the promise of EBP. Nurse Manage. 2012;43(4):19–21.

    Article  Google Scholar 

  29. Scott K, McSherry R. Evidence-based nursing: clarifying the concepts for nurses in practice. J Clin Nurs. 2009;18(8):1085–95.

    Article  PubMed  Google Scholar 

  30. Rycroft-Malone J, Seers K, Titchen A, Harvey G, Kitson A, McCormack B. What counts as evidence in evidence-based practice? J Adv Nurs. 2003;47(1):81–90.

    Article  Google Scholar 

  31. Youngblut JM, Brooten D. Evidence-based nursing practice: why is it important? AACN Clin Issues. 2001;12(4):468–76.

    Article  CAS  PubMed  Google Scholar 

  32. Age UK. [cited 2015 November]. Available from:

  33. (DH) DoH. [cited 2015 November]. Available from:

  34. Colquhoun HL, Levac D, O'Briend KK, Straus S, Tricco AC, Perrier L, et al. Scoping reviews: time for clarity in definition, methods, and reporting. J Clin Epidemiol. 2014;67(12):1291–4.

    Article  PubMed  Google Scholar 

  35. Medical Research Council (MRC). Developing and evaluating complex interventions: new guidance 2008 [cited 2014 September]. Available from:

  36. Arksey H, O'Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8(1):19–32.

    Article  Google Scholar 

  37. Levac D, Colquhoun HL, O'Brien KK. Scoping studies: advancing the methodology. Implement Sci. 2010;5(1):1–9.

    Article  Google Scholar 

  38. Daudt HM, van Mossel C, Scott SJ. Enhancing the scoping study methodology: a large, inter-professional team’s experience with Arksey and O'Malley's framework. BMC Med Res Methodol. 2013;13:48.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Johnston BM. Perceptions of palliative nursing: University of Glasgow; 2002 [cited 2012 September]. Available from:

  40. Cameron D, Johnston B. Development of a questionnaire to measure the key attributes of the community palliative care specialist nurse role. Int J Palliat Nurs. 2015;21(2):87–95.

    Article  PubMed  Google Scholar 

  41. Chochinov HM, Hassard T, McClement S, Hack T, Kristjanson LJ, Harlos M, Sinclair S, Murray A. The patient dignity inventory: a novel way of measuring dignity-related distress in palliative care. J Pain Symptom Manag. 2008;36(6):559–71.

  42. Jacelon CS, Choi J. Evaluating the psychometric properties of the Jacelon attributed dignity scale. J Adv Nurs. 2014;70(9):2149–61.

    Article  PubMed  Google Scholar 

  43. Oosterveld-Vlug MG, Pasman HRW, van Gennip IE, de Vet HCW, Onwuteaka-Phillipsen BD. Assessing the validity and intra-observer agreement of the MIDAM-LTC; an instrument measuring factors that influence personal dignity in long-term care facilities. Health Qual Life Outcomes. 2014;12:17.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Rosenberg M. Society and the adolescent self-image. Princeton: Princeton University Press; 1965.

    Book  Google Scholar 

  45. Foundation TH. Person-centred care made simple. London: 2014.

  46. Osse BHP, Vernooji-Dassen MJFJ, Schadé E, Grol RPTM. A practical instrument to explote patients’ needs in palliative care: the problems and needs in palliative care questionnaire- short version. Palliat Med. 2007;21:391–9.

    Article  PubMed  Google Scholar 

  47. Engleberg R, Downey L, Randall CJ. Psychometric characteristics of a quality of communication questionnaire assessing communication about end-of-life care. J Palliat Med. 2006;9(5):1086–98.

    Article  Google Scholar 

  48. Social Care Institute for Excellence (SCIE). Dignity factod-Communication [cited 2016 May]. Available from:

  49. Schwartz CE, Merriman MP, Reed G, Byock I. Evaluation of the Missoula-VITAS quality of life index- revised: research tool or clinical tool? J Palliat Med. 2005;8(1):121–35.

    Article  PubMed  Google Scholar 

  50. Manthorpe J, Iliffe S, Samsi K, Cole L, Goodman C, Drennan V, et al. Dementia, dignity and quality of life: nursing practice and its dilemmas. Int J Older People Nursing. 2010;5:235–44.

    Article  Google Scholar 

  51. Curtis JR, Patrick DL. Barriers to communication about end-of-life care in AIDS patients. J Gen Intern Med. 1997;12(736–741):736–41.

  52. Curtis JR, Patrick DL, Caldwell E, Greenlee H, Collier AC. The quality of patient-clinician communication about end-of-life care: a study of patients with AIDS and their primary care clinicians. AIDS. 1999;13:1123–31.

    Article  CAS  PubMed  Google Scholar 

  53. Jacelon C. The dignity of elders in an acute care hospital. Qual Health Res. 2003;13(4):543–56.

    Article  PubMed  Google Scholar 

  54. Jacelon C. Managing personal integrity: the process of hospitalization for elders. J Adv Nurs. 2004;46(5):549–57.

    Article  PubMed  Google Scholar 

  55. Bausewein C, Simon ST, Benalia H, Downing J, Mwangi-Powell FN, Daveson BA, et al. Implementing patient reported outcome measures (PROMs) in palliative care - users’ cry for help. Health Qual Life Outcomes. 2011a;9:27.

    Article  PubMed  PubMed Central  Google Scholar 

Download references


The authors would like to thank Melissa Harden (Information Scientist, University of York), who assisted in developing the search strategy and carrying out the searches, and Patience Ogie, a community nurse, who was seconded to the University of Nottingham for 5 months to gain experience of research and, thereby, assist the research team.


This scoping review was conducted as part of an NIHR Development grant Funded by Nottingham City Clinical Commissioning Group through an NIHR Research Capability Funding Award. The study was a 12 month study and ran from May 2015 to April 2016.

Availability of data and materials

The datasets (literature) analysed during the current study are included in the article in tables any further information/data is available from the corresponding author on reasonable request.

Author information

Authors and Affiliations



BJ designed the study; BJ, MN, CC, KF, BH were all involved in developing the search strategy, inclusion criteria and critical appraisal; all authors were involved in narrowing down the texts; MN and BJ critically appraised the PROMs; all authors contributed to the manuscript drafts and final version.

Corresponding author

Correspondence to Bridget Johnston.

Ethics declarations

Ethics approval and consent to participate

Not applicable. Ethics was not required this is a literature review article.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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 distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Johnston, B., Flemming, K., Narayanasamy, M.J. et al. Patient reported outcome measures for measuring dignity in palliative and end of life care: a scoping review. BMC Health Serv Res 17, 574 (2017).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: