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Sisse Walløe, Stine Gundtoft Roikjær, Sebrina Maj-Britt Hansen, and 6 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-4211885/v1 This work is licensed under a CC BY 4.0 License Status: Published Journal Publication published 22 Jul, 2024 Read the published version in BMC Health Services Research → Version 1 posted 4 You are reading this latest preprint version Abstract No reviews so far have been conducted to define the constructs of patient-experienced quality in healthcare transitions or to identify existing generic measures of patients’ experience of the quality within healthcare transitions. Our aim was to identify domains relevant for people experiencing healthcare transitions when evaluating the quality of care they have received, map the comprehensiveness of existing PREMs, and evaluate the PREMs’ content validity. The methods was guided by the Joanna Briggs Institutes’ guidance for scoping reviews. The search was performed on 07 December 2021, in the electronic databases Medline (Ovid), Embase (Ovid), and Cinahl (EBSCO). The search identified 16,134 publications, and 172 studies were included for review. We identified 29 PREMs assessing at least one aspect of adults’ experience of transitions in healthcare. Summarising the content, we consider a model with two domains, organisational and human-relational, likely to be adequate. However, a more comprehensive analysis and adequate definition of the construct is needed. None of the PREMs were considered content valid. Healthcare transitions Patient-Reported Experience Measure Patient Experience Quality Scoping Review Figures Figure 1 Figure 2 Figure 3 Background Care management encompasses evaluating individuals' needs and coordinating healthcare services; however, patients struggle with consistency and clarity in care management. 1 Patients’ ability to navigate healthcare systems has implications for the outcome of their treatment 2,3 , and patients’ experiences are associated with clinical effectiveness and safety. 4 Therefore, assessing patients’ experiences with transitions in healthcare is important in determining the quality of healthcare delivery. Patient-reported experience measures (PREM) are intended to be reliable measures of the quality of healthcare services from patients’ perspectives and may support evaluation of the effectiveness, safety, and efficiency of healthcare provision. 5 Several reviews of instruments measuring patient experience of the quality in healthcare transitions have been published. 6–11 In the systematic review by Berbee et al. (2009) they aimed to identify and select an appropriate instrument for measuring the quality of integrated care for patients experiencing chronic illness, but identified no patient-reported experience measure (PREM) that was comprehensive or relevant according to focus group interviews with the patients. 6 Concordantly, in a systematic review for evaluating patient satisfaction in healthcare settings integrating behavioural and medical health services, Black et al. (2021) found that no PREM comprehensively captured all relevant aspects of the integrated healthcare experience. 7 In contrast, Weaver et al. (2017) reviewed concepts, models, and instruments for understanding care continuity in mental health services and suggested a PREM suitable for self-reporting experiences with mental healthcare. 8 In 2011 Fiscella et al. (2011) published a consensus of domains and measures suitable for patient-reported assessment of cancer navigation but also called for an instrument that covered all relevant topics. 9 Likewise, McMurray et al. (2016) identified 25 instruments to assess patients’ experience of rehabilitation services, but none comprehensively measured patient experience across the rehabilitative care continuum. 10 Following this, Quinn et al. (2017) concluded that no instruments adequately assessed veterans’ experience with access and coordination across healthcare settings. 11 No reviews so far have identified a generic PREM that comprehensively measures patients’ experience with the quality of healthcare transitions. 6–13 Therefore, there is a need to identify adequate concepts and measures that can target the patient experience transition in healthcare. The COSMIN group argues that content validity is the most important aspect of patient-reported measures. 14 Content validity refers to a patient-reported measure's relevance, comprehensiveness, and comprehensibility. 15 In other words, to evaluate whether the instrument provides an adequate reflection of the construct to be measured in the context. 14 Although there is some consensus on defining patient experience of healthcare transitions as a multidimensional concept consisting of human-relational and system factors, the conceptualizations found in existing reviews still lack clarity. 6–13 The overall scope of this review was to explore and define domains of the concept of patient-experienced quality in cross-sectoral care for generic patient populations. Further, to map existing methods for generically assessing the quality of transitions in healthcare settings (e.g. between municipality, general practitioner, and hospital). To achieve this, our objectives were: What domains are considered relevant to measure for patients’ experiencing healthcare transitions when evaluating the quality of care they have received? What existing patient-reported experience measures attempt to measure patients’ experience of transitions in healthcare settings? Are any existing patient-reported experience measures adequate (relevant and comprehensive) reflections of patients’ experience of transitions in healthcare settings? Methods The method of this scoping review followed the Joanna Briggs Institutes’ (JBI) guidance for scoping reviews. 16 The article was outlined following JBI guidelines 16 supported by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) Checklist. 17 A pre-registered protocol, including aims, search strategies, and amendments made during the iterative review process 16 , is available via Open Science Framework (OSF). 18 The research question was defined using the SPIDER-model (i.e., Setting, Phenomenon of Interest, Design, Evaluation, Research). 19 The research question encompassed five concepts with predefined definitions and in- and exclusion criteria to ensure identification of eligible studies ( Table 1 ). Table 1 - Research Question Defined by the SPIDER-Model Concepts Inclusion criteria Exclusion criteria S Setting Transitions in healthcare settings Patient transition between at least 2 healthcare settings (municipality, GP, hospital) Single settings such as “In the primary care setting, at the hospital etc.” PI Phenomenon of Interest Patient-experienced quality Patients’ experiences were accounted for or assessed Only healthcare personnel or relatives’ experiences were assessed D Design Qualitative and quantitative research designs. Psychometric studies qualitative studies, quantitative studies, syntheses/reviews Feasibility studies, study protocols, reports E Evaluation PREMs*, patient accounts, narratives, attitudes, perspectives, and experiences of quality. Patient experience of healthcare provision 10,20 Patient satisfaction 21 R Research Type Published, peer-reviewed research reporting data Peer-reviewed, published studies Conference abstracts and meeting notes *Patient-Reported Experience Measure Search The search was performed on 07 December 2021. The electronic databases Medline (Ovid), Embase (Ovid), and Cinahl (EBSCO) were chosen because they cover multiple research areas within healthcare. The search was developed in Embase and translated to Medline and Cinahl as recommended. 22 For the phenomenon of interest, we identified the Mesh term “Patient Satisfaction”. Although we excluded studies reporting on patient satisfaction rather than patient experience, the terms have been used interchangeably, 10 and patient satisfaction thus seemed necessary to include in our search strategy. As the focus on patient's experiences of coherent care seemed to have emerged around late 1990 and early 2000, 23 we searched for literature from 2000. The search strategy was developed from the predefined definitions and criteria with guidance from research librarians ( see full search strategy in Appendix 1 ). Selection of Sources of Evidence Covidence (Veritas Health Innovation, Melbourne, Australia) was used to manage the duplication and screening process. 24 All studies were screened by two independent reviewers, and a total of seven reviewers participated in the screening process. To ensure calibration of the screening process, a consensus meeting was arranged at the beginning of the process as in rapid reviews. 25 During the calibration sessions, in- and exclusion criteria were specified further than the a-priori defined criteria ( Appendix 2 ). In the full-text screening process, we experienced a larger number of articles than expected. In order to focus this review on the a priori defined aims, we decided to; I) report on intervention studies in an independent review, II) exclude mixed-methods studies and original qualitative studies, III) synthesize dimensions found in the included syntheses and reviews rather than report on the original studies. We decided to include syntheses and reviews because reports on qualitative studies were frequent, and relevant themes for patient-experienced quality of healthcare transitions had already been mapped in these meta-syntheses, integrative reviews, or scoping reviews. Data Charting Process A priori-defined data extraction templates were used and are available at OSF. 26 The data charting was done by one author (SW). The first 10 data extractions were validated independently by a research assistant (NH). The data charting table and process were adapted following the pilot extraction. The final data extraction tables are available in Appendix 3 and Appendix 4. Critical Appraisal of Individual Sources of Evidence Although the JBI guidelines for scoping reviews do not warrant critical appraisal, 27 comprehensive (i.e. PREMs including at least five items of the 12 subthemes). PREMs were critically appraised according to the COSMIN Risk of Bias checklist for systematic reviews of Patient-Reported Outcome Measures 14,28,29 to assess content validity 14 (relevance, comprehensiveness, and comprehensibility) from patients’ perspectives. The critical assessment was done independently by two reviewers (SW, LM), and conflicts were discussed until a consensus was reached. When PREMs were mentioned in included publications but not available in the publication, references were followed to the original publications on that PREM. Synthesis of Results We synthesized the data by; I) Summarizing themes identified in the qualitative syntheses and identifying relevant domains ( Appendix 3 and Figure 3 ); II) Identifying PREMs, assessing the PREMs phenomenon of interest, and categorizing and listing the items of the relevant PREMs to assess comprehensiveness ( Appendix 4, Appendix 5 and Table 2 ); III) Assessing the content validity of the most comprehensive PREMs (items related to five or more themes) ( Table 2 ). The process of synthesizing data is also described in figure 1. Figure 1 – Data Synthesis Process Results The search identified 16,134 records ( Figure 2 ), and 172 reports were included after the screening and selection process ( Figure 2 ). In addition to the regular selection process, first author SW divided the reports according to objectives 1 (24 reports) and 2 (148 reports, 35 reports excluded during data extraction, leaving 113 reports for inclusion). This was done because the scientific methods for reports to answer objective 1 needed to be qualitative, and the methods relevant for answering objective 2 needed to be quantitative observational, development, or validation reports. Figure 2 – PRISMA Flowchart Relevant Domains (Results for Objective 1) For objective one, we included 24 reports ( Appendix 6 ), 30–53 which included: 10 (42%) systematic reviews, 34,36,37,40,43,44,46,47,49,51 six (25%) scoping reviews, 32,38,41,48,50,53 Four (17%) meta syntheses, 30,39,52 three (13%) integrated reviews, 33,35,42 one (4%) narrative review, 54 and one (4%) qualitative review 45 that provided information on relevant domains and/or themes for assessing patients´ experiences with care across healthcare settings. The number of identified themes ranged from two 32 to 13, 50 with most articles reporting three themes. 34,39,52,53 When summarizing and describing themes from the included reports, we found that the themes could be organized in two distinct domains; I) A system/organizational domain; II) A human-relational domaine. Each of these domains encompassed six themes; thus, we identified 12 relevant themes as illustrated in Figure 3. Figure 3 – Domains, Themes, and Items Relevant for Assessing Patients’ Experiences of Pathways Across Healthcare Settings. Existing Patient-Reported Experience Measures (Results for Objective 2) For objective two, we included 113 ( Appendix 6 ) 6–13,55–159 reports that described 109 unique PREMs ( Appendix 4 ). However, 80 (73%) PREMs were excluded during data extraction as they referred to other aspects of care quality than transitions between healthcare settings or otherwise deviated from our specified phenomenon ( Appendix 5 ). The Consumer Assessment of Healthcare Providers and Systems (CAHPS) 160–163 questionnaires were most frequently referred to, 6,7,9,11,56,61,63,66 but we did not find the items relevant according to the construct definition in objective 1. The two relevant PREMs that were most frequently referred to were Nijmegen Continuity Questionnaire 8,12,72,77,105,119,151,152 and Patient Assessment of Chronic Illness Care (PACIC). 6,11,12,78,80,85,109,112,164 In the data extraction process, we identified different ways of formulating items. Some items were worded from a medical system perspective on quality i.e. “My physical pain was controlled as well as possible”, 165 whereas others were articulated from a patient-centred perspective i.e. “My treatment fits my needs”. 124 Yet, other items were specific to a certain contextual system infrastructure i.e. “The specialist makes out the first prescription for the treatment he/she prescribes me”, 95 or they were disease-specific. 114 However, we did identify PREMs with a more generic wording such as, “Were there times when you had to repeat information that should have been in your care records?”. 166 Adequate reflection of patients’ experience (results for objective 3) We extracted 29 PREMs that pertained to patient-experience of quality of transitions in healthcare settings. To assess the relevance and comprehensiveness of the identified PREMs, the items of each PREM were plotted according to the 12 subthemes identified for objective 1 ( table 2 ). Twenty-one PREMs had items related to at least five of the 12 subthemes ( table 2 ). To focus our review on the most comprehensive PREMs, we critically appraised the selected 21 PREMs. The Alberta Continuity of Services Scale – Mental Health (ACSS-MH), 124 the Person-Centered Coordinated Care Experience Questionnaire (P3CEQ), 148 and the Patient Experience of Integrated Care Scale (PEICS) 123 had adequate content validity, however, they were disease-specific and/or did not have items in all themes identified in objective 1 ( table 2 ). The remaining 16 PREMs had doubtful or inadequate content validity. Table 2 – Comprehensiveness and Content Validity of Existing PREMs for Assessment of Patients’ Experiences of the Quality of Transitions in Healthcare Settings. Discussion The overall aim of this scoping review was to define the concept of patient-experienced quality in healthcare transitions and map existing content valid PREMs relevant for measuring this concept. We found the construct of patient-reported experience of transitions in healthcare to consist of two domains – system/organization and human-relation. However, in summarizing the 24 qualitative reports for this review, we found some inconsistency and lack of clarity in the conceptualization and understanding of patient-experienced quality in healthcare transitions. Although some reports identified the construct of patient-experienced quality in healthcare transitions to consist of two main domains (organization and human-relational), 8,9,40,47,158 others disagreed 33,50 and leaned towards the Institute of Medicine’s framework for quality with five or more domains. 23 The two-dimensional model is, however, supported by both qualitative conceptualization 40,47 and testing of measurement properties, 8,9,158 whereas the Institiutes of Medicine’s framework is not. In addition to inconsistency in domains, there was a general inconsistency in the number and terminology for themes 32,50 and formulation of items concerning patient-centeredness. 124,165 As items in PREMs may be approached by respondents much the same as a dialogue, 167 we believe a person-centred approach to item formulation may provide the best opportunity for patients to assess quality of care appropriately. Several reports suggest further research into the conceptualization and understanding of patient-experience with care transitions. 32,36,49,54 Due to the variations in how the construct is defined, assessing the content validity of current PREMs becomes challenging. 14,15 Therefore, we support the suggestion of further research into the conceptualization of patient-experienced quality in healthcare transitions. We identified 29 PREMs that reflected at least one relevant aspect of the construct but none that were comprehensive reflections of generic patient populations’ experiences of transitions in healthcare settings. This finding aligns with the conclusion of the included reviews of instruments. 6–13,158,159 It is surprising that we have not identified a content-valid PREM given the large number of reports (113) and unique PREMs (109) included. This may be associated with the lack of clarity in the construct of patient-experienced quality in healthcare transitions. In the future, a generic PREM should be developed to make cross-comparison between studies and healthcare organizations possible. A collective effort to test and use a generice PREM might also support further development and/or understanding of the construct. This, however, would entail a generic approach to item formulation, as seen in P3CEQ, 166 rather than a context-specific approach. 95 It may be a limitation in our study that our search was imprecise with the inclusion of patient satisfaction in the search terms. However, the sensitivity of our search originates from inclusion of patient satisfaction in the search terms, and we consider the strength of this sensitivity to out way the imprecision by securing a comprehensive review. The comprehensiveness of our search resulted in a large number of records to be reviewed, and thus many reviewers to accommodate for time constraints. We attempted to compensate for a potentially low inter-rater reliability with calibration meetings. Despite of this, the number of reviewers may have been a limitation to the inclusion of all relevant, and only relevant reports. Furthermore, our pragmatic decision of excluding original qualitative studies from this review could have been a limitation to the comprehensiveness of our results. Incorporating the 24 qualitative reports has sufficiently advanced our comprehension of the existing literature to address objective 1. This is corroborated by the absence of new themes identified during data extraction from recent reports. The data extraction performed primarily by one reviewer may have caused some imprecision. However, as we have identified more PREMs than the included reviews of instruments, 6–13,158,159 this does not seem to be the case. While our scoping review does exhibit certain limitations, the thoroughness of our search and the inclusive methodology employed in comprehending and evaluating patient-experienced quality during healthcare transitions have nonetheless generated novel and significant insights. In light of our findings, it is plausible that items extracted from the most relevant and comprehensive PREMs, with a focus on generic formulations for infrastructure and disease, would reflect the construct of patient-experienced quality in healthcare transitions adequately. Furthermore, as there is some consensus that quality healthcare transitions occur when organisational structures are flexible and sensitive to patient preferences, 34,39–42,46,53 it seems advantageous to aply this knowledge in item extraction and/or formulation. As described, the construct seems to be unclear or imprecisely defined. Therefore, a process of extracting and/or formulating items should be undertaken systematically and iteratively with patient involvement and openness to re-evaluating the definition of the construct. A PREM revised by the outlined approach may support valid and reliable evaluation of the effectiveness, safety, and efficiency of healthcare provision. Conclusion In the literature, we identified several conceptual models that referred to aspects of patients’ experience with the quality of healthcare transitions. We consider a model with two domains likely to be adequate, however, a more comprehensive analysis and adequate definition of the construct is needed. Twenty-nine PREMs assessing at least one aspect of patients’ experience of transitions in healthcare were identified. However, none of the PREMs were considered content valid to measure patient-experienced quality in healthcare transitions generically. It is possible that items extracted from the identified questionnaires can be combined for a content-valid PREM. We call for further exploration into the construct of patient experience with healthcare transitions and testing of models to produce a content-valid PREM suitable for generic assessment of patients’ experiences with the quality of healthcare transitions. Declarations Ethics approval and consent to participate Not applicable Consent for publication Not applicable Availability of data and materials The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. Competing interests The authors declare that they have no competing interests. Funding The author(s) disclosed receipt of the following financial support for the research, authorship, or publication of this article: This work was supported by the local research fund at Næstved, Slagelse, and Ringsted hospitals; by a program grant for Exercise First from Region Zealand; and a faculty scholarship from Department of Clinical Research at University of Southern Denmark. Authors’ contributions SW devised the systematic search and review process, contributed substantially to the data extraction and mapping process, and revised the manuscript critically. SGR contributed substantially to the devision of the systematic search and review process, and revised the manuscript critically. SMH contributed substantially to the devision of the search and screening process and revised the manuscript critically. GZ and SRM contributed substantially to the review process and revised the manuscript critically. CBK contributed substantially to the data extraction and mapping process and with critical revision of the manuscript. CS, HHL, and LM made substantial contributions to conceptualisation, the systematic search and review process, the data extraction and mapping process, and critically revised the manuscript. Acknowledgements We thank Mette Kring Clausen and Olga Alexandrovna Tchijevitch for reviewing identified literature References Stewart A, MacIntyre G. Care management in the twenty-first centuryPersistent challenges in implementation in the context of the emergence of self-care. J Integr Care 2013; 21: 91–104. Freeman HP, Muth BJ, Kerner JF. Expanding access to cancer screening and clinical follow-up among the medically underserved. Cancer Pract 1995; 3: 19–30. Egan M, Anderson S, McTaggart J. Community navigation for stroke survivors and their care partners: description and evaluation. Top Stroke Rehabil 2010; 17: 183–190. Doyle C, Lennox L, Bell D. A systematic review of evidence on the links between patient experience and clinical safety and effectiveness. BMJ Open 2013; 3: e001570. Weldring T, Smith SMS. Patient-Reported Outcomes (PROs) and Patient-Reported Outcome Measures (PROMs). Health Serv Insights 2013; 6: 61–68. Vrijhoef HJM, Berbee R, Wagner EH, et al. Quality of integrated chronic care measured by patient survey: identification, selection and application of most appropriate instruments. Health Expect 2009; 12: 417–429. Black D, Held ML, Skeesick J, et al. Measures Evaluating Patient Satisfaction in Integrated Health Care Settings: A Systematic Review. Community Ment Health J 2021; 57: 1464–1477. Weaver N, Coffey M, Hewitt J. Concepts, models and measurement of continuity of care in mental health services: A systematic appraisal of the literature. J Psychiatr Ment Health Nurs 2017; 24: 431–450. Fiscella K, Ransom S, Jean-Pierre P, et al. Patient-reported outcome measures suitable to assessment of patient navigation. Cancer 2011; 117: 3603–3617. McMurray J, McNeil H, Lafortune C, et al. Measuring Patients’ Experience of Rehabilitation Services Across the Care Continuum. Part I: A Systematic Review of the Literature. Arch Phys Med Rehabil 2016; 97: 104–120. Quinn M, Robinson C, Forman J, et al. Survey Instruments to Assess Patient Experiences With Access and Coordination Across Health Care Settings: Available and Needed Measures. Med Care 2017; 55: S84–S91. Fernandes S, Fond G, Zendjidjian XY, et al. Measuring the Patient Experience of Mental Health Care: A Systematic and Critical Review of Patient-Reported Experience Measures. Patient Prefer Adherence 2020; Volume 14: 2147–2161. Perriman N, Davis D. Measuring maternal satisfaction with maternity care: A systematic integrative review. Women Birth 2016; 29: 293–299. Terwee CB, Prinsen C a. C, Chiarotto A, et al. COSMIN methodology for evaluating the content validity of patient-reported outcome measures: a Delphi study. Qual Life Res Int J Qual Life Asp Treat Care Rehabil 2018; 27: 1159–1170. Mokkink LB, Terwee CB, Patrick DL, et al. The COSMIN study reached international consensus on taxonomy, terminology, and definitions of measurement properties for health-related patient-reported outcomes. J Clin Epidemiol 2010; 63: 737–745. Peters MDJ, Marnie C, Tricco AC, et al. Updated methodological guidance for the conduct of scoping reviews. JBI Evid Synth 2020; 18: 2119–2126. PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation | Annals of Internal Medicine, https://www.acpjournals.org/doi/10.7326/M18-0850 (accessed 12 January 2023). Tang L, Skou ST, Nissen N, et al. The Exercise First Research Program, https://osf.io/v3ec5/ (2020, accessed 21 June 2023). The SPIDER Tool for Qualitative Evidence Synthesis | NCCMT, https://www.nccmt.ca/knowledge-repositories/search/191 (accessed 16 January 2023). Crow R, Gage H, Hampson S, et al. The measurement of satisfaction with healthcare: implications for practice from a systematic review of the literature. Health Technol Assess Winch Engl 2002; 6: 1–244. Jenkinson C, Coulter A, Bruster S, et al. Patients’ experiences and satisfaction with health care: results of a questionnaire study of specific aspects of care. Qual Saf Health Care 2002; 11: 335–339. Bramer WM, De Jonge GB, Rethlefsen ML, et al. A systematic approach to searching: an efficient and complete method to develop literature searches. J Med Libr Assoc ; 106. Epub ahead of print 4 October 2018. DOI: 10.5195/JMLA.2018.283. Institute of Medicine (US) Committee on Quality of Health Care in America. Crossing the Quality Chasm: A New Health System for the 21st Century . Washington (DC): National Academies Press (US), http://www.ncbi.nlm.nih.gov/books/NBK222274/ (2001, accessed 23 January 2023). McKeown S, Mir ZM. Considerations for conducting systematic reviews: evaluating the performance of different methods for de-duplicating references. Syst Rev 2021; 10: 38. Cochrane Rapid Reviews Methods Group offers evidence-informed guidance to conduct rapid reviews - ClinicalKey, https://www.clinicalkey.com/#!/content/playContent/1-s2.0-S089543562031146X?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS089543562031146X%3Fshowall%3Dtrue&referrer=https:%2F%2Fpubmed.ncbi.nlm.nih.gov%2F (accessed 2 March 2022). Review_protocol_20220404.pdf, https://osf.io/https://osf.io/zwht4 (2022, accessed 21 June 2023). Peters MDJ, Godfrey C, McInerney P, et al. Best practice guidance and reporting items for the development of scoping review protocols. JBI Evid Synth 2022; 20: 953–968. Mokkink LB, de Vet HCW, Prinsen C a. C, et al. COSMIN Risk of Bias checklist for systematic reviews of Patient-Reported Outcome Measures. Qual Life Res Int J Qual Life Asp Treat Care Rehabil 2018; 27: 1171–1179. Prinsen C a. C, Mokkink LB, Bouter LM, et al. COSMIN guideline for systematic reviews of patient-reported outcome measures. Qual Life Res Int J Qual Life Asp Treat Care Rehabil 2018; 27: 1147–1157. Allen J, Hutchinson AM, Brown R, et al. User experience and care for older people transitioning from hospital to home: Patients’ and carers’ perspectives. Health Expect Int J Public Particip Health Care Health Policy 2018; 21: 518–527. Instituto Nacional de Cancerología E.S.E, Arias Rojas M, García-Vivar C, et al. The transition of palliative care from the hospital to the home: a narrative review of experiences of patients and family caretakers. Investig Educ En Enferm ; 33. Epub ahead of print 15 October 2015. DOI: 10.17533/udea.iee.v33n3a12. Asif M, Cadel L, Kuluski K, et al. Patient and caregiver experiences on care transitions for adults with a hip fracture: a scoping review. Disabil Rehabil 2020; 42: 3549–3558. Beattie M, Shepherd A, Howieson B. Do the Institute of Medicine’s (IOM’s) dimensions of quality capture the current meaning of quality in health care? – An integrative review. J Res Nurs 2013; 18: 288–304. Boye LK, Mogensen CB, Mechlenborg T, et al. Older multimorbid patients’ experiences on integration of services: a systematic review. BMC Health Serv Res 2019; 19: 795. Carpenter JG. Hospital Palliative Care Teams and Post-Acute Care in Nursing Facilities: An Integrative Review. Res Gerontol Nurs 2017; 10: 25–34. Davidson L, Scott J, Forster N. Patient experiences of integrated care within the United Kingdom: A systematic review. Int J Care Coord 2021; 24: 39–56. De Regge M, De Pourcq K, Meijboom B, et al. The role of hospitals in bridging the care continuum: a systematic review of coordination of care and follow-up for adults with chronic conditions. BMC Health Serv Res 2017; 17: 550. Foglino S, Bravi F, Carretta E, et al. The relationship between integrated care and cancer patient experience: A scoping review of the evidence. Health Policy 2016; 120: 55–63. Hestevik CH, Molin M, Debesay J, et al. Older persons’ experiences of adapting to daily life at home after hospital discharge: a qualitative metasummary. BMC Health Serv Res 2019; 19: 224. Hohmann NS, McDaniel CC, Mason SW, et al. Patient perspectives on primary care and oncology care coordination in the context of multiple chronic conditions: A systematic review. Res Soc Adm Pharm 2020; 16: 1003–1016. Lawless MT, Marshall A, Mittinty MM, et al. What does integrated care mean from an older person’s perspective? A scoping review. BMJ Open 2020; 10: e035157. Mayo SJ, Ajaj R, Drury A. Survivors’ preferences for the organization and delivery of supportive care after treatment: An integrative review. Eur J Oncol Nurs 2021; 54: 102040. McMurray J, McNeil H, Lafortune C, et al. Measuring Patients’ Experience of Rehabilitation Services Across the Care Continuum. Part II: Key Dimensions. Arch Phys Med Rehabil 2016; 97: 121–30. Oishi A, Murtagh FE. The challenges of uncertainty and interprofessional collaboration in palliative care for non-cancer patients in the community: A systematic review of views from patients, carers and health-care professionals. Palliat Med 2014; 28: 1081–1098. Piccenna L, Lannin NA, Gruen R, et al. The experience of discharge for patients with an acquired brain injury from the inpatient to the community setting: A qualitative review. Brain Inj 2016; 30: 241–251. Sampson R, Cooper J, Barbour R, et al. Patients’ perspectives on the medical primary–secondary care interface: systematic review and synthesis of qualitative research. BMJ Open 2015; 5: e008708. Scholl I, Zill JM, Härter M, et al. An Integrative Model of Patient-Centeredness – A Systematic Review and Concept Analysis. PLoS ONE 2014; 9: e107828. Segan JD, Briggs AM, Chou L, et al. Patient-perceived health service needs in inflammatory arthritis: A systematic scoping review. Semin Arthritis Rheum 2018; 47: 765–777. Sibounheuang P, Olson PS, Kittiboonyakun P. Patients’ and healthcare providers’ perspectives on diabetes management: A systematic review of qualitative studies. Res Soc Adm Pharm 2020; 16: 854–874. Staniszewska S, Boardman F, Gunn L, et al. The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines. Int J Qual Health Care 2014; 26: 151–157. van Servellen G, Fongwa M, Mockus D’Errico E. Continuity of care and quality care outcomes for people experiencing chronic conditions: A literature review. Nurs Health Sci 2006; 8: 185–195. Waibel S, Henao D, Aller M-B, et al. What do we know about patients’ perceptions of continuity of care? A meta-synthesis of qualitative studies. Int J Qual Health Care 2012; 24: 39–48. Youssef A, Chaudhary ZK, Wiljer D, et al. Mapping Evidence of Patients’ Experiences in Integrated Care: A Scoping Review. Gen Hosp Psychiatry 2019; 61: 1–9. Arias Rojas M, García-Vivar C. The transition of palliative care from the hospital to the home: a narrative review of experiences of patients and family caretakers. Investig Educ En Enfermeria 2015; 33: 482–491. Willems LM, Kwakkenbos L, Bode C, et al. Health care use and patients’ perceptions on quality of care in systemic sclerosis. Clin Exp Rheumatol 2013; 31: 64–70. Wells R, Breckenridge ED, Siañez M, et al. Self-Reported Quality, Health, and Cost-Related Outcomes of Care Coordination Among Patients with Complex Health Needs. Popul Health Manag 2020; 23: 59–67. Weinberg DB, Gittell JH, Lusenhop RW, et al. Beyond our walls: impact of patient and provider coordination across the continuum on outcomes for surgical patients. Health Serv Res 2007; 42: 7–24. Vargas I, Waibel S, Vazquez ML, et al. A comprehensive analysis of patients’ perceptions of continuity of care and their associated factors. Int J Qual Health Care 2013; 25: 291–299. Tremblay D, Roberge D, Touati N, et al. Effects of interdisciplinary teamwork on patient-reported experience of cancer care. BMC Health Serv Res 2017; 17: 218. Sisler JJ, Taylor-Brown J, Nugent Z, et al. Continuity of care of colorectal cancer survivors at the end of treatment: the oncology–primary care interface. J Cancer Surviv 2012; 6: 468–475. Sequist TD, Von Glahn T, Li A, et al. Measuring chronic care delivery: patient experiences and clinical performance. Int J Qual Health Care 2012; 24: 206–213. Riley DL, Stewart DE, Grace SL. Continuity of cardiac care: Cardiac rehabilitation participation and other correlates. Int J Cardiol 2007; 119: 326–333. O’Malley AS, Cunningham PJ. Patient experiences with coordination of care: the benefit of continuity and primary care physician as referral source. J Gen Intern Med 2009; 24: 170–7. Noel PH, Barnard JM, Barry FM, et al. Patient experience of health care system hassles: Dual-system vs single-system users. Health Serv Res 2020; 55: 548–555. Mosallam RA, Metwally S. Patients’ views on the quality of transitional care at a health insurance hospital in Alexandria, Egypt. J Egypt Public Health Assoc 2014; 89: 74–80. Mollica MA, Buckenmaier SS, Halpern MT, et al. Perceptions of care coordination among older adult cancer survivors: A SEER-CAHPS study. J Geriatr Oncol 2021; 12: 446–452. Mohr DC, Benzer JK, Vimalananda VG, et al. Organizational Coordination and Patient Experiences of Specialty Care Integration. J Gen Intern Med 2019; 34: 30–36. Kollen BJ, Groenier KH, Berendsen AJ. Patients’ experiences with continuum of care across hospitals. A multilevel analysis of Consumer Quality Index Continuum of Care. Patient Educ Couns 2011; 83: 269–272. Kessing LV, Hansen HV, Ruggeri M, et al. Satisfaction with treatment among patients with depressive and bipolar disorders. Soc Psychiatry Psychiatr Epidemiol 2006; 41: 148–155. Karam M, Lambert A-S, Macq J. Patients’ perceptions of continuity of care across primary care level and emergency departments in Belgium: cross-sectional survey. BMJ Open 2019; 9: e033188. Ireson CL, Scutchfield FD, Slavova S, et al. Bridgingf the care continuum: Patient information needs for specialist referrals. BMC Health Serv Res 2009; 9: 163. Hopstaken JS, van Dalen D, van der Kolk BM, et al. Continuity of care experienced by patients in a multi-institutional pancreatic care network: a pilot study. BMC Health Serv Res 2021; 21: 1–9. Hod R, Maimon O, Zimlichman E. Does Care Transition Matter? Exploring the Newly Published HCAHPS Measure. Am J Med Qual 2020; 35: 380–387. Hincapie AL, Slack M, Malone DC, et al. Relationship Between Patients’ Perceptions of Care Quality and Health Care Errors in 11 Countries: A Secondary Data Analysis. Qual Manag Health Care 2016; 25: 13–21. Guilabert M, Martínez-García A, Sala-González M, et al. Results of a Patient Reported Experience Measure (PREM) to measure the rare disease patients and caregivers experience: a Spanish cross-sectional study. Orphanet J Rare Dis 2021; 16: 67. Fryer A-K, Friedberg MW, Thompson RW, et al. Achieving care integration from the patients’ perspective: Results from a care management program. Healthcare 2016; 4: 36–44. Den Herder-van Der Eerden M, Ebenau A, Payne S, et al. Integrated palliative care networks from the perspectives of patients: A cross-sectional explorative study in five European countries. Palliat Med 2018; 32: 1103–1113. Cramm JM, Nieboer AP. High-quality chronic care delivery improves experiences of chronically ill patients receiving care. Int J Qual Health Care 2013; 25: 689–695. Collett GK, Durcinoska I, Rankin NM, et al. Patients’ experience of lung cancer care coordination: a quantitative exploration. Support Care Cancer 2019; 27: 485–493. Carryer J, Doolan-Noble F, Gauld R, et al. New Zealand patients’ perceptions of chronic care delivery. J Integr Care 2014; 22: 71–80. Carneiro C, Ellis J, Singh S, et al. Patient and Primary Care Practitioner Confidence in and Perceptions of Cancer Treatment Transition and the Shared Care Model of Cancer Care. J Oncol Navig Surviv 2016; 7: 18–24. Burgers JS, Voerman GE, Grol R, et al. Quality and Coordination of Care for Patients With Multiple Conditions: Results From an International Survey of Patient Experience. Eval Health Prof 2010; 33: 343–364. Breton M, Haggerty J, Roberge D, et al. Management continuity in local health networks. Int J Integr Care ; 12. Epub ahead of print 13 April 2012. DOI: 10.5334/ijic.682. Bravi F, Ruscio ED, Frassoldati A, et al. Patient and Health Care Professional Perspectives: A Case Study of the Lung Cancer Integrated Care Pathway. Int J Integr Care 2018; 18: 7. Bower P, Reeves D, Sutton M, et al. Improving care for older people with long-term conditions and social care needs in Salford: the CLASSIC mixed-methods study, including RCT. Health Serv Deliv Res 2018; 6: 1–188. Bortoli A, Daperno M, Kohn A, et al. Patient and physician views on the quality of care in inflammatory bowel disease: Results from SOLUTION-1, a prospective IG-IBD study. J Crohns Colitis 2014; 8: 1642–1652. Boele F, Harley C, Pini S, et al. Cancer as a chronic illness: support needs and experiences. BMJ Support Palliat Care 2019; bmjspcare-2019-001882. Benzer JK, Singer SJ, Mohr DC, et al. Survey of Patient-Centered Coordination of Care for Diabetes with Cardiovascular and Mental Health Comorbidities in the Department of Veterans Affairs. J Gen Intern Med 2019; 34: 43–49. Bentler SE, Morgan RO, Virnig BA, et al. The Association of Longitudinal and Interpersonal Continuity of Care with Emergency Department Use, Hospitalization, and Mortality among Medicare Beneficiaries. PLoS ONE 2014; 9: e115088. Auerbach AD, Kripalani S, Vasilevskis EE, et al. Preventability and Causes of Readmissions in a National Cohort of General Medicine Patients. JAMA Intern Med 2016; 176: 484. Andrew NE, Busingye D, Lannin NA, et al. The Quality of Discharge Care Planning in Acute Stroke Care: Influencing Factors and Association with Postdischarge Outcomes. J Stroke Cerebrovasc Dis Off J Natl Stroke Assoc 2018; 27: 583–590. Alsayali MM, AlSharif K, Al-Sahafi A, et al. Patients’ satisfaction after primary health care centers’ integration with Ministry of Health Hospitals, Jeddah. J Epidemiol Glob Health 2019; 9: 135–142. Aller M-B, Vargas I, Waibel S, et al. Factors associated to experienced continuity of care between primary and outpatient secondary care in the Catalan public healthcare system. Gac Sanit 2013; 27: 207–213. Acosta AM, Lima MADS, Marques GQ, et al. Brazilian version of the Care Transitions Measure: translation and validation. Int Nurs Rev 2017; 64: 379–387. Aller MB, Vargas I, Garcia I, et al. A tool for assessing continuity of care across care levels: an extended psychometric validation of the CCAENA questionnaire. Int J Integr Care ; 13. Epub ahead of print 2 December 2013. DOI: 10.5334/ijic.1160. Badri MA, Attia ST, Ustadi AM. Testing not-so-obvious models of healthcare quality. Int J Health Care Qual Assur 2008; 21: 159–74. Bakshi AB, Wee S-L, Tay C, et al. Validation of the care transition measure in multi-ethnic South-East Asia in Singapore. BMC Health Serv Res 2012; 12: 256. Bentler SE, Morgan RO, Virnig BA, et al. Do claims-based continuity of care measures reflect the patient perspective?. Med Care Res Rev MCRR 2014; 71: 156–73. Bentler SE, Morgan RO, Virnig BA, et al. Evaluation of a patient-reported continuity of care model for older adults. Qual Life Res Int J Qual Life Asp Treat Care Rehabil 2014; 23: 185–93. Berendsen AJ, Groenier KH, de Jong GM, et al. Assessment of patient’s experiences across the interface between primary and secondary care: Consumer Quality Index Continuum of care. Patient Educ Couns 2009; 77: 123–7. Bull MJ, Luo D, Maruyama GM. Measuring continuity of elders’ posthospital care. J Nurs Meas 2000; 8: 41–60. Castle N, Engberg J, Men A. Satisfaction of Discharged Nursing Home Residents. J Appl Gerontol Off J South Gerontol Soc 2018; 37: 1225–1243. Chavez LM, Canino G, Shrout PE, et al. Psychometric evaluation of the Spanish version of CONNECT: a measure of continuity of care in mental health services. Int J Methods Psychiatr Res 2007; 16: 23–33. Clark K, Beatty S, Reibel T. Maternity-care: measuring women’s perceptions. Int J Health Care Qual Assur 2016; 29: 89–99. Cohen Castel O, Dagan E, Keinan-Boker L, et al. Reliability and validity of the Hebrew version of the Nijmegen Continuity Questionnaire for measuring patients’ perceived continuity of care in oral anticancer therapy. Eur J Cancer Care (Engl) 2018; 27: e12913. Coleman EA, Mahoney E, Parry C. Assessing the quality of preparation for posthospital care from the patient’s perspective: the care transitions measure. Med Care 2005; 43: 246–55. Crump H, King J, Graham C, et al. Developing a User Reported Measure of Care Co-ordination. Int J Integr Care 2017; 17: 4. Dolovich LR, Nair KM, Ciliska DK, et al. The Diabetes Continuity of Care Scale: the development and initial evaluation of a questionnaire that measures continuity of care from the patient perspective. Health Soc Care Community 2004; 12: 475–87. Drewes HW, de Jong-van Til JT, Struijs JN, et al. Measuring chronic care management experience of patients with diabetes: PACIC and PACIC+ validation. Int J Integr Care 2012; 12: e194. Eubank BH, Lafave MR, Mohtadi NG, et al. Validation of a tool to assess patient satisfaction, waiting times, healthcare utilization, and cost. Prim Health Care Res Dev 2019; 20: e47. Fulton BR, Sternke EA, Ayala L, et al. Psychometric Testing of a Measure of Patient Experience in an Ambulatory Surgery Setting. J Ambulatory Care Manage 2019; 42: 27–36. Glasgow RE, Wagner EH, Schaefer J, et al. Development and validation of the Patient Assessment of Chronic Illness Care (PACIC). Med Care 2005; 43: 436–444. Graumlich JF, Novotny NL, Aldag JC. Brief scale measuring patient preparedness for hospital discharge to home: Psychometric properties. J Hosp Med 2008; 3: 446–54. Gulliford MC, Naithani S, Morgan M. Measuring continuity of care in diabetes mellitus: an experience-based measure. Ann Fam Med 2006; 4: 548–55. Hadjistavropoulos HD, Biem HJ, Kowalyk KM. Measurement of continuity of care in cardiac patients: reliability and validity of an in-person questionnaire. Can J Cardiol 2004; 20: 883–91. Hadjistavropoulos H, Biem H, Sharpe D, et al. Patient perceptions of hospital discharge: reliability and validity of a Patient Continuity of Care Questionnaire. Int J Qual Health Care J Int Soc Qual Health Care 2008; 20: 314–323. Haggerty JL, Burge F, Pineault R, et al. Management continuity from the patient perspective: comparison of primary healthcare evaluation instruments. Healthc Policy Polit Sante 2011; 7: 139–53. Haggerty JL, Roberge D, Freeman GK, et al. Validation of a generic measure of continuity of care: when patients encounter several clinicians. Ann Fam Med 2012; 10: 443–51. Hetlevik Ø, Hustoft M, Uijen A, et al. Patient perspectives on continuity of care: adaption and preliminary psychometric assessment of a Norwegian version of the Nijmegen Continuity Questionnaire (NCQ-N). BMC Health Serv Res 2017; 17: 760. Husain A, Barbera L, Howell D, et al. Advanced lung cancer patients’ experience with continuity of care and supportive care needs. Support Care Cancer Off J Multinatl Assoc Support Care Cancer 2013; 21: 1351–8. Hwang J-I, Chung J-H, Kim HK. Psychometric properties of transitional care instruments and their relationships with health literacy: Brief PREPARED and Care Transitions Measure. Int J Qual Health Care J Int Soc Qual Health Care 2019; 31: 774–780. Ignatyev Y, Timm J, Heinze M, et al. Development and Preliminary Validation of the Scale for Evaluation of Psychiatric Integrative and Continuous Care-Patient’s Version. Front Psychiatry 2017; 8: 162. Joober H, Chouinard M-C, King J, et al. The Patient Experience of Integrated Care Scale: A Validation Study among Patients with Chronic Conditions Seen in Primary Care. Int J Integr Care 2018; 18: 1. Joyce AS, Adair CE, Wild TC, et al. Continuity of care: validation of a self-report measure to assess client perceptions of mental health service delivery. Community Ment Health J 2010; 46: 192–208. Kiang MV, Singer SJ, Friedberg MW, et al. Development and preliminary validation of the Patient Perceptions of Integrated Care survey. Med Care Res Rev 2013; 70: 143–164. Kowalyk KM, Hadjistavropoulos HD, Biem HJ. Measuring continuity of care for cardiac patients: development of a patient self-report questionnaire. Can J Cardiol 2004; 20: 205–12. Liu L-M, Liu M-T, Sun M-J, et al. Validity and reliability of the Chinese version of the partners at care transitions measure. BMC Health Serv Res 2021; 21: 1284. Lloyd H, Fosh B, Whalley B, et al. Validation of the person-centred coordinated care experience questionnaire (P3CEQ). Int J Qual Health Care J Int Soc Qual Health Care 2019; 31: 506–512. Malik N, Alvaro C, Kuluski K, et al. Measuring patient satisfaction in complex continuing care/rehabilitation care. Int J Health Care Qual Assur 2016; 29: 324–36. Masters S, Giles L, Halbert J, et al. Development and testing of a questionnaire to measure older people’s experience of the Transition Care Program in Australia. Australas J Ageing 2010; 29: 172–8. McAlister FA, Lin M, Bakal J, et al. The Care Transitions Measure-3 Is Only Weakly Associated with Post-discharge Outcomes: a Retrospective Cohort Study in 48,384 Albertans. J Gen Intern Med 2019; 34: 2497–2504. McGuiness C, Sibthorpe B. Development and initial validation of a measure of coordination of health care. Int J Qual Health Care J Int Soc Qual Health Care 2003; 15: 309–318. Mira JJ, Nuno-Solinis R, Guilabert-Mora M, et al. Development and Validation of an Instrument for Assessing Patient Experience of Chronic Illness Care. Int J Integr Care 2016; 16: 13. Noest S, Ludt S, Klingenberg A, et al. Involving patients in detecting quality gaps in a fragmented healthcare system: development of a questionnaire for Patients’ Experiences Across Health Care Sectors (PEACS). Int J Qual Health Care 2014; 26: 240–249. Oikonomou E, Page B, Lawton R, et al. Validation of the Partners at Care Transitions Measure (PACT-M): assessing the quality and safety of care transitions for older people in the UK. BMC Health Serv Res 2020; 20: 608. Parra-Vega I, Marques-Sanchez P, Pelayo-Teran JM, et al. Development and validation of a questionnaire for assessing patients’ perceptions of interprofessional integration in health care. J Interprof Care 2021; 1–7. Peabody M, Bradley KD, Custer M. Assessing the Validity of a Continuum-of-care Survey: A Rasch Measurement Approach. J Appl Meas 2016; 17: 1–13. Radwin LE, Cabral HJ, Seibert MN, et al. Patient-Centered Care in Primary Care Scale: Pilot Development and Psychometric Assessment. J Nurs Care Qual 2019; 34: 34–39. Ramond-Roquin A, Stewart M, Ryan BL, et al. The ‘Patient-centered coordination by a care team’ questionnaire achieves satisfactory validity and reliability. J Interprof Care 2019; 33: 558–569. REYNOLDS J, GADSBY E, RIJKEN M, et al. Measuring Older Peoples’ Experiences of Person-Centred Coordinated Care: Experience and Methodological Reflections from Applying a Patient Reported Experience Measure in SUSTAIN. Int J Integr Care IJIC 2021; 21: 1–17. Rose D, Sweeney A, Leese M, et al. Developing a user-generated measure of continuity of care: brief report. Acta Psychiatr Scand 2009; 119: 320–324. Rucci P, Foglino S, Bravi F, et al. Validation of the OPportunity for Treatment In ONcology (OPTION) questionnaire measuring continuity of care. Eur J Cancer Care (Engl) ; 27. Epub ahead of print 2018. DOI: 10.1111/ecc.12765. Shadmi E, Zisberg A, Coleman EA. Translation and validation of the Care Transition Measure into Hebrew and Arabic. Int J Qual Health Care J Int Soc Qual Health Care 2009; 21: 97–102. Smith LFP. Postnatal care: development of a psychometric multidimensional satisfaction questionnaire (the WOMBPNSQ) to assess women’s views. Br J Gen Pract J R Coll Gen Pract 2011; 61: e628-37. Soares JB, Nogueira MC, Fernandes D, et al. Validation of the Portuguese version of a questionnaire to measure Quality of Care Through the Eyes of Patients with Inflammatory Bowel Disease (QUOTE-IBD). Eur J Gastroenterol Hepatol 2015; 27: 1409–17. Sorra J, Zebrak K, Carpenter D, et al. Development and psychometric properties of surveys to assess patient and family caregiver experience with care transitions. BMC Health Serv Res 2021; 21: 785. Squitieri L, Tsangaris E, Klassen AF, et al. Patient-reported experience measures are essential to improving quality of care for chronic wounds: An international qualitative study. Int Wound J 2020; 17: 1052–1061. Sugavanam T, Fosh B, Close J, et al. Codesigning a Measure of Person-Centred Coordinated Care to Capture the Experience of the Patient: The Development of the P3CEQ. J Patient Exp 2018; 5: 201–211. Teale EA, Young JB. A Patient Reported Experience Measure (PREM) for use by older people in community services. Age Ageing 2015; 44: 667–72. Thompson R, Stevens G, Elwyn G. Measuring Patient Experiences of Integration in Health Care Delivery: Psychometric Validation of IntegRATE Under Controlled Conditions. J Patient Exp 2021; 8: 23743735211007344. Uijen A, Schellevis F, Bosch W, et al. Nijmegen Continuity Questionnaire: Development and testing of a questionnaire that measures continuity of care. J Clin Epidemiol 2011; 64: 1391–9. Uijen AA, Schers HJ, Schellevis FG, et al. Measuring continuity of care: psychometric properties of the Nijmegen Continuity Questionnaire. Br J Gen Pract J R Coll Gen Pract 2012; 62: e949-57. Valaker I, Fridlund B, Wentzel-Larsen T, et al. Adaptation and psychometric properties of the Norwegian version of the heart continuity of care questionnaire (HCCQ). BMC Med Res Methodol 2019; 19: 62. van Melle MA, van Stel HF, Poldervaart JM, et al. The transitional risk and incident questionnaire was valid and reliable for measuring transitional patient safety from the patients’ perspective. J Clin Epidemiol 2019; 105: 40–49. Walker KO, Stewart AL, Grumbach K. Development of a survey instrument to measure patient experience of integrated care. BMC Health Serv Res 2016; 16: 193. Ware NC, Dickey B, Tugenberg T, et al. CONNECT: a measure of continuity of care in mental health services. Ment Health Serv Res 2003; 5: 209–21. Young JM, Walsh J, Butow PN, et al. Measuring cancer care coordination: development and validation of a questionnaire for patients. BMC Cancer 2011; 11: 298. Fillion L, Cook S, Veillette A-M, et al. Professional Navigation Framework: Elaboration and Validation in a Canadian Context. Oncol Nurs Forum 2012; 39: E58–E69. Schick-Makaroff K, Karimi-Dehkordi M, Cuthbertson L, et al. Using Patient- and Family-Reported Outcome and Experience Measures Across Transitions of Care for Frail Older Adults Living at Home: A Meta-Narrative Synthesis. The Gerontologist 2020; 61: e23–e38. Hargraves JL, Hays RD, Cleary PD. Psychometric properties of the Consumer Assessment of Health Plans Study (CAHPS) 2.0 adult core survey. Health Serv Res 2003; 38: 1509–1527. Platonova EA, Saunders WB, Warren-Findlow J, et al. Patient Perceptions of Patient-Centered Medical Home Characteristics and Satisfaction with Free Clinic Services. Popul Health Manag 2016; 19: 324–331. Dyer N, Sorra JS, Smith SA, et al. Psychometric properties of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Clinician and Group Adult Visit Survey. Med Care 2012; 50 Suppl: S28-34. Hays RD, Berman LJ, Kanter MH, et al. Evaluating the psychometric properties of the CAHPS Patient-centered Medical Home survey. Clin Ther 2014; 36: 689-696.e1. Gensichen J, Serras A, Paulitsch MA, et al. The Patient Assessment of Chronic Illness Care questionnaire: evaluation in patients with mental disorders in primary care. Community Ment Health J 2011; 47: 447–453. Cott CA, Teare G, McGilton KS, et al. Reliability and construct validity of the client-centred rehabilitation questionnaire. Disabil Rehabil 2006; 28: 1387–1397. Lloyd H, Jenkinson C, Hadi M, et al. Patient reports of the outcomes of treatment: a structured review of approaches. Health Qual Life Outcomes 2014; 12: 5. Strack and Schwarz; Asking questions: measurement in the social sciences in Ash MG, Sturm T (eds). Psychology’s territories: historical and contemporary perspectives from different disciplines . Mahwah, N.J: Lawrence Erlbaum Associates, 2007. Table Table 2 is available in the Supplementary Files section. Additional Declarations No competing interests reported. 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3","display":"","copyAsset":false,"role":"figure","size":399046,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eDomains, Themes, and Items Relevant for Assessing Patients’ Experiences of Pathways Across Healthcare Settings.\u003c/strong\u003e\u003c/p\u003e","description":"","filename":"Figure320230828.jpg","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/80dba3a9d709d478fbb9a61a.jpg"},{"id":61596973,"identity":"1d17cbd9-a100-4310-813d-112697d36101","added_by":"auto","created_at":"2024-08-01 17:30:56","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":1933485,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/2e251808-9d53-46c6-ab0d-8a2dec8f32e9.pdf"},{"id":54594573,"identity":"2888e555-d604-4a78-963e-2ba2d82c673c","added_by":"auto","created_at":"2024-04-12 18:28:30","extension":"docx","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":21874,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix1.docx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/94953836bb3874a9a23af10c.docx"},{"id":54594594,"identity":"05156338-af19-48b4-945c-3cfb70faa1bd","added_by":"auto","created_at":"2024-04-12 18:28:33","extension":"docx","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":14871,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix2.docx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/a754e0bfe9165e53cecdc091.docx"},{"id":54594641,"identity":"d3dbce7e-c37d-4edd-b9d1-2afa3c75704e","added_by":"auto","created_at":"2024-04-12 18:28:43","extension":"docx","order_by":3,"title":"","display":"","copyAsset":false,"role":"supplement","size":72362,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix320230726.docx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/51927739b11bf22d775bbd65.docx"},{"id":54594605,"identity":"6f7fb94c-8890-41d4-8b2f-d2d82e76b1df","added_by":"auto","created_at":"2024-04-12 18:28:35","extension":"xlsx","order_by":4,"title":"","display":"","copyAsset":false,"role":"supplement","size":13410,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix420230726.xlsx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/1f50f07bbf8809eba6068e32.xlsx"},{"id":54594577,"identity":"c30e4ed9-1d44-4aed-9162-ed1dd5060e43","added_by":"auto","created_at":"2024-04-12 18:28:31","extension":"docx","order_by":5,"title":"","display":"","copyAsset":false,"role":"supplement","size":22249,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix5.docx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/bd928b4b6d0a41bb26c804ec.docx"},{"id":54594590,"identity":"aa246319-384c-4f34-b1ea-9427807e9752","added_by":"auto","created_at":"2024-04-12 18:28:33","extension":"pdf","order_by":6,"title":"","display":"","copyAsset":false,"role":"supplement","size":298085,"visible":true,"origin":"","legend":"","description":"","filename":"Appendix620230728.pdf","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/a9ce7905aa30d69f33a7c3d0.pdf"},{"id":54594564,"identity":"ed5b1064-1dc2-407c-ae07-f4a1c71c36b6","added_by":"auto","created_at":"2024-04-12 18:28:28","extension":"docx","order_by":7,"title":"","display":"","copyAsset":false,"role":"supplement","size":33615,"visible":true,"origin":"","legend":"","description":"","filename":"Table2.docx","url":"https://assets-eu.researchsquare.com/files/rs-4211885/v1/dce2ec95cd4989fbde85832a.docx"}],"financialInterests":"No competing interests reported.","formattedTitle":"Content Validity of Patient-Reported Measures Evaluating Experiences of the Quality of Transitions in Healthcare Settings - A Scoping Review.","fulltext":[{"header":"Background","content":"\u003cp\u003eCare management encompasses evaluating individuals' needs and coordinating healthcare services; however, patients struggle with consistency and clarity in care management.\u003csup\u003e1\u003c/sup\u003e Patients\u0026rsquo; ability to navigate healthcare systems has implications for the outcome of their treatment\u003csup\u003e2,3\u003c/sup\u003e, and patients\u0026rsquo; experiences are associated with clinical effectiveness and safety.\u003csup\u003e4\u003c/sup\u003e Therefore, assessing patients\u0026rsquo; experiences with transitions in healthcare is important in determining the quality of healthcare delivery. Patient-reported experience measures (PREM) are intended to be reliable measures of the quality of healthcare services from patients\u0026rsquo; perspectives and may support evaluation of the effectiveness, safety, and efficiency of healthcare provision.\u003csup\u003e5\u003c/sup\u003e\u003c/p\u003e\n\u003cp\u003eSeveral reviews of instruments measuring patient experience of the quality in healthcare transitions have been published.\u003csup\u003e6\u0026ndash;11\u003c/sup\u003e In the systematic review by Berbee et al. (2009) they aimed to identify and select an appropriate instrument for measuring the quality of integrated care for patients experiencing chronic illness, but identified no patient-reported experience measure (PREM) that was comprehensive or relevant according to focus group interviews with the patients.\u003csup\u003e6\u003c/sup\u003e Concordantly, in a systematic review for evaluating patient satisfaction in healthcare settings integrating behavioural and medical health services, Black et al. (2021) found that no PREM comprehensively captured all relevant aspects of the integrated healthcare experience.\u003csup\u003e7\u003c/sup\u003e In contrast, Weaver et al. (2017) reviewed concepts, models, and instruments for understanding care continuity in mental health services and suggested a PREM suitable for self-reporting experiences with mental healthcare.\u003csup\u003e8\u003c/sup\u003e In 2011 Fiscella et al. (2011) published a consensus of domains and measures suitable for patient-reported assessment of cancer navigation but also called for an instrument that covered all relevant topics.\u003csup\u003e9\u003c/sup\u003e Likewise, McMurray et al. (2016) identified 25 instruments to assess patients\u0026rsquo; experience of rehabilitation services, but none comprehensively measured patient experience across the rehabilitative care continuum.\u003csup\u003e10\u003c/sup\u003e Following this, Quinn et al. (2017) concluded that no instruments adequately assessed veterans\u0026rsquo; experience with access and coordination across healthcare settings.\u003csup\u003e11\u003c/sup\u003e No reviews so far have identified a generic PREM that comprehensively measures patients\u0026rsquo; experience with the quality of healthcare transitions.\u003csup\u003e6\u0026ndash;13\u003c/sup\u003e Therefore, there is a need to identify adequate concepts and measures that can target the patient experience transition in healthcare.\u003c/p\u003e\n\u003cp\u003eThe COSMIN group argues that content validity is the most important aspect of patient-reported measures.\u003csup\u003e14\u003c/sup\u003e Content validity refers to a patient-reported measure's relevance, comprehensiveness, and comprehensibility.\u003csup\u003e15\u003c/sup\u003e In other words, to evaluate whether the instrument provides an adequate reflection of the construct to be measured in the context.\u003csup\u003e14\u003c/sup\u003e Although there is some consensus on defining patient experience of healthcare transitions as a multidimensional concept consisting of human-relational and system factors, the conceptualizations found in existing reviews still lack clarity.\u003csup\u003e6\u0026ndash;13\u003c/sup\u003e\u003c/p\u003e\n\u003cp\u003eThe overall scope of this review was to explore and define domains of the concept of patient-experienced quality in cross-sectoral care for generic patient populations. Further, to map existing methods for generically assessing the quality of transitions in healthcare settings (e.g. between municipality, general practitioner, and hospital). To achieve this, our objectives were:\u003c/p\u003e\n\u003col start=\"1\" type=\"1\"\u003e\n\u003cli\u003e\n\u003cp\u003eWhat domains are considered relevant to measure for patients\u0026rsquo; experiencing healthcare transitions when evaluating the quality of care they have received?\u003c/p\u003e\n\u003c/li\u003e\n\u003cli\u003e\n\u003cp\u003eWhat existing patient-reported experience measures attempt to measure patients\u0026rsquo; experience of transitions in healthcare settings?\u003c/p\u003e\n\u003c/li\u003e\n\u003cli\u003e\n\u003cp\u003eAre any existing patient-reported experience measures adequate (relevant and comprehensive) reflections of patients\u0026rsquo; experience of transitions in healthcare settings?\u003c/p\u003e\n\u003c/li\u003e\n\u003c/ol\u003e"},{"header":"Methods","content":"\u003cp\u003eThe method of this scoping review followed the Joanna Briggs Institutes\u0026rsquo; (JBI) guidance for scoping reviews.\u003csup\u003e16\u003c/sup\u003e The article was outlined following JBI guidelines\u003csup\u003e16\u003c/sup\u003e supported by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) Checklist.\u003csup\u003e17\u003c/sup\u003e A pre-registered protocol, including aims, search strategies, and amendments made during the iterative review process\u003csup\u003e16\u003c/sup\u003e, is available via Open Science Framework (OSF).\u003csup\u003e18\u003c/sup\u003e The research question was defined using the SPIDER-model (i.e., Setting, Phenomenon of Interest, Design, Evaluation, Research).\u003csup\u003e19\u003c/sup\u003e The research question encompassed five concepts with predefined definitions and in- and exclusion criteria to ensure identification of eligible studies (\u003cem\u003eTable 1\u003c/em\u003e).\u003c/p\u003e\n\u003cp\u003eTable 1 - Research Question Defined by the SPIDER-Model\u003c/p\u003e\n\u003ctable border=\"1\" cellspacing=\"0\" cellpadding=\"0\"\u003e\n \u003ctbody\u003e\n \u003ctr\u003e\n \u003ctd width=\"21.65109034267913%\" colspan=\"2\" valign=\"top\"\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003eConcepts\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003eInclusion criteria\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003eExclusion criteria\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"4.049844236760125%\" valign=\"top\"\u003e\n \u003cp\u003eS\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"17.601246105919003%\" valign=\"top\"\u003e\n \u003cp\u003eSetting\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003eTransitions in healthcare settings\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003ePatient transition between at least 2 healthcare settings (municipality, GP, hospital)\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003eSingle settings such as \u0026ldquo;In the primary care setting, at the hospital etc.\u0026rdquo;\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"4.049844236760125%\" valign=\"top\"\u003e\n \u003cp\u003ePI\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"17.601246105919003%\" valign=\"top\"\u003e\n \u003cp\u003ePhenomenon of Interest\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003ePatient-experienced quality\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003ePatients\u0026rsquo; experiences were accounted for or assessed\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003eOnly healthcare personnel or relatives\u0026rsquo; experiences were assessed\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"4.049844236760125%\" valign=\"top\"\u003e\n \u003cp\u003eD\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"17.601246105919003%\" valign=\"top\"\u003e\n \u003cp\u003eDesign\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003eQualitative and quantitative research designs.\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003ePsychometric studies qualitative studies, quantitative studies,\u0026nbsp;\u003c/p\u003e\n \u003cp\u003esyntheses/reviews\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003eFeasibility studies, study protocols, reports\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"4.049844236760125%\" valign=\"top\"\u003e\n \u003cp\u003eE\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"17.601246105919003%\" valign=\"top\"\u003e\n \u003cp\u003eEvaluation\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003ePREMs*, patient accounts, narratives, attitudes, perspectives, and experiences of quality.\u0026nbsp;\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003ePatient experience of \u0026nbsp;healthcare provision\u003csup\u003e10,20\u003c/sup\u003e\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003ePatient satisfaction\u003csup\u003e21\u003c/sup\u003e\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"4.049844236760125%\" valign=\"top\"\u003e\n \u003cp\u003eR\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"17.601246105919003%\" valign=\"top\"\u003e\n \u003cp\u003eResearch Type\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"23.98753894080997%\" valign=\"top\"\u003e\n \u003cp\u003ePublished, peer-reviewed research reporting data\u0026nbsp;\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"26.4797507788162%\" valign=\"top\"\u003e\n \u003cp\u003ePeer-reviewed, published studies\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"27.881619937694705%\" valign=\"top\"\u003e\n \u003cp\u003eConference abstracts and meeting notes\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"100%\" colspan=\"5\" valign=\"top\"\u003e\n \u003cp\u003e*Patient-Reported Experience Measure\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003c/tbody\u003e\n\u003c/table\u003e\n\u003cp\u003eSearch\u003c/p\u003e\n\u003cp\u003eThe search was performed on 07 December 2021. The electronic databases Medline (Ovid), Embase (Ovid), and Cinahl (EBSCO) were chosen because they cover multiple research areas within healthcare. The search was developed in Embase and translated to Medline and Cinahl as recommended.\u003csup\u003e22\u003c/sup\u003e For the phenomenon of interest, we identified the Mesh term \u0026ldquo;Patient Satisfaction\u0026rdquo;. Although we excluded studies reporting on patient satisfaction rather than patient experience, the terms have been used interchangeably,\u003csup\u003e10\u003c/sup\u003e and patient satisfaction thus seemed necessary to include in our search strategy. As the focus on patient\u0026apos;s experiences of coherent care seemed to have emerged around late 1990 and early 2000,\u003csup\u003e23\u003c/sup\u003e we searched for literature from 2000. The search strategy was developed from the predefined definitions and criteria with guidance from research librarians (\u003cem\u003esee full search strategy in Appendix 1\u003c/em\u003e).\u003c/p\u003e\n\u003cp\u003eSelection of Sources of Evidence\u003c/p\u003e\n\u003cp\u003eCovidence (Veritas Health Innovation, Melbourne, Australia) was used to manage the duplication and screening process.\u003csup\u003e24\u003c/sup\u003e All studies were screened by two independent reviewers, and a total of seven reviewers participated in the screening process. To ensure calibration of the screening process, a consensus meeting was arranged at the beginning of the process as in rapid reviews.\u003csup\u003e25\u003c/sup\u003e During the calibration sessions, in- and exclusion criteria were specified further than the a-priori defined criteria (\u003cem\u003eAppendix 2\u003c/em\u003e).\u003c/p\u003e\n\u003cp\u003eIn the full-text screening process, we experienced a larger number of articles than expected. In order to focus this review on the a priori defined aims, we decided to; I) report on intervention studies in an independent review, II) exclude mixed-methods studies and original qualitative studies, III) synthesize dimensions found in the included syntheses and reviews rather than report on the original studies. We decided to include syntheses and reviews because reports on qualitative studies were frequent, and relevant themes for patient-experienced quality of healthcare transitions had already been mapped in these meta-syntheses, integrative reviews, or scoping reviews.\u003c/p\u003e\n\u003cp\u003eData Charting Process\u003c/p\u003e\n\u003cp\u003eA priori-defined data extraction templates were used and are available at OSF.\u003csup\u003e26\u003c/sup\u003e The data charting was done by one author (SW). The first 10 data extractions were validated independently by a research assistant (NH). The data charting table and process were adapted following the pilot extraction. The final data extraction tables are available in Appendix 3 and Appendix 4.\u003c/p\u003e\n\u003cp\u003eCritical Appraisal of Individual Sources of Evidence\u003c/p\u003e\n\u003cp\u003eAlthough the JBI guidelines for scoping reviews do not warrant critical appraisal,\u003csup\u003e27\u003c/sup\u003e comprehensive (i.e. PREMs including at least five items of the 12 subthemes). PREMs were critically appraised according to the COSMIN Risk of Bias checklist for systematic reviews of Patient-Reported Outcome Measures\u003csup\u003e14,28,29\u003c/sup\u003e to assess content validity\u003csup\u003e14\u003c/sup\u003e (relevance, comprehensiveness, and comprehensibility) from patients\u0026rsquo; perspectives. The critical assessment was done independently by two reviewers (SW, LM), and conflicts were discussed until a consensus was reached. When PREMs were mentioned in included publications but not available in the publication, references were followed to the original publications on that PREM.\u003c/p\u003e\n\u003cp\u003eSynthesis of Results\u003c/p\u003e\n\u003cp\u003eWe synthesized the data by; I) Summarizing themes identified in the qualitative syntheses and identifying relevant domains (\u003cem\u003eAppendix 3 and Figure 3\u003c/em\u003e); II) Identifying PREMs, assessing the PREMs phenomenon of interest, and categorizing and listing the items of the relevant PREMs to assess comprehensiveness (\u003cem\u003eAppendix 4, Appendix 5 and Table 2\u003c/em\u003e); III) Assessing the content validity of the most comprehensive PREMs (items related to five or more themes) (\u003cem\u003eTable 2\u003c/em\u003e). The process of synthesizing data is also described in figure 1.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFigure 1 \u0026ndash; Data Synthesis Process\u003c/strong\u003e\u003c/p\u003e"},{"header":"Results","content":"\u003cp\u003eThe search identified 16,134 records (\u003cem\u003eFigure 2\u003c/em\u003e), and 172 reports were included after the screening and selection process (\u003cem\u003eFigure 2\u003c/em\u003e). In addition to the regular selection process, first author SW divided the reports according to objectives 1 (24 reports) and 2 (148 reports, 35 reports excluded during data extraction, leaving 113 reports for inclusion). This was done because the scientific methods for reports to answer objective 1 needed to be qualitative, and the methods relevant for answering objective 2 needed to be quantitative observational, development, or validation reports.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFigure 2 \u0026ndash; PRISMA Flowchart\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eRelevant Domains (Results for Objective 1)\u003c/p\u003e\n\u003cp\u003eFor objective one, we included 24 reports (\u003cem\u003eAppendix 6\u003c/em\u003e),\u003csup\u003e30\u0026ndash;53\u003c/sup\u003e which included: 10 (42%) systematic reviews,\u003csup\u003e34,36,37,40,43,44,46,47,49,51\u003c/sup\u003e six (25%) scoping reviews,\u003csup\u003e32,38,41,48,50,53\u003c/sup\u003e Four (17%) meta syntheses,\u003csup\u003e30,39,52\u003c/sup\u003e three (13%) integrated reviews,\u003csup\u003e33,35,42\u003c/sup\u003e one (4%) narrative review,\u003csup\u003e54\u003c/sup\u003e and one (4%) qualitative review\u003csup\u003e45\u003c/sup\u003e that provided information on relevant domains and/or themes for assessing patients\u0026acute; experiences with care across healthcare settings. The number of identified themes ranged from two\u003csup\u003e32\u003c/sup\u003e to 13,\u003csup\u003e50\u003c/sup\u003e with most articles reporting three themes.\u003csup\u003e34,39,52,53\u003c/sup\u003e When summarizing and describing themes from the included reports, we found that the themes could be organized in two distinct domains; I) A system/organizational domain; II) A human-relational domaine. Each of these domains encompassed six themes; thus, we identified 12 relevant themes as illustrated in Figure 3.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFigure 3 \u0026ndash; Domains, Themes, and Items Relevant for Assessing Patients\u0026rsquo; Experiences of Pathways Across Healthcare Settings.\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eExisting Patient-Reported Experience Measures (Results for Objective 2)\u003c/p\u003e\n\u003cp\u003eFor objective two, we included 113 (\u003cem\u003eAppendix 6\u003c/em\u003e)\u003csup\u003e6\u0026ndash;13,55\u0026ndash;159\u003c/sup\u003e reports that described 109 unique PREMs (\u003cem\u003eAppendix 4\u003c/em\u003e). However, 80 (73%) PREMs were excluded during data extraction as they referred to other aspects of care quality than transitions between healthcare settings or otherwise deviated from our specified phenomenon (\u003cem\u003eAppendix 5\u003c/em\u003e). The Consumer Assessment of Healthcare Providers and Systems (CAHPS)\u003csup\u003e160\u0026ndash;163\u003c/sup\u003e questionnaires were most frequently referred to,\u003csup\u003e6,7,9,11,56,61,63,66\u003c/sup\u003e but we did not find the items relevant according to the construct definition in objective 1. The two relevant PREMs that were most frequently referred to were Nijmegen Continuity Questionnaire\u003csup\u003e8,12,72,77,105,119,151,152\u003c/sup\u003e and Patient Assessment of Chronic Illness Care (PACIC).\u003csup\u003e6,11,12,78,80,85,109,112,164\u003c/sup\u003e\u003c/p\u003e\n\u003cp\u003eIn the data extraction process, we identified different ways of formulating items. Some items were worded from a medical system perspective on quality i.e. \u0026ldquo;My physical pain was controlled as well as possible\u0026rdquo;,\u003csup\u003e165\u003c/sup\u003e whereas others were articulated from a patient-centred perspective i.e. \u0026ldquo;My treatment fits my needs\u0026rdquo;.\u003csup\u003e124\u003c/sup\u003e Yet, other items were specific to a certain contextual system infrastructure i.e. \u0026ldquo;The specialist makes out the first prescription for the treatment he/she prescribes me\u0026rdquo;,\u003csup\u003e95\u003c/sup\u003e or they were disease-specific.\u003csup\u003e114\u003c/sup\u003e However, we did identify PREMs with a more generic wording such as, \u0026ldquo;Were there times when you had to repeat information that should have been in your care records?\u0026rdquo;.\u003csup\u003e166\u003c/sup\u003e\u003c/p\u003e\n\u003cp\u003eAdequate reflection of patients\u0026rsquo; experience (results for objective 3)\u003c/p\u003e\n\u003cp\u003eWe extracted 29 PREMs that pertained to patient-experience of quality of transitions in healthcare settings. To assess the relevance and comprehensiveness of the identified PREMs, the items of each PREM were plotted according to the 12 subthemes identified for objective 1 (\u003cem\u003etable 2\u003c/em\u003e). Twenty-one PREMs had items related to at least five of the 12 subthemes (\u003cem\u003etable 2\u003c/em\u003e). To focus our review on the most comprehensive PREMs, we critically appraised the selected 21 PREMs. The Alberta Continuity of Services Scale \u0026ndash; Mental Health (ACSS-MH),\u003csup\u003e124\u003c/sup\u003e the Person-Centered Coordinated Care Experience Questionnaire (P3CEQ),\u003csup\u003e148\u003c/sup\u003e and the Patient Experience of Integrated Care Scale (PEICS)\u003csup\u003e123\u003c/sup\u003e had adequate content validity, however, they were disease-specific and/or did not have items in all themes identified in objective 1 (\u003cem\u003etable 2\u003c/em\u003e). The remaining 16 PREMs had doubtful or inadequate content validity.\u003c/p\u003e\n\u003cp\u003eTable 2 \u0026ndash; Comprehensiveness and Content Validity of Existing PREMs for Assessment of Patients\u0026rsquo; Experiences of the Quality of Transitions in Healthcare Settings.\u003c/p\u003e"},{"header":"Discussion","content":"\u003cp\u003eThe overall aim of this scoping review was to define the concept of patient-experienced quality in healthcare transitions and map existing content valid PREMs relevant for measuring this concept. We found the construct of patient-reported experience of transitions in healthcare to consist of two domains \u0026ndash; system/organization and human-relation. However, in summarizing the 24 qualitative reports for this review, we found some inconsistency and lack of clarity in the conceptualization and understanding of patient-experienced quality in healthcare transitions. Although some reports identified the construct of patient-experienced quality in healthcare transitions to consist of two main domains (organization and human-relational),\u003csup\u003e8,9,40,47,158\u003c/sup\u003e others disagreed\u003csup\u003e33,50\u003c/sup\u003e and leaned towards the Institute of Medicine\u0026rsquo;s framework for quality with five or more domains.\u003csup\u003e23\u003c/sup\u003e The two-dimensional model is, however, supported by both qualitative conceptualization\u003csup\u003e40,47\u003c/sup\u003e and testing of measurement properties,\u003csup\u003e8,9,158\u003c/sup\u003e whereas the Institiutes of Medicine\u0026rsquo;s framework is not. In addition to inconsistency in domains, there was a general inconsistency in the number and terminology for themes\u003csup\u003e32,50\u003c/sup\u003e and formulation of items concerning patient-centeredness.\u003csup\u003e124,165\u003c/sup\u003e As items in PREMs may be approached by respondents much the same as a dialogue,\u003csup\u003e167\u003c/sup\u003e we believe a person-centred approach to item formulation may provide the best opportunity for patients to assess quality of care appropriately. Several reports suggest further research into the conceptualization and understanding of patient-experience with care transitions.\u003csup\u003e32,36,49,54\u003c/sup\u003e Due to the variations in how the construct is defined, assessing the content validity of current PREMs becomes challenging.\u003csup\u003e14,15\u003c/sup\u003e Therefore, we support the suggestion of further research into the conceptualization of patient-experienced quality in healthcare transitions.\u003c/p\u003e\n\u003cp\u003eWe identified 29 PREMs that reflected at least one relevant aspect of the construct but none that were comprehensive reflections of generic patient populations\u0026rsquo; experiences of transitions in healthcare settings. This finding aligns with the conclusion of the included reviews of instruments.\u003csup\u003e6\u0026ndash;13,158,159\u003c/sup\u003e It is surprising that we have not identified a content-valid PREM given the large number of reports (113) and unique PREMs (109) included. This may be associated with the lack of clarity in the construct of patient-experienced quality in healthcare transitions. In the future, a generic PREM should be developed to make cross-comparison between studies and healthcare organizations possible. A collective effort to test and use a generice PREM might also support further development and/or understanding of the construct. This, however, would entail a generic approach to item formulation, as seen in P3CEQ,\u003csup\u003e166\u003c/sup\u003e rather than a context-specific approach.\u003csup\u003e95\u003c/sup\u003e\u003c/p\u003e\n\u003cp\u003eIt may be a limitation in our study that our search was imprecise with the inclusion of patient satisfaction in the search terms. However, the sensitivity of our search originates from inclusion of patient satisfaction in the search terms, and we consider the strength of this sensitivity to out way the imprecision by securing a comprehensive review. The comprehensiveness of our search resulted in a large number of records to be reviewed, and thus many reviewers to accommodate for time constraints. We attempted to compensate for a potentially low inter-rater reliability with calibration meetings. Despite of this, the number of reviewers may have been a limitation to the inclusion of all relevant, and only relevant reports. Furthermore, our pragmatic decision of excluding original qualitative studies from this review could have been a limitation to the comprehensiveness of our results. Incorporating the 24 qualitative reports has sufficiently advanced our comprehension of the existing literature to address objective 1. This is corroborated by the absence of new themes identified during data extraction from recent reports. The data extraction performed primarily by one reviewer may have caused some imprecision. However, as we have identified more PREMs than the included reviews of instruments,\u003csup\u003e6\u0026ndash;13,158,159\u003c/sup\u003e this does not seem to be the case. While our scoping review does exhibit certain limitations, the thoroughness of our search and the inclusive methodology employed in comprehending and evaluating patient-experienced quality during healthcare transitions have nonetheless generated novel and significant insights.\u003c/p\u003e\n\u003cp\u003eIn light of our findings, it is plausible\u0026nbsp;that items extracted from the most relevant and comprehensive PREMs, with a focus on generic formulations for infrastructure and disease, would reflect the construct of patient-experienced quality in healthcare transitions adequately. Furthermore, as there is some\u0026nbsp;consensus that quality healthcare transitions occur when organisational structures are flexible and sensitive to patient preferences,\u003csup\u003e34,39\u0026ndash;42,46,53\u003c/sup\u003e it seems advantageous to aply this knowledge in item extraction and/or formulation. As described, the construct seems to be unclear or imprecisely defined. Therefore, a process of extracting and/or formulating items should be undertaken systematically and iteratively with patient involvement and openness to re-evaluating the definition of the construct. A PREM revised by the outlined approach may support valid and reliable evaluation of the effectiveness, safety, and efficiency of healthcare provision.\u003c/p\u003e"},{"header":"Conclusion","content":"\u003cp\u003eIn the literature, we identified several conceptual models that referred to aspects of patients\u0026rsquo; experience with the quality of healthcare transitions. We consider a model with two domains likely to be adequate, however, a more comprehensive analysis and adequate definition of the construct is needed.\u003c/p\u003e\n\u003cp\u003eTwenty-nine PREMs assessing at least one aspect of patients\u0026rsquo; experience of transitions in healthcare were identified. However, none of the PREMs were considered content valid to measure patient-experienced quality in healthcare transitions generically. It is possible that items extracted from the identified questionnaires can be combined for a content-valid PREM. We call for further exploration into the construct of patient experience with healthcare transitions and testing of models to produce a content-valid PREM suitable for generic assessment of patients\u0026rsquo; experiences with the quality of healthcare transitions.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003eEthics approval and consent to participate\u003c/p\u003e\n\u003cp\u003eNot applicable\u003c/p\u003e\n\u003cp\u003eConsent for publication\u003c/p\u003e\n\u003cp\u003eNot applicable\u003c/p\u003e\n\u003cp\u003eAvailability of data and materials\u003c/p\u003e\n\u003cp\u003eThe datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.\u003c/p\u003e\n\u003cp\u003eCompeting interests\u003c/p\u003e\n\u003cp\u003eThe authors declare that they have no competing interests.\u003c/p\u003e\n\u003cp\u003eFunding\u003c/p\u003e\n\u003cp\u003eThe author(s) disclosed receipt of the following financial support for the research, authorship, or publication of this article: This work was supported by the local research fund at N\u0026aelig;stved, Slagelse, and Ringsted hospitals; by a program grant for Exercise First from Region Zealand; and a faculty scholarship from Department of Clinical Research at University of Southern Denmark.\u003c/p\u003e\n\u003cp\u003eAuthors\u0026rsquo; contributions\u003c/p\u003e\n\u003cp\u003eSW devised the systematic search and review process, contributed substantially to the data extraction and mapping process, and revised the manuscript critically. SGR contributed substantially to the devision of the systematic search and review process, and revised the manuscript critically. SMH contributed substantially to the devision of the search and screening process and revised the manuscript critically. GZ and SRM contributed substantially to the review process and revised the manuscript critically. CBK contributed substantially to the data extraction and mapping process and with critical revision of the manuscript. CS, HHL, and LM made substantial contributions to conceptualisation, the systematic search and review process, the data extraction and mapping process, and critically revised the manuscript.\u003c/p\u003e\n\u003cp\u003eAcknowledgements\u003c/p\u003e\n\u003cp\u003eWe thank Mette Kring Clausen and Olga Alexandrovna Tchijevitch for reviewing identified literature\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n\u003cli\u003eStewart A, MacIntyre G. Care management in the twenty-first centuryPersistent challenges in implementation in the context of the emergence of self-care. \u003cem\u003eJ Integr Care\u003c/em\u003e 2013; 21: 91\u0026ndash;104.\u003c/li\u003e\n\u003cli\u003eFreeman HP, Muth BJ, Kerner JF. Expanding access to cancer screening and clinical follow-up among the medically underserved. \u003cem\u003eCancer Pract\u003c/em\u003e 1995; 3: 19\u0026ndash;30.\u003c/li\u003e\n\u003cli\u003eEgan M, Anderson S, McTaggart J. Community navigation for stroke survivors and their care partners: description and evaluation. \u003cem\u003eTop Stroke Rehabil\u003c/em\u003e 2010; 17: 183\u0026ndash;190.\u003c/li\u003e\n\u003cli\u003eDoyle C, Lennox L, Bell D. A systematic review of evidence on the links between patient experience and clinical safety and effectiveness. \u003cem\u003eBMJ Open\u003c/em\u003e 2013; 3: e001570.\u003c/li\u003e\n\u003cli\u003eWeldring T, Smith SMS. Patient-Reported Outcomes (PROs) and Patient-Reported Outcome Measures (PROMs). \u003cem\u003eHealth Serv Insights\u003c/em\u003e 2013; 6: 61\u0026ndash;68.\u003c/li\u003e\n\u003cli\u003eVrijhoef HJM, Berbee R, Wagner EH, et al. Quality of integrated chronic care measured by patient survey: identification, selection and application of most appropriate instruments. \u003cem\u003eHealth Expect\u003c/em\u003e 2009; 12: 417\u0026ndash;429.\u003c/li\u003e\n\u003cli\u003eBlack D, Held ML, Skeesick J, et al. Measures Evaluating Patient Satisfaction in Integrated Health Care Settings: A Systematic Review. \u003cem\u003eCommunity Ment Health J\u003c/em\u003e 2021; 57: 1464\u0026ndash;1477.\u003c/li\u003e\n\u003cli\u003eWeaver N, Coffey M, Hewitt J. Concepts, models and measurement of continuity of care in mental health services: A systematic appraisal of the literature. \u003cem\u003eJ Psychiatr Ment Health Nurs\u003c/em\u003e 2017; 24: 431\u0026ndash;450.\u003c/li\u003e\n\u003cli\u003eFiscella K, Ransom S, Jean-Pierre P, et al. Patient-reported outcome measures suitable to assessment of patient navigation. \u003cem\u003eCancer\u003c/em\u003e 2011; 117: 3603\u0026ndash;3617.\u003c/li\u003e\n\u003cli\u003eMcMurray J, McNeil H, Lafortune C, et al. Measuring Patients\u0026rsquo; Experience of Rehabilitation Services Across the Care Continuum. Part I: A Systematic Review of the Literature. \u003cem\u003eArch Phys Med Rehabil\u003c/em\u003e 2016; 97: 104\u0026ndash;120.\u003c/li\u003e\n\u003cli\u003eQuinn M, Robinson C, Forman J, et al. Survey Instruments to Assess Patient Experiences With Access and Coordination Across Health Care Settings: Available and Needed Measures. \u003cem\u003eMed Care\u003c/em\u003e 2017; 55: S84\u0026ndash;S91.\u003c/li\u003e\n\u003cli\u003eFernandes S, Fond G, Zendjidjian XY, et al. Measuring the Patient Experience of Mental Health Care: A Systematic and Critical Review of Patient-Reported Experience Measures. \u003cem\u003ePatient Prefer Adherence\u003c/em\u003e 2020; Volume 14: 2147\u0026ndash;2161.\u003c/li\u003e\n\u003cli\u003ePerriman N, Davis D. Measuring maternal satisfaction with maternity care: A systematic integrative review. \u003cem\u003eWomen Birth\u003c/em\u003e 2016; 29: 293\u0026ndash;299.\u003c/li\u003e\n\u003cli\u003eTerwee CB, Prinsen C a. C, Chiarotto A, et al. COSMIN methodology for evaluating the content validity of patient-reported outcome measures: a Delphi study. \u003cem\u003eQual Life Res Int J Qual Life Asp Treat Care Rehabil\u003c/em\u003e 2018; 27: 1159\u0026ndash;1170.\u003c/li\u003e\n\u003cli\u003eMokkink LB, Terwee CB, Patrick DL, et al. The COSMIN study reached international consensus on taxonomy, terminology, and definitions of measurement properties for health-related patient-reported outcomes. \u003cem\u003eJ Clin Epidemiol\u003c/em\u003e 2010; 63: 737\u0026ndash;745.\u003c/li\u003e\n\u003cli\u003ePeters MDJ, Marnie C, Tricco AC, et al. Updated methodological guidance for the conduct of scoping reviews. \u003cem\u003eJBI Evid Synth\u003c/em\u003e 2020; 18: 2119\u0026ndash;2126.\u003c/li\u003e\n\u003cli\u003ePRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation | Annals of Internal Medicine, https://www.acpjournals.org/doi/10.7326/M18-0850 (accessed 12 January 2023).\u003c/li\u003e\n\u003cli\u003eTang L, Skou ST, Nissen N, et al. The Exercise First Research Program, https://osf.io/v3ec5/ (2020, accessed 21 June 2023).\u003c/li\u003e\n\u003cli\u003eThe SPIDER Tool for Qualitative Evidence Synthesis | NCCMT, https://www.nccmt.ca/knowledge-repositories/search/191 (accessed 16 January 2023).\u003c/li\u003e\n\u003cli\u003eCrow R, Gage H, Hampson S, et al. The measurement of satisfaction with healthcare: implications for practice from a systematic review of the literature. \u003cem\u003eHealth Technol Assess Winch Engl\u003c/em\u003e 2002; 6: 1\u0026ndash;244.\u003c/li\u003e\n\u003cli\u003eJenkinson C, Coulter A, Bruster S, et al. Patients\u0026rsquo; experiences and satisfaction with health care: results of a questionnaire study of specific aspects of care. \u003cem\u003eQual Saf Health Care\u003c/em\u003e 2002; 11: 335\u0026ndash;339.\u003c/li\u003e\n\u003cli\u003eBramer WM, De Jonge GB, Rethlefsen ML, et al. A systematic approach to searching: an efficient and complete method to develop literature searches. \u003cem\u003eJ Med Libr Assoc\u003c/em\u003e; 106. Epub ahead of print 4 October 2018. DOI: 10.5195/JMLA.2018.283.\u003c/li\u003e\n\u003cli\u003eInstitute of Medicine (US) Committee on Quality of Health Care in America. \u003cem\u003eCrossing the Quality Chasm: A New Health System for the 21st Century\u003c/em\u003e. Washington (DC): National Academies Press (US), http://www.ncbi.nlm.nih.gov/books/NBK222274/ (2001, accessed 23 January 2023).\u003c/li\u003e\n\u003cli\u003eMcKeown S, Mir ZM. Considerations for conducting systematic reviews: evaluating the performance of different methods for de-duplicating references. \u003cem\u003eSyst Rev\u003c/em\u003e 2021; 10: 38.\u003c/li\u003e\n\u003cli\u003eCochrane Rapid Reviews Methods Group offers evidence-informed guidance to conduct rapid reviews - ClinicalKey, https://www.clinicalkey.com/#!/content/playContent/1-s2.0-S089543562031146X?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS089543562031146X%3Fshowall%3Dtrue\u0026amp;referrer=https:%2F%2Fpubmed.ncbi.nlm.nih.gov%2F (accessed 2 March 2022).\u003c/li\u003e\n\u003cli\u003eReview_protocol_20220404.pdf, https://osf.io/https://osf.io/zwht4 (2022, accessed 21 June 2023).\u003c/li\u003e\n\u003cli\u003ePeters MDJ, Godfrey C, McInerney P, et al. Best practice guidance and reporting items for the development of scoping review protocols. \u003cem\u003eJBI Evid Synth\u003c/em\u003e 2022; 20: 953\u0026ndash;968.\u003c/li\u003e\n\u003cli\u003eMokkink LB, de Vet HCW, Prinsen C a. C, et al. COSMIN Risk of Bias checklist for systematic reviews of Patient-Reported Outcome Measures. \u003cem\u003eQual Life Res Int J Qual Life Asp Treat Care Rehabil\u003c/em\u003e 2018; 27: 1171\u0026ndash;1179.\u003c/li\u003e\n\u003cli\u003ePrinsen C a. C, Mokkink LB, Bouter LM, et al. COSMIN guideline for systematic reviews of patient-reported outcome measures. \u003cem\u003eQual Life Res Int J Qual Life Asp Treat Care Rehabil\u003c/em\u003e 2018; 27: 1147\u0026ndash;1157.\u003c/li\u003e\n\u003cli\u003eAllen J, Hutchinson AM, Brown R, et al. User experience and care for older people transitioning from hospital to home: Patients\u0026rsquo; and carers\u0026rsquo; perspectives. \u003cem\u003eHealth Expect Int J Public Particip Health Care Health Policy\u003c/em\u003e 2018; 21: 518\u0026ndash;527.\u003c/li\u003e\n\u003cli\u003eInstituto Nacional de Cancerolog\u0026iacute;a E.S.E, Arias Rojas M, Garc\u0026iacute;a-Vivar C, et al. The transition of palliative care from the hospital to the home: a narrative review of experiences of patients and family caretakers. \u003cem\u003eInvestig Educ En Enferm\u003c/em\u003e; 33. Epub ahead of print 15 October 2015. DOI: 10.17533/udea.iee.v33n3a12.\u003c/li\u003e\n\u003cli\u003eAsif M, Cadel L, Kuluski K, et al. Patient and caregiver experiences on care transitions for adults with a hip fracture: a scoping review. \u003cem\u003eDisabil Rehabil\u003c/em\u003e 2020; 42: 3549\u0026ndash;3558.\u003c/li\u003e\n\u003cli\u003eBeattie M, Shepherd A, Howieson B. Do the Institute of Medicine\u0026rsquo;s (IOM\u0026rsquo;s) dimensions of quality capture the current meaning of quality in health care? \u0026ndash; An integrative review. \u003cem\u003eJ Res Nurs\u003c/em\u003e 2013; 18: 288\u0026ndash;304.\u003c/li\u003e\n\u003cli\u003eBoye LK, Mogensen CB, Mechlenborg T, et al. Older multimorbid patients\u0026rsquo; experiences on integration of services: a systematic review. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2019; 19: 795.\u003c/li\u003e\n\u003cli\u003eCarpenter JG. Hospital Palliative Care Teams and Post-Acute Care in Nursing Facilities: An Integrative Review. \u003cem\u003eRes Gerontol Nurs\u003c/em\u003e 2017; 10: 25\u0026ndash;34.\u003c/li\u003e\n\u003cli\u003eDavidson L, Scott J, Forster N. Patient experiences of integrated care within the United Kingdom: A systematic review. \u003cem\u003eInt J Care Coord\u003c/em\u003e 2021; 24: 39\u0026ndash;56.\u003c/li\u003e\n\u003cli\u003eDe Regge M, De Pourcq K, Meijboom B, et al. The role of hospitals in bridging the care continuum: a systematic review of coordination of care and follow-up for adults with chronic conditions. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2017; 17: 550.\u003c/li\u003e\n\u003cli\u003eFoglino S, Bravi F, Carretta E, et al. The relationship between integrated care and cancer patient experience: A scoping review of the evidence. \u003cem\u003eHealth Policy\u003c/em\u003e 2016; 120: 55\u0026ndash;63.\u003c/li\u003e\n\u003cli\u003eHestevik CH, Molin M, Debesay J, et al. Older persons\u0026rsquo; experiences of adapting to daily life at home after hospital discharge: a qualitative metasummary. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2019; 19: 224.\u003c/li\u003e\n\u003cli\u003eHohmann NS, McDaniel CC, Mason SW, et al. Patient perspectives on primary care and oncology care coordination in the context of multiple chronic conditions: A systematic review. \u003cem\u003eRes Soc Adm Pharm\u003c/em\u003e 2020; 16: 1003\u0026ndash;1016.\u003c/li\u003e\n\u003cli\u003eLawless MT, Marshall A, Mittinty MM, et al. What does integrated care mean from an older person\u0026rsquo;s perspective? A scoping review. \u003cem\u003eBMJ Open\u003c/em\u003e 2020; 10: e035157.\u003c/li\u003e\n\u003cli\u003eMayo SJ, Ajaj R, Drury A. Survivors\u0026rsquo; preferences for the organization and delivery of supportive care after treatment: An integrative review. \u003cem\u003eEur J Oncol Nurs\u003c/em\u003e 2021; 54: 102040.\u003c/li\u003e\n\u003cli\u003eMcMurray J, McNeil H, Lafortune C, et al. Measuring Patients\u0026rsquo; Experience of Rehabilitation Services Across the Care Continuum. Part II: Key Dimensions. \u003cem\u003eArch Phys Med Rehabil\u003c/em\u003e 2016; 97: 121\u0026ndash;30.\u003c/li\u003e\n\u003cli\u003eOishi A, Murtagh FE. The challenges of uncertainty and interprofessional collaboration in palliative care for non-cancer patients in the community: A systematic review of views from patients, carers and health-care professionals. \u003cem\u003ePalliat Med\u003c/em\u003e 2014; 28: 1081\u0026ndash;1098.\u003c/li\u003e\n\u003cli\u003ePiccenna L, Lannin NA, Gruen R, et al. The experience of discharge for patients with an acquired brain injury from the inpatient to the community setting: A qualitative review. \u003cem\u003eBrain Inj\u003c/em\u003e 2016; 30: 241\u0026ndash;251.\u003c/li\u003e\n\u003cli\u003eSampson R, Cooper J, Barbour R, et al. Patients\u0026rsquo; perspectives on the medical primary\u0026ndash;secondary care interface: systematic review and synthesis of qualitative research. \u003cem\u003eBMJ Open\u003c/em\u003e 2015; 5: e008708.\u003c/li\u003e\n\u003cli\u003eScholl I, Zill JM, H\u0026auml;rter M, et al. An Integrative Model of Patient-Centeredness \u0026ndash; A Systematic Review and Concept Analysis. \u003cem\u003ePLoS ONE\u003c/em\u003e 2014; 9: e107828.\u003c/li\u003e\n\u003cli\u003eSegan JD, Briggs AM, Chou L, et al. Patient-perceived health service needs in inflammatory arthritis: A systematic scoping review. \u003cem\u003eSemin Arthritis Rheum\u003c/em\u003e 2018; 47: 765\u0026ndash;777.\u003c/li\u003e\n\u003cli\u003eSibounheuang P, Olson PS, Kittiboonyakun P. Patients\u0026rsquo; and healthcare providers\u0026rsquo; perspectives on diabetes management: A systematic review of qualitative studies. \u003cem\u003eRes Soc Adm Pharm\u003c/em\u003e 2020; 16: 854\u0026ndash;874.\u003c/li\u003e\n\u003cli\u003eStaniszewska S, Boardman F, Gunn L, et al. The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines. \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2014; 26: 151\u0026ndash;157.\u003c/li\u003e\n\u003cli\u003evan Servellen G, Fongwa M, Mockus D\u0026rsquo;Errico E. Continuity of care and quality care outcomes for people experiencing chronic conditions: A literature review. \u003cem\u003eNurs Health Sci\u003c/em\u003e 2006; 8: 185\u0026ndash;195.\u003c/li\u003e\n\u003cli\u003eWaibel S, Henao D, Aller M-B, et al. What do we know about patients\u0026rsquo; perceptions of continuity of care? A meta-synthesis of qualitative studies. \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2012; 24: 39\u0026ndash;48.\u003c/li\u003e\n\u003cli\u003eYoussef A, Chaudhary ZK, Wiljer D, et al. Mapping Evidence of Patients\u0026rsquo; Experiences in Integrated Care: A Scoping Review. \u003cem\u003eGen Hosp Psychiatry\u003c/em\u003e 2019; 61: 1\u0026ndash;9.\u003c/li\u003e\n\u003cli\u003eArias Rojas M, Garc\u0026iacute;a-Vivar C. The transition of palliative care from the hospital to the home: a narrative review of experiences of patients and family caretakers. \u003cem\u003eInvestig Educ En Enfermeria\u003c/em\u003e 2015; 33: 482\u0026ndash;491.\u003c/li\u003e\n\u003cli\u003eWillems LM, Kwakkenbos L, Bode C, et al. Health care use and patients\u0026rsquo; perceptions on quality of care in systemic sclerosis. \u003cem\u003eClin Exp Rheumatol\u003c/em\u003e 2013; 31: 64\u0026ndash;70.\u003c/li\u003e\n\u003cli\u003eWells R, Breckenridge ED, Sia\u0026ntilde;ez M, et al. Self-Reported Quality, Health, and Cost-Related Outcomes of Care Coordination Among Patients with Complex Health Needs. \u003cem\u003ePopul Health Manag\u003c/em\u003e 2020; 23: 59\u0026ndash;67.\u003c/li\u003e\n\u003cli\u003eWeinberg DB, Gittell JH, Lusenhop RW, et al. Beyond our walls: impact of patient and provider coordination across the continuum on outcomes for surgical patients. \u003cem\u003eHealth Serv Res\u003c/em\u003e 2007; 42: 7\u0026ndash;24.\u003c/li\u003e\n\u003cli\u003eVargas I, Waibel S, Vazquez ML, et al. A comprehensive analysis of patients\u0026rsquo; perceptions of continuity of care and their associated factors. \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2013; 25: 291\u0026ndash;299.\u003c/li\u003e\n\u003cli\u003eTremblay D, Roberge D, Touati N, et al. Effects of interdisciplinary teamwork on patient-reported experience of cancer care. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2017; 17: 218.\u003c/li\u003e\n\u003cli\u003eSisler JJ, Taylor-Brown J, Nugent Z, et al. Continuity of care of colorectal cancer survivors at the end of treatment: the oncology\u0026ndash;primary care interface. \u003cem\u003eJ Cancer Surviv\u003c/em\u003e 2012; 6: 468\u0026ndash;475.\u003c/li\u003e\n\u003cli\u003eSequist TD, Von Glahn T, Li A, et al. Measuring chronic care delivery: patient experiences and clinical performance. \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2012; 24: 206\u0026ndash;213.\u003c/li\u003e\n\u003cli\u003eRiley DL, Stewart DE, Grace SL. Continuity of cardiac care: Cardiac rehabilitation participation and other correlates. \u003cem\u003eInt J Cardiol\u003c/em\u003e 2007; 119: 326\u0026ndash;333.\u003c/li\u003e\n\u003cli\u003eO\u0026rsquo;Malley AS, Cunningham PJ. Patient experiences with coordination of care: the benefit of continuity and primary care physician as referral source. \u003cem\u003eJ Gen Intern Med\u003c/em\u003e 2009; 24: 170\u0026ndash;7.\u003c/li\u003e\n\u003cli\u003eNoel PH, Barnard JM, Barry FM, et al. Patient experience of health care system hassles: Dual-system vs single-system users. \u003cem\u003eHealth Serv Res\u003c/em\u003e 2020; 55: 548\u0026ndash;555.\u003c/li\u003e\n\u003cli\u003eMosallam RA, Metwally S. Patients\u0026rsquo; views on the quality of transitional care at a health insurance hospital in Alexandria, Egypt. \u003cem\u003eJ Egypt Public Health Assoc\u003c/em\u003e 2014; 89: 74\u0026ndash;80.\u003c/li\u003e\n\u003cli\u003eMollica MA, Buckenmaier SS, Halpern MT, et al. Perceptions of care coordination among older adult cancer survivors: A SEER-CAHPS study. \u003cem\u003eJ Geriatr Oncol\u003c/em\u003e 2021; 12: 446\u0026ndash;452.\u003c/li\u003e\n\u003cli\u003eMohr DC, Benzer JK, Vimalananda VG, et al. Organizational Coordination and Patient Experiences of Specialty Care Integration. \u003cem\u003eJ Gen Intern Med\u003c/em\u003e 2019; 34: 30\u0026ndash;36.\u003c/li\u003e\n\u003cli\u003eKollen BJ, Groenier KH, Berendsen AJ. Patients\u0026rsquo; experiences with continuum of care across hospitals. A multilevel analysis of Consumer Quality Index Continuum of Care. \u003cem\u003ePatient Educ Couns\u003c/em\u003e 2011; 83: 269\u0026ndash;272.\u003c/li\u003e\n\u003cli\u003eKessing LV, Hansen HV, Ruggeri M, et al. Satisfaction with treatment among patients with depressive and bipolar disorders. \u003cem\u003eSoc Psychiatry Psychiatr Epidemiol\u003c/em\u003e 2006; 41: 148\u0026ndash;155.\u003c/li\u003e\n\u003cli\u003eKaram M, Lambert A-S, Macq J. Patients\u0026rsquo; perceptions of continuity of care across primary care level and emergency departments in Belgium: cross-sectional survey. \u003cem\u003eBMJ Open\u003c/em\u003e 2019; 9: e033188.\u003c/li\u003e\n\u003cli\u003eIreson CL, Scutchfield FD, Slavova S, et al. Bridgingf the care continuum: Patient information needs for specialist referrals. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2009; 9: 163.\u003c/li\u003e\n\u003cli\u003eHopstaken JS, van Dalen D, van der Kolk BM, et al. Continuity of care experienced by patients in a multi-institutional pancreatic care network: a pilot study. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2021; 21: 1\u0026ndash;9.\u003c/li\u003e\n\u003cli\u003eHod R, Maimon O, Zimlichman E. Does Care Transition Matter? Exploring the Newly Published HCAHPS Measure. \u003cem\u003eAm J Med Qual\u003c/em\u003e 2020; 35: 380\u0026ndash;387.\u003c/li\u003e\n\u003cli\u003eHincapie AL, Slack M, Malone DC, et al. Relationship Between Patients\u0026rsquo; Perceptions of Care Quality and Health Care Errors in 11 Countries: A Secondary Data Analysis. \u003cem\u003eQual Manag Health Care\u003c/em\u003e 2016; 25: 13\u0026ndash;21.\u003c/li\u003e\n\u003cli\u003eGuilabert M, Mart\u0026iacute;nez-Garc\u0026iacute;a A, Sala-Gonz\u0026aacute;lez M, et al. Results of a Patient Reported Experience Measure (PREM) to measure the rare disease patients and caregivers experience: a Spanish cross-sectional study. \u003cem\u003eOrphanet J Rare Dis\u003c/em\u003e 2021; 16: 67.\u003c/li\u003e\n\u003cli\u003eFryer A-K, Friedberg MW, Thompson RW, et al. Achieving care integration from the patients\u0026rsquo; perspective: Results from a care management program. \u003cem\u003eHealthcare\u003c/em\u003e 2016; 4: 36\u0026ndash;44.\u003c/li\u003e\n\u003cli\u003eDen Herder-van Der Eerden M, Ebenau A, Payne S, et al. Integrated palliative care networks from the perspectives of patients: A cross-sectional explorative study in five European countries. \u003cem\u003ePalliat Med\u003c/em\u003e 2018; 32: 1103\u0026ndash;1113.\u003c/li\u003e\n\u003cli\u003eCramm JM, Nieboer AP. High-quality chronic care delivery improves experiences of chronically ill patients receiving care. \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2013; 25: 689\u0026ndash;695.\u003c/li\u003e\n\u003cli\u003eCollett GK, Durcinoska I, Rankin NM, et al. Patients\u0026rsquo; experience of lung cancer care coordination: a quantitative exploration. \u003cem\u003eSupport Care Cancer\u003c/em\u003e 2019; 27: 485\u0026ndash;493.\u003c/li\u003e\n\u003cli\u003eCarryer J, Doolan-Noble F, Gauld R, et al. New Zealand patients\u0026rsquo; perceptions of chronic care delivery. \u003cem\u003eJ Integr Care\u003c/em\u003e 2014; 22: 71\u0026ndash;80.\u003c/li\u003e\n\u003cli\u003eCarneiro C, Ellis J, Singh S, et al. Patient and Primary Care Practitioner Confidence in and Perceptions of Cancer Treatment Transition and the Shared Care Model of Cancer Care. \u003cem\u003eJ Oncol Navig Surviv\u003c/em\u003e 2016; 7: 18\u0026ndash;24.\u003c/li\u003e\n\u003cli\u003eBurgers JS, Voerman GE, Grol R, et al. Quality and Coordination of Care for Patients With Multiple Conditions: Results From an International Survey of Patient Experience. \u003cem\u003eEval Health Prof\u003c/em\u003e 2010; 33: 343\u0026ndash;364.\u003c/li\u003e\n\u003cli\u003eBreton M, Haggerty J, Roberge D, et al. Management continuity in local health networks. \u003cem\u003eInt J Integr Care\u003c/em\u003e; 12. Epub ahead of print 13 April 2012. DOI: 10.5334/ijic.682.\u003c/li\u003e\n\u003cli\u003eBravi F, Ruscio ED, Frassoldati A, et al. Patient and Health Care Professional Perspectives: A Case Study of the Lung Cancer Integrated Care Pathway. \u003cem\u003eInt J Integr Care\u003c/em\u003e 2018; 18: 7.\u003c/li\u003e\n\u003cli\u003eBower P, Reeves D, Sutton M, et al. Improving care for older people with long-term conditions and social care needs in Salford: the CLASSIC mixed-methods study, including RCT. \u003cem\u003eHealth Serv Deliv Res\u003c/em\u003e 2018; 6: 1\u0026ndash;188.\u003c/li\u003e\n\u003cli\u003eBortoli A, Daperno M, Kohn A, et al. Patient and physician views on the quality of care in inflammatory bowel disease: Results from SOLUTION-1, a prospective IG-IBD study. \u003cem\u003eJ Crohns Colitis\u003c/em\u003e 2014; 8: 1642\u0026ndash;1652.\u003c/li\u003e\n\u003cli\u003eBoele F, Harley C, Pini S, et al. Cancer as a chronic illness: support needs and experiences. \u003cem\u003eBMJ Support Palliat Care\u003c/em\u003e 2019; bmjspcare-2019-001882.\u003c/li\u003e\n\u003cli\u003eBenzer JK, Singer SJ, Mohr DC, et al. Survey of Patient-Centered Coordination of Care for Diabetes with Cardiovascular and Mental Health Comorbidities in the Department of Veterans Affairs. \u003cem\u003eJ Gen Intern Med\u003c/em\u003e 2019; 34: 43\u0026ndash;49.\u003c/li\u003e\n\u003cli\u003eBentler SE, Morgan RO, Virnig BA, et al. The Association of Longitudinal and Interpersonal Continuity of Care with Emergency Department Use, Hospitalization, and Mortality among Medicare Beneficiaries. \u003cem\u003ePLoS ONE\u003c/em\u003e 2014; 9: e115088.\u003c/li\u003e\n\u003cli\u003eAuerbach AD, Kripalani S, Vasilevskis EE, et al. Preventability and Causes of Readmissions in a National Cohort of General Medicine Patients. \u003cem\u003eJAMA Intern Med\u003c/em\u003e 2016; 176: 484.\u003c/li\u003e\n\u003cli\u003eAndrew NE, Busingye D, Lannin NA, et al. The Quality of Discharge Care Planning in Acute Stroke Care: Influencing Factors and Association with Postdischarge Outcomes. \u003cem\u003eJ Stroke Cerebrovasc Dis Off J Natl Stroke Assoc\u003c/em\u003e 2018; 27: 583\u0026ndash;590.\u003c/li\u003e\n\u003cli\u003eAlsayali MM, AlSharif K, Al-Sahafi A, et al. Patients\u0026rsquo; satisfaction after primary health care centers\u0026rsquo; integration with Ministry of Health Hospitals, Jeddah. \u003cem\u003eJ Epidemiol Glob Health\u003c/em\u003e 2019; 9: 135\u0026ndash;142.\u003c/li\u003e\n\u003cli\u003eAller M-B, Vargas I, Waibel S, et al. Factors associated to experienced continuity of care between primary and outpatient secondary care in the Catalan public healthcare system. \u003cem\u003eGac Sanit\u003c/em\u003e 2013; 27: 207\u0026ndash;213.\u003c/li\u003e\n\u003cli\u003eAcosta AM, Lima MADS, Marques GQ, et al. Brazilian version of the Care Transitions Measure: translation and validation. \u003cem\u003eInt Nurs Rev\u003c/em\u003e 2017; 64: 379\u0026ndash;387.\u003c/li\u003e\n\u003cli\u003eAller MB, Vargas I, Garcia I, et al. A tool for assessing continuity of care across care levels: an extended psychometric validation of the CCAENA questionnaire. \u003cem\u003eInt J Integr Care\u003c/em\u003e; 13. Epub ahead of print 2 December 2013. DOI: 10.5334/ijic.1160.\u003c/li\u003e\n\u003cli\u003eBadri MA, Attia ST, Ustadi AM. Testing not-so-obvious models of healthcare quality. \u003cem\u003eInt J Health Care Qual Assur\u003c/em\u003e 2008; 21: 159\u0026ndash;74.\u003c/li\u003e\n\u003cli\u003eBakshi AB, Wee S-L, Tay C, et al. Validation of the care transition measure in multi-ethnic South-East Asia in Singapore. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2012; 12: 256.\u003c/li\u003e\n\u003cli\u003eBentler SE, Morgan RO, Virnig BA, et al. Do claims-based continuity of care measures reflect the patient perspective?. \u003cem\u003eMed Care Res Rev MCRR\u003c/em\u003e 2014; 71: 156\u0026ndash;73.\u003c/li\u003e\n\u003cli\u003eBentler SE, Morgan RO, Virnig BA, et al. Evaluation of a patient-reported continuity of care model for older adults. \u003cem\u003eQual Life Res Int J Qual Life Asp Treat Care Rehabil\u003c/em\u003e 2014; 23: 185\u0026ndash;93.\u003c/li\u003e\n\u003cli\u003eBerendsen AJ, Groenier KH, de Jong GM, et al. Assessment of patient\u0026rsquo;s experiences across the interface between primary and secondary care: Consumer Quality Index Continuum of care. \u003cem\u003ePatient Educ Couns\u003c/em\u003e 2009; 77: 123\u0026ndash;7.\u003c/li\u003e\n\u003cli\u003eBull MJ, Luo D, Maruyama GM. Measuring continuity of elders\u0026rsquo; posthospital care. \u003cem\u003eJ Nurs Meas\u003c/em\u003e 2000; 8: 41\u0026ndash;60.\u003c/li\u003e\n\u003cli\u003eCastle N, Engberg J, Men A. Satisfaction of Discharged Nursing Home Residents. \u003cem\u003eJ Appl Gerontol Off J South Gerontol Soc\u003c/em\u003e 2018; 37: 1225\u0026ndash;1243.\u003c/li\u003e\n\u003cli\u003eChavez LM, Canino G, Shrout PE, et al. Psychometric evaluation of the Spanish version of CONNECT: a measure of continuity of care in mental health services. \u003cem\u003eInt J Methods Psychiatr Res\u003c/em\u003e 2007; 16: 23\u0026ndash;33.\u003c/li\u003e\n\u003cli\u003eClark K, Beatty S, Reibel T. Maternity-care: measuring women\u0026rsquo;s perceptions. \u003cem\u003eInt J Health Care Qual Assur\u003c/em\u003e 2016; 29: 89\u0026ndash;99.\u003c/li\u003e\n\u003cli\u003eCohen Castel O, Dagan E, Keinan-Boker L, et al. Reliability and validity of the Hebrew version of the Nijmegen Continuity Questionnaire for measuring patients\u0026rsquo; perceived continuity of care in oral anticancer therapy. \u003cem\u003eEur J Cancer Care (Engl)\u003c/em\u003e 2018; 27: e12913.\u003c/li\u003e\n\u003cli\u003eColeman EA, Mahoney E, Parry C. Assessing the quality of preparation for posthospital care from the patient\u0026rsquo;s perspective: the care transitions measure. \u003cem\u003eMed Care\u003c/em\u003e 2005; 43: 246\u0026ndash;55.\u003c/li\u003e\n\u003cli\u003eCrump H, King J, Graham C, et al. Developing a User Reported Measure of Care Co-ordination. \u003cem\u003eInt J Integr Care\u003c/em\u003e 2017; 17: 4.\u003c/li\u003e\n\u003cli\u003eDolovich LR, Nair KM, Ciliska DK, et al. The Diabetes Continuity of Care Scale: the development and initial evaluation of a questionnaire that measures continuity of care from the patient perspective. \u003cem\u003eHealth Soc Care Community\u003c/em\u003e 2004; 12: 475\u0026ndash;87.\u003c/li\u003e\n\u003cli\u003eDrewes HW, de Jong-van Til JT, Struijs JN, et al. Measuring chronic care management experience of patients with diabetes: PACIC and PACIC+ validation. \u003cem\u003eInt J Integr Care\u003c/em\u003e 2012; 12: e194.\u003c/li\u003e\n\u003cli\u003eEubank BH, Lafave MR, Mohtadi NG, et al. Validation of a tool to assess patient satisfaction, waiting times, healthcare utilization, and cost. \u003cem\u003ePrim Health Care Res Dev\u003c/em\u003e 2019; 20: e47.\u003c/li\u003e\n\u003cli\u003eFulton BR, Sternke EA, Ayala L, et al. Psychometric Testing of a Measure of Patient Experience in an Ambulatory Surgery Setting. \u003cem\u003eJ Ambulatory Care Manage\u003c/em\u003e 2019; 42: 27\u0026ndash;36.\u003c/li\u003e\n\u003cli\u003eGlasgow RE, Wagner EH, Schaefer J, et al. Development and validation of the Patient Assessment of Chronic Illness Care (PACIC). \u003cem\u003eMed Care\u003c/em\u003e 2005; 43: 436\u0026ndash;444.\u003c/li\u003e\n\u003cli\u003eGraumlich JF, Novotny NL, Aldag JC. Brief scale measuring patient preparedness for hospital discharge to home: Psychometric properties. \u003cem\u003eJ Hosp Med\u003c/em\u003e 2008; 3: 446\u0026ndash;54.\u003c/li\u003e\n\u003cli\u003eGulliford MC, Naithani S, Morgan M. Measuring continuity of care in diabetes mellitus: an experience-based measure. \u003cem\u003eAnn Fam Med\u003c/em\u003e 2006; 4: 548\u0026ndash;55.\u003c/li\u003e\n\u003cli\u003eHadjistavropoulos HD, Biem HJ, Kowalyk KM. Measurement of continuity of care in cardiac patients: reliability and validity of an in-person questionnaire. \u003cem\u003eCan J Cardiol\u003c/em\u003e 2004; 20: 883\u0026ndash;91.\u003c/li\u003e\n\u003cli\u003eHadjistavropoulos H, Biem H, Sharpe D, et al. Patient perceptions of hospital discharge: reliability and validity of a Patient Continuity of Care Questionnaire. \u003cem\u003eInt J Qual Health Care J Int Soc Qual Health Care\u003c/em\u003e 2008; 20: 314\u0026ndash;323.\u003c/li\u003e\n\u003cli\u003eHaggerty JL, Burge F, Pineault R, et al. Management continuity from the patient perspective: comparison of primary healthcare evaluation instruments. \u003cem\u003eHealthc Policy Polit Sante\u003c/em\u003e 2011; 7: 139\u0026ndash;53.\u003c/li\u003e\n\u003cli\u003eHaggerty JL, Roberge D, Freeman GK, et al. Validation of a generic measure of continuity of care: when patients encounter several clinicians. \u003cem\u003eAnn Fam Med\u003c/em\u003e 2012; 10: 443\u0026ndash;51.\u003c/li\u003e\n\u003cli\u003eHetlevik \u0026Oslash;, Hustoft M, Uijen A, et al. Patient perspectives on continuity of care: adaption and preliminary psychometric assessment of a Norwegian version of the Nijmegen Continuity Questionnaire (NCQ-N). \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2017; 17: 760.\u003c/li\u003e\n\u003cli\u003eHusain A, Barbera L, Howell D, et al. Advanced lung cancer patients\u0026rsquo; experience with continuity of care and supportive care needs. \u003cem\u003eSupport Care Cancer Off J Multinatl Assoc Support Care Cancer\u003c/em\u003e 2013; 21: 1351\u0026ndash;8.\u003c/li\u003e\n\u003cli\u003eHwang J-I, Chung J-H, Kim HK. Psychometric properties of transitional care instruments and their relationships with health literacy: Brief PREPARED and Care Transitions Measure. \u003cem\u003eInt J Qual Health Care J Int Soc Qual Health Care\u003c/em\u003e 2019; 31: 774\u0026ndash;780.\u003c/li\u003e\n\u003cli\u003eIgnatyev Y, Timm J, Heinze M, et al. Development and Preliminary Validation of the Scale for Evaluation of Psychiatric Integrative and Continuous Care-Patient\u0026rsquo;s Version. \u003cem\u003eFront Psychiatry\u003c/em\u003e 2017; 8: 162.\u003c/li\u003e\n\u003cli\u003eJoober H, Chouinard M-C, King J, et al. The Patient Experience of Integrated Care Scale: A Validation Study among Patients with Chronic Conditions Seen in Primary Care. \u003cem\u003eInt J Integr Care\u003c/em\u003e 2018; 18: 1.\u003c/li\u003e\n\u003cli\u003eJoyce AS, Adair CE, Wild TC, et al. Continuity of care: validation of a self-report measure to assess client perceptions of mental health service delivery. \u003cem\u003eCommunity Ment Health J\u003c/em\u003e 2010; 46: 192\u0026ndash;208.\u003c/li\u003e\n\u003cli\u003eKiang MV, Singer SJ, Friedberg MW, et al. Development and preliminary validation of the Patient Perceptions of Integrated Care survey. \u003cem\u003eMed Care Res Rev\u003c/em\u003e 2013; 70: 143\u0026ndash;164.\u003c/li\u003e\n\u003cli\u003eKowalyk KM, Hadjistavropoulos HD, Biem HJ. Measuring continuity of care for cardiac patients: development of a patient self-report questionnaire. \u003cem\u003eCan J Cardiol\u003c/em\u003e 2004; 20: 205\u0026ndash;12.\u003c/li\u003e\n\u003cli\u003eLiu L-M, Liu M-T, Sun M-J, et al. Validity and reliability of the Chinese version of the partners at care transitions measure. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2021; 21: 1284.\u003c/li\u003e\n\u003cli\u003eLloyd H, Fosh B, Whalley B, et al. Validation of the person-centred coordinated care experience questionnaire (P3CEQ). \u003cem\u003eInt J Qual Health Care J Int Soc Qual Health Care\u003c/em\u003e 2019; 31: 506\u0026ndash;512.\u003c/li\u003e\n\u003cli\u003eMalik N, Alvaro C, Kuluski K, et al. Measuring patient satisfaction in complex continuing care/rehabilitation care. \u003cem\u003eInt J Health Care Qual Assur\u003c/em\u003e 2016; 29: 324\u0026ndash;36.\u003c/li\u003e\n\u003cli\u003eMasters S, Giles L, Halbert J, et al. Development and testing of a questionnaire to measure older people\u0026rsquo;s experience of the Transition Care Program in Australia. \u003cem\u003eAustralas J Ageing\u003c/em\u003e 2010; 29: 172\u0026ndash;8.\u003c/li\u003e\n\u003cli\u003eMcAlister FA, Lin M, Bakal J, et al. The Care Transitions Measure-3 Is Only Weakly Associated with Post-discharge Outcomes: a Retrospective Cohort Study in 48,384 Albertans. \u003cem\u003eJ Gen Intern Med\u003c/em\u003e 2019; 34: 2497\u0026ndash;2504.\u003c/li\u003e\n\u003cli\u003eMcGuiness C, Sibthorpe B. Development and initial validation of a measure of coordination of health care. \u003cem\u003eInt J Qual Health Care J Int Soc Qual Health Care\u003c/em\u003e 2003; 15: 309\u0026ndash;318.\u003c/li\u003e\n\u003cli\u003eMira JJ, Nuno-Solinis R, Guilabert-Mora M, et al. Development and Validation of an Instrument for Assessing Patient Experience of Chronic Illness Care. \u003cem\u003eInt J Integr Care\u003c/em\u003e 2016; 16: 13.\u003c/li\u003e\n\u003cli\u003eNoest S, Ludt S, Klingenberg A, et al. Involving patients in detecting quality gaps in a fragmented healthcare system: development of a questionnaire for Patients\u0026rsquo; Experiences Across Health Care Sectors (PEACS). \u003cem\u003eInt J Qual Health Care\u003c/em\u003e 2014; 26: 240\u0026ndash;249.\u003c/li\u003e\n\u003cli\u003eOikonomou E, Page B, Lawton R, et al. Validation of the Partners at Care Transitions Measure (PACT-M): assessing the quality and safety of care transitions for older people in the UK. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2020; 20: 608.\u003c/li\u003e\n\u003cli\u003eParra-Vega I, Marques-Sanchez P, Pelayo-Teran JM, et al. Development and validation of a questionnaire for assessing patients\u0026rsquo; perceptions of interprofessional integration in health care. \u003cem\u003eJ Interprof Care\u003c/em\u003e 2021; 1\u0026ndash;7.\u003c/li\u003e\n\u003cli\u003ePeabody M, Bradley KD, Custer M. Assessing the Validity of a Continuum-of-care Survey: A Rasch Measurement Approach. \u003cem\u003eJ Appl Meas\u003c/em\u003e 2016; 17: 1\u0026ndash;13.\u003c/li\u003e\n\u003cli\u003eRadwin LE, Cabral HJ, Seibert MN, et al. Patient-Centered Care in Primary Care Scale: Pilot Development and Psychometric Assessment. \u003cem\u003eJ Nurs Care Qual\u003c/em\u003e 2019; 34: 34\u0026ndash;39.\u003c/li\u003e\n\u003cli\u003eRamond-Roquin A, Stewart M, Ryan BL, et al. The \u0026lsquo;Patient-centered coordination by a care team\u0026rsquo; questionnaire achieves satisfactory validity and reliability. \u003cem\u003eJ Interprof Care\u003c/em\u003e 2019; 33: 558\u0026ndash;569.\u003c/li\u003e\n\u003cli\u003eREYNOLDS J, GADSBY E, RIJKEN M, et al. Measuring Older Peoples\u0026rsquo; Experiences of Person-Centred Coordinated Care: Experience and Methodological Reflections from Applying a Patient Reported Experience Measure in SUSTAIN. \u003cem\u003eInt J Integr Care IJIC\u003c/em\u003e 2021; 21: 1\u0026ndash;17.\u003c/li\u003e\n\u003cli\u003eRose D, Sweeney A, Leese M, et al. Developing a user-generated measure of continuity of care: brief report. \u003cem\u003eActa Psychiatr Scand\u003c/em\u003e 2009; 119: 320\u0026ndash;324.\u003c/li\u003e\n\u003cli\u003eRucci P, Foglino S, Bravi F, et al. Validation of the OPportunity for Treatment In ONcology (OPTION) questionnaire measuring continuity of care. \u003cem\u003eEur J Cancer Care (Engl)\u003c/em\u003e; 27. Epub ahead of print 2018. DOI: 10.1111/ecc.12765.\u003c/li\u003e\n\u003cli\u003eShadmi E, Zisberg A, Coleman EA. Translation and validation of the Care Transition Measure into Hebrew and Arabic. \u003cem\u003eInt J Qual Health Care J Int Soc Qual Health Care\u003c/em\u003e 2009; 21: 97\u0026ndash;102.\u003c/li\u003e\n\u003cli\u003eSmith LFP. Postnatal care: development of a psychometric multidimensional satisfaction questionnaire (the WOMBPNSQ) to assess women\u0026rsquo;s views. \u003cem\u003eBr J Gen Pract J R Coll Gen Pract\u003c/em\u003e 2011; 61: e628-37.\u003c/li\u003e\n\u003cli\u003eSoares JB, Nogueira MC, Fernandes D, et al. Validation of the Portuguese version of a questionnaire to measure Quality of Care Through the Eyes of Patients with Inflammatory Bowel Disease (QUOTE-IBD). \u003cem\u003eEur J Gastroenterol Hepatol\u003c/em\u003e 2015; 27: 1409\u0026ndash;17.\u003c/li\u003e\n\u003cli\u003eSorra J, Zebrak K, Carpenter D, et al. Development and psychometric properties of surveys to assess patient and family caregiver experience with care transitions. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2021; 21: 785.\u003c/li\u003e\n\u003cli\u003eSquitieri L, Tsangaris E, Klassen AF, et al. Patient-reported experience measures are essential to improving quality of care for chronic wounds: An international qualitative study. \u003cem\u003eInt Wound J\u003c/em\u003e 2020; 17: 1052\u0026ndash;1061.\u003c/li\u003e\n\u003cli\u003eSugavanam T, Fosh B, Close J, et al. Codesigning a Measure of Person-Centred Coordinated Care to Capture the Experience of the Patient: The Development of the P3CEQ. \u003cem\u003eJ Patient Exp\u003c/em\u003e 2018; 5: 201\u0026ndash;211.\u003c/li\u003e\n\u003cli\u003eTeale EA, Young JB. A Patient Reported Experience Measure (PREM) for use by older people in community services. \u003cem\u003eAge Ageing\u003c/em\u003e 2015; 44: 667\u0026ndash;72.\u003c/li\u003e\n\u003cli\u003eThompson R, Stevens G, Elwyn G. Measuring Patient Experiences of Integration in Health Care Delivery: Psychometric Validation of IntegRATE Under Controlled Conditions. \u003cem\u003eJ Patient Exp\u003c/em\u003e 2021; 8: 23743735211007344.\u003c/li\u003e\n\u003cli\u003eUijen A, Schellevis F, Bosch W, et al. Nijmegen Continuity Questionnaire: Development and testing of a questionnaire that measures continuity of care. \u003cem\u003eJ Clin Epidemiol\u003c/em\u003e 2011; 64: 1391\u0026ndash;9.\u003c/li\u003e\n\u003cli\u003eUijen AA, Schers HJ, Schellevis FG, et al. Measuring continuity of care: psychometric properties of the Nijmegen Continuity Questionnaire. \u003cem\u003eBr J Gen Pract J R Coll Gen Pract\u003c/em\u003e 2012; 62: e949-57.\u003c/li\u003e\n\u003cli\u003eValaker I, Fridlund B, Wentzel-Larsen T, et al. Adaptation and psychometric properties of the Norwegian version of the heart continuity of care questionnaire (HCCQ). \u003cem\u003eBMC Med Res Methodol\u003c/em\u003e 2019; 19: 62.\u003c/li\u003e\n\u003cli\u003evan Melle MA, van Stel HF, Poldervaart JM, et al. The transitional risk and incident questionnaire was valid and reliable for measuring transitional patient safety from the patients\u0026rsquo; perspective. \u003cem\u003eJ Clin Epidemiol\u003c/em\u003e 2019; 105: 40\u0026ndash;49.\u003c/li\u003e\n\u003cli\u003eWalker KO, Stewart AL, Grumbach K. Development of a survey instrument to measure patient experience of integrated care. \u003cem\u003eBMC Health Serv Res\u003c/em\u003e 2016; 16: 193.\u003c/li\u003e\n\u003cli\u003eWare NC, Dickey B, Tugenberg T, et al. CONNECT: a measure of continuity of care in mental health services. \u003cem\u003eMent Health Serv Res\u003c/em\u003e 2003; 5: 209\u0026ndash;21.\u003c/li\u003e\n\u003cli\u003eYoung JM, Walsh J, Butow PN, et al. Measuring cancer care coordination: development and validation of a questionnaire for patients. \u003cem\u003eBMC Cancer\u003c/em\u003e 2011; 11: 298.\u003c/li\u003e\n\u003cli\u003eFillion L, Cook S, Veillette A-M, et al. Professional Navigation Framework: Elaboration and Validation in a Canadian Context. \u003cem\u003eOncol Nurs Forum\u003c/em\u003e 2012; 39: E58\u0026ndash;E69.\u003c/li\u003e\n\u003cli\u003eSchick-Makaroff K, Karimi-Dehkordi M, Cuthbertson L, et al. Using Patient- and Family-Reported Outcome and Experience Measures Across Transitions of Care for Frail Older Adults Living at Home: A Meta-Narrative Synthesis. \u003cem\u003eThe Gerontologist\u003c/em\u003e 2020; 61: e23\u0026ndash;e38.\u003c/li\u003e\n\u003cli\u003eHargraves JL, Hays RD, Cleary PD. Psychometric properties of the Consumer Assessment of Health Plans Study (CAHPS) 2.0 adult core survey. \u003cem\u003eHealth Serv Res\u003c/em\u003e 2003; 38: 1509\u0026ndash;1527.\u003c/li\u003e\n\u003cli\u003ePlatonova EA, Saunders WB, Warren-Findlow J, et al. Patient Perceptions of Patient-Centered Medical Home Characteristics and Satisfaction with Free Clinic Services. \u003cem\u003ePopul Health Manag\u003c/em\u003e 2016; 19: 324\u0026ndash;331.\u003c/li\u003e\n\u003cli\u003eDyer N, Sorra JS, Smith SA, et al. Psychometric properties of the Consumer Assessment of Healthcare Providers and Systems (CAHPS\u0026reg;) Clinician and Group Adult Visit Survey. \u003cem\u003eMed Care\u003c/em\u003e 2012; 50 Suppl: S28-34.\u003c/li\u003e\n\u003cli\u003eHays RD, Berman LJ, Kanter MH, et al. Evaluating the psychometric properties of the CAHPS Patient-centered Medical Home survey. \u003cem\u003eClin Ther\u003c/em\u003e 2014; 36: 689-696.e1.\u003c/li\u003e\n\u003cli\u003eGensichen J, Serras A, Paulitsch MA, et al. The Patient Assessment of Chronic Illness Care questionnaire: evaluation in patients with mental disorders in primary care. \u003cem\u003eCommunity Ment Health J\u003c/em\u003e 2011; 47: 447\u0026ndash;453.\u003c/li\u003e\n\u003cli\u003eCott CA, Teare G, McGilton KS, et al. Reliability and construct validity of the client-centred rehabilitation questionnaire. \u003cem\u003eDisabil Rehabil\u003c/em\u003e 2006; 28: 1387\u0026ndash;1397.\u003c/li\u003e\n\u003cli\u003eLloyd H, Jenkinson C, Hadi M, et al. Patient reports of the outcomes of treatment: a structured review of approaches. \u003cem\u003eHealth Qual Life Outcomes\u003c/em\u003e 2014; 12: 5.\u003c/li\u003e\n\u003cli\u003eStrack and Schwarz; \u003cem\u003eAsking questions: measurement in the social sciences\u003c/em\u003e in Ash MG, Sturm T (eds). \u003cem\u003ePsychology\u0026rsquo;s territories: historical and contemporary perspectives from different disciplines\u003c/em\u003e. Mahwah, N.J: Lawrence Erlbaum Associates, 2007.\u003c/li\u003e\n\u003c/ol\u003e"},{"header":"Table","content":"\u003cp\u003eTable 2 is available in the Supplementary Files section.\u003c/p\u003e "}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":true,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"
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