Measuring patients' experiences of continuity of care in a primary care context-Development and evaluation of a patient-reported experience measure

被引:3
作者
Ljungholm, Linda [1 ,4 ]
arestedt, Kristofer [1 ,2 ]
Fagerstrom, Cecilia [1 ,2 ]
Djukanovic, Ingrid [1 ]
Ekstedt, Mirjam [1 ,3 ]
机构
[1] Linnaeus Univ, Fac Hlth & Life Sci, Kalmar, Sweden
[2] Dept Res, Kalmar, Reg Kalmar Cty, Sweden
[3] Karolinska Inst, Dept Learning Informat Management & Ethics, Stockholm, Sweden
[4] Linnaeus Univ, Fac Hlth & Life Sci, SE-39182 Kalmar, Sweden
基金
瑞典研究理事会;
关键词
classic test theory; complex care needs; continuity of care; instrument development; primary healthcare; psychometric evaluation; SELF-REPORT MEASURE; HEALTH-CARE; INTERPERSONAL CONTINUITY; QUESTIONNAIRE; ASSOCIATION; PERCEPTIONS; VALIDATION; COSTS;
D O I
10.1111/jan.15792
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
BackgroundContinuity of care is viewed as a hallmark of high-quality care in the primary care context. Measures to evaluate the quality of provider performance are scarce, and it is unclear how the assessments correlate with patients' experiences of care as coherent and interconnected over time, consistent with their preferences and care needs.AimTo develop and evaluate a patient-reported experience measure of continuity of care in primary care for patients with complex care needs.MethodThe study was conducted in two stages: (1) development of the instrument based on theory and empirical studies and reviewed for content validity (16 patients with complex care needs and 8 experts) and (2) psychometric evaluation regarding factor structure, test-retest reliability, internal consistency reliability, and convergent validity. In all, 324 patients participated in the psychometric evaluation.ResultsThe Patient Experienced Continuity of care Questionnaire (PECQ) contains 20 items clustered in four dimensions of continuity of care measuring Information (four items), Relation (six items), Management (five items), and Knowledge (five items). Overall, the hypothesized factor structure was indicated. The PECQ also showed satisfactory convergent validity, internal consistency, and stability.Conclusion/ImplicationsThe PECQ is a multidimensional patient experience instrument that can provide information on various dimensions useful for driving quality improvement strategies in the primary care context for patients with complex care needs.Patient or Public ContributionPatients have participated in the content validation of the items.
引用
收藏
页码:387 / 398
页数:12
相关论文
共 50 条
  • [31] The effects of primary care physician visit continuity on patients' experiences with care
    Rodriguez, Hector P.
    Rogers, William H.
    Marshall, Richard E.
    Safran, Dana Gelb
    JOURNAL OF GENERAL INTERNAL MEDICINE, 2007, 22 (06) : 787 - 793
  • [32] The Effects of Primary Care Physician Visit Continuity on Patients’ Experiences with Care
    Hector P. Rodriguez
    William H. Rogers
    Richard E. Marshall
    Dana Gelb Safran
    Journal of General Internal Medicine, 2007, 22 : 787 - 793
  • [33] Experiences of patient-centred care in alcohol and other drug treatment settings: A qualitative study to inform design of a patient-reported experience measure
    Hinsley, Kathryn
    Kelly, Peter J.
    Davis, Esther
    DRUG AND ALCOHOL REVIEW, 2019, 38 (06) : 664 - 673
  • [34] Differences in Patient-Reported Experiences of Care by Race and Acculturation Status
    Hasnain, Memoona
    Schwartz, Alan
    Girotti, Jorge
    Bixby, Angela
    Rivera, Luis
    JOURNAL OF IMMIGRANT AND MINORITY HEALTH, 2013, 15 (03) : 517 - 524
  • [35] Development of a prototype of a patient-reported outcomes measure for hypospadias care, the Patient Assessment Tool for Hypospadias (PATH)
    Brown, Charlene
    Larson, Kristen
    Cockrum, Brandon
    Hawryluk, Bridget
    Moore, Courtney M.
    Wiehe, Sarah E.
    Chan, Katherine H.
    JOURNAL OF PEDIATRIC UROLOGY, 2024, 20 (06) : 1072 - 1081
  • [36] Patient-reported primary health care experiences in Canada: The challenges faced by Nepalese immigrant men
    Dahal, Rudra
    Bajgain, Bishnu Bahadur
    Thapa-Bajgain, Kalpana
    Adhikari, Kamala
    Naeem, Iffat
    Chowdhury, Nashit
    Turin, Tanvir C.
    JOURNAL OF MIGRATION AND HEALTH, 2024, 9
  • [37] Stakeholder engagement from problem analysis to implementation strategies for a patient-reported experience measure in disability care: A qualitative study on the process and experiences
    van Rooijen, Marjolein
    Lenzen, Stephanie
    Dalemans, Ruth
    Beurskens, Anna
    Moser, Albine
    HEALTH EXPECTATIONS, 2021, 24 (01) : 53 - 65
  • [38] Measuring the Value Functions of Primary Care: Physician-Level Continuity of Care Quality Measure
    Dai, Mingliang
    Pavletic, Denise
    Shuemaker, Jill C.
    Solid, Craig A.
    Phillips, Robert L., Jr.
    ANNALS OF FAMILY MEDICINE, 2022, 20 (06) : 535 - 540
  • [39] Psychometric evaluation of the Urgency NRS as a new patient-reported outcome measure for patients with ulcerative colitis
    Dubinsky, Marla C.
    Shan, Mingyang
    Delbecque, Laure
    Lissoos, Trevor
    Hunter, Theresa
    Harding, Gale
    Stassek, Larissa
    Andrae, David
    Lewis, James D.
    JOURNAL OF PATIENT-REPORTED OUTCOMES, 2022, 6 (01)
  • [40] Development and pilot of a burns-specific patient-reported experience measure
    Hodgkinson, E. L.
    Boullin, P.
    Heary, S.
    Grant, B.
    BURNS, 2019, 45 (07) : 1600 - 1604