Development and Content Validity of a Patient-Reported Experience Measure for Home Dialysis

被引:19
|
作者
Rivara, Matthew B. [1 ,2 ]
Edwards, Todd [3 ]
Patrick, Donald [3 ]
Anderson, Lisa [1 ]
Himmelfarb, Jonathan [1 ,2 ]
Mehrotra, Rajnish [1 ,2 ]
机构
[1] Univ Washington, Kidney Res Inst, Seattle, WA 98104 USA
[2] Univ Washington, Harborview Med Ctr, Dept Med, Div Nephrol, Seattle, WA 98104 USA
[3] Univ Washington, Sch Publ Hlth, Dept Hlth Serv, Seattle, WA 98104 USA
关键词
end stage kidney disease; peritoneal dialysis; hemodialysis;
D O I
10.2215/CJN.15570920
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives The population of patients with kidney failure in theUnited States using home dialysis modalities is growing rapidly. Unlike for in-center hemodialysis, there is no patient-reported experiencemeasure for assessment of patient experience of care for peritoneal dialysis or home hemodialysis. We sought to develop and establish content validity of a patient-reported experience measure for patients undergoing home dialysis using a mixed methods multiple stakeholder approach. Design, setting, participants, & measurements We conducted a structured literature review, followed by concept elicitation focus groups and interviews among 65 participants, including 21 patients on home dialysis, 33 home dialysis nurses, three patient care partners, and eight nephrologists. We generated a list of candidate items for possible measure inclusion and conducted a national prioritization exercise among 91 patients on home dialysis and 39 providers using a web-based platform. We drafted the Home Dialysis Care Experience instrument and conducted cognitive debriefing interviews to evaluate item interpretability, order, and structure. We iteratively refined the measure on the basis of interview findings. Results The literature review and concept elicitation phases supported 15 domains of home dialysis care experience in six areas: communication and education of patients, concern and helpfulness of the care team, proficiency of the care team, patient-centered care, care coordination, and amenities and environment. Focus groups results showed that domains of highest importance for measure inclusion were patient education and communication, care coordination, and personalization of care. Prioritization exercise results confirmed focus group findings. Cognitive debriefing indicated that the finalmeasurewas easily understood and supported content validity. Conclusions TheHomeDialysis Care Experience instrument is a 26-itempatient-reported experiencemeasure for use in peritoneal dialysis and home hemodialysis. The Home Dialysis Care Experience instrument represents the first rigorously developed and content-valid English-language instrument for assessment of patient-reported experience of care in home dialysis.
引用
收藏
页码:588 / 598
页数:11
相关论文
共 50 条
  • [21] Patient-reported experience measure in sickle cell disease
    Chakravorty, Subarna
    Tallett, Amy
    Witwicki, Cara
    Hay, Harriet
    Mkandawire, Catherine
    Ogundipe, Avanelle
    Ojeer, Patrick
    Whitaker, Antonia
    Thompson, Jessica
    Sizmur, Stephen
    Sathyamoorthy, Ganesh
    Warner, John O.
    ARCHIVES OF DISEASE IN CHILDHOOD, 2018, 103 (12) : 1104 - 1109
  • [22] Developing a Patient-Reported Outcome and Experience Measure for Glaucoma
    Scollo, Paolo
    Pujari, Rathin
    Somner, John
    Pesudovs, Konrad
    Shah, Peter
    Rajani, Sajan
    Dufour, Lionel
    Pujari, Reema
    Hassan, Ali
    Hanspal, Inderraj
    Khatib, Tasneem
    Tapply, Ian
    Bourne, Rupert R. A.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2020, 61 (07)
  • [23] Developing a Patient-Reported Experience Measure for Surgical Outpatients
    Seager, A.
    Bukhari, M. A. S.
    BRITISH JOURNAL OF SURGERY, 2015, 102 : 156 - 156
  • [24] Systematic review of development and content validity of patient-reported outcome measures in inflammatory bowel disease: do we measure what we measure?
    van Andel, E.
    Koopmann, B.
    van Asseldonk, D.
    de Boer, N.
    Mokkink, L.
    Noomen, C.
    JOURNAL OF CROHNS & COLITIS, 2019, 13 : S228 - S229
  • [25] Systematic Review of Development and Content Validity of Patient-reported Outcome Measures in Inflammatory Bowel Disease: Do We Measure What We Measure?
    van Andel, Emma M.
    Koopmann, Brechtje D. M.
    Crouwel, Femke
    Noomen, Casper G.
    de Boer, Nanne K. H.
    van Asseldonk, Dirk P.
    Mokkink, Lidwine B.
    JOURNAL OF CROHNS & COLITIS, 2020, 14 (09): : 1299 - 1315
  • [26] Assessing the patient experience of respiratory syncytial virus infection: development of a patient-reported outcome measure
    Romano, Carla
    Finelli, Lyn
    Lewis, Sandy
    Williams, Valerie
    Martin, Emily
    Phillips, Matthew
    Saretsky, Todd L.
    Norquist, Josephine
    HEALTH AND QUALITY OF LIFE OUTCOMES, 2023, 21 (01)
  • [27] Assessing the patient experience of respiratory syncytial virus infection: development of a patient-reported outcome measure
    Carla (DeMuro) Romano
    Lyn Finelli
    Sandy Lewis
    Valerie Williams
    Emily Martin
    Matthew Phillips
    Todd L. Saretsky
    Josephine Norquist
    Health and Quality of Life Outcomes, 21
  • [28] A Practical Guide for Item Generation in Measure Development: Insights From the Development of a Patient-Reported Experience Measure of Compassion
    Sinclair, Shane
    Jaggi, Priya
    Hack, Thomas F.
    McClement, Susan E.
    Cuthbertson, Lena
    JOURNAL OF NURSING MEASUREMENT, 2020, 28 (01) : 138 - 156
  • [29] The Psoriasis Symptom Diary: development and content validity of a novel patient-reported outcome instrument
    Lebwohl, Mark
    Swensen, Andrine R.
    Nyirady, Judit
    Kim, Edward
    Gwaltney, Chad J.
    Strober, Bruce E.
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2014, 53 (06) : 714 - 722
  • [30] DEVELOPMENT AND CONTENT VALIDITY OF THE PATIENT-REPORTED INTRAOCULAR LENS QUESTIONNAIRE (PR-ILQ)
    Shields, A.
    Galipeau, N.
    Chacko, J.
    Mazar, I
    Bowyer, B.
    VALUE IN HEALTH, 2017, 20 (05) : A250 - A250