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Test-retest properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire and its constituent domains.
Chai-Adisaksopha, Chatree; Skinner, Mark W; Curtis, Randall; Frick, Neil; Nichol, Michael B; Noone, Declan; O'Mahony, Brian; Page, David; Stonebraker, Jeffrey; Thabane, Lehana; Crowther, Mark A; Iorio, Alfonso.
Afiliação
  • Chai-Adisaksopha C; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Skinner MW; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Curtis R; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Frick N; Institute for Policy Advancement Ltd, Washington, District of Columbia.
  • Nichol MB; Factor VIII Computing, Berkeley, California.
  • Noone D; National Hemophilia Foundation, New York, New York.
  • O'Mahony B; Sol Price School of Public Policy, University of Southern California, Los Angeles, California.
  • Page D; Irish Haemophilia Society, Dublin, Ireland.
  • Stonebraker J; Irish Haemophilia Society, Dublin, Ireland.
  • Thabane L; Trinity College Dublin, Dublin, Ireland.
  • Crowther MA; Canadian Hemophilia Society, Montreal, Quebec, Canada.
  • Iorio A; Poole College of Management, North Carolina State University, Raleigh, North Carolina.
Haemophilia ; 25(1): 75-83, 2019 Jan.
Article em En | MEDLINE | ID: mdl-30520534
ABSTRACT

BACKGROUND:

The Patient Reported Outcomes, Burdens and Experiences (PROBE) study aims to develop and validate questionnaire for assessing health status in patients with haemophilia and participants without bleeding disorders.

OBJECTIVE:

To investigate the test-retest properties of the PROBE questionnaire.

METHODS:

The PROBE questionnaire covers four domains and is comprised of 29 questions. People with haemophilia (PWH) and participants without bleeding disorder were invited to participate in this study. All participants were asked to complete the PROBE questionnaire three times (paper-based survey on two consecutive days T1 and T2 and then a web-based version T3). Test-retest properties and percentage agreement were analysed.

RESULTS:

A total of 63 participants were enrolled in this study with a median age of 50 (range 17-76) years. Of these, 30 (47.6%) were PWH. On the questions common to PWH and participants without bleeding disorder, Kappa coefficients ranged from 0.69 to 1.00, indicating substantial to almost perfect agreement (T1 vs T2). For haemophilia-related questions (T1 vs T2), Kappa coefficients ranged from 0.5 to 1.0. Of these, 5 of 11 items were in perfect agreement (Kappa = 1.0). The web-based questionnaire (T3) showed substantial to almost perfect agreement with the paper version (T1 test-retest properties were comparable between PWH and individuals without a bleeding disorder).

CONCLUSIONS:

The results suggest that PROBE is a reliable tool to assess patient-reported outcomes for PWH and benchmark data in participants without bleeding disorder. The web-based questionnaire and the standard paper-based version can be used interchangeably.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Efeitos Psicossociais da Doença / Transtornos Herdados da Coagulação Sanguínea / Medidas de Resultados Relatados pelo Paciente Tipo de estudo: Qualitative_research Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Efeitos Psicossociais da Doença / Transtornos Herdados da Coagulação Sanguínea / Medidas de Resultados Relatados pelo Paciente Tipo de estudo: Qualitative_research Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article