The development of the ICIQ-UAB: A patient reported outcome measure for underactive bladder.


Journal

Neurourology and urodynamics
ISSN: 1520-6777
Titre abrégé: Neurourol Urodyn
Pays: United States
ID NLM: 8303326

Informations de publication

Date de publication:
03 2019
Historique:
received: 09 05 2018
revised: 04 12 2018
accepted: 24 01 2019
pubmed: 26 2 2019
medline: 8 2 2020
entrez: 26 2 2019
Statut: ppublish

Résumé

To present the development of the International Consultation on Incontinence Questionnaire-underactive bladder (ICIQ-UAB) as the first patient reported outcome measure for the assessment of the symptoms and impact on the health-related quality of life of UAB developed in-line with the Food and Drug Administration Guidance for Industry. Draft items were developed following 44 semi-structured concept elicitation interviews in the UK and refined using 36 cognitive interviews. A pilot study was designed to assess the draft ICIQ-UAB's initial psychometric properties with 54 patients recruited from European hospitals. Further concept elicitation interviews were also carried out with 11 patients in the US and 10 patients in Japan. All participants had a prior urodynamic diagnosis of detrusor underactivity. The cognitive interviews confirmed the initial items to be understood and interpreted as intended. Pilot testing showed that both internal consistency (Cronbach's α ≥ 0.85) and test-retest reliability (stable patients; intraclass correlation coefficient ≥ 0.88) were high. The interviews in the US and Japan elicited symptoms and impacts that support previous findings in the UK and provided further insight into the experiences of patients in those countries. The developmental ICIQ-UAB was refined using the evidence from all substudies. The validity and reliability of the ICIQ-UAB were supported in a pilot study setting and the wider cultural applicability by the additional interviews in the US and Japan. Following further validation in future clinical trials, the developmental ICIQ-UAB is envisaged as an important tool for the monitoring of future UAB treatment strategies.

Identifiants

pubmed: 30801826
doi: 10.1002/nau.23947
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

996-1004

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Alan D Uren (AD)

Bristol Urological Institute, Bristol, UK.

Nikki Cotterill (N)

Bristol Urological Institute, Bristol, UK.

Christopher Harding (C)

Department of Urology, Freeman Hospital, Newcastle-upon-Tyne, UK.

Christopher Hillary (C)

Department of Urology, Royal Hallamshire Hospital, Sheffield, UK.

Christopher Chapple (C)

Department of Urology, Royal Hallamshire Hospital, Sheffield, UK.

Kathryn Lasch (K)

Pharmerit, Boston, Massachusetts.

Angela Stroupe (A)

Pharmerit, Boston, Massachusetts.

Chinmay Deshpande (C)

Pharmerit, Bethesda, Maryland.

Laure Delbecque (L)

Pharmerit, Rotterdam, The Netherlands.

Gommert Van Koeveringe (G)

Department of Urology, Maastricht University Medical Centre, Maastricht, The Netherlands.

Matthias Oelke (M)

Department of Urology, St. Antonius Hospital, Gronau, Germany.

Mohammed Belal (M)

Department of Urology, Queen Elizabeth Hospital, Birmingham, UK.

Ruud Bosch (R)

Department of Urology, University Medical Centre Utrecht, Utrecht, The Netherlands.

Bertil Blok (B)

Department of Urology, Erasmus Medical Centre, Rotterdam, The Netherlands.

Victor Nitti (V)

Department of Urology, NYU Langone Medical Centre, New York, New York.

Momokazu Gotoh (M)

Department of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Mineo Takei (M)

Harasanshin Hospital, Fukuoka, Japan.

Bruce Crawford (B)

Syneos Health, Tokyo, Japan.

Monique Klaver (M)

Astellas Pharma Europe B.V, Leiden, The Netherlands.

Dominique Bongaerts (D)

Astellas Pharma Europe B.V, Leiden, The Netherlands.

Zalmai Hakimi (Z)

Astellas Pharma Europe B.V, Leiden, The Netherlands.

Ton Kos (T)

Astellas Pharma Europe B.V, Leiden, The Netherlands.

Paul Abrams (P)

Bristol Urological Institute, Bristol, UK.

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