Literature DB >> 26600438

Construction and validation of the chronic acquired polyneuropathy patient-reported index (CAP-PRI): A disease-specific, health-related quality-of-life instrument.

Kelly G Gwathmey1, Mark R Conaway2, Reza Sadjadi1, Amruta Joshi1, Carolina Barnett3, Vera Bril3, Eduardo Ng3, William David4, Karissa Gable5, Jeffrey T Guptill5, Lisa D Hobson-Webb5, Jennifer Dineen6, Michael Hehir7, Thomas H Brannagan8, Esther Byun9, Margaret Adler10, Ted M Burns1.   

Abstract

INTRODUCTION: Generic health-related quality-of-life (HRQOL) patient-reported outcome measures have been used in patients with chronic immune-mediated polyneuropathies. We have created a disease-specific HRQOL instrument.
METHODS: The chronic acquired polyneuropathy patient-reported index (CAP-PRI) was developed and validated in multiple steps. Items were initially generated through patient and specialist input. The performance of the preliminary 20 items was analyzed via a prospective, 5-center study involving chronic immune-mediated polyneuropathy patients.
RESULTS: Data analysis suggested modification to a 15-item scale with 3 response categories rather than 5. The final CAP-PRI was validated in another prospective, 5-center study. The CAP-PRI appeared to be a unidimensional outcome measure that fit the Rasch model in our multicenter cohort. It correlated appropriately with outcome measures commonly used in this patient population.
CONCLUSIONS: The CAP-PRI is a simple disease-specific HRQOL measure that appears to be useful for clinical care and possibly also for clinical trials. Muscle Nerve 54: 9-17, 2016.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  CAP-PRI; chronic inflammatory demyelinating polyneuropathy; immune-mediated polyneuropathy; patient-reported outcome; quality of life

Mesh:

Year:  2015        PMID: 26600438      PMCID: PMC4950873          DOI: 10.1002/mus.24985

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  10 in total

Review 1.  Quality of life and measures of quality of life in patients with neuromuscular disorders.

Authors:  Ted M Burns; Christopher D Graham; Michael R Rose; Zachary Simmons
Journal:  Muscle Nerve       Date:  2012-05-29       Impact factor: 3.217

2.  Understanding the consequences of chronic inflammatory demyelinating polyradiculoneuropathy from impairments to activity and participation restrictions and reduced quality of life: the ICE study.

Authors:  Ingemar S J Merkies; Richard A C Hughes; Peter Donofrio; Vera Bril; Marinos C Dalakas; Kim Hanna; Hans-Peter Hartung; Norman Latov; Pieter A van Doorn; Chunqin Deng
Journal:  J Peripher Nerv Syst       Date:  2010-09       Impact factor: 3.494

3.  Correlates of quality of life in ALS: Lessons from the minocycline study.

Authors:  Jau-Shin Lou; Dan Moore; Paul H Gordon; Robert Miller
Journal:  Amyotroph Lateral Scler       Date:  2010

4.  Randomized controlled trial of intravenous immunoglobulin versus oral prednisolone in chronic inflammatory demyelinating polyradiculoneuropathy.

Authors:  R Hughes; S Bensa; H Willison; P Van den Bergh; G Comi; I Illa; E Nobile-Orazio; P van Doorn; M Dalakas; M Bojar; A Swan
Journal:  Ann Neurol       Date:  2001-08       Impact factor: 10.422

5.  The COSMIN checklist for evaluating the methodological quality of studies on measurement properties: a clarification of its content.

Authors:  Lidwine B Mokkink; Caroline B Terwee; Dirk L Knol; Paul W Stratford; Jordi Alonso; Donald L Patrick; Lex M Bouter; Henrica Cw de Vet
Journal:  BMC Med Res Methodol       Date:  2010-03-18       Impact factor: 4.615

6.  Quality of life complements traditional outcome measures in immune-mediated polyneuropathies.

Authors:  I S J Merkies; P I M Schmitz; F G A van der Meché; J P A Samijn; P A van Doorn
Journal:  Neurology       Date:  2002-07-09       Impact factor: 9.910

7.  Muscle performance relates to physical function and quality of life in long-term chronic inflammatory demyelinating polyradiculoneuropathy.

Authors:  Thomas Harbo; Henning Andersen; Kristian Overgaard; Johannes Jakobsen
Journal:  J Peripher Nerv Syst       Date:  2008-09       Impact factor: 3.494

Review 8.  Outcome measures in immune-mediated neuropathies: the need to standardize their use and to understand the clinimetric essentials.

Authors:  Sonja I van Nes; Catharina G Faber; Ingemar S J Merkies
Journal:  J Peripher Nerv Syst       Date:  2008-06       Impact factor: 3.494

9.  Health-related quality-of-life improvements in CIDP with immune globulin IV 10%: the ICE Study.

Authors:  I S J Merkies; V Bril; M C Dalakas; C Deng; P Donofrio; K Hanna; H-P Hartung; R A C Hughes; N Latov; P A van Doorn
Journal:  Neurology       Date:  2009-04-14       Impact factor: 9.910

10.  Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance.

Authors: 
Journal:  Health Qual Life Outcomes       Date:  2006-10-11       Impact factor: 3.186

  10 in total
  2 in total

1.  Validation of a simple disease-specific, quality-of-life measure for diabetic polyneuropathy: CAPPRI.

Authors:  Kelly G Gwathmey; Reza Sadjadi; William B Horton; Mark R Conaway; Carolina Barnett-Tapia; Vera Bril; James W Russell; Aziz Shaibani; Michelle L Mauermann; Michael K Hehir; Noah Kolb; Jeffrey Guptill; Lisa Hobson-Webb; Karissa Gable; Shruti Raja; Nicholas Silvestri; Gil I Wolfe; A Gordon Smith; Rabia Malik; Rebecca Traub; Amruta Joshi; Matthew P Elliott; Sarah Jones; Ted M Burns
Journal:  Neurology       Date:  2018-05-04       Impact factor: 9.910

2.  A longitudinal evaluation of fatigue in chronic inflammatory demyelinating polyneuropathy.

Authors:  Karissa L Gable; Stojan Peric; Michael W Lutz; Ivo Bozovic; Milutin Petrovic; Aleksandar Stojanov; Ivana Basta; Jeffrey A Allen
Journal:  Brain Behav       Date:  2022-07-21       Impact factor: 3.405

  2 in total

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