Literature DB >> 25523316

Caregiver preferences for emerging duchenne muscular dystrophy treatments: a comparison of best-worst scaling and conjoint analysis.

Ilene L Hollin1, Holly L Peay, John F P Bridges.   

Abstract

BACKGROUND: Through Patient-Focused Drug Development, the US Food and Drug Administration (FDA) documents the perspective of patients and caregivers and are currently conducting 20 public meetings on a limited number of disease areas. Parent Project Muscular Dystrophy (PPMD), an advocacy organization for Duchenne muscular dystrophy (DMD), has demonstrated a community-engaged program of preference research that would complement the FDA's approach.
OBJECTIVE: Our objective was to compare two stated-preference methods, best-worst scaling (BWS) and conjoint analysis, within a study measuring caregivers' DMD-treatment preferences.
METHODS: Within one survey, two preference-elicitation methods were applied to 18 potential treatments incorporating six attributes and three levels. For each treatment profile, caregivers identified the best and worst feature and intention to use the treatment. We conducted three analyses to compare the elicitation methods using parameter estimates, conditional attribute importance and policy simulations focused on the 18 treatment profiles. For each, concordance between the results was compared using Spearman's rho.
RESULTS: BWS and conjoint analysis produced similar parameter estimates (p < 0.01); conditional attribute importance (p < 0.01); and policy simulations (p < 0.01). Greatest concordance was observed for the benefit and risk parameters, with differences observed for nausea and knowledge about the drug-where a lack of monotonicity was observed when using conjoint analysis.
CONCLUSIONS: The observed concordance between approaches demonstrates the reliability of the stated-preference methods. Given the simplicity of combining BWS and conjoint analysis on single profiles, a combination approach is easily adopted. Minor irregularities for the conjoint-analysis results could not be explained by additional analyses and needs to be the focus of future research.

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Year:  2015        PMID: 25523316     DOI: 10.1007/s40271-014-0104-x

Source DB:  PubMed          Journal:  Patient        ISSN: 1178-1653            Impact factor:   3.883


  31 in total

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Authors:  Joachim Marti
Journal:  Soc Sci Med       Date:  2012-03-17       Impact factor: 4.634

Review 2.  Valuing citizen and patient preferences in health: recent developments in three types of best-worst scaling.

Authors:  Terry N Flynn
Journal:  Expert Rev Pharmacoecon Outcomes Res       Date:  2010-06       Impact factor: 2.217

3.  A national profile of health care and family impacts of children with muscular dystrophy and special health care needs in the United States.

Authors:  Lijing Ouyang; Scott D Grosse; Michael H Fox; Julie Bolen
Journal:  J Child Neurol       Date:  2011-09-27       Impact factor: 1.987

4.  Methodological issues in the monetary valuation of benefits in healthcare.

Authors:  Mandy Ryan; Verity Watson; Mabelle Amaya-Amaya
Journal:  Expert Rev Pharmacoecon Outcomes Res       Date:  2003-12       Impact factor: 2.217

5.  The effect of caregiving on women in families with Duchenne/Becker muscular dystrophy.

Authors:  Aileen Kenneson; Janet Kay Bobo
Journal:  Health Soc Care Community       Date:  2010-06-16

6.  Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years - four states, 2007.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2009-10-16       Impact factor: 17.586

7.  Health care utilization and expenditures for children and young adults with muscular dystrophy in a privately insured population.

Authors:  Lijing Ouyang; Scott D Grosse; Aileen Kenneson
Journal:  J Child Neurol       Date:  2008-04-10       Impact factor: 1.987

8.  Best--worst scaling: What it can do for health care research and how to do it.

Authors:  Terry N Flynn; Jordan J Louviere; Tim J Peters; Joanna Coast
Journal:  J Health Econ       Date:  2006-05-16       Impact factor: 3.883

9.  Women's colposcopy experience and preferences: a mixed methods study.

Authors:  Dawn R Swancutt; Sheila M Greenfield; Sue Wilson
Journal:  BMC Womens Health       Date:  2008-01-14       Impact factor: 2.809

Review 10.  The role of corticosteroids in muscular dystrophy: a critical appraisal.

Authors:  Corrado Angelini
Journal:  Muscle Nerve       Date:  2007-10       Impact factor: 3.217

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  25 in total

1.  Using Best-Worst Scaling to Measure Caregiver Preferences for Managing their Child's ADHD: A Pilot Study.

Authors:  Susan dosReis; Xinyi Ng; Emily Frosch; Gloria Reeves; Charles Cunningham; John F P Bridges
Journal:  Patient       Date:  2015-10       Impact factor: 3.883

2.  How important is social support in determining patients' suitability for transplantation? Results from a National Survey of Transplant Clinicians.

Authors:  Keren Ladin; Joanna Emerson; Zeeshan Butt; Elisa J Gordon; Douglas W Hanto; Jennifer Perloff; Norman Daniels; Tara A Lavelle
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3.  The imperative for patient-centred research to develop better quality services in rare diseases.

Authors:  Karen Facey; Helle Ploug Hansen
Journal:  Patient       Date:  2015-02       Impact factor: 3.883

4.  Symposium Title: Preference Evidence for Regulatory Decisions.

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Journal:  Patient       Date:  2018-10       Impact factor: 3.883

5.  Moving from Patient Advocacy to Partnership: A Long and Bumpy Road.

Authors:  Durhane Wong-Rieger
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Review 6.  A Systematic Review Comparing the Acceptability, Validity and Concordance of Discrete Choice Experiments and Best-Worst Scaling for Eliciting Preferences in Healthcare.

Authors:  Jennifer A Whitty; Ana Sofia Oliveira Gonçalves
Journal:  Patient       Date:  2018-06       Impact factor: 3.883

7.  The Ball is in Your Court: Agenda for Research to Advance the Science of Patient Preferences in the Regulatory Review of Medical Devices in the United States.

Authors:  Bennett Levitan; A Brett Hauber; Marina G Damiano; Ross Jaffe; Stephanie Christopher
Journal:  Patient       Date:  2017-10       Impact factor: 3.883

8.  A Latent Class Analysis to Identify Variation in Caregivers' Preferences for their Child's Attention-Deficit/Hyperactivity Disorder Treatment: Do Stated Preferences Match Current Treatment?

Authors:  Xinyi Ng; John F P Bridges; Melissa M Ross; Emily Frosch; Gloria Reeves; Charles E Cunningham; Susan dosReis
Journal:  Patient       Date:  2017-04       Impact factor: 3.883

9.  Prioritizing Parental Worry Associated with Duchenne Muscular Dystrophy Using Best-Worst Scaling.

Authors:  Holly Landrum Peay; I L Hollin; J F P Bridges
Journal:  J Genet Couns       Date:  2015-08-21       Impact factor: 2.537

10.  A Framework for Instrument Development of a Choice Experiment: An Application to Type 2 Diabetes.

Authors:  Ellen M Janssen; Jodi B Segal; John F P Bridges
Journal:  Patient       Date:  2016-10       Impact factor: 3.883

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