Literature DB >> 27649378

Patient-centered benefit-risk assessment in duchenne muscular dystrophy.

Ilene L Hollin1, Holly L Peay2,3, Susan D Apkon4, John F P Bridges1.   

Abstract

INTRODUCTION: This study quantified caregiver and patient preferences for a therapeutic agent with demonstrated pulmonary benefits for Duchenne muscular dystrophy (DMD). Caregiver and patient differences were also explored.
METHODS: A best-worst scaling survey (BWS) was administered to caregivers and patients. Across 9 profiles, respondents selected the best and worst attributes. Utility scores were estimated using mixed logistic regression.
RESULTS: Respondents indicated greatest preference for therapies that maintain their current level of cough strength for 10 years or for 2 years. Preference scores for risks were low: 50% chance of diarrhea and 4 additional blood draws per year.
CONCLUSION: There is a strong preference for pulmonary benefit and willingness to trade off risks and burden to achieve these benefits. In exchange for maintaining cough strength for 10 years, respondents were willing to tolerate high probabilities of diarrhea and additional blood draws. Muscle Nerve 55: 626-634, 2017.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  Duchenne/Becker muscular dystrophy; best-worst scaling; patient preferences; patient-centered benefit-risk assessment; quality of life; regulatory review

Mesh:

Year:  2017        PMID: 27649378     DOI: 10.1002/mus.25411

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


  18 in total

1.  Symposium Title: Preference Evidence for Regulatory Decisions.

Authors:  Juan Marcos Gonzalez; F Reed Johnson; Bennett Levitan; Rebecca Noel; Holly Peay
Journal:  Patient       Date:  2018-10       Impact factor: 3.883

Review 2.  Practical Considerations for Using Online Methods to Engage Patients in Guideline Development.

Authors:  Sean Grant; Glen S Hazlewood; Holly L Peay; Ann Lucas; Ian Coulter; Arlene Fink; Dmitry Khodyakov
Journal:  Patient       Date:  2018-04       Impact factor: 3.883

3.  How Do Members of the Duchenne and Becker Muscular Dystrophy Community Perceive a Discrete-Choice Experiment Incorporating Uncertain Treatment Benefit? An Application of Research as an Event.

Authors:  John F P Bridges; Jui-Hua Tsai; Ellen Janssen; Norah L Crossnohere; Ryan Fischer; Holly Peay
Journal:  Patient       Date:  2019-04       Impact factor: 3.883

4.  Characterizing Enrollment in Observational Studies of Duchenne Muscular Dystrophy by Race and Ethnicity.

Authors:  Alison M Barnard; Samuel L Riehl; Rebecca J Willcocks; Glenn A Walter; Amber M Angell; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2020

5.  Developing and piloting an instrument to prioritize the worries of patients with acute myeloid leukemia.

Authors:  John Fp Bridges; Allison H Oakes; Crystal A Reinhart; Ernest Voyard; Bernadette O'Donoghue
Journal:  Patient Prefer Adherence       Date:  2018-04-27       Impact factor: 2.711

Review 6.  To what degree are orphan drugs patient-centered? A review of the current state of clinical research in rare diseases.

Authors:  Sally Lanar; Catherine Acquadro; James Seaton; Isabelle Savre; Benoit Arnould
Journal:  Orphanet J Rare Dis       Date:  2020-06-03       Impact factor: 4.123

7.  Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents.

Authors:  Holly Landrum Peay; Ryan Fischer; Janice P Tzeng; Sharon E Hesterlee; Carl Morris; Amy Strong Martin; Colin Rensch; Edward Smith; Valeria Ricotti; Katherine Beaverson; Hannah Wand; Carol Mansfield
Journal:  PLoS One       Date:  2019-05-01       Impact factor: 3.240

8.  Nonclinical Exon Skipping Studies with 2'-O-Methyl Phosphorothioate Antisense Oligonucleotides in mdx and mdx-utrn-/- Mice Inspired by Clinical Trial Results.

Authors:  Maaike van Putten; Christa Tanganyika-de Winter; Sieto Bosgra; Annemieke Aartsma-Rus
Journal:  Nucleic Acid Ther       Date:  2019-01-23       Impact factor: 5.486

9.  Patient Involvement in the Lifecycle of Medicines According to Belgian Stakeholders: The Gap Between Theory and Practice.

Authors:  Rosanne Janssens; Eline van Overbeeke; Lotte Verswijvel; Lissa Meeusen; Carolien Coenegrachts; Kim Pauwels; Marc Dooms; Hilde Stevens; Steven Simoens; Isabelle Huys
Journal:  Front Med (Lausanne)       Date:  2018-10-11

10.  Home-Based Monitoring of Pulmonary Function in Patients with Duchenne Muscular Dystroph.

Authors:  Gunnar M Buyse; Christian Rummey; Thomas Meier; Mika Leinonen; Thomas Voit; Craig M McDonald; Oscar H Mayer
Journal:  J Neuromuscul Dis       Date:  2018
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