Literature DB >> 27671699

Development of a patient-reported outcome measure for upper limb function in Duchenne muscular dystrophy: DMD Upper Limb PROM.

K Klingels1,2, A G Mayhew3, E S Mazzone4, T Duong5, V Decostre6, U Werlauff7, E Vroom8, E Mercuri4, N M Goemans9.   

Abstract

AIM: To develop a patient-reported outcome measure (PROM) assessing upper limb function related to activities of daily living (ADL) that cannot be observed in a clinical setting, specifically for patients with Duchenne muscular dystrophy (DMD) across a wide age range, applicable in the different stages of the disease.
METHOD: The developmental process was based on US Food and Drug Administration guidelines. This included item generation from a systematic review of existing tools and expert opinion on task difficulty and relevance, involving individuals with DMD. Cultural aspects affecting ADL were taken into consideration to make this tool applicable to the broad DMD community. Items were selected in relation to a conceptual framework reflecting disease progression covering the full range of upper limb function across different ADL domains.
RESULTS: After pilot testing and iterative Rasch analyses, redundant or clinically irrelevant items were removed. The final questionnaire consists of 32 items covering four domains of ADL (food, self-care, household and environment, leisure and communication). Test-retest reliability was excellent.
INTERPRETATION: A DMD-specific upper limb PROM was developed on the basis of clinical relevance and psychometric robustness. Its main purpose is to document the patient self-reported natural history of DMD and assess the efficacy of interventions.
© 2016 Mac Keith Press.

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Mesh:

Year:  2016        PMID: 27671699     DOI: 10.1111/dmcn.13277

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  11 in total

1.  Assessing the engagement of children and families in selecting patient-reported outcomes (PROs) and developing their measures: a systematic review.

Authors:  Malcolm McNeill; Samantha Noyek; Eshetu Engeda; Nora Fayed
Journal:  Qual Life Res       Date:  2020-11-06       Impact factor: 4.147

2.  Latent process model of the 6-minute walk test in Duchenne muscular dystrophy : A Bayesian approach to quantifying rare disease progression.

Authors:  Janelle L Lennie; John T Mondick; Marc R Gastonguay
Journal:  J Pharmacokinet Pharmacodyn       Date:  2020-01-20       Impact factor: 2.745

Review 3.  The involvement of rare disease patient organisations in therapeutic innovation across rare paediatric neurological conditions: a narrative review.

Authors:  Christina Q Nguyen; Kristine Alba-Concepcion; Elizabeth E Palmer; Jackie L Scully; Nicole Millis; Michelle A Farrar
Journal:  Orphanet J Rare Dis       Date:  2022-04-18       Impact factor: 4.303

Review 4.  Measuring what matters to rare disease patients - reflections on the work by the IRDiRC taskforce on patient-centered outcome measures.

Authors:  Thomas Morel; Stefan J Cano
Journal:  Orphanet J Rare Dis       Date:  2017-11-02       Impact factor: 4.123

Review 5.  Towards a core outcome set for hemorrhoidal disease-a systematic review of outcomes reported in literature.

Authors:  R R van Tol; E van Zwietering; J Kleijnen; J Melenhorst; L P S Stassen; C D Dirksen; S O Breukink
Journal:  Int J Colorectal Dis       Date:  2018-04-22       Impact factor: 2.571

6.  Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy.

Authors:  Claudia Brogna; Lara Cristiano; Tommaso Tartaglione; Tommaso Verdolotti; Lavinia Fanelli; Luana Ficociello; Giorgio Tasca; Roberta Battini; Giorgia Coratti; Nicola Forcina; Roberto De Santis; Giulia Norcia; Sara Carnicella; Cesare Colosimo; Pierre Carlier; Marika Pane; Eugenio Mercuri
Journal:  PLoS One       Date:  2018-06-20       Impact factor: 3.240

7.  "Be an ambassador for change that you would like to see": a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease.

Authors:  Anna Ambrosini; Ros Quinlivan; Valeria A Sansone; Ingeborg Meijer; Guus Schrijvers; Aad Tibben; George Padberg; Maarten de Wit; Ellen Sterrenburg; Alexandre Mejat; Alexandra Breukel; Michal Rataj; Hanns Lochmüller; Raffaella Willmann
Journal:  Orphanet J Rare Dis       Date:  2019-06-07       Impact factor: 4.123

8.  Adapting traditional content validation methods to fit purpose: an example with a novel video assessment and training materials in Duchenne muscular dystrophy (DMD).

Authors:  Michelle K White; Mindy Leffler; Kaitlin Rychlec; Chris Jones; Christine McSherry; Linsey Walker; Mark Kosinski
Journal:  Qual Life Res       Date:  2019-07-13       Impact factor: 4.147

9.  Association of Elbow Flexor MRI Fat Fraction With Loss of Hand-to-Mouth Movement in Patients With Duchenne Muscular Dystrophy.

Authors:  Karin J Naarding; Menno van der Holst; Erik W van Zwet; Nienke M van de Velde; Imelda J M de Groot; Jan J G M Verschuuren; Hermien E Kan; Erik H Niks
Journal:  Neurology       Date:  2021-09-07       Impact factor: 9.910

10.  Update on Standard Operating Procedures in Preclinical Research for DMD and SMA Report of TREAT-NMD Alliance Workshop, Schiphol Airport, 26 April 2015, The Netherlands.

Authors:  Maaike van Putten; Annemieke Aartsma-Rus; Miranda D Grounds; Joe N Kornegay; Anna Mayhew; Thomas H Gillingwater; Shin'ichi Takeda; Markus A Rüegg; Annamaria De Luca; Kanneboyina Nagaraju; Raffaella Willmann
Journal:  J Neuromuscul Dis       Date:  2018
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