
ACCME Accredited Roundtable
Unmet needs in Pompe disease: Highlights from World Muscle Society Congress 2022
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Live Webinar Roundtable Agenda
Unmet needs in Pompe disease: Highlights from World Muscle Society Congress 2022 Date and time: Wednesday 18 January 2023, 15:00 GMT |
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Chair: Professor Jordi Díaz-Manera | |
Introduction | Professor Jordi Díaz-Manera |
Topic 1: Unmet needs and burden of Pompe disease | Mr Allan Muir |
Topic 2: Early diagnosis of Pompe disease | Professor Benedikt Schoser |
Topic 3: Treatments for Pompe disease | Professor Jordi Díaz-Manera |
Q&A | All |
Closing remarks | Professor Jordi Díaz-Manera |
Learning Objectives
This roundtable aims to improve awareness of:
- The current clinical and socioeconomical burden of Pompe disease, and the unmet needs regarding its early diagnosis, management, treatment, and monitoring
- Early Pompe disease diagnosis, understanding the signs and symptoms of infantile- and late-onset Pompe disease, common misdiagnoses, and strategies for confirming a diagnosis
- Treatments for Pompe disease, including enzyme replacement therapy (ERT), and the importance of monitoring disease progression, emphasising the need for a multidisciplinary team and patient involvement to ensure appropriate management
Target Audience
This activity has been designed to meet the educational needs of Neuromuscular specialists, geneticists, neurologists, Lysosomal disease specialists, genetic counsellors, Paediatricians, GPs, and specialist nurses.
Disclosures
USF Health adheres to the Standards for Integrity and Independence in Accredited Continuing Education. All individuals in a position to influence content have disclosed to USF Health any financial relationship with an ineligible organization. USF Health has reviewed and mitigated all relevant financial relationships related to the content of the activity. The relevant financial relationships are listed below. All individuals not listed have no relevant financial relationships.
Meet the roundtable expert panel
Professor Jordi Díaz-Manera
Professor Jordi Díaz-Manera is Professor of Neuromuscular Disorders at Newcastle University, and Honorary Consultant Clinical Geneticist with the Newcastle Hospitals NHS Foundation Trust.
Jordi’s clinical research projects are focused on the characterisation of large cohort of patients with muscular dystrophies, the implementation of quantitative muscle magnetic-resonance imaging (MRI) for the diagnosis and follow-up of patients with muscular diseases, and the development of new outcome measures for clinical trials and natural history studies. His basic research interest focuses on the process of muscle fibre degeneration and the replacement of muscle tissue by fat and fibrosis that takes place in patients with muscular dystrophies.
Disclosures
Jordi Diaz Manera, MD - Advisory board or panel fees from Amicus, Astellas, Sarepta and Sanofi Genzyme. Grants/research support from Boehringer-Ingelheim, Spark, Sanofi and Sarepta. Other financial or material support from Boehringer-Ingelheim.
Mr Allan Muir
As the parent of a son with Pompe disease, Allan has been involved with the Pompe Community for over 30 years. He manages a national charity that supports Glycogen Storage Diseases for 9 years and has chaired the Pompe Support Network for three years. Allan is currently vice-chair of the International Pompe Association.
Disclosures
Allan Muir – Advisory board or panel fees from Amicus Therapeutics, Audentes Therapeutics, AvroBio and Maze Therapeutics.
Professor Benedikt Schoser
Professor Benedikt Schoser is senior consultant at the Friedrich-Baur-Institute, Department of Neurology at the Ludwig-Maximilians-University of Munich, Germany. He is member of the executive board of the World Muscle Society, and member of the European academy of Neurology panel for neuromuscular disorders.
Benedikt is interested in the pathogenesis and histopathology of muscular dystrophies, myotonic dystrophies, and metabolic myopathies. Within the neuromuscular research group at Friedrich-Baur-Institute, he is engaged in morphological and molecular analyses, including neuromuscular animal models. He has a special interest in translational gene therapy of myotonic dystrophies and glycogen storage disorders.
Disclosures
Benedikt Schoser, MD - Advisory board or panel fees from Amicus, Argenx, Astellas, Avrobio, Maze Therapeutics, PepGen, Sanofi and Taysha. Grants/research support from Amicus and Astellas. Speakers bureau fees from Alexion and Kedrion.
Content Reviewer
Reviewer, Rebecca Hurst, MD, no financial interests/relationships or affiliations in relation to this activity.
Staff
USF Health Office of Continuing Professional Development and EPG Health staff have no relevant financial interests/relationships or affiliations in relation to this activity.
Requirements for Successful Completion
In order to receive credit for this activity, participants must review the content and complete the post-test and evaluation form. Statements of credit are awarded upon successful completion of the post-test and evaluation form.
If you have questions regarding credit please contact cpdsupport@usf.edu
Accreditations
Physicians
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through a joint providership of USF Health and EPG Health. USF Health is accredited by the ACCME to provide continuing medical education for physicians.
USF Health designates this enduring activity for a maximum of 0.75 AMA PRA Category 1 CreditTM. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
The European Union of Medical Specialists (UEMS) – European Accreditation Council for Continuing Medical Education (EACCME) has an agreement of mutual recognition of continuing medical education (CME) credit with the American Medical Association (AMA). European physicians interested in converting AMA PRA Category 1 CreditTM into European CME credit (ECMEC) should contact the UEMS (www.uems.eu)
Advanced Practice Providers
Physician Assistants may claim a maximum of 0.75 Category 1 credits for completing this activity. NCCPA accepts AMA PRA Category 1 CreditTM from organizations accredited by ACCME or a recognized state medical society.
The AANPCP accepts certificates of participation for educational activities approved for AMA PRA Category 1 CreditTM by ACCME-accredited providers. APRNs who participate will receive a certificate of completion commensurate with the extent of their participation.
Date of original release: 18 January, 2023. Date credit expire: 17 January, 2024.
If you have any questions regarding credit please contact cpdsupport@usf.edu
This Activity Is Funded By:
An independent medical education grant from Amicus Therapeutics, Inc.
This activity is jointly provided by USF Health and EPG Health.
The information provided by this CE activity is for continuing education purposes only and is not meant to substitute for the independent medical/clinical judgment of a healthcare provider relative to diagnostic and treatment options of a specific patient’s medical condition.
USF is an Equal Opportunity / Affirmative Action / Equal Access Institution.
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