Patients with long-chain fatty oxidation disorders (LC-FAODs) have historically been treated with diet modification and even-carbon medium-chain triglyceride (MCT) supplementation. In this 45-minute, case-based, modular activity, Sandra van Calcar, PhD, RD, LD, and Jerry Vockley, MD, PhD, address key topics, including disease presentation, historical treatment, emerging treatment with triheptanoin, and nutritional planning specific to patients with LC-FAODs. Triheptanoin is an odd-carbon MCT designed to bypass the metabolic block in LC-FAODs, recently approved as an alternative treatment option. The faculty discuss the safety and efficacy of triheptanoin and their real-world experience initiating and optimizing it to bridge critical care gaps in patients with LC-FAODs. They briefly orient learners to a downloadable, point-of-care resource for patient education developed as part of this accredited activity.
This content is also availble as a podcast: You may listen here. In addition, you can access a companion activity focused on interprofessional collaboration here.
| This activity is developed in collaboration with Genetic Metabolic Dietitians International (GMDI) | ![]() |
Course Credit:
0.75 AMA PRA Category 1 CreditsTM
0.75 ANCC Contact Hours
0.75 CA-BRN Contact Hours
0.75 CDR Contact Hours
Dates:
Opens: 2024-11-25
Closes: 2025-11-25
Target Audience:
This activity is intended for metabolic dieticians, nurse practitioners, nurses, and metabolic disease specialists working within Inborn Errors of Metabolism (IEM) clinics in the United States and Canada who care for patients with long chain fatty acid oxidation disorders (LC-FAODs).
This activity is supported by an educational grant from Ultragenyx Pharmaceutical Inc.
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Sandra Carol van Calcar, PhD, RD, LD
Associate Professor of Molecular and Medical Genetics
School of Medicine
Oregon Health and Science University
Portland, Oregon -
Jerry Vockley, MD, PhD
University of Pittsburgh
Cleveland Family Endowed Chair in Pediatric Research
Professor of Human Genetics
UPMC Children's Hospital of Pittsburgh
Chief of Genetic and Genomic Medicine
Director of the Center for Rare Disease Therapy
Pittsburgh, Pennsylvania
