| Literature DB >> 36101815 |
Sandra Sirrs1, Elisa Fabbro2, Annalisa Sechi3.
Abstract
The rapid expansion of the number of adult patients with inherited metabolic diseases (IMDs) has created demand for physicians with expertise in the field of adult metabolic medicine (AMM). Unfortunately, existing accredited training programs in this field are rare, and training programs in pediatric metabolic medicine cannot fully meet the needs of AMM physicians as the types of patients and the problems they face are different in the adult setting. We surveyed a group of working practitioners in AMM for input on what medical expert competencies they feel should be included as part of training programs in AMM. Through a modified Delphi process, 66 physicians from six continents reached consensus on a comprehensive list of training competencies in AMM. This list includes competencies from the fields of adult internal medicine, neurology, medical genetics, and pediatric metabolic medicine but also includes competencies not found in any of those programs, leading to the conclusion that the training needs for specialists in AMM cannot be met from any of these existing programs. We propose that AMM be considered a subspecialty separate from pediatric metabolic medicine and that accredited training programs in AMM be created using these medical expert competencies as part of a broader program design.Entities:
Keywords: adult metabolic medicine; objectives of training; postgraduate medical education; training competencies
Year: 2022 PMID: 36101815 PMCID: PMC9458608 DOI: 10.1002/jmd2.12312
Source DB: PubMed Journal: JIMD Rep ISSN: 2192-8304
FIGURE 1Stages in development of consensus statement for training competencies in adult metabolic medicine
Top ranked competencies in each area
| Area of competency | % of Respondents ranking as very important |
|---|---|
| Area 1: Basic Science in cellular biology and genetics | |
|
| |
| Fluid and electrolyte balance, acid–base regulation, intermediary metabolism and metabolic response to fed and fasting states | 70 |
| Enzymes/proteins: structure/function relationships, cellular distribution, mechanisms of mechanisms of action, control of enzyme activity, role of cofactors, principles of measurement, enzyme kinetics | 58 |
| Demonstrate effective, appropriate, and timely performance of diagnostic procedures relevant to adult metabolic medicine, including but not limited to skin biopsy and lumbar puncture | 57 |
| Area 2: Consultative expertise in Adult Metabolic Medicine | |
| Carry out a comprehensive physical examination including both general and detailed neurological examination | 89 |
|
| |
| Hyperammonemia | 89 |
| Lactic acidemia | 81 |
| Area 3: Clinical expertise in inherited metabolic diseases in adults | |
|
| |
| Hyperammonemia and urea cycle disorders | 89 |
| Lysosomal storage disorders | 87 |
| Disorders of carbohydrate metabolism: glycogen storage diseases, galactosemia, fructose intolerance | 85 |
| Disorders of fatty acid oxidation and carnitine metabolism | 85 |
| Area 4: Appropriate use of laboratory testing | |
|
| |
| Intermediary metabolites (glucose, ammonia, lactate, pyruvate, free fatty acids, homocysteine, ketones) | 85 |
| Amino acids | 83 |
| Organic acids | 83 |
| Carnitine/acylcarnitines | 83 |
| Area 5: Longitudinal care of adults with inherited metabolic disorders | |
| Demonstrate knowledge of the appropriate indications for emergency /crisis management of metabolic disorders | 96 |
| Identify appropriate investigations and timing for clinical, laboratory and imaging investigations for the long term follow up of adults with inherited metabolic diseases | 83 |
| Demonstrate an ability to work in multi‐disciplinary teams with biochemists, dieticians, etc. | 83 |
| Identify the risk of metabolic decompensation in patients who develop new medical problems either related or unrelated to their IMD (e.g., cancer, coronary artery disease, diabetes mellitus, etc.) | 83 |
| Area 6: Treatment | |
| Understand available drug therapies for inherited metabolic disorders including the indications to initiate and discontinue the medications, mechanism of action, and cost | 91 |
| Understand the principles of treatment related to inborn errors of metabolism | 89 |
| Demonstrate an ability to start treatment to manage acute metabolic decompensation while diagnostic investigations are in process | 89 |
| Understand acute and chronic side effects of the specific drug treatments and be able to manage them | 87 |
| Area 7. Management of contraception, pregnancy and lactation | |
| Demonstrate the ability to optimize metabolic control in preconception for planned pregnancies (i.e., PKU) | 89 |
| Demonstrate an ability to provide recommendations to pregnant adults with inherited metabolic diseases on diet, drug therapy, and appropriate investigations | 87 |
| Understand the impact of common inherited metabolic diseases on fertility, maternal and fetal risks in pregnancy, and impact on lactation | 81 |
| Area 8: Transition management | |
| Understand the key issues in engaging young adults during the transition from pediatric to adult services | 68 |
| Understand developmental and behavioral barriers to adherence to treatment regimens in transitional aged youth and appropriate strategies to promote adherence | 62 |
| Outline the concept of patient self‐care and the role of the expert patient | 47 |
| Area 9: Management of complications | |
| Encephalopathy | 74 |
| Acid–base disturbances | 72 |
| Fluid and electrolyte abnormalities | 68 |
| Area 10: Critical appraisal | |
| Apply skills in critical appraisal to the care of adult patients with inherited metabolic disorders | 79 |
| Understand the importance of critical appraisal in the evaluation of therapies for inherited metabolic disorders | 77 |
| Demonstrate the ability to manage uncertainty when faced with incomplete evidence to guide disease management | 70 |
Note: The top three competencies in each of the 10 defined areas are shown. If there were more than three competencies with equivalent rank, all are shown.
Ten competencies receiving the highest ranking—note that the competencies of “hyperammonemia” and “hyperammonemia and urea cycle defects” overlap and are counted as one within the top 10.
Several competencies in nutritional therapy for inherited metabolic diseases (IMDs) were ranked as mandatory or recommended by survey respondents but were ranked below the top 3 so are not shown in this table but can be seen in Appendix S1.
All competencies under Area 10 were ranked as important or very important by more than 90% of survey respondents including those that are not shown in Table 1 but can be seen in the full list of competencies provided in the Appendix S1.