Consensus Guidelines for the Clinical Management of ASMD
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Study Objective
Guideline development process: AGREE II system and classification
- To develop clinical guidelines
- Standard of care for ASMD patients
- Using an SLR and the experiences of multidisciplinary experts (GDG)
Experts’ Recommendations for Classification and Diagnosis of ASMD
Acute neurovisceral, ASMD type A
Hepatosplenomegaly, proatherogenic lipid profile, thrombocytopenia, interstitial lung disease, skeletal involvement, liver disease, cherry red macula, hypotonia, and rapidly progressive neurodegeneration
Chronic neurovisceral, ASMD type A/B
All symptoms of ASMD type A along with delayed growth and puberty, slowly progressive neurodegeneration and cherry red macula (in few patients), and hypotonia
Chronic visceral, ASMD type B
All symptoms of type A/B with the absence of hypotonia and neurodegeneration and few patients with cherry red macula
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Experts’ Recommendations for the Management of ASMD
Multidisciplinary assessment is recommended for all ASMD patients or as needed by:
- Primary care physician
- Metabolic diseases specialist
- Neurologist
Management of ASMD
ERT
- All patients with a confirmed diagnosis of ASMD and significant non-CNS
- Effectiveness of treatment should be monitored
Use of HSCT is experimental
Symptomatic treatment
- CLD should be monitored and treated for gastrointestinal bleeding
- Pulmonary disease may require long-term oxygen therapy
Recommended assessments for all ASMD patients
Assesment | Frequency |
Baseline history | At diagnosis
|
Pulmonary assessment |
|
Musculoskeletal assessment | At diagnosis, then at each visit |
Ophthalmologic evaluation | At diagnosis |
Abbreviations
AGREE: Appraisal of guidelines for research and evaluation; ASM: Acid sphingomyelinase; ASMD: Acid sphingomyelinase deficiency; CLD: Chronic liver disease; CNS: Central nervous system; CT: Computed tomography; DBS: Dried blood spot; ERT: Enzyme replacement therapy; GDG: Guidelines Development Group; HSCT: Hematopoietic stem cell transplantation; NP: Natriuretic peptides; SLR: Systematic literature review; SMPD1: Sphingomyelin phosphodiesterase 1 gene; VUS: Variant of uncertain significance.