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Home - About VASCERN - Structure and Governance - Working Groups - Rare Disease Working Groups - Pediatric and Primary Lymphedema (PPL-WG) - Clinical Decision Support Tools - Patient Pathways
Pediatric and Primary Lymphedema (PPL-WG)
Introduction Diseases covered
Experts & Centers
Experts Centers
Clinical Decision Support Tools
Patient Pathways Do’s and Don’ts Clinical Practice Guidelines (CPGs) adopted Clinical Expert Consensus Statements Written Clinical Outcome Measures
Registry
Research
Clinical Trials and Observational Studies Research Publications
Training and Education
E-Learning Pills of Knowledge (PoK) Webinars

Patient Pathways

Patient Pathways aim to improve the care and management of patients with a rare disease. They include the “red flags” that may lead to the suspicion of the disease, how to reach a definite diagnosis and the management and follow-up recommendations. They are a very important tool used in defining the best patient care and will be further validated and updated when needed.

Result (1)
Pediatric and Primary Lymphedema (PPL) General Patient Pathway V4
October 06 2023

The new version 4 of the General Patient Pathway for Pediatric and Primary Lymphedema.

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