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.
These documents are the deliverables for our Work Package on “Patient Pathways”. Disease (or group of disease)-specific Patient Pathways are being developped by each of VASCERN’s Rare Disease Working Groups (RDWGs).
- The HHT Patient Pathway (issued 11/07/2017) is available here
This pathway has also kindly been translated in French by FAVA-Multi:
Le parcours patient de la maladie de Rendu-Osler ici
Coming soon!!!
The VASCA-WG Patient Pathway on Severe/Rare Infantile Hemangioma (issued 20/03/2019) is available here
German translation here
Italian translation here
Spanish translation here
Swedish translation here
The Capillary Malformation Patient Pathway (issued 29/04/2020) can be found here
The Venous Malformation Patient Pathway (issued 29/04/2020) can be found here
The Lymphatic Malformation Patient Pathway (issued 29/04/2020) can be found here