Hereditary Haemorrhagic Telangiectasia Working Group (HHT-WG)

Patient Pathways

Our Patient Pathways are designed to guide healthcare professionals through the complexities of the care and management of patients with a rare vascular disease, from initial suspicion and diagnosis to treatment, management, and beyond. These pathways aim to:

  • Streamline Diagnosis: Facilitate early and accurate diagnosis through specialized diagnostic criteria and access to expert consultations.
  • Optimize Treatment: Provide comprehensive treatment plans utilizing the latest, evidence-based practices tailored to individual patient needs.
  • Enhance Care Coordination: Ensure seamless coordination between the various healthcare providers, specialists, and support services involved in your care.

Have a look at the HHT pathway below.

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