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Phenotype Submission - Raynaud’s disease or Raynaud's phenomenon

Cohort Definition Name: “Raynaud’s disease or Raynaud’s phenomenon”
Contributor name: Joel N. Swerdel
Contributor OrcId: 0000-0001-9491-2737
Logic Description: First occurrence of Raynaud’s disease or Raynaud’s phenomenon.
Recommended study application: outcome, indication
Assertion statement: This cohort definition was executed on at least one real person-level observational health data source and resulted in a cohort with at least 1 person.
Submitted cohort definition:
raynaud.txt (3.6 KB)

Target Clinical Description

Raynaud’s disease, also known as Raynaud’s phenomenon or Raynaud’s syndrome, is a vascular disorder characterized by episodic and reversible narrowing of the small blood vessels, primarily in the fingers and toes. This vascular constriction, often triggered by cold temperatures or emotional stress, leads to reduced blood flow, causing the affected areas to turn white, blue, and then red. Raynaud’s disease can occur as a primary condition (Raynaud’s disease) or secondary to an underlying condition, such as autoimmune diseases or vascular disorders.

Presentation for Raynaud’s Disease:

  1. Color changes in the fingers and toes in response to cold or stress: white (pallor), blue (cyanosis), and red (hyperemia)
  2. Numbness or tingling sensation in the affected digits
  3. Pain and throbbing as blood flow returns to the area
  4. Episodes typically last minutes to hours
  5. May involve one or more fingers or toes
  6. Potential complications, such as skin ulcers or gangrene (rare in primary Raynaud’s)

Assessment for Raynaud’s Disease:

  1. Clinical evaluation, including a detailed medical history and physical examination
  2. Cold provocation test to reproduce symptoms
  3. Nailfold capillaroscopy to examine nailbed blood vessels
  4. Blood tests to rule out underlying conditions (e.g., autoimmune diseases)
  5. Imaging studies (e.g., Doppler ultrasound) to assess blood flow in affected areas
  6. Assessment of severity and frequency of episodes

Differential Diagnoses for Raynaud’s Disease:

  1. Secondary Raynaud’s phenomenon due to underlying conditions (e.g., systemic sclerosis, lupus)
  2. Frostbite or cold injury
  3. Vascular disorders (e.g., atherosclerosis)
  4. Buerger’s disease (thromboangiitis obliterans)
  5. Thoracic outlet syndrome

Treatment Plan for Raynaud’s Disease:

  1. Lifestyle modifications to avoid triggers (e.g., keeping warm, using gloves)
  2. Stress reduction techniques
  3. Medications to relax blood vessels (e.g., calcium channel blockers, vasodilators)
  4. Avoidance of vasoconstrictive substances (e.g., caffeine, nicotine)
  5. Treatment of underlying conditions if secondary Raynaud’s is present
  6. Digital sympathectomy (surgical procedure) in severe cases

Prognosis for Raynaud’s Disease: The prognosis for individuals with Raynaud’s disease is generally good. Most people can manage their symptoms effectively through lifestyle modifications and, when necessary, medications. While Raynaud’s can be uncomfortable and potentially cause complications like skin ulcers in severe cases, it is not typically life-threatening. However, individuals with secondary Raynaud’s may need ongoing management of the underlying condition. Education and self-care measures are essential for minimizing the impact of Raynaud’s disease on daily life.

Imported to the OHDSI Phenotype Library. It may be expected to be found with id = 780 in the next release. Thank you

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