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Jul 1
9m 10s

Episode 211: Granulomatosis with Polyang...

CORE EM
About this episode

Granulomatosis with Polyangiitis (GPA) – Recognition and Management in the ED

Hosts:
Phoebe Draper, MD
Brian Gilberti, MD

Download One Comment Tags: Rheumatology

Show Notes

Background

  • A vasculitis affecting small blood vessels causing inflammation and necrosis
  • Affects upper respiratory tract (sinusitis, otitis media, saddle nose deformity), lungs (nodules, alveolar hemorrhage), and kidneys (rapidly progressive glomerulonephritis)
  • Can lead to multi-organ failure, pulmonary hemorrhage, renal failure

Red Flag Symptoms:

  • Chronic sinus symptoms
  • Hemoptysis (especially bright red blood)
  • New pulmonary complaints
  • Renal dysfunction
  • Constitutional symptoms (fatigue, weight loss, fever)

Workup in the ED:

  • CBC, CMP for anemia and AKI
  • Urinalysis with microscopy (hematuria, RBC casts)
  • Chest imaging (CXR or CT for nodules, cavitary lesions)
  • ANCA testing (not immediately available but important diagnostically)

Management:

  • Stable patients: Outpatient workup, urgent rheumatology consult, prednisone 1 mg/kg/day
  • Unstable patients: High-dose IV steroids (methylprednisolone 1 g daily x3 days), consider plasma exchange, cyclophosphamide or rituximab initiation, ICU admission

Conditions that Mimic GPA:

  • Goodpasture syndrome (anti-GBM antibodies)
  • TB, fungal infections
  • Lung malignancy
  • Other vasculitides (EGPA, MPA, lupus)
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