Synopsis
Confirm inflammatory relapse, find secondary causes and use slow, steroid-sparing escalation to prevent repeated flares and constriction.
- Recurrent pericarditis is a new episode after a documented first attack and a symptom-free interval, conventionally at least 4-6 weeks.
- Incessant disease continues beyond 4-6 weeks without remission; chronic disease lasts beyond 3 months.
- Do not label every recurrent chest pain inflammatory: document CRP rise, ECG/effusion change or CT/CMR inflammation when criteria are incomplete.
- Recheck TB, bacterial, malignant, autoimmune, post-injury and drug causes when the course is atypical, systemic or treatment-resistant.
- Aspirin/NSAID plus weight-adjusted colchicine for at least 6 months is usual first-line recurrent-disease therapy.
- Avoid an early high-dose steroid reflex; if steroids are necessary, use low-to-moderate dose after excluding infection and taper only after complete remission.
- Steroid-dependent, colchicine-resistant inflammatory disease may qualify for specialist IL-1 blockade; infection screening and a taper plan are mandatory.
- Persistent effusion without inflammatory evidence is not treated automatically with repeated anti-inflammatory courses; reassess haemodynamics and cause.
Key red flags
Rising JVP, tachycardia, pulsus paradoxus, hypotension or echo chamber collapse is an emergency irrespective of chronicity.
Ascites, oedema, Kussmaul sign, pericardial knock or ventricular interdependence needs specialist constriction assessment.