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ClearRounds Health · Cardiology · Quick Reference
Cardiac Sarcoidosis
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Heart Failure & CardiomyopathyAdvancedIn progressOne-page PDF
Suspicion triggers, conduction disease/VT/HF clues, MRI/PET role, immunosuppression referral, ICD considerations.
Last reviewed
Pending initial clinical review
Sources / guidelines to verify
- HRS Expert Consensus on Cardiac Sarcoidosis
- AHA/ACC arrhythmia & device guidelines (ICD indications)
Disclaimer: Educational reference only. Not a substitute for clinician judgment, local protocols, or current guideline review.
One-page reference
Draft content pending the site owner’s clinical review. Verify against the sources above and local protocol before clinical use.
1
What it is / why it matters
- Granulomatous infiltration of myocardium → conduction disease, VT, and heart failure.
- Often accompanies systemic sarcoidosis but can be isolated.
2
Key diagnostic clues
- Unexplained AV block in a patient <60.
- Ventricular tachycardia or new cardiomyopathy.
- Known pulmonary sarcoid with cardiac symptoms; patchy LV dysfunction.
3
Initial workup
- ECG/telemetry, echo, cardiac MRI (late gadolinium enhancement) and/or FDG-PET (active inflammation).
- Evaluate extracardiac sarcoid (chest imaging; biopsy an accessible node when possible).
4
Management framework
- Immunosuppression (corticosteroids ± steroid-sparing agents) for active inflammation, via specialist.
- HF GDMT; low threshold for ICD (VT, high-grade block, or low EF).
- EP referral for ventricular arrhythmia.
5
Red flags / escalate now
- High-grade AV block, VT/VF, or syncope → urgent monitoring + EP/ICD evaluation.
6
Follow-up / monitoring
- PET to track inflammation/treatment response; device checks; multidisciplinary care.
7
Clinic pearls
- Unexplained AV block in a young patient → think sarcoid (and Lyme).
- The ICD threshold is low; MRI and PET are complementary.
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