# Diagnosis and Management of Patients with Cardiac Sarcoidosis by a Regional Specialist Service

**Authors:** Rebecca Godfrey, Otto Fenske, Raj Selvaraju, Ana Frappell, Emine Cicek, Imad Mohamed Imran, Achuth Hosur, Eleonora Manca, Nitasha Singh, Susan Ellery, Victoria Parish, David Hildick-Smith, Jack McCready, Sabina Dizdarevic, Rachel Buxton-Thomas, John Silberbauer, Alexander Liu

PMC · DOI: 10.3390/diseases14020076 · Diseases · 2026-02-17

## TL;DR

A new regional cardiac sarcoidosis service in the UK improved diagnosis and management of patients with better outcomes compared to previous approaches.

## Contribution

A novel regional multi-disciplinary team-based service for cardiac sarcoidosis with improved diagnostic accuracy and clinical outcomes.

## Key findings

- 13 out of 51 referrals met Heart Rhythm Society criteria and were correctly diagnosed with cardiac sarcoidosis.
- 8 out of 38 HRS-negative referrals still received a clinical diagnosis of cardiac sarcoidosis.
- No deaths or heart failure hospitalizations occurred within the first 11 months of service operation.

## Abstract

Background: Cardiac sarcoidosis (CS) is associated with potentially serious complications, including heart failure and life-threatening arrhythmias. The diagnosis and management of CS is multifaceted, requiring a multi-disciplinary team (MDT)-based approach. A new regional CS clinical service was established in Sussex County (UK) in January 2025. This service is based on a core of cardiologists working with a wider MDT, including specialists in pulmonary sarcoidosis, nuclear medicine and cardiac electrophysiology. This study assessed the clinical performance of this new service. Methods: Patients with suspected CS referred to the Sussex CS Service between January and December 2025 were included, as compared to a control cohort of patients referred for CS assessment before the service was conceived. Results: Of the 51 CS service referrals, 13 patients fulfilled the Heart Rhythm Society (HRS) criteria, all of whom were correctly diagnosed with CS, whilst only two out of seven HRS-positive control patients were correctly diagnosed. In the 38 HRS-negative CS service referrals, 8 patients (21%) were still given a clinical CS diagnosis compared to none in the HRS-negative controls. Of the 21 patients diagnosed with CS, 7 (33%) had active myocardial inflammation and 8 (38%) had LV systolic dysfunction. Where indicated, immunosuppressive and heart failure therapies were initiated in all patients. Eight CS patients (38%) underwent implantable cardioverter defibrillator implantation. No deaths or heart failure hospitalisations occurred within the first 11 months. Conclusions: An MDT-based CS service model can provide multi-faceted care to patients, without major short-term adverse outcomes. The service model replicability and long-term outcomes require further assessment.

## Linked entities

- **Diseases:** cardiac sarcoidosis (MONDO:0001707), heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** ventricular tachycardia (MESH:D017180), arrhythmic (OMIM:212500), ventricular tachyarrhythmias (MESH:D014693), EMB (MESH:D004719), pulmonary sarcoidosis (MESH:D017565), heart failure (MESH:D006333), VAs (MESH:D001145), aortic stenosis (MESH:D001024), LV Dysfunction (MESH:D018487), lymphoma (MESH:D008223), HRS (MESH:C000719191), sudden cardiac death (MESH:D016757), cardiac (MESH:D006331), granuloma (MESH:D006099), mediastinal lymphadenopathy (MESH:D008477), COPD (MESH:D029424), cardiomyopathies (MESH:D009202), diabetes mellitus (MESH:D003920), Cardiac sarcoidosis (MESH:D012507), LGE (MESH:C564835), CKD (MESH:D012080), congenital heart disease (MESH:D006330), asthma (MESH:D001249), chronic kidney disease (MESH:D051436), atrioventricular block (MESH:D054537), myocardial fibrosis (MESH:D005355), VA (MESH:C563443), injury to (MESH:D014947), MDT (MESH:D015161), Myocardial Inflammation (MESH:D007249), hypertension (MESH:D006973), deaths (MESH:D003643)
- **Chemicals:** glucose (MESH:D005947), MTP (MESH:D008775), methotrexate (MESH:D008727), gadolinium (MESH:D005682), carbohydrate (MESH:D002241), FDG (MESH:D019788), prednisolone (MESH:D011239), ACEi (-), MRA (MESH:C502936)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939275/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939275/full.md

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Source: https://tomesphere.com/paper/PMC12939275