Evidence map›Paper›PMID 38541919›Full record

ReviewJournal of clinical medicine2024

Cardiac Sarcoidosis-Diagnostic and Therapeutic Challenges.

Dennis Korthals, Michael Bietenbeck, Hilke Könemann, Florian Doldi, David Ventura, Michael Schäfers, Michael Mohr, Julian Wolfes, Felix Wegner, Ali Yilmaz and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Redefining Cardiac Sarcoidosis with Advanced Imaging and Therapeutic Strategies.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Dennis KorthalsDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.
Michael BietenbeckDepartment for Cardiology I, Division of Cardiovascular Imaging, University Hospital Münster, 48149 Münster, Germany.
Hilke KönemannDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.
Florian DoldiDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.ORCID 0000-0002-5237-6283
David VenturaDepartment of Nuclear Medicine, University Hospital Münster, 48149 Münster, Germany.ORCID 0000-0002-4346-2606
Michael SchäfersDepartment of Nuclear Medicine, University Hospital Münster, 48149 Münster, Germany.
Michael MohrDepartment of Hematology, Hemostaseology, Oncology and Pneumology, Division of Pneumology, University Hospital Münster, 48149 Münster, Germany.
Julian WolfesDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.
Felix WegnerDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.ORCID 0000-0001-9087-645X
Ali YilmazDepartment for Cardiology I, Division of Cardiovascular Imaging, University Hospital Münster, 48149 Münster, Germany.
Lars EckardtDepartment for Cardiology II, Electrophysiology, University Hospital Münster, 48149 Münster, Germany.
University Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is a multisystem disorder of unknown etiology. The leading hypothesis involves an antigen-triggered dysregulated T-cell-driven immunologic response leading to non-necrotic granulomas. In cardiac sarcoidosis (CS), the inflammatory response can lead to fibrosis, culminating in clinical manifestations such as atrioventricular block and ventricular arrhythmias. Cardiac manifestations frequently present as first and isolated signs or may appear in conjunction with extracardiac manifestations. The incidence of sudden cardiac death (SCD) is high. Diagnosis remains a challenge. For a definite diagnosis, endomyocardial biopsy (EMB) is suggested. In clinical practice, compatible findings in advanced imaging using cardiovascular magnetic resonance (CMR) and/or positron emission tomography (PET) in combination with extracardiac histological proof is considered sufficient. Management revolves around the control of myocardial inflammation by employing immunosuppression. However, data regarding efficacy are merely based on observational evidence. Prevention of SCD is of particular importance and several guidelines provide recommendations regarding device therapy. In patients with manifest CS, outcome data indicate a 5-year survival of around 90% and a 10-year survival in the range of 80%. Data for patients with silent CS are conflicting; some studies suggest an overall benign course of disease while others reported contrasting observations. Future research challenges involve better understanding of the immunologic pathogenesis of the disease for a targeted therapy, improving imaging to aid early diagnosis, assessing the need for screening of asymptomatic patients and randomized trials.

Indexed as

cardiac sarcoidosiscardiovascular magnetic resonanceimplantable cardioverter–defibrillatorinflammatory cardiomyopathypositron emission tomographysudden cardiac deathventricular arrhythmia

Identifiers

PMID38541919
PMCPMC10970915
OpenAlexW4392845506

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.