Evidence map›Paper›PMID 37456487›Full record

ReviewCureus2023

Immunomodulatory Therapy for Giant Cell Myocarditis: A Narrative Review.

Muhammad Wahdan Naseeb, Victor O Adedara, Muhammad Talha Haseeb, Hareem Fatima, Swapna Gangasani, Kamaljit R Kailey, Moiz Ahmed, Kiran Abbas, Waleed Razzaq, Muhammad M Qayyom and 1 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Giant Cell Myocarditis: Is It Time to Redeploy Cytokine Inhibitors?Mediterranean journal of rheumatology · 2026
    Article
  3. Article
  4. Review
  5. Review
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 5 institutions in 2 countries.

Muhammad Wahdan NaseebInternal Medicine, Dow University of Health Sciences, Karachi, PAK.
Victor O AdedaraMedicine, St. George's University School of Medicine, St. George's, GRD.
Muhammad Talha HaseebInternal Medicine, Shaikh Zayed Hospital, Lahore, PAK.
Hareem FatimaInternal Medicine, Federal Medical College, Islamabad, PAK.
Swapna GangasaniInternal Medicine, New York Medical College (NYMC) St. Mary's General Hospital and Saint Clare's Hospitals, New Jersey, USA.
Kamaljit R KaileyMedicine and Surgery, Gian Sagar Medical College and Hospital, Patiala, IND.
Moiz AhmedCardiology, National Institute of Cardiovascular Diseases, Karachi, PAK.
Kiran AbbasCommunity Health Sciences, Aga Khan University, Karachi, PAK.
Waleed RazzaqInternal Medicine, Services Hospital, Lahore, PAK.
Muhammad M QayyomCardiology Department, ChristianaCare, Newark, USA.
Zain U AbdinMedicine, District Headquarter Hospital, Faisalabad, PAK.
Dow University of Health Sciences · PKNational Institute of Cardiovascular Diseases · PKServices Hospital · PKShaikh Zayed Hospital · PKSt. George's University · GD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giant cell myocarditis (GCM) is a rare, often rapidly progressive, and potentially fatal disease because of myocardium inflammation due to the infiltration of giant cells triggered by infectious as well as non-infectious etiologies. Several studies have reported that GCM can occur in patients of all ages but is more commonly found in adults. It is relatively more common among African American and Hispanic patients than in the White population. Early diagnosis and treatment are critical. Electrocardiogram (EKG), complete blood count, erythrocyte sedimentation rate, C-reactive protein, and cardiac biomarkers such as troponin and brain natriuretic peptide (BNP), echocardiogram, cardiac magnetic resonance imaging (MRI), myocardial biopsy, and myocardial gene profiling are useful diagnostic tools. Current research has identified several potential biomarkers for GCM, including myocarditis-associated immune cells, cytokines, and other chemicals. The standard of care for GCM includes aggressive immunosuppressive therapy with corticosteroids and immunomodulatory agents like rituximab, cyclosporine, and infliximab, which have shown promising results in GCM by balancing the immune system and preventing the attack on healthy tissues, resulting in the reduction of inflammation, promotion of healing, and decreasing the necessity for cardiac transplantation. Without immunosuppression, the chance of mortality or cardiac surgery was 100%. Multiple studies have revealed that a treatment combination of corticosteroids and immunomodulatory agents is superior to corticosteroids alone. Combination therapy significantly increased transplant-free survival (TFS) and decreased the likelihood of heart transplantation, hence improving overall survival. It is important to balance the benefits of immunosuppression with its potentially adverse effects. In conclusion, immunomodulatory therapy adds significant long-term survival benefits to GCM.

Indexed as

azathioprinecyclosporingiant cell myocarditisimmunomodulatoryimmunosuppressive therapyintravenous igivmyocarditis

Identifiers

PMID37456487
PMCPMC10349211
OpenAlexW4380680837

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.