Evidence map›Paper›PMID 19026310›Full record

Trial reportThe American journal of cardiology2008

Usefulness of immunosuppression for giant cell myocarditis.

Leslie T Cooper, Joshua M Hare, Henry D Tazelaar, William D Edwards, Randall C Starling, Mario C Deng, Santosh Menon, G Martin Mullen, Brian Jaski, Kent R Bailey and 3 more

Open access · greenAbstract readClinical TrialMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The American journal of cardiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 3 pooled it
5.6field-weighted citation impact, top 4% 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

102 citing papers in PubMed, 3 syntheses or guidelines pooled it, 312 citations in OpenAlex.

  1. Pooled it
  2. Brazilian Society of Cardiology Guideline on Myocarditis - 2022.Arquivos brasileiros de cardiologia · 2022
    Guideline
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42 more citing papers are in PubMed but not listed here.

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

13 authors at 10 institutions in 1 country.

Leslie T CooperDivision of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA. cooper.leslie@mayo.edu
Joshua M Hare
Henry D Tazelaar
William D Edwards
Randall C Starling
Mario C Deng
Santosh Menon
G Martin Mullen
Brian Jaski
Kent R Bailey
Madeleine W Cunningham
G William Dec
Giant Cell Myocarditis Treatment Trial Investigators
Mayo Clinic · USMayo Clinic in Arizona · USCardiovascular Research Associates · USCleveland Clinic · USColumbia University Irving Medical Center · USHarvard University Press · USOhio Heart & Vascular Center · USSharp Memorial Hospital · USUniversity of Miami · USUniversity of Oklahoma Health Sciences Center · US

Funding

Autoimmune Determinants of Human Cardiac MyosinR56HL056267 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI COOPER, LESLIE T, CUNNINGHAM, MADELEINE W. · 2008 to 2015
$933k
Inflammation and Immunity in Dilated CardiomyopathyR13HL074877 · NHLBI · MAYO CLINIC · PI COOPER, LESLIE T · 2004 to 2004
$13k
Giant Cell Myocarditis Treatment Trial Pilot StudyR01FD001986 · FDA · MAYO CLINIC · PI LESLIE, COOPER · 2005 to 2005
–
FDA HHS FD-RO-1-001986NHLBI NIH HHS R13 HL074877NHLBI NIH HHS R56 HL056267
6 · The paper itself

Abstract

Giant cell myocarditis (GCM) is a rare and highly lethal disorder. The only multicenter case series with treatment data lacked cardiac function assessments and had a retrospective design. We conducted a prospective, multicenter study of immunosuppression including cyclosporine and steroids for acute, microscopically-confirmed GCM. From June 1999 to June 2005 in a standard protocol, 11 subjects received high dose steroids and cyclosporine, and 9 subjects received muromonab-CD3. In these, 7 of 11 were women, the mean age was 60 +/- 15 years, and the mean time from symptom onset to presentation was 27 +/- 33 days. During 1 year of treatment, 1 subject died of respiratory complications on day 178, and 2 subjects received heart transplantations on days 2 and 27, respectively. Serial endomyocardial biopsies revealed that after 4 weeks of treatment the degree of necrosis, cellular inflammation, and giant cells decreased (p = 0.001). One patient who completed the trial subsequently died of a fatal GCM recurrence after withdrawal of immunosuppression. Her case demonstrates for the first time that there is a risk of recurrent, sometimes fatal, GCM after cessation of immunosuppression. In conclusion, this prospective study of immunosuppression for GCM confirms retrospective case reports that such therapy improves long-term survival. Additionally, withdrawal of immunosuppression can be associated with fatal GCM recurrence.

Indexed as

Immunosuppression TherapyAdultAgedAged, 80 and overAzathioprineCyclosporineFemaleGiant CellsHumansImmunosuppressive AgentsMaleMiddle AgedMuromonab-CD3MyocarditisProspective StudiesRegistriesAzathioprineCyclosporineImmunosuppressive AgentsMuromonab-CD3

Identifiers

PMID19026310
PMCPMC2613862
OpenAlexW2039855971

What OpenQuestion holds

Textmetadata
LicenceTDM
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.