Evidence map›Paper›PMID 27112783›Full record

Trial reportClinical research in cardiology : official journal of the German Cardiac Society2016

Betaferon in chronic viral cardiomyopathy (BICC) trial: Effects of interferon-β treatment in patients with chronic viral cardiomyopathy.

Heinz-Peter Schultheiss, Cornelia Piper, Olaf Sowade, Finn Waagstein, Joachim-Friedrich Kapp, Karl Wegscheider, Georg Groetzbach, Matthias Pauschinger, Felicitas Escher, Eloisa Arbustini and 2 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical research in cardiology : official journal of the German Cardiac Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06591260 (Role of Endomyocardial Biopsy and Aetiology-based Treatment in Pediatric Patients with Inflammatory Heart Disease in Arrhythmic and Non-arrhythmic Clinical Presentations), which is not on this map. Cited by 66 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 4 pooled it
9.0field-weighted citation impact, top 2% 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.

NCT06591260 recruitingnot on this map

Role of Endomyocardial Biopsy and Aetiology-based Treatment in Pediatric Patients with Inflammatory Heart Disease in Arrhythmic and Non-arrhythmic Clinical Presentations: an Integrated Approach for the Optimal Diagnostic and Therapeutic Management

Typeobservational_patient_registrySponsorScientific Institute San RaffaeleRan2013 to 2030Enrolled20ConditionsMyocarditis, Ventricular Arrhythmia, Inflammatory Cardiomyopathy, Genetic PredispositionArmssupport treatment, cardiac medical treatment, aetiology-specific treatment, device implant, arrhythmia ablation
3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 4 syntheses or guidelines pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Brazilian Society of Cardiology Guideline on Myocarditis - 2022.Arquivos brasileiros de cardiologia · 2022
    Guideline
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Review
  7. Post-viral myocarditis.Heart failure reviews · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Viral Myocarditis.The Yale journal of biology and medicine · 2024
    Review
  20. Article

6 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

12 authors at 7 institutions in 3 countries.

Heinz-Peter SchultheissDepartment of Cardiology, Campus Benjamin Franklin, Charite-Universitätsmedizin Berlin, Berlin, Germany. heinz-peter.schultheiss@charite.de.
Cornelia PiperKardiologische Klinik, Herz- und Diabetes Zentrum NRW, Bad Oeynhausen, Germany.
Olaf SowadeBayer Health Care AG, Berlin, Germany.
Finn WaagsteinDepartment of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Joachim-Friedrich KappBayer Health Care AG, Berlin, Germany.
Karl WegscheiderInstitut für Biometrie und Epidemiologie, Universitätsklinikum Hamburg Eppendorf, Hamburg, Germany.
Georg GroetzbachBayer Health Care AG, Berlin, Germany.
Matthias PauschingerDepartment of Cardiology, Campus Benjamin Franklin, Charite-Universitätsmedizin Berlin, Berlin, Germany.
Felicitas EscherDepartment of Cardiology, Campus Benjamin Franklin, Charite-Universitätsmedizin Berlin, Berlin, Germany.
Eloisa ArbustiniCentre for Inherited Cardiovascular Diseases and Transplant Research Area, IRCCS Foundation Policlinico San Matteo, Univ di Pavia, Pavia, Italy.
Harald SiedentopBayer Health Care AG, Berlin, Germany.
Uwe KuehlDepartment of Cardiology, Campus Benjamin Franklin, Charite-Universitätsmedizin Berlin, Berlin, Germany.
Bayer (Germany) · DECharité - Universitätsmedizin Berlin · DECS Diagnostics · DEHeart and Diabetes Center North Rhine-Westphalia · DEIstituti di Ricovero e Cura a Carattere Scientifico · ITSahlgrenska University Hospital · SEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic viral infections of the heart are considered one antecedent event leading to progressive dysfunction of the myocardium, often with an impaired prognosis due to a virus- or immune-mediated myocardial injury. Symptomatic treatment does not influence the viral cause of heart failure, and the effect of antiviral treatment has not been determined, yet. METHODS AND

resultsIn this phase II study 143 patients with symptoms of heart failure and biopsy-based confirmation of the enterovirus (EV), adenovirus, and/or parvovirus B19 genomes in their myocardial tissue were randomly assigned to double-blind treatment, and received either placebo (n = 48) or 4 × 10(6) (n = 49) and 8 × 10(6) IU (n = 46) interferon beta-1b (IFN-β-1b) for 24 weeks, in addition to standard heart failure treatment. Patients with active myocarditis or other specific causes of heart failure were excluded. Compared to placebo, virus elimination and/or virus load reduction was higher in the IFN-β-1b groups (odds ratio 2.33, p = 0.048), similarly in both interferon groups and both strata. IFN-β-1b treatment was associated with favourable effects on NYHA functional class (p = 0.013 at follow-up week 12), improvement in quality of life (Minnesota Heart Failure score; p = 0.032 at follow-up week 24) and patient global assessment (follow-up week 12 to follow-up week 24; p = 0.039). The frequency of adverse cardiac events was not higher in the IFN-β-1b groups compared to the placebo group.

conclusionsImmunomodulatory IFN-β-1b treatment is a well-tolerated and safe treatment option, leading to effective virus clearance or reduction of the virus load in patients with chronic viral cardiomyopathy. Favourable clinical effects assess quality of life, NYHA functional class, and patient global assessment. ClinicalTrials.gov identifier: NCT001185250.

Indexed as

Adenoviridae InfectionsAdultAgedAntiviral AgentsBiopsyCardiomyopathiesChronic DiseaseDouble-Blind MethodEnterovirus InfectionsErythema InfectiosumEuropeFemaleHumansInterferon beta-1bMaleMiddle AgedAntiviral AgentsInterferon beta-1bAntiviral therapy, myocardial biopsiesChronic viral cardiomyopathyInterferon beta

Identifiers

PMID27112783
OpenAlexW2344476582

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.