MYOCOVID: Hospital Registry of Acute Myocarditis: Evolution of the Proportion of Positive SARS-COV-2 (COVID19) Cases

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Recruiting
CT.gov ID
NCT04375748
Collaborator
(none)
400
68
18
5.9
0.3

Study Details

Study Description

Brief Summary

To date, the effects of SARS-Cov-2 (Covid-19) on the myocardium and the role it plays in the evolution towards an acute myocarditis are badly understood. The current pandemic of this emerging virus is an opportunity to assess the proportion of acute myocarditis attributable to SARS-Cov-2(Covid-19) and to assess the clinical, biological and imaging presentations, by means of a national prospective multicentre hospital registry of cases of acute myocarditis.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Performing routine care (clinical and paraclinical tests)
  • Diagnostic Test: Examinations for the research:

Detailed Description

Although research on the subject has only recently started developing, the links have already been described between SARS-Cov-2 infection, the severity of the clinical status, and the presence of risk factors or a history of cardiovascular disease (hypertension, diabetes, stroke, etc.). Additionally, depending on the series and definition used for cardiac injury (troponin elevation and/or natriuretic peptides), this concerns 7-29% of patients with a clear predominance in severe patients. The mechanisms behind these troponin elevations and cardiac injury are likely to be multiple and variable depending on clinical presentation,severity and patient history. A significant association was found between troponin elevation, and that of CRP and NtproBNP, suggesting an inflammatory part to this cardiac damage. As with other coronaviruses, SARS-Cov-2 infection can cause massive release of proinflammatory cytokines which can lead to inflammation of the vascular wall. This can be the cause of true instability or even rupture of plaque(type1 infarction) but can also be responsible for tissue hypoxia without rupture of plaque causing myocardial pain (infarction type 2). In addition, there may be areal myocardial inflammation causing acute myocarditis, secondary to the cytokine storm or direct damage to the myocardium by the virus itself. In case of acute coronary syndrome presentation, a coronary exploration should be realized to highlight or eliminate a type 1 infarction, but it is clearly difficult to distinguish between a type 2 suffering (no viral attack direct but suffering from hypotension or hypoxia for example) and inflammatory myocardial damage with or without direct viral myocardial damage (myocarditis). In the context of the viral pandemic at Covid19, although few data exist,it is legitimate to consider the possibility of true arrays of acute inflammatory myocarditis or by direct viral attack which could thus modify the natural history and the prognosis of patients, thus justifying a dedicated diagnosis and treatment. The primary objective was to assess the proportion of positive SARS-Cov-2 cases among the patients included (hospitalized for acute myocarditis). During the study period, this proportion will be assessed at regular intervals, for example every month, or more frequently if the number of patients included varies substantially from one week to another. This will make it possible to trace a development curve for the entire period of the pandemic.

The secondary objectives were (1) to describe the clinical, biological and imaging characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort; (2) to assess the short-term (30 days) and long-term (1 year) prognosis of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort and (3) to identify the factors associated with a 30-day and 1-year prognosis of cases of acute myocarditis.

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Hospital Registry of Acute Myocarditis: Evolution of the Proportion of Positive SARS-COV-2 Cases During the Covid-19 Pandemic, Case Characteristics and Prognoses
Actual Study Start Date :
Apr 15, 2020
Anticipated Primary Completion Date :
Oct 15, 2021
Anticipated Study Completion Date :
Oct 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Patients treated for symptoms of acute myocarditis.

Patients treated in intensive coronary care unit (ICCU) or intensive care unit (ICU), in one of the participating hospitals, for symptoms of acute myocarditis confirmed by a myocardial MRI and/or a CT scan and/or a myocardial biopsy.

Diagnostic Test: Performing routine care (clinical and paraclinical tests)
ECG, standard biology and cardiology tests, and routine transthoracic echocardiography (TTE), MRI

Diagnostic Test: Examinations for the research:
Systematic research by polymerase chain reaction (PCR) for Covid-19 in the blood and in an oro-pharyngeal swab, in addition to the usual immunologic, bacteriological, viral and parasitic tests carried out as part of the routine care of all patients with suspected myocarditis. A 30-days phone call follow-up (vital status) and a systematic 1-year follow-up will be realized (clinic, biology, ECG, TTE, +/- MRI)

Outcome Measures

Primary Outcome Measures

  1. Evolution of the proportion of positive SARS-COV-2 cases. [6 months.]

    Estimate at hospital discharge, over a period of 6 months, the evolution of the proportion of positive SARS-COV-2 cases among patients hospitalized for acute myocarditis in Intensive Cardiac Care Unit or Intensive Care Unit (polyvalent, surgical or medical), in the 19 hospitals participating in the study.

Secondary Outcome Measures

  1. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort; Echocardiographic parameters: Volumes (mm3)

  2. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort ; Echocardiographic parameters: diameters (mm)

  3. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort (Echocardiographic parameters: ventricular diastolic function (mm);

  4. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort (Echocardiographic parameters: ventricular systolic function (mm);

  5. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort ; Echocardiographic parameters: Left atrium volume (mm3);

  6. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort ; Echocardiographic parameters: Maximum velocity of tricuspid valve insufficiency;

  7. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort ; Echocardiographic parameters: Presence and quantification of a valvular regurgitation

  8. Ultrasound characteristics. [1 year]

    Describe at the admission and during the treatment ultrasound characteristics of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort ; Echocardiographic parameters: Presence of a pericardial effusion

  9. Assess prognosis of the acute myocarditis . [The short-term (30 days) and long-term (1 year).]

    Assess the short-term (30 days) and long-term (1 year) prognosis of the acute myocarditis among the positive and negative SARS-Cov-2 patients of the myocarditis cohort. The 30-day prognosis will be defined in function to the outcome: A death, whatever the cause, A cardiovascular arrest with recovery, A cardiogenic shock, An acute lung oedema or One of the events cited above. The 1-year prognosis will be defined in function to the outcome: A death, whatever the cause, The need to resort to transplantation and/or chronic assistance, A rehospitalization for cardiovascular reasons (heart failure, painful relapse, recovered cardiac arrest, myocarditis relapse, ACS), A myocarditis relapse, or one of the events cited above. The 1-year prognosis will also be defined in function to the New York Heart Association (NYHA) class.

  10. The factors associated with acute myocarditis cases . [The short-term (30 days) and long-term (1 year).]

    Identify the factors associated with a 30-day and 1-year prognosis of cases of acute myocarditis cardiovascular (Terminal heart failure, Acute edema of the lung, Cardiogenic shock, Sudden death / Ventricular rhythm disorder Pulmonary embolism, Aortic dissection Infectious endocarditis Stroke) or no cardiovascular (Acute respiratory syndrome, septic shock of non-cardiac origin, cancer, Public road accident, end-stage respiratory failure, insufficiency, end-stage renal Failure)

  11. Biological characteristics [1 year]

    Describe the biological parameters on admission and during the treatment (troponinemia (ng/ml)

  12. Biological characteristics [1 year]

    Describe the biological parameters on admission and during the treatment NtproBNP(pg/ml)

  13. Biological characteristics [1 year]

    Describe the biological parameters on admission and during the treatment CRP(mg/ml)

  14. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Ventricular volumes (ml)

  15. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Systole Diameter

  16. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Diastole Diameter

  17. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Longitudinal deformation of left ventricle;

  18. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Longitudinal deformation of right ventricle;

  19. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Total volume of left ventricular oedema

  20. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Quantification of T2 before contrast agent

  21. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Quantification of T1 before contrast agent

  22. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Perfusion anomalies

  23. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Total volume of early left ventricular alteration

  24. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Total volume of late left ventricular alteration

  25. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Quantification of T1 after contrast agent

  26. Describe at the admission and during the treatment cardiac MRI parameters [1 year]

    Presence of a pericardial effusion

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients treated in ICCU or ICU (polyvalent, surgical or medical), in one of the participating hospitals, for symptoms of acute myocarditis confirmed by a myocardial MRI and/or a CT scan and/or a myocardial biopsy. It seems important to include elderly patients who may be under guardianship or curatorship since these patients seem to present the most severe forms. Additionally, the populations most affected by viral myocarditis are generally adolescents and young adults,which justifies including them in the study too. Pregnant women are a population at potentially greater risk, particularly during the third trimester because of the neuro-hormonal changes inherent in pregnancy. This justifies trying to implement the investigator's knowledge through this observational study.
Exclusion Criteria:
  • Refusal to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cardiology Aix-en-Provence France
2 Reanimation Amiens France
3 Cardiology Angers France
4 Reanimation Angers France
5 Cardiology Avignon France
6 Cardiology Bordeaux France
7 Pediatric cardiology Bordeaux France
8 Reanimation Bordeaux France
9 Cardiology Brest France
10 Cardiology Caen France
11 Pediatric Cardiology Caen France
12 Cardiology Clermont-Ferrand France
13 Pediatric cardilogy Clermont-Ferrand France
14 Reanimation Clermont-Ferrand France
15 Pediatric cardiology Dijon France
16 Cardiology Grenoble France
17 Pediatric cardiology Grenoble France
18 Reanimation Grenoble France
19 Cardiology Lille France
20 Pediatric cardiology Lille France
21 Pediatric cardiology Limoges France
22 Cardiology Lyon France
23 Pediatric cardiology Lyon France
24 Cardiology Marseille France
25 Pediatric cardiology Marseille France
26 Cardiology Metz France
27 Cardiology Montpellier France
28 Millénaire Clinical - Cardiology Montpellier France
29 Pediatric cardiology Montpellier France
30 Reanimation Montpellier France
31 Cardiology Nancy France
32 Cardiology Nancy France
33 Pediatric cardiology Nancy France
34 Cardiology Nantes France
35 Pediatric cardiology Nantes France
36 Cardiology Nice France
37 Pediatric cardiology Nice France
38 Cardiology Nîmes France
39 Cardiology, Henri Mondor Hospital Paris France
40 Cardiology Paris France
41 Cardiology Paris France
42 Henri Mondor Hospital Reanimation Paris France
43 Marie Lannelongue Hospital - Pediatric Cardiology Paris France
44 Marie Lannelongue Hospital Cardiology Paris France
45 Reanimation Paris France
46 Reanimation Paris France
47 Robert Debré Hospital - Pediatric cardiology Paris France
48 Saint Antoine Hospital - Cardiology Paris France
49 Cardiology Poitiers France
50 Reanimation Poitiers France
51 Pediatric cardiology Reims France
52 Cardiology Rennes France
53 Pediatric reanimation Rennes France
54 Cardiology Rouen France
55 Pediatric cardiology Rouen France
56 Pédiatric cardiology Strasbourg France
57 Reanimation Strasbourg France
58 CHU de TOULOUSE Toulouse France 31000
59 Croix du Sud Clinical Toulouse France
60 Pasteur Clinical - Cardiology Toulouse France
61 Pasteur Clinical - Pediatric cardiology Toulouse France
62 Pediatric Cardiology Toulouse France
63 Cardiolgy Tours France
64 Pediatric Cardiology Tours France
65 Cardiology Valenciennes France
66 Cardiology Martinique Martinique
67 Cardiology Mamoudzou Mayotte
68 Pédiatric cardiology Réunion Réunion

Sponsors and Collaborators

  • University Hospital, Toulouse

Investigators

  • Principal Investigator: Clément Delmas, CHU Toulouse, Hôpital Rangueil

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT04375748
Other Study ID Numbers:
  • RC31/20/0139
First Posted:
May 5, 2020
Last Update Posted:
Nov 23, 2020
Last Verified:
Nov 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 23, 2020