NEUMOCAR: Myocardial Injury and Severe Pneumococcal Pneumonia

Sponsor
Alejandro Rodriguez Oviedo , MD (Other)
Overall Status
Terminated
CT.gov ID
NCT03058211
Collaborator
(none)
23
1
22
1

Study Details

Study Description

Brief Summary

Hypothesis: The "novo" cardiovascular events (CVE)in patients with severe community-acquired pneumonia (CAP) are frequent (17%) and could be associated with both direct pneumococcal myocardial invasion, toxin delivery (pneumolysin) or different biomarkers (histones, NETs(neutrophil extracellular traps), IL (Interleukin)-1b,h-Fabp (heart-Fatty acid bindding protein) ).The CVE frequency and its impact on outcome in patients without prior heart disease (CP) has not been studied.

Objectives:1) To determine the incidence of myocardian injury (MI) and CVE in patients with CAP without CP evaluated by non-invasive techniques (Echocardiograph and MRI) and biomarkers levels (Tn-I (Troponin I), h-Fabp, NT-proBNP (N-terminal pro-brain natriuretic peptide) histones, NETs, IL 1b); 2) To assess if DMA and CVE are related to the etiology and their impact on outcome , 3) To investigate the presence of myocardial scarring by MRI and its relationship with etiology and MI, and 4) To identify prognostic factors of DMA and CVE to determine level of risk.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Echocardiography
  • Diagnostic Test: Cardiac Magnetic resonance

Detailed Description

Area: Intensive care unit (ICU) of the participating hospitals. Patients: Forty patients with CAP without heart disease history will be included consecutively (20 patients with pneumococcal CAP and 20 patients with non-pneumococcal CAP).Ten healthy volunteers (controls) are included.

Variables: Epidemiological, clinical and hemodynamic variables are recorded. Presence of MI and CVE measured by echocardiography and by biomarkers will be evaluated during the ICU stay. Presence of scarring miocardic by MRI technique will be determined at month 6 since ICU admission.

Statistical analysis: Categorical (Fisher's exact test) and continuous variables( Wilconxon and Anova) will be used to determine differences between them. The Pearson correlation, ROC (discriminatory power) and logistic regression analysis(independent association) will be used to determine the association between variables and outcome. A p-value of 0.05 will be considered significant.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
23 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Myocardial Injury in Severe Pneumococcal Pneumonia as a Cause of Mortality From Acute Cardiovascular Events
Actual Study Start Date :
Mar 1, 2018
Actual Primary Completion Date :
May 31, 2019
Actual Study Completion Date :
Dec 31, 2019

Arms and Interventions

Arm Intervention/Treatment
pneumococcal pneumonia

Patients with community-acquired pneumonia due to S.pneumoniae. An Echocardiography will be performed to all patients (one per day during 7 days). A Cardiac magnetic resonance (MRI) will be performed during an acute episode and at month 6 since ICU admission. In addition a blood sample will be drawn daily (one per day during 7 days) to measure myocardial injury and inflammation systemic (interleukins) biomarkers.

Diagnostic Test: Echocardiography
Standard protocols
Other Names:
  • Heart resonance magnetic nuclear
  • Diagnostic Test: Cardiac Magnetic resonance
    MRI with late gadolinium increase and T1 mapping
    Other Names:
  • MRI
  • non-pneumococcal pneumonia

    Patients with community-acquired pneumonia due to S.pneumoniae. An Echocardiography will be performed to all patients (one per day during 7 days). A Cardiac magnetic resonance (MRI) will be performed during an acute episode and at month 6 since ICU admission. In addition a blood sample will be drawn daily (one per day during 7 days) to measure myocardial injury and inflammation systemic (interleukins) biomarkers.

    Diagnostic Test: Echocardiography
    Standard protocols
    Other Names:
  • Heart resonance magnetic nuclear
  • Diagnostic Test: Cardiac Magnetic resonance
    MRI with late gadolinium increase and T1 mapping
    Other Names:
  • MRI
  • Outcome Measures

    Primary Outcome Measures

    1. Myocardian injury (scarring) in patients with CAP without cardiac disease (CP)history at 6 months of ICU admission [at 6 months]

      MRI with late gadolinium increase and t1 mapping techniques for to detect myocardial scarring

    2. Heart dysfunction in patients with CAP without cardiac disease (CP)history in the first week of ICU admission [at day 7 of ICU admission)]

      Echocardiography with standard and strain techniques for to detect the presence of decrease in ejection fraction of both vetricules

    Secondary Outcome Measures

    1. Temporal profile of the Troponin I as a cardiac injury biomarker in patients with CAP without cardiac disease (CP)history in the first week of ICU admission [once per day ( days 1 to 7 of ICU admission)]

      Determination of serum troponin-I according to standard technique

    2. Temporal profile of the N-terminal pro-brain natriuretic peptide(NT-proBNP) as a cardiac injury biomarker in patients with CAP without cardiac disease (CP)history in the first week of ICU admission [once per day (days 1 to 7 of ICU admission)]

      Determination of serum N-terminal pro-brain natriuretic peptide(NT-proBNP) according to standard technique

    3. Temporal profile of the heart- fatty acid binding protein (h-Fabp) as a cardiac injury biomarker in patients with CAP without cardiac disease (CP)history in the first week of ICU admission [once per day (days 1 to 7 of ICU admission)]

      Determination of serum heart- fatty acid binding protein (h-Fabp)according to standard technique

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
      • Patients admitted to the ICU due to community-acquired pneumonia according to IDSA/ATS criteria
      • No history of heart diasese
      • Informed consent signed
    Exclusion Criteria:
      • Hospital or ventilator-associated pneumonia
      • Health care-associated pneumonia
      • Viral pneumonia
      • Bacterial/viral coinfection pneumonia
      • History of heart disease
      • Chronic administration of statins
      • Chronic administration of steorids (Prednisolone more 20 mg/day or equivalent)
      • No signed informed consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Critical Care Department - Hospital Universitario de Tarragona Joan XXIII Tarragona Spain 43007

    Sponsors and Collaborators

    • Alejandro Rodriguez Oviedo , MD

    Investigators

    • Principal Investigator: Alejandro H Rodriguez Oviedo, Hospital Universitari de Tarragona Joan XXIII

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Alejandro Rodriguez Oviedo , MD, MD,PhD, Hospital Universitari Joan XXIII de Tarragona.
    ClinicalTrials.gov Identifier:
    NCT03058211
    Other Study ID Numbers:
    • PI16/00486
    First Posted:
    Feb 20, 2017
    Last Update Posted:
    Jul 1, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Alejandro Rodriguez Oviedo , MD, MD,PhD, Hospital Universitari Joan XXIII de Tarragona.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 1, 2021