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D018754: Ventricular Dysfunction

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

Navigate: Clinical Trials and HPO


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug1150 Echocardiography Wiki 0.67
drug3525 Transpulmonary thermodilution Wiki 0.58
drug3193 Standard 12-lead ECG, NT-proBNP, echocardiography Wiki 0.58
Name (Synonyms) Correlation
drug152 Abivertinib Wiki 0.58
drug3221 Standard of Care Wiki 0.09

Correlated MeSH Terms (7)


Name (Synonyms) Correlation
D018487 Ventricular Dysfunction, Left NIH 1.00
D018497 Ventricular Dysfunction, Right NIH 0.58
D006976 Hypertension, Pulmonary NIH 0.29
Name (Synonyms) Correlation
D012769 Shock, NIH 0.24
D012127 Respiratory Distress Syndrome, Newborn NIH 0.05
D055371 Acute Lung Injury NIH 0.05
D012128 Respiratory Distress Syndrome, Adult NIH 0.05

Correlated HPO Terms (0)


Name (Synonyms) Correlation

Clinical Trials

Navigate: Correlations   HPO

There are 3 clinical trials


1 Hemodynamic Characteristics of Patients With SARS-CoV-2: PiCCOVID Study

The outbreak of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been declared a public health emergency of international concern. Hospitalized COVID-19-positive patients requiring ICU care is increasing along with the course of epidemic. A large number of these patients developed acute respiratory distress syndrome (ARDS) according to current data. However, the related hemodynamic characteristic has so far been rarely described.

NCT04337983
Conditions
  1. Coronavirus
  2. SARS-CoV-2
  3. COVID-19
  4. Acute Respiratory Distress Syndrome
  5. Shock
  6. Acute Circulatory Failure
  7. Left Ventricular Dysfunction
  8. Fluid Overload
Interventions
  1. Device: Transpulmonary thermodilution
  2. Device: Echocardiography
MeSH:Respiratory Distress Syndrome, Newborn Respiratory Distress Syndrome, Adult Acute Lung Injury Ventricular Dysfunction Ventricular Dysfunction, Left Shock

Primary Outcomes

Description: Body temperature(°C)

Measure: Body temperature

Time: Through study completion, an estimation of 6 months

Description: Blood pressure in mmHg

Measure: Blood pressure

Time: Through study completion, an estimation of 6 months

Description: Pulse (heart rate) in times/minute

Measure: Pulse (heart rate)

Time: Through study completion, an estimation of 6 months

Description: Respiratory rate in times/minute

Measure: Respiratory rate

Time: Through study completion, an estimation of 6 months

Description: Cardiac index (L/min/m2)

Measure: Data provided by transpulmonary thermodilution-CI

Time: Through study completion, an estimation of 6 months

Description: Global end-diastolic volume(mL/m2)

Measure: Data provided by transpulmonary thermodilution-GEDV

Time: Through study completion, an estimation of 6 months

Description: Extravascular lung water (mL/kg)

Measure: Data provided by transpulmonary thermodilution-EVLW

Time: Through study completion, an estimation of 6 months

Description: Pulmonary vascular permeability index

Measure: Data provided by transpulmonary thermodilution-PVPI

Time: Through study completion, an estimation of 6 months

Measure: Incidence of abnormal laboratory test results

Time: Through study completion, an estimation of 6 months

Secondary Outcomes

Description: Left ventricle ejection fraction, Segmental left ventricle contractility, Speckle tracking data of the left and right ventricles, Dimensions of right and left cavities and Diastolic function of left ventricle

Measure: Incidence of new-onset or reversible systolic left ventricular dysfunction

Time: Through study completion, an estimation of 6 months

Description: The worst extravascular lung water

Measure: Changes of extravascular lung water measured by transpulmonary thermodilution

Time: Change from baseline extravascular lung water at 6 months

Description: The worst pulmonary vascular permeability index

Measure: Changes of pulmonary vascular permeability index measured by transpulmonary thermodilution

Time: Change from baseline extravascular lung water at 6 months

Measure: Correlation between the hemodynamic characteristics and 90-day mortality

Time: Up to 90th day after inclusion
2 Opportunistic Screening for Asymptomatic Left Ventricular Dysfunction in COVID-19 Survivors

Coronavirus Disease 2019 (COVID-19) emerged in December 2019, and in mere few months has resulted in a pandemic of viral pneumonia. Substantial proportion of patients with COVID-19 have biochemical evidence of myocardial injuries during the acute phase. Possible mechanisms including acute coronary events, cytokine storm, and COVID-19 related myocarditis, have been postulated for the cardiac involvement in COVID-19. It is uncertain whether COVID-19 survivors are at risk cardiac dysfunction including cardiac arrhythmia and heart failure. The prospective screening study aims to evaluate the possible latent effects from COVID-19 in COVID-19 survivors. COVID-19 survivors 4-6 weeks after hospital discharge will be recruited from the Infectious Disease clinic, Queen Mary Hospital with standard 12-lead electrocardiogram, serum troponin, NT-proBNP, and standard transthoracic echocardiogram. The outcome measures include (1) new onset cardiac arrhythmia, (2) N Terminal (NT)-proBNP elevation above the diagnostic range of heart failure, and (3) newly detected left ventricular dysfunction.

NCT04355884
Conditions
  1. COVID-19
Interventions
  1. Diagnostic Test: Standard 12-lead ECG, NT-proBNP, echocardiography
MeSH:Ventricular Dysfunction Ventricular Dysfunction, Left

Primary Outcomes

Description: Atrial fibrillation, conduction block

Measure: New-onset cardiac arrhythmia

Time: At the time of screening

Description: Elevated NT-proBNP level above the age-specific diagnostic threshold of heart failure

Measure: Elevation of NT-proBNP

Time: At the time of screening

Description: Left ventricular systolic function

Measure: Left ventricular dysfunction

Time: At the time of screening
3 Cardiac Dysfunction in Critically Ill Patients Infected With COVID-19

Cardiac dysfunction has been reported to be common in patients infected with COVID-19. The aim of this study is to evaluate the clinical importance of cardiac dysfunction in critically ill patients infected with COVID-19.

NCT04524234
Conditions
  1. Covid19
  2. Left Ventricular Dysfunction
  3. Right Ventricular Dysfunction
  4. Pulmonary Hypertension
Interventions
  1. Diagnostic Test: Echocardiography
MeSH:Hypertension, Pulmonary Ventricular Dysfunction Ventricular Dysfunction, Left Ventricular Dysfunction, Right
HPO:Pulmonary arterial hypertension

Primary Outcomes

Description: All cause death

Measure: Mortality

Time: 30 days

Secondary Outcomes

Description: Prevalence of left ventricular dysfunction

Measure: Left ventricular dysfunction

Time: Within 72 hours from admission

Description: Prevalence of right ventricular dysfunction

Measure: Right ventricular dysfunction

Time: Within 72 hours from admission

HPO Nodes


HPO

Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


HPO Nodes


Reports

Data processed on September 26, 2020.

An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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