Score TO Predict SHOCK - STOP SHOCK

Sponsor
Premedix Academy (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05570864
Collaborator
(none)
50,000
1
14
3572.5

Study Details

Study Description

Brief Summary

The goal of this international multicenter study is to develop a scoring system to identify the risk of developing cardiogenic shock (CS) in patients suffering from acute coronary syndrome (ACS) utilising artificial intelligence.

Study hypothesis:

A complex machine learning (ML) model utilising standard patient's admission data predicts the development of cardiogenic shock in patients suffering from acute myocardial infarction better than standard prediction models.

Study objectives:

The primary objective of this study is to further improve predictive parameters of #STOPSHOCK model for prediction of development of cardiogenic shock in patients suffering from acute myocardial infarction.

The secondary objective of this study is to develop a new predictive model for the development of cardiogenic shock in patients suffering from acute myocardial infarction based on larger combined cohort of patients utilising advanced ML algorithms, continuous model performance monitoring and continual learning.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Background:

    Cardiogenic shock is a serious life-threatening condition affecting almost 10% of patients suffering from acute coronary syndrome (ACS). When untreated, it can rapidly progress to collapse of circulation and sudden death. Despite recent improvements in diagnostic and treatment options, mortality remains incredibly high, reaching nearly 50%.

    Currently available mechanical circulatory support devices can replace the function of the heart and/or lungs, thereby essentially eliminating the primary cause. However, cardiogenic shock is not only an isolated decrease in cardiac function but a rapidly progressing multiorgan dysfunction accompanied by severe cellular and metabolic abnormalities. The window for successful treatment is relatively narrow, and when missed, even the elimination of the underlying primary cause is not enough to reverse this vicious circle.

    The ability to identify high-risk patients prior to the development of shock would allow to take pre-emptive measures, such as the implantation of mechanical circulatory support, and thus prevent the development of shock leading to improved survival.

    Rationale:

    The AI-based scoring system could aid in identifying high-risk patients prior to the development of cardiogenic shock. This would allow taking pre-emptive measures, implanting mechanical circulatory support, and thus prevent the development of shock, leading to improved survival.

    For this purpose, a predictive scoring system STOP SHOCK (Score TO Predict SHOCK) was developed. This scoring system showed better prediction compared to standard models. STOP SHOCK was validated on an external cohort of patients with area under the curve (AUC) of 0.844 surpassing other externally validated cardiogenic shock (CS) models (e.g. ORBI score). Furthermore, this model is based on variables that are readily available at the first contact with patients and thus STOPSHOCK can be utilized in emergency room (ER) or ambulance even before catheterization.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    50000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Other
    Official Title:
    Artificial Intelligence Based Predictive Scoring System to Identify the Risk of Developing Cardiogenic Shock (CS) in Patients Suffering From Acute Coronary Syndrome (ACS)
    Anticipated Study Start Date :
    Oct 1, 2022
    Anticipated Primary Completion Date :
    Nov 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Study group (with CS)

    A population of patients acquired from multiple national registries aged > 18 years, admitted for ACS without CS and proceeding to coronary angiography who developed cardiogenic shock (CS).

    Control group (without CS)

    A population of patients acquired from multiple national registries aged > 18 years, admitted for ACS without CS and proceeding to coronary angiography who did not develop cardiogenic shock (CS).

    Outcome Measures

    Primary Outcome Measures

    1. Development of cardiogenic shock [Up to 72 hours]

      Development of cardiogenic shock (CS) in patients suffering from acute coronary syndrome (ACS)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria for study population:
    1. Patients with at least one ICD9 diagnosis code:
    • 41000 - 41092: various versions of Acute myocardial infarction

    • 41189: Other acute and subacute forms of ischemic heart disease, other

    • 4139: Other and unspecified angina pectoris

    1. Patients with at least one ICD9 diagnosis code:
    • 78551: Cardiogenic shock

    • 78550: Shock, unspecified

    1. Patients with at least one ICD9 procedures codes:
    • 0066: Percutaneous transluminal coronary angioplasty [PTCA]

    • 3604: Intracoronary artery thrombolytic infusion

    • 3606: Insertion of non-drug-eluting coronary artery stent(s)

    • 3607: Insertion of drug-eluting coronary artery stent(s)

    • 3609: Other removal of coronary artery obstruction

    • 8855: Coronary arteriography using a single catheter

    • 8856: Coronary arteriography using two catheters

    • 8857: Other and unspecified coronary arteriography

    • 3722: Left heart cardiac catheterization

    • 3723: Combined right and left heart cardiac catheterization

    Inclusion criteria for control group:
    1. Patients with at least one ICD9 diagnosis code:
    • 41000 - 41092: various versions of Acute myocardial infarction

    • 41189: Other acute and subacute forms of ischemic heart disease, other

    • 4139: Other and unspecified angina pectoris

    1. Patients with at least one of the ICD9 procedures codes:
    • 0066: Percutaneous transluminal coronary angioplasty [PTCA]

    • 3604: Intracoronary artery thrombolytic infusion

    • 3606: Insertion of non-drug-eluting coronary artery stent(s)

    • 3607: Insertion of drug-eluting coronary artery stent(s)

    • 3609: Other removal of coronary artery obstruction

    • 8855: Coronary arteriography using a single catheter

    • 8856: Coronary arteriography using two catheters

    • 8857: Other and unspecified coronary arteriography

    • 3722: Left heart cardiac catheterization

    • 3723: Combined right and left heart cardiac catheterization

    Exclusion criteria for control group:
    1. Patients without ICD9 diagnosis codes:
    • 78551: Cardiogenic shock

    • 78550: Shock, unspecified

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Premedix Academy Bratislava Slovakia 81102

    Sponsors and Collaborators

    • Premedix Academy

    Investigators

    • Principal Investigator: Allan Böhm, MD, PhD, MBA, FESC, FJCS, Premedix Academy, Medena 18, 81102 Bratislava, Slovakia

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Premedix Academy
    ClinicalTrials.gov Identifier:
    NCT05570864
    Other Study ID Numbers:
    • 0012022
    First Posted:
    Oct 7, 2022
    Last Update Posted:
    Oct 7, 2022
    Last Verified:
    Oct 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Premedix Academy
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 7, 2022