2DSPER: 2D Strain Echocardiography for Diagnosing Chest Pain in the Emergency Room

Sponsor
Technion, Israel Institute of Technology (Other)
Overall Status
Completed
CT.gov ID
NCT01163019
Collaborator
(none)
700
11
48
63.6
1.3

Study Details

Study Description

Brief Summary

Background: Chest pain (CP) and suspected heart attack is the second most frequent complaint among patients presenting to the emergency department (ED). Present workup involves in-hospital observation for 6 - 48 hours and requires significant resources including imaging tests, some of which are invasive and involve radiation and radio-contrast agents, which can be toxic to the kidney.

CP can result from impaired blood supply to the heart muscle, which may result in impaired contraction of the heart that persists for several days. Bedside echocardiography with semi-automated speckle tracking strain analysis (2D strain) is a novel promising noninvasive tool for the evaluation of heart muscle contraction. 2D strain can be useful for evaluating patients with CP, since it can accurately detect minor impairment in heart muscle contraction that can identify patients with coronary artery disease (CAD) and impending heart attack (coronary arteries are the arteries supplying blood to the heart muscle).

Working hypothesis and aims: The investigators hypothesize that a bedside echo study with normal 2D strain may allow quick and safe ruling out of a heart attack and significant CAD disease as the cause of CP.

The main aim of the study is to validate the investigators preliminary findings in a large number of patients in order to establish whether a normal 2D strain can safely rule out a heart attack or life threatening CAD.

Methods: In a large multi-center study 1200 patients presenting to the ED with acute CP of an unclear cause will undergo echocardiography as close as possible to presentation and not more than 24 hours from cessation of pain. Patients will undergo standard workup by the ED physicians. Standard echocardiographic findings, but not the 2D strain analysis, will be made available to the attending physician. Data from discharge letters, ECGs, blood tests, stress tests, nuclear imaging, heart CT and heart catheterization will be collected. A 6-month follow-up telephone interview will be performed to collect data on survival, heart attacks, re-hospitalization and revascularization (opening heart vessels blockages). 2D strain analysis will be performed off-line in a central laboratory to evaluate the ability of 2D strain to distinguish between patients with CP from heart disease and patients without life threatening heart disease that can be early released home safely.

Expected results: The investigators expect, based on the investigators previous experience, that patients with normal 2D strain will have a very low probability of a heart attack and significant CAD. The investigators further expect these patients to have an excellent 6-month prognosis. This will allow their early and cost-effective discharge.

Importance and Probable implications to Medicine: Reduction in ED patient load and a decrease in unnecessary hospitalizations for CP. Cost and resource savings and elimination of unnecessary imaging studies, some of which are invasive or involve radiation and contrast agents.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    700 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Utility of 2D Strain Echocardiography in Triage of Patients With Chest Pain in the Emergency Department
    Study Start Date :
    Sep 1, 2010
    Actual Primary Completion Date :
    Feb 1, 2014
    Actual Study Completion Date :
    Sep 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Chest pain

    Patients who present to the emergency department with a chief complaint of chest pain and have a moderate pre-test probability for an acute coronary syndrome

    Outcome Measures

    Primary Outcome Measures

    1. Acute coronary syndrome [1 week]

    2. Significant coronary artery disease. [1 week]

    Secondary Outcome Measures

    1. Major adverse cardiac events (MACE - death, MI or revascularization) [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients presenting to the emergency department with chest pain characteristic for ischemia and suspected acute coronary syndrome and at least one of the following:
    • Planned emergency department or chest pain unit observation for at least 6 hours

    • Hospital or chest pain unit admission for suspected acute coronary syndrome

    • Planned coronary CT scan

    1. Age ≥ 45 years old

    2. Normal sinus rhythm

    3. Patient able to give an informed consent

    Exclusion Criteria:
    1. ST elevation MI (≥ 1mm in at least 2 contiguous leads) or unstable patients requiring urgent care

    2. Significant (≥ 1mm ST depression in at least 2 contiguous leads) on initial ECG

    3. Elevated troponin on first examination

    4. History of previous MI, CABG, significant Q waves on ECG or wall motion abnormality on a previous echo

    5. Atrial fibrillation or abundant arrhythmia

    6. CLBBB, Ventricular pacing

    7. Valvular disease of at least moderate severity

    8. Cardiomyopathy

    9. Abnormal septal motion due to right ventricular disease or lung disease

    10. Technically suboptimal echo study (> 2 segments of suboptimal quality from apical views)

    11. Pregnancy

    12. Inadequate strain tracing

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ha'Emek Medical Center, Afula Israel
    2 Soroka University Medical Center Beer Sheva Israel
    3 Hillel Yafe Medical Center Hadera Israel
    4 Lady Davis Carmel Medical Center Haifa Israel
    5 Hadassah-Hebrew University Medical Center, Mount Scopus Jerusalem Israel
    6 Hadassah-University Medical Center, Ein Kerem Jerusalem Israel
    7 Shaare Zedek Medical Center Jerusalem Israel
    8 Rabin Medical Center Petah Tikva Israel
    9 Kaplan Medical Center Rehovot Israel
    10 Chaim Sheba Medical Center Tel Hashomer Israel
    11 Assaf Harofeh Medical Center Zrifin Israel

    Sponsors and Collaborators

    • Technion, Israel Institute of Technology

    Investigators

    • Principal Investigator: Avinoam Shiran, MD, Lady Davis Carmel Medical Center, Technion, Israel Institute of Technology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Avinoam Shiran, Director, Echocardiography, Lady Davis Carmel Medical Center, Technion, Israel Institute of Technology
    ClinicalTrials.gov Identifier:
    NCT01163019
    Other Study ID Numbers:
    • 2DS-CP-ED-MSS-IERG
    First Posted:
    Jul 15, 2010
    Last Update Posted:
    Oct 28, 2014
    Last Verified:
    Oct 1, 2014
    Keywords provided by Avinoam Shiran, Director, Echocardiography, Lady Davis Carmel Medical Center, Technion, Israel Institute of Technology
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 28, 2014