Ethnic Differences in Acute Coronary Syndromes Care in Emergency Departments. (ASCEND)

March 12, 2018 updated by: Martha Mackay, University of British Columbia
When doctors and nurses use accepted guidelines for quickly treating patients who come to the emergency department (ED) with a possible heart attack, patients do better. Research shows that there are racial-identity- and ethnicity-based differences in the symptoms these patients have, when and why they seek care, the treatments they receive, and how well they fare afterwards. There is also Canadian evidence that there may be racial-identity-based disparities in the care some patients receive, and it has been suggested that health professionals may unconsciously treat patients of different racial identities differently. But it is not known if there is racial-identity variation in the care given to Canadian patients with heart attack symptoms in the critical first hours after coming to an ED, or in their experiences of this care. The investigators collected information from the health records of patients who come to EDs with symptoms of heart attack. The investigators recorded events and times such as what provisional diagnosis was assigned to the patient, how often they received pain medication, how long until certain tests were performed and what treatments were offered. The investigators also collected information about things that might affect delivery of care, e.g., the number of doctors and nurses who were on duty. Participants also completed a short questionnaire about their reasons for coming to the hospital, how long they waited before coming and why, and what their experience in the ED was like. The investigators reviewed this information to see if there are racial-identity-based differences in the care received by patients with heart attack symptoms. The findings could identify important disparities, which could in turn inform future projects to correct these disparities, for example, education of health professionals about ethnic differences in ideas of health and illness.

Study Overview

Status

Completed

Detailed Description

The investigators conducted a prospective, observational study in which patients presenting to EDs who were subsequently diagnosed with acute coronary syndrome (ACS) or possible ACS were identified. The investigators collected data related to receiving the accepted standard of care for ACS patients. Information about the participants' initial symptoms, attribution of their symptoms, treatment-seeking choices, and perceptions of the care received in the ED was collected.

Setting and Sample: The investigators conducted the study at three sites: Hospital 1 is in an inner-city, quaternary care, university-affiliated hospital whose ED has approximately 71,000 patient visits annually, about 2,800 of which are patients with symptoms that are potentially due to myocardial ischemia. The medical and nursing staffing levels are staggered based on expected patient volumes, ranging from 15 to 18 registered nurses (RNs) and 1 to 6 physicians at a given time. There are also support staff, including licensed practical nurses, aides; clerks, ECG technicians, etc. There is a designated triage area, staffed continuously by at least one RN. Hospital 2's ED is in a large community hospital in a different health authority. It has 100,000 patient visits annually, approximately 6,500 of which are patients with potentially ischemic symptoms. The medical and nursing staffing levels are similar to the first site, ranging from 19 to 22 registered nurses (RNs) and 1 to 4 physicians at a given time. This site is in a community with a very high proportion of South Asian people (27.5%). Hospital 3 is also a community hospital with fewer ED visits annually, but similar nursing and medical staffing levels. This site is in a community with a very high proportion (52.5%) of people identifying as being of Chinese ancestry.

Procedures: Research assistants (RAs) fluent in English, Mandarin and Cantonese for the tertiary site and one fluent in English and Punjabi for the community site recruited participants.

Recruitment. The RAs identified potential participants, seven days per week, from one of three sources: (1) a list, obtained daily from the ED charge nurse, of all patients admitted to the hospital since the RA's last visit who were triaged with codes related to a possible ACS; (2) the current charge nurse, who identified any patient currently in the ED who met study criteria as signified by the ED physician ordering one of the following: (i) cardiology consult, (ii) cardiac computational tomography, or (iii) 2- or 6-hour repeat cardiac biomarker and ECG, followed by outpatient provocative stress testing; (3) a list, obtained from the stress-testing laboratory, of all patients who had been referred from the ED for urgent (within 48 hours) outpatient stress testing.

Recruitment occurred in the ED, the cardiology units (CCU or telemetry unit) and in the stress-testing laboratory. Potential participants were screened for general eligibility through discussion with the nurse or cardiology technologist. Those believed to be eligible were approached and invited to participate.

Data collection. Data regarding delivery of guideline-based care in the ED were collected from the health record (e.g., time to stretcher, time to ECG, time to first MD assessment, medications administered) and other processes (e.g., occurrence and timing of cardiology consultation, transfer from ED to a critical care area). Data regarding several patient-, environment- and system-related potential covariates were collected from the health record (e.g., mode of arrival at ED; language spoken; accompanied by family/friend; language ability of family/friend; symptoms reported) and ED staffing records (staffing levels). Data pertaining to the entire ED stay were captured.

Participants were asked to respond to a questionnaire, administered by the RA, regarding their decision to seek treatment and their perspectives on their ED care. Ethnicity, racial identity and other sociodemographic data were obtained during the interview.

For those admitted to the hospital, additional data regarding admission unit , procedures offered, refused and undergone, major adverse cardiac events, length of stay and final diagnosis were collected. For participants who were discharged from the ED with referral to outpatient stress testing, we tracked discharge diagnosis, attendance at, and interpretation of the test.

Measures: The primary outcome variable, door-to-ECG time, was defined as the time from triage to first ECG acquisition. The official triage time is the time entered by the triage nurse when the patient is initially evaluated. The time of the first ECG is an electronic time stamp appearing in the clinical information system, entered when the ECG is acquired.

The predictor variables ethnicity and racial identity were measured by self-report.

Other outcome variables and potential confounders:

  1. Time intervals: Several time intervals were measured, based on the official triage time.
  2. Location, nature and severity of reported symptoms: All symptoms reported by participant, as well as their intensity.
  3. Acuity at time of triage: measured using the Canadian Triage and Acuity Score. The participants' presenting complaint was measured using the Canadian Emergency Department Information System standardised codes, in use at the study sites.
  4. Other data: Mode of transport to hospital, accompanied versus alone, noted difficulty with English, presence of interpreter during care
  5. Number and frequency of physician and nurse assessments/interventions.
  6. Measured clinical parameters: All documented observations of ECG rhythm and vital signs.
  7. Medications: Agent, dose, route and time of administration
  8. Diagnostic testing: Timing and frequency of bloodwork and ECGs.
  9. Consultation: Consultation of other medical services.
  10. Patient Disposition.
  11. Patient perspectives: Time of onset, type of symptoms, decisions to seek treatment and reasons for delaying; participants' perspectives on care in ED; other socio-demographic variables
  12. Emergency department contextual factors: Staffing levels for each shift.
  13. Post-ED care: Diagnostic tests and interventions offered and completed after leaving ED, e.g., referral for / offer of / consent to / receipt of angiogram, percutaneous coronary intervention or cardiac surgery; discharge diagnosis; length of hospital stay.

Study Type

Observational

Enrollment (Actual)

448

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • British Columbia
      • Richmond, British Columbia, Canada, V6X 1A2
        • Richmond Hospital
      • Surrey, British Columbia, Canada, V3V 1Z2
        • Surrey Memorial Hospital
      • Vancouver, British Columbia, Canada, V6Z1Y6
        • St. Paul's Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients presenting to Emergency Departments with symptoms suggestive of an acute coronary syndrome.

Description

Inclusion Criteria:

  • 20 years of age or older
  • presented to the ED and are either referred for immediate cardiology consultation or managed according to a standardized protocol for continued observation and referral for follow-up (whether ultimately admitted or not);
  • hemodynamically stable and free of ischemic discomfort for at least one hour
  • spoke English, Mandarin, Cantonese, Punjabi
  • able to provide informed consent.

Exclusion Criteria:

• being cared for by any of the Emergency physicians (3) who were co-investigators

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Asian racial identity
Those who self-report "Asian" or related terms as their racial identity.
South Asian racial identity
Those who self-report "South Asian" or related terms as their racial identity.
Other racial identity
All others, who self-report neither "Asian", "South Asian" or their related terms as their racial identity.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Door to ECG
Time Frame: from hour and minute of admission until the hour and minute of first documented ECG, up to 48 hours
time from Emergency triage to first ECG acquisition
from hour and minute of admission until the hour and minute of first documented ECG, up to 48 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of assessments by health professionals
Time Frame: from hour and minute of admission until the hour and minute of transfer to inpatient unit or discharge from Emergency Department, whichever comes first, up to 48 hours
The number of assessments by physicians and nurses during the ED stay.
from hour and minute of admission until the hour and minute of transfer to inpatient unit or discharge from Emergency Department, whichever comes first, up to 48 hours
Rate of being offered and consenting to coronary angiogram
Time Frame: from date of admission until the date of hospital discharge, up to 100 weeks
Rate of being offered and consenting to coronary angiogram among those having a diagnosis of acute coronary syndrome or myocardial infarction.
from date of admission until the date of hospital discharge, up to 100 weeks
Rate of being offered and consenting to any revascularization procedure
Time Frame: from date of admission until the date of hospital discharge, up to 24 weeks
Rate of being offered and consenting to any revascularization procedure among those having coronary atherosclerotic lesions >/= 70% in any vessel
from date of admission until the date of hospital discharge, up to 24 weeks
ethnic differences in treatment-seeking delay
Time Frame: from hour and minute of first documented symptoms until the hour and minute of first documented help-seeking, up to 168 hours
the time between symptom onset and the decision to seek medical help
from hour and minute of first documented symptoms until the hour and minute of first documented help-seeking, up to 168 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 7, 2013

Primary Completion (ACTUAL)

January 11, 2017

Study Completion (ACTUAL)

April 12, 2017

Study Registration Dates

First Submitted

February 5, 2018

First Submitted That Met QC Criteria

March 6, 2018

First Posted (ACTUAL)

March 13, 2018

Study Record Updates

Last Update Posted (ACTUAL)

March 14, 2018

Last Update Submitted That Met QC Criteria

March 12, 2018

Last Verified

March 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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