Efficacy Evaluation of the HEART Pathway in Emergency Department Patients With Acute Chest Pain

Acute Coronary Syndrome Clinical Trial

— HEART Pathway  

Official title:

Efficacy Evaluation of the HEART Pathway in Emergency Department Patients With Acute Chest Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01665521
• Other study ID #: IRB00021074
• Secondary ID: 12CRP12000001
• Status: Completed
• Phase: N/A
• Start date: September 2012
• Est. completion date: January 15, 2018

Study information

• Verified date: August 2018
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Our research will examine a chest pain care strategy, called the HEART pathway, which is designed to correctly identify Emergency Department patients at high-risk for cardiovascular events, likely to benefit from further testing, and patients at very-low-risk for cardiovascular events, who may be safely discharged home. By using an individual's risk assessment to determining testing, we hope to improve the quality and efficiency of the care delivered to Emergency Department patients with chest pain. Our study will determine if the HEART pathway, which combines a clinical decision rule, the HEART score, and two serial troponin measurements, will reduce stress testing and cardiovascular imaging, decrease hospital length of stay, and reduce cost compared to usual care, while maintaining safety.

Description:

Approximately 8-10 million patients complaining of chest pain present to an Emergency Department (ED) annually in the United States. The total cost of chest pain evaluations has been estimated at $5-10 billion annually, yet only 10% of these patients are ultimately diagnosed with an acute coronary syndrome. American College of Cardiology/ American Heart Association (ACC/AHA) guidelines recommend that patients at low-risk for acute coronary syndrome should receive serial cardiac markers followed by objective cardiac testing (stress testing or cardiac imaging). However, many have questioned the value of objective cardiac testing in all low-risk patients.Cardiac testing for all patients at low-risk for acute coronary syndrome (ACS) is not sustainable from a healthcare quality or economic perspective. In addition to increasing costs, objective cardiac testing is associated with a substantial number of false positive and non-diagnostic tests, which lead to additional unnecessary and often invasive procedures. Implementation of accurate risk stratification care pathways designed to eliminate unnecessary cardiac testing could improve the efficiency and quality of care by decreasing false positive/non-diagnostic testing, radiation, and costs. The HEART pathway, which combines a clinical decision rule, the HEART score, and two serial troponin measurements, is a recently developed care pathway designed to identify chest pain patients for early discharge without objective testing. Primary Hypothesis: The HEART Pathway, when compared to usual care, will reduce 30 day objective cardiac testing, hospital length of stay, and cost, while maintaining patient safety. Methods: Participants (n=282) at risk for ACS will be recruited into a clinical trial from Wake Forest Baptist Medical Center (WFBMC) ED. Patients will be equally randomized to HEART Pathway or Usual Care. HEART Pathway participant's treating physician will follow HEART Pathway guidelines for identifying patients to be admitted to the hospital or observation unit for cardiac testing or to be discharged home without testing. Usual Care participant's treating physicians will decide whether the patients should be discharged home or admitted to the hospital or observation unit based on ACC/AHA guidelines without using the HEART pathway.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 282
• Est. completion date: January 15, 2018
• Est. primary completion date: February 20, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• Age greater than or equal to 21 years
• Chest discomfort or other symptoms consistent with possible ACS
• The treating physician feels the patient could be discharged home if cardiac disease was excluded

Exclusion Criteria:

• New ST-segment elevation in contiguous leads on any electrocardiogram (>/= 1 mV)
• Unstable vitals signs: symptomatic hypotension at the time of enrollment (systolic < 90 mm Hg), tachycardia (HR>120), bradycardia (HR<40), and hypoxemia (<90% pulse-oximetry on room air or normal home oxygen flow rate)
• Terminal diagnosis with life expectancy less than 1 year
• A non-cardiac medical, surgical, or psychiatric illness determined by the provider to require admission, increase risk of objective cardiac testing, or prevent immediate discharge following negative testing.
• Prior enrollment
• Incapacity or unwillingness to provide consent and comply with study procedures
• Non-English speaking Sub-study I & II

Inclusion Criteria:

• ED attending physicians

Exclusion Criteria:

• ED attending physicians who decline to participate

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Chest Pain
• Emergencies

Intervention

Other:
• HEART Pathway
During ED evaluation, patients are randomized to HEART Pathway or usual care arms.

Locations

Country	Name	City	State
United States	Wake Forest Wake Forest University Baptist Medical Center - Emergency Department	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences	American Heart Association

Country where clinical trial is conducted

United States, 

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* Note: There are 55 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Major adverse cardiac events (MACE)		30 Days and 1 Year
Other	Missed MACE	MACE occurring in patients discharged without objective cardiac testing.	30 Days and 1 Year
Other	Provider adherence to the HEART Pathway		Duration of Index Hospitalization, average of 1 to 2 days
Other	Inter-rater reliability of the HEART Pathway		Duration of the Index ED visit, less than 1 day
Primary	Objective cardiac testing (stress testing or cardiac imaging) within 30 days	Rate of objective cardiac testing within 30 days	30 Days
Secondary	Cost, length of stay, recurrent ED visits and non-index hospitalization for chest pain.		30 Days
Secondary	Objective cardiac testing (stress testing or cardiac imaging), cost, length of stay, and recurrent ED visits and non-index hospitalization for chest pain.		1 Year
Secondary	Index objective cardiac testing rate	proportion of patients receiving any stress testing modality, coronary computed tomography angiography, or invasive catheter angiography at the index visit	Duration of Index Hospitalization, average of 1 to 2 days
Secondary	Index Hospital Admission Rate	Proportion of patients hospitalized for admission or observation during the index visit	Duration of Index Hospitalization, average of 1 to 2 days
Secondary	Early discharge rate	Proportion of patients that are discharged from the Emergency Department without meeting the composite endpoint of index hospital admission or index objective cardiac testing	Duration of Index Hospitalization, average of 1 to 2 days
Secondary	Composite of 30 day hospital admission and objective cardiac testing		30 Days

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