The study is a prospective, observational study of patients admitted to the BLOCK COPD network hospitals with acute AMI and Chronic Obstructive Pulmonary Disease (COPD) to determine the prevalence of COPD in patients admitted to the hospital with an acute myocardial infarction (AMI) and to characterize the phenotypic expression and severity of their underlying lung disease. Patients with will be identified via the EMR. 571 participants will be enrolled.
Specific Aim 1. To determine the prevalence of COPD in patients admitted to the hospital with an acute myocardial infarction (AMI) and to characterize the phenotypic expression and severity of their underlying lung disease. Patients admitted to the hospital and who undergo cardiac catheterization for an AMI will be identified through the electronic medical record (EMR). Those with a diagnosis of COPD in the EMR will be offered participation in the study. Baseline characterization will include demographics, smoking history, prior history of exacerbations in the year before admission, supplemental oxygen use, respiratory and cardiac medication use, comorbidities including history of coronary artery disease, heart failure and ejection fraction, and pulmonary function data as available in the EMR. Results of this Aim will provide data about the prevalence and clinical characteristics of COPD in the hospitalized population with AMI in our network. The Aim will also provide an estimate of the number of annual admissions for patients with COPD and AMI. Specific Aim 2. To determine the association between beta-blocker use at discharge and cardiopulmonary outcomes in patients with COPD and AMI. Patients with AMI and EMR-documented COPD will be followed, prospectively from the time of discharge using review of the electronic medical record and as local guidance permits, phone calls at 3 and 6 months. The investigators will determine the associations between beta-blocker use at discharge and the risk for all-cause mortality, recurrent ischemic events, and hospitalization for COPD exacerbation adjusting for baseline characteristics and COPD severity. Because of the coronavirus disease 2019(COVID-19) pandemic and the possibility of limited access to hospitalized patients, the study consists of three options for enrollment. Option 1 or 2 is preferable if local guidance permits. Option 1: A total of 3 visits including 1 in person visit in the hospital and 2 follow up phone calls with EMR review at 3 and 6 months after discharge. Sites may consider alternatives to in person consent and data collection including by telephone or video conference. Option 2: EMR review at the time of hospital admission followed by post-discharge telephone consent and 2 follow up phone calls with EMR review at 3 and 6 months. Option 3: EMR review at the time of hospital admission and follow-up review of the EMR at 3 and 6 months after discharge.
Study Type
OBSERVATIONAL
Enrollment
584
Observational
University of Alabama at Birmingham
Prevalence of COPD in Patients Admitted to the Hospital With an Acute Myocardial Infarction (AMI)
Results of this Aim will provide data about the prevalence of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Forced Expiratory Volume (FEV1), L; Post-bronchodilator
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
FEV1 % Predicted; Post-bronchodilator
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Number of Participants With Prescriptions for Home Oxygen
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Number of Participants That Received a Course of Systemic Corticosteroids and/or Antibiotics in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Number of Courses of Systemic Corticosteroids and/or Antibiotics in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
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Birmingham, Alabama, United States
University of California, San Francisco-Fresno
Fresno, California, United States
LA BioMed at Harbor-UCLA Medical Center
Los Angeles, California, United States
University of California at San Francisco
San Francisco, California, United States
National Jewish Medical & Research Center
Denver, Colorado, United States
North Florida/South Georgia Veterans Health System
Gainesville, Florida, United States
Northwestern University
Chicago, Illinois, United States
Louisiana State University
New Orleans, Louisiana, United States
University of Maryland Baltimore
Baltimore, Maryland, United States
University of Michigan
Ann Arbor, Michigan, United States
...and 14 more locations
Time frame: Baseline
Respiratory Episodes Requiring Care in the Emergency Department in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Respiratory Episodes Leading to Hospitalization in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Number of Hospitalizations in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Respiratory Episodes Requiring Intubation in Past Year
Characterize the phenotypic expression and severity of underlying lung disease. Results of this Aim will provide data about the clinical characteristics of COPD in the hospitalized population with AMI in our network.
Time frame: Baseline
Time to Death, or First Hospitalization or Revascularization Event
Compare the time to death or all-cause hospitalization or revascularization event at 6 months for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers.
Time frame: 6 month follow-up
Risk of Death, Hospitalization or Revascularization Event
Compare the risk of death or all-cause hospitalization at 6 months for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers by analyzing number of participants experiencing events. The number of participants will be reported for this outcome.
Time frame: 6 month follow-up
Time to Cardiovascular Disease (CVD) Related Death or First CVD-related Hospitalization/Revascularization Event
Compare the time to first CVD-related event (revascularization, CVD-related hospitalization, or CVD-related death) for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers by analyzing number of participants experiencing events and time to first event.
Time frame: 6 month follow-up
Risk of Cardiovascular Disease (CVD) Related Death or First CVD-related Hospitalization/Revascularization Event
Compare the risk of CVD-related event (revascularization, CVD-related hospitalization, or CVD-related death) for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers by analyzing number of participants experiencing events and time to first event.
Time frame: 6 month follow-up
Time to Respiratory/COPD-related Death or Hospitalization Event
Compare the time to respiratory/COPD-related death or hospitalization for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers by analyzing the time to first event.
Time frame: 6 month follow-up
Risk of Respiratory/COPD-related Death or Hospitalization Event
Compare the risk of respiratory/COPD-related death or hospitalization for patients with AMI and COPD who were discharged alive on beta-blockers to that of patients not discharged on beta-blockers by analyzing the number of of participants experiencing events.
Time frame: 6 month follow-up