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Role of Data Registries in the Time of COVID-19

Heather M. Alger, Joseph H. Williams, Jason Walchok, Michele Bolles, Gregg C. Fonarow, Christine Rutan

2020Circulation Cardiovascular Quality and Outcomes27 citationsDOI

Abstract

On April 1, 2020, the confirmed global burden of coronavirus disease 2019 (COVID-19) was >900 000 with 46 413 deaths. 1 Despite worldwide calls for social distancing and containment, the incidence of the disease continues to increase.COVID-19 is a respiratory tract infection caused by the novel coronavirus (SARS-CoV-2).Preliminary analyses from the Chinese Center for Disease Control and Prevention indicated an overall case fatality rate of 2.3%; however, the case fatality rate was higher in older adults (14.8% in those 80± years) and 49% of all critical cases. 2 Those with preexisting conditions (cardiovascular disease, diabetes mellitus, chronic respiratory disease, hypertension, and cancer) also had higher case fatality rates. 2 In the United States, 116 million adults have hypertension, 26 million US adults have diabetes mellitus, 9% have preexisting cardiovascular disease 3 and may, therefore, be at greater risk of complications or adverse health outcomes from COVID-19 infection.Many researchers are actively engaged in developing vaccines and therapeutics for COVID-19, 4 and the Food and Drug Administration has provided updated guidance for clinical trials not related to the viral infection during the pandemic. 5Clinical registry data can provide valuable insights into patient characteristics, treatment patterns, and clinical outcomes in patients hospitalized with cardiovascular disease during this time period.While randomized clinical trials are the gold standard for treatments, real-world evidence collected in a patient registry of clinical encounters provides a unique opportunity to potentially study the clinical effectiveness of treatments of COVID-19 in a cardiovascular disease patient population.Beginning early April 2020, COVID-19 specific data elements will be added to each of the American Heart Association's Get With The Guidelines (GWTG) registry modules (Table ).Get With The Guidelines is a voluntary quality improvement program, capturing data on patients hospitalized with atrial fibrillation, coronary artery disease, heart failure, stroke, and in-hospital cardiac arrest.Specifically, health care providers and data abstractors will be able to provide information on active viral or bacterial infections during hospitalization, time-sensitive treatment delays related to personalized protective equipment, and medical history of emerging infectious diseases such as COVID-19 to understand long-term impacts.These data elements are designed to be adaptable and updated quickly in response to future emerging infections.Time-sensitive emergencies, like ST-segment-elevation myocardial infarction, stroke, and cardiac arrest, will undoubtedly be impacted.By collecting data on clinical encounters during this pandemic, we could quantify the real-world impact to inform care during future public health emergencies.Early data from a Hong Kong hospital, comparing ST-segment-elevation myocardial infarction patient door to percutaneous coronary intervention times before and during the COVID-19 outbreak showed treatment delays. 6US first-responders, emergency room clinicians and cath-lab operators may be delayed not only by the need to don personalized

Topics & Concepts

Coronavirus disease 2019 (COVID-19)MedicineGerontologyLibrary scienceInternal medicineComputer scienceInfectious disease (medical specialty)DiseaseCOVID-19 and healthcare impactsAcute Myocardial Infarction ResearchCOVID-19 Clinical Research Studies