Incidence and Predictors of Adverse Events Among Initially Stable ST‐Elevation Myocardial Infarction Patients Following Primary Percutaneous Coronary Intervention

Author:

Amon Jaihoon1,Wong Graham C.23,Lee Terry45ORCID,Singer Joel45ORCID,Cairns John23ORCID,Shavadia Jay S.1,Granger Christopher6ORCID,Gin Kenneth23,Wang Tracy Y.6,van Diepen Sean7ORCID,Fordyce Christopher B.234ORCID

Affiliation:

1. Division of Cardiology University of Saskatchewan Saskatoon Saskatchewan Canada

2. Division of Cardiology University of British Columbia and Vancouver General Hospital Vancouver British Columbia Canada

3. Centre for Cardiovascular Innovation University of British Columbia Vancouver British Columbia Canada

4. Centre for Health Evaluation and Outcome Sciences Vancouver British Columbia Canada

5. School of Population and Public Health University of British Columbia Vancouver British Columbia Canada

6. Duke Clinical Research Institute Duke University School of Medicine Durham NC

7. Division of Cardiology, Department of Medicine and Department of Critical Care Medicine University of Alberta Edmonton Alberta Canada

Abstract

Background Cardiac intensive care units were originally created in the prerevascularization era for the early recognition of ventricular arrhythmias following a myocardial infarction. Many patients with stable ST‐segment–elevation myocardial infarction (STEMI) are still routinely triaged to cardiac intensive care units after a primary percutaneous coronary intervention (pPCI), independent of clinical risk or the provision of critical care therapies. The aim of this study was to determine factors associated with in‐hospital adverse events in a hemodynamically stable, postreperfusion population of patients with STEMI. Methods and Results Between April 2012 and November 2019, 2101 consecutive patients with STEMI who received pPCI in the Vancouver Coastal Health Authority were evaluated. Patients were stratified into those with and without subsequent adverse events, which were defined as cardiogenic shock, in‐hospital cardiac arrest, stroke, re‐infarction, and death. Multivariable logistic regression models were used to determine predictors of adverse events. After excluding patients presenting with cardiac arrest, cardiogenic shock, or heart failure, the final analysis cohort comprised 1770 stable patients with STEMI who had received pPCI. A total of 94 (5.3%) patients developed at least one adverse event: cardiogenic shock 55 (3.1%), in‐hospital cardiac arrest 42 (2.4%), death 28 (1.6%), stroke 21 (1.2%), and re‐infarction 5 (0.3%). Univariable predictors of adverse events were older age, female sex, prior stroke, chronic kidney disease, and atrial fibrillation. There was no significant difference in reperfusion times between those with and without adverse events. Following multivariable adjustment, moderate to severe chronic kidney disease (creatinine clearance <44 mL/min; 13% of cohort) was associated with adverse events (odds ratio 2.24 [95% CI, 1.12–4.48]) independent of reperfusion time, age, sex, smoking status, hypertension, diabetes, and prior myocardial infarction/PCI/coronary artery bypass grafting. Conclusions Only 1 in 20 initially stable patients with STEMI receiving pPCI developed an in‐hospital adverse event. Moderate to severe chronic kidney disease independently predicted the risk of future adverse events. These results indicate that the majority of patients with STEMI who receive pPCI may not require routine admission to a cardiac intensive care unit following reperfusion.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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