New Criteria to Identify Patients at Higher Risk for Cardiovascular Complications After Percutaneous Coronary Intervention
Section snippets
Methods
All consecutive patients who underwent PCI at a large-volume tertiary-care center (Mount Sinai Hospital, New York, New York) between January 2014 and December 2019 were considered for inclusion. Patients presenting with acute ST-elevation myocardial infarction (STEMI) or cardiogenic shock were excluded. In agreement with the risk assessment tool developed by Brener et al,17 each patient was assigned a score obtained by summing the points associated with the following 4 variables: age >80 years
Results
Between January 2014 and December 2019, a total of 22,795 PCI procedures were performed at Mount Sinai Hospital. After the exclusion of repeated procedures, 15,322 unique patients who underwent PCI were identified. Of those, 556 patients meeting the exclusion criteria (STEMI or cardiogenic shock), 389 with missing information on the 4 variables, preventing the score calculation, and 1,688 event-free patients lost from follow-up in the first 30 days were excluded. The final study population
Discussion
We validated the value of a new developed score, including 4 variables, to predict the risk of all-cause death and ischemic or bleeding events at 1 year in a cohort of 12,689 patients who underwent PCI for stable ischemic heart disease or NSTE-ACS. The main findings can be summarized as follows:
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Patients at intermediate (score 2 to 3) or high risk (score ≥4) were older and were more likely to be women, to have cardiovascular co-morbidities, and have a higher CAD complexity than patients at low
Impact on Daily Practice
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Patients at higher risk of complications after (PCI) represent a vulnerable and understudied population. A universal definition to identify these patients is currently lacking.
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Among patients who underwent PCI with stable ischemic heart disease or NSTE-ACS, a score based on 4 variables including age, dialysis, ejection fraction, and multivessel PCI allowed to identify patients at low, intermediate, or high risk of all-cause death, MACE, and major bleeding.
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This score represents a new
Disclosures
Dr. Spirito received a research grant from the Swiss National Science Foundation. Dr. Brener reports consulting and speaking fees from AstraZeneca. Dr. Baber reports speaker honoraria from AstraZeneca and Boston Scientific. Dr. Sharma has received consulting fees or honoraria from Abbott, Boston Scientific, Abiomed, and Cardiovascular Systems, Inc. Dr. Dangas reports institutional research grants from Abbott Laboratories, AstraZeneca, Bayer, Boston Scientific, Medtronic, and Daiichi‐Sankyo;
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Funding: none.
This study was supported by the Zena and Michael A. Wiener Cardiovascular Institute Icahn School of Medicine at Mount Sinai New York, New York.