Elsevier

The American Journal of Cardiology

Volume 189, 15 February 2023, Pages 22-30
The American Journal of Cardiology

New Criteria to Identify Patients at Higher Risk for Cardiovascular Complications After Percutaneous Coronary Intervention

https://doi.org/10.1016/j.amjcard.2022.11.029Get rights and content

A universal definition to identify patients at higher risk of complications after percutaneous coronary intervention (PCI) is lacking. We aimed to validate a recently developed score to identify patients at increased risk of all-cause death after PCI. All consecutive patients from a large PCI registry not presenting with ST-elevation myocardial infarction or cardiogenic shock were included. Each patient was assigned a score obtained by summing the points associated with the following variables: age >80 years (3 points), dialysis (6 points), left ventricular ejection fraction <30% (2 points), and multivessel PCI (2 points). Patients were stratified in 3 groups: low risk (score 0), intermediate risk (score 2 to 3), or high risk (score ≥4). The primary outcome was all-cause death, and the secondary outcomes were major adverse cardiovascular events and major bleeding. Events were assessed at 1 year after PCI. Between January 2014 and December 2019, 12,689 patients underwent PCI. Compared with the 9,884 patients at low risk, those at intermediate and high risk had a fourfold (hazard ratio 3.99, 95% confidence interval 2.95 to 5.38) and ninefold (hazard ratio 9.55, 95% confidence interval 6.89 to 13.2) higher hazard for all-cause death at 1 year, respectively. The score had a good predictive value for all-cause death at 1 year (area under the curve 0.70). The risk of major adverse cardiovascular events and major bleeding increased consistently from the low- to the high-risk group. In conclusion, in patients who underwent PCI for stable ischemic heart disease or non–ST-elevation acute coronary syndrome, a score based on 4 variables well predicted the risk of all-cause death at 1 year.

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:

  • 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

  • Patients at higher risk of complications after (PCI) represent a vulnerable and understudied population. A universal definition to identify these patients is currently lacking.

  • 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.

  • 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;

References (25)

Cited by (3)

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.

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