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Simplifying the ISCHEMIA trial algorithm for clinical practice: Identifying left main coronary artery disease using coronary artery calcium scans - 09/07/21

Doi : 10.1016/j.ahj.2021.05.013 
Joel E. Money, MD a, b, Joseph B. Muhlestein, MD a, b, Steve Mason, PA-C a, Tami L. Bair a, Kirk U. Knowlton, MD a, b, Benjamin D. Horne, PhD, MStat, MPH a, c, Jeffrey L. Anderson, MD a, b,
a Intermountain Medical Center, Intermountain Heart Institute, Intermountain Healthcare, Salt Lake City, UT 
b University of Utah School of Medicine, Department of Internal Medicine, Division of Cardiology, Salt Lake City, UT 
c Division of Cardiovascular Medicine, Department of Medicine, Stanford University, Stanford, CA 

Request reprints: Jeffrey L. Anderson, MD, Intermountain Medical Center Heart Institute, 5121 S. Cottonwood St., Salt Lake City, UT 84107.Intermountain Medical Center Heart Institute5121 S. Cottonwood St.Salt Lake CityUT84107

Riassunto

Background

Several recent trials have evaluated invasive versus medical therapy for stable ischemic heart disease. Importantly, patients with significant left main coronary stenosis (LMCS) were excluded from these trials. In the ISCHEMIA trial, these patients were identified by a coronary CT angiogram (CCTA), which adds time, expense, and contrast exposure. We tested whether a coronary artery calcium scan (CACS), a simpler, less expensive test, could replace CCTA to exclude significant LMCS.

Methods

We hypothesized that patients with ≥50% LMCS would have a LM CACS score > 0. As a corollary, we postulated that a LM CACS = 0 would exclude patients with LMCS. To test this, we searched Intermountain Healthcare's electronic medical records database for all adult patients who had undergone non-contrast cardiac CT for quantitative CACS scoring prior to invasive coronary angiography (ICA). Patients aged <50 and those with a heart transplant were excluded. Cases with incomplete (qualitative) angiographic reports for LMCS and those with incomplete or discrepant LM CACS results were reviewed and reassessed blinded to CACS or ICA findings, respectively.

Results

Among 669 candidate patients with CACS followed by ICA, 36 qualifying patients were identified who had a quantitative CACS score and LMCS ≥ 50%. Their age averaged 71.8 years, and 81% were men. Angiographic LMCS averaged 72% (range 50%-99%). Median time between CACS and ICA was 6 days. Total CACS score averaged 2,383 Agatston Units (AU), range 571-6,636. LM CACS score averaged 197 AU, range 31-610. Importantly, no LMCS patient had a LM CACS score of 0 vs 57% (362/633) of non-LMCS controls (P < .00001).

Conclusions

Our results support the hypothesis that an easily administered, inexpensive, low radiation CACS can identify a large subset of patients with a very low risk of LMCS who would not have the need for routine CCTA. Using CACS to exclude LMCS may efficiently allow for safe implementation of an initial medical therapy strategy of patients with stable ischemic heart disease in clinical practice. These promising results deserve validation in larger data sets.

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© 2021  Pubblicato da Elsevier Masson SAS.
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Vol 239

P. 129-134 - Settembre 2021 Ritorno al numero
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