Cancer-associated type 2 versus type 1 myocardial infarction: A physiology-driven framework for inpatient risk stratification.
Abstract
e23234 Background: Myocardial injury during cancer hospitalizations is frequently labeled as myocardial infarction, although many events reflect supply demand mismatch rather than plaque rupture. Distinguishing Type 2 from Type 1 myocardial infarction may better inform inpatient triage and prognosis. This study compared the burden and outcomes of Type 2 and Type 1 myocardial infarction in hospitalized oncology populations. Methods: A serial cross-sectional analysis was performed using adult hospitalizations with a principal diagnosis of malignancy in the 2018 to 2022 National Inpatient Sample with discharge-level survey weighting. Type 2 myocardial infarction was identified using ICD-10-CM I24.8 and Type 1 myocardial infarction using I21 to I22. Outcomes included in-hospital mortality, shock, all types (R57*), mechanical ventilation, intensive care unit utilization proxy, length of stay, hospitalization cost, and All Patient Refined Diagnosis Related Group (APR-DRG) severity. Survey-weighted multivariable regression compared Type 2 myocardial infarction only with Type 1 myocardial infarction only, adjusting for demographics, payer, ZIP-code income quartile, admission type, cancer subtype, hospital characteristics, and year. Results: Among 961,848 unweighted cancer hospitalizations representing 4,809,239 admissions nationally, Type 2 myocardial infarction occurred in 0.70% and Type 1 myocardial infarction in 1.03%. Mean APR-DRG severity was lower with Type 2 than with Type 1 myocardial infarction (3.38 vs 3.75). Mortality was 14.2% with Type 2 versus 19.1% with Type 1 myocardial infarction. Type 2 myocardial infarction was associated with lower shock (5.5% vs 9.2%), mechanical ventilation (8.3% vs 13.9%), intensive care unit utilization (11.9% vs 18.7%), and extreme severity (7.4% vs 12.8%), as well as shorter length of stay and lower costs. After weight adjustment, Type 2 myocardial infarction remained associated with lower mortality (adjusted odds ratio 0.68, 95% CI 0.62 to 0.75), shock (adjusted odds ratio 0.60, 95% CI 0.52 to 0.68), intensive care unit utilization (adjusted odds ratio 0.61, 95% CI 0.56 to 0.68), mechanical ventilation (adjusted odds ratio 0.58, 95% CI 0.52 to 0.65), extreme severity (adjusted odds ratio 0.28, 95% CI 0.23 to 0.34), shorter length of stay (β −1.16 days), lower costs (β −$5,601), and lower APR-DRG severity (β −0.37) compared with Type 1 myocardial infarction. Conclusions: Among cancer hospitalizations, Type 2 myocardial infarction represents a meaningful national burden with high morbidity but consistently lower severity, resource utilization, and mortality than Type 1 myocardial infarction. These findings support early identification of Type 2 myocardial infarction among cancer hospitalizations to appropriately guide prognosis and treatment rather than uniform escalation for myocardial injury.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (6)
Gevork Seifert
Department of Internal Medicine, Sunrise Health GME Consortium, Las Vegas, NV
Khawaja Momal Hassan
Department of Internal Medicine, Sunrise Health GME Consortium, Las Vegas, NV
Mohammad Hashmi
Daniel Thomas Jones
HCA Sunrise Health GME Consortium - MountainView Hospital, Las Vegas, NV
Kyaw Zin Thein
3Comprehensive Cancer Centers of Nevada, Division of Hematology and Medical Oncology, Las Vegas, United States
Pinak Shah
From Gagnon Cardiovascular Institute, Morristown Medical Center, Morristown, NJ (P.G.); Columbia University Medical Center/New York Presbyterian Hospital (A.S., R.T.H., M.B.L.), the Cardiovascular Research Foundation (D.J.C., R.T.H., B.R., M.B.L.), and Weill Cornell Medicine (B.R.), New York, and St. Francis Hospital and Heart Center, Roslyn (D.J.C.) — all in New York; University of Colorado Health, Medical Center of the Rockies, Loveland (J.B.O.); Laval University, Quebec, QC (P.P.), St. Paul’s Hospital, University of British Columbia, Vancouver (P.B., J.L.), and McMaster University, Hamilton, ON (T.S.) — all in Canada; Vanderbilt University Medical Center, Nashville (B.R.L., K.G.); Emory University, Atlanta (V.B.); the Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University, Stanford (W.F.F.), VA Palo Alto Health Care System, Palo Alto (W.F.F.), California Pacific Medical Center, San Francisco (D.V.D.), Cedars–Sinai Medical Center, Los Angeles (R.R.M.), and Edwards ...