ABSTRACT
Background
Perioperative myocardial infarction (PMI) after noncardiac surgery results in significant morbidity and mortality. While comprehensive management, including imaging and guideline‐directed medical therapy (GDMT), improves outcomes, utilization of these strategies and the impact of physician evaluation on their utilization are unknown. This study evaluates the frequency of cardiology evaluation after PMI and its association with guideline‐recommended care.
Methods
Using IBM MarketScan (2016–2021), we analyzed claims for patients ≥ 45 years old with PMI during or after major noncardiac surgery. We examined the relationship between cardiology evaluation and post‐PMI care using three regression models: (1) a Poisson model for GDMT class prescriptions filled within 3 months post‐discharge, and logistic models for (2) ischemic testing and (3) echocardiography during hospitalization or within 3 months post‐discharge.
Results
Among 5660 patients with PMI (mean age 68, 56.9% male, 27.2% with STEMI), 19% were not evaluated by a cardiologist. Patients with cardiology evaluation were more likely to receive at least one GDMT prescription after PMI (78.8% vs 74.0%, p < 0.001). Cardiology evaluation was also associated with an increased likelihood of ischemic testing (38.2% vs 23.0%, p < 0.001) and echocardiography (75.9% vs 53.6%, p < 0.001).
Conclusion
One in five PMI patients lacks cardiology evaluation, and evaluation is associated with an increased likelihood of recommended management after PMI. Future studies should explore whether cardiology evaluation and management strategies impact patient outcomes.
Keywords: cardiology, consultation, echocardiography, myocardial infarction, perioperative
We analyzed the frequency of cardiology evaluation after perioperative myocardial infarction and its association with management in 5660 patients. One in five patients lacked cardiology evaluation. Cardiology evaluation was associated with an increased likelihood of guideline‐directed medical therapy (78.8% vs 74.0%), ischemic testing (38.2% vs 23.0%), and echocardiography (75.9% vs 53.6%).

1. Introduction
Perioperative myocardial infarction (PMI) is a significant and prevalent complication following noncardiac surgery, with substantial implications for adverse patient outcomes. Studies indicate that PMI occurs in 0.76% to 5% of patients undergoing major noncardiac surgery [1, 2, 3]. The mortality rate within 1 year post‐surgery for patients experiencing PMI ranges from 10% to 37% [4, 5, 6, 7]. Those who survive this acute event remain at an elevated risk for recurrent MI, heart failure, and mortality [6].
Guideline‐directed management of MI patients is critical to improve outcomes. Current guidelines recommend several strategies, including echocardiography, ischemic testing, and guideline‐directed medical therapy (GDMT) [8, 9]. GDMT typically includes antiplatelet agents (aspirin, P2Y12 receptor inhibitors), statins, ACE inhibitors or angiotensin receptor blockers, and beta‐blockers. GDMT has been shown to significantly improve patient outcomes, including reducing mortality, following MI [10, 11, 12].
Despite the established guidelines, there is limited information regarding the real‐world implementation of these management strategies following PMI. Moreover, the frequency of cardiology evaluation in real‐world practice, and the impact cardiology evaluation has on the implementation of these guideline‐based management strategies after PMI is unknown. The gap between guideline recommendations and clinical practice, often referred to as the “implementation gap,” is a well‐recognized phenomenon in cardiovascular care [13, 14, 15]. Identifying and addressing the barriers to guideline adherence in the context of PMI may significantly improve patient care and outcomes.
To address these knowledge gaps, we conducted a study using a U.S. insurance claims database to characterize the management of PMI from 2016 to 2021. This study has two aims: (1) to assess the frequency and patterns of GDMT, cardiac workup strategies, and cardiology evaluation following PMI, and (2) to identify whether cardiology evaluation is associated with the frequency of GDMT and cardiac workup.
2. Methods
2.1. Data Source
Data for these analyses came from the Truven Health MarketScan Databases (2015–2021) [16], which provide deidentified, longitudinal data on medical services and prescription drug claims. These databases include individuals with employer‐sponsored insurance, their dependents, and Medicare‐eligible retirees with supplemental insurance. MarketScan tracks claims across sites and over time, covering approximately 6 million U.S. individuals, with a nationally representative sex distribution (49% male).
2.2. Study Population
Patients aged 45 and older in the Health MarketScan Commercial Claims and Encounters and Medicare Supplemental Databases were included in the study cohort if they (1) had an inpatient admission falling between January 1, 2016 and September 30, 2021, (2) had a major noncardiac operating room procedure as their principal procedure [17, 18], and (3) received a diagnosis of a new myocardial infarction during their admission (Figure 1).
Figure 1.

Study flow diagram showing inclusion and exclusion criteria.
Specifically for criteria (2), admissions with principal procedure codes in Healthcare Cost and Utilization Project procedure classes 3 or 4, corresponding to major diagnostic and major therapeutic procedures, respectively, that did not correspond to procedures involving the heart, great vessels, or coronary vessels, were included (Table S1). For criteria (3), myocardial infarction was defined as a diagnosis corresponding to ICD‐9 code 410 or ICD‐10 code I21. There were no individuals with missing data.
2.3. Outcomes
The primary outcome was the number of GDMT medication classes with prescriptions filled within the 3 months post‐discharge from a hospitalization with a PMI. This time frame was chosen to assess short‐term guideline adherence while allowing for potential delays in follow‐up care and medication initiation or prescription filling. Four medication classes were defined as GDMT classes: platelet inhibitors (consisting of P2Y12 receptor inhibitors or aspirin), statins, ACE inhibitors or angiotensin receptor blockers, and beta blockers, and prescriptions were determined using National Drug Code numbers (Table S2). As MarketScan data only includes records on medications for which prescriptions were written and filled in the outpatient setting, the purchase of aspirin by a patient over‐the‐counter without the use of a prescription would not be captured by MarketScan. Two secondary outcomes were also assessed: (1) stress testing or left heart catheterization within the index admission to 3 months post‐discharge and (2) echocardiography within the same period, both identified using CPT codes (Table S3).
2.4. Patient Characteristics and Covariates
Patient age, sex, and length of stay of the index admission containing a PMI were obtained for each patient. The clinical domain of the principal procedure for the index admission with a PMI was determined for each patient using the Healthcare Cost and Utilization Project Procedure Classes Refined for ICD‐10‐PCS, v2023.1 (Table S1). To ensure statistical stability in our analyses, procedural categories with fewer than 50 patients (Ear, Nose, and Throat Procedures n = 30, Endocrine Procedures n = 23, Eye Procedures n = 9, Peripheral Nervous System Procedures n = 19, Pregnancy‐Related Procedures n = 6, and Skin and Breast Procedures n = 38) were combined into an ‘Other Procedures’ category. This approach avoids unreliable coefficient estimates from categories with very small sample sizes while maintaining clinical relevance in our analyses. Emergent procedures were defined as procedures occurring during an admission initiated with a service subcategory code that corresponded to an Emergency Room visit. The presence of evaluation by a provider falling into a specialty of “cardiology,” “family medicine,” or “internal medicine, not elsewhere classified” was determined separately for each patient during their index admission and for the 3‐month period following discharge. The presence of diagnoses of cardiac complications (supraventricular tachycardia, cardiogenic shock, atrial fibrillation, or acute heart failure) and noncardiac complications (severe sepsis, septic shock, hypovolemic shock, respiratory failure, or pulmonary embolism) made during the index admission were identified using ICD diagnosis codes (Table S4). Preoperative and perioperative risk factors recorded within the year before index admission, including ischemic heart disease, heart failure, chronic kidney disease (CKD) stage 3 or higher, and prior stroke or transient ischemic attack were identified using ICD diagnosis codes (Table S4). The presence of insulin‐dependent diabetes was identified using the presence of a filled outpatient prescription for insulin within the year before index admission. Modified Revised Cardiac Risk Index scores [19] were calculated using the above preoperative risk factors, with CKD 3 or higher as a proxy for creatinine > 2.0 and with high‐risk surgery defined as intraperitoneal, intrathoracic, or supra‐inguinal vascular surgery. The Clinical Classifications Software Refined categories were used to identify the high‐risk surgical procedures (Table S5) [20]. Using ICD codes (Table S4), we classified PMI events based on the diagnostic codes assigned to patients during hospitalization, which included STEMI, NSTEMI, and type 2 myocardial infarction. As these diagnoses are not mutually exclusive, patients may have received multiple MI‐related codes during their admission.
2.5. Statistics
All statistical analyses were completed using R statistical software environment version 4.2.2 [21]. Baseline characteristics were reported as mean and standard deviation (continuous variables) or as proportions (categorical variables). Continuous variables were compared using the Student's t‐tests or ANOVA tests, and categorical variables were compared with chi‐square tests. Due to the non‐normal distribution of length of stay data, we reported this variable as median with interquartile range and used non‐parametric Mann‐Whitney U tests for two‐group comparisons and Kruskal‐Wallis tests for multi‐group comparisons. To address the potential for Type I error due to multiple comparisons, we applied the Benjamini‐Hochberg procedure to control the False Discovery Rate (FDR) at 0.05 for all statistical tests. Statistical significance was considered with an adjusted p‐value less than 0.05.
2.6. Model of Frequency of Guideline Directed Medical Therapy Following Perioperative Myocardial Infarction
We fit a Poisson model with the glm function in R to assess the association between evaluation by a cardiologist physician during or after hospitalization with PMI and the number of GDMT drug categories (platelet inhibitors, ACE inhibitors/ARBs, beta‐blockers, or statins) with filled prescriptions within 3 months post‐discharge after PMI, while accounting for demographics and patient history. We selected Poisson regression because the number of drug categories is a count variable. To verify the appropriateness of this modeling approach, we conducted a Pearson chi‐square test for overdispersion, which showed no evidence of overdispersion (χ² = 5412.21, df = 5659, p = 0.991). The mean number of medication classes was 1.88 with a variance of 1.80, yielding a dispersion ratio of 0.96, which is close to 1.0 and confirms that the Poisson distribution appropriately fits our data.
Covariates included age, sex, length of hospital stay, emergency status of admission, clinical domain of principal procedure, and presence of filled prescriptions for ACE inhibitors/ARBs, beta‐blockers, aspirin, statins, and P2Y12 receptor inhibitors in the year before the index admission. Wald tests were used to assess the significance of each covariate, testing whether coefficients differed from zero, and p‐values were adjusted to an FDR of 0.05 using the Benjamini‐Hochberg procedure.
To assess the clinical significance of differences in GDMT utilization, we analyzed the association between cardiology evaluation and receipt of two or more GDMT medication classes, which represents a clinically meaningful threshold of guideline adherence. We calculated the proportion of patients receiving at least two GDMT medication classes stratified by cardiology evaluation status. The absolute risk difference between groups was determined, along with its 95% confidence interval calculated using the standard error formula for the difference between two proportions. The statistical significance of the difference in proportions was assessed using a chi‐square test.
2.7. Models of the Frequency of Ischemic Testing and Echocardiography Following Perioperative Myocardial Infarction
We created two separate logistic regression models with the glm function in R to evaluate the association between various factors and the likelihood of undergoing specific management strategies in the period spanning the index admission to 3 months following discharge from an admission with a post‐PMI: left heart catheterization or stress testing, and echocardiography. For each model, we included clinical and demographic variables including clinical domain of primary procedure, age, sex, comorbidities (ischemic heart disease, heart failure, chronic kidney disease stage 3 or higher, cerebrovascular disease, and insulin‐dependent diabetes), length of stay, emergency status, cardiac complications, noncardiac complications, evaluation by cardiology, family medicine, and internal medicine physicians, prior use of catheterization, stress tests, and echocardiography in the year before the index admission. The binary outcome variables for the two models were (1) Undergoing catheterization or stress testing during or 3 months after the inpatient stay and (2) Undergoing echocardiography during or 3 months after the inpatient stay. For both models, p‐values for each covariate were derived from Wald tests, and p‐values were adjusted to an FDR of 0.05 using the Benjamini‐Hochberg procedure.
3. Results
3.1. Study Population
A total of 1,093,181 patients underwent a major Noncardiac operating room procedure between January 1, 2016 and September 30, 2021, with 10,324 patients (0.94%) experiencing a PMI. Patients with insufficient insurance coverage (n = 4664) were excluded from the final analysis. The study cohort consisted of reports from hospitalizations for 5660 patients, and characteristics of these patients are presented in Table 1. The mean age was 68 years (SD 12.2 years), and 56.9% (n = 3223) were male. Of PMIs, 27.2% were STEMIs, 58.2% were NSTEMIs, and 19.7% were Type 2 MIs. Only 18.6% (n = 1053) of the admissions were nonelective surgical procedures.
Table 1.
Baseline characteristics among patients with perioperative AMI after major noncardiac surgery.
| Characteristics | Mean/Median/Count |
|---|---|
| Age | 68 (12.2) |
| Length of stay (days) | 8 [4–14] |
| Sex = Male | 3223 [56.9%] |
| Year | |
| 2016 | 1323 [23.4%] |
| 2017 | 1009 [17.8%] |
| 2018 | 746 [13.2%] |
| 2019 | 812 [14.3%] |
| 2020 | 992 [17.5%] |
| 2021 | 778 [13.7%] |
| Urgency of Procedure = Emergent | 1053 [18.6%] |
| Type of surgery | |
| Vascular Procedures | 1472 [26%] |
| Central Nervous System Procedures | 154 [2.72%] |
| Female Reproductive System Procedures | 69 [1.22%] |
| Gastrointestinal System Procedures | 751 [13.3%] |
| General Region Procedures | 138 [2.44%] |
| Hepatobiliary and Pancreas Procedures | 342 [6.04%] |
| Lymphatic and Hemic System Procedures | 67 [1.18%] |
| Male Reproductive System Procedures | 60 [1.06%] |
| Musculoskeletal, Subcutaneous Tissue, and Fascia Procedures | 1907 [33.7%] |
| Respiratory System Procedures | 379 [6.7%] |
| Urinary System Procedures | 196 [3.46%] |
| Other Procedures | 125 [2.21%] |
| Complications occurring during hospitalization with PMI | |
| Cardiac complication | 2037 [36%] |
| Supraventricular tachycardia | 211 [3.73%] |
| Cardiogenic shock | 180 [3.18%] |
| Atrial fibrillation | 1299 [23%] |
| Acute heart failure | 837 [14.8%] |
| Noncardiac complication | 1952 [34.5%] |
| Severe sepsis | 224 [3.96%] |
| Septic shock | 305 [5.39%] |
| Hypovolemic shock | 68 [1.2%] |
| Respiratory failure | 1680 [29.7%] |
| Pulmonary embolus | 231 [4.08%] |
| Evaluation by physician during admission with PMI or in 3 months post discharge | |
| Cardiologist | 4582 [81%] |
| Family Medicine | 3267 [57.7%] |
| Internal Medicine (not elsewhere classified) | 4254 [75.2%] |
| GDMT class prescription filled in 12 months before admission | |
| Aspirin | 261 [4.61%] |
| P2Y12 receptor inhibitor | 1283 [22.7%] |
| ACE inhibitor/ARB | 3009 [53.2%] |
| Beta Blocker | 2954 [52.2%] |
| Statin | 3141 [55.5%] |
| GDMT class prescription filled in 3 months after discharge | |
| Aspirin | 461 [8.14%] |
| P2Y12 receptor inhibitor | 1484 [26.2%] |
| ACE inhibitor/ARB | 2373 [41.9%] |
| Beta Blocker | 3389 [59.9%] |
| Statin | 3156 [55.8%] |
| Prior cardiac evaluation | |
| Cardiac stress testing in year before admission with PMI | 1012 [17.9%] |
| Cardiac stress testing during admission with PMI or in three months after discharge | 698 [12.3%] |
| Left heart catheterization in year before admission with PMI | 705 [12.5%] |
| Left heart catheterization during admission with PMI or in three months after discharge | 1501 [26.5%] |
| Echocardiography in year before admission with PMI | 2305 [40.7%] |
| Echocardiography during admission with PMI or in three months after discharge | 4057 [71.7%] |
| Prior Comorbidities | |
| Ischemic heart disease | 2628 [46.4%] |
| Heart failure | 1366 [24.1%] |
| Insulin‐dependent diabetes mellitus | 993 [17.5%] |
| Stroke or transient ischemic attack | 455 [8.04%] |
| Chronic kidney disease stage 3 or higher | 1095 [19.3%] |
| RCRI score | 1 [0–2] |
Note: Mean (standard deviation) is reported for each numeric variable, and count [percent of total] is reported for each categorical variable. Median [IQR] was reported for length of stay and RCRI score due to the non‐normality of these numeric variables.
Abbreviations: GDMT, guideline‐directed medical therapy; PMI, perioperative myocardial infarction; RCRI, revised cardiac risk index.
Before the index admission, 46.4% (n = 2628) of patients had a history of ischemic heart disease, 24.1% (n = 1366) had heart failure, 8.04% (n = 455) had a prior stroke or transient ischemic attack, 19.3% (n = 1095) had chronic kidney disease stage 3 or higher, and 17.5% (n = 993) had insulin‐dependent diabetes. Patients in the general cohort had a median RCRI score of 1 (Interquartile range = 2) before their operation with a PMI. Regarding pre‐existing medication use in the year before admission, a substantial proportion of patients were on cardiovascular medications before admission: 55.5% (n = 3141) on statins, 53.2% (n = 3009) on ACE inhibitors or ARBs, 52.2% (n = 2954) on beta‐blockers, and 22.7% (n = 1283) on P2Y12 receptor inhibitors. However, only 4.6% (n = 261) of patients had a record of filled aspirin prescriptions.
Cardiac complications were observed in 36% (n = 2037) of patients during the index admission, while noncardiac complications occurred in 34.5% (n = 1952). The most frequently occurring cardiac complications included atrial fibrillation (n = 1299 [23%]) and acute heart failure (n = 837 [14.8%]), while the most frequently occurring noncardiac complication was respiratory failure (n = 1680 [29.7%]) (Table 1).
During the index hospitalization to 3 months post‐discharge, 81.0% (n = 4582) of patients were evaluated by a cardiologist, 75.2% (n = 4254) by an internal medicine physician, and 57.7% (n = 3267) by a family medicine physician. Broken down within this interval of time, during the index hospitalization, 75.6% (n = 4277) of patients were evaluated by a cardiologist, 61.4% (n = 3477) by an internal medicine physician, and 25.8% (n = 1458) by a family medicine physician; and in the 3 months following discharge 55.0% (n = 3144) of patients were evaluated by a cardiologist, 57.0% (n = 3229) by an internal medicine physician, and 50.6% (n = 2862) by a family medicine physician.
3.2. Guideline Directed Medical Therapy Following Perioperative Myocardial Infarction
The overall prescription rate of GDMT was relatively low, with 22.1% of patients receiving no GDMT prescriptions (Table 2). Patients filled prescriptions from a mean of 1.88 GDMT drug categories (SD = 1.34), indicating that while most patients were on at least one GDMT drug, they typically received, on average, only one to two classes of GDMT medication. The most common medication classes with filled prescriptions overall were statins (55.8% of patients), ACE inhibitors/ARBs (41.9% of patients), and Beta‐blockers (59.9% of patients). Only 8.14% of patients filled prescriptions for aspirin.
Table 2.
Characteristics among patients with PMI Who received 0, 1, 2, 3, or 4 GDMT medication classes following PMI.
| Characteristics | Number of GDMT Drug Classes with Prescriptions Filled | Adjusted p‐value | ||||
|---|---|---|---|---|---|---|
| 0 (n = 1251) | 1 (n = 968) | 2 (n = 1374) | 3 (n = 1323) | 4 (n = 744) | ||
| Age | 67.4 (13.2) | 68.7 (12.7) | 68.7 (12.3) | 68.2 (11.4) | 66 (10.5) | < 0.001 |
| Length of stay (days) | 9 [5–18] | 7 [4–13] | 8 [4–14] | 7 [4–12] | 7 [4–12] | < 0.001 |
| Year | < 0.001 | |||||
| 2016 | 313 [25%] | 212 [21.9%] | 287 [20.9%] | 345 [26.1%] | 166 [22.3%] | |
| 2017 | 249 [19.9%] | 181 [18.7%] | 209 [15.2%] | 230 [17.4%] | 140 [18.8%] | |
| 2018 | 161 [12.9%] | 99 [10.2%] | 184 [13.4%] | 175 [13.2%] | 127 [17.1%] | |
| 2019 | 169 [13.5%] | 147 [15.2%] | 214 [15.6%] | 178 [13.5%] | 104 [14%] | |
| 2020 | 191 [15.3%] | 190 [19.6%] | 272 [19.8%] | 221 [16.7%] | 118 [15.9%] | |
| 2021 | 168 [13.4%] | 139 [14.4%] | 208 [15.1%] | 174 [13.2%] | 89 [12%] | |
| Sex = Male | 623 [49.8%] | 498 [51.4%] | 756 [55%] | 849 [64.2%] | 497 [66.8%] | < 0.001 |
| Urgency of Procedure = Emergent | 256 [20.5%] | 193 [19.9%] | 281 [20.5%] | 216 [16.3%] | 107 [14.4%] | < 0.001 |
| Type of surgery | < 0.001 | |||||
| Vascular | 226 [18.1%] | 173 [17.9%] | 356 [25.9%] | 423 [32%] | 294 [39.5%] | |
| Central Nervous System | 42 [3.36%] | 32 [3.31%] | 31 [2.26%] | 35 [2.65%] | 14 [1.88%] | |
| Female Reproductive System | 20 [1.6%] | 12 [1.24%] | 19 [1.38%] | 12 [0.907%] | 6 [0.806%] | |
| Gastrointestinal | 185 [14.8%] | 145 [15%] | 179 [13%] | 154 [11.6%] | 88 [11.8%] | |
| General Region | 21 [1.68%] | 32 [3.31%] | 39 [2.84%] | 28 [2.12%] | 18 [2.42%] | |
| Hepatobiliary and Pancreas | 80 [6.39%] | 78 [8.06%] | 100 [7.28%] | 62 [4.69%] | 22 [2.96%] | |
| Lymphatic and Hemic System | 19 [1.52%] | 11 [1.14%] | 15 [1.09%] | 17 [1.28%] | 5 [0.672%] | |
| Male Reproductive | 12 [0.959%] | 14 [1.45%] | 8 [0.582%] | 17 [1.28%] | 9 [1.21%] | |
| Musculoskeletal, Subcutaneous, and Fascia | 438 [35%] | 343 [35.4%] | 460 [33.5%] | 435 [32.9%] | 231 [31%] | |
| Respiratory System | 150 [12%] | 68 [7.02%] | 85 [6.19%] | 53 [4.01%] | 23 [3.09%] | |
| Urinary System | 31 [2.48%] | 37 [3.82%] | 55 [4%] | 57 [4.31%] | 16 [2.15%] | |
| Other Procedures | 27 [2.16%] | 23 [2.38%] | 27 [1.97%] | 30 [2.27%] | 18 [2.42%] | |
| GDMT class prescription filled in 12 months before admission | ||||||
| Aspirin | 36 [2.88%] | 37 [3.82%] | 46 [3.35%] | 75 [5.67%] | 67 [9.01%] | < 0.001 |
| P2Y12 receptor inhibitor | 135 [10.8%] | 114 [11.8%] | 245 [17.8%] | 433 [32.7%] | 356 [47.8%] | < 0.001 |
| ACE inhibitor/ARB | 343 [27.4%] | 429 [44.3%] | 748 [54.4%] | 908 [68.6%] | 581 [78.1%] | < 0.001 |
| Beta Blocker | 337 [26.9%] | 433 [44.7%] | 785 [57.1%] | 897 [67.8%] | 502 [67.5%] | < 0.001 |
| Statin | 327 [26.1%] | 424 [43.8%] | 856 [62.3%] | 977 [73.8%] | 557 [74.9%] | < 0.001 |
| GDMT class prescription filled in 3 months after discharge | ||||||
| Aspirin | 0 [0%] | 29 [3%] | 84 [6.11%] | 156 [11.8%] | 192 [25.8%] | < 0.001 |
| P2Y12 receptor inhibitor | 0 [0%] | 38 [3.93%] | 197 [14.3%] | 580 [43.8%] | 669 [89.9%] | < 0.001 |
| ACE inhibitor/ARB | 0 [0%] | 208 [21.5%] | 570 [41.5%] | 851 [64.3%] | 744 [100%] | < 0.001 |
| Beta Blocker | 0 [0%] | 425 [43.9%] | 987 [71.8%] | 1233 [93.2%] | 744 [100%] | < 0.001 |
| Statin | 0 [0%] | 271 [28%] | 929 [67.6%] | 1212 [91.6%] | 744 [100%] | < 0.001 |
| Evaluation by physician during admission with PMI or in 3 months post discharge | ||||||
| Cardiologist | 971 [77.6%] | 778 [80.4%] | 1108 [80.6%] | 1095 [82.8%] | 630 [84.7%] | < 0.001 |
| Family Medicine | 675 [54%] | 575 [59.4%] | 817 [59.5%] | 761 [57.5%] | 439 [59%] | 0.033 |
| Internal Medicine (not elsewhere classified) | 914 [73.1%] | 731 [75.5%] | 1059 [77.1%] | 995 [75.2%] | 555 [74.6%] | 0.21 |
Note: p‐values are computed by an ANOVA test for numeric variables and a chi‐square test for categorical variables and adjusted to a false discovery rate of 0.05 using the Benjamini‐Hochberg procedure. Mean (standard deviation) is reported for each numeric variable, and count [percent of total] is reported for each categorical variable. A Kruskal‐Wallis test was performed, and the median [IQR] was reported for the length of stay due to the non‐normality of this variable. An adjusted p‐value less than 0.05 was considered significant.
Abbreviations: GDMT, guideline‐directed medical therapy; PMI, perioperative myocardial infarction.
Cardiology evaluation was significantly associated with an increase in the likelihood of receiving at least one GDMT prescription (78.8% of patients with cardiology evaluation had at least one GDMT prescription vs 74.0% of patients without cardiology evaluation, p < 0.001). Patients who received cardiology evaluation were also significantly more likely to receive prescriptions for two or more GDMT medication classes compared to those without cardiology evaluation (61.8% vs. 56.4%, absolute risk difference 5.4%, 95% CI 2.2–8.7%, p < 0.001). The Poisson regression model showed that cardiology evaluation was associated with an increased number of GDMT prescriptions (OR = 1.10 [95% CI 1.05–1.17], p < 0.001) (Table S6). This indicates that patients who saw a cardiologist filled prescriptions in 1.1 times as many GDMT classes compared to those who did not (mean 1.92 GDMT classes vs 1.73).
3.3. Left Heart Catheterization or Cardiac Stress Testing Following Perioperative Myocardial Infarction
Overall, 35.3% of patients underwent left heart catheterization or cardiac stress testing during or within 3 months after the index hospitalization (Table 3). Patients who had a cardiology evaluation were significantly more likely to undergo these procedures compared to those who did not (38.2% vs 23.0%, p < 0.001).
Table 3.
Characteristics among patients with PMI who did or did not receive ischemic evaluation following PMI.
| Characteristics | Ischemic Evaluation during hospitalization or in 3 months after discharge | Adjusted p‐value | |
|---|---|---|---|
| Yes (n = 2000) | No (n = 3660) | ||
| Age | 66.5 (10.9) | 68.8 (12.8) | < 0.001 |
| Length of stay (days) | 8 [4–14] | 7 [4–14] | 0.018 |
| Year | < 0.001 | ||
| 2016 | 503 [25.2%] | 820 [22.4%] | |
| 2017 | 413 [20.6%] | 596 [16.3%] | |
| 2018 | 265 [13.2%] | 481 [13.1%] | |
| 2019 | 280 [14%] | 532 [14.5%] | |
| 2020 | 307 [15.4%] | 685 [18.7%] | |
| 2021 | 232 [11.6%] | 546 [14.9%] | |
| Sex = Male | 1190 [59.5%] | 2033 [55.5%] | 0.0076 |
| Urgency of Procedure = Emergent | 357 [17.8%] | 696 [19%] | 0.33 |
| Type of surgery | < 0.001 | ||
| Vascular | 657 [32.8%] | 815 [22.3%] | |
| Central Nervous System | 35 [1.75%] | 119 [3.25%] | |
| Female Reproductive System | 27 [1.35%] | 42 [1.15%] | |
| Gastrointestinal | 262 [13.1%] | 489 [13.4%] | |
| General Region | 46 [2.3%] | 92 [2.51%] | |
| Hepatobiliary and Pancreas | 115 [5.75%] | 227 [6.2%] | |
| Lymphatic and Hemic System | 19 [0.95%] | 48 [1.31%] | |
| Male Reproductive | 21 [1.05%] | 39 [1.07%] | |
| Musculoskeletal, Subcutaneous, and Fascia | 587 [29.4%] | 1320 [36.1%] | |
| Respiratory System | 116 [5.8%] | 263 [7.19%] | |
| Urinary System | 63 [3.15%] | 133 [3.63%] | |
| Other Procedures | 52 [2.6%] | 73 [1.99%] | |
| Evaluation by physician during admission with PMI or in 3 months post discharge | |||
| Cardiologist | 1752 [87.6%] | 2830 [77.3%] | < 0.001 |
| Family Medicine | 1216 [60.8%] | 2051 [56%] | 0.0012 |
| Internal Medicine (not elsewhere classified) | 1541 [77%] | 2713 [74.1%] | 0.022 |
| Complications during admission with PMI | |||
| Cardiac complication | 830 [41.5%] | 1207 [33%] | < 0.001 |
| Noncardiac complication | 713 [35.6%] | 1239 [33.9%] | 0.21 |
| Prior cardiac evaluation | |||
| Cardiac stress testing in year before admission with PMI | 344 [17.2%] | 668 [18.3%] | 0.36 |
| Left heart catheterization in year before admission with PMI | 178 [8.9%] | 527 [14.4%] | < 0.001 |
| Echocardiography in year before admission with PMI | 729 [36.4%] | 1576 [43.1%] | < 0.001 |
| Echocardiography during admission with PMI | 1563 [78.1%] | 2037 [55.7%] | < 0.001 |
Note: p‐values are computed by a student's t‐test for numeric variables and a chi‐square test for categorical variables and adjusted to a false discovery rate of 0.05 using the Benjamini‐Hochberg procedure. Mean (standard deviation) is reported for each numeric variable, and count [percent of total] is reported for each categorical variable. A Mann‐Whitney U test was performed, and the median [IQR] was reported for the length of stay due to the non‐normality of this variable. An adjusted p‐value less than 0.05 was considered significant.
Abbreviation: PMI, perioperative myocardial infarction.
The logistic regression model showed that cardiology evaluation was strongly associated with an increased likelihood of catheterization or stress testing (OR = 1.82 [95% CI 1.53–2.18], p < 0.001) (Table S7). Other factors significantly associated with the increased likelihood of these procedures included echocardiography during admission. Notably, prior left heart catheterization in the year before the index admission was associated with a decreased likelihood of follow‐up catheterization or stress testing (OR = 0.55 [95% CI 0.45–0.68], p < 0.001). While the presence of one or more cardiac complications during admission was positively associated with follow‐up catheterization or stress testing (OR = 1.41 [95% CI 1.24–1.60], p < 0.001), the presence of a noncardiac complication was negatively associated with the same outcome (OR = 0.81 [95% CI 0.70–0.93], p = 0.002). Evaluation by a family medicine physician was also significantly associated with an increased likelihood of ischemic testing, though with a smaller effect size (OR = 1.22 [95% CI 1.09–1.38], p < 0.001).
3.4. Echocardiography Following Perioperative Myocardial Infarction
Echocardiography was performed in 71.7% of patients during the index admission or within 3 months of discharge (Table 4). Patients who had cardiology evaluation were significantly more likely to undergo echocardiography compared to those who did not (75.9% vs 53.6%, p < 0.001).
Table 4.
Characteristics among patients with PMI who did or did not receive echocardiography following PMI.
| Characteristics | Echocardiography during hospitalization or in 3 months after discharge | Adjusted p‐value | |
|---|---|---|---|
| Yes (n = 4057) | No (n = 1603) | ||
| Age | 68.3 (12.1) | 67.2 (12.3) | 0.0026 |
| Length of stay (days) | 9 [5–16] | 5 [3–8] | < 0.001 |
| Year | 0.79 | ||
| 2016 | 939 [23.1%] | 384 [24%] | |
| 2017 | 733 [18.1%] | 276 [17.2%] | |
| 2018 | 528 [13%] | 218 [13.6%] | |
| 2019 | 593 [14.6%] | 219 [13.7%] | |
| 2020 | 701 [17.3%] | 291 [18.2%] | |
| 2021 | 563 [13.9%] | 215 [13.4%] | |
| Sex = Male | 2290 [56.4%] | 933 [58.2%] | 0.27 |
| Urgency of Procedure = Emergent | 790 [19.5%] | 263 [16.4%] | 0.011 |
| Type of surgery | < 0.001 | ||
| Vascular | 1155 [28.5%] | 317 [19.8%] | |
| Central Nervous System | 119 [2.93%] | 35 [2.18%] | |
| Female Reproductive System | 44 [1.08%] | 25 [1.56%] | |
| Gastrointestinal | 542 [13.4%] | 209 [13%] | |
| General Region | 93 [2.29%] | 45 [2.81%] | |
| Hepatobiliary and Pancreas | 222 [5.47%] | 120 [7.49%] | |
| Lymphatic and Hemic System | 47 [1.16%] | 20 [1.25%] | |
| Male Reproductive | 39 [0.961%] | 21 [1.31%] | |
| Musculoskeletal, Subcutaneous, and Fascia | 1270 [31.3%] | 637 [39.7%] | |
| Respiratory System | 304 [7.49%] | 75 [4.68%] | |
| Urinary System | 132 [3.25%] | 64 [3.99%] | |
| Other Procedures | 90 [2.22%] | 35 [2.18%] | |
| Evaluation by physician during admission with PMI or in 3 months post discharge | |||
| Cardiologist | 3479 [85.8%] | 1103 [68.8%] | < 0.001 |
| Family Medicine | 2473 [61%] | 794 [49.5%] | < 0.001 |
| Internal Medicine (not elsewhere classified) | 3176 [78.3%] | 1078 [67.2%] | < 0.001 |
| Complications during admission with PMI | |||
| Cardiac complication | 1706 [42.1%] | 331 [20.6%] | < 0.001 |
| Noncardiac complication | 1693 [41.7%] | 259 [16.2%] | < 0.001 |
| Prior cardiac evaluation | |||
| Cardiac stress testing in year before admission with PMI | 643 [15.8%] | 369 [23%] | < 0.001 |
| Cardiac stress testing during admission with PMI | 296 [7.3%] | 50 [3.12%] | < 0.001 |
| Left heart catheterization in year before admission with PMI | 460 [11.3%] | 245 [15.3%] | < 0.001 |
| Left heart catheterization during admission with PMI | 1096 [27%] | 166 [10.4%] | < 0.001 |
| Echocardiography in year before admission with PMI | 1553 [38.3%] | 752 [46.9%] | < 0.001 |
Note: p‐values are computed by a student's t‐test for numeric variables and a chi‐square test for categorical variables and adjusted to a false discovery rate of 0.05 using the Benjamini‐Hochberg procedure. Mean (standard deviation) is reported for each numeric variable, and count [percent of total] is reported for each categorical variable. A Mann‐Whitney U test was performed, and the median [IQR] was reported for the length of stay due to the non‐normality of this variable. An adjusted p‐value less than 0.05 was considered significant.
Abbreviation: PMI, perioperative myocardial infarction.
The logistic regression model demonstrated that cardiology evaluation was strongly associated with an increased likelihood of echocardiography (OR = 2.29 [95% CI 1.93–2.71], p < 0.001) (Table S8). Other factors significantly associated with increased likelihood of echocardiography included cardiac complications and noncardiac complications. Evaluation by a family medicine physician was also significantly associated with an increased likelihood of echocardiography, though with a smaller effect size (OR = 1.35 [95% CI 1.18–1.54], p < 0.001).
4. Discussion
4.1. Frequency of Cardiology Evaluation Following PMI and Association With Increased Management Frequency
In our retrospective cohort study of management of patients with PMI, nearly one in five patients (19%) with PMI did not receive evaluation by a cardiologist during the index hospitalization or within 3 months after discharge. We observed that cardiology evaluation was associated with increased use of guideline‐recommended management including GDMT, ischemic testing, and echocardiography following PMI.
Patients who saw a cardiologist filled prescriptions in more GDMT classes of medications and were significantly more likely to undergo ischemic testing and echocardiography than those who did not. Furthermore, even in cases where the presence of either internal medicine (not elsewhere specified) or family medicine evaluation was also significantly positively associated with the frequency of these management outcomes, cardiology evaluation demonstrated a larger effect size compared to these other specialties. These findings suggest that the lack of specifically cardiology involvement in PMI management may contribute to decreased frequency of guideline‐recommended care, though we cannot directly determine causation given the retrospective nature of the study.
Our findings regarding the impact of cardiology evaluation on GDMT prescriptions and cardiac testing are consistent with previous studies in patients with nonsurgical myocardial infarction or injury. McCarthy et al. (2020) found that cardiology consultation during hospitalization for a type 2 myocardial infarction is associated with an increased likelihood of coronary angiography, stress testing, and transthoracic echocardiography as well as an increased likelihood of being discharged on a statin, clopidogrel, or a beta blocker [22]. Our study extends these findings to the specific context of perioperative myocardial infarction, where management may be complicated by surgical factors.
4.2. Temporal Trends in GDMT Prescription Patterns
Interestingly, we observed a declining trend in the proportion of patients receiving GDMT medications over the study period (2016–2021). This unexpected finding may reflect several possibilities: (1) increasing recognition of Type 2 MI, which may be managed differently than Type 1 MI; (2) growing concerns about bleeding risks associated with antiplatelet therapy in surgical patients; (3) changes in prescribing patterns due to evolving evidence regarding the benefits of GDMT in specific perioperative contexts; or (4) shifts in documentation or billing practices affecting our ability to capture medication use. This trend warrants further investigation in future studies specifically designed to examine temporal changes in PMI management.
4.3. Factors Associated With Likelihood of Ischemic Evaluation Following PMI
The ischemic evaluation model revealed notable patterns in the frequency of left heart catheterization or cardiac stress testing after PMI. Diagnoses that suggested a noncardiac etiology (e.g., sepsis, hypovolemic shock, respiratory failure, or pulmonary embolism) that occurred during the index admission with PMI were associated with a lower likelihood of catheterization or cardiac stress testing. In contrast, cardiac complications, such as heart failure and cardiogenic shock, were positively associated with ischemic evaluation. This pattern, assuming the complications occurred before the PMI, suggests that an increased likelihood of presumed Type 1 MI (i.e., due to plaque rupture and coronary thrombosis) drives further cardiac workup of PMI, while PMI likely due to other causes may not lead to additional coronary evaluation [23]. Furthermore, the presence of left heart catheterization in the year before the index admission was negatively associated with repeat left heart catheterization or cardiac stress testing following PMI, suggesting that knowledge of information regarding coronary disease from prior testing reduces repeat evaluation.
4.4. Echocardiography Is Frequent Following PMI
The echocardiography model showed predominantly positive coefficients across various cardiac and noncardiac comorbidities and complications. This suggests that providers generally view echocardiography as a valuable tool to assess myocardial function in the context of PMI, regardless of the presumed etiology, and this is supported by management guidelines [24]. In addition, the widespread use of echocardiography, with 71.7% of patients undergoing the procedure, may be driven by the need for comprehensive cardiac assessment in these high‐risk patients and the relatively greater access to echocardiography compared to left heart catheterization or cardiac stress testing. This widespread use of echocardiography is also consistent with 2019 Appropriate Use Criteria [24].
4.5. Heterogeneity in Management and Potential Implications
Our study reveals significant heterogeneity in the management of PMI, highlighting the current lack of consensus on optimal care. The observed differences between patients who did and did not receive cardiology evaluation reflect potential disparities in treatment approaches and underscore the critical need for further research to determine best practices and improve outcomes. Patients who experience PMI are at increased risk of subsequent cardiac events [6], emphasizing the importance of effective management strategies for this high‐risk population.
Our findings regarding the potential impact of cardiology evaluation can be considered alongside previous literature examining the implementation of cardiology recommendations. Marques et al. studied 589 hospitalized patients who received cardiology consultations and found that when the primary teams did not adhere to cardiology recommendations, patients had significantly worse outcomes (OR = 10.25 [95% CI 4.45–23.62]) [25]. While their study focused on adherence to recommendations among patients who received cardiology consultation rather than comparing patients with and without cardiology evaluation as in our study, their findings support the broader concept that optimal consultation and implementation of cardiology expertise is associated with better care. Their identification of specific factors associated with increased adherence to recommendations, such as follow‐up notes and verbal reinforcement, suggests potential strategies to improve the implementation of cardiology recommendations in the post‐PMI setting.
It is also worth noting that the evidence base for PMI management remains limited. To date, the only medication specifically evaluated for postoperative MI is dabigatran, as investigated in the MANAGE trial [26]. Our findings provide a foundation for future studies to explore the effectiveness of different management strategies and develop evidence‐based guidelines for PMI management.
4.6. Limitations
Our study has several limitations. The use of claims data limits our ability to assess the clinical decision‐making process and the appropriateness of interventions in individual cases. Therefore, it is difficult to comment on the appropriateness of utilization or lack of utilization of certain management strategies following PMI in this study. Additionally, the lack of additional clinical confirmation of myocardial infarctions and strokes/transient ischemic attacks may have led to misclassification of these events. However, these codes are moderately robust at capturing clinically validated events, as the ICD codes have been validated in prior studies (Table S9) [27, 28, 29, 30, 31, 32, 33]. The capture of cardiac testing may also be incomplete due to our reliance on procedural terminology codes. However, while extensive validation studies of such codes are limited, a recent study examining intraoperative transesophageal echocardiography (TEE) Current Procedural Terminology codes found them to be 99.88% sensitive and 100% specific for the identification of TEE [34]. This suggests procedural codes adequately capture the implementation of major cardiac diagnostic tests.
Our medication analysis likely underestimates the true use of certain therapies, particularly aspirin, as we cannot capture over‐the‐counter medication purchases through claims data. Similarly, we could not assess for medication contraindications, which may have influenced GDMT prescription rates. We are unable to make conclusions about causation, given the retrospective nature of our study. As we excluded patients without insurance coverage in the 3 months following discharge from their hospitalization, we, by definition, excluded patients who died during this period.
5. Conclusions
In conclusion, our study demonstrates variations in the frequency of guideline‐based management strategies for PMI and their association with specialty consultation. By highlighting the positive impact of cardiology evaluation and identifying gaps in current practice, these findings may inform efforts to enhance the quality of care for this high‐risk patient population.
Future research should focus on evaluating the impact of these management strategies on long‐term outcomes for PMI patients. In addition, investigating barriers to implementing guideline‐recommended care and developing interventions to improve adherence to GDMT and appropriate use of diagnostic procedures could help optimize care for patients following PMI.
Ethics Statement
Ethical approval was not sought for the present study because the research utilized secondary data that does not contain individually identifiable information.
Conflicts of Interest
The authors declare no conflicts of interest.
Supporting information
Acknowledgments
AH is supported by a National Institutes of Health training grant under award number T32GM150375. DR is supported by the National Institute on Aging of the National Institutes of Health under award number R03AG078957.
Data Availability Statement
The data that support the findings of this study are available from IBM MarketScan Research Databases. Restrictions apply to the availability of these data, which were used under license for this study. Data are available from https://www.ibm.com/watson/health/resources/ipv-opv/ with the permission of IBM MarketScan Research Databases.
Data used in this study were obtained from IBM MarketScan Research Databases under a licensed agreement. While these data support the study's findings, they are not publicly accessible. Researchers interested in accessing these data must contact IBM MarketScan directly and are subject to licensing restrictions.
References
- 1. Devereaux P. J., Xavier D., Pogue J., et al., “Characteristics and Short‐Term Prognosis of Perioperative Myocardial Infarction in Patients Undergoing Noncardiac Surgery: A Cohort Study,” Annals of Internal Medicine 154 (2011): 523–528. [DOI] [PubMed] [Google Scholar]
- 2. Smilowitz N. R., Gupta N., Guo Y., Berger J. S., and Bangalore S., “Perioperative Acute Myocardial Infarction Associated With Non‐Cardiac Surgery,” European Heart Journal 38 (2017): 2409–2417. [DOI] [PubMed] [Google Scholar]
- 3. Rubin D. S., Lin A. Z., Ward R. P., and Nagele P., “Trends and In‐Hospital Mortality for Perioperative Myocardial Infarction After the Introduction of a Diagnostic Code for Type 2 Myocardial Infarction in the United States Between 2016 and 2018,” Anesthesia & Analgesia 138 (2024): 420–429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Puelacher C., Gualandro D. M., Glarner N., et al., “Long‐Term Outcomes of Perioperative Myocardial Infarction/Injury After Non‐Cardiac Surgery,” European Heart Journal 44 (2023): 1690–1701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Puelacher C., Lurati Buse G., Seeberger D., et al., “Perioperative Myocardial Injury After Noncardiac Surgery: Incidence, Mortality, and Characterization,” Circulation 137 (2018): 1221–1232. [DOI] [PubMed] [Google Scholar]
- 6. Roshanov P. S., Chan M. T. V., Borges F. K., et al., “One‐Year Outcomes After Discharge From Noncardiac Surgery and Association between Predischarge Complications and Death after Discharge: Analysis of the VISION Prospective Cohort Study,” Anesthesiology 140 (2024): 8–24. [DOI] [PubMed] [Google Scholar]
- 7. Beaulieu R. J., Sutzko D. C., Albright J., Jeruzal E., Osborne N. H., and Henke P. K., “Association of High Mortality With Postoperative Myocardial Infarction After Major Vascular Surgery Despite Use of Evidence‐Based Therapies,” JAMA Surgery 155 (2020): 131–137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. O'Gara P. T., Kushner F. G., Ascheim D. D., et al., “2013 ACCF/AHA Guideline for the Management of ST‐Elevation Myocardial Infarction,” Circulation 127 (2013): e362–e425. [DOI] [PubMed] [Google Scholar]
- 9. Amsterdam E. A., Wenger N. K., Brindis R. G., et al., “2014 AHA/ACC Guideline for the Management of Patients With Non–ST‐Elevation Acute Coronary Syndromes,” Circulation 130 (2014): e139–e228. [DOI] [PubMed] [Google Scholar]
- 10. Gouya G., Reichardt B., Ohrenberger G., and Wolzt M., “Survival of Patients Discharged After Acute Myocardial Infarction and Evidence‐Based Drug Therapy,” European Journal of Epidemiology 22 (2007): 145–149. [DOI] [PubMed] [Google Scholar]
- 11. Rogers A. M., Ramanath V. S., Grzybowski M., et al., “The Association Between Guideline‐Based Treatment Instructions at the Point of Discharge and Lower 1‐Year Mortality in Medicare Patients After Acute Myocardial Infarction: The American College of Cardiology's Guidelines Applied in Practice (GAP) Initiative In Michigan,” American Heart Journal 154 (2007): 461–469. [DOI] [PubMed] [Google Scholar]
- 12. Rasmussen J. N., Chong A., and Alter D. A., “Relationship Between Adherence to Evidence‐Based Pharmacotherapy and Long‐Term Mortality After Acute Myocardial Infarction,” Journal of the American Medical Association 297 (2007): 177–186. [DOI] [PubMed] [Google Scholar]
- 13. Shanbhag D., Graham I. D., Harlos K., et al., “Effectiveness of Implementation Interventions in Improving Physician Adherence to Guideline Recommendations in Heart Failure: A Systematic Review,” BMJ Open 8 (2018): e017765. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Winchester D. E., Merritt J., Waheed N., et al., “Implementation of Appropriate Use Criteria for Cardiology Tests and Procedures: A Systematic Review and Meta‐Analysis,” European Heart Journal ‐ Quality of Care and Clinical Outcomes 7 (2021): 34–41. [DOI] [PubMed] [Google Scholar]
- 15. Rubin D. S., Hughey R., Gerlach R. M., Ham S. A., Ward R. P., and Nagele P., “Frequency and Outcomes of Preoperative Stress Testing in Total Hip and Knee Arthroplasty From 2004 to 2017,” JAMA Cardiology 6 (2021): 13–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Adamson D., Chang S., and Hansen L. G., “Health Research Data for the Real World: The MarketScan Databases,” Thomson Healthc (2008): 1–32. [Google Scholar]
- 17. Procedure Classes Refined for ICD‐10‐PCS [Internet] [cited 2024 Jul 28], https://hcup-us.ahrq.gov/toolssoftware/procedureicd10/procedure_icd10.jsp.
- 18. Organization W. H., ICD‐10: International Statistical Classification of Diseases and Related Health Problems: Tenth Revision [Internet] (World Health Organization, 2004), [2024 Jul 28], https://iris.who.int/handle/10665/42980. [Google Scholar]
- 19. Davis C., Tait G., Carroll J., Wijeysundera D. N., and Beattie W. S., “The Revised Cardiac Risk Index in the New Millennium: A Single‐Centre Prospective Cohort Re‐Evaluation of the Original Variables in 9519 Consecutive Elective Surgical Patients,” Canadian Journal of Anesthesia/Journal Canadien D'anesthésie 60 (2013): 855–863. [DOI] [PubMed] [Google Scholar]
- 20. Clinical Classifications Software Refined (CCSR) for ICD‐10‐CM Diagnoses [Internet] , [cited 2024 Aug 16], https://hcup-us.ahrq.gov/toolssoftware/ccsr/dxccsr.jsp.
- 21. R Core Team . R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria [Internet]. (2022), https://www.R-project.org/.
- 22. McCarthy C. P., Olshan D. S., Rehman S., et al., “Cardiologist Evaluation of Patients With Type 2 Myocardial Infarction,” Circulation: Cardiovascular Quality and Outcomes 14 (2021): e007440. [DOI] [PubMed] [Google Scholar]
- 23. Sabatine M. S., “Differentiating Type 1 and Type 2 Myocardial Infarction: Unfortunately, Still More Art Than Science,” JAMA Cardiology 6 (2021): 781. [DOI] [PubMed] [Google Scholar]
- 24. Writing Group Members, Doherty J. U., Kort S., et al., “ACC/AATS/AHA/ASE/ASNC/HRS/SCAI/SCCT/SCMR/STS 2019 Appropriate Use Criteria for Multimodality Imaging in the Assessment of Cardiac Structure and Function in Nonvalvular Heart Disease: A Report of the American College of Cardiology Appropriate Use Criteria Task Force, American Association for Thoracic Surgery, American Heart Association, American Society of Echocardiography, American Society of Nuclear Cardiology, Heart Rhythm Society, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, Society for Cardiovascular Magnetic Resonance, and the Society of Thoracic Surgeons,” Journal of the American Society of Echocardiography 32 (2019): 553–579. [DOI] [PubMed] [Google Scholar]
- 25. Marques A. C., Calderaro D., Yu P. C., et al., “Impact of Cardiology Referral: Clinical Outcomes and Factors Associated With Physicians’ Adherence to Recommendations,” Clinics 69 (2014): 666–671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Devereaux P. J., Duceppe E., Guyatt G., et al., “Dabigatran in Patients With Myocardial Injury after Non‐Cardiac Surgery (MANAGE): An International, Randomised, Placebo‐Controlled Trial,” Lancet 391 (2018): 2325–2334. [DOI] [PubMed] [Google Scholar]
- 27. Merry A. H. H., Boer J. M. A., Schouten L. J., et al., “Validity of Coronary Heart Diseases and Heart Failure Based on Hospital Discharge and Mortality Data in the Netherlands Using the Cardiovascular Registry Maastricht Cohort Study,” European Journal of Epidemiology 24 (2009): 237–247. [DOI] [PubMed] [Google Scholar]
- 28. Pajunen P., Koukkunen H., Ketonen M., et al., “The Validity of the Finnish Hospital Discharge Register and Causes of Death Register Data on Coronary Heart Disease,” European Journal of Cardiovascular Prevention & Rehabilitation 12 (2005): 132–137. [DOI] [PubMed] [Google Scholar]
- 29. Kennedy G. T., Stern M. P., and Crawford M. H., “Miscoding of Hospital Discharges as Acute Myocardial Infarction: Implications for Surveillance Programs Aimed at Elucidating Trends in Coronary Artery Disease,” American Journal of Cardiology 53 (1984): 1000–1002. [DOI] [PubMed] [Google Scholar]
- 30. Austin P. C., Daly P. A., and Tu J. V., “A Multicenter Study of the Coding Accuracy of Hospital Discharge Administrative Data for Patients Admitted to Cardiac Care Units in Ontario,” American Heart Journal 144 (2002): 290–296. [DOI] [PubMed] [Google Scholar]
- 31. Pladevall M., Goff D. C., Nichaman M. Z., et al., “An Assessment of the Validity of ICD Code 410 to Identify Hospital Admissions for Myocardial Infarction: The Corpus Christi Heart Project,” International Journal of Epidemiology 25 (1996): 948–952. [DOI] [PubMed] [Google Scholar]
- 32. Columbo J. A., Daya N., Colantonio L. D., et al., “Derivation and Validation of ICD‐10 Codes for Identifying Incident Stroke,” JAMA Neurology 81 (2024): 875–881. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Tirschwell D. L. and Longstreth W. T., “Validating Administrative Data in Stroke Research,” Stroke 33 (2002): 2465–2470. [DOI] [PubMed] [Google Scholar]
- 34. MacKay E. J., Salmon M. K., Fatuzzo M. R., et al., “Validation of Claims Data for the Identification of Intraoperative Transesophageal Echocardiography During Cardiac Surgery,” Journal of Cardiothoracic and Vascular Anesthesia 35 (2021): 3193–3198. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The data that support the findings of this study are available from IBM MarketScan Research Databases. Restrictions apply to the availability of these data, which were used under license for this study. Data are available from https://www.ibm.com/watson/health/resources/ipv-opv/ with the permission of IBM MarketScan Research Databases.
Data used in this study were obtained from IBM MarketScan Research Databases under a licensed agreement. While these data support the study's findings, they are not publicly accessible. Researchers interested in accessing these data must contact IBM MarketScan directly and are subject to licensing restrictions.
