ORIGINAL RESEARCH article

Front. Surg., 09 September 2021

Sec. Cardiovascular Surgery

Volume 8 - 2021 | https://doi.org/10.3389/fsurg.2021.678806

Incidence and Outcome of Acute Myocardial Infarction in Patients With Aortic Dissection and Risk Factor Control

  • 1. Department of Cardiology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China

  • 2. Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT, United States

  • 3. The Key Laboratory of Remodeling-Related Cardiovascular Disease, Department of Cardiology, Ministry of Education, Beijing Anzhen Hospital, Beijing Institute of Heart Lung and Blood Vessel Disease, Capital Medical University, Beijing, China

  • 4. Department of General Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China

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Abstract

Background and Aims: The contradiction of management modality between acute myocardial infarction(AMI) and aortic dissection(AD) may result in clinical catastrophe. Data on risk factors, incidence, and outcome of AD and AMI are limited, and there have been no studies on the long-term outcomes of AMI in patients with AD. So we aimed to investigate long-term outcomes after AMI in patients with AD, and propose a useful diagnostic paradigm.

Methods: Consecutively enrolled patients with AD and AMI who were referred to our center from 2010 to 2017. Baseline patient characteristics, risk factors, all medical treatments, echocardiographic parameters, laboratory data, and treatment were recorded. All patients were followed up from the first hospitalization until a first heart event, death, or 17 March, 2018.

Results: 0.13% in AMI and 7.49% in AD patients had a concomitant diagnosis of AD and AMI. The average patient age was 53.3 ± 12.1 years and 84.6% were male. The most prevalent vascular risk factors were hypertension (69.2%) and current smoker (64.1%). Of all the 39 patients, 66.7% were managed surgically. Overall in-hospital mortality was 10.3%. The 30-day and 5-year fatality rates were 23.1% and 35.9%, but were higher for female than for male (66.7 vs. 30.3%, log-rank P = 0.045) on 5-year mortality. The overall survival of females was inferior to the males (log-rank P = 0.045).

Conclusions: Patients with AMI and AD exhibit high 5-year fatality rates. For these patients, surgical management tends to have lower mortality. Improved management of hypertension and smoking, may reduce future incidence rates.

Background

Acute myocardial infarction (AMI) and aortic dissection (AD) are both very serious diseases with high rates of morbidity and mortality which have the same manifestations of chest pain. Acute aortic dissection (AAD) is the most common acute aortic condition requiring urgent surgical therapy, (1) with an incidence of about 3 cases in 100,000 per year (2, 3). Complications such as tamponade, aortic valve insufficiency, and malperfusion occur when the aortic side branches are involved (4). Thus, AAD represents a medical and/or surgical emergency (5). Presenting features are similar, and progression to dissection may occur (6–8). While the initiating event is unknown, most patients have a structural abnormality of the arterial wall and/or systemic hypertension (9, 10). Despite improved surgical techniques and perioperative care, 30-day and 5-year mortality remains high, between 15 and 30% (11, 12).

Many patients with AAD are diagnosed and treated as having acute coronary syndrome (ACS), which is a much more frequent condition than AAD (13). The triple rule-out protocol has been described as the one-stop computed tomography (CT) examination for chest pain designed to differentiate ACS, pulmonary embolism, and AAD (14). But there are a small proportion of patients with AD represent with AMI (approximately 1 ~3.6%) at the same time (15). However, clinical pathways of efficient streamlined care, similar to in ACS, have not yet been implemented (14). For cardiologists, prompt treatment with antiplatelet, antithrombotic, and thrombolytic agents is important once AMI is diagnosed. But the contradiction of management modality between AMI and acute aortic dissection may result in clinical catastrophe (16). Moreover, data on risk factors, incidence, and outcome of AD and AMI are limited, and there have been no studies on the long-term outcomes of AMI in patients with AD. This study, therefore, aimed to investigate long-term outcomes after AMI in patients with AD, and propose a useful diagnostic paradigm.

Methods

Study Population and Baseline Characteristics

All patients (age ≥18 years) with AD and AMI who were referred to Anzhen Hospital in Beijing, China, from January 2010 and December 2017, were consecutively enrolled in this study. Aortic dissection was classified according to the Stanford system into type A (involvingg the ascending aorta protximal to left subclavian artery origin) or type B (involving only the descending aorta) (17). AD diagnosis was based on history, imaging study findings, visualization at surgery, and/or postmortem examination (1). AMI was diagnosed if a patient had a cardiac troponin I level >99th percentile with ≥1 of the following: chest pain lasting >20 min or diagnostic serial electrocardiographic changes consisting of new pathological Q waves, new ST-segment-T-wave changes, or new left bundle branch block (18). The exclusion criteria included rheumatic heart disease, severe congestive heart disease, malignant tumor, and use of the oral contraceptive pill or pregnancy. All participants provided written informed consent.

Baseline patient characteristics were recorded from the patients, their hospital records, and their general practice records, details of the clinical event, medication, past medical history, all investigations relevant to their admission, and all interventions occurring subsequent after the event. Standardized clinical history and cardiovascular examination were recorded. Analyzed risk factors included age, sex, body mass index (BMI), current smoker, hypertension, diabetes, and hyperlipidemia. Clinically relevant comorbidities included cardiac failure, atrial fibrillation, known coronary artery disease, prior aortic dissection, prior myocardial infarction, anterior myocardial infarction, known aortic aneurysm, prior stroke/ transient ischemic attack (TIA), carotid artery disease, peripheral artery disease chronic renal insufficiency and prior cardiac surgery. All medical treatments during hospitalization were recorded, including aspirin, clopidogrel, statin, nitrates, diuretic, warfarin, and antihypertensives.

Echocardiographic parameters were assessed using transthoracic echocardiography with the Teichholz method before coronary angiography (19). Parameters analyzed included pericardial effusion, acute aortic valve insufficiency, left ventricular ejection fraction (LVEF), and ascending aortic diameters.

Laboratory data were collected upon admission to the hospital, including levels of total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), creatine kinase-MB (CK-MB), troponin I (TNI), D-Dimer, homocysteine (Hcy) and high-sensitivity C-reactive protein (hs-CRP).

Coronary angiography was performed according to standard criteria. Offline analysis of digital angiograms was performed in the core laboratory using an automated edge detection system (CMS; Medis Medical Imaging Systems, Leiden, the Netherlands). Binary stenosis was defined as stenosis of >50% of the luminal diameter.

Follow-Up and Definition of Endpoints

The follow-up started on the day of admission. In the hospital, major adverse events recorded included death, cardiogenic shock, ventricular tachyarrhythmia (VT), ventricular fibrillation (VF), acute left-sided heart failure, and acute kidney injury (AKI).

After hospital discharge, adverse events including cardiac death, recurrent myocardial infarction (re-MI), hospital re-admission and recurrent angina. If a recurrent vascular event was suspected, the patient was assessed by a clinical research physician. Event rates were defined as the total number of vascular events that led to different clinical presentations during the study period. An extension of a previous dissection was not considered to be a recurrent event if it occurred within 6 months of the first event.

All patients were followed up from the first hospitalization until a first coronary event, death, or 17 March, 2018. Endpoint status was ascertained via clinic visits, medical records, telephone contact, and text messages. For deceased patients, death certificates were obtained, and the next of kin were interviewed to determine when the death occurred. This study conformed to the principles defined in the Declaration of Helsinki. Local ethical committee approval was obtained. All patients provided their informed consent prior to their inclusion in the study.

Statistical Analysis

Continuous variables with normal distributions were expressed as mean ± standard deviation, and compared using one-way ANOVA analysis of variance or Fisher's exact test. Categorical variables were expressed as frequencies with percentages, and compared using the chi-square test where appropriate. The 95% confidence interval (CI) of annual mortality rate was calculated using the binomial approximation. Survival was graphically represented using Kaplan-Meier curves. Differences in survival rates were compared using the log-rank test. Univariate and multivariate Cox proportional hazards models were used to identify study endpoint predictors. Variables with univariate p values < 0.10 were selected for multivariate analysis and expressed as hazard ratios (HRs) with 95% CIs. Multivariate Cox regression analysis was performed using an enter method. The 95% CI of the annual mortality rate was calculated using GraphPad Prism 7 (GraphPad Software Inc., La Jolla, USA). All other analyses were performed using SPSS statistical software, version 25.0 (SPSS Inc., Chicago, USA). All tests were 2-tailed, and statistical significance was defined as p < 0.05.

Results

Demographics and Risk Factors

From 2010 to 2017, 29,015 patients with AMI and 5,202 patients with AD were identified who were hospitalized in Anzhen Hospital. Of these, 39 AMI patients had a concomitant diagnosis of AD (0.13% in AMI vs. 7.49% in AD) (Figure 1). Table 1 shows the demographics and risk factors for AMI patients with AD by sex and by Stanford classification. The average patient age was 53.3 ± 12.1 years and 84.6% were male. Of the 39 patients, 31 (79.5%) were Stanford type A and 8 (20.5%) were Stanford type B. 6 patients had previous aorta dissection during the study period (3 of them are Stanford type A, 3 are Stanford type B); 11 patients had prior MI (9 are Stanford type A, 2 are Stanford type B). The most prevalent vascular risk factors were hypertension (69.2%) and current smoker (64.1%). Hypertension tended to be more common in Type B patients (P = 0.042, Table 1). There were no statistically significant sex differences in risk factors for AMI patients with AD, although men were more likely to be on triple antihypertensive medication (p = 0.040, Table 1). Compared with Type B patients with AMI, Type A patients were less likely to present with ST-elevation myocardial infarction (45.2 vs. 87.5%, P = 0.049) (Table 1). A history of cardiac surgery was present in 14 patients (35.9%). In the hospital, Type A patients had lower rates of medication use compared to Type B patients, including statin (32.3 vs. 75.0%, P = 0.045), aspirin (38.7 vs. 87.5%, P = 0.020), clopidogrel (22.6 vs. 75.0%, P = 0.010) and nitrates (38.7 vs. 87.5%, P = 0.020) (Table 1). 18 (58.1%) of Type A patients had pericardial effusion and 19 (61.3%) of them had acute aortic valve insufficiency, the mean ascending aortic diameter was 46.2 ± 12.1 mm in the Type A group with a range from 24.3 to 69.6 mm. Hcy in male is 1.25-fold of that in female (14.8 ± 2.9 vs. 11.8 ± 1.9, P = 0.021), and higher in type B dissection patients compared with type A group (17.8 ± 3.5 vs. 13.4 ± 2.0, P < 0.001).

Figure 1

Table 1

TotalMaleFemaleP ValueType AType BP Value
n = 39n = 33n = 6n = 31n = B
Mean (SD) age, y53.3 ± 12.151.9 ± 11.960.8 ± 11.30.09852.0 ± 11.458.4 ± 14.10.188
Male, n (%)33 (84.6)25 (80.6)8 (100.0)0.313
BMI, n (%)25.5 ± 3.325.5 ± 3.225.4 ± 3.90.92025.1± 3.527.2 ± 1.80.096
KILLIP≥2, n (%)26 (66.7)21 (63.6)5 (83.3)0.64320 (64.5)6 (75.0)0.694
Risk factors
      Current smoker, n (%)25 (64.1)21 (63.6)4 (66.7)1.00019 (61.3)6 (75.0)0.686
      Hypertension, n (%)27 (69.2)23 (69.7)4 (66.7)1.00019 (61.3)8 (100.0)0.042*
      Diabetes mellitus, n (%)6 (15.4)6 (18.2)0 (0.0)0.5643 (9.7)3 (37.5)0.088
      Dyslipidemia, n (%)8 (20.5)6 (18.2)2 (33.3)0.5836 (19.4)2 (25.0)0.658
      Cardiac failure, n (%)13 (33.3)10 (33.3)3 (50.0)0.3808 (25.8)5 (62.5)0.090
      Atrial fibrillation, n (%)3 (7.7)2 (6.1)1 (16.7)0.4032 (6.5)1 (12.5)0.508
AMI characteristics
      Anterior infarction, n (%)16 (41.0)13 (39.4)3 (50.0)0.67411 (35.5)5 (62.5)0.235
      Inferior infarction, n (%)26 (66.7)22 (66.7)4 (66.7)1.00021 (67.5)5 (62.5)1.000
      ST-segment elevation myocardial infarction, n (%)21 (53.8)20 (60.6)1 (16.7)0.07714 (45.2)7 (87.5)0.049*
Previous vascular disease
      Known coronary artery disease, n (%)13 (33.3)10 (33.3)3 (50.0)0.38012 (38.7)1 (12.5)0.229
      Prior aortic dissection, n (%)6 (15.4)5 (15.2)1 (16.7)1.0003 (9.7)3 (37.5)0.088
      Prior myocardial infarction, n (%)11 (28.2)8 (24.2)3 (50.0)0.3239 (29.0)2 (25.0)1.000
      Known aortic aneurysm, n (%)23 (59.0)20 (60.6)3 (50.0)0.67420 (64.5)3 (37.5)0.235
      Stroke, n (%)5 (12.8)4 (12.1)1 (16.7)1.0004 (12.9)1 (12.5)1.000
      Carotid artery disease, n (%)2 (5.1)2 (6.1)0 (0.0)1.0001 (3.2)1 (12.5)0.372
      Peripheral arterial disease, n (%)1 (2.6)1 (3.0)0 (0.0)1.0001 (3.2)0 (0.0)1.000
Chronic renal insufficiency, n (%)3 (7.7)2 (6.1)1 (16.7)0.4032 (6.5)1 (12.5)0.508
Prior cardiac surgery, n (%)14 (35.9)11 (33.3)3 (50.0)0.64710 (32.3)4 (50.0)0.424
      Aortic valve replacement, n (%)3 (7.7)2 (6.1)1 (16.7)0.4033 (9.7)0 (0.0)1.000
      Descending aorta replacement, n (%)4 (10.3)4 (12.1)0 (0.0)1.0001 (3.2)3 (37.5)0.022*
      Coronary artery bypass graft surgery, n (%)1 (2.6)0 (0.0)1 (16.7)0.1541 (3.2)0 (0.0)1.000
      Percutaneous Coronary Intervention, n (%)5 (12.8)4 (12.1)1 (16.7)1.0004 (12.9)1 (12.5)1.000
      Aortic root surgery, n (%)2 (5.1)1 (3.0)1 (16.7)0.2872 (6.5)0 (0.0)1.000
Medications
      Statin, n (%)16 (41.0)13 (39.4)3 (50.0)0.67410 (32.3)6 (75.0)0.045*
      Aspirin, n (%)19 (48.7)17 (51.5)2 (33.3)0.66112 (38.7)7 (87.5)0.020*
      Clopidogrel, n (%)13 (33.3)10 (33.3)3 (50.0)0.3807 (22.6)6 (75.0)0.010*
      Nitrates, n (%)19 (48.7)17 (51.5)2 (33.3)0.66112 (38.7)7 (87.5)0.020*
      Diuretic, n (%)21 (53.8)20 (60.6)1 (16.7)0.07716 (51.6)5 (62.5)0.702
      Warfarin, n (%)11 (28.2)9 (27.3)2 (33.3)1.00011 (35.5)0 (0.0)0.078
Antihypertensives0.040*0.201
      0, n (%)8 (20.5)8 (24.2)0 (0.0)8 (25.8)0 (0.0)
      1, n (%)9 (23.1)6 (18.2)3 (50.0)8 (25.8)1 (12.5)
      2, n (%)10 (25.6)7 (21.2)3 (50.0)6 (19.4)5 (50.0)
      ≥3, n (%)12 (30.8)12 (36.4)0 (0.0)9 (29.0)3 (37.5)
Echocardiography
      Pericardial effusion, n (%)19 (48.7)16 (48.5)3 (50.0)1.00018 (58.1)1 (12.5)0.044*
      Acute aortic valve insufficiency, n (%)21 (53.8)18 (54.5)3 (50.0)1.00019 (61.3)2 (25.0)0.112
      LVEF ≤ 40, n (%)7 (17.9)6 (18.2)1 (16.7)1.0004 (12.9)3 (37.5)0.137
      Ascending aortic diameters (n = 33)44.4 ± 11.444.7 ± 11.342.7 ± 12.60.69546.2 ± 12.137.5 ± 3.00.001*
Biochemical
      TC, mmol/L3.9 ± 1.04.0 ± 1.13.5 ± 0.60.4614.0 ± 1.03.7 ± 1.20.535
      TG, mmol/L1.6 ± 1.01.5 ± 1.11.7 ± 0.30.7091.6 ± 1.01.6 ± 0.90.852
      HDL, mmol/L1.0 ± 0.61.0 ± 0.71.0 ± 0.20.9851.0 ± 0.70.8 ± 0.30.293
      LDL, mmol/L2.3 ± 0.92.4 ± 0.91.9 ± 0.40.2622.3 ± 0.82.3 ± 1.00.944
      CK-MB, ng/mL150.4 ± 98.6141.3 ± 101.1222.8 ± 17.80.284133.3 ± 99.5210.0 ± 78.00.177
      TNI, ng/mL46.0 ± 30.742.9 ± 30.074.6 ± 27.40.17140.2 ± 29.869.2 ± 25.40.092
      D-DIMER, mg/L1964.8 ± 2720.22209.2 ± 2833.5259.3 ± 406.60.2562276.6 ± 3004.4796.6 ± 439.70.292
      HCY, umol/L14.3 ± 3.014.8 ± 2.911.8 ± 1.90.021*13.4 ± 2.017.8 ± 3.50.000*
      hs-CRP, mg/L18.3 ± 14.119.1 ± 14.013.2 ± 16.30.53618.7 ± 13.517.0 ± 16.60.773

Demographics and risk factors for incident aortic dissection by sex and type.

AMI, acute myocardial infarction; BMI, body mass index; CK-MB, creatine kinase isoenzymes; HCY, homocysteine; HDL, high-density lipoprotein cholesterol; hs-CRP, hypersensitive-c reactive protein; LDL, low-density lipoprotein; LVEF, left ventricular ejection fraction; TC, total cholesterol; TG, triglycerides; TNI, troponin I.

*

P < 0.05.

Presenting Signs, Symptoms and Diagnostic Imaging

Hypertension at initial presentation was more common among patients with Type B dissection (61.3 vs. 100%, P = 0.042). Despite 79.5% of patients being on antihypertensive medication, the control of blood pressure (BP) was poor. Maximum previously recorded systolic BP was ≥180 mmHg (Stage 3) in 51.9% of patients and was similar for type B dissections (52.6%) and type A dissections (50.0%), but tended to be more common in women (75.0%) in comparison with men (47.8%) (Table 2).

Table 2

TotalMaleFemaleP ValueType AType BP Value
n = 39n = 33n = 6n = 31n = B
Hypertension, n (%)27 (69.2)23 (69.7)4 (66.7)1.00019 (61.3)8 (100.0)0.042*
Control under 140/90 mmHg, n (%)17 (43.6)15 (45.5)2 (33.3)0.67915 (48.4)2 (25.0)0.426
Degree0.7821.000
      Stage 1, n (%)7 (25.9)6 (26.1)1 (25.0)5 (26.3)2 (25.0)
      Stage 2, n (%)6 (22.2)6 (26.1)0 (0.0)4 (21.1)2 (25.0)
      Stage 3, n (%)14 (51.9)11 (47.8)3 (75.0)10 (52.6)4 (50.0)
Presenting symptoms0.5140.658
      Chest pain, n (%)31 (79.5)26 (78.8)5 (83.3)25 (80.6)6 (75.0)
      Feelings of pressure or tightness, n (%)5 (12.8)5 (15.2)0 (0.0)4 (12.9)1 (12.5)
      Pain throat/jaw, n (%)2 (5.1)1 (3.0)1 (16.7)1 (3.2)1 (12.5)
      Syncope, n (%)1 (2.6)1 (3.0)0 (0.0)1 (3.2)0 (0.0)
      Auscultated murmur of aortic insufficiency, n (%)12 (30.8)11 (33.3)1 (16.7)0.64511 (35.5)1 (12.5)0.394
Diagnostic imaging of AD0.4670.058
      Computed tomography, n (%)21 (53.8)19 (57.6)2 (33.3)15 (48.4)6 (75.0)
      Echocardiophy, n (%)11 (28.2)8 (24.2)3 (50.0)11 (35.5)0 (0.0)
      Magnetic resonance imaging, n (%)3 (7.7)2 (6.1)1 (16.7)1 (3.2)2 (25.0)
      Coronary angiography, n (%)3 (7.7)3 (9.1)0 (0.0)3 (9.7)0 (0.0)

Presenting symptoms and physical examination of patients with acute myocardial infarction and aortic dissection.

AD, aortic dissection.

*

P < 0.05.

The most frequent presentation is sudden-onset chest pain (79.5%). 17.9% of patients presented with feelings of pressure or tightness or throat/jaw pain (Table 2), which were more similar to symptoms of AMI. Not infrequently, 1 male patients with type A dissection presented with syncope and transient blindness without other neurological findings, 5 type A patients presented with paraparesis or paraplegia.

Most patients had multiple imaging studies performed (Table 2). CT was more often the initial study tool for 53.8% of all the patient, particularly in patients with type B dissection. Echocardiography and magnetic resonance imaging (MRI) were rarely used initially. 3 male patients with type A dissection were not diagnosed until coronary angiography was done.

Angiographic Features, and Treatment Characteristics

Of all the 39 patients, 66.7% (26/39) were managed surgically (Table 3), 16 of them were treated AMI and AD at the same time.

Table 3

Type AType BP Value
n = 31n = 8
Surgical Management, n (%)20 (64.5)6 (75.0)0.694
      On AMI, n (%)19 (61.3)6 (75.0)0.686
      On AD, n (%)17 (54.8)4 (50.0)1.000
      On AMI and AD, n (%)12 (38.7)4 (50.0)0.425
AMI Treatment strategy
Angiographic features
      LAD, n (%)9 (29.0)8 (100.0)0.000*
      LCx, n (%)5 (16.1)5 (62.5)0.016*
      RCA, n (%)22 (71.0)5 (62.5)0.682
      Involvement of the LMCA, n (%)1 (3.2)0 (0.0)1.000
Vascular involvement number0.007*
      Nonstenotic vessels, n (%)5 (16.1)0 (0.0)
      1-vessel disease, n (%)18 (58.1)2 (25.0)
      2-vessel disease, n (%)6 (19.4)1 (12.5)
      3-vessel disease, n (%)2 (6.5)5 (62.5)
Treatment strategy
      Thrombolysis, n (%)2 (6.5)0 (0.0)1.000
      Percutaneous coronary intervention, n (%)6 (19.4)1 (12.5)1.000
      Coronary artery bypass grafting, n (%)13 (41.9)4 (50.0)0.709
      No revascularization, n (%)11 (35.5)3 (37.5)1.000
AD Treatment strategyn = 16n = 2
Procedural times(min)
      Cardiopulmonary bypass209 ± 93451 ± 300.003*
      Cross-clamp118 ± 57149 ± 450.004*
      Selective cerebral perfusion25.0 ± 5.741.0 ± 5.70.467

Angiographic features, and treatment characteristics.

AD, aortic dissection; AMI, acute myocardial infarction; LAD, left anterior descending; LCx, left circumflex; LMCA, left main coronary artery; RCA, right coronary artery.

*

P < 0.05.

The vascular involvement number was significantly different between patients with type A dissection and patients with type B dissection (P = 0.007); patients with type A dissection were more likely to have one vessel involvement than patients with type B dissection (Table 3). Left anterior descending (LAD) and left circumflex (LCx) were more often involved in patients with type B dissection (LAD: 100.0 vs. 29.0%, LCx: 62.5 vs. 16.1%, P < 0.05) (Table 3), however, not all these coronary vascular involvements that need surgical intervention, and the ratio of percutaneous coronary intervention were similar between type A group (19.4%, 6/31) and type B group (12.5%, 1/8, P = 1.000), in addition, the ratio of coronary artery bypass grafting performed in type A patients was no significance different compared with type B patients (41.9%, 13/31 vs. 50%, 4/8, P = 0.709).

A total of 18 open procedures were performed following acute dissection during the study period. Both the cardiopulmonary bypass time (209 ± 93 vs. 451 ± 30) and cross-clamp time (118 ± 57 vs. 149 ± 45) are less in type A dissection group compared with type B group (P < 0.05), however, there is no significant difference in selective cerebral perfusion time between two groups.

In-Hospital Management and Follow-Up

Overall in-hospital mortality was 10.3%. Death all occurred in patients receiving surgery (10.9%). For patients surviving until hospital discharge, the median length of stay was 15.3 ± 11.8 days. Follow-up at 3.02 ± 2.68 years was available for all of the patients, 14 died during the study period. Mortality was highest within the first 7 days of presentation (Figure 2). The 30-day and 5-year fatality rates (Figure 3) were 23.1% and 35.9%, but were higher for female than for male (66.7 vs. 30.3%, log-rank P = 0.045) on 5-year mortality. In patients with incident type A dissection who survived while hospital admission, 30-day mortality was 25.8%. Among those who survived while hospital discharge, subsequent 5-year survival rates were high (61.3% for type A; 75% for type B). After reported, 42.9% of death was caused by cardiac, 28.6% was caused by aortic rupture (Table 4).

Figure 2

Figure 3

Table 4

TotalMaleFemaleP ValueType AType BP Value
n = 39n = 33n = 6n = 31n = 8
In-hospital outcome
      Death, n (%)4 (10.3)2 (6.1)2 (33.3)0.1043 (9.7)1 (12.5)1.000
Complications
      Cardiogenic shock, n (%)6 (15.4)5 (15.2)1 (16.7)1.0004 (12.9)2 (25.0)0.583
      VTA, n (%)4 (10.3)4 (12.1)0 (0.0)1.0002 (6.5)2 (25.0)0.180
      VF, n (%)3 (7.7)2 (6.1)1 (16.7)0.4032 (6.5)1 (12.5)0.508
      Acute left-sided heart failure, n (%)9 (23.1)8 (24.2)1 (16.7)1.0006 (19.4)3 (37.5)0.355
      AKI, n (%)4 (10.3)4 (12.1)0 (0.0)1.0003 (9.7)1 (12.5)1.000
      Length of stay, d15.3 ± 11.816.2 ± 11.610.8 ± 12.90.31613.9 ± 11.020.9 ± 14.00.138
Out-hospital outcome
      Follow-up,y3.02 ± 2.683.3 ± 2.71.5 ± 1.80.1292.8 ± 2.73.9 ± 2.70.336
      Death, n (%)14 (35.9)10 (33.3)4 (66.7)0.16312 (38.7)2 (25.0)0.686
      Aortic rupture, n (%)4 (28.6)2 (20.0)2 (50.0)0.1044 (33.3)0 (0.0)1.000
      Cardiac death, n (%)6 (42.9)4 (12.1)2 (50.0)0.2243 (33.3)2 (100.0)0.583
      MI, n (%)3 (7.7)2 (6.1)1 (16.7)0.4032 (6.5)1 (12.5)0.508
      Re-hospital, n (%)3 (7.7)2 (6.1)1 (16.7)0.4031 (3.2)2 (25.0)0.101
      Recurrent angina, n (%)2 (5.1)2 (6.1)0 (0.0)1.0000 (0.0)2 (25.0)0.038*

In- and out-hospital outcomes.

AKI, acute kidney injury; MI, myocardial infarction; VF, ventricular fibrillation; VT, ventricular tachyarrhythmia.

*

P < 0.05.

Female patients tended to be older (60.8 vs. 51.9, P =0.098) (Table 1) and the overall survival of females was inferior to the males (log-rank P = 0.045; Figure 3). However, it seems that there is no specific difference in mortality between type A and type B dissection (P > 0.05).

Of 31 patients with type A dissection, 20 (64.5%) were managed surgically (Supplementary Table 1). The overall surgical in-hospital mortality was 15.0%; medically treated patients had an in-hospital mortality of 0%. Surgery was not performed in 35.5% of patients with type A dissection because of advanced age, comorbidity, patient refusal, intramural hematoma, and death before planned surgery. Of type B patients, 6 were managed surgically resulting in 1 death (16.7%), 2 were managed medically with 0 death (0%). Patients treated medically had lower mortality in-hospital but as for the long-term outcome, surgical management tends to have lower mortality. Among type A patients, 20 received surgical therapy, of whom 6 death (out-hospital mortality 30.0%), and 11 received medical therapy, of whom 6 died (54.5%); Of type B patients, 1 death (our-hospital mortality 16.7%) occurred after surgery and 1 death (50.0%) happened with medical management.

Cox proportional hazards models for all-cause mortality are shown in Table 5. By sex, the independent determinants of deaths were aortic dissection type (HR: 30.432, 95% CI: 1.092–848.183), prior cardiac surgery (HR: 0.048, 95% CI: 0.003–0.745), auscultated murmur of aortic insufficiency (HR: 18.258, 95% CI: 1.436–232.18), and medications such as nitrates (HR: 0.045, 95% CI: 0.003–0.578) and warfarin (HR: 0.033, 95% CI: 0.001–0.915). As for by type, the independent determinants of deaths were male (HR: 0.001, 95% CI: 9.296–5355.344), prior cardiac surgery (HR: 0.004, 95% CI: 0.001–0.266), and medications such as antihypertensives (HR: 0.036, 95% CI: 0.074–0.915) and warfarin (HR: 0.020, 95% CI: 0.001–0.528).

Table 5

UnivariateMultivariate
HR (95%CI)P ValueHR (95%CI)P Value
By sex
Aortic dissection type0.727 (0.154–3.424)0.68730.432 (1.092–848.183)0.044
Prior cardiac surgery0.097 (0.012–0.774)0.0280.048 (0.003–0.745)0.030
Auscultated murmur of aortic insufficiency2.999 (1.040–8.647)0.04218.258 (1.436–232.18)0.025
On AD0.301 (0.093–0.973)0.045
On AMI and AD0.289 (0.080–1.047)0.059
Antihypertensives0.398 (0.212–0.746)0.004
Nitrates0.243 (0.065–0.902)0.0350.045 (0.003–0.578)0.017
Warfarin0.125 (0.016–0.977)0.0470.033 (0.001–0.915)0.033
By type
Male2.814 (0.841–9.414)0.093223.123 (9.296–5355.344)0.001
KILLIP≥23.891 (0.866–17.472)0.076
Inferior infarction2.803 (0.945–8.310)0.063
Prior cardiac surgury0.241 (0.054–1.086)0.0640.015 (0.001–0.266)0.004
Auscultated murmur of aortic insufficiency2.678 (0.886–8.100)0.081
On AD0.266 (0.083–0.859)0.027
On AMI and AD0.306 (0.084–1.106)0.071
Antihypertensives0.431 (0.237–0.783)0.0060.261 (0.074–0.915)0.036
Aspirin0.316 (0.081–1.231)0.097
Nitrates0.180 (0.037–0.889)0.035
Warfarin0.117 (0.015–0.908)0.0400.018 (0.001–0.528)0.020

Cox regression analysis for death over the follow-up.

AD, aortic dissection; AMI, acute myocardial infarction.

Discussion

Patients suffered from both AMI and AD may be uncommon, but complications occur often and early, and the outcome is frequently fatal. Although clinicians today are better equipped to deal with the complex threat posed by AMI and AD, mortality rates remain high. Besides that, there has not been any research focus on the long-term outcome of AMI patients with AD. The results of our study demonstrated that patients with AMI and AD exhibit high 5-year fatality rates of 35.9%, especially in females (66.7%). For patients with AMI and AD, surgical management tends to have lower mortality.

The pathophysiology of AD is diverse and affected by histopathology and genetic components, (14) which usually results from a tear in the aortic intima. The blood typically propagates rapidly along the length of the aorta and often compromises branch vessels along its path and/or disrupts aortic valve function.

Occasionally, dissection and myocardial infarction may occur concomitantly.

For one reason, AMI may happen when the dissection flap involves the coronary. Iatrogenic acute aortic dissection can also occur during percutaneous coronary intervention. For other reasons, the two diseases just happen on the same patient occasionally. Though the ratio of involvement of LAD and LCx were higher in type B dissection patients compared with type A dissection patients in our results, the indeed needs for surgical intervention were similar between two groups, and both for open surgery or PCI.

In the present study, the overall in-hospital mortality was 10.3% which was relatively low compared with those in the previous studies (1). One reason may result from the improvement of diagnostic equipment and surgical techniques in recent years. Another reason might be that some patients died in the emergency department before a confirmative diagnosis was made. In the IRAD registry, a history of hypertension, which is considered the most common predisposing factor for aortic dissection, was present in more than 70% of patients (20). This was consistent with our study for the most prevalent vascular risk factors were hypertension (69.2%) and current smoker (64.1%). Despite 79.5% of patients being on antihypertensive medication, the control of blood pressure (BP) was poor. Improved primary prevention, in particular, more aggressive management of hypertension and smoking cessation, may reduce future incidence rates, but treatment of resistant or refractory hypertension is likely to remain a challenge.

The Hcy is higher in type B dissection patients compared with type A dissection patients showed in this manuscript, that is consistent with higher incidence of hypertension in type B group in present study. A random clinical trial enrolled 20702 adults confirmed that almost 75% hypertensive patients have elevated Hcy in Chinese population (21, 22), therefore, we thought the higher level of Hcy in type B dissection may result from the higher incidence of hypertension. In addition, Sassi and his colleagues found that Hcy was significantly higher in men than in women (23), that is consistent with our results.

This study has limitations. First, this was a retrospective cohort study, which may underestimate incidence and case fatality by the incomplete inclusion of deaths before hospital admission, which might also bias the assessment of risk factors and predictors of outcome. Second, although this study was the first to fulfill a substantial follow-up of a large series of patients with AMI and AD, its sample size was relatively small in comparison with that of many studies regarding AMI or AD only. Because AMI occurring in patients with AD is a rare condition, it seems impractical for a single center to enroll a large study population with both AMI and HCM. Multicenter studies enrolling much larger study populations are necessary to validate our findings.

Conclusion

Patients with AMI and AD exhibit high 5-year fatality rates. For these patients, surgical management tends to have lower mortality. Improved management of hypertension and smoking may reduce future incidence rates.

Funding

This study was supported by grants from the Chaoyang Hospital (CHPY202051).

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Beijing Anzhen Hospital Ethics Committee. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author contributions

FL and S-CQ contributed to the conception or design of the work. FL, S-CQ, X-CY, and M-LC contributed to the acquisition, analysis, or interpretation of data for the work. FL drafted the manuscript. X-CY and M-LC critically revised the manuscript. All authors gave final approval and agreed to be accountable for all aspects of the work ensuring integrity and accuracy. All authors take responsibility for all aspects of the reliability and freedom from bias of the data presented and their discussed interpretation. All authors contributed to the article and approved the submitted version.

Acknowledgments

This research has been conducted using Beijing Anzhen Hospital database. We are grateful to the Beijing Anzhen Hospital for providing administrative and technical support.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer ZWZ declared a shared affiliation with one of the authors, FL, to the handling editor.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsurg.2021.678806/full#supplementary-material

Supplementary Table 1

Management and outcomes of acute aotric dissection.

    Abbreviations

  • AAD

    Acute aortic dissection

  • ACS

    acute coronary syndrome

  • AMI

    acute myocardial infarction

  • CABG

    coronary artery bypass grafting

  • CI

    confidence interval

  • HRs

    hazard ratios

  • PCI

    percutaneous coronary intervention.

References

  • 1.

    HaganPGNienaberCAIsselbacherEMBruckmanDKaraviteDJRussmanPLet al. The International Registry of Acute Aortic Dissection (IRAD): new insights into an old disease. Jama. (2000) 283:897–903. 10.1001/jama.283.7.897

  • 2.

    OlssonCThelinSStahleEEkbomAGranathF. Thoracic aortic aneurysm and dissection: increasing prevalence and improved outcomes reported in a nationwide population-based study of more than 14,000 cases from 1987 to 2002. Circulation. (2006) 114:2611–8. 10.1161/CIRCULATIONAHA.106.630400

  • 3.

    AcostaSOgrenMBengtssonHBergqvistDLindbladB. and Zdanowski Z. Increasing incidence of ruptured abdominal aortic aneurysm: a population-based study. J Vasc Surg. (2006) 44:237–43. 10.1016/j.jvs.2006.04.037

  • 4.

    NienaberCAPowellJT. Management of acute aortic syndromes. Eur Heart J. (2012) 33:26–35b. 10.1093/eurheartj/ehr186

  • 5.

    PapeLAAwaisMWoznickiEMSuzukiTTrimarchiSEvangelistaAet al. Presentation, diagnosis, and outcomes of acute aortic dissection: 17-year trends from the international registry of acute aortic dissection. J Am Coll Cardiol. (2015) 66:350–8. 10.1016/j.jacc.2015.05.029

  • 6.

    O'GaraPTDeSanctisRW. Acute aortic dissection and its variants Toward a common diagnostic and therapeutic approach. Circulation. (1995) 92:1376–8. 10.1161/01.CIR.92.6.1376

  • 7.

    NienaberCAvon KodolitschYPetersenBLooseRHelmchenUHaverichAet al. Intramural hemorrhage of the thoracic aorta. Diagnostic and therapeutic implications. Circulation. (1995) 92:1465–72. 10.1161/01.CIR.92.6.1465

  • 8.

    YamadaTTadaSHaradaJ. Aortic dissection without intimal rupture: diagnosis with MR imaging and CT. Radiology. (1988) 168:347–52. 10.1148/radiology.168.2.3393653

  • 9.

    RobertsWC. Aortic dissection: anatomy, consequences, and causes. Am Heart J. (1981) 101:195–214. 10.1016/0002-8703(81)90666-9

  • 10.

    LarsonEWEdwardsWD. Risk factors for aortic dissection: a necropsy study of 161 cases. Am J Cardiol. (1984) 53:849–55. 10.1016/0002-9149(84)90418-1

  • 11.

    FannJISmithJAMillerDCMitchellRSMooreKAGrunkemeierGet al. Surgical management of aortic dissection during a 30-year period. Circulation. (1995) 92:Ii113–21. 10.1161/01.CIR.92.9.113

  • 12.

    CrawfordESKirklinJWNaftelDCSvenssonLGCoselliJSSafiHJ. Surgery for acute dissection of ascending aorta Should the arch be included?J Thorac. Cardiovasc Surg. (1992) 104:46–59. 10.1016/S0022-5223(19)34835-4

  • 13.

    RobertsWCVowelsTJKoJM. and Guileyardo JM. Acute aortic dissection with tear in ascending aorta not diagnosed until necropsy or operation (for another condition) and comparison to similar cases receiving proper operative therapy. Am J Cardiol. (2012) 110:728–35. 10.1016/j.amjcard.2012.04.057

  • 14.

    NienaberCACloughRE. Management of acute aortic dissection. Lancet. (2015) 385:800–11. 10.1016/S0140-6736(14)61005-9

  • 15.

    RampoldiVTrimarchiSEagleKANienaberCAOhJKBossoneEet al. Simple risk models to predict surgical mortality in acute type A aortic dissection: the International Registry of Acute Aortic Dissection score. Ann Thorac Surg. (2007) 83:55–61. 10.1016/j.athoracsur.2006.08.007

  • 16.

    HansenMSNogaredaGJHutchisonSJ. Frequency of and inappropriate treatment of misdiagnosis of acute aortic dissection. Am J Cardiol. (2007) 99:852–6. 10.1016/j.amjcard.2006.10.055

  • 17.

    HowardDPBanerjeeAFairheadJFPerkinsJSilverLERothwellPM. Population-based study of incidence and outcome of acute aortic dissection and premorbid risk factor control: 10-year results from the Oxford vascular study. Circulation. (2013) 127:2031–7. 10.1161/CIRCULATIONAHA.112.000483

  • 18.

    BaxJJBaumgartnerHCeconiCDeanVUKCDFagardRet al. Third universal definition of myocardial infarction. Circulation. (2012) 126:2020–35. 10.1161/CIR.0b013e31826e1058

  • 19.

    YangYJFanCMYuanJQZhangHBDuanFJWangZMet al. Long-term survival after acute myocardial infarction in patients with hypertrophic cardiomyopathy. Clin Cardiol. (2017) 40:26–31. 10.1002/clc.22601

  • 20.

    WilsonSKHutchinsGM. Aortic dissecting aneurysms: causative factors in 204 subjects. Arch Pathol Lab Med. (1982) 106:175–80.

  • 21.

    HuoYLiJQinXHuangYWangXGottesmanRFet al. Efficacy of folic acid therapy in primary prevention of stroke among adults with hypertension in China: the CSPPT randomized clinical trial. Jama. (2015) 313:1325–35. 10.1001/jama.2015.2274

  • 22.

    KongXHuangXZhaoMXuBXuRSongYet al. Platelet count affects efficacy of folic acid in preventing first stroke. J Am Coll Cardiol. (2018) 71:2136–46. 10.1016/j.jacc.2018.02.072

  • 23.

    SassiSCosmiBPalaretiGLegnaniCGrossiGMusolesiSet al. Influence of age, sex and vitamin status on fasting and post-methionine load plasma homocysteine levels. Haematologica. (2002) 87:957–64.

Summary

Keywords

acute myocardial infarction, aorta dissection, incidence, long-term outcomes, risk factors

Citation

Liu F, Qian S-C, Jing S, Wang Z, Yang X-C and Chen M-L (2021) Incidence and Outcome of Acute Myocardial Infarction in Patients With Aortic Dissection and Risk Factor Control. Front. Surg. 8:678806. doi: 10.3389/fsurg.2021.678806

Received

16 April 2021

Accepted

26 July 2021

Published

09 September 2021

Volume

8 - 2021

Edited by

Giovanni Mariscalco, University Hospitals of Leicester NHS Trust, United Kingdom

Reviewed by

Hong Liu, Nanjing Medical University, China; Zhen W. Zhuang, Yale University, United States

Updates

Copyright

*Correspondence: Mu-Lei Chen

†These authors have contributed equally to this work

This article was submitted to Heart Surgery, a section of the journal Frontiers in Surgery

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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