Skip to main content
American Heart Journal Plus: Cardiology Research and Practice logoLink to American Heart Journal Plus: Cardiology Research and Practice
. 2022 Dec 19;25:100243. doi: 10.1016/j.ahjo.2022.100243

Outcomes among ST-Elevation Myocardial Infarction (STEMI) patients with cardiogenic shock and COVID-19: A nationwide analysis

Bruce Adrian Casipit a,⁎, Zurab Azmaiparashvili a, Kevin Bryan Lo a, Aman Amanullah b
PMCID: PMC9762040  PMID: 36570777

Abstract

Background

There is paucity of data regarding the characteristics and outcomes of patients admitted for ST Elevation Myocardial Infarction (STEMI) complicated by cardiogenic shock (CS) with concomitant Coronavirus Disease 2019 (COVID-19) infection.

Methods

Using the National Inpatient Sample (NIS) Database for the year 2020, we conducted a retrospective cohort study to investigate the outcomes of patients who sustained STEMI-associated cardiogenic shock (STEMI-CS) with concomitant COVID-19 infection looking at its impact on in-hospital mortality and secondarily at the in-hospital procedure and intervention utilization rates as well as hospital length of stay.

Results

We identified a total of 22,775 patients with STEMI-CS, of which 1.71 % (n = 390/22,775) had COVID-19 infection. Using a stepwise survey multivariable logistic regression model that adjusted for patient and hospital level confounders, concomitant COVID-19 infection among STEMI-CS patients was found to be an independent predictor of overall in-hospital mortality compared to those without COVID-19 (adjusted OR 2.10; 95 % confidence interval [CI], 1.30–3.40). STEMI-CS patients with concomitant COVID-19 infection had similar in-hospital utilization rates for percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG), extracorporeal membrane oxygenation (ECMO), percutaneous and durable left ventricular device, intra-arterial aortic balloon pump (IABP), renal replacement therapy (RRT), mechanical ventilation, as well as similar hospital lengths of stay.

Conclusion

Concomitant COVID-19 infection was associated with higher in-hospital mortality rates among patients with cardiogenic shock related to STEMI but had similar in-hospital procedure and intervention utilization rates as well as hospital length of stay.

Keywords: STEMI, Cardiogenic shock, COVID-19

1. Introduction

Cardiogenic shock (CS) remains to be one of the major complications associated with ST-Elevation Myocardial Infarction (STEMI) [1], and is a leading cause of in-hospital mortality after sustaining an acute myocardial infarction [2]. The emergence of Coronavirus Disease 2019 (COVID-19) infection, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has brought about global concern [3] due to its associated increased morbidity especially in those with severe disease [4]. COVID-19 affects the cardiovascular system through various mechanisms and can bring about acute myocardial injury, myocarditis, acute coronary syndrome, heart failure, arrhythmias, and venous thromboembolism [5]. This potentially places patients with COVID-19 and STEMI complicated by CS (STEMI-CS) at higher risk for increased morbidity and mortality. Although previous studies have shown that COVID-19 infection increases the risk of morbidity and mortality among STEMI-CS patients [6], [7], there is still a paucity of data regarding the outcomes of hospitalized STEMI-CS patients with COVID-19 infection. Further, at the height of the pandemic, there were delays in the presentation of STEMI since patients were more cautious in going to the hospital due to the fear of being exposed to COVID-19. Likewise, there was a decrease in the procedure utilization rates including that of percutaneous coronary intervention (PCI) due to COVID-19 restriction protocols [8]. With this, we aim to investigate the impact of concomitant COVID-19 infection among patients admitted for STEMI-CS in terms of their outcomes including in-hospital mortality, interventional procedure utilization rates as well as hospital length of stay by utilizing a large nationwide database.

2. Methods

We conducted a retrospective cohort study utilizing the 2020 National Inpatient Sample (NIS) database. Briefly, the publicly available NIS of the Health Care Utilization Project (HCUP), sponsored by the Agency for Healthcare Research and Quality (AHRQ), is the largest all-payer inpatient database in the United States that approximates 20-percent stratified sample of all discharges from US community hospitals. The NIS is an annual sample of hospital discharges that provides national estimates of the characteristics of the patients, diagnoses, and hospital-based procedures performed in US acute-care hospitals. All discharges from these hospitals are recorded and weighted to ensure that they are nationally representative. It is estimated to represent >97 % of the US population due to its multistate nature [9].

In our study sample of interest, all patients aged 18 and older who were admitted with a principal diagnosis of STEMI that was complicated by cardiogenic shock during the index hospitalization between January 2020 and December 2020 were included in the analysis. All eligible discharge records that had STEMI and cardiogenic shock as the diagnoses were identified using the International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM). Patients were divided according to the presence or absence of COVID-19 infection. Sociodemographic variables were included. Further, patient comorbidities and medical history were retrieved based on the discharge records containing ICD-10 CM codes for the patient's diagnoses during the index hospitalization and were recorded accordingly. Procedural and interventional variables including PCI, coronary artery bypass graft (CABG), extracorporeal membrane oxygenation (ECMO), percutaneous and durable left ventricular assist device (LVAD), intra-aortic balloon pump (IABP), renal replacement therapy (RRT) and mechanical ventilation were identified using their respective procedure and intervention codes. (See Supplementary Table 1 for ICD-10-CM codes used in this study.)

The main clinical outcome of interest in this study was to investigate the impact of COVID-19 infection on in-hospital mortality. Secondary outcomes included other factors associated with inpatient mortality among patients with STEMI-CS, the influence of COVID-19 infection on the utilization rates of in-hospital interventions and procedures (coronary intervention rates, mechanical circulatory support rates, renal replacement therapy rates and mechanical ventilation rates), and length of stay among patients with STEMI-CS.

All data analyses were performed using StataBE 17.0 (StataCorp, College Station, Texas). The NIS is based on a complex sampling design that includes stratification, clustering, and weighing. This facilitates analysis to produce nationally representative results, variance estimates, and p values. Continuous variables were presented as median and interquartile range (IQR) as well as mean ± standard error (SE) where appropriate. Categorical variables were presented as numbers and/or percentages. Proportions were compared using the chi-square test, and continuous variables were compared using the student t-test. Survey univariable and multivariable logistic and linear regression analysis were used to calculate both adjusted and unadjusted odds ratios (ORs) for the primary and secondary outcomes. Outcomes were adjusted for potential patient and hospital level confounders, including age, gender, race, Charlson Comorbidity Index, median income, hospital bed size, hospital location, and teaching status, insurance type, and comorbidities. The variables were entered into the multivariable model were chosen based on the possible association with the outcome of interest on univariate regression analysis with p value <0.2. Survey multivariate linear regression analysis was used for the secondary outcome of hospital length of stay to adjust for possible patient and hospital level confounders as above. Variables were tested for collinearity, odds ratios and beta coefficients with 95 % confidence intervals were provided as appropriate. A p value of <0.05 was considered statistically significant.

3. Results

There were a total of 160,515 hospitalizations with a principal diagnosis of STEMI identified in the NIS database in the year 2020, of which 23,405 had cardiogenic shock during the index hospitalization. Of these, 22,775 met our inclusion criteria. Table 1 summarizes the baseline characteristics of the study population. Patients with concomitant COVID-19 infection accounted for 1.71 % (n = 390/22,775) of the total study population. Further, the median age for those with and without COVID-19 were 63 years (IQR, 57–73 years) and 66 years (IQR, 58–75 years), respectively. Compared to patients admitted without COVID-19 infection, admitted STEMI patients with cardiogenic shock and concomitant COVID-19 infection had similar proportion of females, insurance type, characteristics of admitting hospitals, and prevalence of hypertension, heart failure, obesity, diabetes mellitus, COPD, chronic kidney disease (stage 1–5) and tobacco use (see Table 1). On the contrary, patients admitted with COVID-19 infection were less likely to be white (35.9 % vs 69.6 %, p = 0.00), and had a lower median annual income (39.74 % vs 26.87 %, p = 0.01).

Table 1.

Baseline characteristics of the study population.

Patient characteristics With COVID Without COVID p-Value
Number of patients 390 22,385
Age at index admission, years (IQR) 63 (57–73) 66 (58–75)
Women, no. (%) 34.62 33.37 0.82
Race/ethnicity, no. (%) 0.00
 White 35.9 69.6 0.00
 Black 14.1 8.09 0.06
 Hispanic 29.49 8.91 0.00
 Asian or Pacific Islander 6.41 4 0.29
 Native American 0 0.51 0.54
 Others 7.69 4.49 0.17
Comorbidities (%)
 Hypertension 15.38 23.97 0.10
 Hyperlipidemia 43.59 55.17 0.05
 Heart failure 51.28 54.72 0.56
 Diabetes mellitus 12.82 9.67 0.35
 Obesity 14.1 16.82 0.52
 COPD 8.97 11.64 0.47
  CAD 66.67 77.64 0.02
  CKD, stage 1–4 17.95 20.75 0.53
  ESRD 3.85 3.57 0.90
 Tobacco use 0 1.61 0.29
Interventions/procedures (%)
  PCI 42.31 42.71 0.94
  CABG 5.13 10.52 0.12
Percutaneous left ventricular assist device 11.54 19.16 0.07
Durable left ventricular assist device 0 0.36 0.60
 ECMO 2.56 3.82 0.56
 IABP 37.18 32.97 0.44
 RRT 10.26 5.94 0.10
 Mechanical ventilation 60.26 44.72 0.01
Charlson Comorbidity Index score, no. (%)
 1 15.38 13.78 0.69
 2 17.95 28.5 0.04
 3 66.67 57.72 0.12
Median annual income in patient's zip code, US$, no. (%) 0.00
 $1–$49,999 39.74 26.87 0.01
 $50,000–$64,999 34.62 27.54 0.15
 $65,000–85,999 14.1 23.43 0.05
 ≥$86,000 8.97 2.01 0.01
Insurance type, no. (%) 0.20
 Medicaid 52.56 53.63 0.85
 Medicare 16.67 10.32 0.06
 Private 20.51 26.58 0.21
 Uninsured 3.85 5.56 0.52
 Hospital characteristics
Hospital region, no. (%) 0.80
Northeast 15.38 17.09 0.71
 Midwest 25.64 21.85 0.43
 South 34.62 38.51 0.49
 West 24.36 22.56 0.71
Hospital bed size, no. (%) 0.61
 Small 19.23 15.17 0.32
 Medium 28.21 29.08 0.87
 Large 52.56 55.75 0.58
Location and teaching status of the hospital (%) 0.42
 Rural 2.56 4.18 0.47
 Urban non-teaching 20.51 15.64 0.25
 Urban teaching 76.92 80.19 0.48

COPD: chronic obstructive pulmonary disease, CAD: coronary artery disease, CKD: chronic kidney disease, ESRD: end-stage renal disease, PCI: percutaneous coronary intervention, CABG: coronary artery bypass grafting, ECMO: extracorporeal membrane oxygenation, IABP: intra-aortic balloon pump, RRT: renal replacement therapy.

The overall mortality rate among patients admitted for STEMI complicated by cardiogenic shock was 32.76 % (n = 7460/22,775). Among those with concomitant COVID-19 infection, the mortality rate was significantly higher at 52.56 % (205/390) (p = 0.00). On univariate and multivariate analyses that adjusted for patient and hospital level confounders, concomitant COVID-19 infection was found to be an independent predictor of overall in-hospital mortality (adjusted OR 2.11; 95 % confidence interval [CI], 1.32–3.38). Further, age, female sex, Charlson comorbidity index, lack of insurance, use of LVAD, RRT and ECMO, were significantly associated with increased inpatient mortality in patients with STEMI-CS (see Table 2).

Table 2.

Multivariable logistic regression table of factors associated with in-hospital mortality among patients with STEMI complicated by cardiogenic shock.

Variable Adjusted odds ratio 95 % confidence interval [CI] p value
COVID-19 2.11 1.32–3.38 0.00
Age 1.05 1.04–1.06 0.00
Male, sex Reference
Female, sex 1.22 1.05–1.40 0.01
Charlson Comorbidity Index 1.11 1.05–1.17 0.00
Hospital bed size
 Small-sized Reference
 Medium-sized 1.24 0.99–1.58 0.06
 Large-sized 1.19 0.96–1.48 0.12
Insurance type
 Medicaid Reference
 Medicare 0.96 0.73–1.26 0.75
 Private 0.81 0.66–1.00 0.05
 Uninsured 1.71 1.20–2.44 0.00
Comorbidities
 Hypertension 1.15 0.93–1.41 0.20
 Hyperlipidemia 0.72 0.62–0.83 0.00
 Heart failure 0.50 0.42–0.61 0.00
 CAD 0.78 0.66–0.92 0.00
 Obesity 0.87 0.71–1.07 0.20
 COPD 0.83 0.65–1.06 0.14
 CKD, stage 1–4 0.88 0.55–1.42 0.60
 ESRD 1.06 0.85–1.32 0.61
 Tobacco use 0.67 0.35–1.29 0.23
Procedures and interventions
 PCI 0.69 0.59–0.80 0.00
 CABG 0.41 0.31–0.56 0.00
Percutaneous left ventricular assist device 2.08 1.73–2.51 0.00
 ECMO 2.02 1.33–3.06 0.00
  IABP 0.98 0.84–1.15 0.83
 RRT 2.09 1.52–2.87 0.00
 Mechanical ventilation 3.86 3.30–4.51 0.00

COPD: chronic obstructive pulmonary disease, CAD: coronary artery disease, CKD: chronic kidney disease, ESRD: end-stage renal disease, PCI: percutaneous coronary intervention, CABG: coronary artery bypass grafting, ECMO: extracorporeal membrane oxygenation, IABP: intra-aortic balloon pump, RRT: renal replacement therapy.

For patients admitted with STEMI complicated by cardiogenic shock, the overall utilization rates were as follows: PCI rate was 42.7 %, while the CABG rate of 10.43 %. In addition, ECMO was required in 3.8 % of admitted patients whereas percutaneous and durable LVAD were utilized in 19.03 % and 0.35 % of total admissions, respectively. Additionally, the IABP utilization rate was 33.04 %. Moreover, RRT was required for 6.02 % of admissions. It was found that there was a significantly higher rate of mechanical ventilation among patients with concomitant COVID-19 infection (60.26 % vs 44.72 %) (p = 0.01), however, after adjusting for patient and hospital level confounders, it showed that COVID-19 infection was not a predictor of mechanical ventilation utilization (adjusted OR 1.57; 95 % confidence interval [CI] 0.95–2.57) (see Supplementary Table 2). Overall, there were no significant differences in the rates of PCI, CABG, ECMO, percutaneous and durable left ventricular assist device, IABP, and RRT utilization (see Table 1).

The mean length of stay for admitted patients with STEMI-CS and concomitant COVID-19 infection was significantly longer at 13.33 days (95 % confidence interval [CI] 7.53–19.13) in contrast to 7.47 days (95 % confidence interval [CI] 7.15–7.80) in those without COVID-19 infection (p = 0.05). After a sensitivity analysis, this time excluding the ones with in-patient mortality, the results showed the same significant increase (but longer mean length of stay) in the hospital LOS among those with concomitant COVID-19 infection (22 days [95 % confidence interval [CI] 9.70–34.30]) compared to those without COVID-19 infection (9.12 days [95 % confidence interval [CI] 8.66–9.59]). However, after adjusting for patient and hospital level confounders, this was no longer statistically significant (p = 0.10). Instead, age, female gender, higher number of comorbidities, insurance type (Medicare and uninsured), and being admitted to a large urban teaching hospital were significantly associated with longer length of stay (please see Table 3).

Table 3.

Multivariable logistic regression table of factors associated with hospital length of stay (LOS) among patients with STEMI complicated by cardiogenic shock.

Variable Coefficient 95 % confidence interval [CI] p value
COVID-19 4.11 −0.85–9.07 0.10
Age −0.6 −0.09 to −0.03 0.00
Male Reference
Female −0.78 −1.35 to −0.20 0.01
Race/ethnicity
 White Reference
 Black 0.36 −0.82–1.53 0.55
 Hispanic −0.13 −1.27–1.02 0.83
 Asian or Pacific Islander −0.83 −2.01–0.35 0.17
 Native American −1.90 −3.90–0.11 0.06
 Others −0.36 −1.52–2.24 0.71
Comorbidities
 Hypertension 0.30 −0.34–0.95 0.35
 Hyperlipidemia −0.83 −2.37 to −1.28 0.00
 Heart failure 3.93 3.25–4.61 0.00
 Diabetes mellitus −2.07 −2.85 to −1.29 0.00
 Obesity 0.89 −1.52 to −0.25 0.01
 COPD −2.00 −2.67 to −1.33 0.00
 CAD −1.79 −2.69 to −0.88 0.00
 CKD, stage 1–4 −0.08 −1.32–1.16 0.90
 ESRD 2.46 −0.38–5.30 0.09
 Tobacco use −1.61 −3.29–0.07 0.06
Charlson Comorbidity Index score 0.49 0.20–0.79 0.00
Median annual income in patient's zip code, US$
 $1–$49,999 Reference
 $50,000–$64,999 0.85 0.07–1.63 0.03
 $65,000–85,999 0.33 −0.44–1.09 0.41
 ≥$86,000 0.29 −0.59–1.18 0.52
Insurance type
 Medicaid Reference
 Medicare 2.52 1.04–4.00 0.00
 Private 0.57 −0.20–1.33 0.15
 Uninsured −1.40 −2.53 to −0.27 0.02
Hospital characteristics
Hospital region
 Northeast Reference
 Midwest −0.81 −1.97–0.36 0.18
 South −0.31 −1.37–0.75 0.56
 West −0.96 −2.12–0.21 0.11
Hospital bed size
 Small Reference
 Medium 0.89 0.15–1.64 0.02
 Large 2.57 −2.12–0.21 0.00
Location and teaching status of the hospital
 Rural Reference
 Urban non-teaching −0.16 −1.26–0.95 0.78
 Urban teaching 1.74 0.71–2.77 0.00

COPD: chronic obstructive pulmonary disease, CAD: coronary artery disease, CKD: chronic kidney disease, ESRD: end-stage renal disease.

4. Discussion

This study is, to the best of our knowledge, the first observational report from a nationally representative database on the clinical outcomes among patients hospitalized for STEMI complicated by cardiogenic shock (STEMI-CS) and with concomitant COVID-19 infection. Investigated outcomes include in-hospital mortality, in-hospital procedure and intervention utilization rates, and impact on hospital length of stay. Our analysis suggests that COVID-19 infection is independently associated with increased odds for in-hospital mortality among patients with STEMI-CS. However, there were no significant differences in in-hospital procedure and intervention utilization rates as well as hospital length of stay regardless of COVID-19 status.

A previous study by Kolte et al. [10] showed that the incidence of STEMI-CS in 2010 was 10.1 % which increased to 14.58 % in 2020 based on our findings. This is likely partly due to the delayed presentation of STEMI patients to the hospital in fear of contracting COVID-19 infection [11] which increases their risk for sustaining complications including cardiogenic shock. Further, a recent study by Vallabhajosyula et al. [12] showed that the in-hospital mortality rates decreased from 49.6 % in 2000 to 32.7 % in 2017, owing in part due to the advances in revascularization techniques, evolution of mechanical circulatory support, and the development of protocols for STEMI-CS. However, according to a study by Varshney et al. [7], among STEMI-CS patients with concomitant COVID-19 infection, the mortality rate was noted to be 63 %. Our analysis concurs with previous studies and further highlights the influence of COVID-19 infection on the mortality rate of patients with STEMI-CS. This significant increase in the in-hospital mortality rate among patients with concomitant COVID-19 infection is likely due to the implicating mechanisms of the SARS-CoV-2 virus causing cardiac injury beyond acute coronary syndromes, including stress-induced cardiomyopathy, myocarditis, microvascular dysfunction and thrombosis, and acute decompensation of a known heart failure [13]. Mechanistically, similar to an influenza infection, myocardial injury due to COVID-19 may be related to increased viscosity, enhanced coagulation cascade, proinflammatory effects or direct cytopathic effects of the SARS-CoV-2 virus [14], [15]. Among patients who suffered from STEMI, in addition to the myocardial injury caused by an ischemic event during an acute myocardial infarction, the increased cytokine level during a COVID-19 infection cause further depression of myocardial function leading to the development or worsening of cardiogenic shock [16]. Further, a significant time delay between the diagnosis and intervention of STEMI-CS may occur among COVID-19 patients because the supposed interventions such as primary PCI may entail logistical delays due to protocols imposed for possible transmission to staff and other patients [17]. Moreover, similar to the results of previous studies that were conducted in a pre-COVID-19 era, our study showed that age [18], [19], [20], [21], female gender [19], [22] and being uninsured [23] are still significant predictors of increased mortality among patients with STEMI-CS. This is likely due to the inherent nature of these risk factors related to disparity in healthcare delivery that are prevalent even before the COVID-19 pandemic. Finally, hyperlipidemia, CAD and pre-existing heart failure are the usual traditional risk factors for STEMI and cardiogenic shock. The seemingly paradoxical association with decreased mortality seen in our study might be something related to COVID-19 infection and non-traditional mechanisms leading to cardiogenic shock including COVID-19 associated myopericarditis. COVID-19 associated cardiogenic shock can be very rapid in onset and may be potentially fatal [24]. Also shock states with COVID-19 might be associated with mixed mechanisms of shock including distributive shock [7]. This might translate to those with COVID-19 having higher rates of mortality as opposed to the ones with traditional cardiometabolic risk factors. However, these findings should be interpreted with caution as these are to be considered observational and hypothesis generating.

Various treatment options exist for STEMI-CS patients, and the utilization rates for these procedures and interventions depend on specific patient indications and institutional capability. In a study by Varshney et al. looking at the epidemiology of cardiogenic shock among COVID-19 patients, the PCI rate was 8 % and the total mechanical circulatory support rate was 11 %, of which 7 % had IABP, 6 % had PVAD, and 8 % had ECMO. Further, 19 % of patients underwent RRT and 90 % were mechanically ventilated [7]. Compared to our analysis, except for the mechanical ventilation rate, in-hospital procedure utilization rates were much higher compared to the previous analysis of Varshney et al. [7], and the overall procedure utilization rate was not much different in patients regardless of COVID-19 status. This is likely since STEMI-CS patients would still likely require the same procedures and interventions regardless of their COVID-19 status – in accordance to the true medical need. The differences can also be explained as we specifically only looked at cardiogenic shock per se in a specific subset of patients (with STEMI) while their study also included other forms of combined shock and undetermined shock. Lastly, there could be some degree of underestimation of the outcomes of interest in patients with COVID-19 infection and concomitant STEMI-CS since those who have STEMI-CS may have been too critically ill to be labeled as severe COVID-19 infection, hence, the utilization of certain interventions such as mechanical ventilation among those with COVID-19 may have been underestimated.

Among STEMI-CS patients, the hospital length of stay is determined by several factors including age, severity of the myocardial infarction, and number of significant comorbidities [25]. In a study by Swaminathan et al. [26], STEMI-CS patients had a significantly longer length of stay as compared to those with no cardiogenic shock. Further, patients were generally older, of the female gender and had more comorbidities. Additionally, according to Saad et al., patients with concomitant COVID-19 infection had longer lengths of stay compared to those without COVID-19 [27]. Interestingly, although our study confirmed that age, female gender and higher number of comorbidities lead to longer length of stay, our analysis showed that COVID-19 infection is not a predictor of a longer LOS. However, our study is limited by its ability to infer the severity of both cardiogenic shock and concomitant COVID-19 infection, since an asymptomatic or mild COVID-19 infection may not impact the overall prognosis of STEMI-CS patients, hence will also have little to no impact in the hospital LOS.

Our study has several limitations owing to the use of an administrative dataset and the cross-sectional nature of our study design thereby limiting the ability to capture patient level data including the time to first medical contact, door to device time and time from presentation to the development of cardiogenic shock, all of which could confound the independent association of COVID-19 to the outcomes of interest. Additionally, the database lacks the information regarding the disease severity indicator whether a condition is present on admission or not, and non-availability of a disease state relevant to the outcome of interest. Moreover, underreporting and coding errors might be a source of bias in our analysis [26]. Further, in the absence of radiographic, echocardiographic, and angiographic data, it's not possible to further stratify the severity of cardiovascular illness and the extent of myocardial injury. Moreover, the ICD-10 code for COVID-19 infection was released on April 1, 2020 which potentially missed a significant number of true COVID-19 cases since the pandemic started several months prior. In addition, there could be some underestimation of certain in-hospital events including morbidity indicators such as utilization of invasive ventilation likely due to the challenge of correctly attributing the severity of STEMI-CS or COVID-19 infection to certain disease severity indicators. Furthermore, the seemingly paradoxical association of CAD, heart failure and hyperlipidemia with less mortality and COPD with less mechanical ventilation utilization should be interpreted with caution. Lastly, the study was limited to in-hospital events only, thereby certain complications that may have occurred after hospitalization could have been missed.

5. Conclusion

This study showed that STEMI-CS patients with concomitant COVID-19 infection have higher odds of inpatient mortality compared to those who do not have COVID-19, but they have similar in-hospital procedure and intervention utilization rates as well as hospital lengths of stay.

CRediT authorship contribution statement

Bruce Adrian Casipit: Conceptualization, Methodology, Software, Validation, Formal analysis, Investigation, Data curation, Writing – original draft, Writing – review & editing, Visualization, Project administration. Zurab Azmaiparashvili: Conceptualization, Methodology, Validation, Formal analysis, Investigation, Writing – review & editing, Visualization, Supervision. Kevin Bryan Lo: Conceptualization, Methodology, Software, Validation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing, Visualization, Supervision. Aman Amanullah: Conceptualization, Methodology, Validation, Formal analysis, Investigation, Writing – review & editing, Visualization, Supervision.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.ahjo.2022.100243.

Appendix A. Supplementary data

Supplementary material

mmc1.docx (23.4KB, docx)

References

  • 1.Helgestad O.K.L., Josiassen J., Hassager C., Jensen L.O., Holmvang L., Sørensen A., et al. Temporal trends in incidence and patient characteristics in cardiogenic shock following acute myocardial infarction from 2010 to 2017: a danish cohort study. Eur. J. Heart Fail. 2019 Nov;21(11):1370–1378. doi: 10.1002/ejhf.1566. [DOI] [PubMed] [Google Scholar]
  • 2.Goldberg R.J., Spencer F.A., Gore J.M., Lessard D., Yarzebski J. Thirty-year trends (1975 to 2005) in the magnitude of, management of, and hospital death rates associated with cardiogenic shock in patients with acute myocardial infarction: a population-based perspective. Circulation. 2009 Mar 10;119(9):1211–1219. doi: 10.1161/CIRCULATIONAHA.108.814947. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Soumya R.S., Unni T.G., Raghu K.G. Impact of COVID-19 on the cardiovascular system: a review of available reports. Cardiovasc. Drugs Ther. 2021;35(3):411–425. doi: 10.1007/s10557-020-07073-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Pellicori P., Doolub G., Wong C.M., Lee K.S., Mangion K., Ahmad M., et al. COVID-19 and its cardiovascular effects: a systematic review of prevalence studies. Cochrane Database Syst. Rev. 2021 Mar;11(3) doi: 10.1002/14651858.CD013879. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Goha A., Mezue K., Edwards P., Nunura F., Baugh D., Madu E. COVID-19 and the heart: an update for clinicians. Clin. Cardiol. 2020 Jun 12;43(11):1216–1222. doi: 10.1002/clc.23406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Rodríguez-Leor O., Cid-Álvarez B., Pérez de Prado A., Rossello X., Ojeda S., Serrador A. Impact of COVID-19 on ST-segment elevation myocardial infarction care. The Spanish experience. Rev. Espanola Cardiol. Engl. Ed. 2020 Dec;73(12):994–1002. doi: 10.1016/j.rec.2020.08.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Varshney A.S., Omar W.A., Goodrich E.L., Bhatt A.S., Wolley A.E., Gong J., et al. Epidemiology of cardiogenic shock in hospitalized adults with COVID-19: a report from the American Heart Association COVID-19 cardiovascular disease registry. Circ. Heart Fail. 2021 Dec;14(12) doi: 10.1161/CIRCHEARTFAILURE.121.008477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Yong C.M., Ang L., Welt F.G.P., Gummidipundi S., Henry T.D., Pinto D.S., et al. Cardiac procedural deferral during the coronavirus (COVID-19) pandemic. Catheter. Cardiovasc. Interv. 2020 Nov;96(5):1080–1086. doi: 10.1002/ccd.29262. [DOI] [PubMed] [Google Scholar]
  • 9.Khera R., Krumholz H.M. With great power comes great responsibility: big data research from the National Inpatient Sample. Circ. Cardiovasc. Qual. Outcomes. 2017 Jul;10(7) doi: 10.1161/CIRCOUTCOMES.117.003846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Kolte D., Khera S., Aronow W.S., Mujib M., Palaniswamy C., Sule S., et al. Trends in incidence, management, and outcomes of cardiogenic shock complicating ST-elevation myocardial infarction in the United States. J. Am. Heart Assoc. 2014 Jan 13;3(1) doi: 10.1161/JAHA.113.000590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Clifford C.R., Le May M., Chow A., Boudreau R., Fu A.Y.N., Barry Q., et al. Delays in ST-elevation myocardial infarction care during the COVID-19 lockdown: an observational study. CJC Open. 2020 Dec 15;3(5):565–573. doi: 10.1016/j.cjco.2020.12.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Vallabhajosyula S., Dewaswala N., Sundaragiri P.R., Bhopalwala H.M., Cheungpasitporn W., Doshi R., et al. Cardiogenic shock complicating ST-segment elevation myocardial infarction: an 18-year analysis of temporal trends, epidemiology, management, and outcomes. Shock Augusta Ga. 2022 Mar 1;57(3):360–369. doi: 10.1097/SHK.0000000000001895. [DOI] [PubMed] [Google Scholar]
  • 13.Atri D., Siddiqi H.K., Lang J.P., Nauffal V., Morrow D.A., Bohula E.A. COVID-19 for the cardiologist: basic virology, epidemiology, cardiac manifestations, and potential therapeutic strategies. JACC Basic Transl. Sci. 2020 May;5(5):518–536. doi: 10.1016/j.jacbts.2020.04.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Nguyen J.L., Yang W., Ito K., Matte T.D., Shaman J., Kinney P.L. Seasonal influenza infections and cardiovascular disease mortality. JAMA Cardiol. 2016 Jun 1;1(3):274–281. doi: 10.1001/jamacardio.2016.0433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Kwong J.C., Schwartz K.L., Campitelli M.A., Chung H., Crowcroft N.S., Karnauchow T., et al. Acute myocardial infarction after laboratory-confirmed influenza infection. N. Engl. J. Med. 2018 Jan 25;378(4):345–353. doi: 10.1056/NEJMoa1702090. [DOI] [PubMed] [Google Scholar]
  • 16.Dhakal B.P., Sweitzer N.K., Indik J.H., Acharya D., William P. SARS-CoV-2 infection and cardiovascular disease: COVID-19 heart. Heart Lung Circ. 2020 Jul;29(7):973–987. doi: 10.1016/j.hlc.2020.05.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Kim H.N., Lee J.H., Park H.S., Yang D.H., Jang S.Y., Bae M.H., et al. A case of COVID-19 with acute myocardial infarction and cardiogenic shock. J. Korean Med. Sci. 2020 Jul 8;35(27) doi: 10.3346/jkms.2020.35.e258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Mavrić Z., Zaputović L., Zagar D., Matana A., Smokvina D. Usefulness of blood lactate as a predictor of shock development in acute myocardial infarction. Am. J. Cardiol. 1991 Mar 15;67(7):565–568. doi: 10.1016/0002-9149(91)90892-o. [DOI] [PubMed] [Google Scholar]
  • 19.Leor J., Goldbourt U., Reicher-Reiss H., Kaplinsky E., Behar S. Cardiogenic shock complicating acute myocardial infarction in patients without heart failure on admission: incidence, risk factors, and outcome. SPRINT Study Group. Am. J. Med. 1993 Mar;94(3):265–273. doi: 10.1016/0002-9343(93)90058-w. [DOI] [PubMed] [Google Scholar]
  • 20.Jeger R.V., Radovanovic D., Hunziker P.R., Pfisterer M.E., Stauffer J.C., Erne P., et al. Ten-year trends in the incidence and treatment of cardiogenic shock. Ann. Intern. Med. 2008 Nov 4;149(9):618–626. doi: 10.7326/0003-4819-149-9-200811040-00005. [DOI] [PubMed] [Google Scholar]
  • 21.Dziewierz A., Siudak Z., Rakowski T., Dubiel J.S., Dudek D. Predictors and in-hospital outcomes of cardiogenic shock on admission in patients with acute coronary syndromes admitted to hospitals without on-site invasive facilities. Acute Card. Care. 2010 Mar;12(1):3–9. doi: 10.3109/17482941003637106. [DOI] [PubMed] [Google Scholar]
  • 22.Conde-Vela C., Moreno R., Hernández R., Pérez-Vizcayno M.J., Alfonso F., Escaned J., et al. Cardiogenic shock at admission in patients with multivessel disease and acute myocardial infarction treated with percutaneous coronary intervention: related factors. Int. J. Cardiol. 2007 Dec 15;123(1):29–33. doi: 10.1016/j.ijcard.2006.11.102. [DOI] [PubMed] [Google Scholar]
  • 23.Vallabhajosyula S., Kumar V., Sundaragiri P.R., Cheungpasitporn W., Miller P.E., Harsha Patlolla S., et al. Management and outcomes of acute myocardial infarction-cardiogenic shock in uninsured compared with privately insured individuals. Circ Heart Fail. 2022 May;15(5) doi: 10.1161/CIRCHEARTFAILURE.121.008991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Noone S., Flinspach A.N., Fichtlscherer S., Zacharowski K., Sonntagbauer M., Raimann F.J. Severe COVID-19-associated myocarditis with cardiogenic shock - management with assist devices - a case report & review. BMC Anesthesiol. 2022 Dec 12;22(1):385. doi: 10.1186/s12871-022-01890-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Spencer F.A., Lessard D., Gore J.M., Yarzebski J., Goldberg R.J. Declining length of hospital stay for acute myocardial infarction and postdischarge outcomes: a community-wide perspective. Arch. Intern. Med. 2004 Apr 12;164(7):733–740. doi: 10.1001/archinte.164.7.733. [DOI] [PubMed] [Google Scholar]
  • 26.Swaminathan R.V., Rao S.V., McCoy L.A., Kim L.K., Minutello R.M., Wong S.C., et al. Hospital length of stay and clinical outcomes in older STEMI patients after primary PCI: a report from the National Cardiovascular Data Registry. J. Am. Coll. Cardiol. 2015 Mar 31;65(12):1161–1171. doi: 10.1016/j.jacc.2015.01.028. [DOI] [PubMed] [Google Scholar]
  • 27.Saad M., Kennedy K.F., Imran H., Louis D.W., Shippey E., Poppas A., et al. Association between COVID-19 diagnosis and in-hospital mortality in patients hospitalized with ST-segment elevation myocardial infarction. JAMA. 2021 Nov 16;326(19):1940–1952. doi: 10.1001/jama.2021.18890. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary material

mmc1.docx (23.4KB, docx)

Articles from American Heart Hournal Plus: Cardiology Research and Practice are provided here courtesy of Elsevier

RESOURCES