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Original Article
CPR/Resuscitation
Is two-dimensional echocardiography better than electrocardiography for predicting patient outcomes after cardiac arrest?
Dong Ki Kimorcid, Yong Soo Choorcid, Joochan Kimorcid, Byung Kook Leeorcid, Dong Hun Leeorcid, Eujene Jungorcid, Jeong Mi Moonorcid, Byeong Jo Chunorcid
Acute and Critical Care 2021;36(1):37-45.
DOI: https://doi.org/10.4266/acc.2020.00773
Published online: December 21, 2020

Department of Emergency Medicine, Chonnam National University Hospital, Gwangju, Korea

Corresponding author Yong Soo Cho Department of Emergency Medicine, Chonnam National University Hospital, 42 Jebong-ro, Dong-gu, Gwangju 61469, Korea Tel: +82-62-220-6809 Fax: +82-62-228-7417 E-mail: semi-moon@hanmail.net
• Received: September 24, 2020   • Revised: November 26, 2020   • Accepted: December 4, 2020

Copyright © 2021 The Korean Society of Critical Care Medicine

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Background
    Coronary artery stenosis increases hospital mortality and leads to poor neurological recovery in cardiac arrest (CA) patients. However, electrocardiography (ECG) cannot fully predict the presence of coronary artery stenosis in CA patients. Hence, we aimed to determine whether regional wall motion abnormality (RWMA), as observed by two-dimensional echocardiography (2DE), predicted patient survival outcomes with greater accuracy than did ST segment elevation (STE) on ECG in CA patients who underwent coronary angiography (CAG) after return of spontaneous circulation.
  • Methods
    This was a retrospective observational study of adult patients with CA of presumed cardiac etiology who underwent CAG at a single tertiary care hospital. We investigated whether RWMA observed on 2DE predicted patient outcomes more accurately than did STE observed on ECG. The primary outcome was incidence of hospital mortality. The secondary outcomes were Glasgow-Pittsburgh Cerebral Performance Category scores measured 6 months after discharge and significant coronary artery stenosis on CAG.
  • Results
    Among the 145 patients, 36 (24.8%) experienced in-hospital death. In multivariable analysis of survival outcomes, only total arrest time (P=0.011) and STE (P=0.035) were significant. The odds ratio (OR) and 95% confidence interval (CI), which were obtained by adjusting the total arrest time for survival outcomes, were significant only for STE (OR, 0.40; 95% CI, 0.17–0.94). The presence of RWMA was not a significant factor.
  • Conclusions
    While STE predicted survival outcomes in adult CA patients, RWMA did not. The decision to perform CAG after CA should include ECG under existing guidelines. The use of RWMA has limited benefits in treatment of this population.
The most common cause of cardiac arrest (CA) is acute coronary syndrome (ACS), which accounts for 70% of all CA cases [1-3]. Coronary angiography (CAG) improves both survival and neurological outcomes in CA patients [3-5]. The current guidelines for CA patients recommend that immediate CAG be performed on patients with ST segment elevation (STE) on electrocardiography (ECG); if STE is not detected, CAG should be performed considering account instability, comorbidities, and patient characteristics [5].
In ACS patients, ECG is helpful for prediction of patient outcomes. In several studies of ACS patients who underwent primary percutaneous coronary intervention (PCI), STE was associated with poorer survival-to-hospital discharge rates [6-8]. These results are similar to those in CA patients. In a previous study [9], CA patients who underwent CAG had a low incidence of survival-to hospital discharge when STE was not present because ECG detects coronary artery stenosis. The presence of coronary artery stenosis increases in-hospital mortality rates and leads to poor neurological recovery in CA patients [9]. However, the ability of ECG to predict coronary artery stenosis in CA patients is limited [3,10-12].
When diagnosing coronary artery stenosis in ACS patients, regional wall motion abnormality (RWMA) assessment using two-dimensional echocardiography (2DE) is more useful than STE assessment using ECG [13,14] because RWMA assessment is more sensitive to coronary artery stenosis [11,15]. As in ACS, if RWMA assessment is more capable of diagnosing coronary artery stenosis in CA patients than is STE assessment, it may predict the outcomes of CA patients with greater accuracy than STE assessment using ECG. We investigated whether RWMA assessment using 2DE could predict prognosis more effectively than STE assessment using ECG in CA patients who underwent CAG after return of spontaneous circulation (ROSC).
Study Design and Patients
This was a retrospective observational study of adult CA survivors who were treated at Chonnam National University Hospital in Kwangju, Korea, between January 2006 and December 2018. This study was approved by the Institutional Review Board of the Chonnam National University Hospital (IRB No. CNUH-2020-104); the need for informed consent was waived.
Adult (age ≥18 years) CA patients with presumed cardiac etiology who underwent ECG, 2DE, and CAG immediately after ROSC were included in the study. In patients with CA, including out-of-hospital cardiac arrest (OHCA) and in-hospital cardiac arrest, cardiac etiology was defined as follows [16-18]: CA was presumed to be of cardiac etiology unless it was known or likely to have been caused by trauma, submersion, drug overdose, asphyxia, exsanguination, or any other noncardiac cause as best determined by rescuers. No patients who did not undergo CAG were enrolled in the study because they either died shortly after ROSC or their caregivers withdrew them from treatment. The exclusion criteria were as follows: (1) 2DE performed after CAG and (2) CAG performed at least 24 hours after ROSC [5,9,10] (Figure 1). A total of 145 patients was enrolled.
Measurements
We extracted the following data from the electronic medical records of CA survivors: age; sex; past history; first monitored rhythm; CA etiology; OHCA; presence of a witness on collapse; bystander cardiopulmonary resuscitation (CPR); time to ROSC (time interval from recognition of collapse to ROSC); levels of serum troponin-I, brain natriuretic peptide, and lactate; ST segment change from the initial ECG; RWMA assessment using 2DE; presence of significant stenosis on CAG; and interval from emergency department (ED) presentation to CAG. Data regarding CA, including initial arrhythmia, witnessed arrest status, administration of bystander CPR, comorbidities (if any), and changes from initial ECG findings, were systematically collected upon admission according to Utsteinstyle guidelines [16-18]. The primary outcome in our study was in-hospital mortality. The secondary outcomes were Glasgow-Pittsburgh Cerebral Performance Category (CPC) score measured at 6 months after discharge and significant coronary artery stenosis observed on CAG.
During the study period, all patients received CPR and postCA care according to the advanced cardiac life support guidelines [19,20]. All patients received standard intensive care, including extracorporeal membrane oxygenation and targeted temperature management (TTM), according to institutional protocols. Throughout the study, CAG was performed at the discretion of the attending cardiologist. The timing for CAG was determined by an interventional cardiologist. The decision to perform subsequent PCI or medical treatment was based on the judgment of the attending cardiologist and the angiographic findings of the patients. Significant coronary artery stenosis was defined as stenosis ≥ 70% of one or more major epicardial coronary arteries, except the left main coronary artery, for which ≥ 50% stenosis was considered significant [21,22]. In patients with multivessel disease, revascularization was performed in the culprit vessel only, whereas revascularization for other significant lesions was performed in the elective phase [16].
A cardiologist performed 2DE at bedside in the ED during preparation for CAG. RWMA is defined as hypokinesis, dyskinesis, or akinesis of a segment of the left ventricle compared to the other contracting segments of the chamber [23]. RWMA included all cases of single or multiple hypokinesia, dyskinesia, or akinesia in any of the 17 myocardial segments. ECG was performed upon arrival of the patient at the ED. In the absence of left ventricular hypertrophy and bundle branch block, STE was defined as new STE at the J-point in two continuous leads with a cutoff-point ≥ 1 mm in all leads other than V2–V3, where the following cutoff-points were applied: ≥ 2 mm in males aged ≥ 40 years; ≥ 2.5 mm in males aged < 40 years; and ≥ 1.5 mm in females regardless of age [24].
At 6 months after discharge, neurological outcomes were assessed using the Glasgow-Pittsburgh CPC scale and recorded as CPC 1 (good performance), CPC 2 (moderate disability), CPC 3 (severe disability), CPC 4 (vegetative state), or CPC 5 (brain death or death). We defined a good neurological outcome as a CPC score of 1 or 2 and a poor neurological outcome as a CPC score of 3–5 [25].
Statistical Analysis
Continuous variables were expressed as mean and standard deviation or median and interquartile range based on normality. The Mann-Whitney U-test and independent t-tests were conducted for comparison of continuous variables, as appropriate. Categorical variables were presented as frequency and percentage. Comparisons of categorical variables were performed using the chi-square or Fisher exact test, as appropriate. Multivariable logistic regression analysis was performed to adjust for potential confounders determined by univariable analysis. All variables with P-value < 0.2 in the univariable analysis were included in the multivariable regression analysis. Variables that were significant in multivariable analysis were adjusted for 2DE and RWMA. Odds ratio (OR) with 95% confidence interval (CI) were calculated for survival, good neurological outcome, and coronary artery stenosis. Data were analyzed using R software version 4.0.0 (R Foundation for Statistical Computing, Vienna, Austria). A two-sided significance level of 0.05 was used to determine statistical significance.
Among 145 patients, in-hospital death was observed in 36 (24.8%) (Figure 1), good neurological outcome was observed in 78 (53.8%), and significant stenosis of the coronary artery was observed in 76 (52.4%). The flowchart is shown in Figure 1. In all patients, ECG was performed immediately after the visit, 2DE was performed at 151 minutes (interquartile range, 5 minutes to 589 minutes), and CAG was performed at 318 minutes (interquartile range, 151 minutes to 789 minutes). During 2DE, 105 patients (72.4%) had RWMA. On ECG, 61 patients (42.1%) had STE (Table 1). The incidence of STE differed significantly between the survival and death groups (P=0.037), while RWMA incidence showed no difference between groups (P=0.853). In terms of good neurological outcomes, no difference was observed between RWMA and STE (P=0.995, P=0.817). The incidence of significant coronary artery stenosis was significantly different between the RWMA and STE groups (P<0.001, P=0.004). Other variables related to prognosis of CA patients, such as age, sex, medical history, presence of a witness, CPR administration by a bystander, initial shockable rhythm, and total arrest time, did not differ between the STE and RWMA groups (Table 1).
In univariable analysis of survival, total arrest time, hypertension, OHCA, troponin-I, NT-proB-type natriuretic peptide, and STE had P-values < 0.2, and a multivariable analysis using these variables revealed that only total arrest time (P=0.011) and STE (P=0.035) were significant. The OR and 95% CI obtained after adjusting for significant variables in the multivariable analysis of survival outcomes were only significant for STE (OR, 0.40; 95% CI, 0.17–0.94) (Table 2). In the multivariable analysis of good neurological outcomes, only sex (P=0.013), initial shockable rhythm (P<0.001), and total arrest time (P<0.001) were significant (Table 3). Neither STE nor RWMA was a significant predictor of good neurological outcomes. In the multivariable analysis of stenosis, age (P=0.021), sex (P=0.045), and RWMA (P<0.001) were significant. The OR and 95% CI for stenosis were significant for RWMA (OR, 6.07, 95% CI, 2.37–15.54) (Table 4). The demographic findings of RWMA and no-RWMA in 84 no-STE patients are shown in Supplementary Table 1. In the multivariable analysis, RWMA was only significant for stenosis (OR, 6.01; 95% CI, 1.78–20.21), and there were no significant differences in survival and neurologic outcomes between the two groups (Supplementary Table 2).
STE was independently associated with survival outcomes, whereas RWMA was not. Both STE and RWMA were independent predictors of coronary artery stenosis but not of neurological outcomes.
In the multivariable analysis, total arrest time and STE were significant predictors of survival outcomes. After adjusting for total arrest time, the OR for STE was 0.37 (95% CI, 0.17–0.83). In a previous study [9] of patients with CA, the survival-to-hospital discharge rate was 55.1% (109/198) for all patients with STE, higher than the rate of 41.3% (226/547) in patients without STE (adjusted P=0.007). However, in patients who underwent CAG, the survival-to-hospital discharge rate was 55.7% (107/192) when STE was found and 66.8% (165/247) when it was not (adjusted P=0.01). We studied patients who underwent CAG, and survival was poor when STE was present, consistent with the findings of the previous study [9]. This is likely due to the association of coronary artery stenosis with mortality in CA patients.
In the multivariable analysis of significant coronary artery stenosis, only RWMA and STE were significant. RWMA had a higher OR than STE; however, this did not lead to improved survival. Several studies have shown that it is PCI, not CAG that reduces mortality in CA patients [3,9,11,26,27]. Therefore, CAG is only recommended after CA in patients with significant coronary artery stenosis. However, it is not easy to predict stenosis before CAG [1,10-12,28] because the clinical signs for ischemia caused by significant stenosis are unclear, and the available diagnostic tools are of limited use [1,10-12]. ECG, the most widely-used tool, is a poor predictor of significant stenosis in CA patients [3,10-12]. Significant stenosis was not observed in 20% of STE patients, while it was observed in 25% of patients without STE. This finding suggests the need for further research using other diagnostic tools [3,29]. We assessed the presence of RWMA on 2DE, which is superior to ECG for diagnosis of significant coronary artery stenosis in ACS patients. However, in our study of CA patients, the presence of RWMA did not predict patient survival. This suggests that the characteristics of RWMA differ between CA and ACS.
In the present study, RWMA was observed in 105 patients, whereas STE was observed in 61 patients. This suggests that RWMA can detect stenosis unrelated to survival. In addition, the accuracy of RWMA assessment can decrease due to the presence of Takotsubo syndrome [30], which can occur after CA and is difficult to distinguish from RWMA on 2DE. Postresuscitation myocardial dysfunction (PRMD) occurring after CA can further reduce the accuracy of RWMA assessment. PRMD is reversible myocardial dysfunction caused by global ischemia that occurs during CA, and global myocardial dysfunction is the most common pattern [31,32]. PRMD might have influenced the results of this study and can hinder the ability of physicians to identify RWMA.
In general, cardiac enzymes, such as troponin, predict coronary stenosis and patient outcomes. However, troponin did not show any significant relationships in our study. This observation is consistent with previous reports demonstrating that troponin has a high rate of false negative results (2.5%–7.8%) and is not useful in patients with CA, in contrast with patients with ACS [11]. The treatment strategy for patients with ROSC after CA typically involves CAG and TTM [5]. TTM results in better prognosis when initiated shortly after ROSC, but the optimal timing of CAG, especially in non-ST-elevation myocardial infarction (NSTEMI) patients, remains controversial [2,3,19]. In recent studies of NSTEMI, performing CAG shortly after CA did not show any clear benefit in terms of prognostic measures such as 30-day mortality [2,3,19,29]. In CA patients, CAG also has disadvantages, such as hemodynamic instability, exposure to contrast, and delays in appropriate diagnosis of other possible causes of CA, which can result in incorrect therapeutic decisions [19,29].
We hypothesized that RWMA assessment would help determine whether early CAG should be performed in patients without STE but found that RWMA was a useful predictor of significant coronary artery stenosis rather than of survival outcomes. Therefore, the benefits of 2DE in CA patients were limited. We chose to include only patients who had undergone 2DE prior to CAG. In patients who underwent 2DE after CAG, RWMA findings could differ due to successful PCI. However, we aimed to avoid preconceptions regarding interpretation of RWMA by the cardiologist, a potential consequence of knowing CAG results in advance.
The present study has several limitations. STE was defined according to the Fourth Universal Definition of Myocardial Infarction, so ECG results such as left main or post infarction were classified as no-STE. However, some clinicians have different opinions about these classifications. In our hospital, ECG is performed immediately after arrival at the ED. If STE is observed, CAG is performed as quickly as possible; if there is no STE, the decision to perform CAG is based on patient instability, comorbidities, and characteristics. In the ED, 2DE is performed at bedside during CAG preparation. In our study, STE patients only underwent 2DE if it did not interfere with CAG initiation; thus, selection bias could have been introduced. Since bias is greater in STE, we conducted further analyses of patients with no-STE in an attempt to reduce the impact of this limitation. In addition, since we only targeted patients who underwent CAG, it is possible that patients were selected under the presumption that CAG would be advantageous to their respective prognoses. Our study was limited by the different timings of 2DE and CAG execution. In the future, multicenter trials that address the timing of various procedures in CA patients, such as optimal timing of 2DE implementation, should be conducted.
In conclusion, both RWMA and STE are helpful for prediction of significant coronary artery stenosis. However, while STE predicted survival, RWMA did not. The decision to perform CAG after CA should include ECG results under the existing guidelines. The use of RWMA has limited benefits in treatment of this population.
▪ Both ST segment elevation (STE) and regional wall motion abnormality (RWMA) were independent predictors of coronary artery stenosis but not of neurological outcomes.
▪ In our study of cardiac arrest patients, STE predicted survival, but RWMA did not.
▪ The use of RWMA has limited benefits in treatment of this population.

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

AUTHOR CONTRIBUTIONS

Conceptualization: YSC. Data curation: DKK, JK, YSC, DHL. Formal analysis: YSC, JMM. Methodology: JK, YSC. Project administration: DKK, JK, BJC. Visualization: YSC, JMM, BJC. Writing–original draft: DKK, JK, BKL. Writing–review & editing: BKL, DHL, YSC.

This study was supported by a grant (CRI 18008-1) from the Chonnam National University Hospital Biomedical Research Institute.
Supplementary materials can be found via https://doi.org/10.4266/acc.2020.00773.
Supplementary Table 1.
Demographic findings of the no-STE patients
acc-2020-00773-suppl1.pdf
Supplementary Table 2.
Multivariable logistic regression analysis for each outcome of no-STE patients
acc-2020-00773-suppl2.pdf
Figure 1.
Flowchart of the patient selection process. ECG: electrocardiography; TTE: transthoracic echocardiography; CAG: coronary angiography; 2DE: two-dimensional echocardiogram; STE: ST elevation; RWMA: regional wall motion abnormality.
acc-2020-00773f1.jpg
Table 1.
Demographic findings of the study population according to 2DE and ECG findings
Characteristics 2DE
ECG
RWMA (n=105) No-RWMA (n=40) P-value STE (n=61) No-STE (n=84) P-value
Demographics
Age (yr) 60.1 (51.0–71.1) 59.6 (52.0–66.6) 0.483 60.0 (51.0–67.1) 61.5 (52.0–72.1) 0.467
Male sex 79 (75.24) 30 (75.00) 0.999 49 (80.33) 60 (71.43) 0.303
Medical history
Hypertension 46 (43.81) 19 (47.50) 0.832 27 (44.26) 38 (45.24) 0.999
Diabetes mellitus 32 (30.48) 4 (10.00) 0.019 14 (22.95) 22 (26.19) 0.802
Coronary artery disease 15 (14.29) 2 (5.00) 0.206 4 (6.56) 13 (15.48) 0.166
Chronic kidney disease 8 (7.62) 1 (2.50) 0.449 3 (4.92) 6 (7.14) 0.842
Dyslipidemia 5 (4.76) 2 (5.00) 0.999 3 (4.92) 4 (4.76) 0.999
Arrest characteristics
Out of hospital cardiac arrest 58 (55.24) 29 (72.50) 0.088 30 (49.18) 57 (67.86) 0.036
Witnessed status 82 (78.10) 32 (80.00) 0.981 48 (78.69) 66 (78.57) 0.999
Bystander CPR 92 (87.62) 33 (82.50) 0.596 54 (88.52) 71 (84.52) 0.656
Initial shockable rhythm 65 (61.90) 27 (67.50) 0.665 46 (75.41) 46 (54.76) 0.018
Time from collapse to ROSC (min) 15.0 (7.0–30.0) 19.0 [11.0–36.0) 0.140 15.0 (10.0–30.0) 16.5 (5.5–34.5) 0.950
Laboratoryfinding
Troponin-I (ng/ml) 1.35 (0.23–8.98) 0.63 (0.14–5.87) 0.132 1.15 (0.14–13.13) 1.03 (0.23–6.50) 0.561
proBNP (pg/ml) 677.6 (108.0–5232.0) 310.8 (39.6–1311.0) 0.018 253.5 (56.4–2482.0) 565.7 (119.8–4992) 0.104
Ejection fraction 39.35±13.53 60.14±11.58 <0.001 41.30±15.59 47.84±15.79 0.014
Coronary angiography
Door-to-balloon time 134.0 (75.0–225.0) 203.5 (110.5–330.5) 0.022 90.0 (40.0–135.0) 208.0 (129.0–330.5) <0.001
Significant stenosis 68 (64.76) 8 (20.00) <0.001 41 (67.21) 35 (41.67) 0.004
Successful PCI 58 (55.24) 7 (17.50) <0.001 39 (63.93) 26 (30.95) <0.001
Treatment
ECMO 10 (9.52) 3 (7.50) 0.955 9 (14.75) 4 (4.76) 0.074
TTM 44 (41.90) 12 (30.00) 0.261 19 (31.15) 37 (44.05) 0.161
Outcome
Survival 78 (74.29) 31 (77.50) 0.853 40 (65.57) 69 (82.14) 0.037
Good neurologic outcome 57 (54.29) 21 (52.50) 0.995 34 (55.74) 44 (52.38) 0.817

Values are presented as median (interquartile range), number (%), or mean±standard deviation.

2DE: two-dimensional echocardiography; ECG: electrocardiography; RWMA: regional wall motion abnormality; STE: ST elevation; CPR: cardiopulmonary resuscitation; ROSC: return of spontaneous circulation, proBNP: NT-proB-type natriuretic peptide; PCI: percutaneous coronary intervention; ECMO: extracorporeal membrane oxygenation; TTM: targeted temperature management.

Table 2.
Logistic regression analysis for survival outcomes
Parameter Univariable
Multivariable
OR (95% CI) P-value OR (95% CI) P-value
Hypertension 1.89 (0.86–4.16) 0.113 1.93 (0.82–4.52) 0.130
Out of hospital cardiac arrest 1.73 (0.81–3.69) 0.160 1.75 (0.66–4.68) 0.264
Time from collapse to ROSC 0.98 (0.96–1.00) 0.048 0.97 (0.95–0.99) 0.011
Troponin-I 0.99 (0.98–1.00) 0.131 1.00 (0.98–1.01) 0.407
proBNP 1.00 (1.00–1.00) 0.071 1.00 (1.00–1.00) 0.076
ECG (ST elevation) 0.41 (0.19–0.89) 0.025 0.40 (0.17–0.94) 0.035
2DE (RWMA) 0.84 (0.35–1.99) 0.689 NA NA

OR: odds ratio; CI: confidence interval; ROSC: return of spontaneous circulation; proBNP: NT-proB-type natriuretic peptide; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality; NA: not applicable.

Table 3.
Logistic regression analysis for good neurological outcomes
Parameter Univariable
Multivariable
OR (95% CI) P-value OR (95% CI) P-value
Sex 3.07 (1.39–6.78) 0.006 3.44 (1.29–9.17) 0.013
Chronic kidney disease 0.10 (0.01–0.79) 0.029 0.13 (0.01–1.34) 0.087
Dyslipidemia 5.50 (0.65–46.86) 0.119 5.85 (0.42–82.22) 0.190
Witnessed status 2.18 (0.97–4.91) 0.061 1.11 (0.40–3.09) 0.834
Bystander CPR 3.17 (1.14–8.79) 0.027 0.66 (0.18–2.44) 0.536
Initial shockable rhythm 3.01 (1.49–6.10) 0.002 4.46 (1.84–10.79) <0.001
Time from collapse to ROSC 0.95 (0.92–0.97) <0.001 0.93 (0.91–0.96) <0.001
ECG (ST elevation) 1.14 (0.59–2.22) 0.689 NA NA
2DE (RWMA) 1.07 (0.52–2.23) 0.847 NA NA

OR: odds ratio; CI: confidence interval; CPR: cardiopulmonary resuscitation; ROSC: return of spontaneous circulation; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality; NA: not applicable.

Table 4.
Logistic regression analysis for coronary artery stenosis
Parameter Univariable
Multivariable
OR (95% CI) P-value OR (95% CI) P-value
Age 1.02 (1.00–1.05) 0.052 1.04 (1.01–1.07) 0.021
Sex 1.78 (0.83–3.82) 0.139 2.56 (1.02–6.45) 0.045
Hypertension 1.56 (0.80–3.01) 0.190 1.55 (0.71–3.39) 0.269
Troponin-I 1.02 (1.00-1.04) 0.094 1.02 (0.99-1.04) 0.182
ECG (ST elevation) 2.87 (1.44–5.71) 0.003 1.88 (0.86–4.12) 0.116
2DE (RWMA) 7.35 (3.07–17.58) <0.001 6.07 (2.37–15.54) <0.001

OR: odds ratio; CI: confidence interval; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality.

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    • Just the Facts: Management of return of spontaneous circulation after out-of-hospital cardiac arrest
      Hashim Kareemi, Ariel Hendin, Christian Vaillancourt
      Canadian Journal of Emergency Medicine.2023; 25(7): 580.     CrossRef

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      Is two-dimensional echocardiography better than electrocardiography for predicting patient outcomes after cardiac arrest?
      Acute Crit Care. 2021;36(1):37-45.   Published online December 21, 2020
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    Is two-dimensional echocardiography better than electrocardiography for predicting patient outcomes after cardiac arrest?
    Image
    Figure 1. Flowchart of the patient selection process. ECG: electrocardiography; TTE: transthoracic echocardiography; CAG: coronary angiography; 2DE: two-dimensional echocardiogram; STE: ST elevation; RWMA: regional wall motion abnormality.
    Is two-dimensional echocardiography better than electrocardiography for predicting patient outcomes after cardiac arrest?
    Characteristics 2DE
    ECG
    RWMA (n=105) No-RWMA (n=40) P-value STE (n=61) No-STE (n=84) P-value
    Demographics
    Age (yr) 60.1 (51.0–71.1) 59.6 (52.0–66.6) 0.483 60.0 (51.0–67.1) 61.5 (52.0–72.1) 0.467
    Male sex 79 (75.24) 30 (75.00) 0.999 49 (80.33) 60 (71.43) 0.303
    Medical history
    Hypertension 46 (43.81) 19 (47.50) 0.832 27 (44.26) 38 (45.24) 0.999
    Diabetes mellitus 32 (30.48) 4 (10.00) 0.019 14 (22.95) 22 (26.19) 0.802
    Coronary artery disease 15 (14.29) 2 (5.00) 0.206 4 (6.56) 13 (15.48) 0.166
    Chronic kidney disease 8 (7.62) 1 (2.50) 0.449 3 (4.92) 6 (7.14) 0.842
    Dyslipidemia 5 (4.76) 2 (5.00) 0.999 3 (4.92) 4 (4.76) 0.999
    Arrest characteristics
    Out of hospital cardiac arrest 58 (55.24) 29 (72.50) 0.088 30 (49.18) 57 (67.86) 0.036
    Witnessed status 82 (78.10) 32 (80.00) 0.981 48 (78.69) 66 (78.57) 0.999
    Bystander CPR 92 (87.62) 33 (82.50) 0.596 54 (88.52) 71 (84.52) 0.656
    Initial shockable rhythm 65 (61.90) 27 (67.50) 0.665 46 (75.41) 46 (54.76) 0.018
    Time from collapse to ROSC (min) 15.0 (7.0–30.0) 19.0 [11.0–36.0) 0.140 15.0 (10.0–30.0) 16.5 (5.5–34.5) 0.950
    Laboratoryfinding
    Troponin-I (ng/ml) 1.35 (0.23–8.98) 0.63 (0.14–5.87) 0.132 1.15 (0.14–13.13) 1.03 (0.23–6.50) 0.561
    proBNP (pg/ml) 677.6 (108.0–5232.0) 310.8 (39.6–1311.0) 0.018 253.5 (56.4–2482.0) 565.7 (119.8–4992) 0.104
    Ejection fraction 39.35±13.53 60.14±11.58 <0.001 41.30±15.59 47.84±15.79 0.014
    Coronary angiography
    Door-to-balloon time 134.0 (75.0–225.0) 203.5 (110.5–330.5) 0.022 90.0 (40.0–135.0) 208.0 (129.0–330.5) <0.001
    Significant stenosis 68 (64.76) 8 (20.00) <0.001 41 (67.21) 35 (41.67) 0.004
    Successful PCI 58 (55.24) 7 (17.50) <0.001 39 (63.93) 26 (30.95) <0.001
    Treatment
    ECMO 10 (9.52) 3 (7.50) 0.955 9 (14.75) 4 (4.76) 0.074
    TTM 44 (41.90) 12 (30.00) 0.261 19 (31.15) 37 (44.05) 0.161
    Outcome
    Survival 78 (74.29) 31 (77.50) 0.853 40 (65.57) 69 (82.14) 0.037
    Good neurologic outcome 57 (54.29) 21 (52.50) 0.995 34 (55.74) 44 (52.38) 0.817
    Parameter Univariable
    Multivariable
    OR (95% CI) P-value OR (95% CI) P-value
    Hypertension 1.89 (0.86–4.16) 0.113 1.93 (0.82–4.52) 0.130
    Out of hospital cardiac arrest 1.73 (0.81–3.69) 0.160 1.75 (0.66–4.68) 0.264
    Time from collapse to ROSC 0.98 (0.96–1.00) 0.048 0.97 (0.95–0.99) 0.011
    Troponin-I 0.99 (0.98–1.00) 0.131 1.00 (0.98–1.01) 0.407
    proBNP 1.00 (1.00–1.00) 0.071 1.00 (1.00–1.00) 0.076
    ECG (ST elevation) 0.41 (0.19–0.89) 0.025 0.40 (0.17–0.94) 0.035
    2DE (RWMA) 0.84 (0.35–1.99) 0.689 NA NA
    Parameter Univariable
    Multivariable
    OR (95% CI) P-value OR (95% CI) P-value
    Sex 3.07 (1.39–6.78) 0.006 3.44 (1.29–9.17) 0.013
    Chronic kidney disease 0.10 (0.01–0.79) 0.029 0.13 (0.01–1.34) 0.087
    Dyslipidemia 5.50 (0.65–46.86) 0.119 5.85 (0.42–82.22) 0.190
    Witnessed status 2.18 (0.97–4.91) 0.061 1.11 (0.40–3.09) 0.834
    Bystander CPR 3.17 (1.14–8.79) 0.027 0.66 (0.18–2.44) 0.536
    Initial shockable rhythm 3.01 (1.49–6.10) 0.002 4.46 (1.84–10.79) <0.001
    Time from collapse to ROSC 0.95 (0.92–0.97) <0.001 0.93 (0.91–0.96) <0.001
    ECG (ST elevation) 1.14 (0.59–2.22) 0.689 NA NA
    2DE (RWMA) 1.07 (0.52–2.23) 0.847 NA NA
    Parameter Univariable
    Multivariable
    OR (95% CI) P-value OR (95% CI) P-value
    Age 1.02 (1.00–1.05) 0.052 1.04 (1.01–1.07) 0.021
    Sex 1.78 (0.83–3.82) 0.139 2.56 (1.02–6.45) 0.045
    Hypertension 1.56 (0.80–3.01) 0.190 1.55 (0.71–3.39) 0.269
    Troponin-I 1.02 (1.00-1.04) 0.094 1.02 (0.99-1.04) 0.182
    ECG (ST elevation) 2.87 (1.44–5.71) 0.003 1.88 (0.86–4.12) 0.116
    2DE (RWMA) 7.35 (3.07–17.58) <0.001 6.07 (2.37–15.54) <0.001
    Table 1. Demographic findings of the study population according to 2DE and ECG findings

    Values are presented as median (interquartile range), number (%), or mean±standard deviation.

    2DE: two-dimensional echocardiography; ECG: electrocardiography; RWMA: regional wall motion abnormality; STE: ST elevation; CPR: cardiopulmonary resuscitation; ROSC: return of spontaneous circulation, proBNP: NT-proB-type natriuretic peptide; PCI: percutaneous coronary intervention; ECMO: extracorporeal membrane oxygenation; TTM: targeted temperature management.

    Table 2. Logistic regression analysis for survival outcomes

    OR: odds ratio; CI: confidence interval; ROSC: return of spontaneous circulation; proBNP: NT-proB-type natriuretic peptide; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality; NA: not applicable.

    Table 3. Logistic regression analysis for good neurological outcomes

    OR: odds ratio; CI: confidence interval; CPR: cardiopulmonary resuscitation; ROSC: return of spontaneous circulation; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality; NA: not applicable.

    Table 4. Logistic regression analysis for coronary artery stenosis

    OR: odds ratio; CI: confidence interval; ECG: electrocardiography; 2DE: two-dimensional echocardiogram; RWMA: regional wall motion abnormality.


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