In-Hospital and One-Year Outcomes of Patients after Early and Late Resuscitated Cardiac Arrest Complicating Acute Myocardial Infarction—Data from a Nationwide Database
by
, , , and
Robert Kowalik
1,†, 
Marek Gierlotka
2,†,
Krzysztof Ozierański
1,*,
Przemysław Trzeciak
3,
Anna Fojt
1,
Piotr Feusette
2,
Agnieszka Tycińska
4,
Grzegorz Opolski
1,
Marcin Grabowski
1 and
Mariusz Gąsior
3 1
First Department of Cardiology, Medical University of Warsaw, 02-097 Warsaw, Poland
2
Department of Cardiology, Institute of Medical Sciences, University of Opole, 45-401 Opole, Poland
3
3rd Department of Cardiology, Faculty of Medical Sciences in Zabrze, Silesian Centre for Heart Diseases in Zabrze, Medical University of Silesia in Katowice, 41-800 Zabrze, Poland
4
Department of Cardiology, Medical University of Bialystok, 15-276 Bialystok, Poland
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
J. Clin. Med. 2022, 11(3), 609; https://doi.org/10.3390/jcm11030609
Submission received: 3 December 2021
/
Revised: 19 January 2022
/
Accepted: 21 January 2022
/
Published: 26 January 2022
(This article belongs to the Special Issue New Frontiers in Electrocardiography, Cardiac Arrhythmias, and Arrhythmogenic Disorders)
Abstract
:The prognostic role of early (less than 48 h) resuscitated cardiac arrest (ErCA) complicating acute myocardial infarction (AMI) is still controversial. The present study aimed to analyse the short-term and one-year outcomes of patients after ErCA and late resuscitated cardiac arrest (LrCA) compared to patients without cardiac arrest (CA) complicating AMI. Data from the prospective nationwide Polish Registry of Acute Coronary Syndromes (PL-ACS) were used to assess patients with resuscitated cardiac arrest (rCA) after AMI. Baseline clinical characteristics and the predictors of all-cause death were assessed. The all-cause mortality rate, complications, performed procedures, and re-hospitalisations were assessed for the in-hospital period, 30 days after discharge, and 6- and 12-month follow-ups. Among 167,621 cases of AMI, CA occurred in 3564 (2.1%) patients, that is, 3100 (87%) and 464 (13%) patients with ErCA and LrCA, respectively. The mortality rates in the ErCA vs. LrCA and CA vs. non-CA groups were as follows: in-hospital: 32.1% vs. 59.1% (p < 0.0001) and 35.6% vs. 6.0% (p < 0.0001); 30-day: 2.2% vs. 3.2% (p = 0.42) and 9.9% vs. 5.2% (p < 0.0001); 6-month: 9.2% vs. 17.9% (p = 0.0001) and 12.3% vs. 21.1% (p < 0.0001); and 12-month: 12.3% vs. 21.1% (p = 0.001) and 13% vs. 7.7% (p < 0.0001), respectively. ErCA (hazard ratio (HR): 1.54, confidence interval (CI):1.28–1.89; p < 0.0001) and LrCA (HR: 2.34, CI: 1.39–3.93; p = 0.001) increased the risk of 12-month mortality. During the 12-month follow-up, patients after LrCA more frequently required hospitalisation due to heart failure compared to patients after ErCA. ErCA was related to a higher hospitalisation rate due to coronary-related causes and a higher rate of percutaneous coronary intervention. An episode of LrCA was associated with higher in-hospital and long-term mortality compared to ErCA. ErCA and LrCA were independent risk factors for one-year mortality.
1. Introduction
In recent decades, the incidence of cardiac arrest (CA) prior to hospital admission has decreased due to the fast reperfusion strategy and pharmacotherapy [1,2]. Despite this, acute myocardial infarction (AMI) is still the leading cause of life-threatening ventricular arrhythmias and CA [1,3,4]. Approximately 6–8% of patients develop hemodynamically unstable sustained ventricular tachycardia (VT) or ventricular fibrillation (VF) during the acute phase of AMI [1]. The predictors of CA differ regarding the time after AMI onset [5]. The in-hospital mortality rate of AMI is 10.5%, and it depends mainly on age and baseline clinical presentation (e.g., signs of heart failure, completeness of coronary revascularisation, and the occurrence of CA) [6]. CA requires an early introduction of guideline-recommended therapy and qualification for an implantable cardioverter–defibrillator (ICD) for the secondary prevention of sudden cardiac death (SCD), usually in patients presenting with CA occurring 48 h after AMI onset [1]. The available data suggest that patients after resuscitated CA (rCA) during hospitalisation for AMI are at a higher risk of in-hospital and post-discharge adverse events [7]. However, the prognostic role of early rCA (ErCA) (less than 48 h from the onset of AMI), particularly in long-term observations, is still controversial, and new biomarkers could improve risk stratification [8]. It is postulated that early CA is related to possible reversible causes of CA, such as acute ischemia, acute heart failure, and/or electrolyte disturbances, inducing malignant ventricular arrhythmia, and it has no impact on long-term prognosis, similar to patients without a CA episode [9].
Further data on the significance of ErCA are warranted for better early and long-term risk stratification. The present study aimed to compare the short-term and 12-month outcomes of patients after ErCA and late rCA (LrCA) to patients without CA complicating AMI.
2. Methods
2.1. Study Design
Data from the prospective nationwide Polish Registry of Acute Coronary Syndromes (PL-ACS) from 2005 to 2014 were used for the analysis. The registry was designed to gather comprehensive data on the management and long-term outcomes of AMI patients in Poland. A detailed description of the database and the methods used have been previously published [10]. In brief, the ongoing registry is linked to the government and National Health Fund data, which is the only public healthcare insurer in Poland. Data were collected using questionnaires, including demographics, medical history, clinical condition on admission, type of AMI, related procedures, and treatment. The all-cause mortality rate was assessed for the in-hospital period, 30 days after discharge, and 6-month and 12-month follow-ups. At the one-year follow-up, data on re-hospitalisations (e.g., heart failure, recurrent AMI or CA, stroke), procedures (e.g., coronary angiography, percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG), ablation, cardiac device implantation), and cardiac rehabilitation were gathered. For one-year outcome analyses, only patients with CA after AMI, who survived the index hospitalisation, were included. All analyses were performed for patients with CA (ErCA and LrCA), as well as for patients without CA complicating AMI.
The present study is a retrospective analysis of the prospective Polish Registry of Acute Coronary Syndromes (PL-ACS), which is a nationwide official government registry within the Polish health system: https://isap.sejm.gov.pl/isap.nsf/DocDetails.xsp?id=WDU20180001063 (accessed on 2 December 2021). Therefore, official approval of the study was not required from the Ethics Committee.
2.2. Definitions
ErCA patients were defined as those with CA within the first 48 h of AMI onset, regardless of whether the CA appeared during the pre-hospital or in-hospital phase. LrCA patients were defined as those with CA after the first 48 h of the onset of AMI.
2.3. Statistical Analysis
Continuous variables were presented as means (SD) or median values and interquartile ranges (IQRs) and compared between the groups by means of a Student’s t-test or Mann–Whitney U test according to data distribution, respectively. Categorical data were presented as numbers of patients and percentages and compared with the use of the χ2 test with Pearson modification. Logistic regression was used to define predictors of in-hospital mortality and rCA occurrence during AMI among survivors.
The associations between the analysed groups and follow-up outcomes were analysed using the unadjusted and adjusted Kaplan–Meier method for multiple group comparisons. Adjusted survival and hazard ratios were calculated using the inverse probability method. A p value of less than 0.05 was considered statistically significant. All reported p values are two-sided. Analyses were performed with the use of Statistica version 13 (TIBCO Software Inc., Palo Alto, CA, USA (2017)) and R version 4.0.3 (R Foundation for Statistical Computing, Vienna, Austria).
3. Results
3.1. Study Population
The study included 167,621 cases of AMI from the 2009–2014 period. CA occurred in 3564 (2.1%) patients, that is, 3100 (87%) and 464 (13%) patients with ErCA and LrCA, respectively. Compared to the non-CA group, patients with an rCA episode were younger, more predominantly male, smokers, and more likely to have a diagnosis of STEMI, and they had more intra-hospital complications. In addition, compared to the non-CA group, patients after rCA were more likely to have a history of stroke, ischemic heart disease, and heart failure chronic obstructive pulmonary disease. Patients with rCA less frequently had a history of hypertension, hypercholesterolemia, and a previous AMI compared to the non-CA group (Table S1).
From the ErCA group and the LrCA group, 2106 patients and 190 patients, respectively, survived until discharge from the hospital. There was no difference between the groups regarding gender. The LrCA patients were older (67.9 (±12.3) vs. 63.1 (±11.5) years old (p < 0.001)), had a lower left ventricular ejection fraction (38 (±13) vs. 44 (±12)%), and a longer hospital stay, and they more often required implantation of a pacemaker or ICD during the index hospitalisation compared to the ErCA patients. In the ErCA group, myocardial infarction with ST-segment elevation was more frequent, while in the LrCA group, myocardial infarction without ST-segment elevation was more frequent. The ErCA patients were more likely to have Killip–Kimball class 4 during hospitalisation, as well as coronary angiography. Additionally, the LrCA group had a pulmonary oedema, recurrent AMI, and massive bleeding with blood transfusion episodes more often during the index hospitalisation. Both groups received optimal guideline-recommended therapy. There was no difference in pharmacotherapy at discharge, except for diuretics, vitamin K antagonists, and antidiabetic medications, which were more commonly prescribed in the LrCA group. The detailed clinical characteristics of both groups are presented in Table 1, Table 2, Table 3 and Table 4.
3.2. In-Hospital and One-Year Observation Results
The overall mortality in AMI patients was higher in the CA group than in patients without CA: 35.6% and 6.0% in hospital, 2.3% and 1.1% at 30 days, 9.9% and 5.2% at 6 months, and 13% and 7.7% at 12 months (all p < 0.0001), respectively. There was no statistically significant difference in 30-day mortality between the ErCA and LrCA groups (2.2% vs. 3.2%; p = 0.42). At the 6- and 12-month follow-up periods, all-cause mortality was higher in the LrCA patients than in the ErCA patients (17.9% vs. 9.2%; p = 0.0001 and 21.1% vs. 12.3%; p = 0.001, respectively). Detailed data on the one-year outcomes are presented in Table 5 and Supplementary Materials.
In a multivariable model adjusted for all relevant risk factors, both ErCA (HR 1.54; 1.28–1.89; p < 0001) and LrCA (HR 2.34; CI 1.39–3.93; p = 0.001) increased the risk of one-year death compared to patients without CA after AMI (Figure 1).
In the multivariable analysis, the occurrence of an LrCA episode was also the second strongest factor (after Killip class 4) associated with an over 10-fold increase in the risk of in-hospital death (HR 10.30; CI 8.02–13.20; p < 0.0001), whereas ErCA increased the risk almost 2.5-fold (HR 2.35; CI 2.1–2.63; p < 0.0001) (Figure S1). The factors associated with an increased risk of CA occurrence after AMI are presented in Figure S2.
During the one-year observation, the ErCA patients were more frequently hospitalised due to chronic coronary syndrome, coronary angiography, and PCI when compared to the LrCA patients. The latter group was more likely to be hospitalised due to heart failure (17.9% vs. 10.8%; p = 0.003). Interestingly, only 17.9% of patients in the LrCA group underwent cardiac rehabilitation compared to 27.5% (p = 0.004) of the ErCA group. Figure S3 presents 1-year survival, re-hospitalisations, and procedures in AMI patients discharged home who survived cardiac arrest (early or late) compared to patients without cardiac arrest.
A comparison of the calculated relative risk of different re-hospitalisations associated with the type of CA is presented in Figure 2.
4. Discussion
The main observation of the present study is that ErCA, as a complication of AMI, is an independent prognostic factor of one-year mortality. ErCA, after adjustment of many factors influencing statistical significance, increases the risk of death in the 12-month follow-up (adjusted HR = 1.5).
The available data do not show a clear assessment of the impact of ErCA on the long-term prognosis of patients after AMI. Our study shows the influence of ErCA on mortality, which may be important for future recommendations for the secondary prevention of cardiac arrest.
In one of the thrombolysis-era studies based on data from the GISSI-2 database, both early and late CA episodes increased in-hospital mortality (2.5 times and 4 times, respectively), while they had no significant effect on mortality in the 6-month follow-up [11]. The results from one of the prospective cohort studies by Bougouin et al. showed that patients with AMI complicated by early ventricular fibrillation had a similar number of sudden cardiac death events during the 5-year follow-up to the group without ventricular fibrillation [12].
After an ErCA episode, which occurred within an established time of less than 48 h from the onset of AMI, the patients were classified as a non-homogeneous group with a different prognosis. This group included both patients who survived out-of-hospital CA (OHCA) and in-hospital CA (IHCA) prior to coronary reperfusion and those who had an arrhythmia during or after reperfusion. OHCA patients had by far the worst prognosis. It was demonstrated by Nair et al. that only 4% of patients from this group survived until discharge from the hospital [13].
A recent study by Podolecki et al. showed that the risk of death in long-term observation was associated with the occurrence of life-threatening ventricular arrhythmia only in the pre-reperfusion period [14]. However, this effect on long-term prognosis lost its significance after excluding patients who died within the first 30 days from admission. A similar effect of pre-reperfusion CA on long-term prognosis has also been shown in two other studies by Piccini et al. and Liang et al. [15,16]. Moreover, all three cited papers showed a significantly increased effect of early ventricular arrhythmias on in-hospital mortality [14,15,16].
Interestingly, the assessment of the effect of ventricular arrhythmia during revascularisation procedures gives conflicting results in terms of short-term prognosis, but most of the studies did not show an increase in mortality in the long-term follow-up [17].
Based on the current analysis, mainly LrCA, but also ErCA, is one of the strongest predictors of in-hospital and one-year mortality. LrCA increased the risk of in-hospital death by more than 10-fold (4-fold more than in the ErCA group). This observation is in line with the results of previously published papers [14,18], which showed that the occurrence of late ventricular arrhythmia is associated with a higher risk of in-hospital death by over 8-fold. In terms of the long-term prognosis, the occurrence of late ventricular arrhythmia increased the risk of death in long-term observation by nearly 3.5 times [14]. Another study by Mehta et al. showed that at any stage of follow-up, mortality in the LrCA group remained at a higher level than in the ErCA group [19]. This last observation is in line with our results. There were no differences in mortality in the 30-day observation between the ErCA and LrCA groups in our study, but the mortality was significantly higher in the LrCA group at 6- and 12-months post-hospital discharge.
We did not analyse the rhythm presentation of CA, but we collected data about the ICD and CRT-D implantation rate. In general, VF or VT is a main mechanism of CA in MI (about 80%) [9]. In our study, only 14.2% patients after LrCA, who survived until discharge from the hospital, had an implanted ICD or CRT-D, which suggests a high percentage of non-defibrillated rhythms of CA, probably due to the high percentage of severe in-hospital complications.
The next important finding from our study is the fact that ErCA episodes occur more often in younger patients. This observation was also confirmed in the study by Sulzgruber et al. [20]. This study found an inverse correlation of patient age with the risk of developing ventricular arrhythmia in the acute phase of AMI. In addition, in this study, and in that of Piccini et al., diabetes and hypertension were found to be paradoxically protective against ventricular arrhythmias in the ErCA group [15]. This observation also coincides with the results of the present research. It could be assumed that the pharmacological treatment (beta-blockers, angiotensin-converting enzyme inhibitors, and statins) frequently used in these diseases might be responsible for such an effect.
Another important observation comes from the 12-month follow-up. The patients after ErCA were more often admitted to the hospital due to coronary events (chronic coronary syndromes, unstable angina, or recurrent AMI). They were also referred to coronary angiography and PCI more frequently than patients after LrCA. These results emphasise the importance of optimising medical care in this group.
Finally, it is worth emphasising the importance of early revascularisation strategies, which were significantly less frequently used in the LrCA group. Consequently, a significant increase in the number of repeated AMI and more frequent cardiogenic shock were observed in this study. Perhaps this observation partially explains the problem of such highly unfavourable short- and long-term prognoses of patients in older age groups treated for AMI complicated by CA.
5. Limitations
The results of the present study need to be interpreted considering some limitations. This was a retrospective analysis of an observational registry, which may result in a selection error. The ErCA group was analysed as a homogenous group without consideration of the diversity of this population, thus creating significant differences in prognosis. In the registry, we did not collect data on the rhythm presentation of CA and the timing to the return of spontaneous circulation, which are important in terms of predicting recovery from CA. To reduce the important influences of these factors, we only analysed patients who recovered after CA (resuscitated CA), and we focused on the long-term outcomes. There was a lack of data on treatment methods and the degree of neurological dysfunction of the out-of-hospital CA patients.
6. Conclusions
Both ErCA and LrCA were independent risk factors for one-year mortality. An episode of LrCA was associated with higher in-hospital and one-year mortality than ErCA. The ErCA patients were younger and had less comorbidities than LrCA patients. Further well-designed studies are required to identify clinical outcomes after ErCA (OHCA and IHCA) in long term follow-ups.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcm11030609/s1, Figure S1: Multivariate logistic regression model of factors affecting in-hospital mortality in the whole cohort of patients; Figure S2: Risk factors of the occurrence of resuscitated cardiac arrest (both early or late) in the cohort of patients that survived in-hospital period multivariate logistic regression model; Figure S3: 1-year survival (A), rehospitalizations (B-H) and procedures (I-K) in acute myocardial infarction patients discharged home who survived cardiac arrest (early or late) compared to patients without cardiac arrest; Table S1: Baseline clinical characteristics of patients without cardiac arrest and with ErCA and LrCA in the whole cohort of patients with acute myocardial infarction.
Author Contributions
Conceptualization, R.K., M.G. (Marek Gierlotka) and K.O.; Data curation, R.K., M.G. (Marek Gierlotka), K.O., P.T., A.F., P.F., A.T., G.O., M.G. (Marcin Grabowski) and M.G. (Mariusz Gąsior); Formal analysis, R.K., M.G. (Marek Gierlotka) and K.O.; Investigation, R.K. and M.G. (Marek Gierlotka); Methodology, R.K., M.G. (Marek Gierlotka), K.O., P.T., A.F., P.F., A.T., G.O., M.G. (Marcin Grabowski) and M.G. (Mariusz Gąsior); Project administration, R.K. and M.G. (Marek Gierlotka); Supervision, R.K. and M.G. (Marek Gierlotka); Validation, M.G. (Marek Gierlotka) and M.G. (Marcin Grabowski); Visualization, R.K., M.G. (Marek Gierlotka) and K.O.; Writing—original draft, R.K., M.G. (Marek Gierlotka) and K.O.; Writing—review & editing, R.K., M.G. (Marek Gierlotka), K.O., P.T., A.F., P.F., A.T., G.O., M.G. (Marcin Grabowski) and M.G. (Mariusz Gąsior). All authors have read and agreed to the published version of the manuscript.
Funding
PL-ACS Registry was funded by Ministry of Health. This research received no external additional funding.
Institutional Review Board Statement
Ethical review and approval were waived for this study due to retrospective analysis of the prospective Polish Registry of Acute Coronary Syndrome.
Informed Consent Statement
Patient consent was waived due to retrospective analysis of PL-ACS Registry.
Data Availability Statement
No data available.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Ibanez, B.; James, S.; Agewall, S.; Antunes, M.J.; Bucciarelli-Ducci, C.; Bueno, H.; Widimský, P. 2017 ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation: The Task Force for the management of acute myocardial infarction in patients presenting with ST-segment elevation of the European Society of Cardiology (ESC). Eur. Heart J. 2018, 39, 119–177. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Poloński, L.; Gasior, M.; Gierlotka, M.; Kalarus, Z.; Cieśliński, A.; Dubiel, J.S.; Opolski, G. Polish Registry of Acute Coronary Syndromes (PL-ACS). Characteristics, treatments and outcomes of patients with acute coronary syndromes in Poland. Kardiol. Pol. 2007, 65, 861–872. [Google Scholar] [PubMed]
- Nadolny, K.; Zyśko, D.; Obremska, M.; Wierzbik-Strońska, M.; Ładny, J.R.; Podgorski, M.; Gałązkowski, R. Analysis of out-of-hospital cardiac arrest in Poland in a 1-year period: Data from the POL-OHCA registry. Kardiol. Pol. 2020, 78, 404–411. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kowalik, R.J.; Fojt, A.; Ozierański, K.; Peller, M.; Andruszkiewicz, P.; Banaszewski, M.; Opolski, G. Results of targeted temperature management of patients after sudden out-of-hospital cardiac arrest: A comparison between intensive general and cardiac care units. Kardiol. Pol. 2020, 78, 30–36. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Piccini, J.P.; Zhang, M.; Pieper, K.; Solomon, S.D.; Al-Khatib, S.M.; Van de Werf, F.; Pfeffer, M.A.; McMurray, J.J.; Califf, R.M.; Velazquez, E.J. Predictors of sudden cardiac death change with time after myocardial infarction: Results from the VALIANT trial. Eur. Heart J. 2010, 31, 211–221. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wojtyniak, B.; Gierlotka, M.; Opolski, G.; Rabczenko, D.; Ozierański, K.; Gąsior, M.; Zdrojewski, T. Observed and relative survival and 5-year outcomes of patients discharged after acute myocardial infarction: The nationwide AMI-PL database. Kardiol. Pol. 2020, 78, 990–998. [Google Scholar] [CrossRef] [PubMed]
- Gorenek, B. Blomstrom Lundqvist C, European Heart Rhythm Association, Acute Cardiovascular Care Association, European Association of Percutaneous Cardiovascular Interventions. Cardiac arrhythmias in acute coronary syndromes: Position paper from the joint EHRA, ACCA, and EAPCI task force. Europace 2014, 16, 1655–1673. [Google Scholar] [PubMed]
- Tymińska, A.; Kapłon-Cieślicka, A.; Ozierański, K.; Budnik, M.; Wancerz, A.; Sypień, P.; Filipiak, K.J. Association of galectin-3 and soluble ST2 with in-hospital and 1-year outcomes in patients with ST-segment elevation myocardial infarction treated with primary percutaneous coronary intervention. Pol. Arch. Intern. Med. 2019, 129, 770–780. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Alahmar, A.E.; Nelson, C.P.; Snell, K.I.; Yuyun, M.F.; Musameh, M.D.; Timmis, A.; Samani, N.J. Resuscitated cardiac arrest and prognosis following myocardial infarction. Heart 2014, 100, 1125–1132. [Google Scholar] [CrossRef] [PubMed]
- Gierlotka, M.; Gasior, M.; Poloński, L.; Piekarski, M.; Kamiński, M. Projekt, załozenia metodyczne oraz logistyka Ogólnopolskiego Rejestru Ostrych Zespołów Wieńcowych (PL-ACS) [Project, logistics and methodology of the National Registry of Acute Coronary Syndrome (PL-ACS)]. Kardiol. Pol. 2005, 62 (Suppl. 1), I13–I21. [Google Scholar] [PubMed]
- Volpi, A.; Cavalli, A.; Santoro, L.; Negri, E.; GISSI-2 Investigators. Incidence and prognosis of early primary ventricular fibrillation in acute myocardial infarction—Results of the Gruppo Italiano per lo Studio della Sopravvivenza nell’Infarto Miocardico (GISSI-2) database. Am. J. Cardiol. 1998, 82, 265–271. [Google Scholar] [CrossRef]
- Bougouin, W.; Marjon, E.; Puymirat, E.; Defaye, P.; Celermajer, D.S.; Le Heuzey, J.Y.; FAST-MI Registry Investigators. Incidence of sudden cardiac death after ventricular fibrillation complicating acute myocardial infarction: A 5—years cause-of-death anlysis of the FAST-AMI 2005 registry. Eur. Heart J. 2014, 35, 116–122. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Nair, S.U.; Lundbye, J.B. The use of hypothermia therapy in cardiac arrest survivors. Ther. Hypothermia Temp. Manag. 2011, 1, 9–21. [Google Scholar] [CrossRef]
- Podolecki, T.S.; Lenarczyk, R.K.; Kowalczyk, J.P.; Jedrzejczyk-Patej, E.K.; Chodor, P.K.; Mazurek, M.H.; Kalarus, Z.F. Risk stratification for complex ventricular arrhythmia complicating ST-segment elevation myocardial infarction. Coron. Artery Dis. 2018, 29, 681–686. [Google Scholar] [CrossRef] [PubMed]
- Piccini, J.P.; Berger, J.S.; Brown, D.L. Early sustained ventricular arrhythmias complicating acute myocardial infarction. Am. J. Med. 2008, 121, 797–804. [Google Scholar] [CrossRef] [PubMed]
- Liang, J.J.; Fender, E.A.; Cha, Y.M.; Lennon, R.J.; Prasad, A.; Barsness, G.W. Long-term outcomes in survivor of early ventricular arrhythmias after acute ST-elevation and non-ST-elevation myocardial infarction treated with percutaneous coronary interventions. Am. J. Cardiol. 2016, 117, 709–713. [Google Scholar] [CrossRef] [PubMed]
- Mehta, R.H.; Harjai, K.J.; Grines, C.L.; Stone, G.W.; Boura, J.; Cox, D. Primary Angioplasty in Myocardial Infarction (PAMI) Investigators. Sustained ventricular tachycardia or fibrillation in the cardiac catheterization laboratory among patients receiving primary percutaneous coronary intervention: Incidence, predictors, and outcomes. J. Am. Coll. Cardiol. 2004, 43, 1765–1772. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Orvin, K.; Eisen, A.; Goldenberg, I.; Gottlieb, S.; Kornowski, R.; Matetzky, S.; Haim, M. Outcome of contemporary acute coronary syndrome complicated by ventricular tachyarrhythmia. Europace 2016, 18, 219–226. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Mehta, R.H.; Yu, J.; Piccini, J.P.; Tcheng, J.E.; Farkouh, M.E.; Reiffel, J.; Stone, G.W. Prognostic significance of postprocedural sustained ventricular tachycardia or fibrillation in patients undergoing primary percutaneous coronary intervention (from the HORIZONS-AMI Trial). Am. J. Cardiol. 2012, 109, 805–812. [Google Scholar] [CrossRef] [PubMed]
- Sulzgruber, P.; Schnaubelt, S.; Koller, L.; Goliasch, G.; Niederdöckl, J.; Simon, A.; Niessner, A. Cardiac arrest as an age-dependent prognosticator for long-term mortality after acute myocardial infarction: The potential impact of infarction size. Eur. Heart J. Acute Cardiovasc. Care 2019, 8, 153–160. [Google Scholar] [CrossRef] [PubMed]
Figure 1.
Central illustration. Risk of death from any reason for patients discharged home after resuscitated cardiac arrest during acute myocardial infarction.
Figure 1.
Central illustration. Risk of death from any reason for patients discharged home after resuscitated cardiac arrest during acute myocardial infarction.
Figure 2.
Relative risk of 1-year re-hospitalisation.
Table 1.
Baseline clinical characteristics of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
Table 1.
Baseline clinical characteristics of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
| Variable | Non-CA N = 154,266 | rCA N = 2296 | p Value | ErCA N = 2106 | LrCA N = 190 | p Value |
|---|---|---|---|---|---|---|
| Age, years, mean (SD) | 65.8 (11.9) | 63.5 (11.7) | <0.0001 | 63.1 (11.5) | 67.9 (12.3) | <0.0001 |
| Age ≥ 65 years | 80,187 (52%) | 990 (43.1%) | <0.0001 | 875 (41.6%) | 115 (60.5%) | <0.0001 |
| Age ≥ 75 years | 41,892 (27.2%) | 476 (20.7%) | <0.0001 | 413 (19.6%) | 63 (33.2%) | <0.0001 |
| Age ≥ 85 years | 7548 (4.9%) | 68 (3%) | <0.0001 | 52 (2.5%) | 16 (8.4%) | <0.0001 |
| Male gender | 98,794 (64.1%) | 1578 (68.9%) | <0.0001 | 1449 (68.9%) | 129 (67.9%) | 0.77 |
| From home admission | 88,130 (57.2%) | 1461 (63.7%) | <0.0001 | 1344 (63.9%) | 117 (61.6%) | 0.53 |
| Transfer from other hospital | 66,041 (42.8%) | 834 (36.3%) | <0.0001 | 761 (36.2%) | 73 (38.4%) | 0.53 |
| Hipercholesterolemia | 64,577 (41.9%) | 879 (38.3%) | 0.0006 | 798 (37.9%) | 81 (42.6%) | 0.2 |
| Hypertension | 112,427 (72.9%) | 1440 (62.7%) | <0.0001 | 1311 (62.3%) | 129 (67.9%) | 0.12 |
| Obesity | 31,882 (20.7%) | 445 (19.4%) | 0.13 | 402 (19.1%) | 43 (22.6%) | 0.24 |
| Diabetes mellitus | 38,799 (25.9%) | 474 (21.5%) | <0.0001 | 406 (20.1%) | 68 (37%) | <0.0001 |
| Smoking (current or past) | 91,654 (59.4%) | 1480 (64.5%) | <0.0001 | 1371 (65.1%) | 109 (57.4%) | 0.033 |
| Current smoker | 45,942 (29.8%) | 800 (34.8%) | <0.0001 | 761 (36.1%) | 39 (20.5%) | <0.0001 |
| Ischemic heart disease diagnosed before AMI | 21,800 (14.1%) | 394 (17.2%) | <0.0001 | 347 (16.5%) | 47 (24.7%) | 0.004 |
| Family history of CAD | 17,452 (11.3%) | 266 (11.6%) | 0.68 | 239 (11.4%) | 27 (14.2%) | 0.24 |
| History of heart failure | 11,821 (7.7%) | 215 (9.4%) | 0.002 | 182 (8.6%) | 33 (17.4%) | <0.0001 |
| History of stroke | 5689 (3.7%) | 114 (5%) | 0.001 | 104 (4.9%) | 10 (5.3%) | 0.84 |
| Chronic kidney disease | 9256 (6%) | 149 (6.5%) | 0.33 | 122 (5.8%) | 27 (14.2%) | <0.0001 |
| Peripheral artery disease | 7026 (4.6%) | 122 (5.3%) | 0.084 | 111 (5.3%) | 11 (5.8%) | 0.76 |
| Chronic obstructive pulmonary disease | 6031 (3.9%) | 120 (5.2%) | 0.0013 | 107 (5.1%) | 13 (6.8%) | 0.3 |
| Prior myocardial infarction | 19,708 (12.8%) | 259 (11.3%) | 0.036 | 364 (17.3%) | 39 (20.5%) | 0.26 |
| Prior PCI | 27,128 (17.6%) | 403 (17.6%) | 0.97 | 232 (11%) | 27 (14.2%) | 0.18 |
| Prior CABG | 5090 (3.3%) | 80 (3.5%) | 0.62 | 72 (3.4%) | 8 (4.2%) | 0.57 |
| NSTEMI | 83,073 (53.9%) | 721 (31.4%) | <0.0001 | 645 (30.6%) | 76 (40%) | 0.008 |
| STEMI | 71,194 (46.1%) | 1575 (68.6%) | <0.0001 | 1461 (69.4%) | 114 (60%) | 0.008 |
| CA before admission | 0 (0%) | 1169 (50.9%) | <0.0001 | 1160 (55.1%) | 9 (4.7%) | <0.0001 |
| ECG heart rate, bpm, mean (SD) | 79.1 (24.3) | 846 (27.7) | <0.0001 | 84.3 (27.7) | 88 (28.1) | 0.078 |
| Sinus rhythm | 140,391 (91.6%) | 1918 (83.6%) | <0.0001 | 1775 (84.4%) | 143 (75.3%) | 0.0012 |
| Atrial fibrillation | 8692 (5.7%) | 197 (8.6%) | <0.0001 | 167 (7.9%) | 30 (15.8%) | 0.0002 |
| Other rhythm | 2421 (1.6%) | 147 (6.4%) | <0.0001 | 136 (6.5%) | 11 (5.8%) | 0.72 |
| Normal QRS | 127,755 (83.5%) | 1765 (77.4%) | 0.0012 | 1625 (77.7%) | 140 (74.1%) | 0.25 |
| LBBB | 5843 (3.8%) | 117 (5.1%) | 0.057 | 106 (5.1%) | 11 (5.8%) | 0.65 |
| RBBB | 5255 (3.4%) | 95 (4.2%) | <0.0001 | 81 (3.9%) | 14 (7.4%) | 0.02 |
| Other QRS abnormalities | 14,184 (9.3%) | 303 (13.3%) | <0.0001 | 279 (13.3%) | 24 (12.7%) | 0.8 |
| Normal ST segment | 12,279 (8%) | 79 (3.4%) | <0.0001 | 66 (3.1%) | 13 (6.8%) | 0.007 |
| ST-segment elevation | 69,412 (45.2%) | 1526 (66.5%) | <0.0001 | 1422 (67.6%) | 104 (54.7%) | 0.0003 |
| ST-segment depression | 36,818 (24%) | 359 (15.6%) | <0.0001 | 320 (15.2%) | 39 (20.5%) | 0.053 |
| Negative T waves | 14,164 (9.2%) | 87 (3.8%) | <0.0001 | 77 (3.7%) | 10 (5.3%) | 0.27 |
| Other ST-segment abnormalities | 19,835 (12.9%) | 233 (10.2%) | <0.0001 | 209 (9.9%) | 24 (12.6%) | 0.24 |
| Systolic BP, mmHg, median (IQR) | 140 (120–155) | 120 (100–140) | <0.0001 | 120 (100–140) | 130 (110–142) | 0.11 |
| Killip class 1 | 12,1579 (79.3%) | 1217 (53.1%) | <0.0001 | 1107 (52.6%) | 110 (57.9%) | 0.16 |
| Killip class 2 | 20,415 (13.3%) | 501 (21.8%) | <0.0001 | 451 (21.4%) | 50 (26.3%) | 0.12 |
| Killip class 3 | 3728 (2.4%) | 118 (5.1%) | <0.0001 | 106 (5%) | 12 (6.3%) | 0.45 |
| Killip class 4 | 1988 (1.3%) | 370 (16.1%) | <0.0001 | 361 (17.2%) | 9 (4.7%) | <0.0001 |
Abbreviations: ACE-I—angiotensin-converting enzyme inhibitor; AMI—acute myocardial infarction; ARB—angiotensin receptor blocker; CA—cardiac arrest; CABG—coronary artery bypass grafting; CAD—coronary artery disease; ErCA—early resuscitated cardiac arrest; CRT-D—cardiac resynchronisation therapy defibrillator; CRT-P—cardiac resynchronisation therapy pacemaker; Cx—circumflex artery; IABP—intra-aortic balloon pump; ICD—implantable cardioverter–defibrillator; ECG—electrocardiogram; IQR—interquartile range; LAD—left anterior descending; LBBB—left bundle branch block; LM—left main; LMWH—low-molecular-weight heparin; LrCA—late resuscitated cardiac arrest; NSTEMI—nonST-segment myocardial infarction; PCI—percutaneous coronary intervention; RCA—right coronary artery; RBBB—right bundle branch block; rCA—resuscitated cardiac arrest; SD—standard deviation; STEMI—ST-segment myocardial infarction; TIMI—the thrombolysis in myocardial infarction risk score; VSD—ventricular septal defect.
Table 2.
In-hospital treatment and procedures of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
Table 2.
In-hospital treatment and procedures of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
| Variable | Non-CA N = 154,266 | rCA N = 2296 | p Value | ErCA N = 2106 | LrCA N = 190 | p Value |
|---|---|---|---|---|---|---|
| Thrombolysis | 521 (0.4%) | 23 (11%) | <0.0001 | 20 (1%) | 3 (1.7%) | 0.39 |
| Glycoprotein IIb/IIIa inhibitors | 33,532 (21.7%) | 881 (38.4%) | 0.0032 | 814 (38.7%) | 67 (35.3%) | 0.36 |
| Anticoagulation (not associated with PCI) | 79,366 (51.8%) | 1259 (54.9%) | 0.013 | 1147 (54.5%) | 112 (59%) | 0.24 |
| Coronary angiography | 141,438 (91.7%) | 2137 (93.2%) | 0.7 | 1967 (93.5%) | 170 (89.5%) | 0.036 |
| Infarct-related artery—RCA | 42,924 (30.3%) | 759 (35.5%) | <0.0001 | 708 (36%) | 51 (30%) | 0.2 |
| Infarct-related artery—LM | 2877 (2%) | 74 (3.5%) | 0.00031 | 63 (3.2%) | 11 (6.5%) | 0.025 |
| Infarct-related artery—LAD | 48,046 (34%) | 806 (37.7%) | <0.0001 | 730 (37.1%) | 76 (44.7%) | 0.049 |
| Infarct-related artery—Cx | 27,891 (19.7%) | 342 (16%) | 0.29 | 321 (16.3%) | 21 (12.4%) | 0.18 |
| Infarct-related artery—bypass | 1530 (1.1%) | 18 (0.8%) | <0.0001 | 16 (0.8%) | 2 (1.2%) | 0.62 |
| PCI | 118,119 (76.6%) | 1956 (85.2%) | <0.0001 | 1802 (85.6%) | 154 (81.1%) | 0.096 |
| TIMI 1 before PCI | 72,425 (63.1%) | 1450 (77.7%) | <0.0001 | 1344 (78.5%) | 106 (68.8%) | 0.006 |
| TIMI 3 after PCI | 107,885 (93.6%) | 1704 (91.3%) | 0.044 | 1569 (91.6%) | 135 (87.7%) | 0.098 |
| CABG | 4297 (2.8%) | 48 (2.1%) | <0.0001 | 46 (2.2%) | 2 (1.1%) | 0.44 |
| Pacemaker | 810 (0.5%) | 36 (1.6%) | <0.0001 | 28 (1.3%) | 8 (4.2%) | 0.0022 |
| ICD | 243 (0.2%) | 60 (2.6%) | <0.0001 | 34 (1.6%) | 26 (13.7%) | <0.0001 |
| CRT-D | 25 (0%) | 7 (0.3%) | <0.0001 | 6 (0.3%) | 1 (0.5%) | 0.91 |
| ICD or CRT-D | 268 (0.2%) | 67 (2.9%) | <0.0001 | 40 (1.9%) | 27 (14.2%) | <0.0001 |
| Blood transfusion | 4912 (3.2%) | 213 (9.3%) | <0.0001 | 171 (8.1%) | 42 (22.1%) | <0.0001 |
| Ablation | 24 (0%) | 4 (0.2%) | 0.28 | 4 (0.2%) | 0 (0%) | 0.76 |
| Heart valve surgery | 286 (0.2%) | 2 (0.1%) | <0.0001 | 2 (0.1%) | 0 (0%) | 0.39 |
| IABP | 1382 (0.9%) | 167 (7.3%) | <0.0001 | 150 (7.1%) | 17 (9%) | 0.35 |
For abbreviations, see Table 1.
Table 3.
In-hospital complications of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
Table 3.
In-hospital complications of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
| Variable | Non-CA N = 154,266 | rCA N = 2296 | p Value | ErCA N = 2106 | LrCA N = 190 | p Value |
|---|---|---|---|---|---|---|
| Massive bleeding | 1638 (1.1%) | 114 (5%) | <0.0001 | 93 (4.4%) | 21 (11.1%) | <0.0001 |
| Recurrent myocardial infarction | 274 (0.2%) | 28 (1.2%) | <0.0001 | 19 (0.9%) | 9 (4.7%) | <0.0001 |
| Stroke | 241 (0.2%) | 31 (1.4%) | <0.0001 | 29 (1.4%) | 2 (1.1%) | 0.97 |
| Pulmonary edema | 1088 (0.7%) | 102 (4.4%) | <0.0001 | 87 (4.1%) | 15 (7.9%) | 0.016 |
| Cardiogenic shock | 661 (0.4%) | 227 (9.9%) | <0.0001 | 204 (9.7%) | 23 (12.1%) | 0.28 |
| Hospital CA | 0 (0%) | 1216 (53.0%) | <0.0001 | 1026 (48.7%) | 190 (100%) | <0.0001 |
| Mechanical complication: heart rupture | 28 (0%) | 5 (0.2%) | 0.0037 | 4 (0.2%) | 1 (0.5%) | 0.89 |
| Mechanical complication: mitral regurgitation | 42 (0%) | 3 (0.1%) | 0.54 | 3 (0.1%) | 0 (0%) | 0.6 |
| Mechanical complication: VSD | 25 (0%) | 0 (0%) | <0.0001 | 0 (0%) | 0 (0%) | 1.00 |
| Mechanical complication: heart rupture or VSD | 51 (0%) | 5 (0.2%) | <0.0001 | 4 (0.2%) | 1 (0.5%) | 0.89 |
| Mechanical complications (all) | 92 (0.1%) | 8 (0.4%) | <0.0001 | 7 (0.3%) | 1 (0.5%) | 0.84 |
For abbreviations, see Table 1.
Table 4.
Discharge data of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
Table 4.
Discharge data of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
| Variable | Non-CA N = 154,266 | rCA N = 2296 | p Value | ErCA N = 2106 | LrCA N = 190 | p Value |
|---|---|---|---|---|---|---|
| LVEF, %, mean (SD) | 47.9 (10.6) | 43.2 (12.0) | <0.0001 | 43.7 (11.8) | 38.4 (12.9) | <0.0001 |
| Hospitalisation length, days, median (IQR) | 5 (3–7) | 7 (4–11) | 0.0031 | 6 (4–10) | 12 (8–19) | <0.0001 |
| Aspirin at discharge | 141,512 (91.7%) | 2069 (90.1%) | 0.0052 | 1893 (89.9%) | 176 (92.6%) | 0.22 |
| P2Y12 inhibitor at discharge | 130,658 (84.7%) | 1955 (85.2%) | 0.55 | 1786 (84.8%) | 169 (89%) | 0.12 |
| Acenocoumarol/warfarin at discharge | 3727 (2.4%) | 68 (3%) | 0.091 | 57 (2.7%) | 11 (5.8%) | 0.016 |
| Beta-blocker at discharge | 128,332 (83.2%) | 1822 (79.4%) | <0.0001 | 1665 (79.1%) | 157 (82.6%) | 0.24 |
| LMWH at discharge | 7399 (4.8%) | 197 (8.6%) | <0.0001 | 176 (8.4%) | 21 (11.1%) | 0.2 |
| ACE-I at discharge | 119,911 (77.7%) | 1693 (73.7%) | <0.0001 | 1554 (73.8%) | 139 (73.2%) | 0.85 |
| ARB at discharge | 3765 (2.4%) | 46 (2%) | 0.18 | 41 (2%) | 5 (2.6%) | 0.71 |
| Fibrate at discharge | 1688 (1.1%) | 18 (0.8%) | 0.16 | 18 (0.9%) | 0 (0%) | 0.39 |
| Statin at discharge | 135,497 (87.8%) | 1966 (85.6%) | 0.0014 | 1803 (85.6%) | 163 (85.8%) | 0.95 |
| Calcium channel blocker at discharge | 14,877 (9.6%) | 133 (5.8%) | <0.0001 | 116 (5.5%) | 17 (9%) | 0.052 |
| Nitrate at discharge | 17,305 (11.2%) | 188 (8.2%) | <0.0001 | 168 (8%) | 20 (10.5%) | 0.22 |
| Diuretic at discharge | 38,629 (25%) | 773 (33.7%) | <0.0001 | 675 (32.1%) | 98 (51.6%) | <0.0001 |
| Diabetes treated with insulin at discharge | 13,410 (8.7%) | 189 (8.2%) | 0.44 | 161 (7.6%) | 28 (14.7%) | 0.0007 |
| Diabetes treated with oral medication at discharge | 14,642 (9.5%) | 154 (6.7%) | <0.0001 | 132 (6.3%) | 22 (11.6%) | 0.0051 |
For abbreviations, see Table 1.
Table 5.
One-year follow-up outcomes of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
Table 5.
One-year follow-up outcomes of patients without cardiac arrest and with ErCA and LrCA after acute myocardial infarction (only patients who were discharged after index hospitalisation).
| Variable | Non-CA N = 154,266 | rCA N = 2296 | p Value | ErCA N = 2106 | LrCA N = 190 | p Value |
|---|---|---|---|---|---|---|
| Mortality after discharge | ||||||
| Death: 30 days | 1765 (1.1%) | 53 (2.3%) | <0.0001 | 47 (2.2%) | 6 (3.2%) | 0.42 |
| Death: 6 months | 7942 (5.2%) | 228 (9.9%) | <0.0001 | 194 (9.2%) | 34 (17.9%) | 0.0001 |
| Death: 12 months | 11,947 (7.7%) | 299 (13.0%) | <0.0001 | 259 (12.3%) | 40 (21.1%) | 0.0006 |
| Re-hospitalisation with main diagnosis | ||||||
| All cause | 88,016 (57.1%) | 1348 (58.7%) | 0.11 | 1224 (58.1%) | 124 (65.3%) | 0.055 |
| Cardiovascular cause | 71,290 (46.2%) | 1095 (47.7%) | 0.15810 | 1000 (47.5%) | 95 (50%) | 0.51 |
| Chronic coronary syndrome | 36,659 (23.8%) | 557 (24.3%) | 0.57925 | 530 (25.2%) | 27 (14.2%) | 0.0007 |
| Unstable angina | 19,390 (12.6%) | 225 (9.8%) | 0.00007 | 213 (10.1%) | 12 (6.3%) | 0.092 |
| Myocardial infarction | 8552 (5.5%) | 109 (4.8%) | 0.09758 | 96 (4.6%) | 13 (6.8%) | 0.16 |
| Chronic coronary syndrome or unstable angina or myocardial infarction | 55,008 (35.7%) | 766 (33.4%) | 0.02262 | 720 (34.2%) | 46 (24.2%) | 0.0052 |
| Heart failure | 12,491 (8.1%) | 262 (11.4%) | <0.0001 | 228 (10.8%) | 34 (17.9%) | 0.0033 |
| Stroke | 2205 (1.4%) | 23 (1%) | 0.08595 | 20 (1%) | 3 (1.6%) | 0.65 |
| Cardiac rehabilitation after 30 days | 32,079 (20.8%) | 541 (23.6%) | 0.00119 | 511 (24.3%) | 30 (15.8%) | 0.0084 |
| Cardiac rehabilitation after 6 months | 35,748 (23.2%) | 592 (25.8%) | 0.00326 | 561 (26.6%) | 31 (16.3%) | 0.0018 |
| Cardiac rehabilitation after 12 months | 37,258 (24.2%) | 614 (26.7%) | 0.00401 | 580 (27.5%) | 34 (17.9%) | 0.004 |
| Re-hospitalisation with procedure | ||||||
| Coronary angiography | 39,549 (25.6%) | 559 (24.4%) | 0.15983 | 528 (25.1%) | 31 (16.3%) | 0.0071 |
| PCI | 31,015 (20.1%) | 376 (16.4%) | 0.00001 | 361 (17.1%) | 15 (7.9%) | 0.001 |
| CABG | 8081 (5.2%) | 112 (4.9%) | 0.44160 | 103 (4.9%) | 9 (4.7%) | 0.92 |
| Pacemaker implantation | 1276 (0.8%) | 18 (0.8%) | 0.82060 | 17 (0.8%) | 1 (0.5%) | 0.99 |
| CRT-P implantation | 51 (0.03%) | 0 (0%) | 0.38355 | 0 (0%) | 0 (0%) | 1.00 |
| ICD implantation | 2171 (1.4%) | 94 (4.1%) | <0.0001 | 83 (3.9%) | 11 (5.8%) | 0.22 |
| CRT-D implantation | 365 (0.2%) | 18 (0.8%) | <0.0001 | 17 (0.8%) | 1 (0.5%) | 0.99 |
| ICD or CRT-D implantation | 2531 (1.6%) | 111 (4.8%) | <0.0001 | 99 (4.7%) | 12 (6.3%) | 0.32 |
For abbreviations, see Table 1.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Kowalik, R.; Gierlotka, M.; Ozierański, K.; Trzeciak, P.; Fojt, A.; Feusette, P.; Tycińska, A.; Opolski, G.; Grabowski, M.; Gąsior, M. In-Hospital and One-Year Outcomes of Patients after Early and Late Resuscitated Cardiac Arrest Complicating Acute Myocardial Infarction—Data from a Nationwide Database. J. Clin. Med. 2022, 11, 609. https://doi.org/10.3390/jcm11030609
AMA Style
Kowalik R, Gierlotka M, Ozierański K, Trzeciak P, Fojt A, Feusette P, Tycińska A, Opolski G, Grabowski M, Gąsior M. In-Hospital and One-Year Outcomes of Patients after Early and Late Resuscitated Cardiac Arrest Complicating Acute Myocardial Infarction—Data from a Nationwide Database. Journal of Clinical Medicine. 2022; 11(3):609. https://doi.org/10.3390/jcm11030609
Chicago/Turabian StyleKowalik, Robert, Marek Gierlotka, Krzysztof Ozierański, Przemysław Trzeciak, Anna Fojt, Piotr Feusette, Agnieszka Tycińska, Grzegorz Opolski, Marcin Grabowski, and Mariusz Gąsior. 2022. "In-Hospital and One-Year Outcomes of Patients after Early and Late Resuscitated Cardiac Arrest Complicating Acute Myocardial Infarction—Data from a Nationwide Database" Journal of Clinical Medicine 11, no. 3: 609. https://doi.org/10.3390/jcm11030609
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
