| Literature DB >> 33283476 |
Uwe Primessnig1,2,3, Burkert M Pieske1,2,3, Mohammad Sherif1.
Abstract
AIMS: This study aimed to evaluate the impact of coronavirus disease 2019 (Covid-19) outbreak on admissions for acute myocardial infarction (AMI) and related mortality, severity of presentation, major cardiac complications and outcome in a tertiary-care university hospital in Berlin, Germany. METHODS ANDEntities:
Keywords: Acute myocardial infarction; Covid-19; NSTEMI; Percutaneous coronary intervention; SARS-CoV-2; STEMI
Mesh:
Year: 2020 PMID: 33283476 PMCID: PMC7835606 DOI: 10.1002/ehf2.13075
Source DB: PubMed Journal: ESC Heart Fail ISSN: 2055-5822
Figure 1Hospitalization and case fatality rate for acute myocardial infarction during Covid‐19 pandemic: (A) reduced number of admissions for acute myocardial infarction (AMI) during early‐Covid‐19 (black bars: e‐COV = 1 March to 30 April) pandemic compared with the pre‐Covid‐19 time (white bars: pre‐COV = 1 January to 29 February). (B) Increased mortality rate in Covid‐19 outbreak compared with pre‐Covid‐19 time: absolute number of admissions for AMI during e‐COV (n = 51) and pre‐COV (n = 96). Data are absolute values or percentage. Statistical analysis was performed with χ 2 tests. Statistical significance was reached with a P < 0.05.
Figure 2Admission for acute myocardial infarction and mortality between January and April 2020 compared with the previous year 2019: (A) There were no differences in hospitalizations for acute myocardial infarction (AMI) on January and February 2020 and 2019, while on March and April 2020, admissions for AMI halved compared with those in 2019. Absolute number of admissions. Grey bars = January to April 2019. White bars = pre‐COV (January to February 2020). Black bars = e‐COV (March to April 2020). (B) Mortality was unchanged in January and February 2020 and 2019; however, in March, mortality rate increased by 10.5% and, in April, by 11.8% in 2020 (Covid‐19 outbreak) compared with 2019. Case fatality rate among patients admitted for AMI in percentage.
Patient characteristics
| Patient characteristics | Pre‐COV ( | e‐COV ( |
|
|---|---|---|---|
| Age | 70 (56.5–76) | 64 (58–72) | 0.06 |
| Sex (male) | 66 (69%) | 36 (70%) | 0.9 |
| Arterial hypertension | 87 (90%) | 47 (92%) | 0.9 |
| Dyslipidaemia | 71 (74%) | 40 (78%) | 0.8 |
| Obesity | 24 (25%) | 15 (29%) | 0.6 |
| Diabetes mellitus | 31 (32%) | 18 (35%) | 0.7 |
| Coronary artery disease | 52 (54%) | 27 (53%) | 0.9 |
| Prior MI | 35 (36%) | 16 (31%) | 0.3 |
| Prior PCI | 49 (51%) | 25 (49%) | 0.9 |
| Prior CABG | 10 (10%) | 4 (8%) | 0.6 |
| Smoker | 43 (45%) | 25 (49%) | 0.7 |
| COPD | 19 (19%) | 7 (14%) | 0.4 |
| Heart failure | 30 (31%) | 19 (37%) | 0.6 |
| Chronic kidney disease | 24 (25%) | 16 (31%) | 0.5 |
CABG, coronary artery bypass graft surgery; CAD, coronary artery disease; CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; MI, myocardial infarction; PCI, percutaneous coronary intervention.
Absolute number of admissions for acute myocardial infarction during early‐Covid‐19 (e‐COV: (n = 51) = 1 March to 30 April) and pre‐Covid‐19 pandemic [pre‐COV: (n = 96) = 1 January to 29 February]. Data are median with inter‐quartile range, absolute values, or percentage. Statistical analysis was performed with Mann–Whitney test or χ 2 test. Statistical significance was reached with a P < 0.05.
Clinical presentation and diagnosis
| Pre‐COV | e‐COV |
| |
|---|---|---|---|
| Clinical presentation | |||
| AMI | 96 | 51 | |
| STEMI | 35 (36%) | 26 (51%) | 0.4 |
| NSTEMI | 61 (64%) | 25 (49%) | 0.3 |
| Resuscitation (CPR) | 21 (22%) | 15 (29%) | 0.4 |
| Cardiogenic shock (CS) | 23 (24%) | 17 (33%) | 0.3 |
| Life‐threatening arrhythmias (VT/Vfib) | 24 (25%) | 16 (31%) | 0.5 |
| Clinical diagnosis | |||
| CAD | 91 (95%) | 49 (96%) | 0.9 |
| TTS | 2 (2%) | 2 (4%) | 0.5 |
| Myocarditis | 3 (3%) | 0 | 0.2 |
AMI, acute myocardial infarction; CAD, coronary artery disease; CPR, cardio‐pulmonary resuscitation; CS, cardiogenic shock; NSTEMI, non‐ST‐elevation MI; STEMI, ST‐elevation MI; TTS, Takotsubo cardiomyopathy syndrome; Vfib, ventricular fibrillation; VT, ventricular tachycardia.
Absolute number of admissions for AMI during early‐Covid‐19 [e‐COV: (n = 51) = 1 March to 30 April] and pre‐Covid‐19 pandemic [pre‐COV: (n = 96) = 1 January to 29 February]. Data are absolute values or percentage. Statistical analysis was performed with χ 2 tests. Statistical significance was reached with a P < 0.05.
Severity of presentation
| Severity of presentation | Pre‐COV (n = 96) | e‐COV (n = 51) |
|
|---|---|---|---|
| Troponin hs (ng/L) | 75 (29–200) | 292 (64–1165) | <0.0001 |
| CK (U/L) | 113 (72–232) | 391 (124–1191) | <0.0001 |
| Patients with LVEF < 45% at first medical contact | 15 (20%) | 19 (45%) | 0.03 |
| Inotropic support | 25 (26%) | 26 (51%) | 0.001 |
| Hemodynamic support (ECMO, Impella) | 10 (10%) | 11 (22%) | 0.1 |
| Invasive ventilation | 22 (23%) | 18 (35%) | 0.2 |
Increased measured high‐sensitivity troponin (troponin hs, ng/L) and creatine kinase (CK, U/L) at first medical contact during early‐Covid‐19 (e‐COV = 1 March to 30 April) pandemic compared with the pre‐Covid‐19 time (pre‐COV = 1 January to 29 February) as a marker for myocardial injury and potentially caused through a prolonged myocardial ischaemic time. Higher percentage of reduced measured left ventricular ejection fraction (LVEF < 45%) during e‐COV compared with pre‐COV at first medical contact. Higher use of inotropic support including dobutamine, epinephrine, norepinephrine, enoximone, and milrinone. Haemodynamic support including veno‐arterial extracorporeal membrane oxygenation system (va‐ECMO) and/or left ventricular microaxial pump system (Impella®). Data are absolute numbers or percentage. Statistical analysis was performed with χ 2 tests or Mann–Whitney test. Statistical significance was reached with a P < 0.05.
Figure 3Time delay in presentation with acute myocardial infarction (AMI) during COVID‐19 pandemic: a higher percentage of ST‐elevation myocardial infarction (STEMI) (A) and non‐ST‐elevation myocardial infarction (NSTEMI) (B) patients presented with a delayed time from symptom onset to first medical contact in e‐COV compared with pre‐COV. (C) Door to balloon time was not significantly changed in STEMI patients during e‐COV compared with pre‐COV. (D) Time from first medical contact to revascularization was significantly prolonged in NSTEMI patients during e‐COV. Black bars: e‐COV = 1 March to 30 April. White bars: pre‐COV = 1 January to 29 February. Data are percentage or minutes. Statistical analysis was performed with χ 2 tests or Mann–Whitney test. Statistical significance was reached with a P < 0.05.
Figure 4Major cardiac complications after acute myocardial infarction (AMI) during Covid‐19 pandemic: major cardiac complications after AMI represented as a composite endpoint of cardio‐pulmonary resuscitation, cardiogenic shock, and life‐threatening arrhythmias (including ventricular tachycardia and ventricular fibrillation) were significantly higher in early‐Covid‐19 (black bars: e‐COV = 1 March to 30 April) pandemic compared with the pre‐Covid‐19 time (white bars: pre‐COV = 1 January to 29 February). Data are percentage. Statistical analysis was performed with χ 2 tests. Statistical significance was reached with a P < 0.05.
Figure 5Myocardial injury and cardiac outcome of acute myocardial infarction (AMI) during Covid‐19 pandemic: (A) creatine kinase with its myocardial isoform (CK‐MB, U/L) and (B) maximum measured creatine kinase (CKmax, U/L) as a marker for total myocardial injury and damage after AMI were elevated during early‐Covid‐19 (black circles: e‐COV = 1 March to 30 April) pandemic compared with the pre‐Covid‐19 time (white circles: pre‐COV = 1 January to 29 February). (E) Significant lower left ventricular ejection fraction (LVEF,%) after AMI during hospitalization and (F) higher levels of NTproBNP (ng/L) as marker for heart failure in e‐COV. Data are mean ± SD. Statistical analysis was performed with Mann–Whitney test. Statistical significance was reached with a P < 0.05.