Results from clinical trials on ST‐elevation myocardial infarction in a historic perspective with some pathophysiological aspects

2003 ◽  
Vol 37 (6) ◽  
pp. 316-323 ◽  
Author(s):  
Jan Erik Otterstad ◽  
Frank Brosstad
2021 ◽  
Vol 42 (Supplement_1) ◽  
Author(s):  
L Oliveira ◽  
C Machado ◽  
C Almeida ◽  
M Fatima Loureiro ◽  
D Martins ◽  
...  

Abstract Background Current European Society of Cardiology guidelines recommend an invasive strategy (IS) for the treatment of non-ST elevation myocardial infarction (NSTEMI) patients, but the clinical trials that support this recommendations included only a few patients with previous coronary artery bypass graft (CABG). Purpose To characterize NSTEMI patients with previous CABG who underwent medical and invasive management and to evaluate the prognostic impact of the type of strategy used. Methods Retrospective analysis of a cohort of patients from a multicenter national registry diagnosed with NSTEMI with a previous history of CABG between 2010 and 2021. Patient's baseline demographics, medical history and in-hospital management data was collected. Outcomes of in-hospital and six months follow-up all-cause mortality were accessed. Results A total of 890 patients were included in the analysis. Of these, 470 were medically managed (MM) – this group included 249 patients (53.1%) who underwent coronary angiography but did not perform any further revascularization. The remaining 420 underwent an invasive strategy (IS) and performed additional revascularization, mainly percutaneous (only 1 patient submitted to reCABG). Mean age was similar (MM 72±10 vs IS 71±10 years, p=0.147) and most patients were male (MM 81.5% vs IS 83.8%, p=0.362). MM patients had more chronic kidney disease (16.7% vs 9.9%, p=0.003), peripheral artery disease (20.5% vs 15.0%, p=0.003) and heart failure (20.5% vs 11.9%, p<0.001). Main presenting symptom was chest pain in both groups, however it was more frequent in the IS group (89.4% vs 94.5%, p=0.006) and dyspnea in the MM patients (6.3% vs 3.1%). Mean left ventricle ejection fraction was similar between groups (MM 49±12% vs IS 50±11%, p=0.290). Although the GRACE risk score was available for only 124 patients, high risk patients (GRACE score >140) were equally distributed among the two groups (55.9% vs 48.2%, p=0.395). An IS was associated with significant lower in-hospital mortality (4.5% vs 1.7%, OR 0.37, 95% CI 0.15–0.87, p=0.018). At six months follow-up an IS was also associated with lower mortality (6.6% vs 2.4%, HR 0.18, 95% CI 0.06–0.52, p=0.002), even after adjusting for the baseline differences (HR 0.41, 95% CI 0.20–0.85, p=0.016). Conclusions In this cohort of patients with NSTEMI and previous CABG, an IS was linked to better outcomes during hospitalization and during six months follow-up. Randomized clinical trials are needed to address this issue. FUNDunding Acknowledgement Type of funding sources: None.


2020 ◽  
Vol 13 (Suppl_1) ◽  
Author(s):  
Brian C Case ◽  
Charan Yerasi ◽  
Yanying Wang ◽  
Brian J Forrestal ◽  
Joshua Hahm ◽  
...  

Objectives: This study aimed to evaluate non-ST-elevation myocardial infarction (NSTEMI) rates, revascularization timing, and mortality rates using the Nationwide Readmissions Database (NRD). Background: Clinical trials have shown improved outcomes with reduced mortality with an early invasive approach for NSTEMI. However, real-world data are lacking. Methods: The study cohort was obtained from the 2016 NRD dataset. We used the International Classification of Diseases, Tenth Revision, to identify patients who underwent diagnostic angiography and subsequently received either percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG). Finally, revascularization timing and mortality rates (in-hospital and 30-day) were extracted. Results: Our analysis included 748,463 NSTEMI admissions in 2016. Of these admissions, 50.1% (374,988) underwent diagnostic angiography with 38.9% (253,492) revascularized: 77.6% (197,945) PCI and 22.4% (57,254) CABG. Patients with more comorbidities tended to have more delayed revascularization. PCI was most commonly performed on the day of admission, 32.9% (65,155). This differs from CABG, which was most commonly performed on Day 3 after admission, 13.7% (7,823). The in-hospital mortality rate increased after Day 1 for PCI patients and after Day 4 for CABG patients, whereas 30-day in-hospital mortality for both populations increased as revascularization was delayed (Figure 1). Conclusions: Our study shows that mortality generally increased as revascularization was delayed, while sicker patients tended to have longer delays until revascularization. However, confounding variables prevent definite causal attribution. Randomized clinical trials are needed to evaluate whether very early revascularization (<90 minutes) is associated with improved long-term outcomes in high-risk patients.


Author(s):  
S. El Kadi ◽  
T. R. Porter ◽  
A. C. van Rossum ◽  
O. Kamp

Abstract Background Treatment of ST-elevation myocardial infarction (STEMI) has improved over the years. Current challenges in the management of STEMI are achievement of early reperfusion and the prevention of microvascular injury. Sonothrombolysis has emerged as a potential treatment for acute myocardial infarction, both for epicardial recanalisation as well as improving microvascular perfusion. This study aims to determine safety and feasibility of sonothrombolysis application in STEMI patients in the ambulance. Methods Ten patients with STEMI will be included and treated with sonothrombolysis in the ambulance during transfer to the PCI centre. Safety will be assessed by the occurrence of ventricular arrhythmias and shock during sonothrombolysis intervention. Feasibility will be assessed by the extent of protocol completion and myocardial visibility. Efficacy will be determined by angiographic patency rate, ST-elevation resolution, infarct size and left ventricular volumes, and function measured with cardiovascular magnetic resonance imaging, and contrast and strain echocardiography. A comparison will be made with matched controls using an existing STEMI database. Discussion Sonothrombolysis is a novel technique for the treatment of cardiovascular thromboembolic disease. The first clinical trials on its use for STEMI have demonstrated promising results. This study will be the first to examine the feasibility of in-ambulance sonothrombolysis for STEMI. Trial registration EU Clinical Trials Register (identifier: 2019-001883-31), registered 2020-02-25.


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