Short Communication - Interventional Cardiology (2022) Volume 14, Issue 5
Clinical effects of percutaneous coronary intervention of chronic total occlusion in noninfarct-related artery after acute myocardial infarction
- Corresponding Author:
- Junbo Ge
Department of Cardiology,
Zhongshan Hospital, Shanghai Institute of Cardiovascular Diseases,
Fudan University,
Shanghai,
China,
E-mail: ge.junbo@zs-hospital.sh.cn
Received date: 29-Aug-2022, Manuscript No. FMIC-22-68208; Editor assigned: 31-Aug-2022, PreQC No. FMIC-22-68208 (PQ); Reviewed date: 14-Sep-2022, QC No. FMIC-22-68208;Revised date: 21-Sep-2022, Manuscript No. FMIC-22-68208 (R);Published date: 28-Sep-2022, DOI: 10.37532/1755-5310.2022.14(5).552
Abstract
The success rate of Percutaneous Coronary Intervention (PCI) in coronary Chronic Total Occlusion (CTO) has improved with technical and technological progress, however, the clinical benefit of CTO PCI is still controversial. In this article, we summarize the clinical studies with long term follow up data investigating the effect of CTO PCI in noninfarct-related artery after acute myocardial infarction.
Keywords
Percutaneous coronary intervention • Chronic total occlusion • Acute myocardial infarction
Description
In the current era, the technical success rate of Percutaneous Coronary Intervention (PCI) of coronary Chronic Total Occlusions (CTOs) has achieved nearly 90%, along with the improvements in techniques, devices and operator’s experiences, as well as the standardization of the procedure [1,2]. However, CTO PCI remains a controversial procedure as its clinical benefit remains to be determined. The Randomized Clinical Trials (RCTs) demonstrated improvement in Quality Of Life (QOL) [3,4] and relieved myocardial ischemic burden [5] in patients underwent CTO PCI compared with Optimal Medical Therapy (OMT), but failed to show recovery of regional wall motion or benefit on Major Adverse Cardiovascular Events (MACEs) in these patients [3-6]. Consequently, the recommendation level of CTO PCI in 2021 ACC/AHA/SCAI Guideline for Coronary Artery Revascularization is IIB [7]. The results of the ongoing ISCHEMIA-CTO (Revascularization or Optimal Medical Therapy of CTO; NCT03563417) may add evidence to the benefit of CTO-PCI in patients with myocardial ischemia.
Recently, clinical studies focused on the effect of CTO PCI in non-culprit arteries of patients with Acute Myocardial Infarction (AMI), as patients with AMI and concurrent CTO had worse clinical outcomes compared with patients with AMI but without CTO [8]. Moreover, Fujimoto Y, et al. demonstrated patients with AMI with CTO in non-culprit arteries had worse clinical outcomes than those with 90% to 99% stenosis in non-culprit arteries during a median follow-up duration of 1.2 years [9], suggesting patients with CTO had more myocardial damage and early revascularization may be considered. However, the long term follow up results of EXPLORE trial failed to confirm the beneficial effect of early CTO PCI on MACE after ST-Segment Elevation Myocardial Infarction (STEMI) [10]. Instead, a significantly higher rate of cardiac death was demonstrated in patients randomized to CTO PCI [10]. The long term follow up data from the randomized EXPLORE trial seems to be contrary to the data from retrospective studies, which demonstrated lower rate of cardiac death in patients in CTO PCI group after AMI (Table 1) [11-14].
Authors | Year published | Study design | Area | Sites | Target | Number of patients | Group | Time interval after IRA PCI | MACE/MACCE definition | J-CTO score | Procedural success | Follow-up duration | Cardiac death | MACE/MACCE |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Elias, et al. [10] | 2018 | Randomized clinical trial | Europe and Canada | 14 centers | STEMI and concurrent CTO | 302 | CTO PCI vs. MT (n=148) (n=154) | 5.0 ± 1.9 days | cardiac death, MI, and CABG | 2 ± 1 vs. 2 ± 1 | 73% | Median 3.9 years | 6% vs. 1% p=0.02 | 13.5% vs. 12.3% p=0.93 |
Valenti, et al. [11] | 2014 | Retrospective | Italy | Single center | STEMI and concurrent CTO | 169 | s-CTO vs. o-CTO (n=58) (n=111) | within 1 month | - | - | 78.40% | Median 3.9 years | 3.7% vs. 14.9% p=0.03 | - |
Choi, et al [12] | 2016 | Retrospective | Korea | 9 centers | AMI and concurrent CTO | 324 | s-CTO vs. o-CTO (n=170) (n=154) | - | all‐cause death, stroke, nonfatal MI, and any revascularization | - | - | Median 3.5 years | 7.6% vs. 20.1% p=0.001 | 15.9% vs. 37.7% p<0.001 |
Yoshida, et al. [13] | 2020 | Retrospective | Japan | Single center | AMI and concurrent CTO | 172 | s-CTO vs. o-CTO (n=65) (n=107) | within 3 months | cardiac death, MI, and CABG | 1(1-2) vs. 1(1-2) | 73.90% | Median 4.1 years | 19.0% vs. 51.9% p=0.004 | 22.7% vs. 57.1% p=0.0002 |
Cui, et al. [14] | 2020 | Retrospective | China | Single center | STEMI and concurrent CTO | 287 | CTO PCI vs. MT (n=91) (n=196) | 8 (5-40) days | all‐cause death, stroke, nonfatal MI, and unplanned revascularization | - | 80.20% | Mean 6.1 years | 4.4% vs. 16.8% - | 22% vs. 46.9% p=0.002 |
Qin, et al. [15] | 2022 | Retrospective | China | Single center | AMI and concurrent CTO | 330 | CTO PCI vs. MT (n=198) (n=132) | within 1 year | all‐cause death, stroke, nonfatal MI, and any revascularization | - | 83.80% | Median 2.6 years | 3.0% vs. 12.1% p=0.004 | 22.2% vs. 37.1% p=0.055 |
Abbreviations: IRA: Infarct Related Artery; PCI: Percutaneous Coronary Intervention; MACE: Major Adverse Cardiacvascular Event; MACCE: Major Adverse Cardiovascular and Cerebrovascular Event; STEMI: ST-Segment Elevation Myocardial Infarction; CTO: Chronic Total Occlusion; MT: Medical Therapy; MI: Myocardial Infarction; CABG: Coronary Artery Bypass Grafting; s-CTO: successful CTO; o-CTO: occluded CTO( MT and failed CTO PCI); AMI: Acute Myocardial Infarction
Table 1: Clinical studies with long term follow up data investigating the effect of percutaneous coronary intervention of chronic total occlusion in noninfarct-related artery after acute myocardial infarction.
It should be noted that the procedural success (73%) in EXPLORE trial was relatively lower than that in retrospective studies published recently (>80%), which may cause underestimation of the value of CTO recanalization [14,15]. Furthermore, the early CTO-PCI (5.0 ± 1.9 days) after primary PCI in EXPLORE may aggravate inflammation and cause adverse left ventricular remodeling.
Conclusion
Therefore, a well-designed randomized clinical trial with reasonable time interval after Infarct Related Artery (IRA) PCI is required to show whether patients may benefit from CTO-PCI after AMI under contemporary techniques and experiences. As patients with AMI and concurrent CTO have high risk of clinical events, the sample size to demonstrate the effect of CTO PCI on hard end points will not be too big.
Nowadays, the technical issue in CTO recanalization is no longer a challenge. We need to identify the group of high-risk patients who will benefit from CTO-PCI in terms of hard cardiovascular outcomes.
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