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. 2021 Jul 7;57(7):694. doi: 10.3390/medicina57070694

Clinical Outcome of Rotational Atherectomy in Calcified Lesions in Korea-ROCK Registry

Kyusup Lee 1, Ji-hoon Jung 2, Myunhee Lee 1, Dae-Won Kim 1, Mahn-Won Park 1, Ik-Jun Choi 3, Jae-Hwan Lee 4, Jang-Hoon Lee 5, Sang-Rok Lee 6, Pil-Hyung Lee 7, Seung-Whan Lee 7, Ki-Dong Yoo 8, Kyeong-Ho Yun 9, Hyun-Jong Lee 10, Sung-Ho Her 8,*
Editor: Tomasz Zieliński
PMCID: PMC8303478  PMID: 34356975

Abstract

Background and Objectives: Data is still limited regarding clinical outcomes of rotational atherectomy (RA) after percutaneous coronary intervention. We sought to evaluate clinical outcomes of RA. Materials and Methods: This multi-center registry enrolled patients who underwent RA during PCI from nine tertiary centers in Korea between January 2010 and October 2019. The primary endpoint was target-vessel failure (TVF; the composite outcome of cardiac death, target-vessel spontaneous myocardial infarction, or target-vessel revascularization). Results: Of 540 patients (583 lesions), the mean patient age was 71.4 ± 0.4 years, 323 patients (59.8%) were men, and 305 patients (56.5%) had diabetes mellitus. Technical success rate was 96.4%. In-hospital major adverse cerebral and cardiac events occurred in 63 cases (10.8%). At 1.5 years, 72 (16.0%) of TVFs were occurred. We evaluated independent predictors of TVF, which included current smoker (hazard ratio (HR), 1.92; 95% confidence interval (CI), 1.17–3.16; p = 0.01), chronic renal disease (HR, 1.87; 95% CI, 1.14–3.08; p = 0.013), history of cerebrovascular attack (HR, 2.14; 95% CI, 1.24-3.68; p = 0.006), left ventricle ejection fraction (HR, 0.98; 95% CI, 0.97–0.999; p = 0.037), and left main disease (HR, 1.94; 95% CI, 1.11–3.37; p = 0.019). Conclusions: From this registry, we demonstrated acceptable success rates, in-hospital and mid-term clinical outcomes of RA in the DES era.

Keywords: percutaneous coronary intervention, rotational atherectomy, drug-eluting stent, clinical outcome

1. Introduction

With the development of device technology, there have been expanded indications of percutaneous coronary intervention (PCI) to more challenging cases. Moreover, as the elderly population increases, we can get a more chance to meet patients with complex calcified coronary lesions in clinical practice [1].

With this current change, methods for modifying calcified coronary lesions have been more and more important (such as a non-compliant balloon, cutting/scoring balloon, orbital atherectomy, intravascular lithotripsy, and rotational atherectomy (RA)) [2,3,4,5]. The RA system is composed of a high-speed rotating diamond-coated burr that modifies calcified lesions. Therefore, it is a useful device for plaque modification of those lesions to facilitate balloon and stent delivery [6,7]. However, in our daily practice, patients qualified for RA are often “non-option” patients due to their comorbidity. Operators should be concerned about procedure-related complications and adverse clinical outcomes [8,9,10,11,12]. With the widespread use of second-generation drug-eluting stents (DES), optimal medical treatment, including statin and intravascular image, there has been a need for updated clinical results of RA in real-world practice. Therefore, we designed this study to introduce our registry and to investigate procedural outcomes, in-hospital events, and clinical outcomes of RA in the DES era.

2. Materials and Methods

2.1. Study Design and Population

The study population consisted of 540 patients (583 lesions) with calcified coronary artery disease (CAD) who underwent PCI using RA between January 2010 and October 2019 at 9 tertiary centers, from the ‘ROtational atherectomy in Calcified lesions in Korea (ROCK)’ registry. Data were collected at each site using a standardized case report form to record demographic and clinical characteristics and procedural and follow-up data. Follow-up data were collected retrospectively, based on medical records and a physician or patient interview. The local ethics committee approved this study of each hospital.

Between 2010 and 2019, consecutive patients with heavily calcific coronary lesions and significant stenosis (stenosis ≥ 70% of vessel diameter) who underwent PCI using RA were retrospectively enrolled from each institutional database. After reviewing angiography, two lesions could not be performed RA were dropped out from the registry. One experienced coronary perforation and cardiac tamponade before the RA procedure. The other could not pass the wire through the target lesion. Chronic kidney disease (CKD) was defined as an estimated glomerular filtration rate <60 mL/min/1.73 m2, as calculated using the Modification of Renal Diet equation from baseline serum creatinine [13].

2.2. Procedure

The treatment strategy, including decisions of performing/timing of RA, burr size, and selection of vascular access, was at the discretion of the attending cardiologists with careful consideration of clinical risk factors, anatomical complexity, patients’ conditions. Standard techniques and management guided all procedures. All RA procedures were performed using the RotablatorTM RA system (Boston Scientific, Marlborough, MA, USA). During RA, pauses in ablation runs and intracoronary nitroglycerin and/or verapamil were used to avoid coronary spasm and slow flow phenomenon. Antiplatelet therapy and peri-procedural anticoagulation were performed following the accepted guidelines [14,15].

2.3. Study Outcomes

The primary endpoint of the study was the occurrence of target-vessel failure (TVF), defined as cardiac death, target-vessel spontaneous myocardial infarction (MI), or target vessel revascularization (TVR). The secondary endpoint was all-cause death, cardiac death, any MI, target-vessel spontaneous MI, any repeat revascularization (RR), TVR, target-lesion revascularization (TLR), stent thrombosis (ST), coronary artery bypass grafting (CABG) surgery, cerebrovascular accident (CVA), and bleeding.

Technical success was defined as the achievement of residual stenosis < 30% in the presence of grade III Thrombolysis in myocardial infarction flow. Procedural success was defined as achieving technical success without in-hospital major adverse cerebral and cardiac events (MACCEs), including in-hospital death, in-hospital CVA, urgent revascularization (CABG or PCI), peri-procedural MI or ST during the index hospitalization period. Procedural complications included cardiac tamponade, coronary perforation, severe coronary dissection, defined from The National Heart, Lung, and Blood Institute classification system as type D, E, and F, temporary pacemaker insertion, contrast-induced nephropathy, or in-hospital bleeding.

We investigated procedure time, radiation dose, and contrast amount to assess procedural efficiency and safety. We also reviewed contrast-induced nephropathy (CIN) after PCI, which was defined as the impairment of kidney function-measured as either a 25% increase in serum creatinine from baseline or a 0.5 mg/dL increase in absolute serum creatinine value within 48–72 h after the procedure.

Death was defined as death from any cause. Target-vessel spontaneous MI was spontaneous MI clearly attributable to the target vessel. Spontaneous MI was defined as any creatine kinase-myocardial band or troponin increase above the upper limit of the normal range with ischemic symptoms or signs during follow-up after discharge. Peri-procedural MI was defined as peak elevations of the creatine kinase-myocardial band of >10-fold above the upper reference limit within 48 h after the procedure [16]. RR was defined as any percutaneous or surgical revascularization in any vessel. TVR was defined as any percutaneous or surgical revascularization of the treated vessel. TLR was defined as any percutaneous or surgical revascularization of the treated lesion. CVA was defined as a focal neurological deficit of central origin lasting >24 h, confirmed by a neurologist and imaging. All clinical events were confirmed by source documentation collected at each hospital and centrally adjudicated by an independent group of clinicians unaware of the revascularization type.

2.4. Statistical Analyses

Continuous variables were presented as mean ± standard deviation (SD) and compared using the Student t-test or Mann–Whitney U test. Categorical variables were presented as counts (percentages) and compared using the chi-square or Fisher exact test, as appropriate. Event rates were estimated on Kaplan–Meier estimates in time-to-first-event analyses, and they were compared using the log-rank test. A univariate Cox regression analysis was performed to obtain the hazard ratio (HR) for clinical outcomes. Then, to find out the independent predictors with the clinical outcomes, a multivariate Cox proportional hazard regression model was performed using important clinical covariates including clinically relevant variables and statistically significant variables with a p-value < 0.1 by univariate analysis. All reported p values were two-sided, and p values < 0.05 were considered statistically significant. Statistical analysis was performed with Statistical Package for Social Sciences, version 18.0.0 (SPSS Inc., Chicago, IL, USA).

3. Results

3.1. Baseline Patient, Lesion, and Procedural Characteristics

From January 2010 to October 2019, a total of 540 patients (583 lesions) who received PCI using RA were enrolled (Figure 1). Baseline patient characteristics are summarized in Table 1. The mean age was 71.4 ± 0.4 years (range, 19–104 years), and 323 (59.8%) patients were male gender. Three hundred five (56.5%) patients had diabetes mellitus. More than 60% of patients were diagnosed with the acute coronary syndrome. The mean left ventricular ejection fraction was 53.0 ± 13.4. Dual antiplatelet therapy (DAPT) and statin were prescribed well at discharge (95.9% and 92.4%, respectively).

Figure 1.

Figure 1

Study Population Flow Chart.

Table 1.

Baseline characteristics of the patients.

Characteristics Mean ± SD, n (%) or
Median (IQR)
(n = 540)
Age (years) 71.4 ± 0.4
Male 323 (59.8)
BMI (kg/m2) 24.2 ± 3.9
Diabetes mellitus 305 (56.5)
Insulin use 72 (13.3)
Hypertension 415 (76.9)
Hyperlipidemia 235 (43.5)
Current smoker 103 (19.1)
Clinical presentation
Silent ischemia 37 (6.9)
Stable angina 176 (32.6)
Unstable angina 175 (32.4)
NSTEMI 133 (24.6)
STEMI 19 (3.5)
Presented as ACS 327 (60.6)
Chronic kidney disease 96 (17.8)
Prior MI 66 (12.2)
Prior PCI 138 (25.6)
Prior CABG 24 (4.4)
Peripheral vascular disease 39 (7.2)
History of heart failure 77 (14.3)
Atrial fibrillation 49 (9.1)
LV EF, % 53.0 ± 13.4
Medication at discharge
Aspirin 529 (98.0)
P2Y12 Inhibitor 530 (98.1)
DAPT 518 (95.9)
B-blocker 381 (70.6)
ACEI/ARB 341 (63.1)
Statin 499 (92.4)
NOAC 17 (2.9)

Values are presented as n (%) or mean ± SD. Abbreviations: SD, standard deviation; IQR, interquartile range; BMI, body mass index; CAD, coronary artery disease; NSTEMI, non-ST elevation myocardial infarction; STEMI, ST-elevation myocardial infarction; ACS, acute coronary syndrome; MI, myocardial infarction; PCI, percutaneous coronary intervention; CABG, coronary artery bypass grafting; LV EF, left ventricle ejection fraction; DAPT, dual antiplatelet therapy; ACEI/ARB, angiotensin-converting-enzyme inhibitor/angiotensin II receptor blocker; NOAC, non-vitamin K oral anticoagulant.

The majority of lesions were classified as type B2 (10.1%) or C (82.3%) according to the American College of Cardiology and the American Heart Association (ACC/AHA) classification. Left anterior descending (LAD), including left main (LM), left circumflex (LCX) coronary artery, and right coronary artery (RCA) was involved in 65.9%, 10.1%, and 24.0%, respectively. LM and multivessel disease included in 14.1% and 80.1%, respectively (Table 2).

Table 2.

Lesion and procedural characteristics.

Characteristics Mean ± SD, n (%) or Median (IQR)
(n = 583)
ACC/AHA classification
Type B2/C 59 (10.1)/480 (82.4)
Target vessel
LAD 384 (65.9)
LCX 59 (10.1)
RCA 140 (24.0)
LM disease 82 (14.1)
Multivessel disease 467 (80.1)
Femoral approach 323 (55.4)
Treatment type
POBA 6 (1.0)
DEB 17 (2.9)
Stent implantation 548 (94.0)
Failure 12 (2.0)
IVUS or OCT 268 (46.0)
Escalation of Burr 91 (15.6)
Maximum Burr size, mm
1.25 157 (26.9)
1.5 308 (52.9)
1.75 107 (18.4)
2.0 10 (1.7)
2.5 1 (0.2)
Access size
5 F 5 (0.9)
6 F 215 (36.9)
7 F 326 (55.9)
8 F 37 (6.3)
Total number of stents 2.38 ± 1.18
Number of stents (target-vessel) 1.66 ± 0.68
Mean stent diameter, mm (target-vessel) 2.99 ± 0.38
Total stent length, mm 69.02 ± 35.66
Stent length, mm (target-vessel) 49.48 ± 21.13

Values are presented as n (%) or mean ± SD. Abbreviations: SD, standard deviation; ACC/AHA, American College of Cardiology/American Heart Association; LAD, left anterior descending; LCX, left circumflex; RCA, right coronary artery; LM, left main; POBA, plain old balloon angioplasty; DEB, drug-eluting balloon; IVUS, intravascular ultrasound; OCT, optical coherence tomography.

Detailed procedural characteristics were described in Table 2. The femoral approach was used in 55.4% of cases, whereas other cases used the radial approach. Stent implantation was performed in 548 (94.0%) patients, plain old balloon angioplasty (POBA) in six (1.0%), and drug-eluting balloon (DEB) in 16 (2.7%). The others (11 [1.9%] patients) could not perform anything due to technical failure. Intravascular ultrasound (IVUS) or optical coherence tomography were used in 46.0% of cases. The most frequently used burr size (maximum) was 1.5 mm (52.9%), followed by 1.25 mm, 1.75 mm, 2.0 mm, and 2.5 mm (26.9%, 18.4%, 1.7%, and 0.2%).

The number of stents per patient and per lesion was 2.38 ± 1.18 and 1.66 ± 0.68. Mean stent diameter, total stent length, and stent length per lesion were 2.99 ± 0.38, 69.02 ± 35.66, and 49.48 ± 21.13, respectively.

3.2. Procedural Outcomes

The rate of technical and procedural success was 96.4% and 86.1%. Procedure time was 63.4 (45.0–97.0) minutes. In addition, the amount of contrast used was 210 mL (interquartile range [IQR)]: 150–300 mL), and the radiation dose was 2685 mGy (IQR: 1512–4800 mGy) (Table 3).

Table 3.

In-hospital Events and Procedural Outcomes.

Mean ± SD, n (%) or Median (IQR)
Technical success 562 (96.4)
Procedural success 508 (87.1)
Contrast amount, mL 210 (150–300)
Procedure time, min 63.4 (45.0–97.0)
Radiation dose, mGy 2685 (1512–4800)
In-hospital MACCEs 62 (10.6)
In-hospital death 11 (1.9)
Procedure-related myocardial infarction 46 (7.9)
Urgent revascularization 9 (1.5)
In-hospital stroke 2 (0.3)
Procedural Complications
Cardiac tamponade requiring intervention 3 (0.5)
Coronary perforation 11 (1.9)
Severe coronary dissection immediate after RA procedure * 35 (6.0)
Temporary pacemaker during RA procedure 19 (3.3)
Contrast-Induced Nephropathy 19 (3.3)
In-hospital bleeding 27 (4.6)

* Type D, E, and F, defined from The National Heart, Lung, and Blood Institute (NHLBI) classification system. MACCE, major adverse cardiac and cerebral event; RA, rotational atherectomy; SD, standard deviation; IQR, interquartile range.

As shown in Table 3, in-hospital major adverse cerebral and cardiac events (MACCEs) occurred in 62 cases (10.6%), mainly driven by peri-procedural myocardial infarction (46 cases, 7.9%). In-hospital death and in-hospital CVA occurred in 11 (1.9%) and 2 (0.3%) patients. Severe coronary dissection (Type D, E, and F) and coronary perforation occurred in 35 (6.0%) and 11 (1.9%) cases. Cardiac tamponade requiring intervention occurred in 3 cases (0.5%). Urgent revascularization was needed in nine patients (1.5%; 2 CABG; 7 PCI).

3.3. Clinical Outcomes

Median follow-up duration was 1.5 (IQR, 0.7–2.9) years. At 1.5 years, 72 TVFs (16.0%) occurred and all-cause death occurred in 37 (8.4%), cardiac death in 33 (6.9%), spontaneous MI in 18 (4.2%), target-vessel spontaneous MI in 9 (2.1%), any RR in 53 (12.8%), TVR in 41 (9.8%), TLR in 34 (8.2%), CVA in 10 (2.0%), and ST in 6 (1.2%) (Figure 2). One patient underwent urgent CABG at 11 days after the index procedure.

Figure 2.

Figure 2

Kaplan-Meier Curves for Clinical Outcomes at 18 months.

We evaluated independent predictors of TVF, which included current smoker (hazard ratio [HR], 1.92; 95% confidence interval (CI), 1.17–3.16; p = 0.01), chronic renal disease (HR, 1.87; 95% CI, 1.14–3.08; p = 0.013), history of cerebrovascular attack (HR, 2.14; 95% CI, 1.24–3.68; p = 0.006), left ventricle ejection fraction (HR, 0.98; 95% CI, 0.97–0.999; p = 0.037), and left main disease (HR, 1.94; 95% CI, 1.11–3.37; p = 0.019) (Table 4).

Table 4.

Univariable and multivariable cox regression analysis of independent predictors of target-vessel failure.

Univariate Multivariate *
Variables HR (95% CI) p HR (95% CI) p
Age 0.99 (0.97–1.01) 0.43
Male gender 1.12 (0.74–1.70) 0.59
Current smoker 1.67 (1.06–2.65) 0.028 1.92 (1.17–3.16) 0.01
HTN 0.97 (0.60–1.57) 0.91
Diabetes mellitus 1.39 (0.91–2.11) 0.13
Hyperlipidemia 0.59 (0.38–0.92) 0.018
Chronic kidney disease 2.12 (1.34–3.35) 0.001 1.87 (1.14–3.08) 0.013
Family history of CAD 1.50 (0.37–6.11) 0.57
Prior MI 0.60 (0.28–1.29) 0.19
Prior PCI 1.10 (0.69–1.73) 0.70
Prior CABG 0.91 (0.33–2.48) 0.85
History of cerebrovascular attack 2.15 (1.32–3.50) 0.002 2.14 (1.24–3.68) 0.006
Peripheral artery disease 1.69 (0.88–3.25) 0.12
Atrial fibrillation 1.54 (0.82–2.90) 0.18
LV EF (%) 0.98 (0.96–0.99) 0.003 0.98 (0.97–0.999) 0.037
Presented as ACS 1.61 (1.03–2.51) 0.035 1.54 (0.95–2.51) 0.08
MVD 0.95 (0.56–1.61) 0.86
LM disease 1.68 (1.02–2.75) 0.041 1.94 (1.11–3.37) 0.019
Mean stent diameter per target vessel 0.97 (0.55–1.71) 0.92
Total number of stents 1.23 (1.04–1.44) 0.014 1.19 (0.996–1.41) 0.06
Total stent length 1.007 (1.001–1.012) 0.026

* adjusted by age, gender, current smoker, diabetes mellitus, chronic kidney disease, history of cerebrovascular attack, LV EF, presented as an acute coronary syndrome, left main disease, the total number of stents, and total stent length HR, hazard ratio; CI, confidence interval; HTN, hypertension; CAD, coronary artery disease; MI, myocardial infarction; PCI, percutaneous coronary intervention; CABG, coronary artery bypass grafting surgery; LV EF, left ventricle ejection fraction; ACS, acute coronary syndrome; MVD, multivessel disease; LM, left-main.

3.4. Subgroup Analysis among Patients that Received PCI Successfully According to Clinical Presentation

To demonstrate the high mortality rate of our registry (27.1% during the entire follow-up period, 0–10.1 years), we performed a subgroup analysis of patients who received PCI successfully (n = 541). We investigated the long-term clinical outcomes according to clinical presentation (ACS versus stable angina). Kaplan–Meier curves showed poorer clinical outcomes regarding the TVF and mortality in ACS group compared to stable angina group (21.7% vs. 14.5%, log-rank p = 0.005; 14.1% vs. 6.8%, log-rank p < 0.001, respectively) (Supplement Figure S1). Multivariable cox regression analysis revealed that ACS was an independent predictor of mortality (HR, 1.94; 95% CI, 1.002–3.75; p = 0.049) (Supplement Table S3).

4. Discussion

Major findings from our study were as follows: (1) Technical and procedural success rate of RA was acceptable in heavily calcified and diffuse coronary lesions; (2) RA during PCI was safe and efficient for revascularization regarding in-hospital MACCEs and procedural complications, as well as procedural outcomes (procedure time, contrast amount, or radiation dose); (3) the independent predictors of TVF were identified from our registry.

This ‘ROtational atherectomy in Calcified lesions in Korea (ROCK)’ registry is the largest, all-comer, multi-center registry, including patients undergoing RA in Korea. Patients who were received PCI were implanted with drug-eluting stents (DESs), especially 2nd generation DES, except for one patient with 1st generation DES, which might reflect the clinical outcomes of RA in the 2nd-generation DES era. As described previously, DAPT and statin were prescribed above 90% of the study population, which would reflect that these patients were treated as current guidelines [14,17,18].

All cases except for a few chronic total occlusion or in-stent restenosis cases were calcified and diffuse disease, represented by 82.4% of lesions classified as type C (ACC/AHA classification). In 38% of cases, RA was done due to unsuccessful 2.0 mm sized or bigger balloon predilatation. In the others, RA was done promptly based on the operator's decision. It was based on angiographic findings, the calcification arc revealed by intravascular images, the friction of smaller balloons or wires, etc. Although, we provided data of acceptable efficacy outcomes regarding success rate and procedural outcomes. We achieved final TIMI 3 in 96.4% of all cases, similar to the previous studies [1,12,19,20,21]. The absolute values of procedure time and contrast amount were smaller compared to the previous study [20].

The study population consisted of patients with advanced coronary atherosclerosis and high comorbidity. Indeed, diabetes mellitus accounted for more than half of the study population, and more than 80% were multivessel diseases. From the current guideline, for revascularization of multivessel disease accompanied by diabetes, we should consider CABG [22,23]. However, because of high-risk peri-operative mortality and morbidity and patients’ preference, operators chose the PCI with RA instead of CABG for those patients in this registry. Although, in-hospital MACCEs and procedural complications showed feasible and acceptable results compared to other previous studies [1,12,19,20,21]. However, in-hospital MACCEs were developed in 10.6% of our registry, mainly driven by peri-procedural MI, which showed higher events than previous studies. We thought plausible explanations as follows; (1) because we included more than 60% of ACS patients; (2) events were recorded according to 10 times elevation of the cardiac enzyme (CK-MB) with medical records, would be over-estimated. Coronary perforation occurred in 1.9% of cases, consistent with previous studies (0.5–2.3%) [12,19,20,21].

As shown in Table 5, our study showed relatively high mortality similar to that of the J2T Multicenter registry [1]. We found one possible explanation from baseline clinical demographics in both of the two studies, which might be due to a large proportion (more than 50%) of the acute coronary syndrome (ACS). Our subgroup analysis demonstrated ACS was an independent predictor of mortality among patients who received PCI successfully.

Table 5.

Comparison with previous studies of rotational atherectomy including technical success and follow-up clinical outcomes.

All Study Population Era Technical Success, % Follow-Up Duration All-Cause Death, % TVR, % TLR, % ST, % CVA, %
Okai et al. [1] 1090 DES 96.2 3.8 (IQR 1.9–6.1) years 24.2 21.4 16.2 1.3 4.7
Kawamoto et al. [20] 985 8.8% BMS91.2% DES 99.1 2 years 9.5 19.8 16.6 1.8 1.0
Cortese et al. [21] 1397 17% POBA40.7% BMS42% DES 99.3 2.4 (0.8–5.7) years 6.4 - 11.7 1.4 -
Rathore et al. [19] 516 24.2% BMS75.8% DES 99.4 6–9 months - - 14.4 0.8 * -
Abdel-Wahab et al. [12] 205 DES 98.0 1.3 (0.08–7) years 9.0 11.2 7.9 1.0 -
Our study ** 540 DES 96.4 1.5 (IQR 0.7–2.9) years 8.4 9.8 8.2 1.2 2.0

* Includes only late stent thrombosis. ** Event rates at 18 months were estimated on Kaplan–Meier estimates in time-to-first-event analyses. TVR, target-vessel revascularization; TLR, target-lesion revascularization; ST, stent thrombosis; CVA, cerebrovascular accident; DES, drug-eluting stent; IQR, interquartile range; BMS, bare metal stent; POBA, plain old balloon angioplasty.

Patients received 2nd-generation DES were included in 36.3% (J2T Multicenter registry) [1] and 69.3% (ROTATE registry) [20]. In our registry, as mentioned above, we included 99.8% of 2nd-generation DES among patients treated with stent implantation. This homogeneity of implanted stents is the unique and valuable strength of our registry. Moreover, nearly half of the cases were performed procedures with intravascular image guidance. We could evaluate the benefit of intravascular guidance in RA with our data.

TVF occurred in 16.0% at 1.5 years, which showed acceptable clinical outcomes to previous studies considering that our study population consisted of more elderly patients, ACS patients, including ST-elevation MI, and the long-term follow-up period. We summarized clinical outcomes compared with previous studies of RA (Table 5).

Limitation

Our study has several limitations. This was a non-randomized, observational, single-arm, retrospective study. Due to the relatively large number of centers included in the study over the long study period, there may be confounders that have not been accounted for. Second, the registry included a relatively limited number of patients and insufficient follow-up duration to evaluate the long-term clinical outcomes. Third, parameters of lesion complexity (such as SYNTAX score or quantitative coronary angiography) were not available. Therefore, our findings should be further evaluated after reassessing those parameters.

5. Conclusions

Our study has provided a large registry for in-hospital and long-term clinical outcomes of RA in the 2nd-generation DES era, which showed acceptable success rates, in-hospital, and long-term clinical outcomes.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/medicina57070694/s1, Figure S1: Kaplan-Meier curves for 3-year clinical outcomes according to clinical presentation., Table S1: Clinical characteristics according to clinical presentation among patients received PCI successfully., Table S2: Lesion and procedural characteristics according to clinical presentation among patients received PCI successfully., Table S3: Multivariable Cox Regression Analysis of Independent Predictors of all-cause death.

Author Contributions

K.L. designed the study, collected data, analyzed the data, drafted and revised the manuscript, drew figures; J.-h.J., M.L., D.-W.K., M.-W.P., I.-J.C., J.-H.L. (Jae-Hwan Lee), J.-H.L. (Jang-Hoon Lee), S.-R.L., P.-H.L., S.-W.L., K.-D.Y., K.-H.Y., and H.-J.L. (Jang-Hoon Lee) collected data; S.-H.H. designed the study, collected data, validated data, and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by grants from the Nuri Cardiovascular Society Foundation of South Korea.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board of Daejeon St. Mary’s Hospital (DC19REDI0066 and 30 July 2019).

Informed Consent Statement

Patient consent was waived due to retrospective design of this study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The data presented in this study are available on request from the corresponding author.


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