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Article

Clinical Outcomes and Prognostic Factors in Complex, High-Risk Indicated Procedure (CHIP) and High-Bleeding-Risk (HBR) Patients Undergoing Percutaneous Coronary Intervention with Sirolimus-Eluting Stent Implantation: 4-Year Results

by
Maciej Tyczyński
1,
Adam Kern
2,
Patryk Buller
3,
Wojciech Wańha
4,
Robert J. Gil
5 and
Jacek Bil
1,*
1
Department of Invasive Cardiology, Center of Postgraduate Medical Education, 02-508 Warsaw, Poland
2
Department of Cardiology and Internal Medicine, School of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland
3
Department of Cardiology, Provincial Integrated Hospital, 09-400 Plock, Poland
4
Department of Cardiology and Structural Heart Diseases, Medical University of Silesia, 40-635 Katowice, Poland
5
Department of Cardiology, State Medical Institute of the Ministry of Interior and Administration, 02-508 Warsaw, Poland
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2023, 12(16), 5313; https://doi.org/10.3390/jcm12165313
Submission received: 26 July 2023 / Revised: 9 August 2023 / Accepted: 14 August 2023 / Published: 15 August 2023
(This article belongs to the Special Issue Interventional Cardiology: Current Challenges in Clinical Practice)
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Abstract

:
We aimed to characterize the performance and safety of percutaneous coronary intervention (PCI) in complex, high-risk indicated procedure (CHIP) and high-bleeding-risk (HBR) patients at a 4-year follow up. We included all consecutive patients who underwent PCI with the sirolimus-eluting coronary stent Alex Plus (Balton, Poland) between July 2015 and March 2016. We analyzed various baseline demographic and clinical characteristics, laboratory data, and clinical outcomes. We enrolled 232 patients in whom 282 stents were implanted, including 81 patients meeting the CHIP criteria and 76 patients meeting the HBR criteria. In the whole population, the mean age was 68 ± 11 years, and 23.7% were females. Most procedures were performed from radial access (83.2%) using a 6F guiding catheter (95.7%). The lesions were mostly predilated (61.6%), and postdilatation was performed in 37.9%. The device success was 99.6% (in one case, a second stent was required due to heavy calcifications). Additional stents were deployed in 39% of cases due to edge dissection (6.9%), side branch stenting (5.2%), or diffuse disease (26.9%). Myocardial infarction (MI) type 4a was revealed in 2.2% of cases. At 4 years, the MACE rates for the whole population and for CHIP and HBR patients were 23.3%, 29.6%, and 27.6%, respectively. CHIP patients had a higher risk of MACEs (29.6% vs. 19.9%, HR 1.69, p = 0.032) and cardiac death (11.1% vs. 4.6%, HR 2.50, p = 0.048). There were no differences for MI (7.4% vs. 6.6%, p = 0.826) and TLR (18.5% vs. 12.6%, p = 0.150). HBR patients were also characterized by a higher risk of MACEs (27.6% vs. 21.2%, HR 1.84, p = 0.049) and cardiac death (17.1% vs. 1.9%, HR 9.61, p < 0.001). There were no differences for MI (7.9% vs. 6.4%, p = 0.669) and TLR (11.8% vs. 16.0%, p = 0.991). PCI in CHIP and HBR patients is feasible with a low rate of periprocedural complications. Nevertheless, CHIP and HBR patients are at a high risk of future adverse events and require strict surveillance to improve outcomes.

Graphical Abstract

1. Introduction

Since 1977, tremendous progress has been made in percutaneous coronary intervention (PCI) techniques and the stents used. Unfortunately, the problem of in-stent restenosis (ISR) is still ongoing despite the invention of drug-eluting stents (DESs) and their continuous improvement. Approximately 10% of all PCI procedures are performed yearly because of ISR [1], and ISR significantly impacts long-term clinical outcomes in patients undergoing PCI. In the NCDR registry having the data of 653,304 patients, PCI due to ISR was performed in 10.2% of cases. Patients undergoing PCI due to ISR were characterized by a worse prognosis. Those patients had a higher rate of major adverse cardiovascular and cerebrovascular events (MACCEs) at 36-month follow up, including a higher incidence of all-cause death, myocardial infarction (MI), or target lesion revascularization (TLR) [2].
In many patients, ISR presents as an acute coronary syndrome without persistent ST-segment elevation. Although DESs have reduced the risk of ISR by 60% compared to bare metal stents (BMSs), the ISR problem remains significant and increases exponentially with the number of reinterventions. Moreover, as the follow up lengthens (i.e., 5–10 years), the late catch-up phenomenon in ISR rates is observed between DESs and BMSs [3].
Various clinical and procedural (considering a lesion, a stent, or a procedure itself) factors are associated with unfavorable outcomes. Comorbidities (diabetes, dyslipidemia, chronic kidney disease) or massive coronary artery calcifications might play a significant role [4,5]. Similarly, the type of stent is also of enormous importance. The thickness of stent struts affects the degree of damage to the arterial wall at the time of implantation and the local blood rheology after stent deployment. As a result, this affects the strength of the inflammatory response at the target lesion, reendothelialization, strut coverage, and neointima formation. Stent underexpansion, malapposition, and the leaving of so-called stent gaps are also linked with an elevated risk of ischemic complications [6,7,8,9]. In 2019, a new restenosis classification was proposed, considering intravascular imaging and available treatment options [10].
With an aging population and improvements in technology, we treat more and more difficult patients both in terms of bleeding as well as ischemic complications. To tackle this issue and better characterize it in further studies, new terms have been defined such as high-bleeding-risk (HBR) patients and patients undergoing complex, high-risk indicated procedures (CHIPs) [11,12]. The abovementioned factors associated with ISR also pose a challenge in CHIP patients to obtain optimal procedural as well as long-term outcomes. In CHIP patients, to obtain the optimal outcome, often, additional interventions are required, such as using rotational atherectomy or orbital atherectomy, which makes the procedures even more difficult and associated with a higher risk of periprocedural complications [13,14]. Moreover, more and more frequently, CHIP patients undergo PCI with the simultaneous use of percutaneous left ventricular assist devices [15,16].
CHIP patients pose the highest challenge in modern PCI; however, in the past 20 years, ischemic events after PCI halved (from 18.4% to 9.1%), and out-of-hospital bleeding doubled (from 2.5% to 5%). The proper identification of HBR patients and bleeding prevention became a priority in modern cardiology. This is because bleeding episodes, even if not linked directly with poor outcomes, evoke worse medication adherence and quality-of-life deterioration [17].
We aimed to characterize the performance and safety of PCI with second-generation sirolimus-eluting stents with a biodegradable polymer in CHIP and HBR patients at a 4-year follow up.

2. Materials and Methods

2.1. Study Design and Participants

We obtained data retrospectively from the hospital database and analyzed all consecutive patients who underwent PCI with sirolimus-eluting coronary stent Alex Plus (Balton, Poland) implantation between July 2015 and March 2016. We included patients undergoing PCI in the setting of chronic coronary syndrome as well as acute coronary syndrome. Additionally, we differentiated two subgroups, i.e., complex, high-risk indicated procedure (CHIP) patients and high-bleeding-risk (HBR) patients.
We compared various baseline demographic and clinical characteristics, laboratory data (see Section 2.4), and clinical outcomes (see Section 2.5) at a 4-year follow up in the whole population and in the CHIP and HBR subgroups.

2.2. CHIP and HBR Subgroup Criteria

CHIP patients were characterized as having at least one clinical criterion and one anatomical high-risk criterion [11,18]. The clinical criteria were as follows: advanced age (≥75 years), diabetes mellitus, heart failure with left ventricular ejection fraction ≤ 35%, acute coronary syndrome, previous cardiac surgery, peripheral vascular disease, advanced chronic kidney disease (estimated glomerular filtration rate < 30 mL/min/1.73 m2), chronic obstructive pulmonary disease, concomitant severe aortic valvulopathy, or severe mitral regurgitation. The anatomical criteria were as follows: unprotected left main disease, degenerated saphenous vein grafts, severely calcified lesions requiring rotational atherectomy, last patent conduit, or chronic total occlusion in a patient with multivessel disease.
HBR patients were characterized based on the Academic Research Consortium for High Bleeding Risk (ARC-HBR). Patients were considered HBR if at least one major or two minor criteria were met [12]. The ARC-HBR criteria were adopted since they provide reliable predictions for major bleeding also in acute coronary syndrome patients [19] and they are not inferior to other scores such as PRECISE-DAPT [20].

2.3. Alex Plus Stent Characteristics

The Alex Plus stent platform is made of cobalt–chromium alloy (L605) with a strut thickness of 70 μm. The sirolimus concentration is 1.3 μg/mm2, and the drug is released from a biodegradable polymer in a process lasting for 8 weeks [21,22]. The stent’s nominal diameter and length ranges are 2.0–5.0 mm and 8.0–40.0 mm, respectively. The stent can be overexpanded during postdilatation (3.5 mm → 4.3 mm; 4.0 mm → 4.7 mm; 5.0 mm → 6.0 mm).

2.4. Data Collection

We gathered demographic, clinical, periprocedural, and laboratory data from the hospital database. We collected information on comorbidities such as arterial hypertension, dyslipidemia, diabetes mellitus, prior PCI, prior MI, chronic kidney disease (defined as eGFR < 60 mL/min/1.73 m2), prior coronary artery bypass grafting (CABG), prior stroke, peripheral artery disease, chronic obstructive pulmonary disease (COPD), and smoking. Additionally, we analyzed data on PCI: planned vs. urgent, lesion location, lesion type (A, B1, B2, C according to AHA/ACC classification [23]), and periprocedural complications. Additionally, the SYNTAX (https://syntaxscore.org accessed on 10 April 2023), SYNTAX II [24], and EuroScore II (https://www.euroscore.org accessed on 12 April 2023) were calculated. Moreover, we collected information on echocardiographic parameters (left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter, intraventricular septal diameter, posterior wall diameter diastolic, left atrial diameter, tricuspid annular plane systolic excursion) and laboratory findings assessed at admission: complete blood count with differential (white blood cells (WBCs), red blood cells (RBCs), hemoglobin (Hgb), platelets (PLTs)), creatine kinase (CK), CK-MB, creatinine, troponin T, estimated glomerular filtration rate (eGFR), glucose, glycated hemoglobin (HbA1c), and lipid profile. We also obtained information on the medications at discharge. We obtained long-term data by phone contact and from the hospital database. If no phone contact was possible, we obtained data on the patient’s status from the National Health Fund.

2.5. Study Endpoints

The primary study endpoint was to compare the 4-year rate of major cardiovascular adverse events (MACEs) defined as joined rates of cardiac death, MI, and target lesion revascularization (TLR). The secondary endpoints included all-cause death, cardiac death, MI, and TLR rates at 1, 2, 3, and 4 years.

2.6. Statistical Methods

Descriptive statistics are shown as mean, standard deviation, minimum, median, interquartile range, and maximum for continuous variables and as count and percent for categorical variables. The Pearson’s chi-squared test or the Fisher’s exact test was performed to compare categorical variables between two groups (e.g., CHIP and non-CHIP patients). The Fisher’s exact test was used when at least one of the subgroups had count = 0. The Wilcoxon rank sum test was performed to compare continuous variables between two groups (e.g., CHIP and non-CHIP patients). A p-value < 0.05 was considered statistically significant.
Kaplan–Meier estimators with 95% CI were calculated to compare the 4-year survival curves for various endpoints between groups (e.g., CHIP and non-CHIP patients). If a given endpoint occurred for a particular patient more than once in a 4-year follow-up period, then survival time was assumed as the time to the first occurrence of this endpoint. Notably, in the case of a MACE (a composite endpoint), the survival time was assumed as the time to the first occurrence of either cardiac death, MI, or TLR.
Univariable and multivariable Cox regression (Cox proportional hazards model) was performed to compare survival rates between groups. The multivariable Cox regression model was chosen in stepwise selection with a backward elimination algorithm with a significance level = 0.1. Results regarding the hazard ratio (HR) and 95% confidence intervals for HR are presented.
Statistical analyses were performed using R software version 4.2.1 (2022-06-23 ucrt)—“Funny-Looking Kid” Copyright (C) 2022, The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (64-bit).

3. Results

3.1. Patient Inclusion

In the analyzed period, we identified 872 PCI procedures. Amongst these, we identified 250 patients with 307 Alex Plus stent labels in the procedure books. However, in four patients (five stents), Alex Plus stents were not implanted (one device failure—no possibility to deliver the stent to the target lesion due to calcification and tortuosity, four stents not implanted due to fatal cardiac arrest). Moreover, we excluded 14 patients (20 stents) due to in-hospital death unrelated to the sirolimus-eluting stent deployment. Ultimately, we analyzed 232 patients in whom 282 stents were implanted. Additionally, we identified 81 patients meeting the CHIP criteria and 76 patients meeting the HBR criteria (Figure 1).

3.2. Baseline Characteristics

In the whole population, the mean age was 68 ± 11 years and 23.7% were females. The PCI procedures in 38.4% of cases were performed in the acute setting. The following comorbidities were the most prevalent: arterial hypertension (91.8%), dyslipidemia (76.3%), prior PCI (56%), prior MI (48.7%), and diabetes type 2 (41.8%). The mean LVEF was 49.5 ± 10.5% (Table 1).
As stated earlier, the CHIP definition was met by 81 patients. The median number of fulfilled clinical criteria was four (IQR 2–7), and the median number of fulfilled anatomical criteria was two (IQR 1–3). The CHIP patients were older (70 ± 11 vs. 67 ± 11 years, p = 0.027) and characterized by higher rates of MI as a reason for PCI (p = 0.003), diabetes (p = 0.002), and dyslipidemia (p = 0.008). Similarly, the HBR patients were older (77 ± 8 vs. 63 ± 9 years, p < 0.001) and characterized by higher rates of diabetes type 2 (p < 0.001) and chronic kidney disease (p < 0.001). Differences between the CHIP vs. non-CHIP and the HBR and non-HBR subgroups are presented in Supplementary Tables S1 and S2.
The laboratory findings are shown in Table 2. Additional data are also presented in Supplementary Tables S3 and S4. The CHIP patients were characterized by lower red blood cells (p = 0.038) and lower LDL values (p = 0.042). At the same time, the HBR patients were characterized by lower red blood cells (p < 0.001), hemoglobin values (p < 0.001), total cholesterol (p < 0.001), LDL values (p < 0.001), triglycerides (p = 0.007) and eGFR (p < 0.001).

3.3. Procedure Characteristics

In the whole study population, most lesions were located in the right coronary artery (38.8%), followed by the left anterior descending artery (31%) and the left circumflex artery (26.3%). The lesions were mostly complex—type C lesions accounted for 39.2% of cases. Coronary bifurcations were treated in 9.9% of cases. The mean SYNTAX PCI score was 32.9 ± 11.0 (Table 3). Most procedures were performed from radial access (83.2%) using a 6F guiding catheter (95.7%). The lesions were mostly predilated (61.6%), and postdilatation was performed in 37.9% of cases. The mean nominal parameters of the Alex Plus stent were 3.2 ± 0.5 mm × 21.2 ± 10.9 mm. The device success was 99.6% (in one case, a second stent was required due to heavy calcifications). Additional stents were deployed in 39% of cases due to edge dissection (6.9%), side branch stenting (5.2%), or diffuse disease (26.9%). MI type 4a was revealed in 2.2% of cases (Table 3).
The CHIP patients had more procedures within the left main (0.7 vs. 9.9%), more complex lesions (type C: 31.8% vs. 53.1%, p = 0.014), and larger implanted Alex Plus stents (3.1 ± 0.5 × 18.3 ± 7.0 mm vs. 3.3 ± 0.5 × 26.7 ± 14.3 mm) as well as more frequent additional stent implantations (12.7% vs. 87.7%, p < 0.001). The rate of coronary dissection was higher in the CHIP patients than in the non-CHIP ones (13.6% vs. 3.3%, p = 003), with similar rates of MI type 4a (1.2% vs. 2.7%, p = 0.66). There were no statically significant differences in periprocedural complications in the HBR vs. the non-HBR groups (dissection: 3.9% vs. 8.3%, p = 0.216 and MI type 4a: 1.3 vs. 2.6%, p = 0.999) (Supplementary Tables S5 and S6).
The medications at discharge are presented in Table 4 as well as Supplementary Tables S7 and S8. All patients received acetylsalicylic acid and P2Y12 inhibitors (clopidogrel—92.2%). The other key medications were as follows: beta-blockers (96.1%), ACEI/ARB (97.4%), and statins (99.1%).

3.4. Four-Year Outcomes

The detailed rates of MACEs, death, cardiac death, MI, and TLR at 12, 24, 36, and 48 months are presented in Table 5 and Figure 2. At 4 years, the MACE rates for the whole population, CHIP, HBR, and CHIP + HBR were 23.3%, 29.6%, 27.6%, and 31.4%, respectively.
CHIP patients had a higher risk of MACEs (29.6% vs. 19.9%, HR 1.69, p = 0.032) and cardiac death (11.1% vs. 4.6%, HR 2.50, p = 0.048). There were no differences for MI (7.4% vs. 6.6%, p = 0.826) and TLR (18.5% vs. 12.6%, p = 0.150). At 12 months, in non-CHIP patients (n = 151), the rates were as follows: cardiac death—3.3% (n = 5), TLR—5.3% (n = 8), and MI—3.3% (n = 5). Similarly, at 48 months, in non-CHIP patients (n = 151), the rates were as follows: cardiac death—7 (4.6%), TLR—12.5% (n = 19), and MI—6.6% (n = 10).
HBR patients were also characterized by a higher risk of MACEs (27.6% vs. 21.2%, HR 1.84, p = 0.049) and cardiac death (17.1% vs. 1.9%, HR 9.61, p < 0.001). There were no differences for MI (7.9% vs. 6.4%, p = 0.669) and TLR (11.8% vs. 16.0%, p = 0.991).

3.5. Multivariable Cox Regression Analysis

Finally, the Cox analysis identified predictive factors for MACEs and TLR at 48 months. The final results of the multivariable analyses are provided in Table 6 for MACEs, and those for TLR are presented in Table 7 (univariable analyses are presented in Supplementary Tables S9–S14). For the whole population, the predictive factors of MACEs were lesion in the LM (HR 3.88), calcification (HR 2.70), second stent implantation (HR 2.06), EuroScore II > 5% (HR 2.87), and prior PCI (HR 2.09).
In CHIP patients, prior CABG (HR 3.02) and chronic kidney disease (HR 5.07) increased the MACE rate, but beta-blockers significantly reduced the risk (HR 0.001). In the case of HBR patients, EuroScore II 3–5% (HR 4.12), cardiogenic shock (HR 13.0), and hypoglycemic drug use (HR 5.30) were independent predictors for MACEs.

4. Discussion

Our study showed that PCI with Alex Plus stent in CHIP and HBR patients is feasible with a low rate of periprocedural complications and a device success of over 99%. Nevertheless, CHIP and HBR patients are at high risk of future adverse events and require strict surveillance to improve outcomes.
In our study, at 4 years, the MACE rates for the whole population, CHIP, HBR, and CHIP + HBR were 23.3%, 29.6%, 27.6%, and 31.4%, respectively. When analyzing the results in detail, we can also distinguish the non-complex group of patients treated with Alex Plus (non-CHIP). At 12 months, in non-CHIP patients (n = 151), the rates were as follows: cardiac death—3.3% (n = 5), TLR—5.3% (n = 8), and MI—3.3% (n = 5). Similarly, at 48 months, in non-CHIP patients (n = 151), the rates were as follows: cardiac death—7 (4.6%), TLR—12.5% (n = 19), and MI—6.6% (n = 10). Nevertheless, this non-CHIP subgroup included HBR patients, which could also negatively influence the results. One of the reasons could be the limited use of new potent antiplatelets in HBR patients [25]. The first year’s results are important since, as Eccleston et al. showed, unplanned early hospitalization following PCI, particularly in <30 days, was linked with a significantly higher incidence of MACEs at long-term follow up [26].
Sirolimus-eluting stents (SESs) have already been proven to be effective. In STEMI patients, Sakurai et al. confirmed that primary PCI with SESs was linked with reduced all-cause death and TLR rates without increased rates of recurrent MI or definite stent thrombosis compared to BMSs. Up to 48 months, SESs secured a significant reduction in TLR (OR 0.44, p < 0.001) and all-cause death (OR 0.62, p = 0.049) compared to BMSs [27]. Nevertheless, nowadays, BMSs are rarely used, and we should compare Alex Plus’s performance with that of other second-generation SESs. Table 8 summarizes studies showing the long-term results of patients undergoing PCI with SESs identified in PubMed in the last 10 years.
As stressed earlier in our study, the CHIP group was characterized by the worst outcomes, with a cardiac death rate of 11.1% and a TLR rate of 18.5% at 4 years. This is in accordance with the available literature since CHIP patients are characterized by both worse periprocedural as well as long-term outcomes [28]. Nevertheless, in our paper, the CHIP patients were not characterized by high periprocedural complications. Regarding periprocedural complications, we should not forget about bleeding, especially in HBR patients. In our study, 83.2% of procedures were performed from radial access. Other authors show that one of the options to decrease the bleeding risk even further is to use distal radial artery access. Such access might be beneficial for HBR patients but is also feasible in CHIP patients [29,30].
Table 8. Clinical outcomes at long-term follow in studies on PCI with SESs.
Table 8. Clinical outcomes at long-term follow in studies on PCI with SESs.
StudyCommentsDeathCardiac DeathTLRMI
Our study: whole 10.8%6.9%14.7%6.9%
Our study:
Non-complex		Including HBR8.6%4.6%12.5%6.6%
Our study: CHIP 14.8%11.1%18.5%7.4%
Murray [31]-18.8%---
Riku [32]5 yrs FU non-complex vs. complex PCI7.0 vs. 12.2%2.9 vs. 5.4%9.8 vs. 22%1.4 vs. 3.1%
Buiten [33]3 yrs FU
SES/EES/ZES		-2.4%/2.5%/2.5%7%/9.5%/10%3.3%/3.9%/4.2%
Maeng [34]EES/SES12/9.5%8.3/4.8%5.6/9.5%1.9/7.6%
Olesen [35]5 yrs FU ZES/SES16/17.9%6.5/7.1%14.8/4.8%8.9/7.1%
Wijns [36]ZES/SES5.5/6%2.9/3.4%9/8.6%4.6/5.8
Sato [37]5 yrs FU
DM/non-DM		7.1/8.9%2.4/2.7%9.4/8.9%4.7/0%
Stefanini [38]BP-DES/DP-SES9.3/10%5.2/5.9%12/13.7%6/6.8%
TLR—target lesion revascularization; MI—myocardial infarction; FU—follow up; PCI—percutaneous coronary intervention; SES—sirolimus-eluting stent; ZES—zotarolimus-eluting stent; EES—everolimus-eluting stent; DM—diabetes mellitus; BP—biodegradable polymer; DP—durable polymer.
As presented in the identified studies with follow up from 3 to 5 years (follow up precisely 4 years), the cardiac death rate of patients with SESs deployed was 2.9–7.1% (3.4–5.9%); the MI rate was 1.4–7.6% (5.8–7.6%), and the TLR rate was 7–22% (8.6–13.7%). The results for Alex Plus in non-complex PCI (as most studies represented similar populations) fall within those ranges, i.e., cardiac death rate—4.6%, MI rate—6.6%, and TLR rate—12.5%. In our study, the highest TLR rate was observed in the CHIP group (18.5%), and as presented in the study by Riku et al., the TLR rate in the complex PCI group was 22% [32].
Interestingly, Riku et al. also presented outcomes up to 10 years [32]. As one could presume, the TLR rate was significantly higher in the complex PCI group than in the non-complex PCI group (29.4% vs. 13.0%, p = 0.001). Late TLR cases were observed over 10 years at a rate of 2.4% per year in the complex PCI group and at 1.1% per year in the non-complex PCI group. The cardiac death rate was higher in the complex PCI group than in the non-complex PCI group, particularly after 4 years (15.8% vs. 7.5%, p = 0.031). Worth stressing is the fact that sudden death was the major reason for cardiac death beyond 4 years in patients from the complex PCI group.
Brenner et al. proposed a more straightforward CHIP-PCI classification, dividing patients into low-risk, intermediate-risk, and high-risk PCI. The 12-month all-cause death rates in those three groups were 1.24%, 2.47%, and 10.86%, respectively (p < 0.001) [39].
The Alex Plus is a sirolimus-eluting stent with a biodegradable polymer. This may be an advantage since, recently, Mattke et al. showed that biodegradable polymer (BP) SESs compared to durable polymer (DP) EESs, were associated with 2603 fewer deaths per one million patients over 48 months. This corresponded with a relative risk reduction of 6% [40]. Although de Waha et al. showed that BP DESs and DP SESs were characterized by comparable clinical outcomes at 4 years, the stent thrombosis rate was significantly lower in patients with BP DESs [41].
Finally, it is crucial to identify risk factors that could negatively impact the outcomes in patients undergoing PCI with second-generation DESs. Here, we identified the following. For the whole population, the predictive factors of MACEs were lesion in the left main (HR 3.88), calcifications (HR 2.70), second stent implantation (HR 2.06), EuroScore II > 5% (HR 2.87), and prior PCI (HR 2.09). In CHIP patients, prior CABG (HR 3.02) and chronic kidney disease (HR 5.07) increased the MACE rate, but beta-blockers significantly reduced the risk (HR 0.001). In the case of HBR patients, EuroScore II 3–5% (HR 4.12), cardiogenic shock (HR 13.0), and hypoglycemic drug use (HR 5.30) were independent predictors increasing the MACE risk. The predictive factors for TLR were a bit different. In the whole population, there were lesions in the left main (HR 14.9), calcifications (HR 3.07), and second stent implantation (HR 4.09). In the CHIP subgroup, prior CABG (HR 3.94) was the only predictive factor, and in the HBR subgroup, there were postdilatation (HR 5.62), smoking (HR 5.70), and use of alpha-adrenolytics (HR 5.22). In the HBR group, male sex (HR 0.15) was the only factor decreasing the TLR risk.
Fujimoto et al. showed that pulmonary disease, active malignancy, unstable hemodynamics, hemodialysis, left ventricular ejection fraction, and valvular disease significantly increased the MACE risk [42]. In their other paper, the same group showed that frailty (OR 2.04, 95% CI 1.10–3.75, p = 0.022), unstable hemodynamics (OR 5.75, 95% CI 1.21–27.20, p = 0.027), and immunosuppressive drugs (OR 3.04, 95% CI 1.25–7.38, p = 0.014) were linked with the increased risk of major complications in CHIP patients [43]. Interestingly, Guldener et al., applying machine learning and self-organizing maps, identified additional ISR risk factors such as age, BMI, dyslipidemia, chronic artery occlusion, clinical presentation (STEMI vs. NSTEMI vs. elected PCI), baseline TIMI flow in the treated coronary artery, prior PCI, lesion length, and residual diameter stenosis post-PCI [44].
We think that future studies, especially performed on a large scale, should answer the question of whether all drugs (sirolimus, everolimus, zotarolimus, biolimus A9) are equally effective when used during PCI in CHIP and HBR patients.

Study Limitations

Our study has the recognized limitations of registries and observational studies. The lack of randomization might have led to selection bias, even if partially mitigated by the consecutive patient enrolment. Moreover, the moderate size of this study’s population and the limitations in follow-up data gathering could have also influenced the results.

5. Conclusions

CHIP patients pose the highest challenge in modern PCIs. However, in the past 20 years, ischemic events after PCI halved (from 18.4% to 9.1%), and out-of-hospital bleeding doubled (from 2.5% to 5%). Our study showed that PCI with a second-generation sirolimus-eluting stent in CHIP and HBR patients is feasible with a reasonable rate of periprocedural complications, including low rates of MI type 4a. The MACE rates at 4 years support the performance and safety of this stent in those populations. Nevertheless, CHIP and HBR patients are at high risk of future adverse events and require strict surveillance to improve outcomes.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/jcm12165313/s1, Supplementary Table S1. Baseline characteristics: CHIP vs. non-CHIP. Supplementary Table S2. Baseline characteristics: HBR vs. non-HBR. Supplementary Table S3. Laboratory test findings CHIP vs. non-CHIP. Supplementary Table S4. Laboratory test findings HBR vs. non-HBR. Supplementary Table S5. Lesion and procedure characteristics CHIP vs. non-CHIP. Supplementary Table S6. Lesion and procedure characteristics HBR vs. non-HBR. Supplementary Table S7. Medications at discharge CHIP vs. non-CHIP. Supplementary Table S8. Medications at discharge HBR vs. non-HBR. Supplementary Table S9. Univariable Cox regression for MACE: the whole population. Supplementary Table S10. Univariable Cox regression for TLR: the whole population. Supplementary Table S11. Univariable Cox regression for MACE: CHIP population. Supplementary Table S12. Univariable Cox regression for TLR: CHIP population. Supplementary Table S13. Univariable Cox regression for MACE: HBR population. Supplementary Table S14. Univariable Cox regression for TLR: HBR population.

Author Contributions

Conceptualization, M.T. and J.B.; methodology, M.T. and J.B.; investigation, P.B., M.T., A.K. and W.W.; data curation, J.B. and R.J.G.; writing—original draft preparation, M.T. and J.B.; writing—review and editing, M.T. and W.W.; supervision, R.J.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study’s protocol was reviewed and approved by the Independent Ethics Committee of the Central Clinical Hospital of the Ministry of Interior and Administration in Warsaw (No. 64/2020 of 22 April 2020).

Informed Consent Statement

Patient consent was waived due to the retrospective nature of this study.

Data Availability Statement

Data are available from the corresponding author on request.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Study flow chart.
Figure 1. Study flow chart.
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Figure 2. Kaplan–Meier curves showing event-free survival in CHIP and HBR patients. MI—myocardial infarction; TLR—target lesion revascularization.
Figure 2. Kaplan–Meier curves showing event-free survival in CHIP and HBR patients. MI—myocardial infarction; TLR—target lesion revascularization.
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Table 1. Baseline characteristics.
Table 1. Baseline characteristics.
ParameterWhole Population
n = 232 (%)		CHIP
n = 81 (%)		HBR
n = 76 (%)
Females55 (23.7)22 (27)25 (33)
Age [years]68 ± 1170 ± 1177 ± 8
Acute coronary syndrome type at presentation
     UA31 (13.4)13 (16.0)11 (14.5)
     NSTEMI26 (11.2)16 (19.8)11 (14.5)
     STEMI32 (13.8)13 (16.0)10 (13.2)
Cardiogenic shock6 (2.6)3 (3.7)3 (3.9)
Arterial hypertension213 (91.8)76 (93.8)71 (93.4)
Diabetes type 297 (41.8)45 (55.6)44 (57.9)
Dyslipidemia177 (76.3)70 (86.4)61 (80.3)
Prior myocardial infarction113 (48.7)42 (51.9)43 (56.6)
Prior PCI130 (56.0)48 (59.3)49 (64.5)
Prior CABG22 (9.5)12 (14.8)11 (14.5)
Chronic kidney disease42 (18.1)16 (19.8)27 (35.5)
Prior stroke17 (7.3)6 (7.4)10 (13.2)
Peripheral artery disease25 (10.8)12 (14.8)9 (11.8)
Chronic obstructive pulmonary disease13 (5.6)6 (7.4)6 (7.9)
Echocardiographic parameters
     LVEDd [mm]50.4 ± 9.052.0 ± 7.951.5 ± 8.5
     IVSd [mm]11.4 ± 2.111.4 ± 2.411.6 ± 1.7
     PWDd [mm]10.5 ± 1.610.6 ± 1.910.5 ± 1.6
     LA [mm]40.4 ± 5.941.0 ± 6.043.2 ± 5.8
     TAPSE [mm]22.0 ± 4.322.2 ± 4.521.3 ± 4.8
     LVEF [%]49.5 ± 10.548.9 ± 10.447.0 ± 12.2
     Severe mitral regurgitation6 (3.1)2 (2.7)4 (6.1)
     Severe aortic regurgitation1 (0.5)00
     Severe aortic stenosis4 (2.1)3 (4.1)3 (4.5)
UA—unstable angina; NSTEMI—non-ST-elevation myocardial infarction; STEMI—ST-elevation myocardial infarction; PCI—percutaneous coronary intervention; CABG—coronary artery bypass grafting; LVEDd—left ventricular end-diastolic diameter; IVSd—intraventricular septal diameter; PWDd—posterior wall diastolic diameter; LA—left atrium; TAPSE—tricuspid annular plane systolic excursion; LVEF—left ventricular ejection fraction.
Table 2. Laboratory test findings.
Table 2. Laboratory test findings.
ParameterWhole Population
n = 232		CHIP
n = 81		HBR
n = 76
White blood cells [109/L]8.5 ± 2.78.6 ± 2.38.0 ± 2.2
Hemoglobin [g/dL]13.4 ± 1.713.1 ± 1.712.1 ± 1.9
Red blood cells [1012/L]4.4 ± 0.54.3 ± 0.54.1 ± 0.6
Platelets [109/L]222.9 ± 65215.8 ± 63222.5 ± 64.7
Glucose [md/dL]136.4 ± 64.9154.8 ± 75.3148.3 ± 77.4
HbA1c [%]6.3 (6.0–7.3)6.6 (6.1–7.3)6.4 (6.0–7.1)
Total cholesterol [md/dL]163.9 ± 50.9161.5 ± 60.6143.4 ± 41.4
HDL [md/dL]45.7 ± 14.644.0 ± 43.544.7 ± 13.1
LDL [md/dL]89.8 ± 40.583.0 ± 42.676.0 ± 35.8
Triglycerides [md/dL]142 ± 33.9170.7 ± 89.9113.1 ± 62.3
Creatine [md/dL]1.1 ± 0.71.2 ± 0.91.4 ± 0.8
eGFR70.5 ± 23.267.4 ± 23.456.6 ± 20.4
TnI at admission [ng/mL]108 (15.8–235)211.5 (28.2–754.5)62.5 (19.0–1446)
Max. TnI [ng/mL]1110 (49.8–11,573)1263 (88.2–13,371)372 (44.0–8802)
CK134.5 (84–326)169 (75–319)118 (72–334)
CK max173 (90–473)183 (80–390)156 (74–363)
CK-MB18 (13.5–30)20 (13–34.5)18 (13–29.8)
CK-MB max22.5 (15–48.5)26.5 (14.2–68)23.5 (14.2–40)
Results presented as mean ± standard deviation or median (interquartile range); CK—creatine kinase.
Table 3. Lesion and procedure characteristics.
Table 3. Lesion and procedure characteristics.
ParameterWhole Population
n = 232 (%)		CHIP
n = 81 (%)		HBR
n = 76 (%)
Lesion location
       LM9 (3.9)8 (9.9)5 (6.6)
       LAD72 (31)21 (25.9)31 (40.8)
       LCx61 (26.3)16 (19.8)14 (8.4)
       RCA90 (38.8)36 (44.4)29 (38.2)
       VG6 (2.6)6 (7.4)2 (2.6)
Lesion type
       A38 (16.4)12 (14.8)14 (18.4)
       B166 (28.4)17 (21)24 (31.6)
       B237 (15.9)9 (11.1)8 (10.5)
       C91 (39.2)43 (53.1)30 (39.5)
Heavy calcification18 (7.8)9 (11.1)6 (7.9)
Coronary bifurcation23 (9.9)12 (14.8)6 (7.9)
SYNTAX13.9 ± 8.716.0 ± 8.414.8 ± 9.2
SYNTAX II PCI32.9 ± 11.035.6 ± 10.140.3 ± 10.5
SYNTAX II CABG29.1 ± 10.829.9 ± 10.528.4 ± 10.5
EuroScore II1.6 (0.9–3.3)2.5 (1.3–4.3)3.6 (1.8–6.6)
Lesion predilatation143 (61.6)47 (58.0)48 (63.2)
Stent diameter [mm]3.2 ± 0.53.3 ± 0.53.1 ± 0.5
Stent length [mm]21.2 ± 10.926.7 ± 14.320.3 ± 8.8
Stent pressure [atm]15.3 ± 2.715.5 ± 2.615.4 ± 2.5
2nd stent90 (39)71 (87.7)34 (44.7)
Stent postdilatation88 (37.9)34 (42.0)54 (35.8)
Access site
       Transradial193 (83.2)64 (79)56 (73.7)
       Transfemoral43 (18.5)19 (23.5)20 (26.3)
Guiding catheter
       6F222 (95.7)76 (93.8)71 (93.4)
       7F11 (4.7)5 (6.2)5 (6.6)
Dissection16 (6.9)11 (13.6)3 (3.9)
MI type 4a5 (2.2)1 (1.2)1 (1.3)
LM—left main; LAD—left anterior descending artery; LCx—left circumflex artery; RCA—right coronary artery; VG—vein graft.
Table 4. Medications at discharge.
Table 4. Medications at discharge.
ParameterWhole Population
n = 232 (%)		CHIP
n = 81 (%)		HBR
n = 76 (%)
Acetylsalicylic acid232 (100)81 (100)76 (100)
P2Y12
       Clopidogrel214 (92.2)74 (91.4)72 (94.7)
       Prasugrel1 (0.4)1 (1.2)0
       Ticagrelor17 (7.3)6 (7.4)4 (5.3)
Beta-blocker223 (96.1)80 (98.8)73 (96.1)
Ca-blocker53 (22.8)21 (25.9)12 (15.8)
Angiotensin-converting enzyme inhibitor190 (81.9)66 (81.5)60 (78.9)
Angiotensin receptor blocker36 (15.5)14 (17.3)13 (17.1)
Diuretic125 (53.9)51 (63)61 (80.3)
Mineralocorticoid receptor antagonist48 (20.7)16 (19.8)20 (26.3)
Nitrates13 (5.6)8 (9.9)7 (9.2)
Vitamin K antagonist17 (7.3)4 (4.9)16 (21.1)
Novel oral anticoagulant11 (4.7)5 (6.1)10 (13.1)
Statin230 (99.1)81 (100)76 (100)
Hypoglycemic medications62 (26.7)29 (35.8)23 (30.3)
Insulin33 (14.2)20 (24.7)18 (23.7)
Table 5. Outcomes at 4 years.
Table 5. Outcomes at 4 years.
YearDeathCardiac DeathTLRMIMACE
Whole population (n = 232)
1st year17 (7.3)11 (4.7)18 (7.8)9 (3.9)27 (11.6)
2nd year19 (8.2)13 (5.6)28 (12.1)11 (4.7)39 (16.8)
3rd year21 (9.1)15 (6.5)31 (13.4)11 (4.7)44 (18.9)
4th year25 (10.8)16 (6.9)34 (14.7)16 (6.9)54 (23.3)
CHIP (n = 81)
1st year9 (11.1)6 (7.4)10 (12.3)4 (4.9)14 (17.3)
2nd year10 (12.3)7 (8.6)13 (16.1)4 (4.9)18 (22.2)
3rd year11 (13.6)8 (9.9)14 (17.3)4 (4.9)20 (24.7)
4th year12 (14.8)9 (11.1)15 (18.5)6 (7.4)24 (29.6)
HBR (n = 76)
1st year11 (14.5)9 (11.8)6 (7.9)5 (6.6)13 (17.1)
2nd year13 (17.1)10 (13.2)8 (10.5)5 (6.6)16 (21.1)
3rd year15 (19.7)12 (15.8)9 (11.8)5 (6.6)19 (25.0)
4th year17 (22.4)13 (17.1)9 (11.8)6 (7.9)21 (27.6)
CHIP + HBR (n = 35)
1st year8 (22.9)6 (17.1)4 (11.4)3 (8.6)8 (22.9)
2nd year10 (28.6)7 (20.0)4 (11.4)3 (8.6)9 (25.7)
3rd year12 (34.3)8 (22.9)4 (11.4)3 (8.6)9 (25.7)
4th year14 (40.0)9 (25.7)4 (11.4)4 (11.4)11 (31.4)
Values presented as n (%). TLR—target lesion revascularization; MI—myocardial infarction; MACE—major adverse cardiovascular event; CHIP—complex, high-risk indicated procedure; HBR—high bleeding risk.
Table 6. Multivariable analysis for MACEs.
Table 6. Multivariable analysis for MACEs.
CharacteristicMultivariable Analysis for MACEs
HR95% CIp
Whole population (n = 232)
Lesion in left main3.881.42, 10.60.008
Calcification2.701.17, 6.230.020
Second stent2.061.11, 3.840.023
EuroScore II
<3——
3–51.920.83, 4.420.125
>52.871.32, 6.230.008
Prior PCI2.091.03, 4.210.040
CHIP (n = 81)
Prior CABG3.021.02, 8.920.045
Chronic kidney disease5.071.44, 17.90.011
Beta-blocker0.000.00, 0.06<0.001
Diuretics3.020.80, 11.40.103
HBR (n = 76)
EuroScore II
<3——
3–54.121.16, 14.60.028
>52.190.67, 7.190.196
Cardiogenic shock13.01.99, 85.40.007
Smoking2.620.94, 7.260.065
Hypoglycemic drugs5.301.90, 14.80.001
CHIP—complex, high-risk indicated procedure; HBR—high bleeding risk; PCI—percutaneous coronary intervention; CABG—coronary artery bypass grafting.
Table 7. Multivariable analysis for TLR.
Table 7. Multivariable analysis for TLR.
CharacteristicMultivariable Analysis for TLR
HR95% CIp
Whole population (n = 232)
Lesion in left main14.93.95, 56.2<0.001
Calcification3.071.12, 8.370.029
Second stent4.091.72, 9.750.001
CHIP (n = 81)
Prior CABG3.941.15, 13.50.029
HBR (n = 76)
Male sex0.150.03, 0.710.017
Postdilatation5.621.06, 29.90.043
Smoking5.701.02, 31.70.047
Alpha-adrenolytic5.221.04, 26.30.045
CHIP—complex, high-risk indicated procedure; HBR—high bleeding risk; CABG—coronary artery bypass grafting.
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MDPI and ACS Style

Tyczyński, M.; Kern, A.; Buller, P.; Wańha, W.; Gil, R.J.; Bil, J. Clinical Outcomes and Prognostic Factors in Complex, High-Risk Indicated Procedure (CHIP) and High-Bleeding-Risk (HBR) Patients Undergoing Percutaneous Coronary Intervention with Sirolimus-Eluting Stent Implantation: 4-Year Results. J. Clin. Med. 2023, 12, 5313. https://doi.org/10.3390/jcm12165313

AMA Style

Tyczyński M, Kern A, Buller P, Wańha W, Gil RJ, Bil J. Clinical Outcomes and Prognostic Factors in Complex, High-Risk Indicated Procedure (CHIP) and High-Bleeding-Risk (HBR) Patients Undergoing Percutaneous Coronary Intervention with Sirolimus-Eluting Stent Implantation: 4-Year Results. Journal of Clinical Medicine. 2023; 12(16):5313. https://doi.org/10.3390/jcm12165313

Chicago/Turabian Style

Tyczyński, Maciej, Adam Kern, Patryk Buller, Wojciech Wańha, Robert J. Gil, and Jacek Bil. 2023. "Clinical Outcomes and Prognostic Factors in Complex, High-Risk Indicated Procedure (CHIP) and High-Bleeding-Risk (HBR) Patients Undergoing Percutaneous Coronary Intervention with Sirolimus-Eluting Stent Implantation: 4-Year Results" Journal of Clinical Medicine 12, no. 16: 5313. https://doi.org/10.3390/jcm12165313

APA Style

Tyczyński, M., Kern, A., Buller, P., Wańha, W., Gil, R. J., & Bil, J. (2023). Clinical Outcomes and Prognostic Factors in Complex, High-Risk Indicated Procedure (CHIP) and High-Bleeding-Risk (HBR) Patients Undergoing Percutaneous Coronary Intervention with Sirolimus-Eluting Stent Implantation: 4-Year Results. Journal of Clinical Medicine, 12(16), 5313. https://doi.org/10.3390/jcm12165313

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