Fibrinolysis Therapy Combined with Deferred PCI versus Primary Angioplasty for STEMI Patients During the COVID-19 Pandemic: Preliminary Results from a Single Center.

INTRODUCTION: The efficacy of fibrinolysis therapy with deferred percutaneous coronary angioplasty (FPCI) versus primary angioplasty (PPCI) during the coronavirus disease 2019 (COVID-19) pandemic is unclear when medical quarantine is needed. PATIENTS AND METHODS: Acute ST segment elevation myocardial infarction (STEMI) patients underwent PPCI after finishing the screening protocol from January 23, 2020 to June 10, 2020 while FPCI was applied when COVID-19-confirmed cases reoccurred in Beijing near our hospital from June 11, 2020 to July 20, 2020. The door-to-balloon time (DTB) or door-to-needle time (DTN) as well as in-hospital adverse clinical outcomes were compared between the two groups. A propensity score-matched (PSM) analysis was performed to diminish the potential influence of confounding factors on the clinical outcomes.
RESULTS: A total of 126 STEMI patients underwent PPCI after finishing the screening protocol and 17 patients received FPCI before PSM. Patients who received FPCI were younger than patients who underwent PPCI (50.8±14.0 versus 64.1±14.2 years, p=0.001), and chronic kidney disease (CKD) was less common in FPCI patients than in patients who underwent PPCI (0% versus 24.6%, p=0.024). The DTN was significantly shorter than DTB (25.8±4.2 versus 61.1±10.7, p=0.000) before PSM. The DTN was significantly shorter than DTB (26.9±4.2 versus 64.9±23.6, p=0.000); however, the incidence rate of in-hospital ischemia and bleeding adverse clinical outcomes were comparable between the two groups after PSM.
CONCLUSION: Fibrinolysis therapy combined with deferred PCI can reduce the ischemia time and has a similar in-hospital adverse clinical outcome rate compared with patients who underwent primary PCI during the COVID-19 pandemic.

Introduction

The novel coronavirus 2019 (COVID-19) was considered as a global pandemic by World Health Organization (WHO) since March 2020.1 Due to its highly contagious features, necessary quarantine and social distance is important in preventing cross-infection.2 Health-care facilities, as high-risk regions, applied screening protocols to avoid nosocomial infection.3 Not only the patients with chronic conditions are affected, but patients with acute conditions are also compromised during this pandemic.4 The negative impact of the COVID-19 pandemic on the management of acute ST segment elevation myocardial infarction (STEMI) has been demonstrated by multiple studies with a reduction of catheter activation and increased systemic delay.5,6

Current guidelines highlighted the importance of primary percutaneous coronary intervention (PCI) on the management of STEMI because of its superiority of achieving higher rate of TIMI-3 grade flow and lower rate of re-infarction than fibrinolysis therapy.7,8 But this recommendation is based on the normal performance of health-care facilities. In fact, fibrinolysis therapy was recommended as the first-line reperfusion therapy (RT) during the COVID-19 pandemic in China, especially in high risk locations. Primary PCI was considered when STEMI patients finished the screening protocol including medical history, blood test and chest computed tomography (CT).9 Previous studies have demonstrated that fibrinolysis therapy should be considered when prolonged PCI delay is expected.10–12 Which is the better RT for STEMI patients during the COVID-19 pandemic is still unclear.

Beijing Tiantan Hospital, Capital Medical University applied two different RTs according to dynamic change of the cross-infection risk. From January 23, 2020 to June 10, 2020, we performed PPCI in STEMI patients after the patients finished a screening protocol when the overall cross-infection risk was relatively low in Beijing. Fibrinolysis therapy combined with a deferred angioplasty within 24 hours (FPCI) was applied between June 11, 2020 and July 20, 2020 when the second outbreak of COVID-19 began and confirmed COVID-19 patients emerged with possible disease origination from a market nearby our hospital.

We retrospectively collected and analyzed the clinical data of these two groups of patients, and compared the door-to-balloon time (DTB) and door-to-needle time (DTN) as well as the in-hospital adverse clinical outcomes including ischemia and bleeding events.

The study protocol was approved by the Ethics Committee of the Beijing Tiantan Hospital, Capital Medical University. The study was implemented in complete concordance with the tenets of the Declaration of Helsinki on human research. Informed consent was obtained from the study participants.

Patients and Methods

Study Design and Participants

This single center retrospective study was conducted in Beijing Tiantan Hospital, Capital Medical University, Beijing, China. Patients aged 18 years or older diagnosed with acute STEMI within 24 hours after symptom onset in our center from January 23, 2020 to July 20, 2020 were consecutively enrolled. The diagnosis of STEMI was according to the current guidelines, summarized as myocardial ischemia symptoms associated with ST-segment elevation >2 mm in V2–V3 or >1 mm in other contiguous leads, or a new (or presumed-to-be new) left bundle branch block. Patients who refused or did not undergo PCI, patients with acute myocardial infarction due to stent thrombosis or those with mechanical complications were excluded. The study flow chart is demonstrated in Figure 1.

Figure 1

Study flow chart.

Clinical information including demographic characteristics, comorbidities and prior medications was collected and analyzed. Clinical manifestation on admission including heart function by Killip classification, on-admission hypotension or cardiac shock was evaluated by professional cardiologists. Risk stratification was evaluated by the Global Registry of Acute Coronary Events (GRACE) and the Thrombolysis in Myocardial Infarction (TIMI) scoring systems, which are widely used to predict the incidence of in-hospital clinical adverse events.13,14 The severity of coronary anatomy was scored by Syntax (Synergy between Percutaneous Coronary Intervention with Taxus and Cardiac Surgery) which is a well-accepted scoring system to evaluate the severity of coronary stenosis.15 Laboratory test results which include the peak cardiac troponin I during hospitalization, B-type natriuretic peptide (BNP) on admission, left ventricular ejection fraction (LVEF) on admission were also collected and analyzed.

Screening Protocol Before STEMI Patients Received RT in Beijing Tiantan Hospital During the COVID-19 Pandemic

STEMI patients who underwent primary PCI had to finish a screening protocol before he or she underwent PPCI between January 31, 2020 and June 10, 2020. If the patient had fever or a suspected medical contact history of Hubei province, then fibrinolysis therapy would be applied. If the patient had no sign of infection and no relevant medical contact history, the patient could undergo primary PCI after finishing the screening tests including whole blood count and chest CT. FPCI was applied from June 11, 2020 to July 20, 2020, when a negative result of nucleic acid as well as blood test and chest CT test results were necessary before performing PCI. Nucleic acid was examined by reverse-transcription polymerase chain reaction (RT-PCR) assay. None of the patients who underwent primary PCI were confirmed with COVID-19 infection in our study.

Study Endpoints

The door-to-needle (DTN) and door to balloon (DTB) times were compared between FPCI patients and PPCI patients. The in-hospital clinical outcomes including ischemia events and bleeding events were also compared. The ischemia events included major adverse cardiac event (MACE), all-cause of death, cardiac death, non-fatal myocardial infarction, stroke, any revascularization, stent thrombosis, new renal replacement therapy. MACE was defined as the composite of death, myocardial infarction, and revascularization. All deaths were considered cardiac related unless an unequivocal non-cardiac cause could be established. Myocardial infarction was defined by the presence of clinical symptoms associated with electrocardiogram (ECG) changes or abnormal imaging findings indicative of myocardial infarction and an increase in creatine kinase myocardial band fraction above the upper normal limits or an increase in troponin-I above the 99th percentile. Cardiac death was defined as any death due to cardiac or procedure-related causes. Stroke was defined as the presence of a new neurological disorder with signs or symptoms persisting for 24 h and confirmed by imaging examination. Any revascularization was defined as a repeat PCI or coronary bypass surgery. Stent thrombosis was diagnosed by recommendations from the Academic Research Consortium.16 In-hospital adverse events were retrieved from electronic medical records.

Treatment Protocol of FPCI and PPCI

Treatment protocol of FPCI: Fibrinolysis therapy was performed in the emergency department using alteplase after excluding contraindications and completion of informed consent. Alteplase was administered (15 mg intravenous bolus and 0.75 mg/kg for 30 min, 0.5 mg/kg for 60 min, the total amount is no more than 100 mg) in combination with low-molecular enoxaparin (30 mg intravenous bolus, subcutaneous injection of 1 mg/kg after 15 min and 1 mg/kg every 12 h). A deferred PCI within 24 hours was performed when the negative results of blood test, chest CT as well as nucleic acid test came out. Treatment protocol of PPCI: PPCI was performed after finishing the screening protocol including medical contact history, blood test, chest CT. PCI was done by trained interventionists by standard technique. The access route, application of devices including thrombus aspiration catheter, intra-aortic balloon counter-pulsation (IABP), temporary pacemaker as well as the use of a glycoprotein IIb/IIIa inhibitor (GPI) and anticoagulation medications were all left to the discretion of the operator. All of the patients were prescribed with dual antiplatelet therapy (DAPT) as well as angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blocker (ARB), β-blockers, statins and other medical therapies as the guidelines recommended.

Statistical Analysis

Categorical variables were presented as numbers and frequencies (percentages) and were compared using chi-square test or Yate’s continuity correction for expected counts per category < 5. Continuous variables were expressed as mean SD±mean or median (quartile 1, quartile 3) based on normality assumption and were compared using the independent sample t-test or Mann–Whitney test, as appropriate. A logistic regression model with propensity scores matching (PSM) of 1:2 ratio was created with variables that were associated with in-hospital clinical outcomes to balance patient characteristics between FPCI and PPCI patients. A p value of <0.05 was considered to be significant. Statistical analysis was performed using Statistical Package for the Social Sciences version 22.0 (SPSS Inc., Chicago, IL) and PSM was performed with EmpowerStats 2.20 (X&Y Solutions Inc., Boston, MA, USA).

Result

A total of 143 patients were enrolled in this study, of whom 17 patients received FPCI and 126 underwent PPCI before PSM, 9 and 18 patients received FPCI and PPCI after PSM respectively. The process of PSM is shown in Figure 2.

Figure 2

The process of propensity score-matched analysis.

The baseline clinical demographic and characteristics comparison results before and after PSM are shown in Table 1. As shown, FPCI patients were younger than PPCI patients (50.8±14.0 versus 64.1±14.2 years, p=0.001) before PSM. Also, we observed a significantly lower rate of diagnoses of chronic kidney disease (CKD) in FPCI patients compared with PPCI patients (0% versus 24.6%, p=0.024) before PSM. There were no significant differences regarding the demographic and clinical characteristics between the two groups after PSM.

Table 1

Comparison of the Baseline Demographic and Clinical Characteristics Between the FPCI and PPCI Patients

Variables	Before PSM			After PSM#
	FPCI (n=17)	PPCI (n=126)	P-value	FPCI (n=9)	PPCI (n=18)	P-value
Age/year	50.8±14.0	64.1±14.2	0.001	60.67 ± 10.97	58.00 ± 11.49	0.569
Male (n,%)	14(82.4)	82(65.1)	0.181	6(66.7)	15(83.3)	1.000
Smoking (n,%)	8(47.1)	44(34.9)	0.421	3 (33.3)	9 (50)	0.681
Hypertension (n,%)	9(52.9)	61(48.4)	0.799	7 (77.8)	8 (44.4)	0.218
Diabetes (n,%)	6(35.3)	55(43.7)	0.607	4 (44.4)	4 (44.4)	1.000
Dyslipidemia (n,%)	10(58.8)	45(35.7)	0.109	3 (33.3)	10 (55.6)	0.496
CKD (n,%)	0(0)	31(24.6)	0.024	0 (0)	2 (11.1)	0.795
PMI (n,%)	3(17.6)	20(15.9)	0.738	1 (11.1)	4 (22.2)	0.861
Premature CAD (n,%)	5(29.4)	14(11.1)	0.053	2 (22.2)	1 (5.6)	0.516
HF (n,%)	2(11.8)	21(16.7)	1.000	2(22.2)	5(27.8)	1.000
AF (n,%)	2(11.8)	20(15.9)	1.000	1(11.1)	2(11.1)	1.000
Prior PCI (n,%)	2(11.8)	14(11.1)	1.000	0(0)	1(5.6)	1.000
Prior CABG (n,%)	0(0)	2(1.6)	1.000	0(0)	0(0)	1.000
ACEI or ARB (n,%)	0(0)	21(16.7)	0.077	0 (0)	2 (11.1)	0.795
β-blockers (n,%)				1 (11.1)	1 (5.6)	1.000
Statins (n,%)	5(29.4)	42(33.3)	1.000	2 (22.2)	5 (27.8)	1.000

Notes: #The following variables were used in the propensity score (PSM) model: age, sex, history of diabetes, hypertension, dyslipidemia, family history of premature coronary artery disease, smoking, previous myocardial infarction, CKD, AF, HF, previous PCI, previous CABG, previous use of ACEI or ARB, β-blockers, statins. Bold character indicates that the P value is <0.05.

Abbreviations: FPCI, fibrinolysis therapy combined with deferred PCI; PPCI, primary PCI; PSM, propensity score-matched method; CKD, chronic kidney disease; PMI, previous myocardial infarction; CAD, coronary artery disease; AF, atrial fibrillation; HF, heart failure; PCI, percutaneous coronary intervention; CABG, coronary artery bypass surgery; ACEI, angiotensin-converting enzyme inhibitor; ARB, angiotensin receptor blocker.

The comparison of angiographic and PCI characteristics between FPCI and PPCI patients before and after PSM is shown in Table 2. Before PSM, both pre- and post-procedure TIMI flow were higher in FPCI patients compared with PPCI patients (p=0.000 and 0.040, respectively). The GRACE and Syntax risk scores were lower in FPCI patients compared with PPCI patients (157.8±9.5 versus 169.9±20.3, p=0.000 and 24.0 [19.5–26.5] versus 27.5 [22.0–33.0], p=0.040, respectively). Also, the rate of application of thrombus aspiration catheter, vasopressure as well as GPI were lower in FPCI patients compared with PPCI patients (0% versus 22.2%, p=0.025;23.5% versus 53.8%, p=0.020;82.4% versus 96.8%, p=0.037, respectively). There were no significant differences regarding the angiographic and PCI characteristics between FPCI and PPCI patients after PSM except for the higher rate of TIMI-3 flow before procedure in TPIC patients (p=0.000).

Table 2

Comparison of Angiographic and Percutaneous Coronary Intervention Characteristics Between the FPCI and PPCI Patients

Variables	Before PSM			After PSM#
	FPCI (n=17)	PPCI (n=126)	P-value	FPCI (n=9)	PPCI (n=18)	P-value
Infarct-related artery
Left main (n,%)	0(0)	1(0.8)		0(0)	0(0)
LAD (n,%)	11(64.7)	76(60.3)		5(55.6)	12(66.7)
LCX (n,%)	2(11.8)	13(10.3)		2(22.2)	3(16.7)
RCA (n,%)	4(23.5)	36(28.6)		2(22.2)	3(16.7)
Saphenous vein graft (n,%)	0(0)	0(0)	0.757	0(0)	0(0)	0.668
Location of infraction
Anterior (n,%)	12(70.6)	78(61.9)		6(66.7)	12(66.7)
Inferial (n,%)	5(29.4)	45(35.7)		3(33.3)	5(27.8)
Lateral (n,%)	0(0)	3(2.4)	0.456	0(0)	1(5.6)	0.940
Pre-procedural TIMI grade
0	2(11.8)	110(87.3)		0(0)	15(83.3)
1	0(0)	11(8.7)		0(0)	3(16.7)
2	0(0)	3(2.4)		0(0)	0(0)
3	15(88.2)	2(1.6)	0.000	9(100)	0(0)	0.000
Post-procedural TIMI grade
0	0(0)	0(0)		0(0)	0(0)
1	0(0)	5(4.0)		0(0)	1(5.6)
2	0(0)	21(16.7)		0(0)	4(22.2)
3	17(100)	100(79.4)	0.040	9(100)	13(72.2)	0.235
Risk stratification
TIMI risk score	5(4–6)	5(5–6)	0.172	5.0(4–6)	5.5(5–6)	0.322
GRACE risk score	157.8 ±9.5	169.9 ± 20.3	0.000	155.8± 10.4	166.6± 23.7	0.112
Syntax score	24.0(19.5–26.5)	27.5(22–33)	0.009	22.4±5.7	27.0±7.0	0.104
Stent deployment	17(100)	126(100)	1.000	9(100)	18(100)	1.000
Intra-operation procedure
Thrombus aspiration	0(0)	28(22.2)	0.025	0(0)	3(16.7)	0.529
IABP (n,%)	1(5.9)	34(27.0)	0.072	1(11.1)	4(22.2)	0.636
Temporary pacemaker (n,%)	0(0)	6(4.8)	1.000	0(0)	0(0)	1.000
Vasopressors (n,%)	4(23.5)	69(54.8)	0.020	3(33.3)	10(55.6)	0.420
Cardiogenic shock (n,%)	3(17.6)	17(13.5)	0.708	2(22.2)	2(11.1)	0.582
GPI (n,%)	14(82.4)	122(96.8)	0.037	7(77.8)	18(100)	0.103

Notes: #The following variables were used in the propensity score (PSM) model: age, sex, history of diabetes, hypertension, dyslipidemia, family history of premature coronary artery disease, smoking, previous myocardial infarction, CKD, AF, HF, previous PCI, previous CABG, previously use of ACEI or ARB, β-blockers, statins. Bold character indicates that the P value is <0.05.

Abbreviations: FPCI, fibrinolysis therapy combined with deferred PCI; PPCI, primary PCI; PSM, propensity score-matched method; LAD, left anterior descending artery; LCX, left circumflex artery; RCA, right coronary artery; GRACE, Global Registry of Acute Coronary Events; Syntax, Synergy Between Percutaneous Coronary Intervention With Taxus and Cardiac Surgery; IABP, intra-aortic balloon counter-pulsation; GPI, glycoprotein IIb/IIIa inhibitor.

The comparison of DTN in FPCI patients and DTB in PPCI patients as well as the ischemia and bleeding events between these two groups before and after PSM is shown in Table 3. The in-hospital adverse clinical outcome was comparable between the two groups regarding the in-hospital ischemia events. The bleeding events score was also comparable between the two groups except for the higher rate of minor bleeding events before PSM. However there was no significant difference in bleeding events between these two groups after PSM.

Table 3

Comparison of Door-to-Balloon/Needle Time and In-Hospital Adverse Clinical Outcomes Between the FPCI and PPCI Patients

Variables	Before PSM			After PSM#
	FPCI (n=17)	PPCI (n=126)	P-value	FPCI (n=9)	PPCI (n=18)	P-value
DTB/DTN (min)	25.8± 4.2	61.1±10.7	0.000	26.9± 4.2	64.9± 23.6	0.000
All-cause of death (n,%)	0 (0)	9 (7.1)	0.599	0 (0)	1(5.6)	1.000
Cardiac death (n,%)	0 (0)	9 (7.1)	0.599	0 (0)	1(5.6)	1.000
MACE (n,%)	0 (0)	12 (9.5)	0.361	0 (0)	1(5.6)	1.000
Non-fatal myocardial infarction (n,%)	0 (0)	5 (4)	1.000	0 (0)	0 (0)	NA
Stroke (n,%)	0 (0)	1 (0.8)	1.000	0 (0)	0 (0)	NA
Any revascularization (n,%)	0 (0)	1 (0.8)	1.000	0 (0)	0 (0)	NA
Stent thrombosis (n,%)	0 (0)	1 (0.8)	1.000	0 (0)	0 (0)	NA
Major bleeding§ (n,%)	0 (0)	0 (0)	NA	0 (0)	0 (0)	NA
Moderate bleeding§ (n,%)	1 (5.9)	0 (0)	0.119	1 (11.1)	0 (0)	0.333
Minor bleeding§ (n,%)	5 (29.4)	6 (4.8)	0.004	2 (22.2)	3 (16.7)	1.000

Notes: #The following variables were used in the propensity score model: age, sex, history of diabetes, hypertension, dyslipidemia, family history of coronary artery disease, smoking, previous myocardial infarction, chronic kidney disease (CKD), atrial fibrillation (AF), heart failure (HF), previous PCI, previous coronary artery bypass surgery (CABG), previously usage of ACEI or ARB, β-blockers, statins. §Bleeding event is defined by the Global Use of Strategies to Open Occluded Arteries (GUSTO) definition of bleeding. Bold character indicates that the P value is <0.05.

Abbreviations: FPCI, fibrinolysis therapy combined with deferred PCI; PPCI, primary PCI; PSM, propensity score-matched method; MACE, major adverse cardiac event.

Discussion

In this single-center retrospective observational study, a shorter DTN time is observed in FPCI patients compared with PPCI patients in STEMI patients during the COVID-19 pandemic in our center. Although the incidence rate of minor bleeding event is higher in TPIC patients compared with PPCI patients, a similar rate of in-hospital ischemia and bleeding events is observed between the two groups after adjusting the relative risk factors using PSM method (Figure 3).

Figure 3

Graphic demonstration of the main results.

The proper RT for STEMI patients is still in debate during the COVID-19 pandemic. How to balance the risk of cross-infection and timely and effective blood flow restoration is an important issue for health-care providers.17 Fibrinolysis therapy is believed to have a lower rate of TIMI-2 flow and higher rate of re-infarction compared with PPCI, not to mention the potential bleeding risk caused by fibrinolysis agents.7,8 However, this conclusion is based on the normal performance of clinical practice. In fact, fibrinolysis therapy is the preferred RT recommended by the Chinese Cardiovascular Association.9 But primary PCI is still the preferred RT in some countries when isolated catheter lab, patient ward as well as personal protective equipment (PPE) is available.18–20 Acentralized and specific “Hub” is also demonstrated to be effective to perform PPCI when the systemic delay is not significantly prolonged.21,22

Beijing Tiantan Hospital applied different RT for STEMI patients during the COVID-19 pandemic according to the overall risk of cross-infection. When the overall risk of cross-infection was relatively low in our hospital, we applied PPCI after STEMI patents finished the screening protocol. FPCI was applied when the risk of cross-infection was elevated in our hospital.

The first finding of our study is that the DTN time is significantly shorter than D2B time both before and after PSM. Systemic delay is significantly prolonged during the COVDI-19 pandemic.23 Daniels et al. believed that the PPCI treatment delays increased during the COVID-19 pandemic, even among COVID-19 negative patients because of the screening protocols. They thought that fibrinolysis therapy might reduce the system delay, which is consistent with our finding.24

The second finding of our study is that a higher post-procedural TIMI flow was observed in FPCI patients. It is known that no-reflow or slow re-flow is associated with worse clinical outcomes.25–27 The EARLY-MYO Trial (Early Routine Catheterization After Alteplase Fibrinolysis Versus Primary PCI in Acute ST-Segment-Elevation Myocardial Infarction) demonstrated that for patients with STEMI presenting ≤6 hours after symptom onset and with an expected PCI-related delay, fibrinolysis therapy with half-dose alteplase and deferred PCI offers more complete myocardial reperfusion when compared with PPCI, which was similar to our finding.28

The third finding of our study is that there are no significant differences in the in-hospital ischemia and bleeding events in the two groups after PSM. Multiple studies compared fibrinolysis therapy and PPCI in STEMI patients. Rashid et al. demonstrated that fibrinolysis strategy was associated with similar rates of the composite of mortality, re-infarction, or stroke as compared with PPCI, however, there was a propensity for more bleeding with a fibrinolysis strategy in a real-world study.10 Armstrong et al. enrolled STEMI patients who presented within 3 hours after symptom onset and who were unable to undergo primary PCI within 1 hour, these patients were randomly divided into fibrinolysis therapy and primary PCI; it turns out that pre-hospital fibrinolysis with timely coronary angiography resulted in effective reperfusion in patients with early STEMI who could not undergo primary PCI within 1 hour after the first medical contact. However, fibrinolysis was associated with a slightly increased risk of intracranial bleeding.11 Strategic Reperfusion Early After Myocardial Infarction (STREAM) trial enrolled patients with STEMI presenting ≤3 hours of symptom onset with an expected time delay from first medical contact (FMC) to PPCI >1 hour, and showed no significant difference in the primary cardiovascular events at 30-day and 1-year follow-up between PPCI and fibrinolysis patients.12 A meta-analysis which enrolled four trials and 1570 patients indicated that deferred PCI was associated with a lower incidence of no-reflow and similar all-cause mortality after 34 months follow up compared with PPCI.29 Recently, Danchin et al. reported that 28% of all patients who underwent late PCI (>120 min from ECG) have poorer 5-year outcomes compared with patients who received fibrinolysis therapy alone.30 All of these studies are consistent with our findings. However, the 16 years follow-up result of the Danish Trial in Acute Myocardial Infarction 2 (DANAMI-2) showed that PPCI produced better clinical outcomes compared with fibrinolysis therapy, but this partially was a result of longer delay times compared with other studies.31,32

In conclusion, our study for the first time demonstrated that FPCI had better post-procedure TIMI flow and similar incidence rate of in-hospital ischemia and bleeding events after PSM when necessary screening protocol is needed. Due to the limited number of participants and short-time follow-up period, the conclusion still needs to be validated in future studies.