IMR Press / RCM / Volume 24 / Issue 3 / DOI: 10.31083/j.rcm2403080
Open Access Systematic Review
Prognostic Value of Preoperative Assessment of Left Ventricular Function in Patients Undergoing Percutaneous Coronary Intervention
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1 Department of Cardiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 100730 Beijing, China
*Correspondence: sunkaii@gmail.com (Kai Sun)
Rev. Cardiovasc. Med. 2023, 24(3), 80; https://doi.org/10.31083/j.rcm2403080
Submitted: 27 October 2022 | Revised: 29 November 2022 | Accepted: 5 December 2022 | Published: 6 March 2023
Copyright: © 2023 The Author(s). Published by IMR Press.
This is an open access article under the CC BY 4.0 license.
Abstract

Background: Patients may experience a decline in cardiac function even after successful percutaneous coronary intervention (PCI). It is apparent that the assessment of left ventricular (LV) function before PCI is often overlooked. The purpose of this review is to explore the significance of LV function assessment before PCI by comparing the differences in short- and long-term PCI outcomes between patients with different LV ejection fraction (LVEF) stratified preoperatively. Methods: PubMed and Scopus were searched to identify potential studies from January 1, 2001 through January 1, 2022. Results: A total of 969,868 participants in 33 studies at different stratifications of baseline LVEF were included in this review and their PCI outcomes were stratified for analysis. The hazard ratio of all-cause mortality within 30 days, one year and greater than 1 year after PCI between patients with abnormal and normal LVEF were 2.96 [95% CI, 2.2, 3.98], 3.14 [95% CI, 1.64, 6.01] and 3.08 [95% CI, 2.6, 3.64]; moderately impaired LV function versus normal were 2.32 [95% CI, 1.85, 2.91], 2.04 [95% CI, 1.37, 3.03], 1.93 [95% CI, 1.54, 2.44]; poor LV function versus normal were 4.84 [95% CI, 3.83, 6.1], 4.48 [95% CI, 1.37, 14.68], 6.59 [95% CI, 4.23, 10.27]. Conclusions: A moderate or severe reduction in patients’ LVEF may have a serious impact on PCI prognosis. We strongly advocate for adequate assessment of LVEF before PCI as this will assist in choosing the optimal revascularization and postoperative treatment, thereby reducing short- and long-term mortality.

Keywords
percutaneous coronary intervention
left ventricular ejection fraction
prognostic
1. Introduction

Since percutaneous coronary intervention (PCI) was introduced in 1977 [1], important advances have been made. Early and long-term outcomes of PCI have been improved with the advent of lower profile balloons, bare-metal stent (BMS), drug eluting stent (DES), improved guide-wire support, increased use of adjuvant drugs and hemodynamic support devices. Recent studies have shown that increased use of PCI reperfusion has led to a decrease in acute coronary syndrome (ACS) mortality. In patients with ST segment elevation myocardial infarction (STEMI), primary PCI can limit infarct size and preserve left ventricular (LV) systolic function [2, 3]. Despite being highly effective in reducing the need for repeat revascularisation compared with BMS, early-generation DES were associated with an increased risk of late (>1 year) thrombotic events due to an excess of stent thrombosis [4, 5, 6]. Currently, new-generation DES feature lower antiproliferative drug loads, thinner stent metallic struts and more biocompatible durable or biodegradable polymers than previous devices [7, 8].

PCI is a mature technology that is highly utilized in clinical practice. Lack of evaluation of the LV function before PCI may result in the failure to select the optimal revascularization protocol. In a 2021 network meta-analysis by Yujiro Yokoyama et al. [9], coronary-artery bypass grafting (CABG) remained the treatment of choice in patients with coronary artery disease and low LV ejection fraction (LVEF). Studies have shown that approximately one-third of patients who undergo PCI [10, 11, 12] suffered from LV dysfunction—an important predictor of post PCI death and major adverse cardiac events (MACE) [13, 14]. PCI does not improve or maintain cardiac function in all STEMI patients with data demonstrating that 4.7–8.6% of patients may experience a decline in cardiac function after successful primary PCI [15, 16]. Therefore, the stratification of LVEF risk assessment before PCI is particularly important but often overlooked. According to the audit of European Association for Percutaneous Cardiovascular Intervention in the UK, only 46% of patients undergoing PCI had ever received LV classification [10]. According to the Mayo Clinic, information on LV function is available in only 60% cases [17] with the main reason being that PCI is increasingly performed in the setting of ACS that requires timely intervention [18, 19]. Comprehensive clinical assessment is sacrificed for the sake of expediency, resulting in insufficient time to assess LV function before PCI. Congestive heart failure (CHF) after STEMI PCI is the primary reason behind the increase in morbidity and mortality [20]. Patients at high risk for CHF need to be identified to select more appropriate post infarction therapies. We believe that LV assessment is helpful for patient risk stratification, even in the context of ACS. This ensures the preoperative awareness of the high-risk nature of the surgery and facilitates the proper revascularization [21].

This study aims to explore the significance of LV function assessment before PCI by comparing the differences in short- and long-term PCI outcomes between patients with different LVEF levels stratified preoperatively along with raising the importance of the evaluation of LVEF before PCI.

2. Materials and Methods

The protocol was registered on INPLASY (INPLASY202220031) and is available on inplasy.com (https://doi.org/10.37766/inplasy2022.2.0031). Our systematic review was consistent with the PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) statement [22].

2.1 Data Sources and Searches

PubMed and Scopus were searched to identify potential studies from January 1, 2001 through January 1, 2022 (Supplementary Method M1) There were no language restrictions. The reference list of previous systematic reviews [23, 24, 25, 26] was scrutinized.

2.2 Study Selection and Eligibility Criteria

We included observational studies or secondary analysis of intervention studies that reported prognosis of PCI. Outcomes of studies needed to be stratified according to LVEF. Two investigators performed title/abstract screening independently from each other. Following this, the full-text of potentially eligible studies was accessed by two investigators for determining eligibility and data extraction. Data evaluated included study design, age, gender, grouping rules, sample size, patients, country, follow-up periods, and study results. If the article did not provide data results, we used free software Engauge-digitizer (Version 12.1, Mark Mitchell, Baurzhan Muftakhidinov and Tobias Winchen et al.) [27] to obtain data from figures present [28]. We assessed study quality using items from the Newcastle-Ottawa Quality Assessment Scale (NOS) [29].

2.3 Outcome and Data Synthesis

The primary outcome was all-cause mortality stratified according to LVEF at baseline. The secondary outcomes were MACE and cardiac mortality in-hospital or long-term. We conducted random-effects or fix-effects meta-analysis of outcomes for which at least 2 studies contributed data. Categorical data were expressed as the pooled odds ratio (OR) or Hazard ratio (HR) with their 95% CIs using the inverse variance method. Heterogeneity was evaluated using both the χ2 test and the I2 statistic. Publication bias was assessed using the Begg rank correlation test and the Egger weighted linear regression test for implementation strategies with at least 10 studies. All statistical tests were two sided and used a significance level of p < 0.05. We used STATA 15 (StataCorp, College Station, TX, USA) for all statistical analyses.

2.4 Subgroup Analysis

We analyzed three subgroups. (1) Patients with heart failure (New York Heart Association or Killip class >1) at baseline, heart failure with reduced ejection fraction (HFrEF) versus heart failure with preserved ejection fraction (HFpEF). (2) Patients undergoing elective PCI for chronic total occlusion (CTO). (3) STEMI patients.

3. Results
3.1 Literature Search

We identified 9786 studies by database searching and 106 additional articles by reference tracking, of which 33 met inclusion criteria with resultant 969,868 patients. The flowchart of the article search and selection process is demonstrated in Fig. 1.

Fig. 1.

Flowchart of study selection.

3.2 Study Characteristics

Of the 33 studies included, two were secondary analyses of randomized controlled trials [13] with the remaining 31 being observational studies (12 prospective and 19 retrospective). Participants in 6 studies [13, 14, 30, 31, 32, 33] were exclusively patients with STEMI, in 3 studies [34, 35, 36] participants were exclusively patients with CTO, and 3 studies [31, 37, 38] were patients with baseline heart failure. Thirteen studies [11, 30, 31, 32, 37, 38, 39, 40, 41, 42, 43, 44, 45] reported the prognostic outcomes during hospitalization, 14 studies [14, 33, 34, 35, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55] reported the prognostic outcomes for greater than or equal to one year, and 6 studies [10, 13, 36, 56, 57, 58] reported the prognostic outcomes in both short and long term. The characteristics of the included studies are detailed (Table 1, Ref. [10, 11, 13, 14, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58]). The average NOS score of all included studies was 7.6 points, with 2 studies having a minimum score of 5 [32, 34] and 3 studies having score of 6 [30, 40, 43] (Supplementary Table 1). Five studies [30, 32, 34, 40, 43] were of low quality because they had too small sample sizes to be representative of the average level of the community, and confounders were not well controlled during the compassrison process, resulting in low comparability.

Table 1.Characteristics of included studies.
Study Year Study design Age Male stratified LVEF% Sample size Patients Country Follow up
Alidoosti [46] 2008 Prospective Observational 56.1 69.0% <40, 41–49, 50 2030 Patients with low, intermediate and high ejection fraction Iran long-term
Banga [30] 2019 Retrospective Observational 61.8 (12.9) 74.3% <50, 50 249 Patients with STEMI treated with primary PCI USA in-hospital
Daneault [13] 2013 Secondary analysis of open-label, randomized trial 60.3 (54.6–72.3) 69.3% <40, 40 2430 Patients with STEMI treated with primary PCI USA 3-year
Doshi [31] 2019 Retrospective Observational 65.6 (13.4) 65.0% <50, 50 31,180 hospitalisations undergoing STEMI-PCI USA in-hospital
El Awady [34] 2020 Prospective Observational 61.1 (8.2) 76.0% <40, 40–49, 50 75 patients undergoing CTO PCI Egypt 6 months
Galassi [35] 2017 Prospective Observational <35, 35–50, 50 839 patients undergoing elective PCI of CTOs Italy 6 months
Holper [47] 2006 Prospective Observational 69.2 54.5% <50, 50 4697 patients undergoing PCI USA 1 year
Jiang [48] 2017 Prospective Observational <50, 50 10,490 patients undergoing PCI China 2 year
Jiang [37] 2019 Retrospective Observational 68.6 (12.1) 69.8% <40, 40–50, 50 1270 hospitalised patients with AMI undergoing emergency PCI China in-hospital
Marui [49] 2014 Prospective Observational 69.7 (9.7) <50, 50 1432 patients undergoing first myocardial revascularization Japan 5 years
Sardi [56] 2012 Retrospective Observational 68.6 (11.7) 75.8% <25, 25–40, 41–50, 50 5337 patients undergoing PCI USA 1 year
Shiga [50] 2009 Prospective Observational 66 (12) 73.7% 30, 30–40, >40 4122 patients with AMI, who were discharged alive Japan 5 years
Son [51] 2016 Retrospective Observational 66.8% 60, >60 319 patients who underwent successful PCI Korea 1 year
Sutton [52] 2016 Retrospective Observational 78 (71–84) 57.3% 35, 35–45, 45–55, 55 82,558 patients who underwent successful PCI USA 1 year
Toma [36] 2017 Prospective Observational 66 (11) 87.0% 40, >40 2002 patients undergoing elective CTO PCI Germany 2 years
Vakili [32] 2014 Prospective Observational 63.5 (12.6) 65.2% 25, 25–50, 50 401 patients with STEMI who underwent primary angioplasty Iran in-hospital
Wang [38] 2017 Prospective Observational 64.20 ± 10.75 79.2% <40, 40–50, 50 1647 patients who had HF, and undergoing PCI/CAG in-hospital
Ye [39] 2018 Retrospective Observational 62.18 (10.31) 69.9% <50, 50 1600 patients who have undergone PCI China in-hospital
Zhong [53] 2020 Prospective Observational 63.69 (8.10) 87.5% <50, 50 301 patients who underwent successful PCI China 1 year
Alaswad [40] 2018 Retrospective Observational 69.57 (11.29) 75.3% 35, >35 891 patients undergoing PCI USA in-hospital
Biondi-Zoccai [57] 2011 Retrospective Observational 74.2 (9.2) 76.1% <30, 30–45, >45 975 patients undergoing PCI Italy median of 18.2 months
De Silva [10] 2012 Retrospective Observational 65.7 (57.4–73.4) 73.7% <30, 30–49, >50 2328 patients undergoing PCI UK long-term
Gao [58] 2013 Prospective Observational 59.9 (11.1) 83.2% <40, 40 4335 patients undergoing PCI China 36 months
Halkin [54] 2005 Retrospective Observational 62 (53–71) 72.9% <40, 40–50, 50–60, >60 1620 AMI USA 1 year
Jackson [41] 2018 Retrospective Observational 68 (12) 77.0% <30, 30–50, >50 260,726 patients who received PCI UK 1 month
Keelan [11] 2003 Retrospective Observational 72.3% 40, 41–49, 50 1158 patients who underwent PCI USA in-hospital
Kwok [42] 2015 Retrospective Observational 73.5% <30, 30–49, 50 246,840 patients who received PCI UK 30 days
Levi [55] 2016 Retrospective Observational 72 (12) 73.0% <30, 30–50, 50 974 patients who underwent an elective PCI Israel 5 years
Mamas [14] 2014 Retrospective Observational 68.5 (68.3–68.6) 77.4% <30, 30–50, >50 230,464 patients undergoing PCI for elective STEMI and non-STEMI UK 5 years
Marsico [43] 2003 Retrospective Observational 67 (27–89) 79.2% 35, >35 2488 patients who underwent PTCA Italy in-hospital
Singh [44] 2007 Retrospective Observational 66.9 (12.1) 69.0% <20, 20–39, 40–59, 60 7457 patients who underwent PCI USA in-hospital
van der Vleuten [33] 2008 secondary analysis of two randomized controlled trials 59.8 (12.0) 77.8% <35, 35–55, >55 924 patients with STEMI treated with PCI Israel 2.5 years
Wallace [45] 2009 Retrospective Observational 63.8 (11.7) 67.5% <25, 26–35, 36–45, 46–55, >55 55,709 patients who underwent PCI USA in-hospital
Studies 33 969,868
AMI, acute myocardial infarction; CTO, chronic total occlusion; LVEF, left ventricular ejection fraction; PCI, percutaneous coronary intervention; PTCA, Percutaneous Transluminal Coronary Angioplasty; STEMI, ST-elevation myocardial infarction.
3.3 Definition of LVEF Stratification

Normal LVEF is defined as LVEF 50% with and abnormal LVEF being defined as LVEF <50%. Abnormal LVEF is classified into moderately impaired LV function (LVEF 30–49%) and poor LV function (LVEF <30%). Because stratification according to LVEF slightly varied from study to study, the definition of stratification fluctuated + or –5% in our combined analysis.

3.4 All-Cause Mortality

The hazard ratios of all-cause mortality within 30 days (or in-hospital), in one year and over a period more than 1 year after PCI between patients with abnormal and normal LVEF were 2.96 [95% CI, 2.2, 3.98], 3.14 [95% CI, 1.64, 6.01] and 3.08 [95% CI, 2.6, 3.64]. The hazard ratios of all-cause mortality within 30 days (or in-hospital), in one year and over a period more than 1 year after PCI between patients with moderately impaired LV function and patients with normal LVEF were 2.32 [95% CI, 1.85, 2.91], 2.04 [95% CI, 1.37, 3.03], 1.93 [95% CI, 1.54, 2.44]. The hazard ratios of all-cause mortality within 30 days (or in-hospital), in one year and over a period more than 1 year after PCI between patients with poor LV function and patients with normal LVEF were 4.84 [95% CI, 3.83, 6.1], 4.48 [95% CI, 1.37, 14.68], 6.59 [95% CI, 4.23, 10.27] (Table 1, Supplementary Figs. 1–9). The above comparisons suggested that the poorer baseline LV function was a major source for all-cause PCI mortality.

3.5 Incidence of MACE

The odds ratios of MACE occurrence within 30 days (or in-hospital), in 1 year and over a period greater than 1 year after PCI between patients with abnormal and normal LVEF were 1.9 [95% CI, 1.65, 2.2], 1.71 [95% CI, 1.13, 2.59], and 1.37 [95% CI, 1.14, 1.65]. The odds ratios of MACE occurrence within 30 days (or in-hospital), in 1 year and over a long-term of period greater than 1 year after PCI between patients with moderately impaired LV function and patients with normal LVEF were 1.35 [95% CI, 1.27, 1.43], 1.194 [95% CI, 0.96, 1.48], and 1.15 [95% CI, 0.879, 1.52]. The odds ratios of MACE occurrence within 30 days (or in-hospital), in 1 year and over a period greater than 1 year after PCI between patients with poor LV function and patients with normal LVEF were 2.41 [95% CI, 2.04, 2.85], 1.47 [95% CI, 1.03, 2.081], and 2.31 [95% CI, 1.46, 3.66] (Table 2, Supplementary Figs. 10–18). The above comparisons suggest that the risk of MACE occurrence in 1 year or over a period greater than 1 year after PCI in patients with modestly impaired LV function was not different from that in patients with normal LVEF, but was greater in patients with poor baseline LV function than that in patients with normal LVEF.

Table 2.Outcomes.
Outcomes Comparisons (stratified according to LVEF at baseline) Follow-up HR [95% CI] p-value Studies Samples
All-cause mortality abnormal vs normal 30-day 2.96 [2.2, 3.98] 0.000 96.3% 13 813,975
All-cause mortality abnormal vs normal 1-year 3.14 [1.64, 6.01] 0.000 99.7% 8 324,723
All-cause mortality abnormal vs normal long-term 3.08 [2.6, 3.64] 0.000 88.5% 7 237,097
All-cause mortality moderate vs normal 30-day 2.32 [1.85, 2.91] 0.000 80.8% 9 807,277
All-cause mortality moderate vs normal 1-year 2.04 [1.37, 3.03] 0.000 98.1% 7 320,026
All-cause mortality moderate vs normal long-term 1.93 [1.54, 2.44] 0.000 89.1% 5 235,665
All-cause mortality poor vs normal 30-day 4.84 [3.83, 6.1] 0.000 77.8% 7 797,443
All-cause mortality poor vs normal 1-year 4.48 [1.37, 14.68] 0.000 99.8% 5 317,248
All-cause mortality poor vs normal long-term 6.59 [4.23, 10.27] 0.000 96.7% 5 235,665
MACE abnormal vs normal 30-day 1.9 [1.65, 2.2] 0.000 76.3% 7 521,584
MACE abnormal vs normal 1-year 1.71 [1.13, 2.59] 0.011 61.2% 3 6477
MACE abnormal vs normal long-term 1.37 [1.14, 1.65] 0.001 0.0% 4 14,334
MACE moderate vs normal 30-day 1.35 [1.27, 1.43] 0.000 2.3% 4 515,998
MACE moderate vs normal 1-year 1.19 [0.96, 1.48] 0.107 0.0% 2 6176
MACE moderate vs normal long-term 1.15 [0.87, 1.52] 0.329 0.0% 3 3844
MACE poor vs normal 30-day 2.41 [2.04, 2.85] 0.000 61.3% 4 515,998
MACE poor vs normal 1-year 1.46 [1.03, 2.08] 0.036 0.0% 2 6176
MACE poor vs normal long-term 2.31 [1.46, 3.66] 0.000 0.0% 2 1814
Cardiac death <40 vs >40 30-day 7.54 [2.7, 21.06] 0.000 56.1% 2 6765
Cardiac death <40 vs >40 1-year 4.51 [1.96, 10.38] 0.000 0.0% 2 8457
Cardiac death <40 vs >40 long-term 6.51 [4.25, 9.97] 0.000 51.2% 3 10,887
CTO-Death abnormal vs normal all 3.3 [2.53, 4.29] 0.000 0.0% 2 2841
CTO-MACE abnormal vs normal all 1.6 [1.34, 1.9] 0.000 0.0% 3 2916
STEMI-Death abnormal vs normal 30-day 4.36 [1.52, 12.5] 0.000 96.9% 4 264,475
STEMI-Death abnormal vs normal 1-year 5.22 [3.87, 7.04] 0.000 92.8% 3 233,818
STEMI-Death abnormal vs normal long-term 3.83 [3.35, 4.37] 0.000 82.7% 3 233,818
STEMI-MACE abnormal vs normal 30-day 3.78 [2.54, 5.64] 0.000 0.0% 2 2679
HF-Death HFrEF vs HFpEF 30-day 1.36 [1.15, 1.6] 0.000 0.0% 3 34,097
CTO, chronic total occlusion; HF, heart failure; HFrEF, HF with reduced ejection fraction; HFpEF, HF with preserved ejection fraction; HR, Hazard ratio; LVEF, left ventricular ejection fraction; MACE, major adverse cardiac events; STEMI, ST-elevation myocardial infarction.
Bold italics mean no statistical significance.
3.6 Cardiovascular Mortality

Due to the paucity of study data, in this study the outcomes were pooled based on a cutoff value of 40% for the baseline LVEF. The hazard ratios of cardiovascular mortality within 30 days, in 1 year and over a period greater than 1 year after PCI between patients with baseline LVEF <40% and patients with baseline LVEF 40% were 7.54 [95% CI, 2.7, 21.06], 4.507 [95% CI, 1.96, 10.38], 6.51 [95% CI, 4.25, 9.97]. The results indicate that patients with baseline LVEF <40% have a higher risk of short- and long-term cardiovascular mortality after PCI (Table 2, Supplementary Figs. 19–21).

3.7 Subgroup Analysis

Among patients undergoing elective CTO PCI, patients with abnormal LVEF had significantly higher all-cause mortality than that of patients with normal LVEF, HR = 3.30 [95% CI, 2.53, 4.29], and the incidence of MACE was significantly increased, OR = 1.60 [95% CI, 1.34, 1.90]. Among patients undergoing STEMI PCI, patients with abnormal LVEF had significantly higher 30-day, 1-year, and long-term all-cause mortality compared to patients with normal LVEF, with HR = 4.36 [95% CI, 1.52, 12.5], 5.22 [95% CI, 3.87, 7.04], and 3.83 [95% CI, 3.35, 4.37]. Compared with HFpEF, patients with HFrEF undergoing PCI were significantly noted to have an increased all-cause mortality, HR = 1.36 [95% CI, 1.14, 1.60] (Table 2, Supplementary Figs. 22–28).

3.8 Publication Bias

Publication bias was assessed using funnel plots and asymmetry of the funnel plot was evaluated with the Egger regression test for implementation strategies with at least 10 studies. We found publication bias in the comparison of 30-day all-cause mortality in patients with abnormal versus normal LVEF (Supplementary Fig. 29).

4. Discussion

A total of 969,868 participants in 33 studies [10, 11, 13, 14, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58] at different stratification of baseline LVEF were included in this study and their PCI outcomes were stratified for analysis. This study found that lower baseline LVEF was associated with higher risk of all-cause mortality after PCI. Patients with a moderate level of LVEF had a 2.32-fold increased risk of all-cause mortality within 30 days and a 1.93-fold increased risk of all-cause mortality over 1 year compared with patients with a normal LVEF. Compared with patients with normal LVEF, the HR of 30-day all-cause mortality was 4.84 and the HR of over 1-year all-cause mortality was 6.59 in patients with poor LVEF. We also investigated cardiovascular mortality in patients with LVEF below 40%. Our study demonstrated that patients with LVEF below 40% had 7.54 times higher 30-day cardiovascular mortality and 6.54 times higher cardiovascular mortality over 1 year compared with patients with LVEF above 40%. This data supports that reduced LVEF is an important contributing factor to the prognosis of all-cause mortality, especially to cardiovascular death after PCI.

Studies have suggested that our findings may be related to the following reasons: (1) patients with reduced LV function are mostly elderly diabetic patients with a history of acute myocardial infarction and a higher possibility of cardiogenic shock; (2) with the decrease of LV function, the shear forces in the stented segment decreases, increasing the possibility of thrombosis [59, 60]; (3) with the decline of cardiac function, the incidence of renal insufficiency, which is a known risk factor for stent thrombosis, increases. In view of this, adequate preoperative evaluation of LVEF and the pursuit of optimal revascularization may be of great significance for the outcomes of these patients. Some guidelines recommend CABG as a revascularization strategy for patients with poor ejection fraction. The European Society Of Cardiology Guidelines indicate that CABG is superior to PCI, whereas the US guidelines only recommend CABG and have no comment on PCI [61, 62]. CABG is more likely to achieve complete revascularization than PCI [63]. Full revascularization can more effectively reduce the burden of myocardial ischemia, thereby reducing the risk of both sudden death and cardiac death. Moreover, CABG is better for blood supply in the distal vascular bed with full revascularization achieved after CABG resulting in better outcomes to patients [64]. However, PCI is still widely used due to its operational ease and patients’ own choice. Especially in the context of ACS, evaluation of LVEF before PCI becomes even more important when clinicians are challenged to complete surgery within 72 [18] or 48 hours [19]. Understanding LV dysfunction can provide insight into the possible complexity of the intended PCI, thus providing a basis for preoperative preparation and medical optimization of patients. Meanwhile, this ensures that all team members understand the high-risk nature of the case before starting the procedure, and deploy percutaneous LV assist device in advance, such as axial flow pumpor intra-aortic balloon counter-pulsation. Moreover, identifying high-risk patients facilitates postoperative care, understanding postoperative changes in LVEF, and increases the use of more appropriate postinfarction therapies, such as optimal doses of angiotensin receptor blockers, aldosterone antagonists, or angiotensin converting enzyme inhibitors [65, 66]. The ESC Clinical Practice Guidelines advise that all patients with STEMI undergo a systematic echocardiographic assessment to assess LV function before discharge from the hospital. For patients with LVEF 40%, the guidelines call for an early re-evaluation within 6–12 weeks after leaving the hospital to assess the need for device-based interventions [67, 68]. Data support that the assessment of LVEF before PCI (including ACS patients) is extremely significant for the success of PCI and the improvement of patients’ postoperative survival.

Our subgroup analysis of CTO PCI patients suggests that CTO patients with abnormal LVEF have a 3.3-fold increased risk of mortality and a 1.6-fold increased risk of MACE compared with CTO patients with normal LVEF. PCI may provide significant clinical benefit for CTO [69]. Although the applicability of CTO PCI to symptomatic patients has been generally accepted by guidelines and consensus [70], CTO PCI has another important potential benefit, that is improved LV function. Preoperative assessment of LVEF is necessary to assess the improvement in LV function. According to Galassi et al. [35] and Tajstra et al. [71], a higher prevalence of peripheral vascular disease, chronic kidney disease, and diabetes mellitus in patients with CTO and low LVEF significantly increases the surgical risk. Preoperative LVEF assessment is critical to identify high-risk patients who are to undergo CTO PCI. CTO PCI is a relatively complex procedure, and blocking side branches during CTO PCI is associated with a high risk of coronary perforation and perforation tamponade [72] as well as periprocedural myocardial infarction [73, 74]. The use of the antegrade crossing techniques in CTO recanalization may be preferable because the retrograde crossing techniques have been associated with a high risk of procedural complications [74, 75] and surgical perioperative myocardial infarction. However, preservation of bifurcations and recanalization of complex CTOs often require retrograde techniques [76, 77]. CTO PCI relies heavily on operator experience, so preoperative LVEF evaluation is necessary to fully understand the patient’s condition and the difficulty of operation.

Our subgroup analysis of HF patients showed that the 30-day mortality in HFrEF patients was 1.36 times higher than that in HFpEF patients. Although the data volume is small, it can still be seen that HFrEF patients have a poor prognosis. Currently, there are no clear guidelines for the role of PCI in the treatment of HFrEF. Therefore, for HF patients, pre-PCI LVEF assessment is needed to identify HFrEF patients and select appropriate treatment strategies.

Our findings have some limitations. The stratification criteria of LVEF were not completely consistent across the included studies, and relatively broad criteria were used to classify LVEF into normal, moderate and poor levels, which may account for the higher heterogeneity (Table 2). The time span of our included studies was 20 years and during this time many advances have been made in PCI technology, which may also be one of the reasons for the high heterogeneity among studies in different years. Therefore, the effect sizes in the meta-analysis of all-cause mortality should be interpreted with caution. However, a random effects model has been used to minimize the bias associated with high heterogeneity.

5. Conclusions

Our study suggests that a moderate or severe reduction in patients’ LVEF may have a serious impact on PCI prognosis. Therefore, we strongly advocate for adequate assessment of LVEF before PCI (regardless of ACS) in order to choose the optimal revascularization and postoperative treatment resulting in reduced short- and long-term mortality.

Abbreviations

ACS, acute coronary syndrome(s); BMS, bare-metal stent; CABG, coronary artery bypass grafting; CHF, Congestive heart failure; CTO, chronic total occlusion; DES, drug eluting stent; HF, heart failure; HFpEF, HF with preserved ejection fraction; HFrEF, HF with reduced ejection fraction; HR, Hazard ratio; LV, left ventricular; LVEF, left ventricular ejection fraction; MACE, major adverse cardiac events; NOS, Newcastle-Ottawa Quality Assessment Scale; OR, odds ratio; PCI, percutaneous coronary intervention; STEMI, ST-elevation myocardial.

Author Contributions

MY—Writing - Original draft preparation. FG—Formal analysis. YY—Data curation, Validation. ZJ—Data curation, Validation. KS—Writing - Reviewing and Editing. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript.

Ethics Approval and Consent to Participate

Not applicable.

Acknowledgment

Not applicable.

Funding

This research received no external funding.

Conflict of Interest

The authors declare no conflict of interest.

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