Complete Revascularization of Stable STEMI Patients Offers a Significant Benefit if Done During the Index PCI, but Not if It's Done as a Staged Procedure.

BACKGROUND: Complete revascularization (CR) of hemodynamically stable STEMI improves outcomes when compared to culprit-only PCI. However, the optimal timing for CR (CR during index PCI [iCR] versus staged PCI [sCR]) is unknown. sCR is defined as revascularization of non-culprit lesions not done during the index procedure (mean 31.5±24.6 days after STEMI). Our goal was to determine whether iCR was the superior strategy when compared to sCR.
METHODS: A systematic review of Medline, Cochrane, and Embase was performed for RCTs reporting outcomes of stable STEMI patients who had undergone CR. Only RCTs with a clearly defined timing of CR, for the classification into iCR and sCR, and a follow-up of at least 12 months were included. Seven RCTs comprising 6647 patients (mean age:62.9±1.4 years, male sex:79.4%) met these criteria and were included.
RESULTS: After a mean follow-up of 25.1±9.4 months, iCR was associated with a significant reduction in cardiovascular mortality (risk ratio [RR] 0.48, 95% confidence interval [CI] 0.26-0.90, p=0.02, relative risk reduction [RRR] 52%) and non-fatal reinfarctions (RR 0.42, 95% CI 0.25-0.70, p=0.001, RRR: 58%). sCR showed a significant reduction in non-fatal reinfarctions only (RR 0.68, 95% CI 0.54-0.85, p=0.0008, RRR: 32%). There was no difference in the safety outcome of contrast-induced nephropathy between groups.
CONCLUSION: iCR of stable STEMI patients is associated with a significant reduction in cardiovascular death and a trend towards reduction in all-cause mortality. These benefits are not seen in sCR. Both strategies are associated with a reduction in non-fatal reinfarctions.

Introduction

Percutaneous coronary intervention (PCI) is the treatment of choice for ST-elevation myocardial infarction (STEMI), receiving a class I, Level of Evidence (LOE): A, recommendation in the 2013 ACCF/AHA guidelines for the management of ST-elevation myocardial infarction.1 Around 50% of patients presenting with STEMI have multivessel coronary artery disease (MVCAD), defined as ≥50% stenosis in a non-culprit coronary artery during index angiography.2 MVCAD in patients with STEMI carries a higher MACE risk than single vessel disease and as a result, many RCT’s have focused on whether treatment of non-culprit lesions is beneficial.

The 2013 guidelines, which gave a class III LOE B indication (meaning harm) to primary PCI of non-culprit MVCAD in stable STEMI patients, were derived from limited, and often conflicting, data.1 The subsequent publication of several randomized control trials (RCT) showed that complete revascularization (CR) of MVCAD in stable STEMI patients, either during index PCI (iCR) or as a staged procedure (sCR), might improve outcomes.3–5 This prompted a reassessment of the 2013 guidelines.

This process culminated with the publication of the 2015 ACC/AHA/SCAI Focused Update on Primary Percutaneous Coronary Intervention for Patients With ST-Elevation Myocardial Infarction, where CR was changed from a class III recommendation (harm) to a class IIb LOE B-R (moderate quality evidence from 1 or more RCTs).6

However, there was still hesitancy in adopting these guidelines into clinical practice due to the relatively small number of patients enrolled in previous RCTs, the lack of single hard outcomes reaching statistical significance (dependence on composite outcomes), and the absence of a recommendation on the exact timing of CR (iCR vs sCR). A recently published, large multicenter RCT, the COMPLETE trial (Complete Revascularization with Multivessel PCI for Myocardial Infarction),7 enrolled 4041 patients with a median follow-up of 3 years. It showed benefit in two coprimary composite outcomes (first coprimary composite of cardiovascular (CV) death or myocardial infarction (MI) (hazard ratio [HR] 0.74, 95% confidence interval [CI] 0.60–0.91, p=0.004), and second coprimary composite outcome of cardiovascular (CV) death, MI or ischemia-driven revascularization (HR 0.51, 95% CI 0.43–0.61, P<0.001) when CR strategy was performed. However, this study also failed to show significant benefit for CR with regards to individual hard outcomes of CV death (HR 0.93, 95% CI 0.65–1.32) or all-cause mortality (HR 0.91, 95% CI 0.69–1.20).7

A recent meta-analysis by Pavasini et al showed a significant benefit of CR vs culprit-lesion only strategy in CV death (HR 0.62, 95% CI 0.39–0.97, p=0.04) and repeat MI (HR 0.65, 95% CI 0.53–0.80, p<0.0001) but failed to demonstrate a significant benefit in all-cause mortality (HR 0.81, 95% CI 0.60–1.10, p=0.18).8 A previous meta-analysis and meta-regression by Pasceri et al9 showed a significant total mortality benefit in CR compared to culprit-lesion only revascularization (Relative Risk [RR] 0.62, 95% CI 0.39–0.97). However, that analysis included two RCTs (Hamza et al and HELP AMI)10,11 that are not generalizable due to a strict inclusion criteria (Hamza et al with diabetic patients only),11 or outdated technology (HELP AMI with heparin-coated stents).10

Given the aforementioned lack of clarity regarding the optimal timing for CR and its true effects on clinically relevant outcomes, we decided to perform a systematic review and meta-analysis of all available RCTs that met our criteria to try to ascertain if the timing of CR (either iCR or sCR when compared with a culprit-lesion only strategy) had any impact on single, hard outcomes of all-cause mortality, CV death or non-fatal reinfarction). A secondary goal of this meta-analysis was to determine if there were any differences in safety outcomes of contrast-induced nephropathy between iCR and sCR.

Methods

The present meta-analysis was performed according to Cochrane Collaboration and Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statements.12 This meta-analysis was registered in PROSPERO with registration number CRD42020155116.

Search Strategy

We searched PubMed, Embase, and Cochrane Central Register of Clinical Trials (Cochrane Library, Issue 02, 2017) databases from January 2008 through November 2020 to identify RCTs comparing a CR vs culprit-lesion only strategy in stable patients presenting with STEMI.

We used the following terms: (“complete revascularization”) AND (“STEMI” OR “ST-elevation myocardial infarction”). Language was restricted to papers in English only. The reference lists of identified articles were also exhaustively reviewed for additional sources.

Eligibility Criteria

Studies with the following characteristics were considered eligible: (A) RCTs comparing CR vs culprit-lesion only in stable patients with STEMI; (B) clearly identified the timing of the CR strategy (either iCR or sCR); (C) compared the event rates of all-cause mortality, CV death and non-fatal reinfarction between the two groups; (D) compared the rates of strokes and CIN between groups; (F) had a follow-up period of at least 12 months.

Case reports, editorials, reviews, non-randomized studies and expert opinions were excluded from our analysis. Abstracts presented in major international conferences that have not been published as full papers were not considered in our analysis.

Primary Outcome and Composite Safety Outcome

The primary outcomes of this study were (A) All-cause mortality (B) CV death, and (C) non-fatal reinfarction. The safety outcome was contrast-induced nephropathy (CIN).

CV death was defined as all deaths with a clear cardiovascular or unknown cause. Reinfarction was defined using the Fourth Universal Definition of Myocardial Infarction.13 CIN was defined as an elevation of serum creatinine of ≥25% or ≥0.5 mg/dl (44 μmol/l) from baseline within 48 h.14

Data Extractions and Quality Appraisal

Two investigators (R.C.C.R and S.M.I.R.) independently screened all titles, abstracts and manually searched the full text versions of all relevant studies that fulfilled the inclusion criteria. References of the retrieved articles were independently reviewed for further identification of potentially relevant studies. Disagreements were resolved by consensus after discussion (R.C.C.R and S.M.I.R.). We extracted characteristics of each study including methodology and baseline patient characteristics, CV deaths, non-fatal reinfarction, stroke rate, and CIN rate. If the abovementioned information was not readily available in the written article, the principal investigator of that particular study was contacted to supply pertinent information.

Quality Assessment

The quality and reporting of the included RCTs were assessed using the Cochrane Risk of Bias Tool.15 Six categories were included in the analysis [A] Selection bias: systematic differences between baseline characteristics of the groups that are compared; [B] Performance bias: systematic differences between groups in the care that is provided, or in exposure to factors other than the interventions of interest; [C] Detection bias: systematic differences between groups in how outcomes are determined. Blinding of outcome assessors may reduce the risk that knowledge of which intervention was received, rather than the intervention itself, affects outcome measurement; [D] Attrition bias: systematic differences between groups due to withdrawals from a study. Withdrawals from the study lead to incomplete outcome data; [E] Reporting bias: systematic differences between reported and unreported findings; [F] Other biases: other sources of bias that are relevant only in certain circumstances. Quality of the included RCTs was summarized visually.

Statistical Analysis

Descriptive statistics are presented as number of cases (n) for dichotomous and categorical variables. Statistical analysis was performed in line with recommendations from the Cochrane Collaboration and PRISMA guidelines, using Review Manager (RevMan version 5.4, the Cochrane Collaboration, 2020).15 Heterogeneity was assessed using the I2 statistics, which is the proportion of total variation observed among the studies attributable to differences between studies rather than sampling error (chance). Data were summarized across groups using the Mantel-Haenszel Risk Ratio (RR) Fixed-Effect model if I2<25.16 We considered I2<25% as low and I2≥75% as high. The Random-Effects Model was used if I2≥25%. Publication bias was estimated visually by funnel plots.15

Results

A total of 204 studies were identified using the specified search criteria (Figure 1). After evaluation of these studies based on titles and abstracts, 10 RCTs were further analyzed in their full-text version, 3 of which were excluded to result in 7 RCTs that fulfilled all inclusion criteria. These 7 RCTs incorporated a total of 6647 participants (79.4% male, average age 62.9± 1.4 years, mean follow-up period 25.1±9.4 months). Other RCTs were excluded due to a lack of information relevant to our study questions, narrow population (Hamza et al RCT of diabetic patients only11 limiting generalizability, outdated technology that is no longer routinely used (HELP-AMI) with its heparin-coated stents),10 or because of insufficient follow-up (less than 12 months).

Figure 1

Study selection. Process of study selection.

Characteristics of Included Studies

The baseline characteristics of the included trials are summarized in Table 1. Complete revascularization during index PCI was undertaken in 744 participants (11.2%), whereas CR was done as a staged procedure in 2475 participants (37.2%). Culprit-vessel only PCI was done in 3430 participants (51.6%). The mean age was 62.9±1.4 years; 79.4% were males. The mean follow-up period was 25.1± 9.4 months.

Table 1

Baseline Characteristics of Included RCTs

Study Name	n	Culprit-Only PCI	Index CR (iCR)	Staged CR (sCR)	Time Before sCR	Median Follow-Up (Months)	Mean Age	Male Sex	Diabetes	Hypertension	Current Smoker	Previous MI
COMPARE-ACUTE 201727	885	590	295	0	NA	12	61.5	683	137	418	407	70
COMPLETE 20197	4041	2025	0	2016	No later than 45 days after randomization	36	62	3225	787	2009	1606	NP
CVLPRIT 20154	296	146	150	0	NA	12	65	240	39	105	87	12
DANAMI-3-PRIMULTI 20153	627	313	0	314	Average 2 days after STEMI	27	63.5	506	71	276	311	44
Ghani 201228	121	41	0	80	No later than 3 weeks after STEMI	36	61.5	97	7	38	54	7
Politi 200929	214	84	65	65	Average 56.8±12.9 days after STEMI	30	65	166	41	124	NP	NP
PRAMI 20135	465	231	234	0	NA	23	62	363	83	187	221	35

Notes: COMPARE-ACUTE 2017: Fractional Flow Reserve–Guided Multivessel Angioplasty in Myocardial Infarction. COMPLETE 2019: Complete Revascularization with Multivessel PCI for Myocardial Infarction. CVLPRIT 2015: Randomized Trial of Complete Versus Lesion-Only Revascularization in Patients Undergoing Primary Percutaneous Coronary Intervention for STEMI and Multivessel Disease. DANAMI-3-PRIMULTI 2015: Complete revascularization versus treatment of the culprit lesion only in patients with ST-segment elevation myocardial infarction and multivessel disease (DANAMI-3—PRIMULTI): an open-label, randomized controlled trial. Ghani 2012: Treatment of non-culprit lesions detected during primary PCI: long-term follow-up of a randomized clinical trial. Politi 2009: A randomized trial of target-vessel versus multi-vessel revascularization in ST-elevation myocardial infarction: major adverse cardiac events during long-term follow-up. PRAMI 2013: Randomized Trial of Preventive Angioplasty in Myocardial Infarction.

Abbreviations: NA, Not Applicable; RCT, randomized control trial; PCI, percutaneous coronary intervention; pCR, Complete Revascularization performed during the primary PCI; sCR, Complete Revascularization performed as a staged procedure; MI, Myocardial Infarction; STEMI, ST-elevation myocardial infarction.

Quality Assessment and Publication Bias

Funnel plots did not suggest publication bias for the selected outcomes (Figure 2). All the RCTs included in this meta-analysis had good methodological quality indicating “low risk of bias” (Figure 3).

Figure 2

Funnel Plots – (A) all-cause mortality of complete revascularization during index PCI (B) cardiovascular mortality of staged complete revascularization (C) reinfarction events of complete revascularization during index PCI (D) reinfarction events of complete revascularization during staged complete revascularization. Primary complete revascularization: Revascularization done at the time of primary percutaneous catheter intervention (PCI). Staged complete revascularization: Revascularization done at a different time than the primary PCI.

Figure 3

Risk of bias summary: review authors’ judgements about each risk of bias item for each included study. COMPARE-ACUTE 2017: Fractional Flow Reserve–Guided Multivessel Angioplasty in Myocardial Infarction. COMPLETE 2019: Complete Revascularization with Multivessel PCI for Myocardial Infarction. CVLPRIT 2015: Randomized Trial of Complete Versus Lesion-Only Revascularization in Patients Undergoing Primary Percutaneous Coronary Intervention for STEMI and Multivessel Disease. DANAMI-3-PRIMULTI 2015: Complete revascularization versus treatment of the culprit lesion only in patients with ST-segment elevation myocardial infarction and multivessel disease (DANAMI-3—PRIMULTI): an open-label, randomized controlled trial. Ghani 2012: Treatment of non-culprit lesions detected during primary PCI: long-term follow-up of a randomized clinical trial. Politi 2009: A randomized trial of target-vessel versus multi-vessel revascularization in ST-elevation myocardial infarction: major adverse cardiac events during long-term follow-up. PRAMI 2013: Randomized Trial of Preventive Angioplasty in Myocardial Infarction.

Impact of Complete Revascularization on All-Cause Mortality

There was a non-significant, but remarkable trend towards an all-cause mortality benefit in the iCR group when compared with the culprit-only group: iCR (RR 0.63, 95% CI 0.40–1.00, p=0.05). No significant difference was seen in the sCR group when compared with the culprit-only group (RR 0.92, 95% CI 0.57–1.49, p=0.75) (Figure 4).

Figure 4

Forest Plot – all-cause mortality (A) complete revascularization during index PCI (B) staged complete revascularization. Diamond indicates overall summary estimate for the analysis (width of the diamond represents the 95% CI); width of the shaded square, size of the population. Fixed-effect model was used for this outcome during index PCI as I2<25; random effects model was used for the staged complete revascularization outcome given I2≥25.

Impact of Complete Revascularization on Cardiovascular Mortality

There was a statistically significant reduction in cardiovascular mortality in the iCR group, when compared to the culprit-lesion only group (RR 0.48, 95% CI 0.26–0.90, p=0.02), with a relative risk reduction (RRR) of 52% (Figure 5). There was no benefit seen in the sCR group (RR 0.73, 95% CI 0.38–1.41, p=0.35).

Figure 5

Forest Plot – cardiovascular mortality (A) complete revascularization during index PCI (B) staged complete revascularization. Diamond indicates overall summary estimate for the analysis (width of the diamond represents the 95% CI); width of the shaded square, size of the population. Fixed-effect model was used for this outcome during index PCI as I2<25; random effects model was used for the staged complete revascularization outcome given I2≥25.

Impact of Complete Revascularization on Non-Fatal Reinfarction

We found a statistically significant reduction in non-fatal reinfarctions in both complete revascularization groups, regardless of timing, when compared with the culprit-only strategy. The iCR group (RR 0.42, 95% CI 0.25–0.70, p=0.001), with a relative risk reduction (RRR) of 58% (Figure 6), whereas the sCR group (RR 0.68, 95% CI 0.54–0.85, p=0.0008) with a RRR of 32%. In the sCR cohort, the statistical weight of the COMPLETE trial is responsible for the significant decrease in reinfarctions.

Figure 6

Forest Plot – non-fatal reinfarction (A) complete revascularization during index PCI (B) staged complete revascularization. Diamond indicates overall summary estimate for the analysis (width of the diamond represents the 95% CI); width of the shaded square, size of the population. Fixed-effect model was used in both outcomes as I2<25.

Safety Outcome of Contrast-Induced Nephropathy

There was no significant difference in outcomes between the complete revascularization groups and the culprit-lesion only group: iCR (RR 0.67, 95% CI 0.16–2.82, p=0.58) and sCR (RR 0.83, 95% CI 0.83–2.17, p=0.23) (Figure 7).

Figure 7

Forest Plot –safety outcome of contrast-induced nephropathy (A) complete revascularization during Index PCI (B) staged complete revascularization. Diamond indicates overall summary estimate for the analysis (width of the diamond represents the 95% CI); width of the shaded square, size of the population. Fixed-effect model was used in both outcomes as I2<25.

Discussion

Complete revascularization of MVCAD in patients who present with a hemodynamically stable STEMI has been shown to be beneficial when compared with a culprit-vessel only strategy in previously published meta-analyses.8,9 In a recently published meta-analysis by Atti et al, complete revascularization was associated with a significantly decreased reinfarction rate (RR 0.69, 95% CI 0.50–0.95) and repeat revascularization (RR 0.34, 95% CI 0.25–0.44) with no benefit in the other studied efficacy outcomes (all-cause mortality and cardiovascular mortality).17 However, the vast majority of the previous meta-analyses pooled together data from papers and populations that underwent complete revascularization during the index PCI as well as those who did so as a staged procedure after the culprit lesion was treated, without distinction regarding timing.

We performed this meta-analysis to determine whether the timing of CR (iCR vs sCR), has an impact on cardiovascular mortality, non-fatal reinfarction, and all-cause mortality. With our findings, we have demonstrated that iCR is superior to sCR because it lowers CV mortality and shows a beneficial, yet non-significant trend in all-cause mortality, when compared to culprit-only revascularization in stable patients presenting with STEMI. This is important and relevant for a number of reasons.

Firstly, it challenges current day practice in which sCR is more commonly performed than iCR. In a large cohort study by Secemsky et al using the National Cardiovascular Data Registry CathPCI Registry from the third quarter of 2009 to the first quarter of 2018,18 multivessel PCI was performed in n=138,380 STEMI patients. Of these, 30.8% (n=42,629) had multivessel PCI performed during the index procedure, 31.6% (n=43,696) were done as staged procedures during the index admission and 37.6% (n=52,055) had multivessel PCI done within 45 days of discharge.18 The same fact can be observed in our meta-analysis, where 77% of the patients underwent a staged complete revascularization while only 23% underwent complete revascularization during the index PCI.

sCR is likely popular because high quality data regarding the optimal timing does not exist at this time, as even a recent review article by Bossard and Mehta puts in evidence – the interventional community agrees on the benefits of performing a complete revascularization of this patient population, but there is a lack of clear guidance regarding the best timing.19 Also, performing a sCR vs iCR is believed in routine clinical practice to lower the risk of CIN, a belief that is refuted by the findings of our metanalysis, which showed that no significant difference exists in CIN between the two strategies.

Next, our analysis shows a trend towards benefit in all-cause mortality when iCR is compared to culprit only (RR 0.63, 95% CI 0.40–1.00, p=0.05) which is not seen when sCR was compared to culprit only (RR 0.92, 95% CI 0.57–1.49, p=0.75). To date, no RCT has ever shown an all-cause mortality benefit with complete revascularization, possibly because no trials have previously been powered to detect this difference. The CR arm in the COMPLETE trial consisted only of sCR (acknowledged by the authors as a limitation of the trial)7 and its results were consistent with our meta-analysis as it failed to show a benefit in CV mortality or all-cause mortality.7

Lastly, complete revascularization during the index PCI has the potential to be more convenient for the patient, depending on their clinical condition, and might even potentially decrease healthcare costs. sCR is often done later during the index hospitalization, which increases the length of stay and potentially further increases healthcare costs.20 Alternatively, patients are discharged and electively readmitted for the sCR, which can be inconvenient for the patient. Furthermore, this can be challenging to coordinate if patients have poor socioeconomic backgrounds or low health literacy.21

Our meta-analysis updates the findings presented by Pasceri et al, which tried to ascertain the best timing of complete revascularization to achieve optimal outcomes.9 They used a composite outcome of death and MI and determined that complete revascularization during index PCI was associated with a significant benefit in the primary composite outcome.9 A recent meta-analysis by Bainey et al22 compared the outcomes of complete revascularization of STEMI patients compared with a culprit-only strategy, showing significant benefit in cardiovascular death (Odds Ratio [OR], 0.69 [95% CI, 0.48–0.99]; P = 0.05) and in the composite outcome of cardiovascular death and new MI (OR, 0.69 [95% CI, 0.55–0.87]; P = 0.001). However, this paper did not study the differences in outcomes between complete revascularization during primary PCI vs complete revascularization as a staged procedure.22

The difference in CV death and mortality might be due to the early occurrence of MACE events, many of which have been found to occur within the first two to three weeks after index revascularization.4 This period is often shorter than the average time to sCR after the index PCI seen in clinical practice. Another hypothesis is that the iCR can improve perfusion to hibernating myocardium and areas of watershed infarction sooner, leading to improved LV function and subsequently, improved clinical outcomes.23 Of note, a pilot study assessing the usefulness of the SYNTAX II (SII) score in patients presenting with a STEMI and cardiogenic shock showed that SII was superior to SYNTAX score by using a receiver-operator curve, with the 2 higher tertiles of SII having a worse in-hospital mortality that the lower tertile.24

Despite the findings above that suggest iCR is superior, we do identify one practical limitation in performing iCR: catheterization lab schedule. There might be scenarios where multiple emergent cases require the attention of the interventionalist and from a real-world, cath lab logistics perspective it is simply more feasible to perform sCR.

Limitations

Our meta-analysis has several limitations: the included studies had different inclusion and exclusion criteria, the majority of the patients enrolled into the studies were male, which might cause them to not represent the true effect of either strategy on female sex patients, and race, a strong predictor of severity of heart disease, with black women faring particularly worse and suffering more severe CAD than other sex and ethnic groups.25

Lastly, this meta-analysis included RCTs with hemodynamically stable patients only and these results cannot be extrapolated to STEMI patients presenting with cardiogenic shock, who do not benefit from a iCR strategy.26

Conclusion

Complete revascularization during index PCI of stable STEMI patients is associated with a statistically significant reduction in cardiovascular death and a non-significant trend towards a reduction in all-cause mortality compared to culprit-lesion-only revascularization, at 25.1±9.4 months follow-up. These benefits are not seen in staged complete revascularization. Both strategies are associated with a reduction in non-fatal reinfarctions and do not have a significant difference in CIN rates. A RCT comparing iCR to sCR with sufficient statistical power is needed to confirm our findings.