Objective We hypothesised that, compared with culprit-only primary percutaneous coronary intervention (PCI), additional preventive PCI in selected patients with ST-elevation myocardial infarction with multivessel disease would not be associated with iatrogenic myocardial infarction, and would be associated with reductions in left ventricular (LV) volumes in the longer term.
Methods In the preventive angioplasty in myocardial infarction trial (PRAMI; ISRCTN73028481), cardiac magnetic resonance (CMR) was prespecified in two centres and performed (median, IQR) 3 (1, 5) and 209 (189, 957) days after primary PCI.
Results From 219 enrolled patients in two sites, 84% underwent CMR. 42 (50%) were randomised to culprit-artery-only PCI and 42 (50%) were randomised to preventive PCI. Follow-up CMR scans were available in 72 (86%) patients. There were two (4.8%) cases of procedure-related myocardial infarction in the preventive PCI group. The culprit-artery-only group had a higher proportion of anterior myocardial infarctions (MIs) (55% vs 24%). Infarct sizes (% LV mass) at baseline and follow-up were similar. At follow-up, there was no difference in LV ejection fraction (%, median (IQR), (culprit-artery-only PCI vs preventive PCI) 51.7 (42.9, 60.2) vs 54.4 (49.3, 62.8), p=0.23), LV end-diastolic volume (mL/m2, 69.3 (59.4, 79.9) vs 66.1 (54.7, 73.7), p=0.48) and LV end-systolic volume (mL/m2, 31.8 (24.4, 43.0) vs 30.7 (23.0, 36.3), p=0.20). Non-culprit angiographic lesions had low-risk Syntax scores and 47% had non-complex characteristics.
Conclusions Compared with culprit-only PCI, non-infarct-artery MI in the preventive PCI strategy was uncommon and LV volumes and ejection fraction were similar.
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Patients with acute ST-elevation myocardial infarction (STEMI) and multivessel coronary artery disease have an increased risk of adverse outcomes,1 ,2 however, the optimal management of non-culprit lesions is controversial. Following primary percutaneous coronary intervention (PCI), additional PCI of non-culprit-artery lesions might prevent recurrent ischaemia and adverse cardiac events.1 ,2 On the other hand, it may cause complications, including iatrogenic myocardial infarction secondary to the PCI procedure through coronary microembolisation leading to a larger overall infarct burden.3 ,4 Evidence of harm associated with non-culprit-artery PCI in large registries5 ,6 and systematic reviews7 underpins the caution in current guideline recommendations regarding routine PCI of non-culprit-artery lesions during primary PCI.8–10
In the randomised trial of preventive angioplasty in myocardial infarction (PRAMI; ISRCTN7302848111), immediate preventive PCI of angiographically significant non-culprit-artery stenoses in 465 patients with STEMI and multivessel disease reduced the incidence of the composite primary outcome (cardiac death, non-fatal myocardial infarction (MI), refractory angina) by 14% at 2 years.
Similar results have recently been reported in the complete versus culprit lesion-only PRimary PCI trial (CvLPRIT) (ISRCTN70913605) trial,12 but in the DANAMI-3-PRIMULTI trial the benefit of complete revascularisation was driven by significantly fewer repeat revascularisations, because all-cause mortality and non-fatal reinfarction did not differ between groups.13 Taken together, the relative risk reduction of the primary composite outcome in these three trials ranges from 45% to 65%.11–13 On the other hand, these trials were not powered to assess cardiac mortality and the performance and timing of non-culprit vessel PCI after primary PCI remains an open and controversial question. In 203 patients in the culprit cardiac magnetic resonance (CMR) substudy there was a statistically significant increase in non-infarct-related artery MI in the complete revascularisation group but total infarct size was not significantly different compared with an infarct related artery (IRA) only strategy.14 Specifically, questions still remain about the risk of iatrogenic MI secondary to the additional PCI procedures increasing infarct size overall, and the associations between non-culprit PCI and left ventricular (LV) ejection fraction and volumes in the longer term.
We hypothesised that, compared with culprit-only primary PCI, additional preventive PCI in selected STEMI patients with multivessel disease would (1) not be associated with iatrogenic myocardial infarction secondary to the preventive PCI procedures and (2) would have a similar infarct size. CMR is the reference diagnostic imaging method for the assessment of infarct size15 and LV volumes.16 In a prespecified CMR substudy, we prospectively assessed infarct size and LV volumes. CMR has potential to be clinically useful for the assessment of procedure-related MI, which cannot otherwise be reliably detected using a troponin elevation or the electrocardiogram in the setting of acute STEMI.
The PRAMI CMR substudy took place in the Golden Jubilee National Hospital, Clydebank and the Freeman Hospital, Newcastle. Both of these hospitals are regional cardiac centres. Acute STEMI management follows contemporary guidelines. Aspiration thrombectomy, direct stenting, antithrombotic drugs and other therapies were administered according to clinical judgement and in line with the guidelines.8–10 Further details are available in the online supplement.
CMR scans were performed during the index hospitalisation within (median, IQR) 3 (1, 5) days post-randomisation and repeated 209 (189, 957) days after primary PCI.
CMR image acquisition
Information about MRI acquisition is provided in the online supplement.
CMR image analysis
Image analysis was performed using a core laboratory with dedicated CMR software (Siemens Syngo VE32D and Argus, Erlangen, Germany). CMR data were anonymised and then analysed in a random order by a CMR-trained cardiologist (KM) who was blinded to the treatment group assignment and all other clinical and health outcome data. Image quality was assessed using Likert scale quality scores.
Infarct definition and size
The myocardial mass of late gadolinium was quantified using computer-assisted planimetry as a hyperintense region over five SDs the signal intensity of remote (see online supplement).
Adverse remodelling was defined as an increase in LV end-diastolic volume and end-systolic volume ≥20% on the follow-up CMR scan versus baseline early post-MI.
Non-infarct-related artery infarcts
Areas of non-infarct-artery late gadolinium enhancement were additionally classified as likely to be acute or chronic based on the presence of myocardial wall thickness (reduced (thinned) versus increased (thick/swollen) and oedema (yes/no) on T2-weighted sequences. This was done by two observers (KM and CB). T2-weighted CMR was not used to assess the area-at-risk as two sequences: a bright-blood T2-weighted ACUT2E method (acquisition for cardiac unified T2 oedema)17 and a T2 mapping method using an investigational prototype were used during the length of this study.
Quantitative coronary analysis
The coronary angiograms underwent quantitative coronary analysis (QCA) of culprit and non-culprit lesions. The analyses were performed by an interventional cardiologist (BWH) who was blinded to the CMR and who had not been involved in any other aspect of the study. The QCA analyses were performed on a Centricity CA 1000 Cardiac Review 1.0 workstation (GE Healthcare, Buckinghamshire, UK).
The primary outcome was the change in LV end-systolic volume index (mL/m2) revealed by CMR at follow-up versus baseline. A prioritised secondary outcome was the occurrence of myocardial infarction in the territory of a non-culprit lesion treated by preventive PCI (ie, iatrogenic myocardial infarction) (see online supplementary material methods).
Sample size calculation
For a between-group treatment difference of 3.0 mL/m2 for the within-subject change in LV end-systolic volume index at follow-up versus baseline and an SD of 4.5 mL/m2 then 37 subjects with evaluable data would be required in each group to refute the null hypothesis of no difference with 80% power and a two-sided test of significance level (α=0.05).
Categorical variables were expressed as number and percentage of patients. Categorical variables were analysed using a χ2 test, or a Fisher's exact test if any of the expected cell sizes were <5. Most continuous variables had a skewed distribution and are therefore presented as median and IQR, and analysed using Mann-Whitney statistical tests. Statistical analysis was not carried out on baseline characteristics as per the CONSORT statement recommendation.18
We also carried out a multivariate regression analysis model, adjusting log-corrected total infarct size between groups for MI location (anterior vs non-anterior), time to reperfusion, age of participants at presentation, thrombolysis in myocardial infarction (TIMI) score (pre-PCI), Rentrop score (pre-PCI) and diabetes mellitus status.
Of 465 subjects enrolled in six sites in the PRAMI trial, 219 (47%) were enrolled in two hospitals in Glasgow and Newcastle. Of these, 84 (38%) participants (mean age 60.4 SD 11.1 years, 77% male) (table 1) underwent CMR at baseline during the first week post-MI. Figure 1 illustrates the flow diagram of the randomised participants, including the reasons for not undergoing CMR.
The participants were evenly distributed between the randomised groups (n=42 (50%) culprit-artery-only PCI; n=42 (50%) preventive PCI). The time from symptom onset to PCI was longer in the culprit-only group (average time 330±332 min) than in the preventive PCI group (273±248 min) but this difference was not statistically significant (p=0.38). Their clinical characteristics are described in table 1.
The Syntax scores of the randomised participants were consistent with non-complex coronary disease (table 2). The Syntax and APPROACH scores and the American Heart Association classification of lesion complexity were similar in both groups.
Preventive PCI reduced the angiographic burden of disease and extent of myocardial jeopardy, as revealed by the post-PCI Syntax and APPROACH scores, respectively (table 2).
At baseline, 80 (95%) of the cine imaging, and 73 (87%) of late gadolinium enhancement (LGE) imaging were of high quality. At follow-up, 68 (94%) of the cine imaging, and 68 (94%) of the LGE imaging were of high quality. At baseline 2 (2%) of the T2 weighted imaging and LGE were missing (see online supplementary table S1).
LV ejection fraction and volumes, and remodelling were similar in each of the randomised groups at baseline and follow-up (table 3; see online supplementary table S2). The timing of CMR was similar between the groups (table 3; see online supplement).
The primary outcome (cardiac death, non-fatal MI and refractory angina) had occurred in four participants assigned to preventive PCI and in seven participants assigned to culprit-artery-only PCI (table 4).
Infarct size and distribution revealed by late gadolinium enhancement imaging were similar in each of the randomised groups at baseline and at follow-up (table 3). Two patients did not have late gadolinium enhancement acquisitions. One of the patients randomised to culprit-artery-only PCI had an eGFR <30 mL/min/1.73 m2 and thus IV gadolinium contrast agent was not administered. One of the patients randomised to preventive PCI could not tolerate the CMR scan, so scanning was terminated after acquisition of the cine sequences.
On multivariate regression analysis, there was still no significant difference in infarct size between patients randomised to preventive PCI and culprit-artery-only PCI (p=0.74). Using the same model approach but with log-transformed infarct-artery infarct size instead of total infarct size, this model yielded a between-group p value of 0.95.
On the baseline CMR scans, four patients randomised to preventive PCI had evidence of late gadolinium enhancement in the territory of a non-culprit-artery treated by PCI (table 3; figure 2). In two of these cases, this abnormality was associated with myocardial wall thinning on cine acquisitions and thus these infarcts were considered chronic. The two patients randomised to culprit-artery-only PCI who had evidence of remote zone scar did not have oedema on T2-weighted imaging, and on cine acquisitions had the myocardium was thinned. These abnormalities were considered to be chronic infarction.
The main findings in the PRAMI CMR substudy were that, in line with our first hypothesis, the incidence of iatrogenic myocardial infarction in the preventive PCI group was uncommon (4.8%), and appears to be lower than the incidence of non-infarct-artery MI (17%) in the population of patients who underwent CMR in the CvLPRIT trial.14 Infarct size was similar between groups within the first week after randomisation, even after adjustment for confounders. Second, LV volumes and ejection fraction were similar acutely and in the longer term, suggesting that differences in LV remodelling are unlikely to explain the benefits of preventive PCI observed in the PRAMI trial.
Strengths and limitations of the current study and results
The strengths of our study include the use of multimodality CMR to assess infarct characteristics, including non-infarct-artery MI and LV remodelling.19 Second, the CMR substudy participants represented one-third of the PRAMI trial population in the participating centres, and their clinical characteristics were broadly similar to those of the overall trial population.11 As in the main trial, by chance, anterior myocardial infarction was more common in the infarct-artery-only PCI group. On the other hand, the APPROACH Lesion Score for myocardial jeopardy, and coronary plaque characteristics, were similar between the groups. The comparatively long duration of follow-up was intended to align with that of the overall trial and thus reflect longer-term changes in infarct size and LV remodelling. We also assessed clinical characteristics associated with PCI-related complications20–22 (table 1).
The main limitation of our study is the sample size. The study is underpowered to detect between-group differences in LV end-systolic volume (<3.0 mL/m2), LV ejection fraction and infarct size. We used oedema imaging qualitatively to identify areas of acute injury, however, we did not quantify the area-at-risk and myocardial salvage index, as two different T2-weighted sequences were used during the course of the study (see online supplement). CMR information on deceased patients was lacking.
Insights into the potential benefit of preventive PCI
The LV volumes and ejection fraction in the surviving patients who completed CMR follow-up were similar in each of the groups. While a type 2 error is not discounted, these CMR results support the possibility that the benefit of the immediate preventive PCI strategy in PRAMI may be mediated by prevention of recurrent spontaneous cardiac events by immediate PCI, in line with the main results of PRAMI11 and CvLPRIT.12 Our results are uniformly consistent with those observed in the larger CvLPRIT CMR substudy14 that involved 205 randomised participants. In that study, as in our own, there were no between-group difference in LV volumes and ejection fraction or infarct size, on baseline and follow-up CMR.23 ,24 Missing CMR data from deceased patients are a relevant gap since one mechanism of benefit of preventive PCI may be prevention of fatal MI and cardiac death.
Importance of the timing of enrolment and randomisation: before versus after culprit-artery PCI and relevance to clinical practice
Based on our angiographic analysis, the non-culprit lesions had low-risk Syntax scores and 47% had non-complex characteristics (table 2), implying selection of lower risk lesions for immediate preventive PCI. In PRAMI, participant eligibility was based on the presence of non-culprit lesions that were deemed by the cardiologist to be amenable to PCI and therefore enrolment after successful culprit-artery PCI was at operator discretion. In other words, preventive PCI was performed in patients in whom the operator believed additional immediate PCI would be feasible, safe and successful. The 4.8% incidence of iatrogenic MI in the preventive PCI group in our PRAMI CMR study was lower than in other reports23 ,24 (eg, 12% incidence of iatrogenic MI in the CvLPRIT CMR substudy). Importantly, the study design of the PRAMI11 and CvLPRIT12 trials differed. Based on our CMR findings, PRAMI has a low incidence of procedure-related MI, unlike in CvLPRIT. This difference may be explained by randomisation before culprit-artery PCI in CvLPRIT and so operators being required by protocol to revascularise lesions that they might otherwise not have treated on technical grounds (be the procedure acute or staged within the index admission), implying higher risk procedures that inevitably would be associated with a higher risk of complications and procedure-related MI. By contrast in PRAMI, the protocol invoked the trial intervention after successful culprit-artery PCI and only in patients who had an artery amenable to PCI (and that was appropriately interpreted to be ‘at that time’). So in PRAMI, there was flexibility to treat lesions (or not) whereas in CvLPRIT, the operator did not have that choice. This is further reflected in the lower incidence of microvascular obstruction in our study group (21%) when compared with other imaging studies in STEMI.14 ,25 ,26 This would suggest that the patient group was lower risk, with an associated lower event rate. The comparatively low incidence of microvascular obstruction in our study population may be one contributing factor for the incidence of adverse health outcomes, since microvascular obstruction is a complication post-STEMI that portends an adverse prognosis.27 ,28
From the perspective of clinical translation to every day practice, this difference lends support for clinicians to focus on non-infarct-related artery lesions that are amenable to preventive PCI and with the decision taking place in the cardiac catheter laboratory immediately after successful culprit-artery PCI. On the other hand, patients with higher risk clinical characteristics or more complex non-infarct-artery disease could be deferred for staged inpatient revascularisation. We think this strategy more closely represents how preventive PCI might be adopted by clinicians in real-life clinical practice.
Clinical relevance of the CMR findings: contemporary guidelines and current trials
The guidelines of the European Society of Cardiology on myocardial revascularisation state that ‘Immediate revascularization of significant non-culprit lesions during the same procedure as primary PCI of the culprit vessel may be considered in selected patients’ (IIb recommendation, Level of Evidence: B).8 The North American guidelines now have a similar IIb recommendation.10
There are two other clinical trials comparing culprit-only PCI to complete revascularisation in patients with STEMI and multi-vessel disease (MVD). The complete versus culprit-only revascularisation to treat multivessel disease after primary PCI for STEMI (COMPLETE; NCT01740479; estimated sample size 3900 patients)29 is designed to assess whether a strategy of complete revascularisation involving staged PCI of all suitable non-infarct-related artery lesions is superior to a strategy of culprit lesion-only revascularisation in reducing the composite outcome of cardiovascular death or MI in patients with MVD who have undergone successful culprit lesion primary PCI for STEMI. The comparison between fractional flow reserve (FFR)-guided revascularisation versus conventional strategy in ACUTE STEMI patients with MVD (COMPARE-ACUTE; NCT01399736; estimated sample size 885)30 has broadly similar objectives as COMPLETE, but is a smaller in scale. These trials should provide meaningful evidence to inform clinicians and practice guidelines on the optimal management of STEMI patients with MVD.
The PRAMI CMR substudy involved a limited proportion of the total number of participants in the main trial PRAMI trial, reflecting the fact that two of the six centres participated in the CMR study. Further studies are warranted. The distributions of some of the characteristics of participants in the substudy, for example, anterior infarct location, departs from those of the main trial population. The number of clinical events in the substudy is lower than in the main trial. Because of changes in the availability of oedema imaging methods, two T2-weighted CMR methods were used during the lifetime of the project, making quantitative assessment of area-at-risk and myocardial salvage not feasible. Two of the patients did not have late gadolinium CMR imaging (one in the culprit-only PCI group and one in the preventive PCI group). Measurement of cardiac biomarkers (eg, serial troponin testing) was not part of the PRAMI trial protocol. There was heterogeneity in the duration of follow-up due to logistical reasons.
We have performed an exploratory CMR substudy in the PRAMI participants. We conclude that the benefit from a preventive PCI strategy was unrelated to infarct size or LV remodelling, although the strength of this conclusion is tempered by the fact that study was underpowered to detect differences in these parameters. Further studies are required.
What is already known on this subject?
Percutaneous coronary intervention (PCI) in patients with acute ST-elevation myocardial infarction (STEMI) and multivessel coronary disease is associated with improved clinical outcomes. However, doubt remains about the benefit of preventative PCI of other coronary arteries in addition to culprit vessel revascularisation.
What might this study add?
In this preventive angioplasty in myocardial infarction (PRAMI) cardiac magnetic resonance substudy, compared with culprit-only percutaneous coronary intervention (PCI), immediate preventive PCI of additional vessels was associated with a low incidence of iatrogenic myocardial infarction (n, % (culprit-artery-only PCI vs preventive PCI), 0 (0) vs 2 (5), p=0.15) with no difference at follow-up in left ventricular (LV) ejection fraction or LV volumes.
How might this impact on clinical practice?
A routine strategy of immediate preventive percutaneous coronary intervention is a reasonable approach in selected patients with acute ST-elevation myocardial infarction and multivessel coronary disease.
We thank the staff and patients who participated in this study. We thank the National Health Service for supporting the costs of the CMR scans. We thank Dr Christie McComb for letting us use her image quality assessment system. We also thank Dr Craig Buckley, Mr Peter Weale and Mr Patrick Revell, Siemens Healthcare, Frimley, UK, who provided technical support. We thank the R&D Department of the Golden Jubilee National Hospital for supporting this study.
Contributors CB and KGO made substantial contributions to conception and design. DC, ARP, MM, RD, RW, RJE, MCP, MMcE, HE, KGO and CB made substantial contributions to acquisition of data. KM, BWH, JMcC, KGO and CB made substantial contributions to the analysis and interpretation of data. KM, KGO and CB drafted the article. All authors were involved in revising it critically for important intellectual content. All authors gave final approval of the version to be submitted and any revised version. CB is responsible for the overall content as guarantor.
Funding CB was supported by the Scottish Funding Council. KM is supported by a Fellowship from the British Heart Foundation (FS/15/54/31639). BWH was supported by British Heart Foundation Project Grant PG/14/97/31263. National Health Service (Scotland) supported the costs of the CMR scans.
Competing interests CB holds a research agreement with Siemens Healthcare through the University of Glasgow. Relationships with industry: The University of Glasgow holds a research agreement with Siemens Healthcare
Ethics approval UK National Research Ethics Service.
Provenance and peer review Not commissioned; externally peer reviewed.
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