Choosing the right model for STEMI care in India – Focus should remain on providing timely fibrinolytic therapy, for now

Primary percutaneous coronary intervention (PCI) is the treatment of choice for the management of acute ST segment elevation myocardial infarction (STEMI), when it can be provided within 120 min of diagnosis1-3. The timely provision of primary PCI presents major logistical challenges. In countries like the United States, which has a large number of cardiac catheterization facilities, many patients with STEMI do not present to PCI-capable hospitals4. These patients are then transferred for primary PCI, but only about a fifth of them achieve the recommended transfer-in door-to-balloon time of ≤90 min5. Consequently, based on the evidence from recent randomized trials, guidelines recommend fibrinolytic therapy followed by elective PCI between 2 and 24 h (a pharmaco-invasive strategy), for patients who are unlikely to receive timely primary PCI2,3. In India, there are far fewer PCI-capable hospitals providing round-the-clock primary PCI facilities than in most developed countries, and the vast majority of patients with STEMI present to non-PCI-capable hospitals. As a result, only about 5-10 per cent of patients with STEMI, who are eligible for reperfusion, undergo primary PCI6. Even in the States with well-developed healthcare infrastructure, the proportion of patients undergoing primary PCI is less than 15 per cent6,7. It would therefore appear that a pharmaco-invasive strategy is ideally suited for a country like India. Some investigators have recently created hub-and-spoke networks to facilitate transfer of patients to PCI-capable hospitals with a view to improving the rates of primary and pharmaco-invasive PCI in the State of Tamil Nadu. Based on the limited observational data obtained from this experience8, there is a movement to scale up this model nationally. We believe that such a model will be costly to implement and is unlikely to yield the expected benefits to patients who suffer a STEMI in this country. Here, we draw on the pathobiology of acute coronary occlusion and on the available data on Indian patients presenting with STEMI, to demonstrate why a focus on improving primary and pharmaco-invasive PCI may be misguided. Myocardium dies rapidly after coronary occlusion Both experimental and clinical data suggest that the amount of salvageable, reversibly injured myocardium reduces exponentially following coronary occlusion. In anaesthetized dogs, nearly 40 per cent of myocardium became nonviable 40 min after occlusion, rapidly progressing to 57 per cent at three hours and 71 per cent at six hours9. This rapid loss of viability is also mirrored by a rapid fall in the relative benefits of fibrinolytic therapy with time to treatment10. In meta-analyses of the fibrinolytic therapy trials, the proportional mortality reduction with fibrinolysis was 26 per cent in patients treated within three hours, falling to 18 per cent for those treated between four and six hours, and just 14 per cent between seven and 12 h11. This is depicted in the Figure. The curves suggest that for reperfusion therapy to be effective, it has to be provided within 3-6 h (corresponding to the steep portion of the curve). Treatment beyond six hours (in the flat portion of the curve) yields far less benefit.Figure: Relationship between time from coronary occlusion and experimental and clinical measures of myocardial salvage. Figure depicts remaining salvageable myocardium (blue dots) with time following experimental coronary occlusion9 and relative mortality reduction with fibrinolytic therapy (red dots) in relation to time from symptom onset10 , 11. Figure recreated from published data9 - 11. STEMI, ST elevation myocardial infarction.Indian patients with STEMI present late In India, the time from symptom onset to presentation to a treating hospital is the main component of pre-hospital delay among patients with STEMI. Typically, patients present beyond 5-6 h after symptom onset and as late as 10-13 h (Table I)7,12-16. In a large registry from the State of Kerala, over 40 per cent of patients presented beyond six hours after symptom onset6. This may be due to several factors, including a failure to recognize the seriousness of symptoms, non-availability of ambulance services and onward referral without treatment at the point of first medical contact (FMC)7. Delays may also be due to the difficult terrain making transport times long. For example, the median time from symptom onset to presentation was 13 h in the Himachal Pradesh ACS Registry14. Therefore, on average, Indian patients with STEMI present in the flat portion of the myocardial salvage curve (Figure), where the effect of even the most efficient reperfusion modalities may be minimal. Further, between 35 and 65 per cent of patients present beyond 12 h and do not receive any reperfusion therapy. Consequently, the largest benefits are likely to accrue from policies and interventions which aim to reduce this pre-hospital delay.Table I: Time from symptom onset to presentation and fibrinolysis in Indian patients with STEMIPharmaco-invasive therapy is useful only in patients who present early The primary mechanism of benefit of elective angioplasty performed within 24 h after fibrinolysis is likely through the prevention of re-occlusion that occurs in about 10 per cent of patients after fibrinolytic therapy17. For example, in the Trial of Routine Angioplasty and Stenting after Fibrinolysis to Enhance Reperfusion in Acute Myocardial Infarction, the difference in the composite primary outcome was driven by the reduction in recurrent ischaemia or infarction in the patients who underwent elective angioplasty after fibrinolysis18. Parenthetically, for prevention of re-occlusion of the infarct-related artery to make a difference, sufficient myocardium must be salvaged by the preceding fibrinolytic therapy. A review of the trials of pharmaco-invasive therapy suggests that the time from symptom onset to presentation is typically less than two hours, with fibrinolysis being provided shortly thereafter (Table II)18-24. Therefore, the evidence for the benefit of pharmaco-invasive therapy comes exclusively from patients who present in the steep portion of the myocardial salvage curve (Figure). There is currently no evidence to indicate that patients who present beyond 2-3 h after symptom onset, particularly those who present in the flat portion of the myocardial salvage curve, will benefit from a pharmaco-invasive approach.Table II: Time from symptom onset to presentation and fibrinolysis in patients enrolled in the randomized trials of pharmaco-invasive therapy compared to fibrinolysisTowards evidence-based programmes and policy Treatment of STEMI presents a good example of a situation where evidence generated elsewhere cannot be extrapolated indiscriminately to the Indian context. There is a need to generate high-quality evidence locally to inform policy. Observational data have well-known limitations and must not be the sole basis for designing new programmes, particularly when, as in this case, major increases in healthcare spending are involved. The transfer of all patients to PCI-capable hospitals involves provisioning for new transport and catheterization laboratory infrastructure and workforce. Secondly, programme objectives should be chosen based on local needs and the best available evidence. Given that most patients across the country present late after symptom onset, and that a substantial number of them do not receive any fibrinolytic therapy, it is obvious that the most appropriate point of focus of any STEMI treatment programme should be on these two metrics. There is overwhelming evidence to suggest that this would yield the greatest improvement in patients’ outcome11. Having multiple additional objectives can have the unanticipated consequence of undermining the primary focus. For example, in the Tamil Nadu STEMI model (which was aimed at facilitating transport for primary PCI or pharmaco-invasive PCI), the proportion of patients receiving fibrinolytic therapy actually reduced (from 67 to 50%) after implementation of the programme, without increasing the overall rate of reperfusion8. These patients were presumably transferred for primary PCI, but it is unclear from the published data if this was performed in a timely manner. This may be a reflection of the ‘reperfusion paradox’ that has been observed in the context of choosing between primary PCI and fibrinolysis4. Armstrong and Boden4 noted that in a futile attempt to offer timely primary PCI, the opportunity for timely fibrinolysis was being foregone. Finally, India is a large country with major differences in healthcare infrastructure between the States (and even districts). Therefore, a one-size-fits-all model of STEMI care for the country would be misguided and wasteful. Based on the available evidence, we suggest that any model of STEMI care in India should have the principal objectives of improving the rates of fibrinolysis, and reducing the time from symptom onset to FMC, and treatment. These can be achieved by ensuring the performance of ECGs at the point of FMC, enable their prompt interpretation (by on-site or off-site personnel) and prompt initiation of bolus fibrinolytic therapy. This approach has resulted in a near doubling of the proportion of patients who received fibrinolytic therapy in the ICMR STEMI-ACT Programme in Shimla (36.7 to 60.2% one year after implementation; unpublished data from annual report submitted to the ICMR). Programmes can be selectively upgraded (at the district or State levels) to include transfer of patients for elective PCI after fibrinolysis, once timely fibrinolysis is routinely provided (time from symptom onset to treatment between 2 and 4 h). However, if investigators believe that a pharmaco-invasive strategy may be appropriate even at longer times to fibrinolysis, they should produce strong evidence in the form of pragmatic randomized trials. Such an approach offers the best way forward for improving STEMI care in India. Financial support & sponsorship: None. Conflicts of Interest: None.