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Editorial

Should Interventional Cardiologists Treat Ischemic Strokes? A Global Perspective

November 2002
Need for stroke interventionists. More than 750,000 strokes occur annually in the United States.1,2 Currently, stroke is the third leading cause of death (60.2 deaths per 100,000 population) and the leading cause of severe neurological disability in our nation. As the elderly segment of the population continues to grow, the stroke death rate has the potential to reach epidemic proportions. Historically, ischemic stroke has been a disease entity approached in terms of prevention and palliation. The phrase “brain attack” is being used more frequently as recent advances have reshaped the focus to an active role in terms of acute intervention. As with the coronary circulation, the duration of ischemia and degree of collateral circulation have the greatest influence on morbidity and mortality in stroke. Early intervention can potentially limit the devastation caused by a stroke, but is it possible for the several hundred neurointerventionists currently in practice to expeditiously evaluate, treat and care for this volume of patients? Clearly, it is impossible. Thus, the interventional treatment of stroke continues to suffer from, among other problems, the lack of sufficiently trained physicians to supply the necessary expeditious care that these patients require. The logical source. Ideally, dedicated neurointerventionists with extensive experience in all minimally invasive intracranial techniques would perform invasive therapies for acute stroke. Currently, there are at most several hundred trained neurointerventionists nationwide. To provide 24-hour coverage for all major medical centers, several thousand more physicians would need to be trained. The relatively small number of elective neurointerventional procedures performed annually could not support the number of specialists required to provide invasive therapy for and manage the care of patients with acute stroke. Thus, the mass training of neurointerventional specialists to provide the majority of invasive acute stroke interventions is not feasible. Fortunately, an infrastructure for the provision of emergent endovascular care already exists. By contrast to the relatively uncommon elective neurointerventional procedure, more than 1 million coronary angioplasty procedures are performed annually in the United States, supporting over 2,000 procedure rooms and nearly 8,000 interventional cardiologists.3 The incorporation of a “brain attack” program into an existing primary angioplasty program for myocardial infarction (MI) would require no additional personnel other than a stroke neurologist. Most contemporary cardiac catheterization laboratories are equipped with the digital subtraction and road-mapping capabilities necessary to perform intracranial work. Techniques employed in the intervention of acute stroke, such as clot removal and angioplasty with stent placement, are similar to those already familiar to the interventional cardiologist, thus minimizing the time required to learn a new skill set. For example, more than 60% of cardiac catheterization laboratories have physicians who perform angioplasty, and most of these laboratories provide emergent angioplasty for acute MI.3 Additionally, interventional cardiologists have gained much insight into the utility and practicality of thrombolytic and anticoagulant therapies. As recent studies have confirmed the safe and effective implementation of primary angioplasty in centers without surgical backup, the proportion of interventional cardiologists will continue to rise.4,5 In addition to the aforementioned reasons supporting the training of cardiologists for acute stroke intervention, it should be remembered that a majority of strokes are the result of cardiac or aortic disease. Cardiologists are often involved in the treatment of patients at risk for stroke and are in an ideal position to provide this care.6,7 Coronary artery disease is a leading cause of death in patients who experience transient ischemic attacks (TIA) or stroke. Fifty consecutive patients with TIA or stroke were studied to determine the prevalence of coronary artery disease, and 29 of these patients had significant coronary artery disease.8 These patients typically are followed by cardiologists for their predisposing heart disease. In one study of 300 consecutive patients with acute focal brain ischemia who underwent a clinical examination by a cardiologist in conjunction with routine electrocardiography, Holter-electrocardiography, and echocardiography, a total of 188 patients had a potential cardiac source of embolism.9 In addition to the coexistent medical conditions that increase the risk for stroke, there is an inherent risk in performing coronary angiography. The stroke rate associated with the performance of 20,924 cardiac catheterizations for interventional procedures was 0.12%.10 The rate of acute neurological complications resulting from cardiac catheterization procedures (n = 3,648) in children was 0.38%.11 This rate is likely attributable to congenital anomalies of the heart and great vessels, with which pediatric interventional cardiologists are intimately familiar. In our opinion, optimal care is to institute interventional stroke treatment as soon as possible, necessitating that cardiologists begin treatment. Evidence for intraarterial therapy. Favorable results of the National Institute of Neurological Disorders and Stroke (NINDS) study12 demonstrating the benefits of intravenous recombinant tissue plasminogen activator (t-PA, alteplase) in patients who present within 3 hours of the onset of acute ischemic stroke led to approval of this agent by the Food and Drug Administration (FDA) in 1996. However, the results of the European Cooperative Acute Stroke Studies (ECASS)13,14 and the Standard Treatment with Alteplase to Reverse Stroke (STARS) trial15 indicated that intravenous therapy was not recommended for use in an unselected population of acute ischemic stroke patients in that both reported rates of major morbidity and death higher than 50% after intravenous therapy (Table 1). The unsatisfactory results of current intravenous therapy have spawned several studies examining the effectiveness of intraarterial therapy.16,17 In the Prolyse in Acute Cerebral Thromboembolism (PROACT) I trial,16 patients with acute ischemic stroke resulting from MCA occlusion and onset of symptoms within 6 hours were treated with intraarterial infusions of recombinant pro-urokinase (r-pro UK). Recanalization rates (TIMI grade 2 or 3) were 58% in the r-pro UK group, which were, remarkably, more than four times those in the placebo group. PROACT I determined the safety of intraarterial pro-urokinase and led to the conduct of PROACT II17 to determine the effectiveness of this therapy. In the second trial, the recanalization rates (TIMI grade 2 or 3) were 66% in the r-pro UK group and 18% in the placebo group. A 15% absolute increase in favorable outcome, as defined by modified Rankin score, was greater in the treatment arm than in the placebo arm. The advantages of the intraarterial approach for thrombolysis are clear. First, angiography localizes the vascular territory of the lesion and determines whether there is persistent occlusion or autogenous recanalization (Figure 1). Second, direct transcatheter delivery of the thrombolytic agent (i.e., t-PA or reteplase) to the occlusion is accomplished without systemic administration (a lesser amount of the drug can actually be used) (Figure 2). Visual appreciation of clot dissolution or recalcitrance provides clinicians with the information necessary to determine if adjuvant mechanical means are necessary to recanalize the vessel (Figures 3–5). Currently, significant disadvantages to the intraarterial approach are the paucity of physicians capable of performing the procedure and the increased risk of direct vascular injury and/or intracranial hemorrhage. Recognition of the symptoms as indicative of a stroke and rapid triage of the patient to a center where he or she can receive treatment continue to be of primary concern. In addition to the intraarterial studies conducted, several studies have examined the effectiveness of a combination of intravenous and intraarterial thrombolysis in patients with acute ischemic stroke.18–22 The results are summarized in Table 2. The notion that large vessel occlusions (e.g., those of the intracranial ICA or the M1 segment of the middle cerebral artery) respond poorly to intravenous therapy, coupled with the knowledge that intravenous therapy can be initiated faster than intraarterial therapy, helped lay the foundation for the combination intraarterial-intravenous approach. On the basis of promising results derived from several small pilot studies, the NINDS funded a Phase II pilot study, the Interventional Management of Stroke (IMS) trial.23 The safety and efficacy of initiating a combination of intravenous and intraarterial t-PA therapies within 3 hours of symptom onset in 80 ischemic stroke patients with an NIHSS score > 10 was examined. Dosing regimens involved 0.6 mg/kg of intravenously administered t-PA over 30 minutes (15% as a bolus) followed by intraarterially administered t-PA at a dose of up to 22 mg over the course of 2 hours if thrombus was identified by a cerebral angiogram. Recanalization rates of 40% were observed with a 16% rate of mortality. Mechanical disruption of clot in combination with intraarterial thrombolysis has great potential benefit for the treatment of acute ischemic stroke, just as it has for the treatment of acute MI. In a study by Qureshi et al. in which combination therapy was used for the treatment of 19 patients with acute ischemic stroke, complete or near-complete recanalization was seen in 16 patients (84%), twelve had neurological improvement and 3 had intracranial hemorrhages.24 Future directions. Educational, political and economic obstacles exist to the incorporation of interventional cardiologists into invasive acute stroke programs. First, training programs must be created to transfer the appropriate skills to interventional cardiologists for safe and effective acute stroke therapy. These skills could be acquired during additional fellowship training or an apprenticeship, at which time interventional cardiologists would work with stroke neurologists and stroke interventionists. Second, political obstructions to the involvement of interventional cardiology by other specialties must be lifted. Even where neurointerventional specialists practice, few institutions will ever have enough trained personnel to adequately provide for uninterrupted stroke-call coverage. Neurointerventionists will need to be receptive to this concept. Without their leadership, the large-scale implementation of invasive therapy for acute stroke will be difficult to realize. Third, a national effort to make the public aware of the signs of acute stroke and the importance of early presentation must be reemphasized. Recent studies have shown that transfer from a community hospital to a major medical center for primary angioplasty is effective therapy for acute MI.25 The same may be true for acute cerebral infarction. Expeditious transfer to faculties capable of providing intraarterial therapy would dramatically broaden the applicability of this therapy to the general population. Implementation of pharmacologic or other therapies for neuroprotection may extend the therapeutic window of opportunity. Finally, reimbursement for such therapy must be commensurate with the substantial expense of implementing such a program. The potential benefits are significant and such therapy may prove to be cost effective as the health care expenditure for stroke is exorbitant. Significant cost savings will be gained by stroke prevention and treatment as opposed to stroke care and rehabilitation. From an educational standpoint, cardiologists must master a significant amount of anatomy and neurology if they are to be involved in the treatment of acute stroke. The ability to perform a rapid neurologic examination that localizes and defines the stroke as focal, global, bulbar, capsular, thalamic or cortical is crucial in choosing an appropriate treatment plan. Understanding symptom progression and whether it is caused by edema, hypoperfusion or infarct extension must also be a priority of the training program. Although the skill set is basically the same as with cardiac catheterization, cerebral vessels are more tortuous and delicate than those in the coronary circulation and have a lower threshold for manipulation. However, these limits would be easily learned by the interventional cardiologist. Structured training programs that focus on the early intervention of stroke could readily provide the cardiologist with the necessary neurological and anatomical knowledge to effectively treat stroke. Such programs, organized and maintained in a cooperative effort by neurointerventionists and cardiologists, would bridge the gap that we will undoubtedly face in the near future. “The interplay of cardiac and neurologic concerns demonstrates how a collaboration of neurologists and cardiologists can yield rewarding results in resolving some of the more difficult problems in clinical medicine.”26 Acknowledgment. We thank Paul H. Dressel for preparation of the illustrations and the staff at Kaleida Gates Hospital Library for assistance with literature searches and reference articles.
1. www.cdc.gov/nchs/fastats/stroke.htm. In: National Center for Health Statistics: 2000. 2. www.stroke.org/pages/brain_cost.cfm. In: National Stroke Association: 2002. 3. Sheldon WC. Trends in cardiac catheterization laboratories in the United States. Cathet Cardiovasc Intervent 2001;53:40–45. 4. Aversano T, Aversano LT, Passamani E, et al. Thrombolytic therapy vs. primary percutaneous coronary intervention for myocardial infarction in patients presenting to hospitals without on-site cardiac surgery: A randomized controlled trial. JAMA 2002;287:1943–1951. 5. Singh M, Ting HH, Berger PB, et al. Rationale for on-site cardiac surgery for primary angioplasty: A time for reappraisal. J Am Coll Cardiol 2002;39:1881–1889. 6. Weinberger J. Prevention of ischemic stroke. Curr Treat Options Cardiovasc Med 2002;4:393–403. 7. Weinberger J. Prevention of ischemic stroke. Curr Cardiol Rep 2002;4:164–171. 8. Rokey R, Rolak LA, Harati Y, et al. Coronary artery disease in patients with cerebrovascular disease: A prospective study. Ann Neurol 1984;16:50–53. 9. Hornig CR, Haberbosch W, Lammers C, et al. Specific cardiological evaluation after focal cerebral ischemia. Acta Neurol Scand 1996;93:297–302. 10. Plehn JF, Davis BR, Sacks FM, et al. Reduction of stroke evidence after myocardial infarction with pravastatin: The Cholesterol and Recurrent Events (CARE) study. The CARE Investigators. Circulation 1999;99:216–223. 11. Liu XY, Wong V, Leung M. Neurologic complications due to catheterization. Pediatr Neurol 2001;24:270–275. 12. The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group. Tissue plasminogen activator for acute ischemic stroke. N Engl J Med 1995;333:1581–1587. 13. Hacke W, Kaste M, Fieschi C, et al. Intravenous thrombolysis with recombinant tissue plasminogen activator for acute hemispheric stroke. The European Cooperative Acute Stroke Study (ECASS). JAMA 1995;274:1017–1025. 14. Hacke W, Kaste M, Fieschl C, et al. Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Second European-Australasian Acute Stroke Study Investigators. Lancet 1998;352:1245–1251. 15. Albers GW, Bates VE, Clark WM, et al. Intravenous tissue-type plasminogen activator for treatment of acute stroke: The Standard Treatment with Alteplase to Reverse Stroke (STARS) study. JAMA 2000;283:1145–1150. 16. del Zoppo GJ, Higashida RT, Furlan AJ, et al. PROACT: A phase II randomized trial of recombinant pro-urokinase by direct arterial delivery in acute middle cerebral artery stroke. PROACT Investigators. Prolyse in Acute Cerebral Thromboembolism. Stroke 1998;29:4–11. 17. Furlan A, Higashida R, Wechsler L, et al. Intraarterial pro-urokinase for acute ischemic stroke. The PROACT II study: A randomized controlled trial. Prolyse in Acute Cerebral Thromboembolism. JAMA 1999;282:2003–2011. 18. Ernst R, Pancioli A, Tomsick T, et al. Combined intravenous and intra-arterial recombinant tissue plasminogen activator in acute ischemic stroke. Stroke 2000;31:2552–2557. 19. Hill MD, Barber PA, Demchuk AM, et al. Acute intravenous-intra-arterial revascularization therapy for severe ischemic stroke. Stroke 2002;33:279–282. 20. Keris V, Rudnicka S, Vorona V, et al. Combined intraarterial/intravenous thrombolysis for acute ischemic stroke. Am J Neuroradiol 2001;22:352–358. 21. Lewandowski CA, Frankel M, Tomsick TA, et al. Combined intravenous and intra-arterial r-TPA versus intra-arterial therapy for acute ischemic stroke: Emergency Management of Stroke (EMS) Bridging Trial. Stroke 1999;30:2598–2605. 22. Suarez JI, Zaidat OO, Sunshine JL, et al. Endovascular administration after intravenous infusion of thrombolytic agents for the treatment of patients with acute ischemic strokes. Neurosurgery 2002;50:251–260. 23. Broderick J. The Interventional Management of Stroke (IMS) Study: Preliminary results. In: The 7th International Symposium on Thrombolysis and Acute Stroke Therapy. Lyon, France: 2002. 24. Qureshi AI, Siddiqui AM, Suri MFK, et al. Aggressive mechanical clot disruption and low-dose intra-arterial third-generation thrombolytic agent for ischemic stroke. A prospective study. Neurosurgery (in press). 25. Grines CL, Westerhausen DR Jr., Grines LL, et al. A randomized trial of transfer for primary angioplasty versus on-site thrombolysis in patients with high-risk myocardial infarction: The Air Primary Angioplasty in Myocardial Infarction study. J Am Coll Cardiol 2002;39:1713–1719. 26. Kantor HL, Krishnan SC. Cardiac problems in patients with neurologic disease. Cardiol Clin 1995;13:179–208.

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