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BMJ 2003;326:1379-1381 (21 June), doi:10.1136/bmj.326.7403.1379
Ever D Grech, consultant cardiologist, assistant professor
Health Sciences Centre and St Boniface Hospital, Winnipeg, Manitoba, Canada, University of Manitoba, Winnipeg
David R Ramsdale, consultant cardiologist
Cardiothoracic Centre, Liverpool
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Although thrombolysis is the commonest form of treatment for acute myocardial infarction, it has important limitations: a rate of recanalisation (restoring normal flow) in 90 minutes of only 55% with streptokinase or 60% with accelerated alteplase; a 5-15% risk of early or late reocclusion leading to acute myocardial infarction, worsening ventricular function, or death; a 1-2% risk of intracranial haemorrhage, with 40% mortality; and 15-20% of patients with a contraindication to thrombolysis.
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Primary angioplasty (also called direct angioplasty) mechanically disrupts the occlusive thrombus and compresses the underlying stenosis, rapidly restoring blood flow. It offers a superior alternative to thrombolysis in the immediate treatment of ST segment elevation myocardial infarction. This differs from sequential angioplasty, when angioplasty is performed after thrombolysis. After early trials of thrombolytic drugs, there was much interest in "adjunctive" angioplasty (angioplasty used as a supplement to successful thrombolysis) as this was expected to reduce recurrent ischaemia and re-infarction. Later studies, however, not only failed to show any advantage, but found higher rates of major haemorrhage and emergency bypass surgery. In contrast, "rescue" (also known as "salvage") angioplasty, which is performed if thrombolysis fails to restore patency after one to two hours, may confer benefit.
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The information provided by immediate coronary angiography is valuable in determining subsequent management. Patients with severe three vessel disease, severe left main coronary artery stenosis, or occluded vessels unsuitable for angioplasty can be referred for bypass surgery. Conversely, patients whose arteries are found to have spontaneously recanalised or who have an insignificant infarct related artery may be selected for medical treatment, and thus avoid unnecessary thrombolytic treatment.
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Disadvantages
The morbidity and mortality associated with primary angioplasty is operator
dependent, varying with the skill and experience of the interventionist, and
it should be considered only for patients presenting early (< 12 hours
after acute myocardial infarction).
Procedural complications are more common than with elective angioplasty for chronic angina, and, even though it is usual to deal only with the occluded vessel, procedures may be prolonged. Ventricular arrhythmias are not unusual on recanalisation, but these generally occur while the patient is still in the catheterisation laboratory and can be promptly treated by intravenous drugs or electrical cardioversion. Right coronary artery procedures are often associated with sinus arrest, atrioventricular block, idioventricular rhythm, and severe hypotension. Up to 5% of patients initially referred for primary angioplasty require urgent coronary artery bypass surgery, so surgical backup is essential if risks are to be minimised.
There are logistical hurdles in delivering a full 24 hour service. Primary angioplasty can be performed only when adequate facilities and experienced staff are available. The time from admission to recanalisation should be less than 60 minutes, which may not be possible if staff are on call from home. However, recent evidence suggests that, even with longer delays, primary angioplasty may still be superior to thrombolysis.
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A catheterisation laboratory requires large initial capital expenditure and has substantial running costs. However, in an existing, fully supported laboratory operating at high volume, primary angioplasty is at least as cost effective as thrombolysis.
Although stenting the lesion seemed an attractive answer, it was initially thought that deploying a stent in the presence of thrombus over a ruptured plaque would provoke further thrombosis. However, improvements in stent deployment and advances in adjunctive pharmacotherapy have led to greater technical success. Recent studies comparing primary stenting with balloon angioplasty alone have shown that stented patients have significantly less recurrent ischaemia, reinfarction, and subsequent need for further angioplasty. Economic analysis has shown that, as expected, the initial costs were higher but were offset by lower follow up costs after a year.
However, one study (Stent-PAMI) showed that stenting was associated with a small (but significant) decrease in normal coronary flow and a trend towards increased six and 12 month mortality. This led some to examine the use of adjunctive glycoprotein IIb/IIIa inhibitors as a solution.
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Stenting and glycoprotein IIb/IIIa inhibitors
The first study (CADILLAC) to examine the potential benefits of
glycoprotein IIb/IIIa inhibitors combined with stenting showed that abciximab
significantly reduced early recurrent ischaemia and reocclusion due to
thrombus formation. There was no additional effect on restenosis or late
outcomes compared with stenting alone. The slightly reduced rate of normal
coronary flow that had been seen in other studies was again confirmed, but did
not translate into a significant effect on mortality.
Another study (ADMIRAL) examined the potential benefit of abciximab when given before (rather than during) primary stenting. Both at 30 days' and six months' follow up, abciximab significantly reduced the composite rate of reinfarction, the need for further revascularisation, and mortality. In addition, abciximab significantly improved coronary flow rates immediately after stenting, which persisted up to six months with a significant improvement in residual left ventricular function.
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| Further reading Fibrinolytic Therapy Trialists' (FTT) Collaborative Group. Indications for fibrinolytic therapy in suspected acute myocardial infarction: collaborative overview of early mortality and major morbidity results from all randomised trials of more than 1000 patients. Lancet 1994;343: 311-22[CrossRef][ISI][Medline] Keeley EC, Boura JA, Grines CL. Primary angioplasty versus intravenous thrombolytic therapy for acute myocardial infarction: a quantitative review of 23 randomised trials. Lancet 2003;361: 13-20[CrossRef][ISI][Medline] De Boer MJ, Zijlstra F. Coronary angioplasty in acute myocardial infarction. In: Grech ED, Ramsdale DR, eds. Practical interventional cardiology. 2nd ed. London: Martin Dunitz, 2002: 189-206 Lieu TA, Gurley RJ, Lundstrom RJ, Ray GT, Fireman BH, Weinstein MC, et al. Projected cost-effectiveness of primary angioplasty for acute myocardial infarction. J Am Coll Cardiol 1997;30: 1741-50[Abstract]
Grines CL, Cox DA, Stone GW, Garcia E, Mattos LA,
Giambartolomei A, et al, for the Stent Primary Angioplasty in Myocardial
Infarction Study Group. Coronary angioplasty with or without stent
implantation for acute myocardial infarction. N Engl J
Med 1999;341:
1949-56
Montalescot G, Barragan P, Wittenberg O, Ecollan P, Elhadad
S, Villain P, et al. Platelet glycoprotein IIb/IIIa inhibition with coronary
stenting for acute myocardial infarction. N Engl J Med
2001;344:
1895-903
Stone GW, Grines CL, Cox DA, Garcia E, Tcheng JE, Griffin
JJ, et al. Comparison of angioplasty with stenting, with or without abciximab,
in acute myocardial infarction. N Engl J Med
2002;346:
957-66 |
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