Mechanical Intervention for Ischemic Stroke
Mechanical Intervention for Ischemic Stroke
Proof in 1995 that tissue plasminogen activator (tPA) substantially improves the neurological outcome of stroke patients heralded a new era in stroke research.1 The discovery changed the face of clinical neuroscience in several ways. First, it showed that stroke, the third highest cause of death in the US, was a treatable condition.With the simple administration of an intravenous drug, patients who would otherwise have only supportive medical care could actually enjoy improved outcomes.
Second, by bringing a new optimism to physicians and scientists, this discovery has attracted numerous clinical scientists to the field of stroke.Third, the use of intravenous tPA led to the creation of primary stroke centers in the US.2 This center designation allows a community to triage pre-hospital patients directly to centers that treat stroke with tPA and away from hospitals that lack these resources. The era of intravenous tPA alone, however, is in transition as newer interventional therapies are becoming conventional.With the US Food and Drug Administration (FDA) clearance in 2004 of the first medical device to mechanically open large intracranial arteries by endovascular means (the Concentric Retriever), there has been increased enthusiasm for treating stroke by direct mechanical intervention, and most recently there has been a call for the designation of comprehensive stroke centers to treat the most severe forms of stroke.3
The call by thought-leaders in stroke for creation of comprehensive stroke centers signifies a solid endorsement that more aggressive endovascular techniques have an important role in stroke therapy. This endorsement stems from two main lines of evidence: large vessel occlusions (basilar, carotid terminus, middle cerebral artery) portend a poor prognosis with a mortality of 53–92%;4–7 and only 20% of untreated patients achieve a good neurological outcome at three months.1 Although tPA can improve this outcome, it is clear that intravenous (IV) tPA restores perfusion of large vessels at most one in five times, and less than half of patients have a good neurological outcome.1 This is likely due to the relatively larger clot burden of large vessel occlusions, the difficulty of delivering a high concentration of tPA directly to the clot when it is administered intravenously, and the relatively low concentration of plasminogen within the clot itself. At least one of these challenges can be mitigated—by instilling a plasminogen activator directly into the clot via catheter, recanalization rates are higher. The Prolyse in Acute Cerebral Thromboembolism (PROACT)-II study found that, for middle cerebral artery occlusions, recanalization rates of 66% can be seen and neurological outcomes statistically improve.8 However, attempts to thrombolyse clots within other arteries (carotid terminus and basilar artery) have proven more difficult. Also, many patients have contraindications for plasminogen activators like recent surgery, trauma, or bleeding disorders, limiting their broad application.
Endovascular thrombectomy is an innovative strategy to open intracranial vessels with a mechanical device introduced via catheter from the groin. The technique carries the intuitive appeal that opening a cerebral vessel quickly by mechanical means could be used in any patient with a large vessel occlusion, including those with tPA contraindications, and in any large vessel regardless of clot burden. The efficacy and safety of this technique was reported in the Mechanical Embolus Removal in Cerebral Ischemia (MERCI) trial, whereby the Concentric Retriever was tested in patients within eight hours of stroke symptom onset.9 The Retriever is a soft, helically shaped, tapered nitinol wire that is delivered into the arterial clot via catheter, then removed from the body with the clot to restore blood flow.The device was found to restore vascular patency in 48% of patients, all of whom were ineligible for tPA. This trial provided data to the FDA to clear the device for clinical use in 2004, and it became the first ever device cleared for use in acute ischemic stroke. Both the PROACT-II8 and MERCI9 studies considered together provide evidence that restoring perfusion improves patient outcome and endovascular techniques have a place in the management of stroke.
2. Alberts M J, Hademenos G, Latchaw RE, et al., - Recommendations for the establishment of primary stroke centers. Brain Attack Coalition; , JAMA (2000);283: pp. 3,102 3,109.
3. Alberts M J, Latchaw R E, Selman W R, et al., - Recommendations for comprehensive stroke centers: a consensus statement from the Brain Attack Coalition; , Stroke (2005);36: pp. 1,597 1,616.
4. Jansen O, von Kummer R, Forsting M, et al., - Thrombolytic therapy in acute occlusion of the intracranial internal carotid artery bifurcation; ,Am. J. Neuroradiol. (1995);16: pp. 1,977 1,986.
5. Bruckmann H, Ferbert A, del Zoppo GJ, et al.,- Acute vertebral-basilar thrombosis.Angiologic-clinical comparison and therapeutic implications; , Acta Radiol. (1986);369 Suppl: pp. 38 42.
6. Brandt T, von Kummer R, Muller-Kuppers M, Hacke W,- Thrombolytic therapy of acute basilar artery occlusion.Variables affecting recanalization and outcome; , Stroke (1996);27: pp. 875 881.
7. Hacke W, Schwab S, Horn M, et al., - Malignant middle cerebral artery territory infarction: clinical course and prognostic signs; , Arch. Neurol. (1996);53: pp. 309 315.
8. Furlan A, Higashida R,Wechsler L et al., - Intra-arterial prourokinase for acute ischemic stroke. The PROACT II study: a randomized controlled trial. Prolyse in Acute Cerebral Thromboembolism; , JAMA (1999);282: pp. 2,003 2,011.
9. Smith W S, Sung G, Starkman S, et al., - Safety and efficacy of mechanical embolectomy in acute ischemic stroke: results of the MERCI trial; , Stroke (2005);36: pp. 1,432 1,438.
10. Smith WS, - Results of the Multi MERCI trial; , Stroke (2006);37: pp. 711 712.
11.IMS Trial Investigators, - Combined intravenous and intra-arterial recanalization for acute ischemic stroke: the Interventional Management of Stroke study; , Stroke (2004);35: pp. 904 911.
12. Investigators II, - Preliminary results of the IMS II trial; , Stroke (2006);37: p. 708.
13. Lees K R, Zivin J A,Ashwood T, et al.,- NXY-059 for acute ischemic stroke; , N. Engl. J. Med. (2006);354: pp. 588 600.
Specialities:
- Neurology
- ADHD
- Advanced Parkinson's Disease
- Anxiety Disorder
- Brain Cancer
- Cerebrovascular Disease
- Dementia
- Epilepsy
- Mood Disorders
- Motor/Movement Disorder
- Multiple Sclerosis
- Neuroimaging
- Neurosurgery
- Obsessive-Compulsive Disorder
- Pain/Headache
- Parkinson's Disease
- Psychiatry
- Schizophrenia
- Sleep Disorder
- Stroke
- 16 February 2012
- 1 March 2012
- 1 March 2012










