Techniques in cerebral protection

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Abstract

Carotid angioplasty and stenting is a valid alternative option to conventional carotid endarterectomy in the treatment of carotid artery stenosis. During the stenting process, however, distal embolization can occur with neurological consequences. To avoid this, cerebral protection devices have been introduced.

Three principal types of protection system have been developed: distal balloon occlusion, distal filters and proximal protection with or without reversal of flow.

As protection devices became the focus of interest by manufactures and physicians, several trials are going on worldwide to analyze the characteristics of each of them and to evaluate their efficacy to reduce the rate of distal embolization.

Introduction

Carotid artery stenting (CAS) is considered a valid therapeutic option for the treatment of the stenoses of the extracranial carotid artery. However, it has an incidence of neurological complications due to distal embolization which ranges from 3.2 to 10% [1], [2].

To reduce the rate of periprocedural neurological complications, various systems of cerebral protection have been proposed; the purpose of these systems is to capture the emboli before they reach the brain.

The first system was described by Théron [3] in 1990, who introduced the concept employing temporary balloon occlusion of the distal internal carotid artery (ICA) during percutaneous transluminal angioplasty.

After this initial experience, several studies have been carried out using different protection devices, which showed a reduction of the neurological periprocedural complication rate. The global carotid artery stent registry described a perioperative stroke and death rate of 5.9 and 2.23%, respectively, in those procedures performed without and with protection devices [4].

Boltuch et al. [5] evaluated 651 patients treated both with (N = 180) and without (N = 471) cerebral protection and found better results for the protected population: technical success 99% versus 95%; complication rate 10% versus 18.3%; TIA 2.8% versus 3.2%; MAE 0.6% versus 2.1%.

Cerebral protection devices (CPD) can be divided into three different types: filters, distal occlusion balloons and proximal protection systems.

In filter systems, flow is maintained and emboli are captured and removed together with the device by retraction of the system. Balloon occlusion devices and proximal protection system block flow in the ICA and emboli are aspirated before balloon deflation and catheter removal.

In this paper, we described the more commonly used CPDs, the techniques of use, and the potential technical and clinical complications.

Section snippets

Distal occlusion balloons

Distal occlusion balloons represent the first class of protection devices used routinely in clinical practice.

They consist of a 0.014 in guide-wire equipped with a distal balloon that is inflated through a small channel present within the wire.

Once the lesion is crossed with the guide-wire, the balloon is positioned above the lesion and inflated to completely occlude the ICA, thus avoiding the passage of microemboli. After treatment of the lesion by angioplasty and stenting, a catheter is

Discussion

Cerebral protections cannot prevent all embolic events that may occur during the different steps of CAS procedures. Up-to-date data on device effectiveness are still limited and results of clinical studies and experimental evaluations of protection devices are controversial [9], [10]. Further details about their effectiveness are discussed elsewhere in this issue.

Despite the fact that CPDs have been used in clinical practice for several years, they are still “young” devices and they are subject

Summary

Carotid artery angioplasty and stenting procedures always produce distal embolization, although most embolization does not produce clinical sequelae. Several studies have proved that the use of cerebral protection devices drastically reduces the incidence of distal microembolization.

References (17)

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