Proximal protection devices could be the first choice for most carotid artery stenting procedures

Original title: Evaluation of proximal protection devices during carotid artery stenting as the first choice for embolic protection. Reference: Hornung M et al. EuroIntervention. 2014; Epub ahead of print.

This series of the Frankfurt CardioVascular Center included 124 consecutive patients undergoing carotid angioplasty with proximal protection. The first 92 patients received the Gore Flow Reversal System (WL Gore; Flagstaff, AZ). After this device became unavailable the Mo.Ma Ultra was used (Medtronic; Minneapolis, MN).

After procedure, all patients were prescribed 100 mg of aspirin indefinitely, and 75 mg of clopidogrel daily for at least 30 days. 21% of the population presented a symptomatic lesion; mean time between index neurological event and stenting was 50.5 days.

Predilation was necessary in 33.1% of lesions and most commonly employed stents were the Protege (Ev3 Endovascular; Plymouth, MN; 56.5%) and the Xact (Abbott Vascular; Santa Clara, CA; 24.2%).

The primary end point, a combination of new transitory ischemic accident and minor or major stroke within 30 days, was observed in one patient only. This patient had no procedural complications but suffered a stent thrombosis 9 days after discharge.

Transitory neurological symptoms due to intolerance of antegrade flow interruption during balloon occlusion were observed in 10 patients (8.1%), but were promptly and completely solved once flow was reestablished.

Only 2 patients were not able to benefit from the proximal embolic protection device, which had a technical success of 98.4%. None of these patients presented neurological complications.

Conclusion

Proximal protection devices are safe and can be used as first choice for embolic protection during carotid artery stenting. 

Editorial Comment

Neurological complications rate with proximal protection (both in the meta-analysis and the current series) is lower than rates reported by the majority of studies comparing carotid stenting with distal protection vs endarterectomy. Outcomes of this study, from one center only, with very few expert operators, may not be transferable to other centers. 

SOLACI.ORG

More articles by this author

Endovascular Treatment of Iliofemoral Disease for the Improvement of Heart Failure with Preserved Ejection Fraction

Peripheral artery disease (PAD) is a significant risk factor in the development of difficult-to-treat conditions, such as heart failure with preserved ejection fraction (HFpEF)....

Chronic Thromboembolic Pulmonary Hypertension: Treatment Outcomes According to a Worldwide Registry

Chronic thromboembolic pulmonary hypertension (CTEPH) is a highly limiting condition that, despite its moderate incidence, significantly impacts patient prognosis and quality of life. The...

Contemporary Outcomes of Acute Limb Ischemia Endovascular Revascularization

Acute limb ischemia (ALI) is a vascular emergency with high mortality rate. It has been defined as a sudden occlusion of limb perfusion compromising...

TCT 2024 | SIRONA: Randomized Study Comparing Sirolimus-Coated vs Paclitaxel-Coated Balloon Angioplasty in Femoropopliteal Disease

This prospective, randomized, multicenter, investigator-initiated non-inferiority study compared the use of sirolimus-coated balloon (MagicTouch) vs paclitaxel-coated balloon in endovascular treatment.  The primary objective was to...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...