The patient was given clopidogrel (300 mg) before the procedure and unfractionated heparin (5000 IU) intra-arterially after vascular access was achieved. A self-expanding 8-6x30 mm tapering stent was implanted in the left ICA without the use of an emboli protection device. Furthermore, the procedure was accomplished without any additional implementation, and angiography revealed no residual stenosis (Figure 1a). Intravenous heparin infusion (1000 IU/h) was initiated following the stent implantation along with the oral administration of aspirin (100 mg). In addition, the activated clotting time (ACT) was kept at over 200 seconds during the procedure. Afterwards, however, the heparin dosage was increased to 1500 IU/h because the ACT was measured at 179 seconds. Dysarthria and right hemiparesis appeared 30 minutes after the procedure, and acute stent occlusion was revealed via a Doppler evaluation (Figure 1b). Following this, right hemiplegia occurred, and the patient lost consciousness. An urgent angiographic evaluation of the aortic arch was then performed in the hybrid operating room, and this supported the diagnosis of acute in-stent occlusion; therefore, the patient underwent an urgent operation (Figure 1c). A carotid endarterectomy and primary repair were also performed after the removal of the stent during the same procedure. We discovered that the stent was totally occluded with thrombus, but there was no fracture or kinking (Figure 2).
Figure 2: (a) The occluded stent along with (b) the endarterectomy material.
The patient was extubated uneventfully in the postoperative third hour. Her platelet counts (preoperative: 193,000/mm3, early postoperative: 161,000/mm3, postoperative day one: 163,000/mm3, and postoperative day four: 163,000/mm3) did not markedly change in the follow-up period, so the heparin-induced thrombocytopenia was excluded. Additionally, there were no signs of neurological deficit after the surgery, and the patient was discharged on the fourth postoperative day without any complications.
Adequate follow-up to assess the patients’ postoperative neurological status in the intensive care unit (ICU) is necessary in order to be aware of acute changes that might need urgent treatment. When a stroke occurs during stent implantation, early diagnosis and treatment with fibrinolysis is crucial for recovery.[8] In addition, surgical removal of the stent or a thrombectomy with aspiration can be performed for acute in-stent thrombosis, but this is only suitable for hybrid operating rooms because a Fogarty catheter cannot be used due to the risk of stent dislocation when the patient is undergoing a thrombectomy.[9] Furthermore, endovascular procedures used to treat extracranial lesions and acute in-stent thrombosis might cause distal embolization. In addition, it is a very time-consuming procedure. Removing the stent after clamping the distal thrombosed part prevents embolic complications, which then allows for the safe removal of the this part of the stent. Alternative treatment strategies that might be employed include thrombolitic therapy for intracranial occlusions and surgery for extracranial lesions.[9]
Performing carotid artery stenting in hybrid operating rooms allows for sufficient time for the surgery without complications, and there is a smaller chance that the stenting procedure will fail. Treatment for acute in-stent occlusion is similar to that for acute complications associated with endarterectomies since both decrease neurological morbidity.[9] Furthermore, a carotid artery stent can be easily removed in the periprocedural period because there is no inflammation or fibrosis in the arterial wall.[10]
In our facility, we carefully monitor patients who undergo carotid artery stenting in the ICU during the period of heparin infusion. In this case, by establishing an accurate diagnosis as soon as the symptoms occurred and performing an early reoperation, we probably saved the life of our patient. Acute stent occlusion can be identified and treated sooner in a hybrid operating room. Our patient was extubated without any complications and revealed no neurological morbidity.
Declaration of conflicting interests
The authors declared no conflicts of interest with
respect to the authorship and/or publication of this
article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
1) Naylor AR. Endarterectomy versus carotid stenting. Br J
Surg 2012;99:149-51.
2) Arya S, Pipinos II, Garg N, Johanning J, Lynch TG,
Longo GM. Carotid endarterectomy is superior to carotid
angioplasty and stenting for perioperative and long-term
results. Vasc Endovascular Surg 2011;45:490-8.
3) Cohen DJ, Stolker JM, Wang K, Magnuson EA, Clark WM,
Demaerschalk BM, et al. Health-related quality of life after
carotid stenting versus carotid endarterectomy: results from
CREST (Carotid Revascularization Endarterectomy Versus
Stenting Trial). J Am Coll Cardiol 2011;58:1557-65.
4) Bosiers M, Peeters P, Deloose K, Verbist J, Sprouse RL
2nd. Selection of treatment for patients with carotid artery
disease: medication, carotid endarterectomy, or carotid
artery stenting. Vascular 2005;13:92-7.
5) Iancu A, Grosz C, Lazar A. Acute carotid stent thrombosis:
review of the literature and long-term follow-up. Cardiovasc
Revasc Med 2010;11:110-3.
6) Nazzal M, Abbas J, Nazzal M, Afridi S, Ritter M. Fractured
internal carotid artery stent. Vascular 2008;16:179-82.
7) Oxley TJ, Dowling RJ, Mitchell PJ, Davis S, Yan B.
Antiplatelet resistance and thromboembolic complications in
neurointerventional procedures. Front Neurol 2011;2:83.
8) Parodi FE, Schonholz C, Parodi JC. Minimizing complications of carotid stenting. Perspect Vasc Surg
Endovasc Ther 2010;22:117-22.