Purpose Transverse sinus stenosis is commonly seen in patients with idiopathic intracranial hypertension. It is not clear whether it is the cause or the result of idiopathic intracranial hypertension. Stenting for idiopathic intracranial hypertension has been carried out in several prior series. Our goal was to evaluate the clinical and imaging follow-up results of patients with idiopathic intracranial hypertension that underwent stenting for this condition at our center. Materials and Methods We reviewed the clinical, venographic and follow-up imaging data in patients who underwent elective transverse sinus stenting during the period from 2011 to 2017. Results In total, 18 patients with idiopathic intracranial hypertension were identified. The mean lumbar cerebrospinal fluid opening pressure recorded was 408 mmH20. Overall, 16 patients met the inclusion criteria and underwent transverse sinus stenting. At venography, the mean pressure gradient across the dominant transverse sinus stenosis was 21 mmHg. The pressure gradient immediately after stenting in all of those measured was negligible. Following stenting, headaches improved in 10 of the 16 cases, with persistent headaches in four patients, one of which had persistent baseline migraines. All cases showed resolution of the papilledema on follow up. Follow-up imaging with computed tomography venography showed that the stents remained widely patent. The follow up in clinic was done for a mean period of 35.5 months. Follow up with computed tomography venography was done for a mean of 10.3 months. Conclusion Venous sinus stenting is a safe and effective procedure. It relieves papilledema in all cases and improves headaches in most cases.
Key Clinical MessageThirty-seven-year old female with hydrocephalus managed by a ventriculoatrial (VA) shunt presented with upper body edema, dysphagia, and headache. Imaging demonstrated thrombosis of the superior vena cava (SVC). Direct catheter thrombolysis led to resolution of thrombus burden. Superior vena cava thrombosis is a rare consequence of VA shunting and must be managed emergently.
Background Endovascular treatment of large complex morphology aneurysms is challenging. High recanalization rates have been reported with techniques such as stent-assisted coiling and balloon-assisted coiling. Flow diverter devices have been introduced to improve efficacy outcomes and recanalization rates. Thromboembolic complications and in-device stenosis are certainly more worrisome when treatment of bilateral internal carotid arteries has been performed. This study aimed to report our experience with mid-term imaging follow-up of staged bilateral Pipeline embolization device placement for the treatment of bilateral internal carotid artery aneurysms. Methods We reviewed the clinical, angiographic, and follow-up imaging data in all consecutive patients treated with bilateral internal carotid artery aneurysms who underwent elective Pipeline embolization. Results Six female patients were treated, harboring a total of 13 aneurysms. Of these, 60% were asymptomatic. Diplopia and headache were the most common symptoms. The most common location was the paraclinoid segment (6/13), including by cavernous segment (4/13) and ophthalmic segment (2/13). Successful delivery of the device was achieved in 12 cases. Difficult distal access precluded the deployment of the device in one case. The treatment was always staged with at least eight weeks' difference between the two procedures. All aneurysm necks were covered completely. There were no periprocedural complications. Angiographic follow-up ranged between 3 and 12 months, and computed tomography angiogram follow-up ranged between 2 and 24 months. Complete aneurysm occlusion was achieved in all cases. Conclusion In our series, Pipeline deployment for the treatment of bilateral internal carotid artery aneurysms in a staged fashion is safe and feasible. Mid-term imaging follow-up showed permanent occlusion of all the treated aneurysms.
PurposeTransverse sinus stenosis is commonly seen in patients with idiopathic intracranial hypertension (IIHT). It is not clear whether it is the cause or the result of IIHT. Stenting for IIHT has been done in several prior series. Our goal was to evaluate the clinical and imaging follow up results of patients with IIHT that underwent stenting for this condition at our Centre.Materials and MethodsWe reviewed the clinical, venographic and follow up imaging and imaging data in patients who underwent elective transverse sinus stenting during the period from 2011 to 2016.ResultsSeven patients with IIHT were identified, of which one had associated dural AVF and hence was excluded from the study. The mean lumbar CSF opening pressure recorded was 370 mm of H20. At venography, the mean pressure gradient across the dominant transverse sinus stenosis was 17 mm of Hg (range of 10–23 mm of Hg). The pressure gradient immediately after stenting in all of those measured was negligible. Following stenting, headache improved in 3 of the 6 cases, with persistent headache in 2, of which one had persistent baseline migraine. One patient had complete relief of their headache. All cases showed no papilledema on follow up. Follow up imaging with CT venography showed that the stents remained widely patent. Follow-up in clinic was done for a mean period of 35.5 months (range 4 months to 65 months). Follow up with CT venography was done for a mean of 10.3 months (range 2 months to 36 months). Time to stenting was done with a mean of 4.6 months (2 months to 9 months).ConclusionVenous sinus stenting is a safe procedure. It helps to relieve papilledema in all cases with significant improvement of headaches in most cases.Disclosures
J. Kovoor: None. J. Tejada: None. K. Riley: None. R. Shastri: None.
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