The fate of cranial neuropathy after flow diversion for carotid aneurysms

Author:

Brown Benjamin L.1,Lopes Demetrius2,Miller David A.1,Tawk Rabih G.1,Brasiliense Leonardo B. C.1,Ringer Andrew3,Sauvageau Eric4,Powers Ciarán J.5,Arthur Adam6,Hoit Daniel6,Snyder Kenneth7,Siddiqui Adnan7,Levy Elad7,Hopkins L. Nelson7,Cuellar Hugo8,Rodriguez-Mercado Rafael9,Veznedaroglu Erol10,Binning Mandy10,Mocco J11,Aguilar-Salinas Pedro12,Boulos Alan13,Yamamoto Junichi13,Hanel Ricardo A.4

Affiliation:

1. Department of Neurosurgery, Mayo Clinic, Jacksonville, Florida;

2. Department of Neurosurgery, Rush University Medical Center, Chicago, Illinois;

3. Department of Neurosurgery, University of Cincinnati, Ohio;

4. Lyerly Neurosurgery, Baptist Health, Jacksonville, Florida;

5. Department of Neurological Surgery, The Ohio State University, Columbus, Ohio;

6. Semmes Murphey Neurologic and Spine Institute, Semmes Murphey Clinic, Memphis, Tennessee;

7. Department of Neurosurgery, University of Buffalo, New York;

8. Department of Neurosurgery, Louisiana State University, Shreveport, Louisiana;

9. Department of Neurosurgery, University of Puerto Rico Medical Sciences, San Juan, Puerto Rico;

10. Capital Institute for Neurosciences, Capital Health, Trenton, New Jersey;

11. Department of Neurological Surgery, Vanderbilt University, Nashville, Tennessee;

12. National Institute of Medical Sciences and Nutrition, Salvador Zubiran, Mexico City, Mexico; and

13. Department of Neurosurgery, Albany Medical Center, Albany, New York

Abstract

OBJECT The authors sought to determine whether flow diversion with the Pipeline Embolization Device (PED) can approximate microsurgical decompression in restoring function after cranial neuropathy following carotid artery aneurysms. METHODS This multiinstitutional retrospective study involved 45 patients treated with PED across the United States. All patients included presented between November 2009 and October 2013 with cranial neuropathy (cranial nerves [CNs] II, III, IV, and VI) due to intracranial aneurysm. Outcome analysis included clinical and procedural variables at the time of treatment as well as at the latest clinical and radiographic follow-up. RESULTS Twenty-six aneurysms (57.8%) were located in the cavernous segment, while 6 (13.3%) were in the clinoid segment, and 13 (28.9%) were in the ophthalmic segment of the internal carotid artery. The average aneurysm size was 18.6 mm (range 4–35 mm), and the average number of flow diverters placed per patient was 1.2. Thirty-eight patients had available information regarding duration of cranial neuropathy prior to treatment. Eleven patients (28.9%) were treated within 1 month of symptom onset, while 27 (71.1%) were treated after 1 month of symptoms. The overall rate of cranial neuropathy improvement for all patients was 66.7%. The CN deficits resolved in 19 patients (42.2%), improved in 11 (24.4%), were unchanged in 14 (31.1%), and worsened in 1 (2.2%). Overtime, the rate of cranial neuropathy improvement was 33.3% (15/45), 68.8% (22/32), and 81.0% (17/21) at less than 6, 6, and 12 months, respectively. At last follow-up, 60% of patients in the isolated CN II group had improvement, while in the CN III, IV, or VI group, 85.7% had improved. Moreover, 100% (11/11) of patients experienced improvement if they were treated within 1 month of symptom onset, whereas 44.4% (12/27) experienced improvement if they treated after 1 month of symptom onset; 70.4% (19/27) of those with partial deficits improved compared with 30% (3/10) of those with complete deficits. CONCLUSIONS Cranial neuropathy caused by cerebral aneurysm responds similarly when the aneurysm is treated with the PED compared with open surgery and coil embolization. Lower morbidity and higher occlusion rates obtained with the PED may suggest it as treatment of choice for some of these lesions. Time to treatment is an important consideration regardless of treatment modality.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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