Intervention
Endovascular balloon test occlusion with qualitative or quantitative cerebral blood flow and/or carotid artery pressure measurements have been successfully used to assess the hemodynamic risk of permanent or temporary carotid arterial occlusion. This assessment couples the 20-minute clinical occlusion test with a qualitative or quantitative test. Patients who cannot tolerate a balloon occlusion test of the internal carotid may require an extracranial-to-intracranial bypass and subsequent reevaluation before indirect treatment is initiated. The type of bypass is directly related to the flow deficiency.
Patients with frankly failing results during the clinical balloon occlusion test are at the greatest risk and pose the greatest challenge. Patients with an aneurysm in the cavernous sinus in whom the balloon occlusion test fails should be treated during extracranial-intracranial bypass surgery with a superficial temporal artery graft or a saphenous vein graft. The rate of blood flow supplied by a superficial temporal artery is 20-60 mL/min; this may not be enough to accommodate a normal blood flow of 75-120 mL/min through a middle cerebral artery. No collateral blood supply flows through the posterior and anterior communicating arteries. Higher flow rates may be achieved with a saphenous vein graft bypass.
During the past decade, the endovascular treatment of intracranial aneurysms has developed extensively. The original indication—the treatment of giant unclippable intracranial aneurysms— has been extended to include small aneurysms and those that have recently ruptured. The introduction of coils, stents, and newer materials allows for successful treatment of many intracranial aneurysms. Depending on the location, configuration, and characteristics of the aneurysm, consideration should be given to a surgical obliteration or endovascular treatment of an intracranial aneurysm.
It is the author's opinion that a team approach involving the neurosurgeon and the endovascular neuroradiologist is of paramount importance for the successful treatent of these patients. In many patients with intracranial aneurysm, a complex endovascular approach that takes into consideration the use of detachable coils, stents, balloons, and aneurysm neck remodeling increases the probability of a successful aneurysm occlusion. The use of hydrogel-coated coils for the endovascular treatment of intracranial aneurysms offers the theoretical advantages of increased volumetric occlusion, thrombus stabilization, and improved neointimal healing.6,7,8,10,18
After the initial diagnosis of an intracerebral aneurysm, when symptoms or TCD ultrasonographic findings suggest vasospasm, repeat angiography definitively depicts the presence, severity, and location of the vasospasm and the status of the aneurysm. Therapy for the regions of narrowing may then be performed with either balloon angioplasty or an infusion of vasodilators, such as papaverine.
Following subarachnoid aneurysmal hemorrhage, endovascular treatment of vasospasm should be implemented in patients who develop clinical or radiologic symptoms of brain ischemia, in conjunction with increased Doppler velocities, despite maximal medical treatment.5,24 Treatment may be either pharmacologic or mechanical. Calcium and phosphodiesterase inhibitors may be administered. In Europe, intravasular nimodipine is widely used; in North America, nicardipine and verapamil are the major agents used, because intravenous nimodipine has not been approved by the FDA.
Papaverine was the drug of choice in the past; however, papaverine is now considered less desirable owing to its short duration of vasodilatation and the risk of aggravation of increased intracranial pressure. Balloon angioplasty has a long-lasting effect but may be applied only in cases involving spasm of proximal vessels. Complications of its use are rare but may be life threatening. The author recommends the use of a combined approach, including the intra-arterial administration of pharmacologic agents and the use of balloon angioplasty. I also recommend that the approach be maintained and that repeat angioplasty procedures be performed as often as the patient's condition warrants it.5,6,7,25,26,27,28,29,30,31,32
Medicolegal Pitfalls
- With endovascular procedures, complications often occur during puncture. Subintimal threading of the catheter or needle may cause dissection syndromes and subsequent ischemic complications. Neck hematomas may develop, requiring termination of the procedure. Occasionally, a thrombus develops in the punctured artery, requiring surgery on an emergency basis. Neurologic deficits may occur during primary vessel puncture.
- During cerebral angiography, complications include arterial dissection and delayed arterial occlusion; arterial rupture; hemorrhagic infarction; and displacement of the surgical clips from the aneurysmal necks.
- During balloon angioplasty, ischemic complications may occur as a result of excessive occlusion times. Stenosis may also occur because the diameter of the noninflated balloon is equivalent to the vessel's diameter. In this situation, the balloon adds to ischemia of the vasospasm before dilation. Occasionally, the procedure is performed in a patient whose blood flow has been critically reduced before dilation. Only short periods of vasodilation are tolerated. The most feared complication of angioplasty is separation of the balloon from the catheter and its distal migration into the intracranial arterial tree; this most often occurs when a detachable balloon is used to occlude the aneurysm. To prevent ischemic complications, the smallest possible balloon and catheter and be selected, and they should be attached firmly. Dilations should be performed rapidly. Hemorrhagic complications occur because of rupture of the primary vessel or aneurysm.
- Aneurysmal rupture during cerebral angiography may occur as a result of traction, the performance of maneuvers near the aneurysmal neck, or catheter misplacement in the neck of an aneurysm that increases dynamic pressures in the aneurysm. One should always be prepared to perform open craniotomy promptly if the aneurysm ruptures. If a thrombus obstructs the vessel, a fibrinolytic such as urokinase or tissue plasminogen should be used immediately.
- A major source of complications of direct surgical treatment of aneurysms is ischemia. Because of the critical nature of the neural structures supplied by the perforating branches, especially during the surgical treatment of posterior circulation aneurysms, occlusion of the perforating vessels typically causes dramatic symptoms. Maneuvers that ensure the identification and liberation of all perforating branches from the aneurysm sac before clip placement are of paramount importance. Inspection after clip positioning is also crucial to ensure that any proximal vessels continue to fill. Major arterial branch occlusions, although less common, have dramatic consequences as well. These problems most often occur as a result of poor clip placement.
- The morbidity and mortality rates of intraoperative rupture during the surgical treatment of intracranial aneurysms can be significant. The operating surgeon must have access to vascular control; in addition, the surgeon should have a practiced set of steps to avoid this complication and should treat it as quickly and efficiently as possible. Techniques to reduce the incidence of intraoperative aneurysm rupture include the use of sharp dissection and complete dissection of the lesion before any attempt at clip placement. Should intraoperative rupture occur, tamponade is usually the quickest and most effective method of initial management. If tamponade fails to significantly reduce the hemorrhage, temporary arterial occlusion should be considered.
- Cranial nerve deficits are well-recognized deficits that occur after the treatment of intracranial aneurysms. The most common cranial nerve deficit in the treatment for basilar bifurcation or posterior communicating artery aneurysms is a temporary third cranial nerve palsy that results in ptosis and ophthalmoplegia. The likely cause is surgical manipulation. Deficits are usually short lived, and most patients recover within 3 months. Other causes include injury from poor clip placement.
- The frequency of acute hydrocephalus during the first 3 days after aneurysmal SAH is approximately 20%. The proportion of patients who have acute hydrocephalus concurrent with intraventricular hemorrhage is 35-65%. Treatment options for patients with SAH and acute hydrocephalus include observation and ventricular drainage. In patients who are asymptomatic in the early postbleeding period, observation in the presence of ventricular dilatation appears justified; approximately 1 in 3 patients have neurologic deterioration in the following few days.
- Among other injuries, the obstruction of venous drainage is a consequence of excessive retraction or injury to the bridging veins. Obstruction may result in the development of hemorrhagic infarction.
More on Brain, Aneurysm |
| Overview: Brain, Aneurysm |
| Imaging: Brain, Aneurysm |
Follow-up: Brain, Aneurysm |
| Multimedia: Brain, Aneurysm |
| References |
| « Previous Page | Next Page » |
References
Biousse V, Newman NJ. Aneurysms and subarachnoid hemorrhage. Neurosurg Clin N Am. Oct 1999;10(4):631-51. [Medline].
Inci S, Spetzler RF. Intracranial aneurysms and arterial hypertension: a review and hypothesis. Surg Neurol. Jun 2000;53(6):530-40; discussion 540-2. [Medline].
Juvela S, Porras M, Poussa K. Natural history of unruptured intracranial aneurysms: probability of and risk factors for aneurysm rupture. J Neurosurg. Sep 2000;93(3):379-87. [Medline].
Inci S, Erbengi A, Ozgen T. Aneurysms of the distal anterior cerebral artery: report of 14 cases and a review of the literature. Surg Neurol. Aug 1998;50(2):130-9; discussion 139-40. [Medline].
Nguyen TN, Raymond J, Roy D, Chagnon M, Weill A, Iancu-Gontard D, et al. Endovascular treatment of pericallosal aneurysms. J Neurosurg. Nov 2007;107(5):973-6. [Medline].
Gruber A, Killer M, Bavinzski G, Richling B. Clinical and angiographic results of endosaccular coiling treatment of giant and very large intracranial aneurysms: a 7-year, single-center experience. Neurosurgery. Oct 1999;45(4):793-803; discussion 803-4. [Medline].
Moret J, Ross IB, Weill A, Piotin M. The retrograde approach: a consideration for the endovascular treatment of aneurysms. AJNR Am J Neuroradiol. Feb 2000;21(2):262-8. [Medline].
Mitha AP, Wong JH, Lu JQ, Morrish WF, Hudon ME, Hu WY. Communicating hydrocephalus after endovascular coiling of unruptured aneurysms: report of 2 cases. J Neurosurg. Jun 2008;108(6):1241-4. [Medline].
Peluso JP, van Rooij WJ, Sluzewski M, Beute GN, Majoie CB. Posterior inferior cerebellar artery aneurysms: incidence, clinical presentation, and outcome of endovascular treatment. AJNR Am J Neuroradiol. Jan 2008;29(1):86-90. [Medline].
Pereira AR, Sanchez-Peña P, Biondi A, Sourour N, Boch AL, Colonne C, et al. Predictors of 1-year outcome after coiling for poor-grade subarachnoid aneurysmal hemorrhage. Neurocrit Care. 2007;7(1):18-26. [Medline].
Bruno A, Carter S, Qualls C, Nolte KB. Incidence of spontaneous subarachnoid hemorrhage among Hispanics and non-Hispanic whites in New Mexico. Ethn Dis. Winter 1997;7(1):27-33. [Medline].
Anderson GB, Steinke DE, Petruk KC, et al. Computed tomographic angiography versus digital subtraction angiography for the diagnosis and early treatment of ruptured intracranial aneurysms. Neurosurgery. Dec 1999;45(6):1315-20; discussion 1320-2. [Medline].
Brown JH, Lustrin ES, Lev MH, et al. Reduction of aneurysm clip artifacts on CT angiograms: a technical note. AJNR Am J Neuroradiol. Apr 1999;20(4):694-6. [Medline].
Hashimoto H, Iida J, Hironaka Y, et al. Use of spiral computerized tomography angiography in patients with subarachnoid hemorrhage in whom subtraction angiography did not reveal cerebral aneurysms. J Neurosurg. 92(2):278-83. [Medline].
Marro B, Valery CA, Bitard A, et al. Intracranial aneurysm on CTA: demonstration using a transparency volume-rendering technique. J Comput Assist Tomogr. Jan-Feb 2000;24(1):96-8. [Medline].
Sahel M, Ourrad E, Zouaoui A, et al. [3D-CT angiography with volume rendering technique in the intracerebral aneurysms]. J Radiol. Feb 2000;81(2):127-32. [Medline].
Velthuis BK, Van Leeuwen MS, Witkamp TD, et al. Computerized tomography angiography in patients with subarachnoid hemorrhage: from aneurysm detection to treatment without conventional angiography. J Neurosurg. Nov 1999;91(5):761-7. [Medline].
Bendel P, Koivisto T, Könönen M, Hänninen T, Hurskainen H, Saari T, et al. MR imaging of the brain 1 year after aneurysmal subarachnoid hemorrhage: randomized study comparing surgical with endovascular treatment. Radiology. Feb 2008;246(2):543-52. [Medline].
Brown BM, Soldevilla F. MR angiography and surgery for unruptured familial intracranial aneurysms in persons with a family history of cerebral aneurysms. AJR Am J Roentgenol. Jul 1999;173(1):133-8. [Medline].
Kahara VJ, Seppanen SK, Ryymin PS, et al. MR angiography with three-dimensional time-of-flight and targeted maximum-intensity-projection reconstructions in the follow-up of intracranial aneurysms embolized with Guglielmi detachable coils. AJNR Am J Neuroradiol. Sep 1999;20(8):1470-5. [Medline].
Leclerc X, Lucas C, Godefroy O, et al. Preliminary experience using contrast-enhanced MR angiography to assess vertebral artery structure for the follow-up of suspected dissection. AJNR Am J Neuroradiol. Sep 1999;20(8):1482-90. [Medline].
Stroobandt G, Duprez T, Menard E. Clinical and MRI long term evolution of intracavernous and carotid ophtalmic artery aneurysms, treated by common carotid ligation. Acta Neurochir (Wien). 1999;141(10):1075-82. [Medline].
Wong JH, Mitha AP, Willson M, Hudon ME, Sevick RJ, Frayne R. Assessment of brain aneurysms by using high-resolution magnetic resonance angiography after endovascular coil delivery. J Neurosurg. Aug 2007;107(2):283-9. [Medline].
Mitsos AP, Corkill RA, Lalloo S, Kuker W, Byrne JV. Idiopathic aneurysms of distal cerebellar arteries: endovascular treatment after rupture. Neuroradiology. Feb 2008;50(2):161-70. [Medline].
Hasan D, Lindsay KW, Vermeulen M. Treatment of acute hydrocephalus after subarachnoid hemorrhage with serial lumbar puncture. Stroke. Feb 1991;22(2):190-4. [Medline].
Kim BM, Kim DI, Shin YS, Chung EC, Kim DJ, Suh SH, et al. Clinical outcome and ischemic complication after treatment of anterior choroidal artery aneurysm: comparison between surgical clipping and endovascular coiling. AJNR Am J Neuroradiol. Feb 2008;29(2):286-90. [Medline].
Kremer C, Groden C, Hansen HC, et al. Outcome after endovascular treatment of Hunt and Hess grade IV or V aneurysms: comparison of anterior versus posterior circulation. Stroke. Dec 1999;30(12):2617-22. [Medline].
Lempert TE, Malek AM, Halbach VV, et al. Endovascular treatment of ruptured posterior circulation cerebral aneurysms. Clinical and angiographic outcomes. Stroke. Jan 2000;31(1):100-10. [Medline].
Lownie SP. Coil occlusion of basilar bifurcation aneurysms: the shape of things to come. Can J Neurol Sci. Aug 1999;26(3):170-1. [Medline].
Newell DW, Elliott JP, Eskridge JM, Winn HR. Endovascular therapy for aneurysmal vasospasm. Crit Care Clin. Oct 1999;15(4):685-99, v. [Medline].
Nichols DA. Endovascular therapy as the preferred method of treatment for "surgical" aneurysms: what must happen for this to become reality?. AJNR Am J Neuroradiol. Sep 1999;20(8):1391-2. [Medline].
Perneczky A, Boecher-Schwarz HG. Endoscope-assisted microsurgery for cerebral aneurysms. Neurol Med Chir (Tokyo). 1998;38 Suppl:33-4. [Medline].
Batjer HH. Controversies in neurosurgery: summary and perspective. Clin Neurosurg. 1999;45:205-7. [Medline].
Carvi y Nievas MN. Poor-grade subarachnoid hemorrhage patients: the use of nimodipine and other optional treatments. Neurol Res. Oct 1999;21(7):649-52. [Medline].
Ekelund A, Saveland H, Reinstrup P, Brandt L. Additional colloids have only a minor haemodilutive effect after surgery for aneurysmal subarachnoid haemorrhage. Br J Neurosurg. Aug 1999;13(4):399-404. [Medline].
Firat MM, Cekirge S, Saatci I, et al. Guglielmi detachable coil treatment of a partially thrombosed giant basilar artery aneurysm in a child. Neuroradiology. Feb 2000;42(2):142-4. [Medline].
Frank EH, Horgan M. An endoscopic aneurysm clip applicator: preliminary development. Minim Invasive Neurosurg. Jun 1999;42(2):89-91. [Medline].
Geevarghese SK, Powers T, Marsh JW, Pinson CW. Screening for cerebral aneurysm in patients with polycystic liver disease. South Med J. Dec 1999;92(12):1167-70. [Medline].
Hemphill JC 3rd, Gress DR, Halbach VV. Endovascular therapy of traumatic injuries of the intracranial cerebral arteries. Crit Care Clin. Oct 1999;15(4):811-29. [Medline].
Hutter BO, Kreitschmann-Andermahr I, Mayfrank L, et al. Functional outcome after aneurysmal subarachnoid hemorrhage. Acta Neurochir Suppl (Wien). 1999;72:157-74. [Medline].
Iizuka Y, Maehara T, R. [Endovascular neurointervention for cerebral aneurysm]. Nippon Igaku Hoshasen Gakkai Zasshi. 60(3):65-70. [Medline].
Karinen P, Koivukangas P, Ohinmaa A, et al. Cost-effectiveness analysis of nimodipine treatment after aneurysmal subarachnoid hemorrhage and surgery. Neurosurgery. Oct 1999;45(4):780-4; discussion 784-5. [Medline].
Kato M, Kaku Y, Okumura A, et al. Thrombosed unruptured cerebral aneurysm causing brain infarction followed by subarachnoid hemorrhage--case report--. Neurol Med Chir (Tokyo). Sep 2005;45(9):472-5. [Medline].
Kirkpatrick PJ, McConnell RS. Screening for familial intracranial aneurysms. BMJ. Dec 11 1999;319(7224):1512-3. [Medline].
Makoui AS, Smith DA, Evans AJ, Cahill DW. Early aneurysm recurrence after technically satisfactory Guglielmi detachable coil therapy: is early surveillance needed? Case report. J Neurosurg. Feb 2000;92(2):355-8. [Medline].
Mariani L, Bianchetti MG, Schroth G, Seiler RW. Cerebral aneurysms in patients with autosomal dominant polycystic kidney disease--to screen, to clip, to coil?. Nephrol Dial Transplant. Oct 1999;14(10):2319-22. [Medline].
Molyneux A, Kerr R. Endovascular aneurysm treatment and the incidence of vasospasm. AJNR Am J Neuroradiol. May 1999;20(5):944-5. [Medline].
Muizelaar JP, Zwienenberg M, Rudisill NA, Hecht ST. The prophylactic use of transluminal balloon angioplasty in patients with Fisher Grade 3 subarachnoid hemorrhage: a pilot study. J Neurosurg. 91(1):51-8. [Medline].
Nagashima H, Okudera H, Orz Y, et al. Endovascular treatment of basilar trunk aneurysm associated with fenestration of the basilar artery. Neurosurg Rev. Dec 1999;22(4):219-21. [Medline].
Nakagawa T, Hashi K, Kurokawa Y, Yamamura A. Family history of subarachnoid hemorrhage and the incidence of asymptomatic, unruptured cerebral aneurysms. J Neurosurg. Sep 1999;91(3):391-5. [Medline].
Ohaegbulam SC, Dujovny M, Ausman JI, et al. Ethnic distribution of intracranial aneurysms. Acta Neurochir (Wien). 1990;106(3-4):132-5. [Medline].
Pierot L, Boulin A, Visot A, et al. Postoperative aneurysm remnants: endovascular treatment as an alternative to further surgery. Neuroradiology. May 1999;41(5):315-9. [Medline].
Prandini MN, Lacanna SN, Tella OI, Bonatelli AP. Aneurysm growth after brain tumor removal: case report. Arq Neuropsiquiatr. Sep 2004;62(3A):722-4. [Medline].
Sciubba DM, Gallia GL, Recinos P, et al. Intracranial aneurysm following radiation therapy during childhood for a brain tumor. Case report and review of the literature. J Neurosurg. Aug 2006;105(2 Suppl):134-9. [Medline].
Sheehan JP, Polin RS, Sheehan JM, et al. Factors associated with hydrocephalus after aneurysmal subarachnoid hemorrhage. Neurosurgery. Nov 1999;45(5):1120-7; discussion 1127-8. [Medline].
Shimoda M, Oda S, Shibata M, et al. Results of early surgical evacuation of packed intraventricular hemorrhage from aneurysm rupture in patients with poor-grade subarachnoid hemorrhage. J Neurosurg. Sep 1999;91(3):408-14. [Medline].
SHSG. Risks and benefits of screening for intracranial aneurysms in first- degree relatives of patients with sporadic subarachnoid hemorrhage. The Magnetic Resonance Angiography in Relatives of Patients with Subarachnoid Hemorrhage Study Group. N Engl J Med. Oct 28 1999;341(18):1344-50. [Medline].
Steiger HJ, Medele R, Bruckmann H, et al. Interdisciplinary management results in 100 patients with ruptured and unruptured posterior circulation aneurysms. Acta Neurochir (Wien). 1999;141(4):359-66; discussion 366-7. [Medline].
Taniguchi M, Takimoto H, Yoshimine T, et al. Application of a rigid endoscope to the microsurgical management of 54 cerebral aneurysms: results in 48 patients. J Neurosurg. Aug 1999;91(2):231-7. [Medline].
terBrugge KG. Neurointerventional procedures in the pediatric age group. Childs Nerv Syst. Nov 1999;15(11-12):751-4. [Medline].
Thomas JE, Armonda RA, Rosenwasser RH. Endosaccular thrombosis of cerebral aneurysms: strategy, indications, and technique. Neurosurg Clin N Am. Jan 2000;11(1):101-21, ix. [Medline].
Ujiie H, Tachibana H, Hiramatsu O, et al. Effects of size and shape (aspect ratio) on the hemodynamics of saccular aneurysms: a possible index for surgical treatment of intracranial aneurysms. Neurosurgery. Jul 1999;45(1):119-29; discussion 129-30. [Medline].
Vespa PM, Gobin YP. Endovascular treatment and neurointensive care of ruptured aneurysms. Crit Care Clin. Oct 1999;15(4):667-84. [Medline].
Wagner KR, Zuccarello M. Local brain hypothermia for neuroprotection in stroke treatment and aneurysm repair. Neurol Res. Apr 2005;27(3):238-45. [Medline].
Wardlaw JM, White PM. The detection and management of unruptured intracranial aneurysms. Brain. 123 (Pt 2):205-21. [Medline].
Yonekawa Y, Kaku Y, Imhof HG, et al. Posterior circulation aneurysms. Technical strategies based on angiographic anatomical findings and the results of 60 recent consecutive cases. Acta Neurochir Suppl (Wien). 1999;72:123-40. [Medline].
Yoshioka H, Inagawa T, Tokuda Y, Inokuchi F. Chronic hydrocephalus in elderly patients following subarachnoid hemorrhage. Surg Neurol. Feb 2000;53(2):119-24; discussion 124-5. [Medline].
Further Reading
Keywords
brain aneurysm, cerebral aneurysm, abnormal arterial dilatation, intracranial aneurysm, berry aneurysm, endovascular procedures, radiological diagnoses, Guglielmi detachable coil, GDC
Follow-up: Brain, Aneurysm