TY - JOUR
T1 - Comparison of the risk of oculomotor nerve deficits between detachable balloons and coils in the treatment of direct carotid cavernous fistulas.
AU - Tsai, Yu-Hsia
AU - Wong, HF
AU - Weng, HH
AU - Chen, YL
PY - 2010
Y1 - 2010
N2 - Among 48 patients with DCCFs treated with endovascular embolization at our institution between March 2004 and May 2009, 38 patients were included in this review. Patients who underwent trapping procedures, a second intervention within 2 weeks, or any procedure that included n-BCA infusion were excluded. Twenty of the enrolled patients were treated with transarterial balloons and the other 18, with GDCs.
Five patients (25%) in the balloon group and none in the coil group had oculomotor nerve deficits within 2 weeks. The rate of procedure-related oculomotor nerve deficit was significantly higher in the balloon group than in the coil group (P = .048). There were no significant differences in terms of procedure-related mortality/morbidity or initial angiographic results between the 2 groups.
The risk of procedure-related oculomotor nerve deficit in the treatment of DCCFs was significantly lower when using a GDC than with a detachable balloon. GDCs may, therefore, be considered as feasible, effective, and safe for DCCFs as detachable balloons.
Transarterial balloon embolization used to be the preferred method for treating DCCFs; however, a strayed, overinflated, or migrated balloon may lead to oculomotor palsy. This investigation compared the use of detachable balloons and GDCs, which were previously used only in cases of balloon-technique failure and are now increasingly used as a first-line treatment for DCCFs, in terms of the risk of oculomotor nerve deficit, mortality/morbidity, and initial angiographic results.
AB - Among 48 patients with DCCFs treated with endovascular embolization at our institution between March 2004 and May 2009, 38 patients were included in this review. Patients who underwent trapping procedures, a second intervention within 2 weeks, or any procedure that included n-BCA infusion were excluded. Twenty of the enrolled patients were treated with transarterial balloons and the other 18, with GDCs.
Five patients (25%) in the balloon group and none in the coil group had oculomotor nerve deficits within 2 weeks. The rate of procedure-related oculomotor nerve deficit was significantly higher in the balloon group than in the coil group (P = .048). There were no significant differences in terms of procedure-related mortality/morbidity or initial angiographic results between the 2 groups.
The risk of procedure-related oculomotor nerve deficit in the treatment of DCCFs was significantly lower when using a GDC than with a detachable balloon. GDCs may, therefore, be considered as feasible, effective, and safe for DCCFs as detachable balloons.
Transarterial balloon embolization used to be the preferred method for treating DCCFs; however, a strayed, overinflated, or migrated balloon may lead to oculomotor palsy. This investigation compared the use of detachable balloons and GDCs, which were previously used only in cases of balloon-technique failure and are now increasingly used as a first-line treatment for DCCFs, in terms of the risk of oculomotor nerve deficit, mortality/morbidity, and initial angiographic results.
KW - Adult
KW - Arteriovenous Fistula/mortality
KW - Arteriovenous Fistula/radiography
KW - Arteriovenous Fistula/therapy
KW - Carotid Artery Diseases/radiography
KW - Carotid Artery, Internal/radiography
KW - Cavernous Sinus/radiography
KW - Cerebral Angiography
KW - Embolization, Therapeutic/adverse effects
KW - Embolization, Therapeutic/instrumentation
KW - Embolization, Therapeutic/mortality
KW - Female
KW - Humans
KW - Male
KW - Middle Aged
KW - Morbidity
KW - Oculomotor Nerve Injuries
KW - Retrospective Studies
KW - Risk Factors
KW - Treatment Outcome
KW - Young Adult
U2 - 10.3174/ajnr.A2009
DO - 10.3174/ajnr.A2009
M3 - Journal Article
C2 - 20150310
SN - 0195-6108
VL - 31
SP - 1123
EP - 1126
JO - American Journal of Neuroradiology
JF - American Journal of Neuroradiology
IS - 6
ER -