Jk. Song et al., Surgical and endovascular treatment of spinal dural arteriovenous fistulas: long-term disability assessment and prognostic factors, J NEUROSURG, 94(2), 2001, pp. 199-204
Object. The authors assessed clinical outcomes of patients with treated spi
nal dural arteriovenous fistulas (DAVFs) and investigated prognostic factor
s.
Methods. Thirty consecutive patients with spinal DAVFs were treated at the
authors' institution during the past 15 years: seven underwent surgery; sev
en underwent surgery after failed embolization; and 16 underwent embolizati
on alone. The outcomes of gait and micturition disability were analyzed. Fo
llow up averaged 3.4 years (range month-11.8 years). Age, duration of sympt
oms, pre and postintervention magnetic resonance (MR) imaging findings, and
preintervention disability were correlated with outcome.
Seventeen patients (57%) experienced improved gait, 12 (40%) were unchanged
, and one (3%) was worse. In 11 patients (37%) micturition function was imp
roved, in 15 (50%) it was unchanged, and in four (13%) it was worse. Gait d
isability, as measured by the Aminoff-Logue Scale, was significantly improv
ed after treatment, from 3.4 +/- 1.4 (average +/- standard deviation) to 2.
7 +/- 1.5 (p = 0.007). Mean micturition disability scores decreased, but no
t significantly, from 1.9 +/- 1 to 1.6 +/- 1.1 (p = 0.20). Preintervention
gait disability was not associated with improvement except for patients wit
h Aminoff-Logue Scale Grade 4 disability (eight of nine improved; p = 0.024
). For patients treated within 13 months of symptom onset, mean micturition
disability decreased (p = 0.035). No association was found between clinica
l improvement and age, a symptom duration less than 30 months, or pre- and
postintervention MR imaging-documented spinal cord edema.
Conclusions. Spinal DAVF treatment significantly improved patients' mean ga
it disability score by almost one grade at last follow up. The mean micturi
tion disability score was not significantly improved, unless treatment was
performed within 13 months of symptom onset. Longer and more uniform follow
-up study is needed to determine if improved and stabilized clinical outcom
es are sustained.