OBJECTIVE: To investigate the long-term surgical outcome of Brown syndrome using an intraoperative adjustable superior oblique (SO) tendon suture spacer. DESIGN: Retrospective case series. PARTICIPANTS: Thirteen patients with congenital unilateral Brown syndrome operated on at the Wolfe Eye Clinic from 2001 through 2007. METHODS: Retrospective analysis of consecutive patients managed with the SO suture spacer followed up for at least 10 months. MAIN OUTCOME MEASURES: Surgical intervention for patients having severe or moderate forms of Brown syndrome. Postoperative effect on abnormal head posture, vertical strabismus in primary gaze, vertical strabismus into affected side gaze, and elevation in adduction. RESULTS: The mean duration of follow-up was 30 months (range, 10-72 months). Abnormal head posture improved from 13 degrees (range, 0 degrees -30 degrees ) to 0.4 degrees (range, 0 degrees -5 degrees ). Vertical strabismus in primary gaze improved from -10Delta (range, 0Delta to -35Delta) to 2.8Delta (range, -16Delta to 16Delta). Vertical in side gaze improved from -20Delta (range, -35Delta to -8Delta) to -1.5Delta (range, -20Delta to 18Delta). Elevation in adduction improved from -3.5 (range, -4 to -2) to -0.4 (range, -2 to 4). Four patients had an overcorrection and 2 patients experienced an increasing late effect. In no patient did a late under correction develop. CONCLUSIONS: The SO suture spacer procedure alleviated abnormal head positions in patients with Brown syndrome by improving vertical strabismus in primary position and in the affected field of gaze while avoiding overcorrection in contralateral gaze. The benefits of the procedure persisted over time.
OBJECTIVE: To investigate the long-term surgical outcome of Brown syndrome using an intraoperative adjustable superior oblique (SO) tendon suture spacer. DESIGN: Retrospective case series. PARTICIPANTS: Thirteen patients with congenital unilateral Brown syndrome operated on at the Wolfe Eye Clinic from 2001 through 2007. METHODS: Retrospective analysis of consecutive patients managed with the SO suture spacer followed up for at least 10 months. MAIN OUTCOME MEASURES: Surgical intervention for patients having severe or moderate forms of Brown syndrome. Postoperative effect on abnormal head posture, vertical strabismus in primary gaze, vertical strabismus into affected side gaze, and elevation in adduction. RESULTS: The mean duration of follow-up was 30 months (range, 10-72 months). Abnormal head posture improved from 13 degrees (range, 0 degrees -30 degrees ) to 0.4 degrees (range, 0 degrees -5 degrees ). Vertical strabismus in primary gaze improved from -10Delta (range, 0Delta to -35Delta) to 2.8Delta (range, -16Delta to 16Delta). Vertical in side gaze improved from -20Delta (range, -35Delta to -8Delta) to -1.5Delta (range, -20Delta to 18Delta). Elevation in adduction improved from -3.5 (range, -4 to -2) to -0.4 (range, -2 to 4). Four patients had an overcorrection and 2 patients experienced an increasing late effect. In no patient did a late under correction develop. CONCLUSIONS: The SO suture spacer procedure alleviated abnormal head positions in patients with Brown syndrome by improving vertical strabismus in primary position and in the affected field of gaze while avoiding overcorrection in contralateral gaze. The benefits of the procedure persisted over time.