Nguyen Michael T B, Cheung Crystal S Y, Hunter David G, Wan Michael J, Gise Ryan
From the Department of Ophthalmology (M.T.B.N., D.G.H., R.G.), Boston Children's Hospital, Boston, Massachusetts, USA; Department of Ophthalmology, Harvard Medical School (M.T.B.N., D.G.H., R.G.), Boston, Massachusetts, USA.
Department of Ophthalmology (C.S.Y.C., M.J.W.), Hospital for Sick Children, Toronto, Ontario, Canada; Department of Ophthalmology, University of Toronto (C.S.Y.C., M.J.W.), Toronto, Ontario, Canada.
Am J Ophthalmol. 2025 Apr;272:1-7. doi: 10.1016/j.ajo.2024.12.025. Epub 2025 Jan 3.
Botulinum toxin is an alternative to conventional strabismus surgery for treatment of acute, acquired, comitant esotropia (AACE). Previous studies suggest that the 2 treatment approaches may be equally effective for 6 months. The purpose of our study was to determine whether botulinum toxin remains as effective as strabismus surgery for 36 months after treatment.
Multicenter, retrospective, nonrandomized, comparative, clinical, noninferiority study.
Setting: Two tertiary care pediatric hospitals.
76 children with AACE followed for at least 36 months after treatment.
Treatment with either botulinum toxin ("BTX group") or strabismus surgery ("surgery group").
Success rate at 36 months (horizontal deviation of 10 prism diopters or less and evidence of binocular vision).
There were 44 patients in the BTX group and 32 patients in the surgery group with a median deviation of 35 PD in both groups (range 10-55). The duration of general anesthesia (6 versus 71 min, P < .0001) and time in the postanesthesia care unit (40 versus 95 min, P < .0001) were significantly shorter in the BTX group. At 36 months, the success rate was 72% in the BTX group and 56% in the surgery group with a similar median deviation and median stereoacuity. BTX was noninferior to surgery at 36 months (95%CI for difference in success rate (BTX minus surgery) was -5% to +38%). At 36 months, the median time from esotropia onset to any intervention was 6.5 months without treatment success and 4 months in those with treatment success (P < .05).
CONCLUSIONS/RELEVANCE: Botulinum toxin was noninferior to strabismus surgery in the treatment of AACE at 36 months while reducing the duration of general anesthesia. Longer delay from esotropia onset to treatment was an independent risk factor for worse sensorimotor outcomes irresepctive of the type of treatment.
肉毒杆菌毒素是治疗急性获得性共同性内斜视(AACE)的传统斜视手术的替代方法。先前的研究表明,这两种治疗方法在6个月内可能同样有效。我们研究的目的是确定治疗36个月后肉毒杆菌毒素是否仍与斜视手术一样有效。
多中心、回顾性、非随机、比较性临床非劣效性研究。
地点:两家三级儿科医院。
76例AACE患儿,治疗后随访至少36个月。
肉毒杆菌毒素治疗(“BTX组”)或斜视手术(“手术组”)。
36个月时的成功率(水平斜视度为10棱镜度或更小且有双眼视觉证据)。
BTX组有44例患者,手术组有32例患者,两组的中位斜视度均为35棱镜度(范围10 - 55)。BTX组的全身麻醉持续时间(6分钟对71分钟,P <.0001)和麻醉后监护病房停留时间(40分钟对95分钟,P <.0001)明显更短。36个月时,BTX组的成功率为72%,手术组为56%,中位斜视度和中位立体视锐度相似。BTX在36个月时不劣于手术(成功率差异(BTX减去手术)的95%置信区间为 - 5%至 + 38%)。36个月时,内斜视发作至任何干预的中位时间在未成功治疗的患者中为6.5个月,在成功治疗的患者中为4个月(P <.05)。
结论/意义:肉毒杆菌毒素在治疗AACE 36个月时不劣于斜视手术,同时缩短了全身麻醉持续时间。内斜视发作至治疗的延迟时间越长是感觉运动预后较差的独立危险因素,与治疗类型无关。