Crawford Alvin H, Strub William M, Lewis Ronald, Gabriel Keith R, Billmire David A, Berger Thomas, Crone Kerry
Department of Pediatric Orthopaedic Surgery, Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, Ohio 45229-3039, USA.
Spine (Phila Pa 1976). 2003 Feb 1;28(3):260-6. doi: 10.1097/01.BRS.0000042234.98512.BE.
A retrospective cohort study was used to investigate a group of neonates with myelomeningocele who had a kyphectomy performed in conjunction with dural sac closure during the first few days of life.
To assess the effectiveness of operative intervention in the neonatal period to correct the kyphotic deformity in the patient with myelomeningocele and to monitor its long-term results.
Orthopedic management originally focused on the immediate treatment of the kyphotic deformity in the infant with myelomeningocele. However, there has been a movement toward postponing surgical treatment of the kyphos until a later age. This study included the longest follow-up of the largest group of neonates that a single surgeon has managed surgically since the treatment of this condition was originally described.
The radiographic and clinical results for all neonates treated with a kyphectomy at the time of myelomeningocele closure between 1980 and 2000 were analyzed.
Neonatal kyphectomy was performed on nine males and two females. The average preoperative kyphotic angle measured 67 degrees. The average initial correction was 77 degrees, and the average loss of correction at follow-up assessment was 55 degrees. There were no serious complications, and wound closure was successful in all patients. One patient required a repeat kyphectomy and posterior spinal fusion at the age of 9 years and 2 months. The average follow-up period was 7 years and 4 months (range 44-174 months).
Kyphectomy performed at the time of dural sac closure in the neonate is a safe procedure with excellent initial correction. Eventual recurrence is expected despite the procedure. However, it occurs in the form of a longer, more rounded deformity that is less technically demanding.
采用回顾性队列研究,调查一组患有脊髓脊膜膨出的新生儿,他们在出生后的头几天接受了椎体后凸切除术并同时进行硬脊膜囊闭合术。
评估新生儿期手术干预矫正脊髓脊膜膨出患者脊柱后凸畸形的有效性,并监测其长期效果。
骨科治疗最初侧重于对患有脊髓脊膜膨出的婴儿的脊柱后凸畸形进行即时治疗。然而,现在有一种趋势是将脊柱后凸的手术治疗推迟到较晚年龄。本研究纳入了自最初描述这种疾病的治疗方法以来,由单一外科医生手术治疗的最大一组新生儿的最长随访数据。
分析了1980年至2000年间所有在脊髓脊膜膨出闭合时接受椎体后凸切除术的新生儿的影像学和临床结果。
9名男性和2名女性接受了新生儿椎体后凸切除术。术前平均脊柱后凸角度为67度。平均初始矫正角度为77度,随访评估时平均矫正丢失角度为55度。无严重并发症,所有患者伤口闭合均成功。1例患者在9岁2个月时需要再次进行椎体后凸切除术和后路脊柱融合术。平均随访时间为7年4个月(范围44 - 174个月)。
新生儿硬脊膜囊闭合时进行椎体后凸切除术是一种安全的手术,初始矫正效果良好。尽管进行了该手术,但最终仍会复发。然而,复发表现为一种更长、更圆的畸形,技术要求较低。