P. A. Petersen, R. M. Marcon, O. B. Letaif, R. G. Oliveira, T. E. Passos de Barros Filho, A. F. Cristante, Spine Group, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
R. M. Marcon, O. B. Letaif, M. A. Mello Santos, A. F. Cristante, Associação de Assistência à Criança Deficiente, Hospital Abreu Sodré, São Paulo, Brazil.
Clin Orthop Relat Res. 2020 Jan;478(1):104-111. doi: 10.1097/CORR.0000000000000976.
Lumbar kyphosis is a complex spinal deformity occurring in approximately 8% to 20% of patients with myelomeningocele. The resulting gibbosity may cause pressure ulcers, difficulty lying down in the supine position and sitting on the ischia without support, decreasing quality of life (QOL). Surgery is generally performed to correct kyphosis and maintain vertebral alignment, but high complication rates have been reported. Despite satisfactory radiological results, the impact of surgery and its complications on health-related QOL (HRQOL) has not yet been established.
QUESTIONS/PURPOSES: Among children with myelomeningocele undergoing corrective surgery for lumbar kyphosis: (1) What is the risk of complications and reoperation after this procedure? (2) Does this procedure improve HRQOL scores in these patients?
Between 2012 and 2013, five surgeons at three centers treated 32 patients for myelomeningocele-related kyphosis with kyphectomy and posterior instrumentation. During that period, all surgeons used the same indications for the procedure, which were progressive postural decompensation and chronic ulceration at the apex of the deformity. Data were prospectively collected, and all patients who underwent surgery were considered in this retrospective study. The legal guardians of one patient declined to sign the informed consent form, resulting in 31 patients included. A total of 9.7% (3 of 31) were lost to follow-up before the 2-year period, and the remaining 90.3% (28 of 31) were seen at a mean of 3 years (± 9 months) after surgery. The average age was 10 years, 7 months (± 21 months) at the time of surgery. The patients had a mean kyphosis angle of 130° ± 36° before surgery. This technique involved posterior fixation using S-shaped rods inserted through the foramina of S1 and pedicle screws inserted in the thoracic spine. The patients' caregivers answered both the generic and specific (neuromuscular module) Pediatric Quality of Life Inventory questionnaires preoperatively and 2 years postoperatively. The minimum clinically important difference (MCID) considered for the instruments used was 5.
Reoperation was performed in 68% of patients (19 of 28), mostly to treat deep infection. In all, 18% of patients (five of 28) underwent implant removal to control infection. Eleven percent (three of 28) had a loss of reduction and pseudarthrosis. The HRQOL increased from 71 ± 11 preoperatively to 76 ± 10 postoperatively (p < 0.001), resulting in a 5-point increase (95% CI 3 to 7) in the generic questionnaire score and from 71 ± 13 to 79 ± 11 (p < 0.001), resulting in an 8-point increase (95% CI 5 to 10) in the neuromuscular Paediatric Quality of Life Inventory questionnaire score, mainly in the physical health domain on both questionnaires.
Kyphectomy was associated with a high risk of complications and reoperations and did not seem to deliver a substantial clinical benefit for patients who underwent the procedure. Most of our HRQOL score improvements were below the minimum clinically important difference for the Pediatric Quality of Life Inventory questionnaires. Although it seems that surgeons lack a better surgical alternative when facing the challenging health impairments these patients suffer, efforts should be made to improve the technique and reduce surgical complications. Additionally, patients and caregivers should be advised of the high reoperation rate and notified that the procedure may not result in a better QOL and should thus be avoided when possible. Future studies should verify whether decreasing the complication rate could imply improvement in the HRQOL of these patients after surgery.
Level IV, therapeutic study.
腰椎后凸是一种复杂的脊柱畸形,约发生在 8%至 20%的脊髓脊膜膨出患者中。由此产生的畸形可能导致压疮,仰卧位和坐骨无支撑坐下困难,降低生活质量(QOL)。一般通过手术来矫正脊柱后凸并维持脊柱的排列,但已有报道手术并发症发生率较高。尽管影像学结果满意,但手术及其并发症对健康相关生活质量(HRQOL)的影响尚未确定。
问题/目的:在接受腰椎后凸矫正手术的脊髓脊膜膨出患儿中:(1)该手术的并发症和再次手术风险如何?(2)该手术是否能改善这些患者的 HRQOL 评分?
2012 年至 2013 年,三个中心的 5 位外科医生采用后路截骨和脊柱内固定治疗 32 例与脊髓脊膜膨出相关的脊柱后凸。在此期间,所有外科医生都采用相同的手术适应证,即脊柱进行性后凸和畸形顶点慢性溃疡。前瞻性收集数据,所有接受手术的患者均纳入本回顾性研究。一名患者的法定监护人拒绝签署知情同意书,导致 31 名患者入组。9.7%(3/31)的患者在 2 年随访前失访,其余 90.3%(28/31)的患者在术后平均 3 年(±9 个月)时接受随访。平均年龄为 10 岁,7 个月(±21 个月)时接受手术。患者术前的脊柱后凸角平均为 130°±36°。该技术采用 S 形棒经 S1 椎间孔插入和胸椎椎弓根螺钉固定。患者的照护者在术前和术后 2 年均回答通用和特定(神经肌肉模块)小儿生活质量问卷。所使用的工具的最小临床重要差异(MCID)被认为是 5。
68%(19/28)的患者进行了再次手术,主要是为了治疗深部感染。28%的患者(5/28)因感染而取出了植入物。11%的患者(3/28)出现了复位丢失和假关节。HRQOL 从术前的 71±11 分增加到术后的 76±10 分(p<0.001),通用问卷评分增加了 5 分(95%CI 3 到 7),神经肌肉小儿生活质量问卷评分从 71±13 分增加到 79±11 分(p<0.001),增加了 8 分(95%CI 5 到 10),主要在两个问卷的生理健康领域。
后路截骨术与较高的并发症和再次手术风险相关,对接受该手术的患者似乎没有带来实质性的临床获益。我们的大多数 HRQOL 评分改善都低于小儿生活质量问卷的最小临床重要差异。尽管似乎当面对这些患者所遭受的具有挑战性的健康损害时,外科医生缺乏更好的手术替代方案,但应努力改进技术并减少手术并发症。此外,应告知患者及其照护者再次手术率较高,并告知他们该手术可能不会提高 QOL,因此在可能的情况下应避免进行该手术。未来的研究应验证是否降低并发症发生率可以改善这些患者术后的 HRQOL。
IV 级,治疗性研究。