From the ISICO (Italian Scientific Spine Institute), Milan, Italy (FDF, FZ, SD); Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy (SN); and IRCCS Fondazione Don Gnocchi, Milan, Italy (SN).
Am J Phys Med Rehabil. 2018 May;97(5):346-356. doi: 10.1097/PHM.0000000000000861.
The aim of the study was to provide a meta-analysis of current literature concerning the natural history of idiopathic scoliosis during growth.
A comprehensive search of Medline, Embase, And Scopus databases was conducted up to November 2016. Eligible works were prospective or retrospective studies that enrolled patients with infantile idiopathic scoliosis, juvenile idiopathic scoliosis, or adolescent idiopathic scoliosis, followed up without any treatment from the time of detection. A meta-analysis for proportion was performed. The following studies were grouped per diagnosis: infantile idiopathic scoliosis, juvenile idiopathic scoliosis, and adolescent idiopathic scoliosis.
Of the 1797 citations screened, we assessed 61 full-text articles and included 13 of these (2301 participants). Three studies included infantile idiopathic scoliosis patients (347 participants), five studies included a mixed population of juvenile idiopathic scoliosis and adolescent idiopathic scoliosis (1330 participants), and five studies included adolescent idiopathic scoliosis patients only (624 participants). The random pooled estimated progression rate was 49% (95% confidence interval = 1%-97%) for infantile idiopathic scoliosis, 49% in a mixed group of patients affected by juvenile idiopathic scoliosis or adolescent idiopathic scoliosis (95% confidence interval = 19%-79%), and 42% in adolescent idiopathic scoliosis (95% confidence interval = 11%-73%).
During growth, idiopathic scoliosis tends to progress in a high percentage of cases. The progression rate varies according to the age at diagnosis, with infantile scoliosis being the most unpredictable. There are many confounders, such as age, Risser sign and baseline Cobb angles that were not consistent among studies, making the data very heterogeneous.
本研究旨在对当前关于特发性脊柱侧凸生长过程中自然史的文献进行荟萃分析。
对 Medline、Embase 和 Scopus 数据库进行了全面检索,检索时间截至 2016 年 11 月。纳入标准为前瞻性或回顾性研究,纳入患者为婴儿型特发性脊柱侧凸、青少年特发性脊柱侧凸或青少年特发性脊柱侧凸,自检出后未接受任何治疗进行随访。进行了比例的荟萃分析。根据诊断对以下研究进行分组:婴儿型特发性脊柱侧凸、青少年特发性脊柱侧凸和青少年特发性脊柱侧凸。
在筛选出的 1797 条引用文献中,我们评估了 61 篇全文文章,并纳入了其中的 13 篇(2301 名参与者)。有 3 项研究纳入了婴儿型特发性脊柱侧凸患者(347 名参与者),5 项研究纳入了混合了青少年特发性脊柱侧凸和青少年特发性脊柱侧凸患者的群体(1330 名参与者),5 项研究仅纳入了青少年特发性脊柱侧凸患者(624 名参与者)。随机汇总估计的进展率为婴儿型特发性脊柱侧凸为 49%(95%置信区间=1%-97%),混合组青少年特发性脊柱侧凸或青少年特发性脊柱侧凸患者为 49%(95%置信区间=19%-79%),青少年特发性脊柱侧凸为 42%(95%置信区间=11%-73%)。
在生长过程中,特发性脊柱侧凸在很大比例的病例中倾向于进展。进展率因诊断时的年龄而异,婴儿型脊柱侧凸最具不可预测性。存在许多混杂因素,如年龄、Risser 征和基线 Cobb 角在研究之间并不一致,这使得数据非常异质。