D'Amato C R, Griggs S, McCoy B
Department of Orthopaedic Surgery, Brown University School of Medicine, Providence, Rhode Island, USA. Charles_D'
Spine (Phila Pa 1976). 2001 Sep 15;26(18):2006-12. doi: 10.1097/00007632-200109150-00014.
A prospective study was conducted of 102 consecutive female patients with adolescent idiopathic scoliosis. Those patients with Risser 0, 1, and 2 met the criteria for inclusion and were treated only with the Providence brace.
To report the authors' experience with a hypercorrective nighttime brace and to evaluate the results with respect to risk factors for progression. Second, the study compares results with expectations from the natural history as reported by others.
Compliance with full-time brace treatment for adolescent idiopathic scoliosis has been a problem. Since the introduction of the Milwaukee brace, alternatives such as low-profile braces, reduced wearing schedules, and nighttime only bracing have been tried. However, many factors influence the success or failure besides compliance. These include in-brace correction, brace design, and the orthotist's skills. This is the first report of the results of treatment with a new nighttime brace that is made with CAD/CAM technology that can achieve higher initial in-brace corrections than other reported methods.
Results were analyzed with respect to curve size, curve pattern, maturity, and level of the primary curve apex. Both compliant and noncompliant patients were included in the analysis. A univariate analysis was done on those factors thought to influence success with bracing using the Pearson chi2 test.
The average initial in-brace correction with a supine radiograph was 96% for major curves and 98% for minor curves. Seventy-five patients (74%) did not progress >5 degrees and 27 patients (26%) progressed > or =6 degrees or went on to surgery. Twenty-nine percent of Risser 0 or 1 patients progressed and 17% of patients Risser 2 progressed. The risk of progression anticipated by natural history data, which included all curve patterns, was 68% for Risser 0 and 1 and 23% for Risser 2. Risser 3 and 4 patients were excluded from the study. Seventy-six percent of patients with curve apexes between T8 and L1 had successful outcomes using the Providence brace. This is compared with a 74% success rate in the prospective Scoliosis Research Society study of patients wearing a thoraco lumbar sacral orthosis for 16 hours per day with curve apexes between T8 and L1. With the Providence brace, 63% of thoracic curves and 65% of double curves were successful. Ninety-four percent of lumbar curves and 93% of thoracolumbar curves were successful.
Excellent initial in-brace correction of adolescent idiopathic scoliosis was observed with this computer-designed and manufactured recumbent brace. Patients with high apex curves cephalad to T8 (n = 31) had a success rate of 61% compared with a success rate of 79% (n = 71) if the apex was at or below T9. Compared with previous natural history and the prospective study data, the Providence brace is effective in preventing progression of adolescent idiopathic scoliosis for curves <35 degrees. It was effective for larger curves with a low apex. The authors' experience with patients with curves >35 degrees (n = 8) is too small to validate its effectiveness for larger curves with a higher apex.
对102例连续的青少年特发性脊柱侧凸女性患者进行了一项前瞻性研究。那些Risser分级为0、1和2级的患者符合纳入标准,仅接受普罗维登斯支具治疗。
报告作者使用一种过度矫正夜间支具的经验,并评估与进展危险因素相关的结果。其次,该研究将结果与其他人报告的自然病史预期结果进行比较。
青少年特发性脊柱侧凸患者对全时支具治疗的依从性一直是个问题。自密尔沃基支具问世以来,人们尝试了多种替代方法,如低轮廓支具、缩短佩戴时间以及仅夜间佩戴支具等。然而,除了依从性之外,许多因素会影响治疗的成败。这些因素包括支具内矫正、支具设计以及矫形师的技术。这是关于一种采用CAD/CAM技术制造的新型夜间支具治疗结果的首次报告,该支具能够实现比其他报告方法更高的初始支具内矫正。
针对曲线大小、曲线类型、成熟度以及主曲线顶点水平对结果进行了分析。分析纳入了依从和不依从的患者。使用Pearson卡方检验对那些被认为会影响支具治疗成功的因素进行了单因素分析。
仰卧位X线片显示,主曲线的平均初始支具内矫正为96%,次曲线为98%。75例患者(74%)进展未超过5度,27例患者(26%)进展超过或等于6度或接受了手术。Risser 0或1级患者中有29%进展,Risser 2级患者中有17%进展。自然病史数据预期的进展风险,包括所有曲线类型,Risser 0和1级为68%,Risser 2级为23%。Risser 3和4级患者被排除在研究之外。曲线顶点在T8和L1之间的患者中,76%使用普罗维登斯支具获得了成功结果。相比之下,脊柱侧凸研究学会的前瞻性研究中,每天佩戴胸腰骶矫形器16小时、曲线顶点在T8和L1之间的患者成功率为74%。使用普罗维登斯支具时,63%的胸段曲线和65%的双主曲线治疗成功。94%的腰段曲线和93%的胸腰段曲线治疗成功。
使用这种计算机设计和制造的卧位支具观察到青少年特发性脊柱侧凸的初始支具内矫正效果极佳。顶点位于T8上方的高顶点曲线患者(n = 31)成功率为61%,而顶点在T9或以下的患者成功率为79%(n = 71)。与先前的自然病史和前瞻性研究数据相比,普罗维登斯支具对小于35度的曲线有效预防青少年特发性脊柱侧凸进展。对于低顶点的较大曲线也有效。作者对曲线大于35度患者(n = 8)的经验太少,无法验证其对高顶点较大曲线的有效性。