Radiographic Outcome Following Treatment of Residual Hip Dysplasia with Pemberton Versus Salter Osteotomy: Comparison of Results in Patients Followed to Skeletal Maturity.

IF 4.4 1区 医学 Q1 ORTHOPEDICS
Daniel J Sucato, Case E Brabham, Adriana De La Rocha, David A Podeszwa, Lori A Karol
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引用次数: 0

Abstract

Background: Salter osteotomy (SO) and Pemberton acetabuloplasty (PA) are procedures to treat skeletally immature patients with developmental dysplasia of the hip (DDH). The purpose of this study was to compare the radiographic results and rate of residual dysplasia (RD) after treatment with SO and with PA.

Methods: This was a retrospective analysis of pediatric patients treated with either SO or PA for DDH between 1980 and 2013 who were skeletally mature at the time of follow-up. The preoperative and postoperative acetabular index (AI) and postoperative lateral center-edge angle (LCEA) and anterior center-edge angle (ACEA) were collected. RD was defined as an LCEA or ACEA of <20° or an acetabular inclination (AIn) of >15° at skeletal maturity. Continuous variables were compared between treatment groups with 2-sample t tests, and categorical variables were compared using chi-square tests. Multivariable analysis was used to identify risk factors for RD with p < 0.05.

Results: The study included 113 hips in 102 patients with a mean follow-up of 10.5 years. The SO group had 73 hips treated at a mean patient age of 5.4 years, and the PA group had 40 hips treated at a mean age of 5.3 years. The preoperative AI did not differ between the treatment groups (32.2° versus 31.3°, p = 0.658), nor did the immediate postoperative AI (20.0° versus 20.2°, p = 0.459). At the time of final follow-up, the SO group had a significantly smaller AIn (8.6° versus 13.2°, p = 0.001), a trend toward a greater LCEA (26.2° versus 21.6°, p = 0.056), and a similar ACEA (24.1° versus 26.1°, p = 0.808). By the abovementioned definition, 36 hips (31.9%) had evidence of RD, with a lower rate in the SO group (26.0% versus 42.5%, p = 0.07). Patients who had a positive family history of hip dysplasia were more likely to have RD (odds ratio = 4.311, 95% confidence interval = 1.125 to 16.528).

Conclusions: Patients with RD could be effectively treated with either SO or PA, with overall good radiographic outcomes. However, SO achieved a better AI and may thus yield better long-term health of the affected hip.

Level of evidence: Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.

用Pemberton和Salter截骨术治疗残余髋关节发育不良的放射学结果:骨骼成熟患者随访结果比较。
背景:Salter截骨术(SO)和Pemberton髋臼成形术(PA)是治疗骨骼发育不成熟的髋关节发育不良(DDH)患者的手术。本研究的目的是比较SO和PA治疗后的影像学结果和残余发育不良(RD)率:这是一项回顾性分析,研究对象是1980年至2013年间接受SO或PA治疗的DDH儿科患者,这些患者在随访时骨骼已发育成熟。收集了术前和术后髋臼指数(AI)、术后外侧中心边缘角(LCEA)和前侧中心边缘角(ACEA)。RD的定义是骨骼成熟时LCEA或ACEA达到15°。治疗组间连续变量的比较采用 2 样本 t 检验,分类变量的比较采用卡方检验。采用多变量分析来确定P<0.05的RD风险因素:研究包括102名患者的113个髋关节,平均随访时间为10.5年。SO组有73个髋关节接受了治疗,患者平均年龄为5.4岁;PA组有40个髋关节接受了治疗,患者平均年龄为5.3岁。治疗组之间的术前AI没有差异(32.2°对31.3°,P = 0.658),术后即刻AI也没有差异(20.0°对20.2°,P = 0.459)。在最终随访时,SO 组的 AIn 明显较小(8.6°对 13.2°,p = 0.001),LCEA 有增大的趋势(26.2°对 21.6°,p = 0.056),ACEA 相似(24.1°对 26.1°,p = 0.808)。根据上述定义,36 个髋关节(31.9%)有 RD 证据,其中 SO 组的比率较低(26.0% 对 42.5%,p = 0.07)。有阳性髋关节发育不良家族史的患者更有可能患有RD(几率比=4.311,95%置信区间=1.125至16.528):RD患者可以通过SO或PA得到有效治疗,且总体放射学效果良好。结论:RD患者接受SO或PA治疗均可获得有效的影像学效果,但SO获得的AI效果更好,因此可改善受影响髋关节的长期健康状况:证据等级:治疗三级。有关证据级别的完整描述,请参阅 "作者须知"。
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来源期刊
CiteScore
8.90
自引率
7.50%
发文量
660
审稿时长
1 months
期刊介绍: The Journal of Bone & Joint Surgery (JBJS) has been the most valued source of information for orthopaedic surgeons and researchers for over 125 years and is the gold standard in peer-reviewed scientific information in the field. A core journal and essential reading for general as well as specialist orthopaedic surgeons worldwide, The Journal publishes evidence-based research to enhance the quality of care for orthopaedic patients. Standards of excellence and high quality are maintained in everything we do, from the science of the content published to the customer service we provide. JBJS is an independent, non-profit journal.
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