A new test (Sacco Manni test 3) of congenital dysplasia of the HIP: A Cross Sectional and Analytic Study

S. Bernardino
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Abstract

Purpose Or Objective: Without a prompt diagnosis, congenital dysplasia of the hip in newborns can lead severe sequelae. Current screening strategies emphatize the use of ORTOLANI AND BARLOW tests, yet they exhibit low sensibility. The purpose of this study is to evaluate for a new test as a screening tool for congenital dysplasia of the hip. Methods: to evaluate the new test, a cross sectional and analytic study was performed with a non-probabilistic sampling method. Patients with either a positive ORTOLANI AND BARLOW TESTS were evaluated with the new test (Sacco Manni test 3) and hip ultrasounds. Controls were infants With negative ORTOLANI AND BARLOW and SACCOMANNI TESTs and also had an ultrasound performed. Results: CONGENITAL dysplasia of the hip was confirmed in 83 to 130 cases (64%), and 2 of 130 controls (2%). The new test had a sensitivity of 76% AND A specificity of 94% as compared to the ORTOLANI AND BARLOW TESTS (sensitivity 31 to 32 %, specificity 93 to 100% (p inferior to 0,05). Conclusion: this new test could serve as another clinical tool for the initial screening of congenital dysplasia of the hip in in fans or newborns. Its promising results against traditional screening procedures might potentially impact diagnosis and prognosis for patients with congenital dysplasia of hip.
先天性髋关节发育不良的一种新测试(sacacco Manni测试3):横断面和分析研究
目的或目的:如果不及时诊断,新生儿先天性髋关节发育不良可导致严重的后遗症。目前的筛查策略强调使用ORTOLANI和BARLOW测试,但它们表现出低敏感性。本研究的目的是评估一种新的测试作为先天性髋关节发育不良的筛查工具。方法:采用非概率抽样方法进行了横断面分析研究,以评价新的检验方法。ORTOLANI和BARLOW试验阳性的患者用新的试验(Sacco Manni试验3)和髋关节超声进行评估。对照组为ORTOLANI, BARLOW和SACCOMANNI试验阴性的婴儿,也进行了超声检查。结果:先天性髋关节发育不良83 ~ 130例(64%),对照组130例中2例(2%)。与ORTOLANI和BARLOW试验相比,新试验的灵敏度为76%,特异性为94%(灵敏度为31%至32%,特异性为93%至100%)。结论:该方法可作为先天性髋关节发育不良患者或新生儿早期筛查的又一临床工具。它对传统筛查程序的有希望的结果可能潜在地影响先天性髋关节发育不良患者的诊断和预后。
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