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A new anatomic locking plate for the treatment of posterolateral tibial plateau fractures

机译:一种新的解剖型锁定钢板治疗胫骨后外侧平台骨折

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Posterolateral tibial plateau fractures have become more common, and their treatment is of great importance to knee function. Additionally, there is no available literature detailing specialized anatomic locking plate for tibial plateau fractures. Therefore, the aim of the study was to evaluate the safety and clinical efficacy of an innovative anatomic locking plate for treatment of posterolateral tibial plateau fractures. Between March 2014 and January 2016, 12 patients with posterolateral tibial plateau fracture underwent surgery with the anatomic locking plate for the posterolateral tibial plateau via the posterolateral approach. Relevant operational data for clinical evaluation were collected. The mean follow-up time was 26?months, and the mean age was 35?years for 12 patients. The mean interval between the time of injury and the surgery was 6.1?days. Radiological fracture union was evident in all patients at 12?weeks. During surgery, the blood loss ranged from 100 to 300?mL, and the duration ranged from 55 to 90?min. The Tegner–Lysholm functional score ranged from 85 to 97 at the final follow-up. Moreover, the final Rasmussen functional score ranged from 25 to 29, and Rasmussen anatomical score ranged from 13 to 18. The newly designed anatomic locking plate for the posterolateral tibial plateau provided adequate fixation along the posterolateral tibial plateau. It proved to be safe and effective in a small-sample-size population (12 patients) during a 12- to 34-month follow-up.
机译:胫骨平台后外侧骨折已变得更加普遍,其治疗对膝关节功能至关重要。另外,没有可利用的文献详细描述用于胫骨平台骨折的专用解剖锁定板。因此,该研究的目的是评估一种创新的解剖型锁定板治疗胫骨后外侧平台骨折的安全性和临床疗效。在2014年3月至2016年1月之间,通过后外侧入路对12例胫骨后外侧平台骨折患者进行了解剖锁定钢板治疗胫骨后外侧平台的手术。收集了用于临床评估的相关操作数据。 12例患者的平均随访时间为26个月,平均年龄为35岁。受伤时间与手术时间之间的平均间隔为6.1天。 12周时所有患者均出现放射性骨折愈合。在手术过程中,失血量为100至300?mL,持续时间为55至90?min。在最后的随访中,Tegner-Lysholm功能评分从85到97不等。此外,最终的拉斯穆森氏功能评分为25至29,拉斯穆森氏解剖评分为13至18。新设计的胫骨后外侧解剖锁定板沿胫骨后外侧高原提供了充分的固定。在12到34个月的随访中,它被证明对小样本人群(12例患者)是安全有效的。

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