Personalised opening wedge high tibial osteotomy with patient-specific plates and instrumentation accurately controls coronal correction and posterior slope: Results from a prospective first case series

胫骨高位截骨术 医学 冠状面 楔形(几何) 仪表(计算机编程) 骨关节炎 口腔正畸科 地质学 眼科 计算机科学 物理 解剖 光学 操作系统 病理 替代医学
作者
Stefano Zaffagnini,Giacomo Dal Fabbro,Gian Andrea Lucidi,Piero Agostinone,Claudio Belvedere,Alberto Leardini,Alberto Grassi
出处
期刊:Knee [Elsevier BV]
卷期号:44: 89-99 被引量:8
标识
DOI:10.1016/j.knee.2023.07.011
摘要

Background Patient specific devices represent a promising tool to improve accuracy and simplify high tibial osteotomy (HTO) procedures. The current study aims to assess accuracy of the correction of alignment and posterior tibial slope (PTS), and provide patient reported outcomes (PROMs) of a new personalised cutting guide and fixation plate (TOKA) system for HTO in patients with medial osteoarthritis (OA) and varus knee. Methods 25 patients (mean age 54.4 years) with medial OA and varus knee malalignment who underwent HTO with the TOKA system were prospectively evaluated pre-operatively, 1, 3, 6 and 12-months follow-up. Standing long-leg and lateral radiographs of the knee were used to assess the hip-knee-ankle (HKA) angle and the PTS, respectively. Accuracy was defined as the difference in planned minus achieved correction. The patient reported outcomes collected were the KOOS score, EQ5D, KSS score, and VAS pain scores. All statistical analyses were performed using IBM SPSS Statistics for Windows. Results The mean preoperative HKA was 170.7° (SD ± 3.2°); the mean postoperative HKA was 177.4° (SD ± 2.9°). The overall mean difference between planned and achieved correction in terms of HKA was 2.1° (SD ± 2.0°). The mean difference between planned and achieved PTS was 0.2° (SD ± 0.4°). All the assessed PROMs had a significant (p < 0.001) increase from the pre-operative value to postoperative evaluation and showed a significant (p < 0.001) improvement with follow-up time. Conclusions TOKA personalised HTO system showed accurate correction in terms of both coronal and sagittal alignment, and excellent patient reported outcomes. Level of evidence: 4, prospective case series. Registration in public trial registry: registered at ClinicalTrial.gov [NCT04574570].
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