Colorado Joint Replacement, Denver, CO; Department of Orthopaedic Surgery, The Johns Hopkins University, Baltimore, MD.
Colorado Joint Replacement, Denver, CO; Department of Orthopaedic Surgery, University of North Carolina, Chapel Hill, NC.
J Arthroplasty. 2021 Jul;36(7):2319-2324. doi: 10.1016/j.arth.2021.01.049. Epub 2021 Jan 23.
Patients with a preoperative varus deformity >8 degrees are at increased risk of aseptic loosening after total knee arthroplasty. This study analyzes the effect of a tibial stem on the rate of aseptic loosening in patients with a severe preoperative varus deformity.
Patients with a preoperative varus deformity of >8 degrees and 2-year minimum follow-up with a stemmed tibial component (n = 67) were matched 1:2 to patients with a similar preoperative varus deformity with a standard tibial component (n = 134). Radiolucent lines were measured on the tibia at 6 weeks, 1 year, and 2 years postoperatively using the Knee Society Radiographic Evaluation System. Failure was defined as revision due to aseptic loosening of the tibial component. Outcomes were evaluated using Student's t-tests and log-rank tests.
Patients with tibial stems had greater preoperative deformity (12.9 vs 11.3 degrees, P = .004). There was no difference in postoperative alignment (1.7 vs 2.1 degrees varus, P = .25) or tibial component angle (1.8 vs 2.1 degrees varus, P = .33). Patients with stems were more likely to have more constraint (44.8% vs 1.5%, P < .001). Progression of radiolucent lines >2 mm was observed in 17.6% (23/134) vs 5.97% (4/67) of patients in the stem group (P = .03). Rates of aseptic loosening were lower in the stem group (0% vs 5.15%, P = .05).
Despite worse preoperative deformity and higher utilization of constraint, tibial stem use in patients with severe preoperative varus deformity resulted in lower rates of aseptic loosening. Prophylactic use of stems in these patients may help increase implant survival.
术前内翻畸形>8 度的患者在全膝关节置换术后发生无菌性松动的风险增加。本研究分析胫骨柄对严重术前内翻畸形患者无菌性松动发生率的影响。
将 67 例术前内翻畸形>8 度且至少随访 2 年、使用带柄胫骨组件的患者与 134 例术前内翻畸形相似、使用标准胫骨组件的患者进行 1:2 匹配。使用膝关节学会放射学评估系统在术后 6 周、1 年和 2 年测量胫骨上的透亮线。因胫骨组件无菌性松动而翻修为失败。使用学生 t 检验和对数秩检验评估结果。
带柄胫骨组患者术前畸形更严重(12.9°比 11.3°,P=0.004)。术后对线无差异(1.7°比 2.1°内翻,P=0.25)或胫骨组件角度无差异(1.8°比 2.1°内翻,P=0.33)。带柄胫骨组患者更有可能采用更高的约束(44.8%比 1.5%,P<0.001)。在胫骨柄组中,有 17.6%(23/134)的患者出现>2mm 的透亮线进展,而在无柄胫骨组中,有 5.97%(4/67)的患者出现(P=0.03)。胫骨柄组的无菌性松动发生率较低(0%比 5.15%,P=0.05)。
尽管术前畸形更严重且采用更高约束的概率更高,但在严重术前内翻畸形患者中使用胫骨柄可降低无菌性松动的发生率。在这些患者中预防性使用胫骨柄可能有助于提高植入物的存活率。