首页> 外文期刊>Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA >One-year clinical and MR imaging outcome after partial meniscal replacement in stabilized knees using a collagen meniscus implant
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One-year clinical and MR imaging outcome after partial meniscal replacement in stabilized knees using a collagen meniscus implant

机译:使用胶原蛋白半月板植入物稳定膝关节部分半月板置换后的一年临床和MR成像结果

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Purpose: The purpose of the study was to evaluate the clinical and radiological outcomes after medial/lateral collagen meniscus substitution (CMI) at 12 months postoperatively. Methods: Sixty-seven patients (m:f = 47:20, mean age 36 ± 10 years) underwent arthroscopic CMI after previous subtotal medial (n = 55) or lateral meniscectomy (n = 12) due to persistent joint line pain (n = 25) or to prophylactic reasons (n = 42). Clinical follow-up consisted of IKDC score, Tegner score, Lysholm score, and visual analog scale for pain and satisfaction (preinjury, preoperatively, and 12 months postoperatively; follow-up rate 90 %). MRI scans were analyzed according to the Genovese criteria. Results: Nineteen patients (29 %) showed a normal (A), 35 nearly normal (B), 5 abnormal (C), and 1 patient severely abnormal total IKDC score (D). The median Tegner preinjury score was 7 (range 2-10) and at follow-up 6 (range 2-10). The mean Lysholm score before surgery was 68 ± 20 and 93 ± 9 at follow-up. Preoperatively, the mean VAS pain was 4. 4 ± 3. 1 and 2. 0 ± 1. 0 at follow-up. Clinical failure of the CMI occurred in 3 patients (n = 1 infection, n = 1 failure of the implant, n = 1 chronic synovitis). On MRI, the CMI was completely resorbed in 3 patients (5 %), partially resorbed in 55 (92 %), and entirely preserved in 3 (5 %) patients. In 5 patients (8 %) the CMI was isointense, in 54 (90 %) slightly and 1 (2 %) highly hyperintense. 43 (72 %) patients showed an extrusion of the CMI implant of more than 3 mm. Conclusions: Significant pain relief and functional improvement throughout all scores at 1 year was noted. The CMI undergoes significant remodeling, degradation, resorption, and extrusion in most of the patients. No difference in outcomes between the medial and lateral CMI was observed. Level of evidence: Prospective therapeutic study, Level IV.
机译:目的:本研究的目的是评估术后12个月内/外侧胶原半月板置换(CMI)后的临床和放射学结果。方法:67例患者(m:f = 47:20,平均年龄36±10岁)由于持续的关节痛(n)而在先前的小计内侧(n = 55)或半月板半月板切除术(n = 12)后接受了关节镜CMI。 = 25)或出于预防原因(n = 42)。临床随访包括IKDC评分,Tegner评分,Lysholm评分和视觉模拟评分表,用于评估疼痛和满意度(受伤前,术前和术后12个月;随访率90%)。根据热那亚标准对MRI扫描进行分析。结果:19例患者(29%)表现正常(A),35例几乎正常(B),5例异常(C)和1例严重异常的IKDC总评分(D)。 Tegner损伤前中位评分为7(范围2-10),而随访时为6(范围2-10)。术前平均Lysholm评分为68±20和93±9。术前平均VAS疼痛为4. 4±3. 1和2. 0±1. 0。 CMI的临床衰竭发生在3例患者中(n = 1感染,n = 1植入物衰竭,n = 1慢性滑膜炎)。在MRI上,CMI在3例患者(5%)中被完全吸收,在55例(92%)中被部分吸收,在3例(5%)中被完全保留。在5例患者(8%)中,CMI为等强度,在54例(90%)中为轻度,而1例(2%)为高强度。 43名(72%)患者显示CMI植入物的挤出超过3毫米。结论:在1年的所有评分中,均显示出明显的疼痛缓解和功能改善。在大多数患者中,CMI经历了重大的重塑,降解,吸收和挤压。在内侧和外侧CMI之间未观察到结局差异。证据级别:前瞻性治疗研究,级别IV。

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