Buttaro Martin, Comba Fernando, Piccaluga Francisco
Hip Surgery Unit, Institute of Orthopaedics Carlos E. Ottolenghi, Italian Hospital, Buenos Aires, Argentina.
Clin Orthop Relat Res. 2007 Aug;461:74-80. doi: 10.1097/BLO.0b013e318073c290.
We explored the role of vancomycin-supplemented cancellous bone allografts in hip revision surgery. We evaluated the incorporation of these allografts in 18 pigs' radiographs, histology, and immunohistochemistry. High-quality radiographs, histologic examination, and immunologic expression of metalloproteinase-13 and transforming growth factor-beta 2 indicated vancomycin did not considerably affect bone graft incorporation. Elution, bioactivity, and nephrotoxicity were subsequently tested in 20 patients who underwent hip reconstruction with this method. Local active bactericidal levels of vancomycin reached 1400.5 microg/mL (average 5-point level, 367.19 microg/mL). Vancomycin was present in urine until day 15 without any sign of nephrotoxicity. Clinical analysis was performed in 30 patients whose hips underwent reconstruction with vancomycin-supplemented cancellous bone allograft. At a minimum 2-year followup, infection control was attained in 29 of 30 patients (reinfection rate, 3.3%; 95% confidence interval, 0.08-17%) without evidence of graft resorption. Histologic observations performed in two patients whose hips were reconstructed with this technique were similar to the ones reported in nonsupplemented bone allografts. Our findings encourage the continued use of vancomycin-supplemented bone allografts in reconstructive orthopaedic surgery.
我们探讨了万古霉素补充的松质骨同种异体移植在髋关节翻修手术中的作用。我们通过18头猪的X线片、组织学和免疫组织化学评估了这些同种异体移植的融合情况。高质量的X线片、组织学检查以及金属蛋白酶-13和转化生长因子-β2的免疫表达表明万古霉素对骨移植融合没有显著影响。随后,我们对20例采用该方法进行髋关节重建的患者进行了洗脱、生物活性和肾毒性测试。万古霉素的局部活性杀菌水平达到1400.5微克/毫升(平均5个时间点水平,367.19微克/毫升)。万古霉素在尿液中一直存在至第15天,没有任何肾毒性迹象。我们对30例采用万古霉素补充的松质骨同种异体移植进行髋关节重建的患者进行了临床分析。在至少2年的随访中,30例患者中有29例实现了感染控制(再感染率为3.3%;95%置信区间为0.08-17%),且没有移植骨吸收的证据。对2例采用该技术进行髋关节重建的患者进行的组织学观察与未补充骨同种异体移植的报告结果相似。我们的研究结果鼓励在重建骨科手术中继续使用万古霉素补充的骨同种异体移植。