School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Orthopedics and Traumatology, Taipei Veterans General Hospital, Taipei, Taiwan.
BMC Musculoskelet Disord. 2022 Sep 10;23(1):853. doi: 10.1186/s12891-022-05802-y.
Deep surgical site infection (DSSI) is one of the most challenging complications in lumbar fusion surgery. Few investigations examined the effect of vancomycin powder mixed with autogenic bone graft (ABG) and bone substitutes on preventing DSSI in degenerative lumbar fusion surgeries as well as any interference with bony fusion. The aim of the study was to investigate the effects of ABG along with bone substitutes as a local vancomycin delivery system on preventing DSSI in lumbar instrumented fusion and compared with those who did not use vancomycin powder.
From January, 2015 through December, 2015, a one-year prospective study using vancomycin powder mixed with ABG and bone substitute for degenerative lumbar fusion surgeries as vancomycin (V) group, 1 gm vancomycin for 2 and 3-level, and 2 gm for more than 3-level instrumentation. From December, 2013 through December 2014, patients received degenerative lumbar fusion surgeries without using vancomycin before the vancomycin protocol were retrospectively enrolled as non-vancomycin (NV) group. Vancomycin concentration was checked at post-operative days 1 and 3 for both the serum and drainage. Patients' demographic data, microbiology reports, fusion status and functional outcomes were evaluated.
One hundred and ten patients were enrolled prospectively in the V group, and 86 for the NV group. After an average 41 months follow-up (range, 36-54), 3 patients (3.48%) developed postoperative DSSIs in the NV group, thereby requiring revision surgeries and parenteral antibiotics treatment versus no DSSIs (0%, 0/100) in the V group. (p = 0.048). The postoperative serum vancomycin levels were undetectable and no vancomycin related side effects was encountered. The mean vancomycin concentration of drainage at postoperative days 1 and 3 were 517.96 ± 174.4 and 220.14 ± 102.3 μg/mL, respectively. At final follow-up, there was no statistical difference observed in terms of clinical and radiologic outcomes.
Our vancomycin protocol may reduce the incidence of DSSI in degenerative lumbar fusion surgery without affecting bony fusion.
Level III ambispective comparative study.
深部手术部位感染(DSSI)是腰椎融合术最具挑战性的并发症之一。很少有研究调查万古霉素粉末与自体骨移植物(ABG)和骨替代物混合在预防退行性腰椎融合手术中的 DSSI 以及对骨融合的任何干扰方面的效果。本研究旨在探讨 ABG 与骨替代物作为局部万古霉素输送系统在预防腰椎器械融合中的效果,并与未使用万古霉素粉末的患者进行比较。
从 2015 年 1 月至 2015 年 12 月,前瞻性研究使用万古霉素粉末与 ABG 和骨替代物混合治疗退行性腰椎融合术作为万古霉素(V)组,2 级和 3 级各用 1 克万古霉素,3 级以上用 2 克万古霉素。从 2013 年 12 月至 2014 年 12 月,在万古霉素方案之前接受退行性腰椎融合术的患者回顾性纳入未使用万古霉素的非万古霉素(NV)组。术后第 1 天和第 3 天检测血清和引流液中的万古霉素浓度。评估患者的人口统计学数据、微生物学报告、融合状态和功能结果。
前瞻性纳入 V 组 110 例,NV 组 86 例。平均随访 41 个月(范围 36-54 个月)后,NV 组 3 例(3.48%)术后发生深部手术部位感染,需行翻修手术和静脉抗生素治疗,而 V 组无深部手术部位感染(0%,0/100)(p=0.048)。术后血清万古霉素水平无法检测,未发现万古霉素相关副作用。术后第 1 天和第 3 天引流液中的万古霉素平均浓度分别为 517.96±174.4 和 220.14±102.3μg/mL。末次随访时,临床和影像学结果无统计学差异。
我们的万古霉素方案可能降低退行性腰椎融合术深部手术部位感染的发生率,而不影响骨融合。
III 级前瞻性比较研究。