Sawin P D, Dickman C A, Crawford N R, Melton M S, Bichard W D, Sonntag V K
Department of Neurological Surgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona 85013, USA.
J Neurosurg. 2001 Jan;94(1 Suppl):76-81. doi: 10.3171/spi.2001.94.1.0076.
The use of corticosteroid agents during the healing phase after spinal arthrodesis remains controversial. Although anecdotal opinion suggests that corticosteroids may inhibit bone fusion, such an effect has not been substantiated in clinical trials or laboratory investigations. This study was undertaken to delineate the effect of exogenous corticosteroid administration on bone graft incorporation in an experimental model of posterolateral lumbar fusion.
An established, well-validated model of lumbar intertransverse process spinal fusion in the rabbit was used. Twenty-four adult New Zealand white rabbits underwent L5-6 bilateral posterolateral spinal fusion in which autogenous iliac crest bone graft was used. After surgery, the animals were randomized into two treatment groups: a control group (12 rabbits) that received intramuscular injections of normal saline twice daily and a dexamethasone group (12 rabbits) that received intramuscular dexamethasone (0.05 mg/kg) twice daily. After 42 days, the animals were killed and the integrity of the spinal fusions was assessed by radiography, manual palpation, and biomechanical testing. In seven (58%) of the 12 control rabbits, solid posterolateral fusion was achieved. In no dexamethasone-treated rabbits was successful fusion achieved (p = 0.003). Tensile strength and stiffness of excised spinal segments were significantly lower in dexamethasone-treated animals than in control animals (tensile strength 91.4+/-30.6 N and 145.3+/-48.2, respectively, p = 0.004; stiffness 31.4+/-11.6 and 45.0+/-15.2 N/mm, respectively, p = 0.02).
The corticosteroid agent dexamethasone inhibited bone graft incorporation in a rabbit model of single-level posterolateral lumbar spinal fusion, inducing a significantly higher rate of nonunion, compared with that in saline-treated control animals.
脊柱融合术后愈合阶段使用皮质类固醇药物仍存在争议。尽管有观点认为皮质类固醇可能会抑制骨融合,但这种效应在临床试验或实验室研究中尚未得到证实。本研究旨在确定在腰椎后外侧融合的实验模型中外源性给予皮质类固醇对骨移植融合的影响。
采用已建立的、经过充分验证的兔腰椎横突间脊柱融合模型。24只成年新西兰白兔接受L5-6双侧后外侧脊柱融合术,术中使用自体髂嵴骨移植。术后,将动物随机分为两个治疗组:对照组(12只兔)每天两次肌肉注射生理盐水;地塞米松组(12只兔)每天两次肌肉注射地塞米松(0.05mg/kg)。42天后,处死动物,通过X线摄影、手动触诊和生物力学测试评估脊柱融合的完整性。12只对照兔中有7只(58%)实现了坚实的后外侧融合。地塞米松治疗的兔中无一例成功融合(p = 0.003)。地塞米松治疗的动物切除的脊柱节段的拉伸强度和刚度显著低于对照动物(拉伸强度分别为91.4±30.6N和145.3±48.2N,p = 0.004;刚度分别为31.4±11.6和45.0±15.2N/mm,p = 0.02)。
在单节段腰椎后外侧脊柱融合的兔模型中,皮质类固醇药物地塞米松抑制了骨移植融合,与生理盐水治疗的对照动物相比,导致不愈合率显著更高。