The causes of failure of lumbar transpedicular spinal instrumentation and fusion - A prospective study

被引:19
|
作者
Hadjipavlou, A
Enker, P
Dupuis, P
Katzman, S
Silver, J
机构
[1] Department of Orthopaedics, University of Texas, Galveston, IN
[2] Department of Orthopaedic Surgery, North Shore University Hospital, Manhassett, NY
[3] Department of Orthopaedic Surgery, Sir Mortimer B Davis Jewish Gen. H., McGill University, Montreal, Que.
[4] Department of Orthopaedics, Medical Centre of Port St Lucie, Florida
[5] Maimonides Medical Center, New York, NY
[6] Department of Orthopaedics, University of Texas, Medical Branch, Galveston
关键词
D O I
10.1007/s002640050024
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
A prospective study was made of 101 patients who underwent transpedicular spinal instrumentation and fusion of the lumbar spine. All were reviewed by art independent observer: The objectives were to determine the causes of clinical failure and to recommend preventive measures. Forty-two primary and 59 revision operations were performed. The average age was 46 years and follow up 4 years. The variable screw placement and Cotrel-Dubousset systems were used Posterior lumbar interbody fusion was carried out in 24 patients. The outcome was satisfactory after primary operations in 67% and after revisions in 46%. Nerve root injuries due to screw placement occurred in 4% (2% permanent and 2% transient). Instrumentation-induced foraminal stenosis developed in 2%. Proper surgical technique can avoid these complications. Predictive factors for failure are: abnormal psychology, symptomatic epidural fibrosis, inadequate decompression of lateral stenosis, surgical complications and the use of allografts.
引用
收藏
页码:35 / 42
页数:8
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