TY - JOUR
T1 - The incidence of adjacent segment disease after lumbar discectomy
T2 - A study of 751 patients
AU - Bydon, Mohamad
AU - Macki, Mohamed
AU - Kerezoudis, Panagiotis
AU - Sciubba, Daniel M.
AU - Wolinsky, Jean Paul
AU - Witham, Timothy F.
AU - Gokaslan, Ziya L.
AU - Bydon, Ali
N1 - Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Introduction The objective of this study is to determine the incidence and prognostic factors of adjacent segment disease (ASD) following first-time lumbar discectomy (LD). Methods We retrospectively reviewed all neurosurgical patients who underwent first-time LD for degenerative lumbar disease from 1990 to 2012. ASD was defined as a clinical and radiographic progression of degenerative spinal disease that required surgical decompression (with or without fusion) at the level above or below the index discectomy. Adjusted odds ratios were calculated from multivariable logistical regression controlling for sex and age, as well as postoperative sensory deficit, motor deficit, back pain, neurogenic claudication, and radiculopathy. Results Of the 751 patients who underwent single-level LD, the cumulative reoperation rate for degenerative spinal disease was 10.79%. The incidence of ASD requiring reoperation was 4% over 3.11 years. More specifically, the incidence of adjacent level discectomy was 1.86% over 3.45 years. The annualized reoperation rate for ASD was 1.35% (1.35 ASD reoperations per 100 person-years). The 63.33% incidence of cranial ASD requiring reoperation was statistically significantly higher than the 40.00% incidence of caudal ASD requiring reoperation. Following multivariable logistical regression, the strongest (and only) statistically significant predictor of ASD requiring reoperation was lower extremity radiculopathy after the index discectomy operation (OR = 14.23, p < 0.001). Conclusions In the first series on ASD following first-time LD without fusion, the rate of reoperation for ASD was 4% and the cumulative reoperation rate 10.79%. Rostral ASD is more common than caudal ASD and lower extremity radiculopathy is the strongest predictor of ASD.
AB - Introduction The objective of this study is to determine the incidence and prognostic factors of adjacent segment disease (ASD) following first-time lumbar discectomy (LD). Methods We retrospectively reviewed all neurosurgical patients who underwent first-time LD for degenerative lumbar disease from 1990 to 2012. ASD was defined as a clinical and radiographic progression of degenerative spinal disease that required surgical decompression (with or without fusion) at the level above or below the index discectomy. Adjusted odds ratios were calculated from multivariable logistical regression controlling for sex and age, as well as postoperative sensory deficit, motor deficit, back pain, neurogenic claudication, and radiculopathy. Results Of the 751 patients who underwent single-level LD, the cumulative reoperation rate for degenerative spinal disease was 10.79%. The incidence of ASD requiring reoperation was 4% over 3.11 years. More specifically, the incidence of adjacent level discectomy was 1.86% over 3.45 years. The annualized reoperation rate for ASD was 1.35% (1.35 ASD reoperations per 100 person-years). The 63.33% incidence of cranial ASD requiring reoperation was statistically significantly higher than the 40.00% incidence of caudal ASD requiring reoperation. Following multivariable logistical regression, the strongest (and only) statistically significant predictor of ASD requiring reoperation was lower extremity radiculopathy after the index discectomy operation (OR = 14.23, p < 0.001). Conclusions In the first series on ASD following first-time LD without fusion, the rate of reoperation for ASD was 4% and the cumulative reoperation rate 10.79%. Rostral ASD is more common than caudal ASD and lower extremity radiculopathy is the strongest predictor of ASD.
KW - Adjacent level discectomy
KW - Adjacent segment disease
KW - Lumbar discectomy
KW - Reoperation
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U2 - 10.1016/j.jocn.2016.09.027
DO - 10.1016/j.jocn.2016.09.027
M3 - Article
C2 - 27765560
AN - SCOPUS:85005900975
SN - 0967-5868
VL - 35
SP - 42
EP - 46
JO - Journal of Clinical Neuroscience
JF - Journal of Clinical Neuroscience
ER -