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132S Proceedings of the NASS 25th Annual Meeting / The Spine Journal 10 (2010) 1S–149S
RESULTS: Two (6.5%) in 31 patients were diagnosed as RLS after sur-
gery. The average onset of symptoms was third days after surgery. The
symptoms were relieved by oral iron supplements and dopaminergic ago-
nists and spontaneously disappeared within postoperative 3 months. In all
patients, Hb and serum iron showed immediately significant drops after
surgery and slowly recovered during postoperative 3 months. The patients
with RLS showed lower preoperative Hb (13.0 vs. 14.1), serum ferritin (48
vs. 120 ng/mL) and more decrease of serum iron at postoperative 2nd and
5th day (83% vs. 70%, 74% vs. 65%) than those of patients without RLS
(Figure 1). Age, sex, number of fusion levels, amount of EBL and postop-
erative drainage, use and amount of transfusion did not have statistically
significant effect on developing RLS after surgery.
CONCLUSIONS: Acute decrease of serum iron by the perioperative
bleeding can cause a secondary RLS and transient leg pain after posterior
decompression and fusion. The symptoms are developed within postoper-
ative 1 week and spontaneously resolved according to recovery of serum
iron. Lower preoperative serum ferritin might be risk factors of postoper-
ative RLS.
FDA DEVICE/DRUG STATUS: This abstract does not discuss or include
any applicable devices or drugs.
doi: 10.1016/j.spinee.2010.07.340
P65. The Effects of Age, Sex, Race, and Weight on the Rate
of Intervertebral Disc Degeneration
Krzysztof Siemionow, MD1, Howard An, MD1, Koichi Masuda, MD2,
Gunnar Andersson, MD1, Gabriella Cs-Szabo, PhD1; 1Rush University
Medical Center, Chicago, IL, USA; 2University of California, San Diego,
San Diego, CA, USA
BACKGROUND CONTEXT: Intervertebral disc (IVD) degeneration is
believed to begin as early as the second decade of life, and is viewed by
most as an inevitable consequence of ageing. Age, sex, race, weight and
lumbar level are some of the factors that play a role in IVD degeneration.
The rate at which IVDs degenerate has not been established.
PURPOSE: The purpose of this study was to find the rate of IVD degen-
eration with ageing and to establish if there is a difference between lumbar
levels. Knowing the annual rate of IVD degeneration could result in im-
proved clinical decision making.
STUDY DESIGN/SETTING: A magnetic resonance imaging (MRI)
study of fresh cadaver lumbar spines.
METHODS: Complete lumbar spine segments (T11/12 to S1) which were
harvested from fresh cadavers underwent MRI. The nucleus pulposus,
annulus fibrosus, cartilaginous and bony end-plate, and the peripheral ver-
tebral body were assessed with MRI and IVD degeneration was graded by
two observers from grade 1 (nondegenerated)-grade 5 (severely degener-
ated) based on a scale developed by Thompson et al. Age, sex, race, weight
were recorded and used for statistical analysis. Statistical analysis was per-
formed using simple and multiple linear regression as well as simple mean
comparisons using analysis of variance and t-tests.
RESULTS: 435 cadaver spines and 1684 IVDs were available for analysis.
There were 302 male and 133 females. The age range was 14–81, average
age was 60.5. Regression analysis revealed that age predicted deterioration
at all lumbar levels and that the L5/S1 IVD degenerated at a significantly
faster rate of 0.040/year compared to 0.031, 0.032, 0.031, 0.028 for L12,
L23, L34, L45, respectively. Multiple regression analysis revealed that
sex and weight had no significant effect on IVD degeneration whereas
non-Caucasian race was associated with lower Thompson score at L12,
L23, L34.
CONCLUSIONS: The relatively early degeneration at L5-S1 in all races
and less degeneration in the upper lumbarmotion segments in non-Caucasian
race needs further investigation.Other factors such as sagittal alignment, fac-
et joint arthritis, and genetic predisposition may also play a role in IVD
degeneration.
All referenced figures and tables will be available at the Annual Mee
FDA DEVICE/DRUG STATUS: This abstract does not discuss or include
any applicable devices or drugs.
doi: 10.1016/j.spinee.2010.07.341
P66. Biomechanics of Disc Arthroplasty: What Can Be Done to
Improve Results: Present and Future Perspectives
Leonardo Oliveira, BSc1, Luis Marchi, MD2, Etevaldo Coutinho, MD2,
Luiz Pimenta, MD, PhD2; 1Universidade Federal de Sao Paulo, Sao Paulo,
Brazil; 2Instituto de Patologia da Coluna, Sao Paulo, Brazil
BACKGROUND CONTEXT: Current lumbar total disc replacement
(TDR) devices require an anterior approach for implantation.The anterior ap-
proach to place lumbar TDR devices has inherent biomechanical limitations
and surgical risks. Within the possible intraoperative issues are: the damage
to various abdominal structures, such to the grand vessels, to bowel compo-
nents and to the sympathetic neural plexus, without mentioning the long dis-
charge and rehabilitation time. Besides the surgical risks, there is resection of
the anterior longitudinal ligament (ALL). Placement of a TDR device from
a true lateral (XLIF) approach allows for easier, less invasive access to the
disc space, as has been shown in reports of XLIF for fusion procedures. Lat-
eral implantation of TDR also preserves the stabilizing ligaments, which are
a natural restraint to excessive rotations and translations, and thereby help to
minimize facet stresses. Importantly, implantation from a lateral approach
leaves greater opportunity for safer revision surgery, if necessary, by avoiding
scarring of anterior vasculature.Additionally, the footprint of the lateral TDR
device capitalizes on the biomechanical support of the ring apophysis.
PURPOSE: To present the clinical and radiological results of a true lateral
implantation of total disc replacement.
STUDY DESIGN/SETTING: Prospective, non randomized clinical trial
to evaluate the safety and effective of the lateral total disc replacement im-
planted by the XLIF approach.
PATIENT SAMPLE: Patients included 16 males and 20 females, average
age 43 yrs (24–60).
OUTCOMEMEASURES: VAS pain scores improved from an average of
9.3 at pre-op to 2.27 after 3 years. Oswestry Disability Index improved
from an average of 57 at pre-op to 16.5 after 3 years.
METHODS: A TDR device designed for implantation through a true
lateral, retroperitoneal, transpsoas approach (XLIF) was implanted in 36
patients with discography-confirmed 1- or 2-level DDD. Clinical and
radiographic outcomes assessments were prospectively collected.
RESULTS: Surgeries included 14 1-level, 3 2-level, and 19 hybrid TDR/
ALIF cases. The surgery was performed through a 4 cm lateral incision in
an average of 134 minutes (90–300) and with an average 58 cc blood loss
(30–150). There was no intra-op or post-op complications. Postoperative
x-rays showed good device placement, with restoration of disc height,
foraminal volume, and sagittal balance. All patients were up and walking
within 12 hours of surgery
CONCLUSIONS:Mid-term results of a laterally placed TDR device dem-
onstrate maintenance of pain relief and functional improvement. The ben-
efits of this technique – minimal morbidity, avoiding mobilization of the
great vessels, preserving the anterior longitudinal ligament, biomechani-
cally stable orientation, and broader revision options - suggest a promising
new direction for TDR procedures.
FDA DEVICE/DRUG STATUS: XLTDR: Investigational/Not approved.
doi: 10.1016/j.spinee.2010.07.342
P67. A Comparative Study of Posterior Fixation in Acute Unstable
Thoracolumbar Injuries by Monoaxial and Polyaxial Pedicle Screws
Rajeshwar N. Srivastava, MD; King Georges Medical College, CSM
Medical University, Lucknow, India
BACKGROUND CONTEXT: The pedicle offers a strong point of at-
tachment of the posterior elements to the vertebral body and pedicle
ting and will be included with the post-meeting online content.