M. Ito et al., THE EFFECT OF PULSED ELECTROMAGNETIC-FIELDS ON INSTRUMENTED POSTEROLATERAL SPINAL-FUSION AND DEVICE-RELATED STRESS SHIELDING, Spine (Philadelphia, Pa. 1976), 22(4), 1997, pp. 382-388
Study Design. This study was designed to examine stress-shielding effe
cts on the spine caused by rigid implants and to investigate the effec
ts of pulsed electromagnetic fields on the instrumented spine. Objecti
ves. To investigate the effects of pulsed electromagnetic fields on po
sterolateral spinal fusion, and to determine if osteopenia induced by
rigid instrumentation can be diminished by pulsed electromagnetic fiel
ds. Summary of Background Data. Although device-related osteopenia on
vertebral bodies is of a great clinical importance, no method for prev
enting bone mineral loss In vertebrae by stiff spinal implants has bee
n effective. Methods. Twenty-eight adult beagles underwent L5-L6 desta
bilization followed by posterolateral spinal fusion. The study was div
ided into four groups: 1) Group CNTL: without instrumentation, without
pulsed electromagnetic fields, 2) Group PEMF: without Steffee, with p
ulsed electromagnetic fields, 3) Group INST: with Steffee, without pul
sed electromagnetic fields, 4) Group PEMF + INST: with Steffee, with p
ulsed electromagnetic fields. At the end of 24 weeks, the dogs were ki
lled, and L4-L7 segments were tested biomechanically without instrumen
tation. Radiographs and quantitative computed tomography assessed the
condition of the fusion mass. Results. Stress shielding was induced in
the anterior vertebral bodies of L6 with the Steffee plates; bone min
eral density Was increased with the addition of pulsed electromagnetic
fields, regardless of the presence or absence of fixation. A decrease
in flexion and bending stiffness was observed in the Group INST; puls
ed electromagnetic fields did increase the flexion stiffness regardles
s of the presence or absence of fixation, although this was not statis
tically significant. Conclusions. Use of pulsed electromagnetic fields
has the potential to minimize device-related vertebral bone mineral l
oss.