Failed Fusion Clinical Trial - Orthofix SPINALSTIM 5212CM Manual De Instrucciones

Consistent users (n=64) of the device in this phase had an initial success
rate of 92.2% with a success rate of 70% after four years (a 24% reduction).
Inconsistent users (n=34) and the entire placebo group (n=97) had an initial
success rate of 65% with a success rate of 50% after four years (again, a 24%
reduction). Long-term follow-up data indicates the success rate differentials
between active and placebo units are maintained over time. Long-term,
consistent SpinalStim device users benefit with a 40% increase in fusion
success, when compared to inconsistent and placebo device users. Based on
this analysis, the reduction in long-term success rates appears unrelated to
treatment with the SpinalStim device. During this four year period, 10% of the
original patients in the randomized double-masked phase were lost to
follow-up and are not reflected in these success rates.

Failed Fusion Clinical Trial

The SpinalStim device was also tested for nonoperative salvage in patients
presenting with established pseudarthrosis of lumbar fusion in an open trial.
Without concomitant regrafting, 67% of these cases reached a successful
fusion with consistent (an average of at least 2 hours per day) PEMF
treatment.
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The four year success rates for these patients in the open trial, non-operative
salvage phase for all subjects (consistent and inconsistent users combined)
was 39% (n=119) as compared with 57% in this phase of the original clinical
trial (i.e., one year postoperative). Consistent users (n=93) of the device in this
phase had a success rate of 44% after four years. Inconsistent users (n=26) of
the device in this phase had a success rate of 19% after four years.
The reduction in success rates from the time of commercial marketing
compared with those at four years showed a similar percentage decrease
(31%) to those in the randomized double-masked trial. During this four year
period, 6% of the original patients in the open phase were lost to follow-up
and are not reflected in these success rates.
Mooney, V., "A Randomized Double-Blind Prospective Study of the Efficacy of Pulsed Electromagnetic
1
Field for Interbody Lumbar Fusions", SPINE, Vol. 15, No. 7, P708, 1990.
Mooney V. Pulsed electromagnetic fields: an adjunct to interbody spinal fusion surgery in the high
2
risk patient. Surg Technol Int 1993, 2:405-410
Simmons, JW, Hayes, MA, Christensen, KD, Dwyer, AP, Koulisis, CW, Kimmich, SJ: "The Effect of
3
Postoperative Pulsed Electromagnetic Fields on Lumbar Fusion: Open Trial Study". Presented at the
Annual Meeting of the North American Spine Society, Quebec City, Canada, 2 July 1989.
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