Clinical outcomes of the Dynesys dynamic neutralization system: 1-year preliminary results

Author:

Welch William C.1,Cheng Boyle C.1,Awad Tariq E.11,Davis Reginald2,Maxwell James H.3,Delamarter Rick4,Wingate Jeffrey K.5,Sherman John6,Macenski M. Mason7

Affiliation:

1. 1University of Pittsburgh Medical Center–Health System, Presbyterian University Hospital, Pittsburgh, Pennsylvania;

2. 2Suez Canal University, Ismailia, Egypt;

3. 3Greater Baltimore Medical Center, Baltimore, Maryland;

4. 4Scottsdale Spine Care, Scottsdale, Arizona;

5. 5The Spine Institute, Santa Monica, California;

6. 7Twin Cities Orthopaedic, Minneapolis, Minnesota and

7. 8Zimmer Spine, Minneapolis, Minnesota

Abstract

Object In this study the authors present the preliminary clinical outcomes of dynamic stabilization with the Dynesys spinal system as part of a multicenter randomized prospective Food and Drug Administration (FDA) investigational device exemption (IDE) clinical trial. Methods This study included 101 patients from six IDE sites (no participants were omitted from the analysis) who underwent dynamic stabilization of the lumbar spine with the Dynesys construct. Patient participation was based on the presence of degenerative spondylolisthesis or retrolisthesis (Grade I), lateral or central spinal stenosis, and their physician's determination that the patient required decompression and instrumented fusion for one or two contiguous spinal levels between L-1 and S-1. Participants were evaluated preoperatively, postoperatively at 3 weeks, and then at 3-, 6-, and 12-month intervals. The 100-mm visual analog scale was used to score both lower-limb and back pain. Patient functioning was evaluated using the Oswestry Disability Index (ODI), and the participants' general health was assessed using the Short Form-12 questionnaire. Overall patient satisfaction was also reported. One hundred one patients (53 women and 48 men) with a mean age of 56.3 years (range 27–79 years) were included. The mean pain and function scores improved significantly from the baseline to 12-month follow-up evaluation, as follows: leg pain improved from 80.3 to 25.5, back pain from 54 to 29.4, and ODI score from 55.6 to 26.3%. Conclusions The early clinical outcomes of treatment with Dynesys are promising, with lessening of pain and disability found at follow-up review. Dynesys may be preferable to fusion for surgical treatment of degenerative spondylolisthesis and stenosis because it decreases back and leg pain while avoiding the relatively greater tissue destruction and the morbidity of donor site problems encountered in fusion. However, long-term follow-up care is still recommended.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Neurology (clinical),General Medicine,Surgery

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