Spinal cord stimulation failure: evaluation of factors underlying hardware explantation

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  • 1 Department of Neurosurgery, University of Cincinnati College of Medicine;
  • 2 Mayfield Clinic, Cincinnati, Ohio; and
  • 3 Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, Utah
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OBJECTIVE

Spinal cord stimulation has been shown to improve pain relief and reduce narcotic analgesic use in cases of complex refractory pain syndromes. However, a subset of patients ultimately undergoes removal of the spinal cord stimulator (SCS) system, presumably because of surgical complications or poor efficacy. This retrospective study addresses the paucity of evidence regarding risk factors and underlying causes of spinal cord stimulation failures that necessitate this explantation.

METHODS

In this retrospective single-center review, 129 patients underwent explantation of SCS hardware during a 9-year period (2005–2013) following initial placement at the authors’ institution or elsewhere. Medical history, including indication of implantation, device characteristics, revision history, and reported reasons for removal of hardware, were reviewed.

RESULTS

The 74 (57%) women and 55 (43%) men were a median of 49 years old (IQR 41–61 years) at explantation; the median time to explantation was 20 months (IQR 7.5–45.5 months). Thoracic or upper lumbar leads were placed in 89.9% of patients primarily for the diagnosis of postsurgical failed–back surgery syndrome (70.5%), chronic regional pain syndrome (14.7%), and neuropathic pain (8.5%). More than half of patients were legally disabled. Initial postoperative reduction in pain was reported in 81% of patients, and 37.8% returned to work. Among 15 patients with acute postsurgical complications (12 infections, 2 hemorrhages, 1 immediate paraplegia), the median time to removal was 2 months. Primary reasons for hardware removal were lack of stimulation efficacy (81%), electrode failure due to migration (14%), and allergic reactions to implanted hardware in 2 patients. The 72 patients who underwent formal psychiatric evaluation before implantation were affected by high rates of major depression (64%), anxiety (34%), posttraumatic stress disorder (PTSD) (12%), drug or alcohol abuse (12%), and physical or sexual abuse (22%).

CONCLUSIONS

The authors’ findings provide insight regarding the mechanisms of spinal cord stimulation failure that resulted in total removal of the implanted system. The relationship between spinal cord stimulation failure and certain psychiatric disorders, such as PTSD, depression, and anxiety, is highlighted. Ultimately, this work may shed light on potential avenues to reduce morbidity and improve patient outcomes.

ABBREVIATIONS CRPS = complex regional pain syndrome; FBSS = failed–back surgery syndrome; PTSD = posttraumatic stress disorder; SCS = spinal cord stimulator.

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Contributor Notes

Correspondence George T. Mandybur: Mayfield Clinic, Cincinnati, OH. gmandybur@mayfieldclinic.com.

INCLUDE WHEN CITING Published online October 4, 2019; DOI: 10.3171/2019.6.SPINE181099.

S.K.P. and Y.M.G. contributed equally to this work.

Disclosures The authors report no conflict of interest concerning the materials or methods used in this study or the findings specified in this paper.

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