Abstract
Increased attention has surrounded spinal cord stimulation’s (SCS) long-term effectiveness and methods to improve patient selection. SCS trialing with documentation of pain relief ≥ 50% as a prerequisite for implantation is commonly utilized, which was reinforced by government agencies (e.g., FDA).1 However, the utility, reporting protocols, and evidence surrounding the long-term prognostic value of trialing are questioned.2,3 The purpose of this study is to analyze the influence of SCS trial reported pain results to accurately predict short, intermediate, and long-term pain outcomes, as well as identify possible patient-specific confounding variables.
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