Study Design. Prospective questionnaire development and validation study. Objective. To develop and validate a new “Forgotten Spine Surgery Score for Cervical Spine Surgery” (FS3-C) to assess patient outcomes after CDR beyond the traditional measures: the ability to forget the presence of the implanted disc in daily life. Summary of Background Data. The Forgotten Joint Score (FJS) has demonstrated superior discrimination in high-functioning total joint arthroplasty patients due to low ceiling and floor effects compared to legacy patient-reported outcome measures (PROMs). To date, there is no similar outcome measure to assess “forgottenness” following spine surgery. Such measures may be critical for evaluating subtle differences in high-performance surgeries like cervical disc replacement (CDR). Methods. A 20-item pilot questionnaire was developed based on published patient expectations and expert opinion, utilizing a 5-point Likert scale. This was administered to 41 patients who underwent primary one- or two-level CDR (minimum 3-month follow-up, 2016-2023) for item selection and internal validity assessment. The final 12-item FS3-C was validated in 97 patients and correlated with the neck disability index (NDI) to determine convergent validity. Results. In the pilot cohort (mean age 44.7±7.9 y), four items were excluded due to high missing responses or ceiling effects. In the pilot cohort (mean age 44.7±7.9 y), four items were excluded due to high missing responses or ceiling effects. The remaining 16 items demonstrated high internal consistency (Cronbach’s alpha 0.95-0.96). Pairwise correlation analysis reduced the questionnaire to 12 items. In the validation cohort (mean age 44.3±9.0 y, 56.7±24.2 mo post-surgery), FS3-C demonstrated high internal consistency with minimal ceiling effects. Mean FS3-C and NDI scores were 86.4±18.9 and 9.8±12.6, respectively, with strong correlation (r=-0.606, P <0.001). Conclusion. The FS3-C demonstrates high internal consistency, low ceiling effects, and strong convergent validity with NDI, enabling spine surgeons to evaluate CDR success beyond traditional symptom improvement measures. Level of Evidence. II
Simon et al. (Wed,) studied this question.
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