ArticleCureus2025
Association Between Public Insurance and Quality of Life Outcomes in Surgically Treated Adolescent Idiopathic Scoliosis.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- A retrospective case-series of adolescent idiopathic scoliosis patients with 5 to 15 years follow-up after segmental pedicle screw instrumentation.North American Spine Society journal · 2026Article
- Structural Drivers of Race and Sex Disparities in Adolescent Idiopathic Scoliosis Care: A Narrative Review.Current reviews in musculoskeletal medicine · 2026Review
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe role of social determinants of health is becoming increasingly studied in orthopedic diseases. In adolescent idiopathic scoliosis (AIS), patients with public insurance have been shown to have larger Cobb angles, longer waits for surgery, and longer hospitalizations, although the literature is conflicting. We do not yet know how insurance type is associated with patient quality of life (QOL) in AIS patients who require surgical management.
methodsThis retrospective cohort study was conducted among AIS patients surgically managed with posterior spinal fusion (PSF). The primary independent variable was insurance type, classified as public or private. For patient-reported outcomes, we used the Scoliosis Research Society Patient Outcome Questionnaires, which synthesizes patient responses into scores for pain, mental health, self-image, functioning, satisfaction, and total QOL. Patients completed surveys throughout the preoperative and postoperative periods.
resultsAmong 263 patients who underwent PSF, 188 (71%) were publicly insured and 75 (29%) were privately insured. Between groups, significant differences were noted for race (P<0.001) and ethnicity (P = 0.01), but no other demographic or preoperative characteristics. Publicly insured patients reported significantly worse preoperative scores for function (3.85 vs 4.11, P = 0.008), pain (3.88 vs 4.31, P = 0.001), self-image (3.18 vs 3.51, P = 0.003), mental health (3.81 vs 4.21, P = 0.002), and total QOL (3.63 vs 3.97, P<0.001). Postoperatively, publicly insured patients continued to report worse scores for pain at six weeks (3.73 vs 3.98, P = 0.03) and six months (4.16 vs 4.40, P = 0.04), and worse mental health scores at six weeks (3.97 vs 4.23, P = 0.03), six months (4.06 vs 4.30, P = 0.05), and one year (4.04 vs 4.36, P = 0.03).
conclusionsPublicly insured patients were found to have worse QOL metrics in nearly all domains prior to surgery and for pain and mental health after surgery. Equalization of function, self-image, and total QOL metrics postoperatively suggests that access to appropriate surgical interventions may help mitigate some, but not all, of these preoperative differences. This study provides Level III evidence, based on a retrospective cohort design.
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