Comorbidity-Specific Risk of Revision Following Single-Level Degenerative Spinal Fusion (2010-2023)

Study Design. Retrospective cohort. Objective. To evaluate the associations of 28 preoperative comorbidities with all-cause and etiology-specific revisions (pseudarthrosis, mechanical failure, adjacent segment disease [ASD], infection) following single-level degenerative spinal fusion. Summary of Background Data. Revision following spinal fusion for degenerative spinal disease remains frequent and costly. While technical factors are well studied, the extent to which preoperative comorbidities differentially predispose to specific revision etiologies is unclear. Materials and Methods. Using the PearlDiver Mariner170 claims database (2010–2023), we identified adults undergoing single-level degenerative spinal fusion and followed them for 2 years for reoperation. All-cause and etiology-specific revisions were defined by CPT/ICD codes. Preoperative comorbidities were analyzed using multivariable cox proportional hazards models adjusted for age, sex, and all comorbidities. Bonferroni correction set significance at P ≤0.00036. Results. Among 399,186 patients (mean age 59.7±13.0; 56.7% female; mean CCI 1.4±1.2), anaemia (HR 1.33), osteoporosis (HR 1.31), substance-related disorders (HR 1.25), and depression (HR 1.19) conferred the greatest risk of all-cause revision. Type 2 diabetes (HR 1.07) and essential hypertension (HR 1.14) had smaller but significant effects. Etiology-specific analyses showed that osteoporosis, anaemia, depression, and substance-related disorders were consistently associated with increased risk across pseudarthrosis, mechanical failure, and ASD. Mechanical failure was additionally associated with hypertension (HR 1.20) and diabetes (HR 1.28), which were not significant in the other revision subtypes. In contrast, ASD revisions were uniquely associated with osteoarthritis (HR 1.26). No comorbidity was significantly associated with infection-related revision. All hazard ratios were significant at P <0.001 unless otherwise specified. Conclusion. In this national cohort of patients, osteoporosis, anaemia, depression, and substance-related disorders emerged as significant predictors of non-infectious revision within two years. Hypertension and type 2 diabetes conferred more modest risks for mechanical failure. These findings support the integration of comorbidity-informed risk stratification into preoperative planning and highlight the potential optimization to minimize revisions and enhance clinical outcomes.

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Journal
Spine
Published
2026-09-28
DOI
https://doi.org/10.1097/brs.0000000000005888
Primary Topic
Spine and Intervertebral Disc Pathology
Type
article
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article

Comorbidity-Specific Risk of Revision Following Single-Level Degenerative Spinal Fusion (2010-2023)

William C. Eward, Anand Veeravagu, Sravisht Iyer, Andrew J. Schoenfeld et al.
Spine
Spine and Intervertebral Disc Pathology
article

Comorbidity-Specific Risk of Revision Following Single-Level Degenerative Spinal Fusion (2010-2023)

William C. Eward, Anand Veeravagu, Sravisht Iyer, Andrew J. Schoenfeld, Mihir S. Dekhne, Dhiraj J. Pangal, Arman Kishan, Gregory S. Kazarian, Raffi S. Avedian, Harmon Singh Khela, Alex Hernandez Manriquez, Sami H. Tuffaha, Peter G. Passias, Alan H. Daniels, Han Jo Kim
article en

Abstract

Study Design. Retrospective cohort. Objective. To evaluate the associations of 28 preoperative comorbidities with all-cause and etiology-specific revisions (pseudarthrosis, mechanical failure, adjacent segment disease [ASD], infection) following single-level degenerative spinal fusion. Summary of Background Data. Revision following spinal fusion for degenerative spinal disease remains frequent and costly. While technical factors are well studied, the extent to which preoperative comorbidities differentially predispose to specific revision etiologies is unclear. Materials and Methods. Using the PearlDiver Mariner170 claims database (2010–2023), we identified adults undergoing single-level degenerative spinal fusion and followed them for 2 years for reoperation. All-cause and etiology-specific revisions were defined by CPT/ICD codes. Preoperative comorbidities were analyzed using multivariable cox proportional hazards models adjusted for age, sex, and all comorbidities. Bonferroni correction set significance at P ≤0.00036. Results. Among 399,186 patients (mean age 59.7±13.0; 56.7% female; mean CCI 1.4±1.2), anaemia (HR 1.33), osteoporosis (HR 1.31), substance-related disorders (HR 1.25), and depression (HR 1.19) conferred the greatest risk of all-cause revision. Type 2 diabetes (HR 1.07) and essential hypertension (HR 1.14) had smaller but significant effects. Etiology-specific analyses showed that osteoporosis, anaemia, depression, and substance-related disorders were consistently associated with increased risk across pseudarthrosis, mechanical failure, and ASD. Mechanical failure was additionally associated with hypertension (HR 1.20) and diabetes (HR 1.28), which were not significant in the other revision subtypes. In contrast, ASD revisions were uniquely associated with osteoarthritis (HR 1.26). No comorbidity was significantly associated with infection-related revision. All hazard ratios were significant at P <0.001 unless otherwise specified. Conclusion. In this national cohort of patients, osteoporosis, anaemia, depression, and substance-related disorders emerged as significant predictors of non-infectious revision within two years. Hypertension and type 2 diabetes conferred more modest risks for mechanical failure. These findings support the integration of comorbidity-informed risk stratification into preoperative planning and highlight the potential optimization to minimize revisions and enhance clinical outcomes.

Spine
Hospital for Special Surgery (US), Harvard University (US), Johns Hopkins University (US), Duke University (US), Brown University (US), Johns Hopkins Medicine (US), Duke Medical Center (US), Stanford Medicine (US), Mass General Brigham (US), Columbia University (US), University of Pennsylvania (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 11%
Spine and Intervertebral Disc Pathology
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