Complex Adult Deformity Surgery (CADS)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Index or spine revision surgery for complex adult spinal deformity.
- Who it may be relevant to
- Registry conditions: Adult Spinal Deformity, Scoliosis, Kyphosis, Sagittal Imbalance. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States, Canada
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Multi-Center Prospective Evaluation of Complex Adult Spinal Deformity Surgery
Overview
Evaluate surgical treatment outcomes and identify best practice guidelines for complex adult spinal deformity (ASD) patients, including radiographic and clinical outcomes, surgical and postoperative complications, risk factors for and revision surgery rates, and the role of standard work to improve patient outcomes and reduce surgical and postoperative complications.
Detailed description
Specific Aims:
• Evaluate surgical treatment outcomes and identify best practice guidelines for complex adult spinal deformity (ASD) patients, including radiographic and clinical outcomes, surgical and postoperative complications, risk factors for and revision surgery rates, and the role of standard work to improve patient outcomes and reduce surgical and postoperative complications.
a. Complex ASD patients will be defined based upon clinical, radiographic and/or procedural criteria identified in an analysis of the existing ISSG ASD database: i. Magnitude of coronal and/or sagittal spinal deformity ≥75th percentile of patients in the ISSG database.
ii. Clinical or Radiographic parameters that corresponded to patients in the ISSG database that had complications requiring revision spine surgery and/or patients that had hospital length of stay \>9 days.
iii. Procedures involving 3 column osteotomies and/or anterior column reconstruction (ACR) of the spine
* Develop and validate a standardized, universal complications classification system for spine surgery * Evaluate perioperative blood management approaches, transfusion requirements, including variance in thresholds for blood transfusion and associated complications for adult spinal deformity surgery * Assess impact of opioid use and pain management on patient cost, complications and outcomes * Evaluate optimal opioid and analgesic usage and protocols for standard work development * Evaluate clinical outcomes utilizing legacy patient reported outcome measures (PROMs) including modified Oswestry Disability Index (mODI), Scoliosis Research Society Questionnaire 22r (SRS-22r), Veterans RAND-12 (VR-12), and numeric pain rating scale (NRS) and compare the results of these legacy PROMs to outcomes scores as measured by the NIH Patient Reported Outcomes Measurement Information System (PROMIS) - PROMIS Anxiety, Depression, Pain Interference, Physical Function, and Social Satisfaction. Secondary aims for PROM research for this study include
1. Validation of the PROMIS tool for ASD 2. Establish a core set of PROMs for best practice guidelines for ASD 3. Evaluate patient reported outcome variance for ASD according to SRS-Schwab spine deformity type including variance in baseline PROM domains impacted and variance in improvement in PROM domains 4. Evaluate ASD outcomes compared to population norms and investigate/develop appropriate measures of clinically significant improvement * Evaluate clinical outcomes stratifying by patient chronological and physiological age * Evaluate measures to quantify patient physiological age including patient frailty for ASD and validate a frailty measurement system for ASD * Evaluate the role of functional tests in patient's baseline frailty assessment including hand manometer and Edmonton Frail Scale. See appendix, pages 17 \& 18 for details. * Evaluate the contribution of patient frailty to patient outcomes, cost of care, disability, and complications * Evaluate if patient frailty is a static measure or if frailty is a dynamic measure that can be improved through "pre-habilitation" and if the according associations with reductions in frailty correlate with reductions of cost, complications, and improvement in outcomes * Evaluate cost variance for ASD surgery according to patient, institution, and geographical region and evaluate the cost effectiveness of surgical intervention for ASD * Evaluate incidence of and risk factors for mental health (MH) compromise among ASD patients and establish best practice guidelines for assessing MH for ASD patients * Evaluate the association of MH with surgical complications, outcomes, hospital length of stay and cost for ASD surgery * Evaluate the association of social health surgical complications, outcomes, hospital length of stay and cost for ASD surgery and risk factors for routine (home) discharge vs. skilled nursing facility (SNF)/rehabilitation facility * Broaden the evaluation of the surgically treated ASD patient to maximize evaluation of the entirety of the episode of care to include steps that can be taken prior to surgery including "prehabilitation," pain management, and MH care to improve treatment outcomes, reduce cost, reduce hospital length of stay, reduce non-routing discharge and reduce early and late complications * Establish a core set of standard work guidelines to clinically and radiographically evaluate and treat ASD patients and evaluate the utility of standard work to improve outcomes for ASD and formulate best practice guidelines for surgical treatment of ASD * Develop predictive analytic algorithms to risk stratify for best/worst outcomes, complications, sentinel events, and economic loss for ASD surgery
Interventions
- Procedure Index or spine revision surgery for complex adult spinal deformity
Surgical interventions will be patient specified by treating surgeon.
Primary outcome measures
- Scoliosis Research Society (SRS) 22r [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Oswestry Disability Index (ODI) [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Veterans RAND 12 Item Health Survey (VR-12) [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Radiographic Evaluation [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Anxiety [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Depression [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Physical Function [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Social Role Satisfaction [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Social Satisfaction (DSA) [Time frame: Change from Preop to 3 months and 1, 2, 5 & 10 year follow-up]
Secondary outcome measures (3)
- Edmonton Frail Scale [Time frame: Change from Preop to 3months and 1, 2, 5 & 10 year follow-up]
- Canadian Study of Health and Aging (CSHA) [Time frame: Change from Preop to 3months and 1, 2, 5 & 10 year follow-up]
- Adverse Events [Time frame: 3 months and 1, 2, 5 & 10 year post treatment]
Eligibility criteria
Criteria:
Inclusion criteria
- Diagnosis of adult congenital, degenerative, idiopathic or iatrogenic spinal deformity
- Full body EOS radiographic assessment (sagittal and coronal visualization from skull to foot)
- Complex patients are defined as and meeting any one of the subsequent criteria:
- Radiographic criteria:
- PI-LL ≥ 25 degrees
- TPA ≥ 30 degrees
- SVA>15cm
- Thoracic scoliosis ≥ 70 degrees
- Thoracolumbar/lumbar scoliosis ≥ 50 degrees
- Global coronal malalignment >7cm
- Procedural criteria:
- Posterior spinal fusion > 12 levels
- 3 column osteotomy or ACR
- Geriatric criteria:
- Age >65 years and minimum 7 levels of spinal instrumentation during surgery
Exclusion criteria
- Age <18 years of age
- Active spine tumor or infection
- Deformity due to acute trauma
- Neuromuscular conditions/diseases (Parkinson's, Multiple Sclerosis, Post-polio syndrome)
- Syndromic scoliosis
- Inflammatory arthritis/auto immune diseases (Rheumatoid arthritis, Lupus, Ankylosing Spondylitis)
- Prisoners
- Women who are pregnant
- Non English speaking patients
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 17 centers
- Shiley Center for Orthopaedic Research and Education at Scripps Clinic — La Jolla
- University of California, Davis, Department of Orthopedic Surgery — Sacramento
- UCSF, Department of Neurosurgery — San Francisco
- Denver International Spine Center, Rocky Mountain Hospital for Children and Presbyterian S — Denver
- University of Kansas, Department of Orthopedic Surgery — Kansas City
- Norton Leatherman Spine Center — Louisville
- Spine Institute of Louisiana — Shreveport
- John Hopkins University, Department of Orthopedic Surgery — Baltimore
- … and 9 more centers
Canada · 1 center
- Toronto Western — Toronto
Publications
- Boutros M, Assi A, Diebo BG, Prince G, Karam M, Daher M, Ames CP, Bess S, Daniels AH, Gupta MC, Hostin R, Kim HJ, Klineberg EO, Lenke LG, Nunley PD, Passias PG, Schwab FJ, Shaffrey CI, Smith JS, Lafage R, Lafage V; International Spine Study Group. A New Normative Zone for Acetabular Anteversion Positioning in ASD Patients. J Orthop Res. 2026 Mar;44(3):e70171. doi: 10.1002/jor.70171. PMID 41761562
- Passias PG, Tretiakov P, Onafowokan OO, Das A, Lafage R, Smith JS, Line BG, Nayak P, Diebo B, Daniels AH, Gum JL, Hamilton DK, Buell TJ, Soroceanu A, Scheer JK, Eastlack RK, Mullin JP, Schoenfeld AJ, Mundis GM, Hosogane N, Yagi M, Mummaneni PV, Chou D, Fu KM, Than KD, Anand N, Okonkwo DO, Wang MY, Klineberg E, Kebaish KM, Lewis S, Hostin R, Gupta M, Lenke L, Kim HJ, Ames CP, Shaffrey CI, Bess S, S PMID 39576989
Identifiers
NCT: NCT04194138 · 2123