Faculty Bibliography

STUDY DESIGN/METHODS:Single institution retrospective clinical review. OBJECTIVE:To investigate the relationship between levels fused and clinical outcomes in patients undergoing open and minimally invasive surgical (MIS) lumbar fusion. SUMMARY OF BACKGROUND DATA/BACKGROUND:Minimally invasive spinal fusion aims to reduce the morbidity associated with conventional open surgery. As multilevel arthrodesis procedures are increasingly performed using MIS techniques, it is necessary to weigh the risks and benefits of multilevel MIS lumbar fusion as a function of fusion length. METHODS:Patients undergoing <4 level lumbar interbody fusion were stratified by surgical technique (MIS or open), and grouped by fusion length: 1-level, 2-levels, 3+ levels. Demographics, Charlson Comorbidity Index (CCI), surgical factors, and perioperative complication rates were compared between technique groups at different fusion lengths using means comparison tests. RESULTS:Included: 361 patients undergoing lumbar interbody fusion (88% transforaminal, 14% lateral; 41% MIS). Breakdown by fusion length: 63% 1-level, 22% 2-level, 15% 3+ level. Op-time did not differ between groups at 1-level (MIS: 233 min vs. Open: 227, P = 0.554), though MIS at 2-levels (332 min vs. 281) and 3+ levels (373 min vs. 323) were longer (P = 0.033 and P = 0.231, respectively). While complication rates were lower for MIS at 1-level (15% vs. 30%, P = 0.006) and 2-levels (13% vs. 27%, P = 0.147), at 3+ levels, complication rates were comparable (38% vs. 35%, P = 0.870). 3+ level MIS fusions had higher rates of ileus (13% vs. 0%, P = 0.008) and a trend of increased adverse pulmonary events (25% vs. 7%, P = 0.110). MIS was associated with less EBL at all lengths (all P < 0.01) and lower rates of anemia at 1-level (5% vs. 18%, P < 0.001) and 2-levels (7% vs. 16%, P = 0.193). At 3+ levels, however, anemia rates were similar between groups (13% vs. 15%, P = 0.877). CONCLUSION/CONCLUSIONS:MIS lumbar interbody fusions provided diminishing clinical returns for multilevel procedures. While MIS patients had lower rates of perioperative complications for 1- and 2-level fusions, 3+ level MIS fusions had comparable complication rates to open cases, and higher rates of adverse pulmonary and ileus events. LEVEL OF EVIDENCE/METHODS:3.

Background/UNASSIGNED:Regional and segmental changes of the lumbar spine have previously been described as patients transition from standing to sitting; however, alignment changes in the cervical and thoracic spine have yet to be investigated. So, the aim of this study was to assess cervical and thoracic regional and segmental changes in patients with thoracolumbar deformity versus a nondeformed thoracolumbar spine population. Methods/UNASSIGNED:This study was a retrospective cohort study of a single center's database of full-body stereoradiographic imaging and clinical data. Patients were ≥ 18 years old with nondeformed spines (nondegenerative, nondeformity spinal pathologies) or thoracolumbar deformity (ASD: PI-LL > 10°). Patients were propensity-score matched for age and maximum hip osteoarthritis grade and were stratified by Scoliosis Research Society (SRS)-Schwab classification by PI-LL, SVA, and PT. Patients with lumbar transitional anatomy or fusions were excluded. Outcome measures included changes between standing and sitting in global alignment parameters: sagittal vertical axis (SVA), pelvic incidence minus lumbar lordosis (PI-LL), pelivc tilt (PT), thoracic kyphosis, cervical alignment, cervical SVA, C2-C7 lordosis (CL), T1 slop minus CL (TS-CL), and segmental alignment from C2 to T12. Another analysis was performed using patients with cervical and thoracic segmental measurements. Results/UNASSIGNED: = .009) segments. Conclusions/UNASSIGNED:Nondeformity patients and ASD patients have significant differences in mobility of global spinopelvic parameters as well as segmental regions in the cervical and thoracic spine between sitting and standing. This study aids in our understanding of flexibility and compensatory mechanisms in deformity patients, as well as the possible impact on unfused segments when considering deformity corrective surgery.

BACKGROUND CONTEXT: Psychiatric diagnoses (PD) present a significant burden on elective surgery patients and may have potentially dramatic impacts on outcomes. As ailments of the spine can be particularly debilitating, the effect of PD on outcomes was compared between elective spine surgery patients and other common elective orthopedic surgery procedures. PURPOSE: Investigate the rates of PD in elective orthopedic procedures. STUDY DESIGN/SETTING: Retrospective review of the National Inpatient Database 2007-2013. PATIENT SAMPLE: A total of 15,434,393 weighted hospital discharges. OUTCOME MEASURES: Rates of PD, post-operative complications, length of stay (LOS), cost to charge (CCR), discharge location, and death.
METHOD(S): Inclusion criteria: elective orthopedic surgery procedures from 2007-2013 as defined by ICD-9-CM codes. Exclusion criteria: emergency, trauma, or non-elective surgery. Patients were grouped as shoulder, elbow, hand, spine, hip, knee, or foot/ankle. Descriptive statistics assessed demographics. Rates of DSM-IV PD, as classified by single-level C

BACKGROUND CONTEXT: As surgery is increasingly recommended for patients with neurologic deterioration secondary to central cord syndrome (CCS), it is important to investigate the relationship between time to surgery and patient outcomes. The merits of early vs delayed surgical treatment remain controversial in the literature. PURPOSE: Investigate associations between time to surgical intervention and surgical outcomes for CCS patients STUDY DESIGN/SETTING: Retrospective review of Healthcare Cost and Utilization Project's Nationwide Inpatient Sample (NIS) PATIENT SAMPLE: A total of 9,246 weighted inpatient discharges. OUTCOME MEASURES: Complication rates, discharge destination, length of hospital stay (LOS).
METHOD(S): CCS patients (ICD-9 codes 952.03, 952.08, 952.13, 952.18) were isolated in the NIS database 2005-2013. Operative patients were grouped by time to intervention: same day as admission, 1-day delay, 2-day, 3-day, 4-7 days, 8-14 days, and >14 days. As appropriate, analysis of variance and chi-squared tests compared demographics, Charlson Comorbidity Index (CCI) scores, surgical details, LOS, discharge status, periop complications and total charges across patient groups. Controlling for age, CCI and concurrent traumatic fractures, binary logistic regression assessed surgical timing associated with increased odds of perioperative complication, using same-day patients as a reference group (odds ratio [95% confidence interval]).
RESULT(S): Included: 6,734 CSS patients (59+/-16yrs, 26%F, mean CCI: 1.2+/-1.6). Overall rate of surgical treatment was 64.1%, with rates of surgery increasing from 2005 (50.0%) to 2013 (73.0%, p<0.001). The most common mechanisms of injury were falls (30.3%), pedestrian accidents (6.9%), assault (3.2%) and bicycle-related injury (2.7%). Of the patients that underwent surgery, 52.0% underwent fusion (62.4% 2-3 levels, 33.2% eight-levels, 0.5% 9+ levels), 30.1% discectomy, and 13.8% other exploration/decompression of the spinal canal. Breakdown by time to procedure was: 38.5% same day, 16.1% 1 day, 9.6% 2 days, 7.5% 3 days, 16.2% 4-7 days, 8.3% 8-14 days, and 2.7% >14 days. Timing groups did not differ in trauma status at admission (shock or hemorrhage, p=0.261); however, age differed between groups (min: 1 day [58+/-15 years], max: >14 days [63+/-13 years], p<0.001). Relative to other groups, same-day patients had the lowest LOS (7.7+/-9.8 days vs 9.4-37.3 days, p<0.001) highest rates of home discharge (42.09% vs 30.9%-14.4%, p<0.001). Same-day patients showed a trend of lower perioperative neurologic complications (0.4%) than 1-day (0.6%) and 2-day (1.0%) patients, while patients delayed 3+ days had the lowest (0.1%, p=0.144). Patients delayed >14 days to surgery had increased odds of periop cardiac (7.0 [1.6-30.0]) and infection (6.1 [2.2-16.3]) complications. All timing groups beyond 3 days showed increased odds of VTE: 4-7 days (3.0 [1.6-5.5]), 8-14 days (3.0 [1.4-6.3]), 14+ days (5.6 [2.3-13.6]). Same-day surgery was also associated with lower total hospital charges than delayed surgery ($87,741 vs $118,815-$272,901, p<0.001).
CONCLUSION(S): Patients undergoing surgery for CCS on the same day as admission showed significantly lower odds of complication, hospital charges, and higher rates of discharge to home than patients that experienced a delay to operation. In contrast, patients delayed >14 days to surgery were associated with inferior outcomes, including increased odds of cardiac complication and infection. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: The Roussouly Classification system of sagittal spinal shape and the SRS-Schwab adult spinal deformity (ASD) classification system have become important indicators of spine deformity. No prior studies have examined the outcomes of matching both Roussouly type and improving in Schwab modifiers postoperatively. PURPOSE: Evaluate outcomes of matching Roussouly Type and improving in Schwab modifier following ASD surgery. STUDY DESIGN/SETTING: Retrospective review of single-center ASD database. PATIENT SAMPLE: A total of 103 ASD patients. OUTCOME MEASURES: Roussouly types, Schwab modifiers, Health Related Quality of Life scores(HRQLs): Minimal Clinical Important Difference for ODI, EQ5D, VAS Leg &Back Pain.
METHOD(S): Surgical ASD patients (SVA>=5cm, PT>=25degree, or TK >=60degree, >3 levels fused) >=18 years old with available baseline (BL) radiographic data at baseline (BL) and 1-year (1Y) were isolated in the single-center Comprehensive Spine Quality Database (Quality). Patients were grouped by two Roussouly types: (1)"theoretical" Roussouly type(Type 1: PI<45degree, LL apex below L4; Type 2: PI<45degree, LL apex above L4 L4-L5 space; Type 3: 45degree60degree); (2) "current" Roussouly type (1: SS<35degree, LL apex below L4; 2: PI<35degree, LL apex above L4-L5 space; 3: 35degree45degree), as previously published. One year (1Y) matched Roussouly: preoperative mismatched (Between 'actual' and 'theoretical' patients that matched at 1Y. Schwab modifiers at BL were identified: non-, moderate and severe deformity (0, +, ++) for PT, SVA, and PI-LL. Schwab improvement was defined as a decrease in a modifier at one year.
RESULT(S): A total of 103 ASD patients (61.8yrs, 63.1%F, 30kg/m2). By surgical approach, 79.6% posterior, 10.7% combined, 2.9% anterior). Average levels fused: 4.6. BL breakdown of 'current; Roussouly type: 28% Type 1, 25.3% Type 2, 32.0% Type 3, 14.7% Type 4. BL Roussouly mismatch: 65.3%. Breakdown BL Schwab modifiers: PT (0: 8.7%, +: 41.7%, ++: 49.5%), SVA (0: 29.7%, +: 20.3%, ++: 50%), PI-LL mismatch (0: 28.2%, +: 25.2%, ++: 46.6%). At one year, 19.2% of patients matched Roussouly target type, while according to Schwab modifiers, 12.6% improved in SVA, 42.7% in PI-LL, and 45.6% in PT. Patients who both met Roussouly type and improved in a Schwab by the modifiers: 9 PT (8.7%), 8 PI-LL (7.8%), 2 SVA (1.9%). There were 2 patients (1.9%) who met their Roussouly type and improved in all 3 Schwab modifiers. One year (1Y) matched Roussouly patients improved more in HRQLs (MCID for ODI, EQ5D, VAS Leg/Back Pain), when compared to mismatched Roussouly, but was not significant(P>0.05). Match Roussouly and improvement in PT Schwab met MCID for EQ5D significantly more (33.3% vs 10.6%, p=0.050). Matched Roussouly and PI-LL Schwab had more patients meet MCID for all HRQLs, yet none were significant, p>0.05. Matched Roussouly and improvement in SVA Schwab met MCID for ODI significantly more (p=0.024).
CONCLUSION(S): Patients who both matched Roussouly sagittal spinal type and improved in SRS-Schwab modifiers had superior patient-reported outcomes at 1-year. Utilizing both classification systems in surgical decision making can optimize postop patient outcomes. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Bariatric surgery for morbid obesity helps to address common comorbidity burdens, including decreasing rates of myocardial infarction and stroke. The increased mechanical stresses on the spine caused by morbid obesity predispose patients to various spinal pathologies and are concerning for spinal surgeons, with previous studies suggesting poorer outcomes than the general population. The effects of bariatric surgery on diminishing spinal complaints or symptoms have yet to be elucidated in the literature. PURPOSE: To assess the rate in which various spinal symptoms diminish after bariatric surgery. STUDY DESIGN/SETTING: Retrospective analysis of the prospectively collected New York State Inpatient Database (NYSID) years (2004-2013). PATIENT SAMPLE: A total of 4,351 patients who underwent bariatric surgery with at least one identified spinal diagnosis present before bariatric surgery. OUTCOME MEASURES: Time from bariatric surgery until disappearance of specific spinal complaint, percentage of unresolved spinal complaints with 2-year follow-up.
METHOD(S): Retrospective analysis of the prospectively collected (NYSID) years 2004-2013. Patient linkage codes allow identification of multiple and return inpatient stays within the time frame analyzed (720 days). Inclusion criteria were bariatrics surgery patients with one or more visits prior to and after bariatric procedure (excluding pts with <30 days f/u, spine surgery, or new post-bariatric spine pathology) for one of the following common cervical or lumbar spinal diagnoses, queried with ICD-9CM codes: herniation, stenosis, spondylosis, disc degeneration, and spondylolisthesis. Time from bariatric surgery until the patient's respective spinal diagnosis was no longer present was considered resolution of spinal symptoms. Kaplan-Meier survivorship curves assessed rates of resolution within each spinal diagnosis cohort.
RESULT(S): A total of 4,351 bariatric surgery pts with a preop spinal diagnosis by ICD-9 were analyzed. Lumbar pts: 1,049 had stenosis, 774 spondylosis, 648 degeneration, 249 spondylolisthesis, 72 disc herniation. Cervical pts: 581 disc herniation, 376 had stenosis, 366 spondylosis, 236 degeneration. Cumulative resolution rates at 90-day, 180-day, 360-day, and 720-day follow-up were as follows: lumbar stenosis (48%,67.6%,79%,91%), lumbar herniation (61%,77%,86%,93%), lumbar spondylosis (47%,65%,80%,93%), lumbar spondylolisthesis (37%,58%,70%,87%), lumbar degeneration (37%,56%,72%,86%). By cervical region: cervical stenosis (48%,70%,84%,94%), cervical herniation (39%,58%,74%,87%), cervical spondylosis (46%, 70%,83%, 94%), cervical degeneration (44%,64%,78%,89%). Lumbar herniation pts saw significantly higher 90d-resolution than cervical herniation pts (p<0.001). Cervical vs lumbar degeneration resolution rates did not differ @90d (p=0.058), but did @180d(p=0.034). Cervical and lumbar stenosis resolution was similar @90d & 180d, but cervical showed greater resolution by 1 year (p=0.036).
CONCLUSION(S): Over 50% of bariatric patients diagnosed with a cervical or lumbar pathology before weight-loss surgery no longer sought inpatient care for their respective spinal diagnosis by 180 days postop. Lumbar herniation had significantly higher resolution than cervical herniation by 90d, whereas cervical degeneration and stenosis resolved at higher rates than corresponding lumbar pathologies by 180d and 1-year follow-up, respectively. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: The efficacy of surgical intervention for central cord syndrome (CCS) is shown in the literature; however, it is unclear whether disparities in patient presentation and treatment exist between those who initially undergo operative treatment and those who delay operative treatment. PURPOSE: In a population of CCS patients, assess disparities in presentation and treatment between those undergoing immediate surgery and those who delay operative treatment. STUDY DESIGN/SETTING: Retrospective analysis of New York State Inpatient Database years 2004-2013. PATIENT SAMPLE: A total of 1,301 CCS patients (ICD-9 codes 952.03, 952.08, 952.13, 952.18). OUTCOME MEASURES: Time to surgery, length of stay (LOS).
METHOD(S): Patient-specific linkage codes allowed longitudinal tracking of inpatient stays within the study period. Demographics, comorbidities (Charlson Comorbidity Index [CCI]), complications, and surgical factors, including Mirza invasiveness score, were compared between CCS patients that initially underwent surgery (Initial) and patients that delayed operative treatment (Delayed) using Chi-squared tests and independent samples t-tests as appropriate. Similar tests assessed differences in demographics and comorbidity burden between nonoperative patients and surgical crossover patients.
RESULT(S): Included: 1,301 CCS patients (62+/-16 yrs, 27% female). Follow-up rate was 67.3%; mean follow-up time was 515+/-707 days. By level of CCS injury, 61.0% of patients were injured between C1 and C4, 59.2% between C5-C7, 1.0% between T1-T6, and 0.6% between T7-T12. Overall, 800 (61%) patients underwent surgical treatment (procedural breakdown: 80% fusion, 59% decompression, including 38% discectomy and 23% other decompression of the spinal canal). Of the surgical patients, 621 (78%) had surgery at first recorded hospital visit, while 179 (22%) experienced a delay before surgical treatment. For patients that delayed treatment, mean time to surgery was 203+/-358 days. Initial and Delayed patients did not differ in sex (p=0.109) or CCI (p=0.894), though Initial patients were younger than Delayed (60+/-15 yrs vs 63+/-13, p=0.016) and had lower rates of diabetes and valvular disease (both p<0.04). Initial patients underwent more invasive procedures than Delayed (5.1+/-2.6 vs 4.3+/-3.2, p=0.003), including higher rates of fusion (84% vs 71%, p<0.001), but not decompression: overall (59% vs 60%, p=0.816), discectomy (39% vs 35%, p=0.306), other canal decompression (22% vs 27%, p=0.175). LOS was longer for Initial patients (16+/-20 days vs 7+/-10, p<0.001), but complication rates did not differ (all p>0.05). Patients who delayed operative treatment did not differ from nonop patients in age (63+/-13 vs 63+/-17, p=0.802) or CCI (1.04+/-1.49 vs 1.06+/-1.49, p=0.923); however, Delayed patients had higher rates of diabetes (26% vs 18%, p=0.037), neurologic disorders (7% vs 1%, p<0.001), and valvular disease (6% vs 2%, p=0.026) than patients that remained nonoperative.
CONCLUSION(S): Although patients managed with initial surgical treatment of CCS had longer hospital stays and were treated with more invasive procedures, perioperative complications did not differ. Twenty-two percent of CCS patients crossed over from nonoperative to operative treatment, with a mean time to crossover of 203 days. Patients who crossed over to operative care were more comorbid than patients who remained nonoperative, indicating comorbidity burden may play a role in the decision to operate. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Persistent lumbopelvic malalignment following ASD-corrective surgery may impair quality of life and result in persistent pathologic compensation in the lower extremities. Patient-specific age- and BMI-adjusted alignment targets have been proposed to improve alignment outcomes; however, it is unclear whether reaching these postop targets reduces rates of pelvic nonresponse following surgery. PURPOSE: Assess the relationship between pelvic nonresponse to ASD-corrective surgery and persistent lower-extremity compensation. STUDY DESIGN/SETTING: Single center retrospective review. PATIENT SAMPLE: Fifty-eight ASD patients. OUTCOME MEASURES: Sagittal alignment.
METHOD(S): Included: surgical ASD patients with full-spine X-ray imaging at pre- and early postop follow-up (<1Y). Patients were grouped by postop improvement in PT, per SRS-Schwab Classification: those who did not improve (pelvic nonresponders, PNR), and those that did improve (pelvic responders, PR). Groups were propensity score matched for preop PT, and assessed for differences in demographics, surgical factors, and alignment (sagittal spinal and lower extremity) with means comparison tests. Rates of persistent postop lower extremity compensation (defined as no improvement in lower extremity alignment) were compared between groups. Subanalysis assessed the relationship between reaching postop age- and BMI-specific alignment targets and rates of pelvic nonresponse.
RESULT(S): Following propensity score matching, PNR (N=29) and PR (N=29) patients did not differ in age, sex, BMI or preop sagittal spinal alignment (all p>0.05); however, PNR patients presented with less knee flexion (9degree vs 14degree, p=0.043). Groups did not differ in levels fused (10.8 vs 10.8, p=0.974) or osteotomy (93% vs 92%, p=0.902). Postop, PNR patients had inferior lumbopelvic alignment in PT (30degree vs 17degree), PI-LL (17degree vs 3degree), and greater global malalignment for TPA (27degree vs 15degree, all p<0.001). For PNR patients, these changes in alignment were accompanied by greater compensatory anterior hip extension (53mm vs 31mm, p=0.021). PNR patients also showed greater pre- to postop increases in sacrofemoral angle (2degree vs -5degree), and smaller decreases in hip extension (-24mm vs -64mm), pelvic femoral angle (-1.4degree vs -3.8degree), and global sagittal angle (-3.5degree vs -8degree, all p<0.005), indicating persistent lower extremity compensation. PNR patients had higher rates of persistent postop lower extremity compensation for sacrofemoral angle (68% vs 25%), ankle flexion (64% vs 33%), and pelvic shift (28% vs 4%, all p<0.034). PNR and PR groups did not differ in rates of reaching age- and BMI specific ideal postop alignment for PT, SVA, TPA, or PI-LL (all p>0.05). For patients with severe preop SVA deformity, overcorrection relative to ideal postop PT targets was associated with lower rates of pelvic non-response (under: 12%, match: 18%, over: 71%, p<0.001). Lower rates of nonresponse were observed for patients with severe preop PT deformity overcorrected relative to ideal postop PI-LL (under: 0%, match: 30%, over: 70%, p=0.016).
CONCLUSION(S): Pelvic nonresponders following ASD-corrective surgery had higher rates of persistent compensatory action in the lower extremities. Patients with severe preop PT deformity who were surgically overcorrected with respect to ideal PI-LL had lower rates of postop pelvic nonresponse, indicating that for severely malalignmed patients, existing alignment targets may need to be adjusted to optimize alignment outcomes. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: The Miller et al adult spinal deformity frailty index (ASD-FI) correlates with increased complication risk after surgery; however, its development was not rooted in clinical outcomes, and the 40 factors needed for its calculation limit the index's utility in a clinical setting. PURPOSE: Develop a simplified, weighted frailty index for ASD patients. STUDY DESIGN/SETTING: Retrospective review of prospective ASD database. PATIENT SAMPLE: A total of 50 ASD patients. OUTCOME MEASURES: Health-related quality of life questionnaires: Oswestry Disability Index (ODI), SRS-22r, pain catastrophizing scale, Numerif Rating Scale (NRS) for Leg Pain.
METHOD(S): ASD patients (scoliosis>=20degree, SVA>=5cm, PT>=25degree, or TK >=60degree) with baseline ASD-FI component factors. Component ASD-FI parameters contributing to overall ASD-FI score were assessed via Pearson correlation. Top significant, clinically relevant factors were regressed against ASD-FI score to generate the modified ASD-FI (mASD-FI). Factors comprising the mASD-FI were regressed against the incidence of medical complications; weights for mASD-FI factors were calculated from these regression coefficients via the beta/Sullivan method. Total mASD-FI score was calculated by summing weights of expressed parameters, resulting in a score ranging from 0 to 21. Linear regression correlated ASD-FI and mASD-FI scores, and previously published ASD-FI cutoffs were used to generate corresponding mASD-FI frailty cutoffs: not frail (NF,<7), frail (7-12), severely frail (SF,>12). Analysis of variance assessed the relationship between increasing frailty category and validated baseline measures of patient pain and disability.
RESULT(S): Included: 50 ASD patients (52+/-20yrs, 78% female). All the following preoperative factors correlated with ASD-FI score (all p<0.039), and combined, accounted for 85.0% (p<0.001) of the variation in ASD-FI score: BMI <18.5 kg/m2 or >30 kg/m2 (weight: 5), depression (weight: 5), difficulty climbing stairs (3), presence of >3 medical comorbidities (2), leg weakness (2), difficulty getting dressed (1), bladder incontinence (1), and patient-reported deterioration in health within the past year (1). These factors were used to calculate the overall population's mean mASD-FI score: 5.7+/-5.2. Combined, these factors comprising the mASD-FI showed a trend of predicting the incidence of medical complications (Nagelkerke R2=0.558, Cox & Snell R2=0.399, p=0.065). Overall patient breakdown by mASD-FI frailty category: NF (70%), frail (12%), SF (18%). Increasing frailty category was associated with significant impairments in validated measures of disability, including ODI score (NF: 23.4, frail: 45.0, SF: 49.3, p<0.001), SRS-22r score (NF: 3.5, frail: 2.6, SF: 2.4, p=0.001), pain catastrophizing scale score (NF: 41.9, frail: 32.4, SF: 27.6, p<0.001), and NRS Leg Pain (NF: 2.3, frail: 7.2, SF: 5.6, p=0.001).
CONCLUSION(S): This study modifies an existing ASD frailty index and proposes a weighted, shorter mASD-FI. The mASD-FI relies less on patient-reported variables, and weights component factors by their contribution to adverse outcomes. As increasing mASD-FI score is associated with inferior clinical measures of pain and disability, the mASD-FI may serve as a valuable tool for preoperative risk assessment. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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