Faculty Bibliography

BACKGROUND CONTEXT: Loss of lumbar curvature is often expressed as an angular regional loss. Previous work comparing adult spinal deformity (ASD) lumbar alignment to their age-and-PI adjusted normative value demonstrated that, contrary to general belief, a large proportion of the curvature is lost proximally (L1-L4). This study is a follow-up looking not only at regional angles, but also at the spinal contour collectively. PURPOSE: Investigate the difference of lumbar shape between ASD and age-and-PI adjusted normative values. STUDY DESIGN/SETTING: Retrospective review of an ASD registry. PATIENT SAMPLE: A total of 119 asymptomatic volunteers and 362 ASD patients. OUTCOME MEASURES: Sagittal alignment of the lumbar and thoracolumbar spine measures using vertebra pelvic angle from L5 to T10.
METHOD(S): Before studying ASD patients, 119 asymptomatic volunteers with full-body, free-standing radiographs were used to identify age-and-PI models of each vertebra pelvic angle (VPA) from L5 to T10, a validated methodology characterizing the detailed shape of the spine. Our study cohort was a registry of surgical primary ASD patients without coronal malalignment (SRS-Schwab Type=N). The formulas developed in the asymptomatic population were applied to the ASD group to calculate an age-and-PI normative spine shape for each patient. Loss of lumbar lordosis was defined as the offset between age-and-PI normative value and pre-operative spino-pelvic alignment. Patients were stratified into four groups by the amount of lordosis lost, ranging from "no loss" to "30degree loss." Paired t-tests were performed to compare actual and normative VPA shapes within each group.
RESULT(S): Out of 1,495 patients enrolled in this registry, 453 were primary cases, and 653 were categorized as a Schwab type N, leading to a cohort of 362 patients (age=64.4+/-13, 57.1% F). Pre-operative alignment demonstrated a large variability with a mean PI-LL of 15degree+/-21, distal LL=31degree+/-15, and PI=55degree+/-13. Compared to their age-and-PI normative values, ASD patients demonstrated a significant lordosis loss of 17degree+/-19 with the following distribution: 14.1% no loss (mean: 0.1+/-2.3), 22.9% with 10degree loss (mean: 9.9+/-2.9), 22.1% with 20degree loss (mean: 20.0+/-2.8), and 29.3% with 30degree loss (mean:33.8+/-6.0). Comparison of the VPAs (and therefore the shape) between each LL group and the normative shape demonstrated that the "no loss" patients had a lumbar spine slightly anterior to the normative shape from L4 to T10 (VPA difference of 2degree). The shape of the "small deformity" group (10degree) superimposed on the normative one from L5 to L2 (VPA with p>0.1) and became anterior at the L1 level. As the lordosis loss increased, the offset between ASD and normative shapes began to propagate to the distal levels and became significant extending caudally to the L3 level for the "20degree loss" group and further down to L4 for the more severe group.
CONCLUSION(S): As the deformity progresses and the loss of lordosis increases, the difference between ASD shape and normative shape happens first proximally and then progresses incrementally caudally with increasing deformity. Understanding the spinal contour and the location of this loss, in addition to regional parameters, may be key to achieving a sustainable correction by identifying optimal and personalized post-operative shape. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: As adult spinal deformity (ASD) prevalence increases in our ever-aging population there is a concomitant increase in poor bone quality. ASD surgery is expensive and carries a high complication profile. It is important to optimize modifiable preoperative risk factors, such as osteopenia or osteoporosis. Additional diagnostic modalities such as a DEXA can add cost, delay diagnosis, and can be an additional insurance hurdle. Some studies suggest HU's can be utilized as a proxy for frailty, but it is unclear if this is useful in risk stratification. PURPOSE: Our goal was to evaluate the relationship between bone health as measured by HU's and PJK and identify a HU threshold in which PJK risk is increased. We hypothesize that HU will correlate with occurrence of PJK after ASD surgery. STUDY DESIGN/SETTING: Retrospective review of a prospective, multicenter ASD database. PATIENT SAMPLE: Of 1,330 pts eligible, 997 (74.9%) had complete 2Y follow-up. Of these, 605 meet inclusion criteria with 110 (18.18%) patients having a PJK. OUTCOME MEASURES: Development of PJK within 2 years of surgery.
METHOD(S): Operative ASD patients (scoliosis >20, SVA>5cm, PT>25, or TK>60) with available baseline (BL) and 2-year (2Y) radiographic and HRQL data were included if they had a preop CT. HU were measured from axial views within the cancellous body (x3) at both L1 and UIV with the mean value calculated for each. Threshold linear regression with Bayesian information criteria was utilized to identify optimal cut-offs of risk factors for PJK. Multivariable analysis (MVA) controlled for PJK prophylaxis and surgeon. Additionally, risk factors identified were controlled against each other.
RESULT(S): Threshold regression identified that cut-offs of <125 HU for UIV, >63 years for age, >0.31 for ASD-FI, and >47degree for preoperative T4-12 thoracic kyphosis, and <10 levels fused were predictive of PJK on bivariate analysis (P<0.05 for all). On MVA, age > 63 years old (OR 4.7; P = 0.003), female gender (OR 3.33; P=0.035), HU at UIV vertebrae <125 (2.83; P=0.008), ASD-FI >0.31 (OR 4.02; P=0.011), TK > 46degree (OR 3.75; P=0.003), and < 10 levels fused (OR 3.31; P=0.0310) were associated with increased odds of PJK.
CONCLUSION(S): Bone health as measured by HU appears to be an independent predictor of PJK after ASD surgery, specifically values <125 at the UIV. It also parallels frailty in prediction of PJK and can potentially be used as a proxy for frailty assessment. This can be easily measured and could help with risk stratification in the future. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Previous orthopedic literature has shown that patients with diabetes mellitus (DM) are more likely to develop complications in the postoperative period. To date, however, no study has assessed the specific pre- and postoperative risk factors that may contribute to this association for diabetic patients undergoing adult spinal deformity surgery. PURPOSE: Establish relevant risk factors for postoperative complications in a cohort of diabetic patients undergoing spinal deformity surgery. STUDY DESIGN/SETTING: Single-center retrospective cohort study. PATIENT SAMPLE: A total of 138 patients with DM who underwent spinal deformity surgery at a single academic hospital from 2012-2019. OUTCOME MEASURES: Primary outcomes were the development of any post-operative complications. These complications included the development of neurologic complications, urinary complications, cardiac complications, pulmonary complications, venous thromboembolism (VTE) and surgical site infections (SSI).
METHOD(S): This study is a retrospective cohort review of diabetic patients undergoing spinal deformity surgery, with 5 levels fused at a single academic medical center. Patients' age, BMI, levels fused, pre- and postoperative hemoglobin (Hgb), hematocrit (HCT) and preoperative HbA1C were collected. T-test and chi-square analyses were used to compare relevant outcomes. Significance was set to p<0.05.
RESULT(S): A total of 138 patients with DM met the inclusion criteria and were included in the analysis. Of these, 50.7% of the total cohort developed a postoperative complication within 90 days of the index surgery. Patients who developed postoperative complications were noted to have significantly lower postoperative Hgb (9.82+/-1.46 g/dL vs 10.72+/-1.76 g/dL, p=0.002) postoperative HCT (28.8+/-3.92% vs 32.60+/-4.61%, p<0.001) and significantly greater number of levels fused (9.49+/-3.74 vs 7.47+/-3.16, p=0.001). Diabetic patients who developed cardiac complications had significantly lower postoperative Hgb (9.47+/-1.50 g/dL vs 10.40+/-1.66 g/dL, p=0.021) and HCT (27.87+/-3.16% vs 31.15+/-4.72%, p=0.003) compared with those who did not. Diabetic patients who developed urinary complications were noted to be older on average (72.56+/-8.20 vs 64.43+/-11.70 years, p=0.043), while patients who developed VTE and pulmonary complications were noted to have significantly higher numbers of levels fused (VTE: 14.00+/-3.61 vs 8.37+/-3.51, p=0.007; PC: 10.82+/-4.14 vs 8.29+/-3.49, p=0.025)Finally, diabetic patients who developed a surgical site infection had significantly lower postoperative HCT (26.74+/-3.27% vs 30.86+/-4.64%, p=0.022) than those who did not. Multivariate logistic regression analysis showed that postoperative HCT (OR: 0.765 [0.613-1.098], p=0.001) and number of levels fused (OR: 1.243 [1.084-1.425], p=0.002) were predictive of development of any postoperative complication, when controlled for BMI, age, and and postoperative Hgb. Postoperative HCT was an independent predictor of the development of cardiac complications (OR: 0.827 [0.692-0.989], p=0.037) and SSI (OR: 0.709 [0.528-0.952], p=0.022).
CONCLUSION(S): Postoperative HCT is predictive of the development of postoperative complications in general, and more specifically the development of cardiac complications and surgical site infections. Along with blood-glucose and HbA1C, it should be closely monitored perioperatively in diabetic patients undergoing spinal deformity surgery. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Prophylaxis usage has been established in literature as an important component of minimizing the risk of proximal junctional kyphosis (PJK) and proximal junctional failure (PJF) development. However, literature is scarce on the effects of prophylaxis in patients who have achieved adequate postoperative alignment and those who maintained poor alignment postoperatively. PURPOSE: To investigate how PJK prophylaxis impacts rates of PJK and PJF with and without ideal alignment and the associated cost/cost-effectiveness. STUDY DESIGN/SETTING: Retrospective cohort study of a prospective adult thoracolumbar deformity database. PATIENT SAMPLE: This study included 1,541 patients. OUTCOME MEASURES: Radiographic alignment, patient-reported outcome measures (ODI), cost per QALY.
METHOD(S): Operative adult spinal deformity patients (scoliosis >20degree, SVA>5cm, PT>25degree, or TK>60degree) with an UIV at L1 or below and available baseline (BL) and 2-year (2Y) radiographic and HRQL data were included. "Matched" and "unmatched" alignment refers to the age-adjusted alignment criteria. PJK prophylaxis was defined by usage of cement, hooks or tethers. PJF was defined as PJK with reoperation. Costs were calculated using the PearlDiver database, accounting for additional costs of prophylaxis when applicable, through estimates from Medicare pay scales for services within a 30-day window, including estimates regarding costs of postoperative complications, outpatient healthcare encounters, revisions and medical related readmissions. QALY was calculated using SF6D.
RESULT(S): A total of 738 ASD patients or below met inclusion criteria (59.9yrs+/-14.0, 79%F, BMI: 27.7 kg/m2 +/-6.0, CCI: 1.8 +/-1.7). Surgically, patients had a mean level fused of 11.1+/-4.4, LOS of 7.9 days+/-4.4, EBL of 1577 mL, operative time of 377 min, with 63% undergoing an osteotomy. Forty percent of patients had PJK prophylaxis. Controlling for age, CCI, BL osteoporosis, levels fused, usage of 3CO, UIV, BL SVA and BL PI-LL, patients who were matched postoperatively in PT, SVA, or PI-LL had lowered PJF rates (OR:.5, 95% CI:.28-.86, p=.01) with prophylaxis. Among those unmatched in either SVA, PILL, or PT by 6W, prophylaxis significantly reduced the rates of PJK and PJF as well (p <0.05). ANCOVA controlling for age, CCI, BL osteoporosis, levels fused, usage of 3CO, UIV, BL SVA and BL PI-LL shows patients with ideal age-adjusted alignment and prophylaxis resulted in a lower cost per QALY by 2Y ($399,948 vs $514,228, p <.001). Similarly, in unmatched patients, prophylaxis resulted in a substantially lower cost per QALY by 2Y ($466,409 vs 672, 024, p <.001), primarily due to decreased costs of reoperation and greater improvements in QALY among prophylaxis cohorts.
CONCLUSION(S): Despite additional surgical cost, optimization of radiographic realignment in conjunction with utilization of proximal junctional failure prophylactic techniques achieves ideal cost utility, predominately due to the minimization of mechanical failure related reoperations. Even among those not achieving optimal alignment, junctional prophylactic measures improved cost utility, emphasizing its critical role of minimization of junctional failures to achieve cost efficiency in adult spinal deformity surgery. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: The ACS-NSQIP and SpineSage are both easy to use and readily available online perioperative risk calculators The ACS-NSQIP calculator predicts perioperative complications after surgery, but lacks more spine-specific predictors. The SpineSage platform was developed as a tool built for predicting complications in spine surgery. While a limited number of studies have shown it be predictive of both overall and major medical complications in spine surgery, large external validation studies are limited and none have directly compared NSQIP against SpineSage in the same cohort of spine surgery patients. PURPOSE: Assess the ACS-NSQIP Risk Calculator and SpineSage informatics platform for prediction of perioperative complications in spine surgery STUDY DESIGN/SETTING: Retrospective. PATIENT SAMPLE: A total of 440 patients undergoing thoracolumbar spine with or without fusion. OUTCOME MEASURES: Any complication, serious complication, pneumonia, cardiac, dural tear, SSI, UTI, VTE, reoperation, death and LOS METHODS: Each patient was entered into the ACS-NSQIP and SpineSage calculators and predicted risk for specific complications were directly compared to actual risks. Paired t-tests compared the differences between calculators and their predictability of complications. Patients were ranked based on risk predicted for each complication and the highest tertile for each was isolated. Multivariate regression controlling for age and gender was used to determine if the highest tertile for each risk calculator had predictability in complications following spine surgery.
RESULT(S): Mean LOS 4.2+3 days, EBL 444+300 mL, operative time 256+240 min, and levels instrumented 2.1+2.3. When assessing the four complications predicted by SpineSage there were significant differences in three of the four variables, as SpineSage underpredicted the risk of all and serious-complications (p.5). Both calculator tertiles were trending towards significance for major medical complications (SpineSage: OR: 2.0, [0.94-4.23], p=.073; ACS-NSQIP: OR: 1.8,[0.96-3.48],p=.067). When examining any medical risk, only ACS NSQIP had significant predictability for any medical complication (OR: 2.1, [1.3-3.3]; p=.003).
CONCLUSION(S): Similar to previous studies, the ACS-NSQIP score underpredicted most complications, with the exception of LOS and death. In contrast to previous studies, our data suggest SpineSage was not predictive of actual rates of complications. As both calculators are highly accessible and provide at least some objective perioperative risk data points, we recommend them as a guiding tool but not as an absolute endpoint for clinical decision making as they may be inaccurate and insensitive. Further, higher powered studies elucidating the findings in this study should be conducted. Additionally, the assessment of these calculators for a specific subset of patients, such as deformity, degenerative or pediatrics, can further help guide clinicians regarding the utility of these calculators for their particular patient populations. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Prone LLIF (P-LLIF) is a novel technique allowing for placement of a lateral interbody in the prone position and allowing posterior decompression and revision of posterior instrumentation without repositioning. To date, studies evaluating the P-LLIF have been small single surgeon series. This multicentre retrospective cohort examines perioperative outcomes and complications of single position P-LLIF againsttraditional Lateral LLIF (L-LLIF) technique with patient repositioning in patients undergoing revision lumbar fusion surgery. PURPOSE: To evaluate the feasibility and safety of the single-position P-LLIF technique for revision lumbar fusion surgery. STUDY DESIGN/SETTING: Multicenter retrospective cohort study. PATIENT SAMPLE: A total of 101 patients undergoing revision circumferential fusion with lateral lumbar interbody fusion (LLIF) were included, of which 43 had P-LLIF and 58 had L-LLIF. OUTCOME MEASURES: Outcome measures included levels fused, operative time, estimated blood loss and perioperative complications. Radiographic analysis included lumbar lordosis (LL), pelvic incidence (PI), pelvic tilt (PT), PI-LL mismatch and segmental lumbar lordosis.
METHOD(S): A multicenter retrospective cohort study was performed from 4 institutions from the USA and Australia of patients undergoing revision anterior-posterior lumbar fusion via either: 1) single-position prone LLIF (P-LLIF); or 2) lateral decubitus LLIF with repositioning to prone (L-LLIF) between January 2015 and November 2021. Patients with greater than 4 levels fused were excluded. Demographics, perioperative outcomes, complications and radiological outcomes were compared using independent samples t-tests and chi-squared analyses as appropriate with significance set at p<0.05.
RESULT(S): A total of 101 patients undergoing revision lateral lumbar interbody fusion surgery were included, of which 43 had P-LLIF and 58 had L-LLIF. Age, BMI and CCI were similar between groups. The number of posterior levels fused (2.21 P-LLIF vs 2.66 L-LLIF, p=0.469) and interbody levels fused (1.23 P-LLIF vs 1.25 L-LLIF, p=0.838) were similar between groups. Levels decompressed, posterior column osteotomy and anterior column release were similar between groups. Operative time was significantly less in the P-LLIF group compared to the L-LLIF group (151 vs 206 min, p=0.004). EBL was similar between groups (150 mL P-LLIF vs 182 mL L-LLIF, p=0.31) and there was a trend toward reduced length of stay (2.7 vs 3.3 days, p=0.09). No significant difference was demonstrated in perioperative or postoperative complications between P-LLIF and L-LLIF groups. Radiographic analysis demonstrated no significant differences in preoperative or postoperative sagittal alignment as measured by lumbar lordosis, PI-LL mismatch, or segmental lumbar lordosis between groups.
CONCLUSION(S): P-LLIF significantly improves operative efficiency and may reduce length of stay when compared to L-LLIF and repositioning for revision lumbar fusion. No increase in complications was demonstrated by P-LLIF or trade-offs in sagittal alignment restoration. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Evidence on long-term maintenance of health status in adult spinal deformity (ASD) patients who improve above MCID threshold (MCID+) at 2 years following surgery is limited. PURPOSE: This study aims to: (1) evaluate whether patients who reached MCID+ status at two years postoperatively will maintain MCID+ status at 5 years, (2) identify risk factors associated with maintaining MCID+ status, and (3) Assess whether maintaining MCID+ status at 5 years is associated with satisfaction with surgery. STUDY DESIGN/SETTING: Retrospective review. PATIENT SAMPLE: Patients who underwent adult spinal deformity (ASD) surgery with minimum 5-year follow-up who achieved 2-year MCID in ODI were identified. OUTCOME MEASURES: Maintenance of MCID+ status at 5 years for Oswestry Diability Index (ODI).
METHOD(S): Patients who maintained MCID+ status at 5 years and those who did not formed the comparison groups. Multivariable logistic regression, controlling for age, complications after two years and two-year alignment, was used to identify risk factors associated with the inability to maintain MCID+ status. In a separate multivariable logistic regression, whether maintaining MCID+ status was associated with 5-year surgical satisfaction was assessed.
RESULT(S): Of 633 eligible patients, 339 had 5-year data. Of 133 with both 2- and 5-year data, 70 who achieved 2-year MCID in ODI were included. 30% (21) failed to maintain MCID+ status at 5 years. Preoperatively, 33% (23) were narcotic users, 47% (33) were frail and mean surgical invasiveness was 96.6+/-36.02. On multivariable logistic regression, preoperative variables were assessed: CCI > 3 (OR 5.75; p=0.026), ASA grade > 2 (OR 5.25; p=0.015), anemia (OR 19.74; p=0.009), and cancer (OR 6.46; p=0.015) were associated with increased odds of failure to maintain MCID+ status at 5-year follow-up. Patients who failed to maintain MCID+ status at 5 years had a higher odds of being unsatisfied with the surgery (OR 15.66; p=0.001). Frailty and surgical invasiveness had no significant impact on MCID+ status at 5 years.
CONCLUSION(S): Preoperative comorbid conditions significantly impact patient's long-term ability to maintain the positive gains in health-related quality of life measures from the surgery. Surgeons should continue to monitor and treat the chronic conditions to ensure maintenance of long-term recovery. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Previous reports indicate postoperative complications have minimal impact on long-term outcomes after ASD surgery. Little data has evaluated the impact of complications on specific heath domains during postoperative period. PURPOSE: To evaluate the impact of specific complications on patient reported health domains compared to patients with no complications. STUDY DESIGN/SETTING: Prospective, multicenter, propensity score matched analysis. PATIENT SAMPLE: ASD patients enrolled into a prospective multi-center study. OUTCOME MEASURES: Oswestry Disability Index, Scoliosis Research Society-22r questionnaire (SRS-22r), Short Form-36v2 questionnaire (SF-36), postoperative complications.
METHOD(S): Surgically treated ASD patients enrolled into a multicenter study were assessed for postoperative complications requiring surgery including wound (WOUND), pseudoarthrosis (PSEUDO), neurologic (NEURO) and malalignment (MAL) and matched to patients with no complications (NOCOMP) using inverse probability weighting for demographic, radiographic and surgical variables. Health domains for SRS-22r, and SF-36 were evaluated at regular time intervals, domain scores normalized to the date of revision surgery, and compared to patients with no complications at minimum 2-year follow-up.
RESULT(S): A total of 566 of 1130 were analyzed, average 3.6 yrs (range: 1.9 to 9). WOUND (n=12) compared to NOCOMP (n=390) had worse SF-36 physical function(21.7 vs 27.4), social function(19.6 vs 28.9), general health (-7.3 vs 8.9) and vitality (-0.9 vs 26.6,p < 0.05). PSEUDO (n=64) was worse than NOCOMP for SRS-22r function, 1.4 vs 2.1, and SF-36 social function, (17.1 vs 28.9) (p < 0.05). NEURO (n=28) was worse than NOCOMP for SRS-22r (0.9 vs 2.1), SF-36 bodily pain (14.7 vs 35.7) and social function (13.4 vs 28.9) (p < 0.05). MAL (n=72) was worse than NOCOMP for SRS-22r pain, (2.7 vs 3.4), function (1.2 vs 2.1), self-image (3.0 vs 3.9), SF-36 bodily pain (27.6 vs 35.7), physical function (18.7 vs 27.4), and social function (11.6 vs 28.9) (p < 0.05).
CONCLUSION(S): Counter to previous reports, specific postoperative complications requiring surgery uniquely impact specific health domains, resulting in worse patient reported quality of life compared to ASD patients with no complications. Social function was negatively impacted for all complications, while wound complications negatively impacted patient perceived general health and vitality and patients with malalignment requiring surgery reported worse self-image. These data highlight new findings that postoperative complications have a negative impact on specific aspects of ASD quality of life that can undermine the potential benefits of ASD surgery. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Numerous studies have reported the interplay between spinal deformity and pelvis compensatory mechanisms, but little data exist evaluating the contribution of lower extremity compensation (LE) to maintain upright posture. We hypothesis that hip, knee and ankle compensation is proportional to the severity of the spinal deformity and varies by demographics. PURPOSE: Evaluate the association between spinal alignment and lower limbs compensation. STUDY DESIGN/SETTING: Multicenter, prospective cohort. PATIENT SAMPLE: This study included 288 patients treated for complex adult spinal deformity (ASD) with full body images available. OUTCOME MEASURES: Pelvic retroversion (PT), hip extension (SFA), knee flexion (KA), ankle dorsiflexion (AA), pelvic translation (P.Shift) and patient reported outcomes (ODI, PROMIS and SRS-22).
METHOD(S): Surgical ASD patients were enrolled into a prospective study based on three criteria: deformity severity (PI-LL>25degree, TPA>30degree, SVA>15cm, TCobb>70degree or TLCobb>50degree), procedure complexity (>12 levels fused, 3CO or ACR) and/or age (>65 and >7 levels fused). Associations between lower extremity compensation (hip extension, knee flexion, and ankle dorsiflexion) and the magnitude of spinal deformity, patient demographics, patient frailty, and patient-reported outcomes (ODI, SRS, PROMIS-CAT) were assessed via regressions and partial correlations.
RESULT(S): A total of 288/329 patients met inclusion criteria (60+/-15yo, 70.5% female), had moderate to severe spinal deformity (PI-LL:15+/-24, TPA:24+/-14, SVA:65+/-69mm, lumbar Cobb:34+/-24), and reported high pain (PROMIS pain interference; PI=62.7+/-7.8) and reduced physical function (PROMIS physical function; PF=35.6+/-7.6). Lower extremity compensation included pelvic retroversion (PT:24.1+/- 11.8), hip extension (SFA: 203+/-10.5), knee flexion (KA:5.5+/- 9.6), ankle dorsiflexion (AA: 5.3+/-4.5), and posterior pelvic translation (P.Shift: 30+/-51mm). Overall, lower extremity compensation increased with age (all p <0.001), BMI and frailty (all p <0.001, except SFA). For a similar PT, women had greater hip extension than men (SFA: 206 vs 200, p <0.001), with less KA (3.6 vs. 10.1, p <0.001), AA, and P.Shift. Lower extremity compensation increased with PI (r=0.2-0.45, p <0.001), TPA (r=0.5-0.9, p <0.001) and correlated with PROMS (ODI:0.26 - 0.37, PROMIS PF: -0.28 - -0.39, SRS Acti.: -0.20 - -0.33). When controlling for deformity severity and PI, most associations between lower limbs compensation and PROMS were lost. However, P.Shift and SFA remained weakly correlated with physical scores (ODI and PROMIS PF).
CONCLUSION(S): The recruitment of LE compensation is overall proportional to the severity of adult spinal deformity, with different patterns observed between men and women. Patients achieved similar PT by recruiting different patterns of LE compensation. Hip extension and posterior pelvic translation are independently associated with impairment in patient-reported outcomes. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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BACKGROUND CONTEXT: Adult cervical deformity (ACD) can have profound impact on health-related quality of life (HRQL). Operative treatment for ACD is associated with high complication rates due to the complexity of surgery and the frailty of the patients affected. Very few studies have focused on outcomes of operative ACD treatment. PURPOSE: To assess whether operative treatment for ACD significantly improves HRQL at minimum 2-yr followup. STUDY DESIGN/SETTING: Multicenter, prospective cohort study. PATIENT SAMPLE: Operatively treated ACD patients. OUTCOME MEASURES: Neck Disability Index (NDI), modified Japanese Orthopaedic Association (mJOA), EuroQol-5D (EQ-5D), and numeric rating scale (NRS) for neck and back pain.
METHOD(S): Operatively treated ACD patients were assessed at baseline, standardized follow-up intervals and through direct mailings. Patient-reported outcomes measures (PROMs) included: NDI, mJOA, EQ-5D and NRS for neck and back pain. Complications were classified as perioperative (=30 days) or delayed (>30 days). Analyses focused on patients with minimum 2-yr followup.
RESULT(S): Of 169 ACD patients, the 102 (60%) with minimum 2-yr followup (mean=3.4 yrs, SD=1.9 yrs, range=2 to 8.1 yrs) had a mean age of 62 yrs (SD=11) and 64% were women. Surgical approaches included anterior-only (22.8%), posterior-only (39.6%) and combined (37.6%). The mean numbers of vertebrae fused anteriorly and posteriorly were 4.3 (SD=1.1) and 9.4 (SD=3.4), respectively, with 16% having a 3-column osteotomy. PROMs significantly improved from baseline to last follow-up, including NDI (47.3 to 33.0), mJOA (12.0 to 12.8; for patients with baseline score 0.05). Overall, 58 (56.9%) patients had at least 1 complication, 41 (40.2%) had at least 1 perioperative complication, and 35 (34.3%) had at least 1 delayed complication. The most common complications included dysphagia (18.6%), distal junctional kyphosis (6.9%), instrumentation failure (6.9%), cardiac events (6.9%), dysphonia (4.9%), nerve sensory deficit (3.9%) and respiratory failure (3.9%). For patients with at least 2-yr follow-up, 12 patients underwent a total of 15 reoperations (9 had 1 and 3 had 2). Notably, the 67 patients who did not achieve 2-yr follow-up were similar to study patients based on demographics, comorbidities and baseline PROMs. Reflective of the frailty of this patient population, there were 18 deaths among the 67 patients without minimum 2-yr followup. These deaths occurred between 0.2 and 34.8 months following surgery. Although most occurred at least 6 months after surgery and likely were not directly related to surgery, 4 occurred within 4 months of surgery, including 1 due OSA/narcotics, 1 due to pneumonia, and 2 with unknown causes.
CONCLUSION(S): This multicenter, prospective analysis demonstrates that operative treatment for ACD provides significant improvement of HRQL at minimum 2-yr (mean 3.4-yr) followup. These findings may prove useful for patient counseling in the context of the substantial impact of ACD. Further studies will be needed to assess the long-term durability and cost-effectiveness of surgical treatment for ACD. FDA DEVICE/DRUG STATUS: This abstract does not discuss or include any applicable devices or drugs.
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