Screw density in adult deformity surgery: the upper instrumented level matters

Spine. 2026;51(21):1538-1543

Reducing implant density in adult spinal deformity surgery should not be treated as a uniform strategy. Williams and colleagues found that higher fixation density was associated with fewer mechanical complications, particularly in constructs extending from the pelvis to T10-L2. Their findings support considering the upper instrumented vertebra when planning fixation, while stopping short of proving that fewer screws are safe in longer thoracic constructs.

Study and key findings

This retrospective single-center study included 170 adults undergoing deformity correction with pelvic fixation between 2008 and 2021. Mean age was 66.8 years and mean radiographic follow-up was 4.5 years. All constructs reached L2 or above, and inclusion required at least two years of radiographic follow-up.

Importantly, density counted fixation points, including screws or hooks, divided by instrumented levels; the sacrum and ilium were counted separately. High and low density were defined relative to cohort-specific medians, rather than a universal surgical threshold.

Across the entire cohort, higher density was associated with lower adjusted odds of the combined endpoint of rod fracture or pseudarthrosis (OR 0.40; 95% CI 0.18-0.86). For constructs with an upper instrumented vertebra at T10-L2, higher density was associated with lower odds of this endpoint (OR 0.18; 95% CI 0.05-0.52) and reoperation (OR 0.16; 95% CI 0.04-0.57). No significant associations were demonstrated in constructs reaching T9 or above. Density was not significantly associated with proximal junctional kyphosis.

Interpretation and limitations

These are associations, not evidence that adding screws prevents failure. Only 170 of 253 eligible patients had sufficient follow-up, creating potential selection bias. Surgeon preferences, anatomy and unmeasured confounding may influence both density and outcomes. Small subgroups limit precision, and nonsignificant findings in longer constructs do not establish equivalence or safety.

The analysis stratified whole constructs by their upper endpoint; it did not establish which individual levels can safely be skipped. Median-based categories should not become prescriptive density targets.

Clinical takeaway

Review fixation density alongside construct extent, bone quality and correction requirements. Be cautious about reducing fixation in T10-L2-to-pelvis constructs, but avoid interpreting this study as a mandate to instrument every level or permission to omit specific thoracic screws.

Endoscopic lumbar discectomy: choosing the corridor around the pathology

Neurosurgical Focus. 2026;61(4):E10

The choice between interlaminar and transforaminal endoscopic discectomy depends on the relationship between the surgical corridor and the compressive pathology. This study describes how one experienced surgeon selected these complementary approaches, highlighting the importance of disc level, fragment location, cranial migration, and associated dorsal stenosis. Its principal contribution is an anatomical framework for planning rather than evidence that either technique produces superior outcomes.

Study and key findings

This retrospective series included 426 adults undergoing 438 single-level procedures between 2019 and 2025: 233 interlaminar and 205 transforaminal discectomies. Of the interlaminar procedures, 86.3% were performed at L5–S1; 95.6% of transforaminal procedures were performed at L4–5 or above.

In a matched analysis restricted to L4–5 and higher levels, involving 32 interlaminar and 64 transforaminal procedures, herniation within the canal, cranial migration, and dorsal stenosis were independently associated with selection of the interlaminar approach. The corresponding odds ratios were 19.69, 17.82, and 5.15. These estimates describe approach selection, not the probability of surgical success.

Disability and pain improved in both groups. Mean Oswestry Disability Index scores decreased from 45.2 to 20.8 after interlaminar surgery and from 46.6 to 23.4 after transforaminal surgery. Mean follow-up was 329 days; 41 procedures (9.4%) were followed by additional surgery at the index level.

Interpretation and limitations

At L5–S1, the interlaminar window and potential iliac crest obstruction help explain the predominant posterior route. Nevertheless, foraminal or extraforaminal pathology can favor transforaminal access even at this level. Cranially migrated intracanal fragments and dorsal compression may instead favor interlaminar access, which also permits posterior decompression.

The retrospective, single-surgeon design reflects individual expertise and selection preferences. The small matched sample and wide confidence intervals limit precision. Improvements in both groups cannot establish equivalence, superiority, or a validated selection algorithm.

Clinical takeaway

Plan the approach around the fragment and all relevant sources of compression. Assess migration, foraminal involvement, dorsal stenosis, iliac crest anatomy, and previous surgical scarring alongside the surgeon’s expertise. Disc level is a useful starting point, but should not determine the corridor alone.

Spinal deformity surgery: interpreting the first two weeks of risk

Spine. 2026;51(20):E519-E529

The extent and complexity of deformity correction deserve explicit consideration when discussing perioperative risk. Katayanagi and colleagues identify associations between operative characteristics and complications during the first 14 days, but their registry does not establish that changing approach or staging surgery will independently prevent harm. Understanding the outcome definition is essential before applying its headline complication rate.

Study and key findings

This retrospective analysis used prospectively recorded Japanese registry data from 3,193 patients undergoing fusion of at least three vertebral segments between 2018 and 2022. Mean age was 60.8 years, and approximately three-quarters underwent fusion of six or more segments.

At least one complication occurred in 910 patients (28.5%); 812 (25.4%) had a major complication, and three died. Importantly, blood loss exceeding 1,000 ml was classified as a major complication and occurred in 638 patients (20.0%). Neurological complications occurred in 3.1%.

Adjusted odds of any complication were higher with operative duration exceeding five hours (odds ratio 4.40), three-column osteotomy (3.50), fusion exceeding five levels (1.51), and posterior/transforaminal interbody fusion (1.47). Staged surgery (0.24), lateral lumbar interbody fusion (0.74), and minimally invasive techniques (0.65) were associated with lower odds. Associations were broadly consistent in the long-fusion subgroup.

Interpretation and limitations

These findings support reviewing surgical burden and possible alternatives, not ranking techniques independently of indication. Prolonged surgery may reflect deformity complexity or intraoperative events; five hours is not a validated deadline for completing an operation.

The registry lacked radiographic deformity severity, achieved correction, patient-reported outcomes and several important comorbidities. Residual confounding therefore limits comparisons, particularly the apparently favorable association with staging. The bleeding-based definition substantially influences the composite endpoint, while overlapping major and minor events mean their percentages should not be added. Fourteen-day surveillance cannot characterize delayed infection, pseudarthrosis or later mechanical failure.

Clinical takeaway

Use these data to inform counseling and multidisciplinary planning around anticipated blood loss, fusion extent and osteotomy requirements. Consider staging or less invasive options when anatomically and clinically appropriate, while preserving necessary correction and decompression. Decisions require balancing early procedural burden against durable alignment and function, outcomes this study did not measure.

Mobile spine chordoma: balancing tumor margins against long-term function

J Neurosurg Spine. 2026;45(4):622-631

Preserving nerve roots does not eliminate the risk of long-term weakness after mobile spine chordoma surgery. Xia and colleagues describe how functional outcomes reflect not only intentional root sacrifice but also neural manipulation, recurrence and other treatment-related events. Their series informs individualized discussions about oncological margins and anticipated disability, without establishing equivalence between surgical strategies.

Study and key findings

This retrospective single-center study included 35 patients with cervical, thoracic or lumbar chordomas, with a median age of 55 years and median follow-up of 5.4 years. Twenty-three resections were Enneking appropriate (EA), defined as en bloc R0 removal with an intact capsule; 12 were Enneking inappropriate (EI), involving intralesional resection or capsule violation.

At last follow-up, motor weakness was present in 11/23 EA patients (47.8%) and 5/12 EI patients (41.7%; p > 0.99). Seven of 19 patients without root sacrifice nevertheless had unplanned long-term weakness. All three patients undergoing sacrifice of roots classified as functionally important developed planned long-term weakness.

Pain improved in 26/31 patients who had preoperative pain, although 21/35 still reported pain at follow-up. Ten patients required surgery for complications. Among the 13 patients with unplanned weakness, the authors attributed five cases to tumor progression; other explanations included neural manipulation, spinal cord infarction, stroke and radiation-related injury.

Interpretation and limitations

The practical decision is whether achieving an intact oncological margin justifies sacrificing a particular neural or vascular structure. In seven EI cases, planned intralesional resection reflected concern about unacceptable morbidity from critical-structure sacrifice.

Treatment selection was not randomized, and the groups differed in anatomy and radiotherapy exposure. Small numbers, retrospective documentation, heterogeneous radiation treatment and absent patient-reported outcomes limit interpretation. A nonsignificant comparison does not demonstrate equal functional or oncological safety. The study’s functional-root classification concerns extremity motor function; it should not imply that other roots have no physiological role.

Clinical takeaway

Discuss the expected deficit from each proposed root sacrifice separately from the broader risk of long-term weakness. Integrate tumor extent, vascular involvement, achievable margins, radiotherapy options and patient priorities into multidisciplinary planning. Root preservation is an important objective, but not a guarantee of preserved function.

Nicotine beyond smoking: a risk signal before ALIF

Spine. 2026;51(20):1456-1463

Preoperative assessment before anterior lumbar interbody fusion (ALIF) should look beyond cigarette smoking. Hirpara and colleagues found that coded nontobacco nicotine dependence was associated with more pseudarthrosis and revision surgery. The findings support a broader nicotine history and individualized counseling, but do not establish causation or quantify the risks of individual products.

Study and key findings

This retrospective TriNetX study included patients older than 18 undergoing primary ALIF. Investigators identified nicotine dependence through diagnostic codes while excluding specified tobacco-dependence and tobacco-use codes. Propensity matching produced two groups of 2,296 patients, balanced for demographic factors, relevant comorbidities and recorded surgical characteristics.

At two years, coded pseudarthrosis occurred in 20.1% of patients with nontobacco nicotine dependence versus 11.3% of controls: odds ratio 1.97, 95% confidence interval 1.67-2.33. Revision surgery occurred in 12.1% versus 9.9%: odds ratio 1.25, 95% confidence interval 1.04-1.51. These represent absolute differences of 8.8 and 2.2 percentage points, respectively.

Emergency visits, pneumonia and sepsis were more frequent within 90 days. Cumulative opioid prescriptions were also higher; these measurements should not be interpreted as continuous opioid consumption at two years. Implant failure did not differ significantly.

Interpretation and limitations

The main contribution is identifying a potentially overlooked risk marker, not selecting an alternative approach or implant. Exposure and outcomes depended on administrative coding rather than biochemical verification or standardized imaging review. Residual confounding remains possible despite matching.

The database could not distinguish nicotine delivery methods, dose, frequency or duration. Consequently, the study cannot isolate the effects of vaping, pouches or therapeutic nicotine replacement, nor establish their comparative safety. Detailed ALIF construct subgroups were unavailable. Although the authors advocate perioperative abstinence, their analysis did not test a cessation intervention or establish an effective abstinence interval.

Clinical takeaway

Ask explicitly about non-cigarette nicotine products during ALIF planning and incorporate the findings into shared risk discussions and coordinated preoperative optimization. This observational evidence does not justify a blanket change in fusion technique or an automatic prohibition of prescribed nicotine-replacement treatment; cessation decisions require individualized clinical assessment.

Two versus four screws in ACDF: earlier fusion, but better clinical outcomes?

Spine. 2026;51(20):1427–1434

Zero-profile implants offer different approaches to fixation after anterior cervical discectomy and fusion (ACDF).
This randomized trial compares a two-screw variable-angle device with a four-screw fixed-angle device.
The two-screw group had more radiographic fusion at six months, while the difference was no longer significant at one year.
The study helps distinguish an early imaging advantage from a demonstrated improvement in patient recovery.

Objective

Compare six-month fusion rates, clinical outcomes and complications after single-level ACDF using two zero-profile implant designs.

Methods

Eighty adults were randomized, with allocation concealed until surgery. Seventy-seven were analyzed: 39 received Zero-P VA with two variable-angle screws and 38 received Zero-P with four fixed-angle screws.

Fusion required both dynamic radiographic criteria and CT evidence of bridging bone. Both groups received artificial bone graft and were advised to wear a rigid collar for three months.

Main results

At six months, fusion rates were 69.2% versus 42.1%, favoring the two-screw device (reported P=0.022): an absolute difference of 27.1 percentage points.

At 12 months, reported rates were 91.9% versus 88.9% (P=0.711). JOA, Neck Disability Index and neck/arm pain scores improved in both groups, without significant between-group differences.

Complications occurred in 9/39 (23.1%) versus 8/38 (21.1%). Subsidence or displacement occurred in 6/39 (15.4%) versus 3/38 (7.9%), respectively; this difference was not statistically significant.

Interpretation

The trial supports an advantage in the prespecified six-month radiographic endpoint. It does not demonstrate better pain relief, function or safety.

The comparison changes screw number, angulation and implant mechanics together. Consequently, the result cannot be attributed to screw count alone. Micromotion and load sharing provide a possible explanation, but were not directly tested as mechanisms.

Limitations

This single-center study analyzed completers, without imputation for three patients lost to follow-up. Patients older than 65 years, those with severe osteoporosis and multilevel cases were excluded.

Secondary outcomes were exploratory. The sample cannot establish equivalent safety or exclude meaningful differences in subsidence, while twelve-month follow-up limits conclusions about durability.

Clinical takeaway

Two-screw variable-angle fixation is an option to consider for selected single-level ACDF patients. Earlier radiographic fusion alone does not justify changing collar protocols or return-to-activity advice; these benefits were not tested.

Rethinking sagittal correction in adult spinal deformity

J Neurosurg Spine October 9, 2026

Choosing sagittal correction targets remains a central challenge in adult spinal deformity surgery.
This multicenter study evaluates lumbar alignment together with the relationship between T4 and L1.
It also examines how early junctional compensation can alter postoperative measurements.
The findings favor interpreting spinal shape in the context of fusion extent and caution against excessive correction.

Objective

Evaluate whether L1 pelvic angle (L1PA) and T4–L1 pelvic angle targets are associated with proximal junctional failure (PJF), accounting for early changes above the instrumented spine.

Methods

Retrospective analysis of a prospective multicenter adult deformity registry. Of 861 eligible patients, 661 had complete two-year follow-up and data. The principal comparisons involved 604 patients fused from the ilium to T2–4 (225 patients) or T9–11 (379 patients).

Six-week radiographs were assessed against published alignment targets. A virtual model estimated alignment without early proximal junctional compensation. PJF comprised proximal-extension revision or severe radiographic junctional kyphosis.

Main results

PJF occurred in 108/604 patients (17.9%); 50/604 (8.3%) underwent proximal-extension revision.

In upper-thoracic constructs, PJF rates were 25.6% with L1PA overcorrection, 12.9% within target, and 11.1% with undercorrection (P=0.029). This association persisted after demographic and comorbidity adjustment (P=0.028).

T4–L1 categories alone did not significantly distinguish failure rates in this subgroup (P=0.094).

In lower-thoracic constructs, removing simulated junctional compensation reclassified 175/379 patients (46.2%). The initial association between T4–L1 category and PJF then lost significance (P=0.148).

Interpretation

The most persuasive finding is that six-week alignment may already incorporate compensatory changes or evolving junctional failure. Consequently, a postoperative measurement can reflect both the surgical correction and the spine’s response to it.

The upper-thoracic findings raise concern about overcorrection relative to the studied L1PA formula. They do not establish intentional undercorrection as a superior treatment strategy. Evidence supporting particular combinations of lumbar and thoracic shape remains exploratory.

Limitations

Observational design limits causal inference, and only 76.8% of eligible patients contributed complete two-year data. Immediate postoperative radiographs were unavailable, requiring modeled reconstruction. Spinal flexibility was not directly measured, and patient-reported outcomes were not evaluated in this analysis.

Adjustment included age, sex, BMI and comorbidity burden, leaving potential residual confounding. Numerous authors disclosed industry relationships.

Clinical takeaway

Interpret L1PA and T4–L1 measurements alongside fusion extent and junctional behavior. The study supports caution with excessive lumbar correction and highlights the limitations of applying identical targets to upper- and lower-thoracic constructs.

Mild posterior ligamentum flavum compression: must cervical arthroplasty be excluded?

Spine (Phila Pa 1976). 2026;51(19):1363-1373

Mild posterior ligamentum flavum compression need not automatically exclude cervical disc replacement in otherwise suitable patients. Pezzi and colleagues report improvements in disability and pain after both arthroplasty and anterior cervical fusion. However, their findings predominantly concern mild disease and do not establish equivalent neurological safety or support arthroplasty for severe posterior compression.

Study and key findings

This single-center retrospective study included 228 adults with degenerative cervical myelopathy or myeloradiculopathy undergoing one- or two-level anterior cervical discectomy and fusion (ACDF; 160 patients) or cervical disc replacement (CDR; 68 patients). Median follow-up was 18.9 months.

Among 127 patients with MRI-defined ligamentum flavum involvement, 101 underwent ACDF and 26 underwent CDR. Weighted analysis found no significant difference in Neck Disability Index trajectories between procedures (P=.26). Disability and pain improved after both operations.

Crucially, 24 of the 26 CDR patients with ligamentum flavum involvement had mild buckling; only two had the more severe grade combining buckling and hypertrophy. The evidence for arthroplasty therefore cannot be generalized across compression severities.

Interpretation and limitations

The practical decision is whether mild posterior buckling should independently rule out motion preservation when an anterior procedure is otherwise appropriate. The findings favor assessing severity and overall anatomy rather than applying a blanket exclusion.

Nevertheless, CDR patients were younger, healthier and less severely affected. Statistical weighting did not fully balance the groups, leaving residual confounding despite further adjustment. Nonsignificant differences do not demonstrate equivalence.

Outcomes emphasized patient-reported disability and pain rather than a dedicated neurological myelopathy scale. Similar recovery scores cannot establish identical spinal cord recovery. Postoperative MRI was available in only 86 patients, limiting conclusions about structural changes. The study does not define a ligament-thickness threshold or validate an anterior-versus-posterior decompression algorithm.

Clinical takeaway

Mild ligamentum flavum buckling may be compatible with cervical arthroplasty in carefully selected patients. Severe posterior compression remains insufficiently studied, and favorable patient-reported outcomes should not substitute for assessment of the adequacy of spinal cord decompression.

Paraspinal muscle advancement after posterior cervical fusion: reconstructing the wound, not merely closing it

Journal of Neurosurgery: Spine. 2026;45(4):660-667

Soft-tissue closure deserves consideration as part of the reconstructive strategy in posterior cervical surgery, particularly when instrumentation leaves a substantial wound cavity. Adida and colleagues examine whether advancing the paraspinal musculature is associated with fewer wound complications than conventional closure after posterior cervical decompression and fusion. Their comparison of 508 patients provides a clinically relevant signal of fewer infections and wound-related reoperations in adjusted analyses, while illustrating the difficulty of separating a closure technique from changes in perioperative care. The practical contribution is a rationale for vascularized coverage and dead-space reduction, rather than definitive evidence that one closure method should replace all others.

Objective

To compare wound complications and wound-related reoperations after conventional closure or bilateral paraspinal muscle flap advancement following posterior cervical decompression and fusion.

Methods

The investigators compared 380 patients treated with conventional closure between 2011 and 2022 with a prospectively maintained series of 128 consecutive patients receiving muscle flap advancement between 2023 and 2025 at a single academic quaternary center. Active local or systemic infection and follow-up shorter than three months were exclusion criteria. Indications included degenerative disease, deformity, trauma and malignancy; approximately one fifth of each cohort underwent revision surgery.

Wound events included infection, dehiscence, hematoma and seroma. Wound-related reoperation was recorded per patient. Analyses included time-to-event comparisons and Firth-penalized logistic regression. Importantly, the methods and Table 2 describe adjustment with individual covariates rather than a single model simultaneously controlling for every potential confounder.

Main results

Infection was recorded in 31 of 380 conventional-closure patients and 4 of 128 muscle-flap patients, approximately 8% and 3%. Wound-related reoperation occurred in 47 and 9 patients, approximately 12% and 7%, respectively. The reported regression estimates associated muscle flap closure with lower odds of infection (OR 0.275, 95% CI 0.085-0.702) and wound-related reoperation (OR 0.445, 95% CI 0.198-0.912).

Dehiscence remained similar, at approximately 12% versus 11%. Seroma was numerically more frequent with muscle advancement, approximately 9% versus 5%, without a statistically significant difference. Hardware removal occurred in five conventional-closure patients and no muscle-flap patients. These small event counts do not establish a reliable hardware-retention advantage.

The time-to-event analyses were less conclusive than the logistic models. Log-rank comparisons for infection-free and reoperation-free survival did not reach statistical significance, and the reported Cox estimates had confidence intervals crossing unity. Thus, the evidence does not support describing the benefit as uniformly demonstrated across analytical approaches.

Interpretation

The operative decision is whether to incorporate paraspinal muscle advancement at the index operation to improve coverage of the instrumented cervical wound. The authors describe mobilizing the muscle complex and bringing vascularized tissue into the midline cavity. Their initial Lembert closure imbricated muscle into the defect; the subsequently adopted vest-over-pants configuration overlapped the advanced muscle margins. Both used absorbable sutures, and superficial drainage was described above the reconstructed muscle layer.

These details support a reconstructive concept: address the deep wound cavity and soft-tissue coverage rather than relying solely on superficial approximation. However, the study did not compare the two flap configurations, quantify tension reduction or perfusion, or establish which patients derive the greatest benefit. Its results also cannot define an optimal drain regimen or justify a specific antimicrobial adjunct independently of the overall closure strategy.

Limitations

The cohorts were noncontemporaneous, with retrospective ascertainment in the earlier group and prospective maintenance of the later series. Changes in practice, case selection and complication detection may therefore contribute to the observed associations. The muscle-flap cohort was older, and baseline characteristics were not identical. Limited events and adjustment one covariate at a time leave substantial potential for residual confounding.

Co-interventions are particularly important. Topical vancomycin was used in every muscle-flap case but only most conventional cases, while incisional negative-pressure therapy was introduced during the study and used in 63 muscle-flap patients. The contributions of these measures cannot be isolated. Drain number, duration and removal criteria were not analyzed. The two flap techniques were pooled, and a three-month minimum follow-up does not ensure equivalent long-term observation across cohorts.

The contrast between logistic and time-to-event findings further limits certainty. The study supports an association and a plausible operative rationale, not a causal estimate of how many infections or reoperations muscle advancement itself prevents.

Clinical takeaway

Paraspinal muscle advancement is a promising option for reconstructing the posterior cervical wound after decompression and fusion. The strongest practical message is to plan deep soft-tissue coverage and dead-space management deliberately. This series does not establish universal superiority over conventional closure, favor Lembert over vest-over-pants repair, or determine the independent benefit of drains, topical antibiotics or negative-pressure therapy.

Body mass index in cervical myelopathy surgery: anticipating operative demands without assuming poor recovery

Spine (Phila Pa 1976). 2026;51(19):1354-1362

Body mass index is readily available during preoperative assessment, but its implications for cervical myelopathy surgery are not straightforward. A technically more demanding operation does not necessarily imply less neurological recovery, and similar average outcomes do not establish equal risk for every patient. Okubo and colleagues address this distinction in a prospective Japanese multicenter cohort, relating BMI to operative variables, cervical alignment and two-year clinical outcomes. Their findings associate obesity with longer procedures and greater blood loss, while showing no statistically significant differences in neurological improvement across BMI categories. The principal relevance is to individualized planning and counseling rather than selection of a specific surgical technique.

Objective

To assess the association between BMI and operative demands, perioperative complications, cervical alignment, neurological recovery and patient-reported outcomes after surgery for degenerative cervical myelopathy.

Methods

The study drew on a prospective cohort from ten high-volume spine centers in Japan between 2018 and 2022. Of 1,105 patients identified with degenerative cervical myelopathy, 935 entered the final analysis after exclusions for previous cervical surgery, missing essential information, loss to follow-up or death during observation.

Patients were classified as underweight (BMI below 18.5; n=35), normal weight (18.5-24.9; n=522), overweight (25.0-29.9; n=292), or having obesity (30 or above; n=86). Posterior decompression predominated in every group; anterior and posterior fusion procedures were less frequent. Complications were defined as adverse events within 30 days of surgery.

Assessment included Japanese Orthopaedic Association (JOA) scores, pain ratings, SF-36 physical and mental component scores, neuropathic pain symptoms, and cervical radiographs. Clinical outcomes at two years were compared using general linear models with adjustment for demographic, comorbidity and imaging variables. Models for outcome changes also incorporated operative time, blood loss and postoperative alignment and motion measurements.

Main results

Patients with obesity had mean operative time of 128.3 minutes and blood loss of 91.2 mL, versus 102.1 minutes and 38.1 mL in normal-weight patients; global comparisons across the four groups were significant. OPLL prevalence was 47.7% versus 16.9%. Adjusted JOA improvement was 3.5, 3.2, 2.6 and 3.1 points across ascending BMI categories (P=.129). Reported complication categories did not differ significantly. Obesity remained associated with less cervical lordosis and motion at two years. Between-group differences in pain, SF-36 and neuropathic pain changes were not statistically significant; this does not demonstrate equivalent outcomes.

Interpretation

The decision informed by this study is how BMI contributes to preparation and expectations when clinical and imaging findings already support surgery. Greater operative demands justify attention to associated comorbidities and cervical anatomy, particularly the higher frequency of OPLL, rather than assuming that neurological recovery will be poor. However, the study does not compare approach-selection algorithms or validate a BMI-specific exposure, fixation or closure technique. Persistent differences in alignment and motion also should not be described as surgical failure: they coexisted with neurological improvement. Conversely, favorable average recovery should not be interpreted as eliminating individual perioperative risk.

Limitations

This observational cohort cannot establish the independent causal effect of BMI. Patients with obesity were younger and more frequently had OPLL, diabetes and hypertension. Statistical adjustment reduces some measured confounding but does not resolve unmeasured differences. Moreover, adjusting for operative demands and postoperative radiographic findings may account for intermediate pathways through which BMI could affect outcomes, rather than estimating its total association with recovery.

The analysis included patients selected for surgery and excluded those who died or were lost during follow-up. Consequently, its complication comparisons cannot be generalized to all patients initially considered for surgery or used to establish mortality safety. Care at high-volume Japanese centers and the predominance of posterior decompression further limit extrapolation to other settings or procedure mixes.

Only 35 patients were underweight and 86 had obesity, without a separate analysis of severe obesity classes. Rare complications and modest clinical differences could therefore have been missed. The authors’ post hoc analysis indicated limited power for JOA and mental-component changes; nonsignificant findings are not evidence of equivalence. BMI also does not characterize muscle mass, nutritional status or visceral adiposity. Two years is insufficient to settle long-term adjacent-segment disease, reoperation or progressive alignment changes. Finally, inconsistencies in some tabulated variability labels and secondary outcome intervals warrant caution when interpreting precise estimates.

Clinical takeaway

In this selected surgical cohort, a higher BMI was associated with greater operative demands but not a statistically significant reduction in two-year neurological improvement. The findings argue against treating BMI alone as a reliable predictor of poor recovery. They do not establish a universal BMI threshold for proceeding with surgery, prove equal complication risk, or test whether preoperative weight reduction changes outcomes. Clinical severity, anatomy, comorbidities and the planned operation remain central to individualized assessment.

Domino connectors in adult spinal deformity: greater corrective capacity, but not proven clinical superiority

Journal of Neurosurgery: Spine 2026;45(4):516-526

Combined sagittal and coronal malalignment poses a particular challenge in adult spinal deformity surgery because correction must address both planes without concentrating excessive forces on individual fixation points. Vila and colleagues investigate the side-to-side domino connector as an active correction tool rather than simply a device for linking rods. Their multicenter cohort associates its use with greater correction and better maintained sagittal alignment at two years. However, comparable patient-reported outcomes and a higher rate of rod breakage/pseudarthrosis require a balanced interpretation: improved radiographic correction does not, by itself, establish greater clinical benefit or mechanical safety.

Objective

To compare radiographic correction, complications and patient-reported outcomes after adult spinal deformity surgery with or without a side-to-side domino connector used for correction of combined sagittal and coronal malalignment.

Methods

This retrospective analysis used a prospectively collected database from six European centers. It included 224 patients undergoing instrumented fusion to the pelvis with at least two years of follow-up: 81 with a domino connector and 143 without. Eligibility required a C7-to-central sacral vertical line distance greater than 20 mm together with sagittal malalignment defined by at least one of the study’s pelvic tilt, sagittal vertical axis, thoracic kyphosis or global tilt criteria.

Connector use was selected by the surgeon, often for more severe, rigid deformities. The connector group started with worse biplanar malalignment and underwent pedicle subtraction osteotomy more frequently. Propensity matching produced 69 pairs based on baseline global tilt, coronal displacement, osteotomy use and rod number. A separate analysis compared patients without pedicle subtraction osteotomy. Outcomes included standing radiographs, mechanical and neurological complications, unplanned reoperations, Oswestry Disability Index and Scoliosis Research Society-22 scores.

Main results

In the matched cohort, two-year global tilt was 24.6° with connectors versus 33.1° without, and L1-S1 lordosis was 54.8° versus 49.0°. Final coronal displacement did not differ significantly. In the full cohort, mechanical complications occurred in 41.9% of both groups, but the combined rod-breakage/pseudarthrosis category was higher with connectors: 22.2% versus 9.1% (P=.006). Unplanned reoperation rates were 27.2% versus 34.3%, without a significant difference. Two-year ODI and SRS-22 scores were comparable. Greater lumbar lordosis also persisted in the subgroup without pedicle subtraction osteotomy, although that comparison retained baseline imbalances.

Interpretation

The technical distinction is the intended force direction, referenced to trunk shift rather than simply curve concavity. For distraction-based correction, the authors place the connector on the side of coronal malalignment; for compression during asymmetric osteotomy closure, they place it opposite the shift. Their illustrated sequence establishes lumbopelvic fixation and initial correction through a contoured contralateral rod before connector-assisted adjustment. Intraoperative imaging checks coronal alignment against a pelvic reference. This is a useful framework for planning correction, but force distribution is a proposed mechanical rationale, not proof that the connector independently prevents fixation failure.

Limitations

This was not a randomized comparison, and matching cannot eliminate unmeasured confounding. Deformity rigidity, surgeon preferences, center-specific practice and the heterogeneity of control constructs may affect both correction and complications. Matching addressed selected variables rather than every baseline difference; thoracic kyphosis remained different between matched groups. The subgroup without pedicle subtraction osteotomy likewise does not isolate the device’s intrinsic effect from other corrective maneuvers.

The clearest persistent radiographic advantage was sagittal. Greater correction from a more displaced starting position should not be confused with significantly better final coronal balance. Similarly, comparable ODI and SRS-22 scores do not establish equivalence, but they do mean that superior patient-reported benefit was not demonstrated at two years.

An identical aggregate mechanical complication rate does not neutralize the higher rod-breakage/pseudarthrosis rate. Greater deformity severity and osteotomy use may contribute, but this study cannot establish their causal contribution or exclude a device-related contribution. The absence of reported intraoperative implant complications is also insufficient to establish general safety. The study received industry funding, and several authors disclosed relevant financial relationships. Longer follow-up and prospective comparative evaluation are needed to clarify durability and clinical benefit.

Clinical takeaway

A domino connector can be considered a correction adjunct when managing complex biplanar adult deformity, with its placement determined by the planned compression or distraction mechanism. This study supports its corrective potential, not routine use in every construct, replacement of an indicated osteotomy, or an expectation of better functional outcomes. Planning should retain equal attention to alignment, the lumbopelvic foundation and subsequent mechanical failure risk.

 

Dynamic MRI in cervical myelopathy: when positional compression changes the surgical plan

Neurosurgery 99:928–937, 2026

Planning decompression for degenerative cervical myelopathy requires identifying not only the severity of spinal cord compression but also its distribution across levels and its response to movement. Neutral-position MRI may not fully represent this positional component. In a randomized single-center study, Ajem and colleagues examined whether additional flexion-extension MRI could refine operative planning and improve early neurological recovery. Dynamic imaging frequently changed the intended operation, and reported functional outcomes favored its use at three months. These findings are clinically relevant, but short follow-up and inconsistencies in outcome reporting temper the strength of the conclusions.

Objective

To determine whether adding dynamic MRI to conventional imaging changes surgical planning and improves three-month functional recovery in adults undergoing surgery for degenerative cervical myelopathy.

Methods

The trial was conducted at a single institution between February 2023 and December 2024. Seventy-four patients were randomized in equal groups after an initial surgical plan had been documented using static MRI. The control group proceeded according to that plan; the dynamic group underwent additional imaging that could change the approach, decompression levels or procedure. Eligibility excluded minors, previous spine surgery, spinal trauma or congenital anomalies, and concomitant lumbar stenosis. Most participants had severe myelopathy.

Dynamic imaging used sagittal T2-weighted sequences in flexion and extension on a 3-T scanner. Positioning was individualized and limited by tolerance without provoking neurological symptoms. The operating surgeon and a senior radiologist reviewed the findings, with additional adjudication when necessary. Five experienced surgeons performed the procedures, retaining discretion over the final operation.

The primary outcome was recovery rate derived from modified Japanese Orthopaedic Association (mJOA) scores at three months. Secondary assessments included mJOA scores, Nurick grades, changes in surgical planning and complications. Randomization concerned the imaging strategy, not the surgical approach.

Main results

Dynamic MRI changed the plan in 22/37 patients (59.5%): 12 anterior-to-posterior conversions, one posterior-to-anterior conversion, six increases in decompression levels and three changes from discectomy to corpectomy. Table 4 reports recovery of at least 50% in 34/37 dynamic-imaging patients versus 22/37 controls. Mean recovery rates were 55.42% and 46.76%, respectively; postoperative mJOA scores were 15.47 and 13.77. The reported between-group Nurick difference was not significant. One patient in each imaging group died after posterior surgery. These results require interpretation alongside the reporting limitations below.

Interpretation

The practical contribution is the opportunity to reconsider a documented operation when positional imaging reveals a different distribution of compression. The predominance of anterior-to-posterior conversions shows that dynamic information affected corridor selection as well as decompression extent. However, imaging-driven changes do not establish that every additional compressed level requires surgery. Clinical concordance and individualized review remain essential, and this study does not provide a validated rule for extending decompression. Nor does it isolate which particular change produced better recovery. Its findings support further evaluation of dynamic imaging as a planning adjunct, rather than automatic escalation of surgery.

Limitations

This small, single-center trial provides only three-month follow-up and does not establish durable neurological benefit, improved quality of life or reduced reoperation. Although described as single-blinded, the report does not clearly identify the blinded party or explain allocation concealment. Surgeons necessarily knew the additional imaging findings, and procedure selection was not standardized. Motion artifacts and discomfort may also limit the examination.

Numerical inconsistencies deserve particular attention. The reported P value of .044 for mean recovery rate is not readily reconciled with the sample sizes, means and standard deviations under the independent-samples t-test described in the methods. Recovery-category counts are also difficult to reconcile fully with the reported means and variability. The direction of the findings is therefore more credible as a preliminary signal than the precise magnitude or statistical certainty of benefit.

The anterior-versus-posterior comparison was not randomized: posterior patients had worse baseline mJOA scores and more levels decompressed. It cannot establish that one approach is inherently safer or more effective. Complication percentages in Table 5 do not correspond to the stated approach-group denominators, further limiting quantitative safety comparisons. The two deaths warrant acknowledgment but cannot support an approach-specific risk estimate in this sample.

Clinical takeaway

Dynamic MRI may help refine the choice of approach and decompression extent when positional findings materially change the assessment of cervical cord compression. This trial offers a useful planning signal, not definitive evidence for routine imaging in every patient or decompression of every dynamically narrowed level. Confirmation in larger trials with transparent outcome reporting and longer follow-up is needed.

L4-L5 fusion in the lateral position: choosing between anterior and transpsoas access

Spine 2026;51(19):1381-1389

Access to L4-L5 during single-position lumbar fusion is shaped by the relationship between the disc, iliac crest, psoas, lumbar plexus and major vessels. Huynh and colleagues compare anterior lumbar interbody fusion performed in lateral decubitus with transpsoas lateral interbody fusion, examining whether the anterior route offers a useful alternative without repositioning the patient. Their multicenter findings associate lateral-position ALIF with fewer postoperative complications and greater segmental lordosis, while highlighting the importance of anatomical selection. The study expands the discussion of available corridors, but its observational design does not establish one approach as uniformly safer or more effective.

Objective

To compare complications, reoperations, procedural efficiency and sagittal alignment after L4-L5 lateral-decubitus ALIF (L-ALIF) and transpsoas LLIF during one- or two-level lateral single-position surgery.

Methods

The authors retrospectively reviewed prospectively and consecutively enrolled patients from seven surgeons across Australia, Brazil and the United States. The reported cohort comprised 511 patients: 72 undergoing L4-L5 L-ALIF and 439 undergoing L4-L5 LLIF. Mean ages were approximately 66 and 65 years, respectively. Indications included degenerative spondylolisthesis, foraminal stenosis and postlaminectomy instability or syndrome. Previous lumbar fusion, additional TLIF/PLIF, repositioning and staged surgery were excluded.

Approach selection depended on surgeon preference and anatomy. Three surgeons contributed L-ALIF cases, whereas all seven contributed LLIF cases. Additional fusion could involve L3-L4 using LLIF or L5-S1 using L-ALIF. Both groups received posterior pedicle instrumentation without changing the lateral position.

Follow-up was at least 90 days, with radiographic assessment at 90 days. Propensity matching for age, sex, BMI, diabetes, smoking and number of fused levels generated groups of 72 patients each. Complications were classified using the Clavien-Dindo system; neurological symptoms persisting beyond six weeks were classified as major complications.

Main results

In the matched groups, postoperative complications occurred in 4.2% after L-ALIF versus 19.4% after LLIF (p = 0.004); major complications were 2.8% versus 11.1% (p = 0.049). Ninety-day reoperations did not differ significantly (2.8% versus 8.3%; p = 0.146). Operating time, blood loss and length of stay were also similar after matching. L4-L5 segmental lordosis increased by 6.6° versus 1.8° (p = 0.003). Postoperative L4-S1 lordosis was greater with L-ALIF, but its change from baseline did not differ significantly. These are matched-cohort results, distinct from the larger unmatched comparison.

Interpretation

L-ALIF provides an alternative when the transpsoas corridor is constrained, but replaces plexus-related exposure concerns with vascular mobilization considerations. The study used an access surgeon for anterior exposure and EMG-guided mapping for LLIF; unsafe transpsoas docking prompted abandonment of that approach. These safeguards are part of the reported treatment setting, not optional details that the comparison can separate from outcomes. Importantly, the three vascular injuries in the overall LLIF-labeled group occurred during accompanying L5-S1 ALIF exposure, not the L4-L5 transpsoas approach. They cannot be attributed to LLIF itself.

Limitations

Treatment was not randomized, and the anatomical reasons for choosing each corridor were not adequately captured. Propensity matching balances measured variables but cannot remove this confounding by indication or the influence of surgeon experience. Only three surgeons supplied L-ALIF cases, compared with seven for LLIF.

Two-level operations combine different approaches, limiting attribution of complications to the L4-L5 corridor. Short follow-up and the absence of patient-reported functional outcomes prevent conclusions about durable symptom relief, fusion success or long-term revision risk. Absence of vascular injury in the 72 L4-L5 L-ALIF patients does not establish absence of risk. Multiple statistical comparisons also increase the possibility of false-positive findings, particularly for borderline results.

The publication contains minor reporting discrepancies, including 438 versus 439 LLIF patients in different locations and a segmental lordosis change of 6.8° in the abstract versus 6.6° in Table 5. The figures summarized here follow the main results and matched tables. Several authors disclosed industry relationships relevant to spinal instrumentation.

Clinical takeaway

For lateral single-position L4-L5 fusion, assess both the anterior vascular corridor and the transpsoas neural corridor before choosing the approach. L-ALIF is a reasonable option in experienced hands and may improve segmental lordosis while avoiding psoas-related symptoms. This study supports individualized planning, not a blanket claim that anterior access is safer or that greater radiographic correction guarantees better clinical recovery.

Severe lumbar stenosis: selecting patients for indirect decompression

 

Neurosurgery. 2026;99(4):841-852

Severe lumbar canal narrowing does not necessarily identify a uniform surgical problem: reducible soft-tissue compression differs fundamentally from fixed osseous stenosis. Li and colleagues examine this distinction in a randomized comparison of oblique lateral interbody fusion and conventional transforaminal lumbar interbody fusion. Their findings support considering indirect decompression in carefully selected patients with instability, with perioperative advantages and earlier functional improvement after OLIF. However, the similar disability scores at two years, restrictive eligibility criteria and limitations in reporting argue against interpreting the study as evidence that indirect decompression can routinely replace direct neural decompression.

Objective

To compare clinical recovery, radiographic decompression, fusion and complications after OLIF and open TLIF for single-level severe lumbar stenosis with segmental instability.

Methods

The five-center trial assessed 260 patients and randomized 224 adults, 112 to each procedure, between November 2018 and December 2021. Allocation used computer-generated blocks and sequentially numbered sealed envelopes. Five experienced spine surgeons performed the operations. After five losses to follow-up, analyses included 109 OLIF and 110 TLIF patients with at least two years of follow-up.

Eligibility required symptomatic L2-L5 stenosis classified as Schizas C or D, radiographic instability, failure of at least three months of conservative treatment and a reducible, predominantly soft-tissue mechanism. Symptoms relieved by recumbency were an important selection feature. Fixed bony stenosis, ossified ligamentum flavum, ankylosis, sequestrated disc material, high-grade spondylolisthesis and unfavorable access anatomy were excluded, alongside several other conditions.

OLIF used a retroperitoneal corridor anterior to the psoas, interbody distraction and supplemental fixation. The comparator was conventional open TLIF with direct decompression, not minimally invasive TLIF. Outcomes included ODI, back and leg pain, serial canal measurements, alignment, CT-assessed fusion and complications.

Main results

OLIF had shorter operating time (102.8 versus 138.5 minutes) and lower estimated blood loss (24.8 versus 200.6 mL). ODI favored OLIF at three and six months, but not at two years (11.24 versus 11.95; p = 0.102). Two-year back pain scores favored OLIF; leg pain did not differ significantly. OLIF restored more disc height and segmental lordosis, whereas TLIF achieved greater canal area. Two-year fusion rates were 98.2% versus 95.5%, without significant separation. Recorded complications occurred in 6/109 OLIF and 8/110 TLIF patients; the difference was not significant.

Interpretation

The practical message is to assess whether compression is reducible, rather than choosing decompression solely from the Schizas grade. The OLIF protocol emphasized thorough disc clearance, preservation of the bony endplates, appropriate cage sizing and verification of implant position; endoscopic inspection was described as an adjunct. These components were not independently tested. Progressive canal enlargement after OLIF supports a remodeling mechanism, but does not establish that waiting for remodeling is appropriate for fixed compression or neurological deterioration. The findings support selective use, not a universal preference for OLIF.

Limitations

The trial studied a highly selected population treated by experienced surgeons at five Chinese centers. Its results do not establish effectiveness in multilevel disease, fixed osseous compression, deformity or high-grade spondylolisthesis. The open TLIF comparator also limits extrapolation to contemporary minimally invasive alternatives. Two years is insufficient to establish protection against adjacent-segment disease or long-term construct failure.

Although the authors describe the procedures as equivalent, the reported analysis does not specify an equivalence margin or a formal equivalence framework. A nonsignificant difference therefore should not be treated as proof of equivalence, particularly for uncommon complications. The report provides limited detail on sample-size justification, handling of repeated measurements and multiplicity; the presented analyses exclude the five patients lost to follow-up.

There is also an inconsistency in the description of OLIF fixation: the title and illustrations identify lateral vertebral fixation, whereas parts of the methods refer to pedicle screws and rods. This limits reproducibility of the exact construct. The early between-group ODI differences of approximately five points should not be confused with the larger within-patient improvement thresholds cited by the authors.

Clinical takeaway

Consider OLIF as an option for carefully selected, reducible single-level stenosis with instability when access anatomy and surgical expertise are suitable. This trial supports earlier recovery compared with open TLIF, but does not justify extending indirect decompression to fixed stenosis or claiming superior long-term function. Patient selection remains more important than canal grade alone.

One-and-a-half MIS-TLIF: selective fusion with adjacent-level decompression

Journal of Neurosurgery: Spine. 2026;45(3):339-346

Lumbar stenosis affecting adjacent levels does not necessarily imply that every symptomatic segment requires fusion. The operative challenge is to distinguish the level requiring stabilization from a neighboring stenotic segment that can be decompressed without compromising its mechanical integrity. Farooq and colleagues evaluate a hybrid strategy combining single-level minimally invasive transforaminal lumbar interbody fusion with adjacent-level unilateral laminotomy for bilateral decompression. Their experience provides preliminary clinical support for selective fusion in carefully chosen patients, while emphasizing that preservation of the adjacent segment depends on both preoperative stability and a structure-preserving decompression.

Objective

To assess reoperation after the one-and-a-half MIS-TLIF procedure, particularly subsequent extension of fusion to the adjacent decompressed segment, together with clinical and radiographic outcomes.

Methods

This retrospective single-center series evaluated operations performed by one experienced surgeon between January 2016 and February 2023. Of 36 patients considered, 33 met the inclusion criteria. Mean age was 67.9 years. Patients had degenerative lumbar disease with radiculopathy and mechanical back pain unresponsive to conservative treatment. The strategy combined MIS-TLIF using an expandable cage at the unstable segment with unilateral laminotomy for bilateral decompression (ULBD) at an adjacent stenotic level. The authors specify that adjacent-level decompression was restricted to segments without dynamic instability.

Outcomes included complications, reoperations, back and leg pain, disability and radiographic measures. Median clinical follow-up was 26 months. Complete serial imaging was available for 26 patients, with a median radiographic follow-up of 11.7 months. Fusion assessment relied primarily on standing and dynamic radiographs; CT was used when available rather than obtained routinely.

Main results

Three patients required reoperation (3/33, 9.1%). Two underwent extension of fusion to the previously decompressed adjacent level (2/33, 6.1%), while one underwent revision at the initially instrumented level. These are observed proportions over the reported follow-up, not comparative estimates of risk reduction.

Four patients experienced perioperative complications (12.1%): one CSF leak, one hardware failure, one wound dehiscence and one wound infection. No neurological complications were reported. Mean operative duration was 213.7 minutes, and median hospital stay was 48 hours. Blood loss was recorded in the categories below 50 mL or 50-150 mL in 28 of 33 patients.

Fusion was reported in 25 of the 26 patients with complete imaging (96.2%). Cage subsidence was present in six of these patients at the latest radiographic assessment (23.1%). Disc height and segmental lordosis improved; mean segmental lordosis increased from 14.1 degrees preoperatively to 17.4 degrees immediately after surgery and measured 16.4 degrees at final radiographic follow-up.

Pain and disability scores also improved. Median leg-pain VAS decreased from 5.5 before surgery to 0 at final follow-up. The final mean back-pain VAS was 3.1, compared with a preoperative median of 7.0. Final median ODI was 13.5, compared with a preoperative mean of 42.1. Because the paper reports a mixture of means and medians, these figures should not be subtracted and presented as a uniform average treatment effect.

Interpretation

The most useful surgical distinction is between adjacent stenosis and adjacent instability. This approach does not simply abbreviate a multilevel fusion: it assigns different treatments to levels with different mechanical requirements. The index level receives stabilization, while the adjacent level remains unfused only when it is radiographically stable and suitable for ULBD.

Preservation of the adjacent facets and posterior tension band is central to the rationale. A limited decompression designed to retain these structures cannot be considered mechanically interchangeable with a wide adjacent-level laminectomy. The authors distinguish this indication from bisegmental instability or foraminal stenosis requiring substantial facetectomy, situations in which a two-level fusion may address a different problem. The series does not validate a universal imaging threshold for selecting decompression alone.

The expandable cage introduces a separate technical consideration. The discussion emphasizes endplate preservation and controlled expansion, and the observed subsidence rate warrants attention even in the presence of a high reported fusion rate. Neither these data nor the accompanying illustration establish superiority of a particular cage design or an optimal expansion protocol.

The principal contribution is evidence of feasibility and early durability in a selected cohort. Two adjacent-level fusion extensions over a median of approximately two years are encouraging, but they do not demonstrate prevention of adjacent segment disease. The authors themselves caution that institutional single-level and two-level fusion series had different indications and follow-up periods and are contextual references rather than valid control groups.

Limitations

The study is small, retrospective and confined to one highly experienced surgeon, without a comparative control group. Selection limits applicability to patients with instability at more than one level, high-grade spondylolisthesis, epidural fibrosis or advanced osteoporosis. Seven patients lacked complete serial imaging, and fusion was not routinely confirmed with CT. Clinical and radiographic follow-up durations differ substantially, and the longer-term risk of adjacent-level deterioration remains uncertain. Absence of neurological complications in 33 patients cannot establish a negligible risk. Comparative advantages in morbidity, reoperation or motion preservation remain unproven.

Clinical takeaway

Consider selective fusion as a question of segment-specific pathology: stabilize the level that requires it and assess whether an adjacent stable stenotic level can be adequately decompressed while preserving its supporting structures. This series supports discussing one-and-a-half MIS-TLIF as an option in appropriately selected patients, with explicit counseling about possible later fusion extension. It does not support substituting limited decompression for fusion at a second genuinely unstable segment.

Cervical disc arthroplasty versus fusion: measuring the burden of recovery

Neurosurgery. 2026;99(3):643-653

The outcome of cervical surgery encompasses not only the patient’s condition at one year, but also the disability experienced while recovering. Asada and colleagues examine this distinction by comparing cervical disc replacement with anterior cervical discectomy and fusion using a cumulative, model-based outcome measure. Their findings associate arthroplasty with a lower burden of neck-related disability during the first postoperative year, without a corresponding advantage in cumulative arm pain. This approach adds a useful dimension to preoperative counseling, although its observational design and the limited validation of the new measure require a cautious interpretation.

Objective

To develop and internally evaluate a modified integrated health state (mIHS) measure and compare cumulative postoperative disability after one- or two-level cervical disc replacement (CDR) and anterior cervical discectomy and fusion (ACDF) for degenerative cervical radiculopathy.

Methods

The authors retrospectively analyzed a prospectively collected, multisurgeon institutional registry covering February 2016 to September 2024. Of 1,273 screened patients, 327 were included: 159 underwent ACDF and 168 underwent CDR. Hybrid constructs, procedures involving three or more levels, missing baseline Neck Disability Index (NDI) scores and baseline NDI below 20 were excluded. The cohort flowchart also excluded myelopathy and trauma.

NDI and neck and arm pain scores were collected before surgery and at intervals through 12 months. Postoperative scores were normalized to baseline, and nonlinear mixed-effects models estimated recovery trajectories. The mIHS summarized the area under these modeled trajectories; it is not a conventional NDI point score. Propensity-score overlap weighting balanced measured baseline characteristics. Patients with shorter follow-up remained eligible, with missing postoperative observations handled under a missing-at-random assumption.

Main results

The one-year NDI-based mIHS was lower after CDR than ACDF (2.68 versus 3.71; difference 1.03, 95% CI 0.80-1.25; p < 0.001), corresponding to a 27.7% relative reduction in this modeled measure. Cumulative neck pain also favored CDR; cumulative arm pain did not differ significantly. Two-level CDR had a similar mIHS to one-level CDR, whereas two-level ACDF carried greater cumulative disability than one-level ACDF. These results describe recovery burden, not a 27.7% reduction in the conventional NDI score.

Interpretation – operative relevance

For patients in whom both procedures are appropriate, the findings support discussing the course of recovery alongside the expected endpoint. Preserved segmental motion after CDR offers a plausible explanation, but this study does not establish it as the cause of better recovery. Nor does it justify extending arthroplasty indications, choosing a particular prosthesis or altering decompression technique. The practical contribution is to procedure selection and counseling rather than a new operative maneuver or proof of long-term superiority.

Limitations

Treatment was not randomized. Before weighting, CDR patients were younger and differed in comorbidity, pathology and number of treated levels. Statistical adjustment cannot remove unmeasured confounding, including the reasons a surgeon selected one procedure over another. Postoperative analgesic consumption was not reliably captured.

Excluding low baseline NDI scores limits applicability to patients with milder disability. Model-based estimates depend on assumptions about recovery trajectories and missing data. The mIHS underwent internal validation only, and its minimum clinically important difference remains undefined; statistical separation therefore cannot be equated with an established patient-perceived benefit threshold.

Follow-up was limited to one year. Imaging was incomplete and nonstandardized, making fusion, motion and heterotopic ossification analyses vulnerable to selection bias. The study does not establish comparative long-term revision rates or device-specific safety.

Clinical takeaway

When counseling suitable candidates for cervical arthroplasty or ACDF, discuss how recovery may unfold, not simply the expected one-year result. This study associates CDR with less cumulative neck-related disability, but its novel outcome measure and observational design do not support a universal preference for arthroplasty.

MIS-TLIF Versus Open TLIF in Combined Lumbar Stenosis and Low-Grade Spondylolisthesis: Discharge Timing and Treatment Pricing

Spine 2026;51:1326–1332

Choosing between minimally invasive and open transforaminal lumbar interbody fusion requires balancing adequate decompression and reconstruction against the burden of surgical exposure. In patients with single-level degenerative stenosis and low-grade spondylolisthesis, Krutko and colleagues provide randomized evidence that early functional recovery need not be compromised by a less extensive approach. Their findings favor a selective interpretation: minimally invasive surgery shortened hospitalization and reduced additional analgesic requirements, but did not establish superior clinical outcomes or lower direct costs. Patient selection, incomplete follow-up and the absence of mature fusion results remain central to applying the study.

Objective

To determine whether minimally invasive TLIF was noninferior to open TLIF for improvement in disability at three months, while comparing clinical, perioperative and direct-cost outcomes.

Methods

This single-center, open-label randomized trial enrolled 96 patients between 2022 and 2024, allocating 48 to each technique. Mean age was 55.8 years, and 74% were women. The registered protocol specified ages 40-75 years; the report describes an additional eligibility requirement of lumbar vertebral attenuation above 120 Hounsfield units. Most procedures involved L4-L5. Two surgeons, each with more than 15 years of experience, performed the operations.

The primary endpoint was change in the Oswestry Disability Index (ODI) at three months, with a prespecified noninferiority margin of 12 points. The primary analysis used available observations from the modified intention-to-treat population; a per-protocol analysis excluded major protocol deviations. Secondary measures included pain, satisfaction, complications, hospitalization and direct costs.

Main results

Three-month ODI data were available for 48 minimally invasive and 39 open-surgery patients. The reported difference was 0.4 points (90% CI -5.7 to 6.5), supporting the authors’ noninferiority conclusion; approximately 83% and 82% achieved clinically important improvement.

Hospitalization averaged 8.0 versus 9.5 days (p = 0.005), and additional analgesia was less frequent after minimally invasive surgery (p = 0.026), although direct costs were 10.5% higher. Pain, satisfaction, blood loss, operative duration and complication comparisons were not statistically significant. Six complications occurred overall, with no reoperations during three months.

Interpretation

Approach selection should follow decompression requirements, bone quality and surgical expertise. The minimally invasive technique combined unilateral paramedian exposure, over-the-top decompression and contralateral percutaneous screws; open surgery used midline exposure, laminectomy and bilateral facetectomy. Both groups received two cages and bilateral fixation.

The findings support these constructs in selected single-level disease, not reduced exposure when adequate decompression is uncertain. They do not determine whether fusion is preferable to decompression alone. Higher implant expenditure outweighed shorter hospitalization locally, so the economic result should not be generalized across healthcare systems.

Limitations

The single-center, unblinded design and highly experienced operators limit generalizability. Missing three-month observations were confined to the open group, creating an important risk of attrition bias in a noninferiority trial. The study also recorded five major protocol deviations in each arm. Secondary comparisons were not adjusted for multiplicity, and the small number of complications cannot establish equivalent safety.

The bone-density eligibility threshold restricts extrapolation to patients with poor bone quality. Three-month disability improvement does not establish fusion success, implant durability or long-term freedom from revision. Length of stay and costs reflect the national and institutional healthcare setting.

Clinical takeaway

For selected single-level degenerative stenosis with low-grade spondylolisthesis, MIS-TLIF is supported as an alternative to open TLIF for early functional recovery. Match the approach to decompression requirements, bone quality and operator experience; do not infer superior long-term fusion, fewer complications or lower costs from this trial.

Achieving Alignment and Implant-Specific Goals in Anterior Lumbar Interbody Fusion, and Predictors of Postoperative Intradiscal Lordosis

Operative Neurosurgery 31:431–444, 2026

Planning anterior lumbar interbody fusion requires distinguishing the lordosis built into an implant from the additional correction achieved at the treated segment. Hamouda and colleagues examine how baseline alignment, cage characteristics, operative level and posterior fixation contribute to this relationship. By comparing intraoperative and postoperative imaging, their study also addresses whether the correction obtained during surgery is maintained on standing. The findings support individualized alignment planning, while cautioning against interpreting implant geometry or the choice of construct as an isolated determinant of surgical success.

Objective

To identify predictors of postoperative intradiscal lordosis and its change from baseline after one- or two-level ALIF, and to evaluate the relationship between intraoperative supine alignment and early postoperative standing measurements.

Methods

This retrospective, single-center study included 204 adults treated between 2019 and 2023 at 258 levels: 80 at L4–5 and 178 at L5–S1. Ninety patients underwent stand-alone ALIF and 114 received supplementary posterior instrumentation. Patients with prior lumbar interbody fusion, surgery for trauma, tumor or infection, combined interbody approaches, or pelvic fixation were excluded.

The authors reviewed standing preoperative radiographs, intraoperative images and postoperative standing radiographs, obtained a median of two days after surgery. Measurements included intradiscal lordosis, disc height, spinopelvic alignment, implant dimensions and cage position. Separate regression models evaluated the final intradiscal angle and the change from baseline. Median overall follow-up was 12.4 months, although the principal alignment comparisons concerned the early postoperative period.

Main results

Tables 2 and 3 report a median intradiscal lordosis of 6.7° before surgery and 17.8° postoperatively, with a median individual change of 10.4°. The median gain was 8.1° after stand-alone ALIF and 11.5° with posterior instrumentation. The between-construct difference was significant at L5–S1, but not at L4–5.

Greater cage lordosis, greater baseline intradiscal lordosis, L5–S1 implantation and posterior instrumentation independently predicted a larger postoperative angle. Each additional degree of implant lordosis was associated with 0.62° greater postoperative intradiscal lordosis (95% CI 0.44–0.79). This coefficient describes the adjusted association with the final angle, not the correction gained from baseline.

The separate change model showed that greater preoperative lordosis was associated with less additional correction. Thus, achieving a larger final angle and gaining more lordosis are distinct outcomes.

Intraoperative imaging showed no significant additional increase in intradiscal lordosis after posterior instrumentation compared with the preceding post-ALIF measurement. The authors considered differences in initial correction and maintenance of alignment on standing as possible explanations for the better results in the circumferential group, rather than attributing them solely to posterior corrective maneuvers.

Interpretation — operative relevance

The most useful planning distinction is between the intended final segmental angle and the additional correction required to reach it. A cage’s stated lordosis should not be presented as the expected angular gain. A segment with relatively preserved baseline lordosis may reach a larger final angle while requiring less correction than a more collapsed disc space.

The operative description emphasizes trial selection that provides contact with both vertebral endplates without excessive distraction. This is relevant to the balance between restoring alignment and avoiding an unnecessarily aggressive increase in disc height. The study does not establish a numerical distraction limit or demonstrate that selecting the tallest or most lordotic available implant improves clinical outcomes.

Posterior fixation was associated with greater correction, particularly at L5–S1, but the intraoperative comparisons do not show that the posterior stage itself reliably adds lordosis. The decision to supplement the anterior construct therefore requires the broader stabilization and decompression assessment; the reported group difference is not, by itself, an indication for instrumentation. In the described practice, an open posterior approach was generally used when decompression was also needed, whereas percutaneous fixation was favored when stabilization alone was required.

Finally, intraoperative alignment should be interpreted in relation to postoperative standing measurements. The study supports attention to this transition, but does not provide a validated patient-specific formula for predicting standing correction from a supine image.

Limitations

The retrospective design and nonrandom selection of constructs prevent causal conclusions. Baseline alignment differed between groups, and implant selection and endplate preparation depended on surgeon judgment. The heterogeneous indications also limit the ability to isolate the influence of individual anatomical features or technical maneuvers. Patient-reported outcomes were not available, so greater radiographic correction cannot be equated with better pain relief, function or long-term clinical benefit.

There are internal numerical discrepancies between the abstract, narrative and tables. The overall descriptive values above follow the concordant entries in Tables 2 and 3; conflicting subgroup estimates have not been used to define a quantitative treatment target.

Clinical takeaway

Define the required correction before selecting the implant, distinguish angular gain from final lordosis, and consider the treated level and fixation strategy together. This study supports anatomically informed ALIF planning and assessment of achieved alignment, rather than maximizing cage dimensions or assuming that posterior instrumentation will automatically produce further correction.

Spinal meningiomas: histopathological grading using a benchmark radiomics model with notes on disease control

Neurosurg Focus 61(3):E8, 2026

Could preoperative imaging help anticipate the biological behavior of spinal meningiomas?
This study applies radiomics—quantitative analysis of imaging features—to distinguish tumor pathology groups.
The model showed promising discrimination using open-source tools and internal validation.
Its potential role is to inform counselling, but clinical adoption requires independent testing.

Objective

To develop a preoperative radiomics classifier for spinal meningioma pathology and explore factors associated with disease control.

Methods

Investigators retrospectively reviewed institutional surgical records from 2012–2025. Manually segmented contrast-enhanced images underwent PyRadiomics feature extraction. An ensemble classifier used 10 features and nested cross-validation.

The study’s “high-grade” category combined WHO grade 2 tumors with grade 1 tumors showing atypia; this is not equivalent to conventional WHO high-grade classification.

Main results

Among 74 patients, the model achieved an area under the receiver-operating-characteristic curve of 0.879 and a mean F1 score of 0.748.

The clinical analysis included 55 patients, with median radiographic follow-up of 22.2 months and four recurrences. Subtotal resection was associated with poorer progression-free survival than gross-total resection: HR 10.62 (95% CI 1.46–77.05; P=.019). Institutional abstract

Interpretation

The imaging approach merits further investigation, but discrimination within one institution does not establish performance across scanners, imaging protocols or patient populations. An AUC of 0.879 should not be described as “87.9% diagnostic accuracy.”

The recurrence analysis is exploratory. Its wide confidence interval signals considerable uncertainty, and it does not justify pursuing complete resection at the expense of neurological function.

Limitations

The small retrospective cohort and internal validation limit generalizability. The unconventional pathology grouping complicates comparison with other grading studies. Four recurrence events provide limited support for prognostic modelling.

Publisher and PubMed retrieval failed; verification relied on the authors’ institutional abstract. Full methodological details and supplementary material could not be assessed.

Clinical takeaway

Radiomics is a promising research adjunct for preoperative assessment of spinal meningiomas. This model should not yet determine resection extent, radiation treatment or surveillance schedules without external validation and confirmation of clinical utility.

Surgical Versus Nonoperative Treatment for Adult Spinal Deformity: A Multicenter Propensity Score–Matched Study of Two-Year Patient-Reported Outcomes

Spine 2026;51:1197–1208

Choosing between reconstruction and nonoperative care for adult spinal deformity demands a realistic estimate of benefit rather than radiographic enthusiasm alone. This multicenter analysis uses propensity matching to compare patients with similar measured baseline characteristics. At 2 years, surgery produced substantially greater improvement in disability and scoliosis-specific quality of life. Clinically meaningful benefit was achieved by a much larger proportion of surgical patients, although the cohort was relatively young and only mildly to moderately impaired at baseline. The results strengthen comparative-effectiveness evidence but do not replace individualized discussion of complications and residual confounding.

Objective

To compare 2-year patient-reported outcomes after surgical and nonoperative management of adult spinal deformity while reducing measured treatment-selection bias through propensity-score matching.

Methods

The retrospective comparison used prospectively collected data from an adult spinal-deformity registry at six centers. Of 580 eligible patients, 338 underwent surgery and 242 received nonoperative care. Propensity scores incorporated demographic variables, radiographic alignment measures and baseline Oswestry Disability Index (ODI) and Scoliosis Research Society–22 (SRS-22) scores. One-to-one matching produced 160 balanced pairs.

Main results

At 2 years, mean ODI improvement was −19.4 ± 14.2 points after surgery and −4.2 ± 12.3 with nonoperative care (p<0.001). A clinically meaningful ODI improvement of at least 15 points was achieved by 72% of surgical patients versus 29% of nonoperative patients.

The mean 2-year SRS-22 total score was 3.95 ± 0.67 after surgery and 3.46 ± 0.75 after nonoperative care (p<0.0001). The minimum clinically important difference for the SRS-22 total score was reached by 81.3% and 36.9%, respectively.

Interpretation

Among matched patients, reconstruction was associated with a large and clinically visible improvement beyond that observed with nonoperative management. Propensity matching makes the groups more comparable but cannot recreate randomization. The magnitude of benefit should therefore be presented alongside the patient’s operative risk, deformity phenotype, frailty, goals and probability of complications or revision.

Limitations

Treatment was not randomized, and unmeasured factors such as surgeon judgment, symptoms, patient preference and socioeconomic context may still influence both selection and outcome. The matched cohort had a mean age of about 45 years and mild-to-moderate baseline impairment, limiting extrapolation to older or frailer patients. Two-year follow-up does not capture late mechanical failure, revision burden or durability.

Clinical takeaway

For an appropriately selected adult with symptomatic deformity, surgery offers a substantially greater chance of meaningful 2-year improvement than continued nonoperative care. Use those probabilities in shared decision-making, but pair them with center-specific complication and revision estimates rather than presenting benefit in isolation.