Evidence map›Paper›PMID 42240749›Full record

ArticleNeurosurgical review2026

Early pain relief and segmental realignment after two-stage lateral lumbar interbody fusion (LLIF) with posterior instrumentation in degenerative lumbar pathology.

Meltem Ivren, Basem Ishak, Sebastian Ille, Martin Dugas, Sandro M Krieg, Pavlina Lenga

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Article in Neurosurgical review, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Meltem IvrenDepartment of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Basem IshakDepartment of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Sebastian IlleDepartment of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Martin DugasInstitute of Medical Informatics, Heidelberg University Hospital, Heidelberg, Germany.
Sandro M KriegDepartment of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Pavlina LengaDepartment of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany. pavlina.lenga@med.uni-heidelberg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-stage circumferential fusion incorporating lateral lumbar interbody fusion (LLIF) is increasingly used to treat degenerative lumbar disorders, yet evidence on perioperative safety, clinical benefit, and optimal sequencing remains limited. We evaluated clinical outcomes, radiographic realignment, perioperative morbidity, and predictors of complications in patients undergoing staged LLIF with posterior fixation. We retrospectively reviewed 20 patients (mean age 67.7 years) who underwent two-stage lumbar fusion, either LLIF followed by posterior instrumentation or vice versa. We assessed pain (NRS scale), segmental lordosis (SL), blood loss, ICU and hospital length of stay, and complications. Subgroup analysis compared LLIF-first vs. posterior-first sequencing. Logistic regression identified predictors of complications. Patients showed a median age-adjusted Charlson Comorbidity Index [ACCI] of 3.0. LLIF was performed first in 65%. Mean NRS pain scores improved from 6.5 preoperatively to 4.1 after the first stage (p = 0.006) and to 3.1 after the second (p < 0.001). Early pain relief tended to be greater with LLIF-first (ΔNRS - 2.46 vs. - 1.75). Posterior-first sequencing involved more instrumented levels (median 4 vs. 2, p = 0.014), greater blood loss (628.6 vs. 142.3 mL, p = 0.01), and longer hospitalization (18.9 vs. 10.8 days, p < 0.001). LLIF-first yielded greater intervertebral height gain (6.5 vs. 3.7 mm, p = 0.05). SL improved mainly at upper lumbar levels (+ 6.4°). ACCI was the only independent predictor of complications (OR 2.6 per point; p = 0.045). Staged lateral lumbar interbody fusion with posterior instrumentation appears to be a feasible treatment option for complex degenerative lumbar disease, associated with early pain relief and segmental alignment changes. Performing the interbody fusion as the first stage may offer potential advantages; however, these findings should be interpreted cautiously given the small sample size of our cohort.

Indexed as

Intervertebral Disc DegenerationLumbar VertebraePain ManagementSpinal FusionAgedFemaleHumansMaleMiddle AgedPain MeasurementRetrospective StudiesTreatment OutcomeDegenerative lumbar spine diseaseIndirect decompressionLateral lumbar interbody fusion (LLIF)Staged circumferential fusion

Identifiers

PMID42240749
PMCPMC13236739

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.