Abstract
Background
The rate of degenerative thoracic spinal stenosis (TSS) as underlying pathology for myelopathy is not precisely known, and larger case series are only available for the Asian region. We present one of the largest European series to evaluate rate and clinical outcome after dorsal decompression via a uni- or bilateral approach.
Method
We investigated patients’ characteristics, imaging/surgical parameters, and outcomes with quality-of-life (QOL) in all patients who underwent surgical treatment for TSS between 2013 and 2018 in a university neurosurgical clinic.
Results
From 645 patients with surgery for degenerative spondylotic myelopathy within 6 years, 28 patients (4.3%) suffered from TSS. Median age was 70.4 years with a slight predominance of the female sex (m:f = 1:1.3). The most frequent symptoms (mean duration 7.6 months) were ataxia (61%) and sensory changes (50%). The stenoses (median Naganawa score 3) mostly resulted from a combined osseous/ligamentous hypertrophy and disc prolapse, the majority located below Th8 (75%). Nineteen patients with lateralized compression underwent bilateral decompression via a unilateral approach (fenestration/hemilaminectomy with “undercutting” procedure), and 9 patients with circular pathology underwent bilateral-approached decompression (laminectomy). There were no significant differences of patients’ characteristics, blood loss, operation time, and in-patient stay between both surgical groups. Independent from the mode of surgery, the spinal canal was significantly (p < 0.001) widened (median Naganawa score 0), and pain (p = 0.04), myelopathy (mJOA score p = 0.01), and QOL (Oswestry Disability Index, p = 0.03; SF-36-MCS, p = 0.01) were significantly improved at long-term follow-up (mean 35.1 months).
Conclusions
Non-tumorous myelopathy is caused in about 4% of patients by TSS and can be effectively treated by surgical decompression via both a uni- or bilateral approach.
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Abbreviations
- AP:
-
Anteroposterior
- BI:
-
Barthel Index
- C:
-
Cervical
- CSS:
-
Cervical spinal stenosis
- CSF:
-
Cerebrospinal fluid
- CT:
-
Computed tomography
- HR:
-
Hazard ratio
- i.e.:
-
Id est
- ISI:
-
Increased signal-intensity
- MCID:
-
Minimum clinically important difference
- MCS:
-
Mental component summary
- min.:
-
Minutes
- mJOA score:
-
Modified Japanese Orthopedic Association score (by Benzel)
- ml:
-
Milliliter
- MRI:
-
Magnetic resonance imaging
- no.:
-
Number
- ODI:
-
Oswestry Disability Index
- OLF:
-
Ossification of the ligamentum flavum
- OPLL:
-
Ossification of the posterior longitudinal ligament
- PCS:
-
Physical component summary
- PROM:
-
Patient-reported outcome measure
- QOL:
-
Quality-of-life
- SEM:
-
standard error of measurement
- SF-36:
-
Short Form-36v2® Health Survey
- Th:
-
Thoracic
- TSS:
-
Thoracic spinal stenosis
- VAS:
-
Visual analogue scale
- yrs.:
-
Years
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We are grateful to all patients participating in our study.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by the local Institutional Review Board of the Ludwig-Maximilians-University Munich and agrees with all standards regarding the use of informed consent according to the guidelines of the local Institutional Review Board of the Ludwig-Maximilians-University Munich (Project # 18-259).
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Parts of this paper have been presented orally at the Annual Spine Section Meeting of the German Society of Neurosurgery held in Giessen (Germany) on September 07, 2019, and at the 14th Annual Meeting of the German Spine Society held in Munich (Germany) on November 28, 2019.
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Siller, S., Pannenbaecker, L., Tonn, JC. et al. Surgery of degenerative thoracic spinal stenosis—long-term outcome with quality-of-life after posterior decompression via an uni- or bilateral approach. Acta Neurochir 162, 317–325 (2020). https://doi.org/10.1007/s00701-019-04191-x
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DOI: https://doi.org/10.1007/s00701-019-04191-x