Abstract
Background
To date, there have been little published data on surgical outcomes for patients with PD with thoracolumbar OVF. We conducted a retrospective multicenter study of registry data to investigate the outcomes of fusion surgery for patients with Parkinson’s disease (PD) with osteoporotic vertebral fracture (OVF) in the thoracolumbar junction.
Methods
Retrospectively registered data were collected from 27 universities and their affiliated hospitals in Japan. In total, 26 patients with PD (mean age, 76 years; 3 men and 23 women) with thoracolumbar OVF who underwent spinal fusion with a minimum of 2 years of follow-up were included (PD group). Surgical invasion, perioperative complications, radiographic sagittal alignment, mechanical failure (MF) related to instrumentation, and clinical outcomes were evaluated. A control group of 296 non-PD patients (non-PD group) matched for age, sex, distribution of surgical procedures, number of fused segments, and follow-up period were used for comparison.
Results
The PD group showed higher rates of perioperative complications (p < 0.01) and frequency of delirium than the non-PD group (p < 0.01). There were no significant differences in the degree of kyphosis correction, frequency of MF, visual analog scale of the symptoms, and improvement according to the Japanese Orthopaedic Association scoring system between the two groups. However, the PD group showed a higher proportion of non-ambulators and dependent ambulators with walkers at the final follow-up (p < 0.01).
Conclusions
A similar surgical strategy can be applicable to patients with PD with OVF in the thoracolumbar junction. However, physicians should pay extra attention to intensive perioperative care to prevent various adverse events and implement a rehabilitation regimen to regain walking ability.
Electronic supplementary material
The online version of this article (10.1186/s12891-019-2473-8) contains supplementary material, which is available to authorized users.
Keywords: Parkinson’s disease, Osteoporosis, Vertebral fracture, Spinal fusion, Thoracolumbar spine, Visual analogue scale, Japanese orthopedic association score, Outcome, Perioperative complication, Kyphosis
Background
Parkinson’s disease (PD) is an age-related, neurodegenerative disorder with a prevalence that is increasing as the population ages. It is characterized by motor- and various non-motor symptoms, which, in particular, increases the risk of falls and consequent fragility fractures. A large epidemiological study of community dwelling elderly women reported that people with PD were more likely to sustain a fracture than their peers (hazard ratio, 2.2; 95% confidence interval, 1.6–3.1). [1] This has been caused by a higher chance of both falls and reduced bone mineral density (BMD) in patients with PD. [2] Reduced BMD is common, and can be typically diagnosed using dual X-ray absorptiometry imaging. [3] A recent study of 186 patients with PD at the early stage demonstrated that 11.8 and 41.4% of patients were diagnosed as osteoporosis (T-score less than − 2.5), and osteopenia (T-score between − 1 and − 2.5), respectively. [4] In addition, reduced BMD can be caused by immobility, vitamin D deficiency, use of dopaminergic treatments, and reduced nutritional intake in patients with PD.
Osteoporotic vertebral fracture (OVF) is the most common fragility fracture and frequently causes back pain, neurological symptoms, and spinal deformity. Thoracolumbar OVF is a common spinal disorder in elderly patients, [5, 6] and the number of patients with thoracolumbar OVF undergoing spinal fusion has been increasing in our aging society. Consequently, a large variety of surgical fusion techniques have been used to treat OVF including anterior spinal fusion (ASF) [7, 8]; posterior spinal fusion alone (PSF) [9, 10]; combined anterior and posterior spinal fusion (APSF) [11]; posterior 3 column osteotomy (3CO), including shortening osteotomy [12, 13] or vertebral column resection [14]; and vertebroplasty with posterior spinal fusion (VP + PSF) [13, 15–17]. However, there is little published data on surgical outcomes of spinal fusion for patients with PD with thoracolumbar OVF.
We hypothesized that patients with PD with thoracolumbar OVF suffered from poorer surgical outcomes, including frequency of perioperative complications and quality of life, compared to non-PD patients. To evaluate this hypothesis, we conducted a retrospective review of a multicenter database of patients with OVF in the thoracolumbar spine to clarify the effectiveness and associated problems of fusion surgery for patients with PD.
Methods
This study was reviewed and approved by the institutional review board of all institutions involved. The study was performed by JASA (Japan Association of Spine Surgeons with Ambition) using a retrospective analysis of patients with OVF treated by spinal fusion surgery at 27 university hospitals and their affiliated hospitals. A total of 26 patients with PD (PD group), including 3 men and 22 women, were identified based on the following inclusion criteria: 1) OVF in the thoracolumbar spine (from T10 to L2); 2) existence of neurological impairment, including motor deficit or neuralgia in the lower extremity; 3) underwent instrumented spinal fusion concomitant with autologous bone grafting (excluding stand-alone vertebroplasty and kyphoplasty); and 4) a minimum of 2 years of follow-up after surgery. The diagnosis of PD was based on the United Kingdom Parkinson’s Disease Society Brain Bank Criteria. [18] The average age and body mass index (BMI) at the time of surgery were 75.7 years (range, 67–89 years) and 21.8 kg/m2 (range, 14.2–34.9 kg/m2), respectively. The collapsed vertebral levels were T11, T12, L1, and L2 in 3, 8, 11, and 4 patients, respectively. The surgical procedures consisted of 4 typical techniques: PSF (n = 3), APSF (n = 2), 3CO (n = 9), and VP + PSF (n = 12), and the mean number of fused segments was 4.1 segments (range, 2–8 segments). The mean PD duration was 60.0 ± 50.6 months (range, 0–168 months), and the Hoehn and Yahr stage [19] was stage 1, 2, 3, and 4 in 2, 6, 13, and 5 patients, respectively. Demographic data are shown in Table 1.
Table 1.
PD group | Non-PD group | p value | |
---|---|---|---|
N of patients | 26 | 296 | – |
Age at operation (years) median, [IQR] | 76.0 [8.0] | 75.0 [10.8] | 0.3343 |
Sex [male/female] (N of patients) | 3/23 | 66/230 | 0.1999 |
BMI (kg/m2) median, [IQR] | 22.1 [6.3] | 22.5 [4.7] | 0.1600 |
Vertebral level (N of patients) | T11: 3 | T10: 16 | 0.6112 |
T12: 8 | T11: 25 | ||
L1: 11 | T12: 116 | ||
L2: 4 | L1: 103 | ||
L2: 36 | |||
Surgical procedure (N of patients) | APSF: 2 | ASF: 19 | 0.7176 |
PSF: 3 | APSF: 27 | ||
3CO: 9 | PSF: 37 | ||
VP + PSF: 12 | 3CO: 84 VP + PSF: 129 |
||
Number of fused segment (segment) median, [IQR] | 4.0 [2.0] | 4.0 [2.0] | 0.9534 |
BMD YAM (%) median, [IQR] | 73.0 [25.0] | 69.0 [19.8] | 0.9295 |
Number of patients with existing vertebral fracture [fx/no fx] (N of patients) | 8/18 | 108/188 | 0.7338 |
Number of comorbidity (disease) median, [IQR] | 1.0 [0.0] | 1.0 [1.0] | < 0.0001 |
Follow-up period (month) median, [IQR] | 37.0 [19.0] | 44.0 [28.0] | 0.1787 |
Abbreviation: N number, IQR interquartile range, BMI body mass index, ASF anterior spinal fusion, APSF combined anterior and posterior spinal fusion, PSF posterior spinal fusion, 3CO 3 column osteotomy, VP + PSF vertebroplasty with PSF, BMD bone mineral density, YAM young adult mean, fx fracture
The control group comprised 296 non-PD patients with thoracolumbar OVF (non-PD group) whose data were retrieved from the same database (Table 1); there were no statistically significant differences with respect to age, sex, BMI, distribution of collapsed vertebral levels, distribution of surgical procedures, number of fused segments, and follow-up period between the PD and non-PD groups (p > 0.05 for all comparisons). The outcome measures were compared between the 2 study groups.
Surgical procedure
The surgical procedures comprised various instrumentations or bone grafting techniques used in the retrospective multicenter database. The ASF surgical procedure was performed using a rod or plate system with an iliac or rib bone strut graft or metal cage. The APSF surgical procedure was a combination of ASF using an iliac or fibula strut graft and PSF using a pedicle screw and rod system. The PSF surgical procedure was performed using a pedicle screw and rod system, occasionally using laminar hooks in the uppermost or lowermost instrumented vertebra. The 3CO surgical procedure consisted of PSF as described above and vertebral column resection with reconstruction using a metal cage or eggshell shortening osteotomy through the posterior approach only. For VP + PSF, the surgical procedure consisted of PSF as described above and VP using hydroxyapatite blocks or paste performed via a transpedicular approach.
Evaluation
Surgical invasion, radiographic sagittal alignment, mechanical failure (MF), and clinical outcomes were evaluated from medical charts, plain radiographs, and computed tomography images. The evaluation of surgical invasion included the operation time, intraoperative blood loss, and perioperative complications. Radiographic sagittal alignment included the local kyphosis angle on the lateral view of plain radiographs measured between the upper endplate of the uninvolved vertebra above the affected level and the lower endplate of the uninvolved vertebra below the affected level using the Cobb method (Fig. 1). The evaluation of mechanical failure included the presence of pedicle screw pull-out, cage migration, fracture of the uppermost or lowermost instrumented vertebra, hook dislodgement, and rod fracture. Clinical outcomes were evaluated using the visual analog scale (VAS; ranging from 0 [no symptoms] to 100 [worst symptoms]) for lower back pain and lower extremity pain or numbness; the Japanese Orthopaedic Association Scoring system ([JOA score], ranging from 0 [worst condition] to 15 [best condition]) (Additional file 1); walking ability using the following grading system: grade 1, independent walking; 2, dependent walking with a cane; 3, dependent walking with walker; and 4, unable to walk (requiring a wheelchair); and occurrence of subsequent vertebral fracture. The rate of improvement in both lower back pain and lower extremity pain was assessed with the JOA score using Hirabayashi’s method [20] as follows: ([postsurgical score - presurgical score] / [15 - presurgical score] × 100).
Statistical analysis
All analyses were performed using StatView-J 5.0 software (Abacus Concepts, Berkeley, CA). The changes in investigated parameters before and after surgery were evaluated using the nonparametric Wilcoxon signed-rank test. The changes in continuous and discrete variables between the two groups were compared using the nonparametric Mann-Whitney U test and the chi-squared test, respectively. P < 0.05 was considered to be statistically significant in all analyses.
Results
The results are summarized in Table 2.
Table 2.
PD group | Non-PD group | p value | |
---|---|---|---|
Operation time (min.) median, [IQR] | 214.0 [100.0] | 237.0 [130.5] | 0.4193 |
Intraoperative blood loss (ml) median, [IQR] | 450.0 [627.0] | 402.0 [575.5] | 0.2761 |
Perioperative complication [complication/ no complication] (N of patients) | 10/16 | 45/251 | 0.0063 |
Local kyphosis angle (°) median, [IQR] | |||
Preop. | 27.0 [21.0] | 26.0 [19.0] | 0.9965 |
Postop. | 6.0 [18.0] | 8.0 [13.4] | 0.8072 |
Final | 18.7 [18.0] | 14.0 [18.0] | 0.3357 |
Amount of kyphosis correction | 10.8 [26.1] | 10.0 [16.0] | 0.6611 |
Mechanical failure (%) | 26.9 | 17.9 | 0.7464 |
JOA score improvement rate (%) median, [IQR] | 50.0 [38.5] | 53.8 [39.2] | 0.1074 |
Walking ability (N of patients) | |||
Preop. | Grade1: 2 | Grade1: 16 | 0.1030 |
Grade 2: 1 | Grade 2: 44 | ||
Grade 3: 4 | Grade 3: 86 | ||
Grade 4: 19 | Grade 4: 150 | ||
Final | Grade1: 3 | Grade1: 114 | 0.0007 |
Grade 2: 5 | Grade 2: 92 | ||
Grade 3: 12 | Grade 3: 70 | ||
Grade 4: 6 | Grade 4: 19 | ||
Subsequent vertebral fracture (%) | 38.4 | 35.1 | 0.7338 |
Abbreviation: N number, IQR interquartile range, JOA score, Japanese Orthopaedic Association scoring system
Surgical invasion
There were no significant differences in the operation time and intraoperative blood loss between the 2 groups (p > 0.05 for both comparisons). The PD group showed a higher rate of perioperative complications (odds ratio 3.48; 95% CI 1.488–8.168, p = 0.0060) and frequency of delirium than the non-PD group (PD group: 23.1%, non-PD group: 3.4%)(odds ratio 8.58; 95% CI 2.83–26.009, p < 0.0001) (Table 3).
Table 3.
Perioperative complication | PD group (N of patients) | Non-PD group (N of patients) |
---|---|---|
Overall [incidence] | 10 [38.5%] | 45 [15.2%] |
Intraoperative complication | ||
Surgical site infection | 0 | 7 |
Neurological deficit | 1 | 6 |
Dural tear | 0 | 5 |
Epidural hematoma | 0 | 3 |
Massive hemorrhage (> 5000 ml) | 0 | 1 |
Postoperative complication | ||
Delirium | 6 | 10 |
Cardiac disease | 0 | 4 |
Gastrointestinal disease | 0 | 4 |
Deep venous thrombosis | 1 | 2 |
Urinary tract infection | 1 | 0 |
Pneumonia | 0 | 2 |
Electrolyte abnormality | 0 | 1 |
Decubitus | 1 | 0 |
Abbreviation: N number
Radiographic sagittal alignment
Regarding the correction of the local kyphosis angle after surgery, both groups showed significant correction between the before surgery and the final follow-up (p < 0.05 for both comparisons) (Fig. 1). There were no significant differences in the degree of kyphosis correction between the groups (p > 0.05).
MF
In the PD group, 8 mechanical failures (26.9%) were identified. There were no significant differences in the frequency of mechanical failures between the two groups (Table 4).
Table 4.
Mechanical failure | PD group (N of patients) | Non-PD group (N of patients) |
---|---|---|
Overall [incidence] | 7 [26.9%] | 53 [17.9%] |
Pedicle/vertebral screw pull-out | 4 | 24 |
Intervertebral cage migration | 0 | 9 |
Uppermost vertebral fracture | 2 | 11 |
Lowermost vertebral fracture | 1 | 4 |
Hook dislodgement | 0 | 3 |
Rod fracture | 0 | 2 |
Abbreviation: N number
Clinical outcome
Regarding the severity of neurological symptoms according to the VAS, both groups demonstrated significant improvement in lower back pain and lower extremity pain at the final follow-up (p < 0.05 for all comparisons) (Fig. 2). There were no significant differences in the VAS preoperatively and at the final follow-up between the groups. Both groups demonstrated significant improvement in the JOA score (p < 0.05 for all comparisons) (Fig. 3), and there was no significant difference in the improvement rate between the groups. There were no significant differences in the walking ability grade preoperatively; however, the PD group showed a higher proportion of patients in grades 3 and 4 at the final follow-up (odds ratio 3.788; 95% CI 1.719–8.347, p = 0.0007). Overall, 114 patients (35.4%) sustained a subsequent vertebral fracture and there were no significant differences in the incidence between the groups.
Discussion
In the present study, patients with PD unexpectedly demonstrated acceptable and similar clinical outcomes compared to non-PD patients, including surgical invasion, local kyphosis correction, frequency of instrumentation-related MF, severity of symptoms, and JOA score. On the other hand, patients with PD demonstrated a higher rate of perioperative complications and inferior walking ability after surgery due to characteristic physical conditions related to PD itself.
Frequency of perioperative complications
According to a large, national insurance database, PD was significantly associated with an increased risk for major medical complications (adjusted OR, 1.22; 95% CI, 1.11–1.34) including myocardial infarction, acute renal failure, pulmonary embolism, cerebrovascular accidents, and pneumonia following thoracolumbar fusion surgery. [21] According to another large, nationwide inpatient database, PD was a significant predictor of major postoperative complications (OR, 1.74; 95% CI, 1.37–2.22) including surgical site infection, sepsis, pulmonary embolism, respiratory complications, cardiac events, stroke, and renal failure following spine surgery. [22] In addition, postoperative delirium was more common in patients with PD (30.3%) than in the controls (4.3%), [22] which was in agreement with the present study. Postoperative delirium is a common complication of surgical procedures in the elderly, [23] and acute delirium increases morbidity and mortality leading to prolonged hospitalization. [24, 25] Therefore, physicians should be aware of the various adverse events that may occur, especially due to interruption of anti-parkinsonism drugs following spine surgery. Moreover, a noteworthy finding is that despite the relatively higher risk of potentially fatal parkinsonism-hyperpyrexia syndrome, [26] no such cases occurred in the present study. Needless to say, the establishment of a partnership between orthopedic surgeons and neurologists is essential for perioperative care, and early intervention against adverse events is desirable.
Surgical strategy for patients with PD and OVF in the thoracolumbar junction
Thoracolumbar OVF is a common spinal disorder in elderly patients, [5, 6] which frequently causes neurological symptoms including spinal cord or cauda equina impairment. Based on previous reports, a consensus has emerged that delayed neurological impairment following OVF is primarily caused by instability of the fracture site rather than mechanical neural compression by ectopic bony fragments. [9, 10, 15] Based on the previous studies, patients with PD have higher chance of postoperative complications and unintended revision surgeries after spinal fusion. Additionally, surgically treated patients with PD tend to have poorer outcomes and lower fusion rates, especially in patients who undergo multi-level fusion. [27, 28] A consensus has emerged that long-segment corrective fusion surgery tends to be necessary for global sagittal malalignment, owing to the progressively stooped posture as PD progresses, and the risk of unfavorable biomechanics related to a long lever arm at the lumbosacral junction. [29] Although various surgical procedures have provided acceptable outcomes for thoracolumbar OVF, we hypothesized that patients with PD and thoracolumbar OVF may have poorer surgical outcomes. In the present study, they surprisingly showed acceptable outcomes as assessed by several indicators including frequency of perioperative complications, amount of kyphosis correction, and improvement of the VAS and JOA score. With regard to the walking ability, patients with PD had a higher proportion of non-ambulators and dependent ambulators with walkers, which might be caused by the diminished baseline physical capacity due to PD itself. Therefore, the results of the present study can conclude that the same conventionally used surgical indications are applicable to PD patients with OVF in the thoracolumbar junction.
There are some limitations of this study. First, the study design was retrospective, and the study was based on data review, which did not allow us to evaluate the severity of preoperative vertebral collapse, surgical details, such as choice of approach, use of supplemental anchors, and concomitant decompression procedures, and global spinal alignment. Second, selection bias could not be avoided due to different indications for non-PD and PD patients based on the various motor or non-motor symptoms associated with PD. Third, we could evaluate the PD status according to the simple 5-grade classification, but could not evaluate the severity of motor- or non-motor symptoms associated with PD. Therefore, a prospective study with a larger sample size that provides detailed specific symptoms on PD must be conducted to elucidate the effect of PD on surgical outcomes in patients with OVF. Despite these limitations, this study presents the largest case series evaluating the surgical outcomes in patients with PD and OVF in the thoracolumbar junction; the number of such patients is currently increasing due to unprecedented aging of the population.
Conclusion
Spinal fusion for patients with PD and OVF in the thoracolumbar junction resulted in good radiological and symptomatic improvement, except for frequency of perioperative complications and functional improvement of walking ability, compared to non-PD patients. Moreover, they were similar with regard to prevalence of instrumentation-related MF and subsequent vertebral fracture. The results of this study imply that same conventionally used surgical strategy can be applicable for patients with PD and OVF in the thoracolumbar junction. However, multidisciplinary, intensive perioperative care must be provided by the orthopedic surgeons and neurologists in unison to prevent various adverse events and a rehabilitation regimen implemented to regain the patients’ walking status before the OVF-related injury.
Additional file
Acknowledgements
The authors thank all supporting members of the Japan Association of Spine Surgeons with Ambition (JASA).
Funding
The research did not receive any specific grant from funding agencies.
Availability of data and materials
All relevant data supporting the conclusions are included within the article and tables. The dataset used and analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- ASF
anterior spinal fusion
- BMD
bone mineral density
- JOA
Japanese Orthopaedic Association
- OVF
osteoporotic vertebral fracture
- PD
Parkinson’s disease
- PSF
posterior spinal fusion
- VAS
Visual Analog Scale
Authors’ contributions
KW1; study design, analyses and interpretation of data, draft of manuscript with tables and figures. NH, KI, TH, NE; substantial contributions to conception and critical revision for important intellectual content. TK, YM, HT, AT, TY, KH, KK2, AK, GI, AN, DS, SI1, SO1, TF, SI2, KK4, HM, SS, MH, KK5, YA, MO2, MT, HE, TA, KN, KW2, TH; substantial contributions to study design and data acquisition, KK1, MO1, YS, TI, TY, HF, YN, HS, HN, KT, SY, SA, SU, NY, HO, TD, HI, MM, WS, TN, MS, TF, SO2, KA, KK3, KY, TY, AI, TT, SS, NI, EO, HF, SU, YS, KN; data acquisition. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was approved by the ethics committee of all institutions involved. Informed consent was waivered by the above ethics committee as the present retrospective cohort study involved already existing data and records at the time of investigation, and did not retain personal identifiers of the gathered information.
The ethical committee, Niigata University School of Medicine; reference number 2015-1385
The ethical committee, Osaka University School of Medicine; 11360-3
The ethical committee, Tokyo Medical University; 2605
The ethical committee, Osaka City University School of Medicine; 3170
The ethical committee, Nagasaki University School of Medicine; 17032715
The ethical committee, Tokyo Medical and Dental University; M2016-055
The ethical committee, Kyushu University School of Medicine; 28-359
The ethical committee, Jichi Medical University; A13-82
The ethical committee, Kitasato University School of Medicine; B16-34
The ethical committee, Osaka Medical College; 2169
The ethical committee, Tokai University School of Medicine; 16R-033
The ethical committee, Shinshu University School of Medicine; 3456
The ethical committee, Chiba University School of Medicine; 2481
The ethical committee, Nagoya University School of Medicine; 2016-0177
The ethical committee, Kochi University School of Medicine; 2016-116
The ethical committee, Kanazawa University School of Medicine; 2015-075
The ethical committee, University of Toyama School of Medicine; 21-22
The ethical committee, Akita University School of Medicine; 1879
The ethical committee, Kobe University School of Medicine; 160004
The ethical committee, Nihon University Itabashi Hospital; RK-160913-21
The ethical committee, Hokkaido University School of Medicine; 015-0396
The ethical committee, Iwate Medical University; H28-88
The ethical committee, University of Tsukuba School of Medicine; H27-133
The ethical committee, Hiroshima University School of Medicine; Epi-139
The ethical committee, Keio University School of Medicine; 20110141
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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References
- 1.Dennison EM, Premaor M, Flahive J, Siris ES, Gehlbach SH, Adachi JD, et al. Effect of co-morbidities on fracture risk: findings from the global longitudinal study of osteoporosis in women (GLOW) Bone. 2012;50:1288–1293. doi: 10.1016/j.bone.2012.02.639. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Dobson R, Yarnall A, Noyce AJ, Giovannoni G. Bone health in chronic neurological diseases: a focus on multiple sclerosis and parkinsonian syndromes. Pract Neurol. 2013;13:70–79. doi: 10.1136/practneurol-2012-000435. [DOI] [PubMed] [Google Scholar]
- 3.Zhao Y, Shen L, Ji HF. Osteoporosis risk and bone mineral density levels in patients with Parkinson’s disease: a meta-analysis. Bone. 2013;52:498–505. doi: 10.1016/j.bone.2012.09.013. [DOI] [PubMed] [Google Scholar]
- 4.van den Bos F, Speelman AD, van Nimwegen M, van der Schouw YT, Backx FJ, Bloem BR, et al. Bone mineral density and vitamin D status in Parkinson’s disease patients. J Neurol. 2013;260:754–760. doi: 10.1007/s00415-012-6697-x. [DOI] [PubMed] [Google Scholar]
- 5.Frost HM. Clinical management of the symptomatic osteoporotic patient. Orthop Clin North Am. 1981;12:671–681. [PubMed] [Google Scholar]
- 6.Lee YL, Yip KM. The osteoporotic spine. Clin Orthop Relat Res. 1996;323:91–97. doi: 10.1097/00003086-199602000-00012. [DOI] [PubMed] [Google Scholar]
- 7.Kaneda K, Asano S, Hashimoto T, Satoh S, Fujiya M. The treatment of osteoporotic-posttraumatic vertebral collapse using the Kaneda device and a bioactive ceramic vertebral prosthesis. Spine (Phila Pa 1976) 1992;17:S295–S303. doi: 10.1097/00007632-199208001-00015. [DOI] [PubMed] [Google Scholar]
- 8.Kanayama M, Ishida T, Hashimoto T, Shigenobu K, Togawa D, Oha F, et al. Role of major spine surgery using Kaneda anterior instrumentation for osteoporotic vertebral collapse. J Spinal Disord Tech. 2010;23:53–56. doi: 10.1097/BSD.0b013e318193e3a5. [DOI] [PubMed] [Google Scholar]
- 9.Ataka H, Tanno T, Yamazaki M. Posterior instrumented fusion without neural decompression for incomplete neurological deficits following vertebral collapse in the osteoporotic thoracolumbar spine. Eur Spine J. 2009;18:69–76. doi: 10.1007/s00586-008-0821-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Nakano A, Ryu C, Baba I, Fujishiro T, Nakaya Y, Neo M. Posterior short fusion without neural decompression using pedicle screws and spinous process plates: a simple and effective treatment for neurological deficits following osteoporotic vertebral collapse. J Orthop Sci. 2017;22:622–629. doi: 10.1016/j.jos.2017.03.004. [DOI] [PubMed] [Google Scholar]
- 11.Nakashima H, Imagama S, Yukawa Y, Kanemura T, Kamiya M, Deguchi M, et al. Comparative study of 2 surgical procedures for osteoporotic delayed vertebral collapse: anterior and posterior combined surgery versus posterior spinal fusion with vertebroplasty. Spine (Phila Pa 1976) 2015;40:E120–E126. doi: 10.1097/BRS.0000000000000661. [DOI] [PubMed] [Google Scholar]
- 12.Saita K, Hoshino Y, Higashi T, Yamamuro K. Posterior spinal shortening for paraparesis following vertebral collapse due to osteoporosis. Spinal Cord. 2008;46:16–20. doi: 10.1038/sj.sc.3102052. [DOI] [PubMed] [Google Scholar]
- 13.Kashii M, Yamazaki R, Yamashita T, Okuda S, Fujimori T, Nagamoto Y, et al. Surgical treatment for osteoporotic vertebral collapse with neurological deficits: retrospective comparative study of three procedures—anterior surgery versus posterior spinal shorting osteotomy versus posterior spinal fusion using vertebroplasty. Eur Spine J. 2013;22:1633–1642. doi: 10.1007/s00586-013-2759-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Suzuki T, Abe E, Miyakoshi N, Murai H, Kobayashi T, Abe T, et al. Posterior-approach vertebral replacement with rectangular parallelepiped cages (PAVREC) for the treatment of osteoporotic vertebral collapse with neurological deficits. J Spinal Disord Tech. 2013;26:E170–E176. doi: 10.1097/BSD.0b013e318286fc18. [DOI] [PubMed] [Google Scholar]
- 15.Katsumi K, Hirano T, Watanabe K, Ohashi M, Yamazaki A, Ito T, et al. Surgical treatment for osteoporotic thoracolumbar vertebral collapse using vertebroplasty with posterior spinal fusion: a prospective multicenter study. Int Orthop. 2016;40:2309–2315. doi: 10.1007/s00264-016-3222-3. [DOI] [PubMed] [Google Scholar]
- 16.Uchida K, Nakajima H, Yayama T, Miyazaki T, Hirai T, Kobayashi S, et al. Vertebroplasty-augmented short-segment posterior fixation of osteoporotic vertebral collapse with neurological deficit in the thoracolumbar spine: comparisons with posterior surgery without vertebroplasty and anterior surgery. J Neurosurg Spine. 2010;13:612–621. doi: 10.3171/2010.5.SPINE09813. [DOI] [PubMed] [Google Scholar]
- 17.Sudo H, Ito M, Kaneda K, Abumi K, Kotani Y, Nagahama K, et al. Anterior decompression and strut graft versus posterior decompression and pedicle screw fixation with vertebroplasty for osteoporotic thoracolumbar vertebral collapse with neurologic deficits. Spine J. 2013;13:1726–1732. doi: 10.1016/j.spinee.2013.05.041. [DOI] [PubMed] [Google Scholar]
- 18.Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson’s disease. J Neurol Neurosurg Psychiatry. 1988;51:745–752. doi: 10.1136/jnnp.51.6.745. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Goetz CG, Poewe W, Rascol O, Sampaio C, Stebbins GT, Counsell C, et al. Movement Disorder Society task force report on the Hoehn and Yahr staging scale: status and recommendations. Mov Disord. 2004;19:1020–1028. doi: 10.1002/mds.20213. [DOI] [PubMed] [Google Scholar]
- 20.Hirabayashi K, Maruyama T, Wakano K, Ikeda K, Ishii Y. Postoperative lumbar canal stenosis due to anterior spinal fusion. Keio J Med. 1981;30:133–139. doi: 10.2302/kjm.30.133. [DOI] [PubMed] [Google Scholar]
- 21.Puvanesarajah V, Jain A, Qureshi R, Carstensen SE, Tyger R, Hassanzadeh H. Elective thoracolumbar spine fusion surgery in patients with Parkinson disease. World Neurosurg. 2016;96:267–271. doi: 10.1016/j.wneu.2016.09.014. [DOI] [PubMed] [Google Scholar]
- 22.Oichi T, Chikuda H, Ohya J, Ohtomo R, Morita K, Matsui H, et al. Mortality and morbidity after spinal surgery in patients with Parkinson's disease: a retrospective matched-pair cohort study. Spine J. 2017;17:531–537. doi: 10.1016/j.spinee.2016.10.024. [DOI] [PubMed] [Google Scholar]
- 23.Kobayashi K, Imagama S, Ando K, Ishiguro N, Yamashita M, Eguchi Y, et al. Risk factors for delirium after spine surgery in extremely elderly patients aged 80 years or older and review of the literature: Japan Association of Spine Surgeons with ambition multicenter study. Global Spine J. 2017;7:560–566. doi: 10.1177/2192568217700115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Rockwood K, Cosway S, Carver D, Jarrett P, Stadnyk K, Fisk J. The risk of dementia and death after delirium. Age Ageing. 1999;28:551–556. doi: 10.1093/ageing/28.6.551. [DOI] [PubMed] [Google Scholar]
- 25.Leslie DL, Zhang Y, Holford TR, Bogardus ST, Leo-Summers LS, Inouye SK. Premature death associated with delirium at 1-year follow-up. Arch Intern Med. 2005;165:1657–1662. doi: 10.1001/archinte.165.14.1657. [DOI] [PubMed] [Google Scholar]
- 26.Newman EJ, Grosset DG, Kennedy PG. The parkinsonism-hyperpyrexia syndrome. Neurocrit Care. 2009;10:136–140. doi: 10.1007/s12028-008-9125-4. [DOI] [PubMed] [Google Scholar]
- 27.Sarkiss CA, Fogg GA, Skovrlj B, Cho SK, Caridi JM. To operate or not?: a literature review of surgical outcomes in 95 patients with Parkinson's disease undergoing spine surgery. Clin Neurol Neurosurg. 2015;134:122–125. doi: 10.1016/j.clineuro.2015.04.022. [DOI] [PubMed] [Google Scholar]
- 28.Bourghli A, Guérin P, Vital JM, Aurouer N, Luc S, Gille O, et al. Posterior spinal fusion from T2 to the sacrum for the management of major deformities in patients with Parkinson disease: a retrospective review with analysis of complications. J Spinal Disord Tech. 2012;25:E53–E60. doi: 10.1097/BSD.0b013e3182496670. [DOI] [PubMed] [Google Scholar]
- 29.Watanabe K, Hirano T, Katsumi K, Ohashi M, Shoji H, Hasegawa K, et al. Characteristics of spinopelvic alignment in Parkinson’s disease: comparison with adult spinal deformity. J Orthop Sci. 2017;22:16–21. doi: 10.1016/j.jos.2016.09.013. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All relevant data supporting the conclusions are included within the article and tables. The dataset used and analyzed during the current study are available from the corresponding author on reasonable request.