Objective To evaluate pulmonary function changes in patients with severe scol iosis undergoing anterior release, posterior segmental fixation and fusion, and convex thoracoplasty by resecting a short length of rib. Methods FromJanuary 2006 to July 2007, 16 patients with severe scol iosis were treated with anterior release, posterior segmental fixation and fusion, and convex thoracoplasty by resecting a short length of rib. There were 6 males and 10 females with an average age of 16.9 years (range, 10-24 years). There were 1 case of Lenke 1 curve, 9 cases of Lenke 2 curve, and 6 cases of Lenke 4 curve. The preoperative Cobb angle was (104.8 ± 10.9)° and the preoperative thoracic kyphotic angle was (30.0 ± 4.2)°. The preoperative height of “razor back” deformity was (5.9 ± 1.2) cm. Before operation, the actual value of forced vital capacity (FVC) was (2.04 ± 0.63) L and that of forced expiratory volume in 1 second (FEV1.0) was (1.72 ± 0.62) L. The percentage of actual values to expected ones in FVC was 70% ± 16%, and that in FEV1.0 was 67% ± 15%. All patients had pulmonary function tests before operation and 3, 6, 12, 24 months after operation. Results All wounds healed by first intention. The Cobb angle at 24-month follow-up was (53.4 ± 18.6)° and the correction rate was 49.0% ± 15.3%. The thoracic kyphotic angle at 24-month follow-up was (34.0 ± 2.4)° and the correction rate was 13.3% ± 2.2%. The height of “razor back” deformity at 24-month follow-up was (2.2 ± 0.8) cm. Compared with preoperative level, all these data showed significant differences (P lt; 0.05). At 3 and 6 months, the actual values of FVC and FEV1.0 decl ined, but no significant difference was found (P gt; 0.05). At 12 and 24 months, the actual values of FVC andFEV1.0 were close to the preoperative level (P gt; 0.05). The percentages of actual values to expected ones in FVC and FEV1.0 indicate continued improvement in pulmonary function from the postoperative 3 to 24 months follow-up. Compared with preoperative level, the percentages of actual values in FVC decl ined 19% 3 months postoperatively (P lt; 0.05) and 12% 6 months postoperatively (P lt; 0.05). The percentages of actual values to expected ones in FEV1.0 decl ined 16% 3 months postoperatively (P lt; 0.05), and 10% 6 months postoperatively (P lt; 0.05). The percentages of actual values to expected ones in FVC and FEV1.0 were close to the preoperative level 12 and 24 months after operation (P gt; 0.05). Conclusion In severe scol iosis patients who are treated with anterior release, posterior segmental fixation and fusion, and convex thoracoplasty by resecting a short length of rib, pulmonary function decreases obviously 3-6 months after operation. And it returns to the operative baseline 12-24 months after operation.
Objective To explore the feasibilities, methods, outcomes and indications of atlas pedicle screw system fixation and fusion for the treatment of upper cervical diseases. Methods From October 2004 to January 2006, 17 patients with upper cervical diseases were treated with atlas pedicle screw system fixation and fusion. There were 13 males and 4 females, ageing 19 to 52 years. Of 17 cases, there were 14 cases of atlantoaxial dislocation(including 3 cases of congenital odontoid disconnection，4 cases of old odontoid fracture，2 cases of new odontoid fracture(typeⅡC), 3 cases of rupture of the transverse ligament, and 2 cases of atlas fracture； 2 cases of tumor of C2; 1case of giant neurilemoma of C2,3 with instability after the resection oftumors. JOA score before operation was 8.3±3.0. Results The mean operative time and bleeding amount were 2.7 hours (2.1-3.4 hours) and 490 ml (300-750 ml) respectively. No injuries to the vertebral artery and spinal cord were observed. The medial-superior cortex of lateral mass was penetrated by 1 C1 screw approximately 3 mmwithout affecting occipito-atlantal motions. All patients were followed up 3-18 months. The clinical symptoms were improved in some extents and the screws were verified to be in a proper position, no breakage or loosening of screw and rob occurred. All patients achieved a solid bone fusion after 3-6 months. JOA score 3 months after operation was14.6±2.2. JOA improvement rates were 73%-91%(mean 82%). Conclusion The atlas pedicle screw system fixation and fusion is feasible for the treatment of upper cervical diseases and has betteroutcomes, wider indications if conducted properly.
Objective To introduce operation skill of the spinal wedge osteotomy by posterior approach for correction of severe rigid scol iosis and to discuss the selection of the indications and the range of fusion and fixation. Methods Between July 1999 and January 2009, 23 patients with severe rigid scol iosis were treated with spinal wedge osteotomy by posterior approach, including 16 congenital scol iosis, 5 idiopathic scol iosis, and 2 neurofibromatosis scol iosis. There were 11 males and 12 females with a median age of 15 years (range, 8-29 years). Two patients had previous surgery history. The Cobb’s angles of scol iosis and kyphosis before operation were (85.39 ± 13.51)° and (56.78 ± 17.69)°, respectively. The mean spinal flexibil ity was 14.4% (range, 4.7%-22.5%). The trunk shift was (15.61 ± 4.89) mm. The preoperative CT or MRI showed bony septum in the canal in 2 patients. Results The mean operative time was 241 minutes and the mean blood loss was 1 452 mL. The average fused vertebrae were 10.7 segaments (range, 8-14 segaments). The follow-up ranged from 1 to 4 years with an average of 2 years and 6 months. The postoperative Cobb’s angle of scol iosis was (38.70 ± 6.51)°, the average correction rate was 54.7%. The postoperative Cobb’s angle of kyphosis was (27.78 ± 6.01)°, the average correction rate was 51.0%. The trunk shift was improved to (4.69 ± 1.87) mm, the increased height was 5.2 cm on average (range, 2.8-7.7 cm). The Cobb’s angle of scol iosis was (41.57 ± 6.80)° with an average 2.9° loss of correction at the final follow-up; the Cobb’s angle of kyphosis was (30.39 ± 5.94)° with an average 2.6° loss of correction at the final follow-up; the trunk shift was (4.78 ± 2.00) mm at the final follow-up. There were significant differences (P lt; 0.05) in the Cobb’s angles of scol iosis and kyphosis and the trunk shift between preoperation and postoperation, between preoperation and last follow-up. Four cases had pedicle fracture, 1 had L1 nerve root injury, 2 had superior mesenteric artery syndrome, 1 had exudates of incision, and 2 had temporary dysfunction of both lower extremity. Conclusion Spinal wedge osteotomy by posterior approach is a rel iable and safe surgical technique for correcting severe rigid scol iosis. With segmental pedical screw fixation, both the spinal balance and stabil ity can be restored.
Objective To study the properties of the xenogeneic deproteinized cancellous bone used as a scaffold in the bone tissue engineering andits application to the spinal fusion of the lumbar intertransverse process in agoat. Methods The deproteinized bone was derived from an adult pig’s femoral cancellous bone through the physical and chemical treatments. Its morphological features, constituting components, and biomechanical properties were examined by the scanning electron microscopy, X-ray diffraction analysis, and mechanical experimental instrument. The cell-material complex was observed under the inverted phase contrast microscope to evaluate the adhesion and the growth of the osteoblasts. The experimental model of the spinal fusion of the lumbar intertransverse process was produced in 12 male goats aged 6-8 months, which were divided into two groups. In Group A, the tissue engineered bone constructed by thexenogeneic deproteinized cancellous bone, the recombinant human bone morphogenetic protein 2, and the mesenchymal stem cells was used for the spinal fusion; however, in Group B the autoilium was used. The samples were harvested at 4, 8 and 12 weeks postoperatively, and a series of examinations were performed, including the radiography and the histomorphological assay. Results The deproteinized cancellous bone had a natural pore network system, with an aperture ranging in size from 200 to 500 μm, containing a main organic material ofcollagen and the inorganic material of hydroxyapatite. So, the deproteinized cancellous bone had a good mechanical strength and a good histocompatibility. In Group A, the X-ray examination at different timepoints postoperatively showed that at 4 weeks,the bridging areas of all the fusion sites were not clear, especially on the internal side; at 8 weeks, the upper and lower bridged parts had a narrowed gap, with formation of much continuous bony callus; at 12 weeks, a complete fusion occurred. In the early stage, the material density was slightly lowerin Group A than in Group B, but at 12 weeks the density was almost the same in both the groups. Histological examination in the transplant area showed that at 4 weeks in Group A there was a new bone formation in a multipoint way; at 8 weeks, a “sandwichshaped” new bone wascrossed with the transplanting materials; and at 12 weeks, a medullary cavity was remodeled and a new cancellous bone was formed. The osteogenic process of thetissue engineered bone constructed by the xenogeneic deproteinized cancellous bone scaffold was almost the same as the autoilium osteogenesis. Conclusion The xenogeneic deproteinized cancellous bone is a good material in the bone tissue engineering, which can be used as an osteogenesis scaffold andprovide a stable environment for revascularization and osteoblastic differentiation.
Objective To investigate the stability and the stress distributions of L3-5 fused with three different approaches (interbody, posterolateral and circumferential fusions) and to investigate degeneration of thesegment adjacent to the fused functional spinal unit. Methods A detailed L3-5 three-dimensional nonlinear finite element model of a normal man aged 32 was established and validated. Based on the model, the destabilized model, the interbody, posterolateral and circumferential fusions models of L4-5 were established. After the loadings were placed on all the models, we recorded the angular motions of the fused segment and the Von Mises stress of the adjacent intervertebral disc. Results The circumferential fusion was most stable than the others, and the interbody fusion was more stable than the posterolateral fusion. The maximal Von Mises stress of the adjacent L3,4 intervertebral disc in all the models was ranked descendingly as flexion,lateral bending,torsion and extension. For the three kinds of fusions, the stress increment of the L3,4 intervertebral disc was ranked ascendingly as interbody fusion,posterolateral fusion and circumferential fusion. Conclusion After destabilization of the L4,5 segment, the stability of the circumferential fusionis better than that of the others, particularly under the flexional or extensional loading. The stability of the interbody fusion is better than that of the posterolateral fusion, except for under the flexional loading. The feasibility of adjacent segment degeneration can be ranked descendingly as: circumferential fusion,posterolateral fusion and interbody fusion.
Objective To compare the effectiveness of three different bone grafts [autogenous bone, allogeneic bone, and bone morphogenetic protein (BMP) composite bone] combined with screw system for spinal fusion of degenerative lumbardisease. Methods Between January 2005 and January 2010, 102 cases of degenerative lumbar disease were randomly treated with autogenous bone (group A, n=35), allogeneic bone (group B, n=33), and BMP composite bone (group C, n=34). There was no significant difference in sex, age, disease duration, affected segments, Meyerding grade, preoperative intervertebral space height, and the Japanese Orthopaedic Association (JOA) score among 3 groups (P gt; 0.05). The intervertebral space height, bone fusion rate, and JOA score were compared among 3 groups at different time points. Results All patients of 3 groups were followed up 2 to 5 years, with an average of 3.2 years. At 6 to 24 months after operation, the intervertebral space height significantly increased when compared with preoperative value in 3 groups (P lt; 0.05); the intervertebral space height of groups A and C was significantly greater than that of group B at 6, 12, 18, and 24 months after operation (P lt; 0.05), but no significant difference was found between groups A and C (P gt; 0.05). Bone graft fusion was observed at 6 months in groups A and C and at 12 months in group B; at 24 months, the rate of bone graft fusion was 100% in groups A and C, and 87.88% in group B, showing significant difference (P lt; 0.05). There was significant difference in JOA score between preoperation and postoperative 12th and 24th months (P lt; 0.05); at 12 and 24 months after operation, JOA socre and improving rate of groups A and C were significantly higher than those of group B (P lt; 0.05), but no significant difference was found between groups A and C (P gt; 0.05). Conclusion The effect of BMP composite bone is equivalent to that of autogenous bone graft in treating spinal fusion of degenerative lumbar disease, and they are better than allogeneic bone graft. BMP composite bone can obtain adequate bone grafts without invasive sampling, and has fast fusion and high successful rate.
Objective To evluate the clinical outcome of autograftsof ilium and interbody fusion cage or bone morphogenetic protein(BMP)／artificial bone material／ cage in treating lumbar spondylolisthesis. Methods From January 1997 to January 2004，114 patients with lumbar spondylolisthesis were treated with posterior lumbar interbody fusion and pedicle screw fixation． There were 45 males and 69 females with an average age of 43 years ranging from 32 to 61 years. Of 114patients, 85 cases were classified as degree Ⅰ, 24 cases as degree Ⅱ and 5 cases as degree Ⅲ. The patients were divided into three groups accordingto the material used for interbody fusion: autografts of ilium (group A, n=42), interbody fusion cages(group B, n=36), and BMP／artificial bone material／ cage (group C, n=36)．The clinical and radiographic results of the patients were compared among three groups． Results All patients were followed from 13 to 30 months with an average of 15 months． There were no statistically significant differences in surgical time, blood loss, and disc space height of preoperation(P＞0.05) among three groups. No severe complication occurred in the three groups(P＞0.05). The excellent and good rates in groups A，B and C were 81.0％, 80.6％, and 83.3％ respectively, showing no statisticallysignificant difference(P＞0.05)．The fusion rate of group C(97.0%) was significantly higher than those of group A(81.0%) and group B(83.3%) (P＜0.05) after 1 year of operation．And the average loss of disc space height in groups B and C was significantly lower than that in group A(P＜0.05). Conclusion Higher fusion rate and lower loss of disc space height can beobtained in treating lumbar spondylolisthesis with BMP／artificial bone materiel.It is an effective method in the treatment of spondylolisthesis.
Objective To investigate the osteoblasts effect, compl ications and influencing factors in the appl ication of small freeze-drying allogeneic bone plots mixed autologous bone fragments in spinal surgery, and to compare with autogenous bone graft. Methods From January 2003 to January 2007, 515 cases of spinal injuries were treated. A total of 324 cases weretreated with small freeze-drying allogeneic bone plots mixed with autologous bone grafts (group A), including 211 males and 113 females with an average age of 36 years (18-83 years). There were 182 cases of thoracolumbar vertebra fracture, 68 cases of lumbar spondylol isthesis, 47 cases of lumbar vertebral canal stenosis, 17 cases of cervical disc herniation, 5 cases of cervical spine fracture-dislocation and 5 cases of thoracolumbar vertebra tumor. The weight of bone graft was 10-60 g (mean 30 g). A total of 191 cases were treated with autogenous bone grafting (group B), including 135 males and 56 females with an average age of 32 years (23-78 years). There were 109 cases of thoracolumbar vertebra fracture, 23 cases of lumbar spondylol isthesis, 17 cases of lumbar vertebral canal stenosis, 19 cases of cervical disc herniation, and 23 cases of cervical spine fracture-dislocation. The weight of bone graft was 10-50 g (mean 25 g). Results In group A, effusion of wound increased in 4 cases and the result of bacterial culture was negative; effusion was absorbed after 2 weeks of local irrigation, drainege and cortin management. In group B, no obvious effusion was observed. The follow-up time was 10-36 months (mean 17.4 months) in group A and 8-36 months (mean 16.8 months) in group B. The bone heal ing was achieved in 308 cases within 4-10 months (mean 8.1 months) and in 184 cases within 4-10 months (mean 5.8 months), and the bone fusion rates were 95.06% and 96.34% in groups Aand B, respectively. There was no significant difference in bone fusion rate between groups (P gt; 0.05). According to Mankin and Komender evaluation standard, the response rates were 95.06% and 96.34% in groups A and B, respectively, showing no significant difference (P gt; 0.05). Conclusion Mix-bone grafting has the same effective to autologous bone grafting in bone fusion rate. It could be used as the supplement of the autologous bone inadequacy.
Objective To investigate the relationship between the volume of bone-graft and fusion efficacy in posterior lumbar interbody fusion and internal fixation of spondylolisthesis. Methods Between May 2004 and June 2007, 79 patients with spondylolisthesis were treated with posterior lumbar interbody fusion and internal fixation. The patients were randomly divided into 3 groups according to the volume of bone-graft for interbody fusion: group A (n=27), 5 bone granules/ cm3 on average; group B (n=26), 11 bone granules/cm3 on average; and group C (n=26), 25 bone granules/cm3 on average. There was no significant difference in gender, age, disease duration, affected segment, and the degree of vertebral slip among 3 groups (P gt; 0.05). The volume of bone-graft, the fusion rate, the loss of intervertebral height, and the incidence of internal fixation failure were compared among 3 groups. Results All cases were followed up 24-43 months (mean, 35 months). There were significant differences in volume of bone-graft among 3 groups (P lt; 0.05). There was no significant difference in total volume of bone-graft and Cage height among 3 groups (P gt; 0.05). The Oswestry disability index (ODI) and visual analogue scale (VAS) scores of low back pain and leg pain at last follow-up were significantly decreased when compared with preoperative scores in 3 groups (P lt; 0.05); but no significant difference was found among 3 groups (P gt; 0.05). The fusion rate was significantly higher in group B than in groups A and C, and in group A than in group C at 1 and 2 years after operation (P lt; 0.05). The change values of the intervertebral height were (2.2 ± 1.4), (0.8 ± 1.3), and (2.3 ± 1.6) mm respectively in groups A, B, and C; it was significantly lower in group B than in groups A and C (P lt; 0.05). The degree of vertebral slip at immediately after operation and last follow-up was significantly improved when compared with preoperative one in 3 groups (P lt; 0.05); the loss of vertebral slip in group B was significantly lower than that in groups A and C at last follow-up (P lt; 0.05). After operation, nail breaking occurred in 1 case (3.7%) of group C at 1 year, depinning in 1 case (3.8%) of group A at 2 years, and no nail breaking or depinning in group B. There was no significant difference in the incidence of internal fixation failure among 3 groups (χ2=3.950, P=0.604). Conclusion The application of bone-graft with middle volume (11 bone granules/cm3 on average) in internal fixation and posterior lumbar interbody fusion has a good imageology outcome, which can increase the fusion rate and decrease the loss of intervertebral height.
Objective To evaluate the cl inical results of allogeneic bone graft for interbody fusion in cervical tuberculosis. Methods Between January 2000 and January 2008, 30 cases of cervical tuberculosis were treated with allogeneic (group A, n=15) or autologous (group B, n=15) il iac crest bone graft combined with anterior fixation after radical debridement. In group A, there were 8 males and 7 females with an average age of 38 years; the disease duration was 6 to 14 months; the preoperative kyphosis Cobb angle was (8.6 ± 11.3)°; the preoperative Japanese Orthopaedic Association (JOA) score was 13.0 ± 3.1 for neurological function; and the length of bone graft was 32 mm on average. In group B, there were 9males and 6 females with an average age of 42 years; the disease duration was 4 to 17 months; the preoperative kyphosis Cobb angle was (4.9 ± 7.4)°; the preoperative JOA score 12.3 ± 4.2; and the length of bone graft was 34 mm on average. There was no significant difference in general data between 2 groups (P gt; 0.05). Results The operation time and bleeding volume in group A were significantly less than those in group B (P lt; 0.05). Wound effusion were found in 2 cases of group A, and the other incisions healed by first intention. No infection occurred in group B. In group A, 13 cases were followed up 12-48 months; in group B, 14 cases were followed up 13-46 months. The time of bone graft heal ing in group A [(7.6 ± 2.1) months] was significantly longer than that in group B [(4.2 ± 1.1) months] (t=2.773, P=0.005). The kyphosis Cobb angles were significantly improved at 6 months and last follow-up after operation in 2 groups when compared with that before operation (P lt; 0.05), but no significant difference was found between 2 groups at different time after operation (P gt; 0.05). There was no significant difference in JOA score at 6 months after operation between group A (14.1 ± 2.6) and group B (14.3 ± 2.4) (t=1.655, P=0.162). The improvement rate for neural function were 83.7% in group A and 87.8% in group B, showing no significant difference (χ2=3.150, P=0.071). There was no loosening of internal fixation and recurrence of tuberculosis in 2 groups during follow-up. Five cases had chronic pain at il iac donor sites in group B. According to Bridwell et al. evaluation standard, the bone fusion was satisfactory in 11 cases (84.6%) and unsatisfactory in 2 cases (15.4%) in group A, and was satisfactory for all in 14 cases (100%) in group B. The satisfactory rate of bone fusion showed no significant difference between 2 groups (χ2=2.680, P=0.115).Conclusion Allogeneic bone grafting has a good cl inical result for spinal fusion in cervical tuberculosis surgery, which can treat tuberculosis bone defect effectively.