Development of a per-operative procedure for concentrated bone marrow adjunction in postero-lateral lumbar fusion: radiological, biological and clinical assessment.

PURPOSE: Addition of bone marrow to the bone graft in the postero-lateral lumbar arthrodesis is a widely used technique. Bone marrow brings stem cells and growth factors contained in the platelets, favorable for bone growth. Adjunction of concentrated bone marrow should create better conditions and may increase bone growth. METHODS: Simple blind randomized clinical, prospective, monocentric trial was conducted. Fifteen patients underwent lumbar arthrodesis. During surgery, a fraction of the bone marrow harvested was centrifuged. One side received this concentrate with autologous bone and ceramics; the other side received the same graft with unconcentrated bone marrow. A quantitative study, realised with a volume calculating software on CT-scan images, determined the cortical bone volume in the graft post-operatively and at 3 months. The osteoprogenitor cells, nucleated cells and platelet concentrations were determined. RESULTS: The biological study found an average concentration of six times for the nucleated cells, 3.5 times for the platelets and 2.2 times for the osteoprogenitor cells. The comparison of the mean cortical bone volumes post-operatively and at 3 months was not significantly different. CONCLUSIONS: Despite the concentration obtained, there was no increase of bone growth by adding concentrated bone marrow. However, the number of stem cells in bone marrow was low and maybe a stronger concentration is needed to obtain a difference. The 3D reconstruction of the graft and the analysis of the graft's volume using a novel software was efficient according to the similarity of the graft's volume post-operatively in all patients.

[Correction of stiff thoracic idiopathic adult scoliosis. Prediction from the traction radiograph]. / Réduction des scolioses idiopathiques raides de l'adulte.

PURPOSE OF THE STUDY: The aim of this study was to determine the predictive value of the traction radiograph in adults with stiff curve (preoperative Cobb angle>60 degrees and reduction of less than 35% with traction) thoracic scoliosis. We wanted to compare this predictive value with that observed in reducible scoliosis. MATERIAL AND METHODS: A traction radiograph was obtained using a standard protocol with dynamometric control of the force applied. Patients with stiff scoliosis had 47 thoracic curves and 11 thoracolumbar curves (with primary anterior release for ten thoracic curves and eight thoracolumbar curves) and patients with reducible scoliosis had 56 thoracic curves. Cortre-Dubousset instrumentation was used for treatment in all patients. RESULTS: The postoperative Cobb angle for the stiff curves (without anterior release) was strongly correlated with the preoperative angle with traction (r=0.91; p<0.0001). The correlation between the postoperative Cobb angle and the preoperative Cobb angle without traction was less pronounced (r=0.86; p<0.0001). The traction radiographs were less predictive of the Cobb angle correction than the postoperative Cobb angle. The difference was 17.5+/-7 degrees , which corresponds to a supplementary gain in reduction after surgery. For the thoracic curves alone, the differences between the traction Cobb angle and the postoperative Cobb angle was 14.5 degrees for stiff curves and 6.5 degrees for reducible curves. Furthermore, the correlation between the Cobb angle with traction and the postoperative Cobb angle was stronger for stiff curve thoracic scoliosis (r=0.90) than reducible thoracic scoliosis (r=0.78). DISCUSSION AND CONCLUSION: The standard traction radiographs were highly predictive of postoperative reduction of stiff thoracic and thoracolumbar curves treated by segmental instrumentation. The postoperative result can thus be estimated with a margin of error of +/-7 degrees . For the stiff curves, the postoperative Cobb angle was 17.5 degrees on average less than predicted on the traction radiograph (on average 20% supplementary gain in reduction). This angle gain, which was greater for stiff than reducible curves, corresponds to the determining effect of release occurring with stiff curves. Finally, because of the stronger correlation between the traction Cobb angle and the postoperative Cobb angle for stiff curves, the predictive value of the traction radiograph is greater for stiff curves than for reducible curves. In conclusion, one of the contributions of the traction radiograph, which results from the predictability of the postoperative angle with a small margin of error, is to enable adequate prediction of the postoperative outcome for a given patient or a specific sub-group of patients, e.g. with or without anterior release.

Comparison between total disc replacement and hybrid construct at two lumbar levels with minimum follow-up of two years.

INTRODUCTION: Lower back pain due to degenerative disc disease is a therapeutic challenge in young patients. Although arthrodesis is currently the gold standard for surgical treatment, improvement in total disc replacement techniques makes it possible to preserve segmental mobility with good results in one-level surgery. Nevertheless, the French National Health Authority does not recommend total disc replacement for multilevel surgery. Thus, hybrid constructs that combine one-level disc replacement with arthrodesis have been developed for multilevel indications. HYPOTHESIS: The outcome of two-level lumbar disc arthroplasty does not differ from hybrid constructs. METHODS: The clinical and radiographic outcomes of disc arthroplasty were compared to hybrid constructs for two-level degenerative disc disease in 72 patients after a continuous follow-up of at least 2 years. The patients were divided into two groups that were similar for the indication and type of implants. RESULTS: There was no statistical difference in pain relief (-3.9 points versus -3.5 points for lumbar VAS) or reduction in ODI (-29.5% versus -27.0%) between TDR and hybrid constructs, respectively. There was no statistical difference in range of motion at the level of arthroplasty (8.4° versus 7.6°) and no kinematic dysfunction was identified. The re-operation rate at two years for persistent lumbar pain was respectively 6.7% for two-level disc arthroplasty and 4.3% for hybrid constructs. The complication rate was 4.8% and 8.7% respectively. DISCUSSION: No difference was found in this comparison of two homogeneous series between two-level disc arthroplasty and hybrid constructs for the treatment of degenerative disc disease after two years of follow-up. Two-level disc arthroplasty may be an alternative for young patients depending on an evaluation of long-term results. LEVEL OF EVIDENCE: Cohort observational study level III.

Does the type of sagittal spinal shape influence the clinical results of lumbar disc arthroplasty?

INTRODUCTION: It has been suggested that the indication for lumbar total disc replacement (LTDR) takes into account the local parameters, such as the type of disc disease demonstrated on MRI and the presence or absence of facet joint osteoarthritis. The type of preoperative sagittal curvature could also be taken into account. This study reports the clinical results of LTDRs depending on the type of sagittal spinal alignment. MATERIAL AND METHODS: Eighty patients were included in this prospective study, with a mean age of 41.7years (range, 27-56years). The clinical analysis took into account the lumbar VAS, the Oswestry Disability Index (ODI), and the preoperative frequency of painkiller use, at 1year and at the last follow-up. The satisfaction index, return to work, and willingness to undergo the same treatment were also collected. The radiological study included the analysis of lumbar-pelvic parameters to distribute the patients according to the Roussouly classification. RESULTS: The mean follow-up was 59.1months (range, 14-96months). The type 1 group included four cases. Reduction of the VAS, the ODI score, and the frequency of painkiller use at the last follow-up were significant in type 2 and 3 patients, and non-significant for type 4. Eighty-five percent of type 2 patients and 87.5% of type 3 patients were satisfied or very satisfied with the surgery versus only 68% of the type 4 patients. In addition, 63% of the type 4 patients declared they would be willing to undergo the same treatment again versus 85% of the type 2 patients and 82.5% of the type 3 patients. It should also be noted that 67% of the patients in this series returned to work. DISCUSSION AND CONCLUSION: This study underscores the influence of the type of sagittal curvature on the clinical results of LTDR, with type 4 patients showing inferior clinical results because of a higher rate of residual lower back pain. The indication in LTDR should be reconsidered for discogenic lower back pain in type 4 patients.

Intraoperative determination of lumbar prosthesis endplate lordotic angulation to improve motion.

The aim of total disc replacement (TDR) is to restore and maintain closer-to-physiology motion. Therefore, the factors that influence postoperative intervertebral motion have to be controlled. Factors such as disc height (DH), postoperative segmental lordosis (SL), implant design and positioning are still recognized to be influent. Otherwise, range of motion (ROM) distribution, between flexion and extension, appear to be influenced by obtaining parallel bearing surfaces, which depends on prosthesis endplate lordotic angulation. To assess in vivo the correlation between an intraoperative parameter (intraoperative segmental lordosis: ISL) and a postoperative parameter (postoperative segmental lordosis: PSL). To determine the advantage of ISL measurement on the improvement of the prosthetic endplate lordotic angulation choice. Radiological comparison between intraoperative and postoperative segmental parameters. Fifty-seven patients who received a TDR at one level, L4-L5 or L5-S1, with different prosthetic endplate lordotic angulations (0°, 5°, and 10°). Twenty-one consecutive patients underwent intraoperative measurement (ISL) on a lateral view, with a spacer at the mid-vertebral bony endplates (Group 1). ISL was correlated using a linear correlation test with PSL. Group 1 postoperative prosthesis endplate lordosis (PEL: angle between the bearing surfaces) were compared to those of 46 patients without intraoperative measurement (Group 2). The mean ISL and PSL angles were 12.2° (7-21°) and 13.9° (8-23°), respectively. We observed a strong linear correlation between ISL and PSL (r=0.78, P <0.006). In Group 1, PEL varied between -1° and 11°, and between -3.7° and 17.8° in Group 2. For 80% of the patients in Group 1, the PEL was less than 5°, versus 33% of the patients in Group 2. Only prostheses with PEL less than 5° had a preserved extension curve in ROM distribution (+3°). Intraoperative measurement of ISL has emerged as a key factor in predicting PSL in TDR. The percentage of parallel bearing surfaces was increased by a prosthesis endplate lordotic angulation choice guided by ISL measurement. This study confirmed the advantage of choosing the adequate lordotic angulation of the prosthesis endplate to restore a physiological motion distribution between flexion and extension.

Interpretation and utility of traction radiography in scoliosis surgery. Analysis of patients treated with Cotrel-Dubousset instrumentation.

STUDY DESIGN: An analysis of a standardized method of traction radiography for the evaluation of reducibility of scoliosis. OBJECTIVES: To determine whether and how preoperative fraction radiography can provide objective information and to compare traction radiography with supine side-bending radiography. SUMMARY OF BACKGROUND DATA: Flexibility of scoliosis deformity remains an arbitrary concept. No objective method of preoperative evaluation of reducibility has been established. METHODS: The utility of a standardized method of traction radiography was evaluated in 74 patients with idiopathic scoliosis who were aged 14-22 years and treated with Cotrel-Dubousset instrumentation. RESULTS: In thoracic curves, the postoperative Cobb angle was highly correlated with the preoperative Cobb angle in traction (r = 0.82). However, such correlation was much lower with lumbar curves (r = 0.54). The reducibility of the thoracic curve by traction as expressed by the ratio to the original curve was dependent on the magnitude of the original curve (P = 0.005), and this parameter proved less informative than the absolute angle values. Time-related analysis of 30 patients who were observed for more than 5 years revealed that the high correlation between the preoperative angle of thoracic curves in traction and their postoperative angle decreased with the follow-up time (r = 0.80-0.65). A comparison of traction radiography and supine side-bending radiography showed that these two tests were practically equivalent in terms of evaluating the reducibility of curves. CONCLUSION: The results provide an objective interpretation of traction radiographs for scoliosis.

Changes in the unfused lumbar spine in patients with idiopathic scoliosis. A 5- to 9-year assessment after cotrel-dubousset instrumentation.

STUDY DESIGN: Postoperative changes in the lumbar spine were studied retrospectively in patients with adolescent idiopathic scoliosis who had been treated with Cotrel-Dubousset instrumentation. OBJECTIVE: To examine middle-term changes in the unfused lumbar segments below an instrumented scoliosis fusion. SUMMARY OF BACKGROUND DATA: Scoliosis fusion by the Harrington method is known to be associated with a flat back in the fused area and subsequent degenerative changes in the segments below the fusion. No data have yet been published concerning a segmental instrumentation system. PATIENTS AND METHODS: Thirty patients with idiopathic scoliosis, between the ages of 14 and 22 years at the time of surgery, were observed for 5-9 years after surgery. Activity, pain, complications, and 21 radiographic parameters were assessed. RESULTS: The prevalence of low back pain increased from 3% before surgery to 20% at the final follow-up visit, although in none of the patients was the pain so severe that specific treatment was required. Radiographically, uninstrumented lumbar segments generally were realigned successfully in the frontal plane. Analyses in the sagittal plane revealed tendencies to a gradual increase in lumbar lordosis, anterior-upward tilting of the lowest instrumented vertebra, and posterior shift of the sagittal spinal balance. During the follow-up period, seven patients (23%) developed degenerative changes, including mild junctional kyphosis, retrolisthesis, narrowing of disc spaces, or osteophytes. CONCLUSION: Whereas the overall clinical and radiographic results of surgery were satisfactory, the unfused lumbar segments required careful surveillance, especially in the sagittal plane.

Intraspinal metallosis causing delayed neurologic symptoms after spinal instrumentation surgery.

STUDY DESIGN: Two cases of intraspinal metallosis causing delayed neurologic symptoms secondary to spinal instrumentation surgery are reported. OBJECTIVE: To present an unusual delayed neurologic complication after spinal instrumentation surgery. SUMMARY OF BACKGROUND DATA: Metal-related complications caused by orthopedic implants have long been a concern in the field of arthroplasty or internal fixation of fractures, but no such complications have been reported for spinal instrumentation. METHODS: Retrospective case report of two patients with degenerative scoliosis who presented with delayed neurologic symptoms months to years after uneventful, but without secondary degenerative changes or dislodgement of the implants. RESULTS: In both reported cases, a granulation-tissue mass characterized by marked metallosis had been formed in the spinal canal adjacent to a loosened laminar hook. CONCLUSIONS: Intraspinal metallosis should be kept in mind as a rare cause of delayed neurologic symptoms after spinal instrumentation surgery. With the metal implants in place, myelography was the sole informative examination for diagnosis.

A synthetic porous ceramic as a bone graft substitute in the surgical management of scoliosis: a prospective, randomized study.

STUDY DESIGN: A prospective randomized study. OBJECTIVES: To assess the clinical and radiologic performances of a synthetic ceramic as a bone graft substitute in scoliosis surgery. SUMMARY OF BACKGROUND DATA: Surgery on the skeleton frequently requires harvesting of autogenous bone grafts from the pelvis, but this procedure often is complicated by problems. METHODS: Fifty-eight patients with idiopathic scoliosis, ages 13 to 25 years, were treated by posterior correction and arthrodesis using Cotrel-Dubousset instrumentation. Posterior spinal fusion was performed using local bone grafts combined with autogenous iliac bone grafts in 30 patients, and combined with porous biphasic calcium phosphate ceramic blocks comprising hydroxyapatite and tricalcium phosphate in another 28 patients. The patients were observed for a minimum of 24 months after surgery, with a mean postoperative observation time of 48 months. The results were assessed clinically and radiographically. RESULTS: Patients in the ceramic group had a lower average blood loss than those in the iliac graft group. They also were free from postoperative local complications in the iliac region, which were experienced by a significantly high proportion of patients belonging to the iliac graft group. Radiography demonstrated successful incorporation of the ceramic blocks within 12 months. The correction of the deformity was maintained similarly and satisfactorily in both groups. CONCLUSIONS: These results justify and favor the use of calcium phosphate ceramics as bone graft substitutes for instrumented posterior spinal fusion in teenagers and young adults. Potentially hazardous harvesting of pelvic bone is no longer necessary for such operations.

Influence of local environment on incorporation of ceramic for lumbar fusion. Comparison of laminar and intertransverse sites in a canine model.

OBJECTIVES: To evaluate bone growth into macroporous ceramic in a canine model in terms of the effect at the lumbar spine site (lamina versus transverse process site) and the depth of the area within the ceramic block (peripheral or central areas). SUMMARY OF BACKGROUND DATA: Previous comparative studies have assessed that the efficacy of bone graft substitutes for spine fusion depends on their physicochemical properties and on the mechanical environment, but rarely on the grafting site at the lumbar spine level. METHODS: Posterior and lateral arthrodesis using pedicular instrumentation was performed at L2, L3, and L4 with a parallelepipedic ceramic block in an experimental group of dogs. A second group of dogs was fused with only autogenous bone graft to compare the fusion stiffness obtained with this material with the stiffness obtained with ceramic. Dogs were studied for 9 months. A biomechanical test and histomorphometric analysis were conducted. RESULTS: With the biomechanical test, no significant differences were found between ceramic and autogenous bone. The percentage of newly formed bone was higher (P < 0.0001) at the lamina (26.52 +/- 6.45%) than at the transverse process site (17.33 +/- 2.54%). For both locations, the highest amount of newly formed bone was observed in the area of close contact between ceramic and bone, and the lowest was observed in central areas (24.6 +/- 5.9% for the laminar site, 14.79 +/- 1.75% for the transverse process site). CONCLUSION: This animal study, which replicated the human procedure in posterolateral lumbar fusion, showed a significant difference of ceramic incorporation between laminar and intertransverse sites. This histomorphometric analysis also confirmed the relationship between bone in-growth and ceramic thickness and ceramic contact area with bone.

Successful monitoring of neurogenic mixed evoked potentials elicited by anterior spinal cord stimulation through thoracoscopy during spine surgery.

STUDY DESIGN: Neurogenic mixed evoked potentials were recorded after thoracoscopic spinal cord stimulation in patients undergoing video-assisted spine surgery. OBJECTIVE: To demonstrate the feasibility and value of thoracoscopic spinal cord monitoring. SUMMARY OF BACKGROUND DATA: Video-assisted thoracic surgery recently has been proposed as a new technique for thoracic spine surgery. It can be used for anterior spinal release of patients with severe spinal deformities and for thoracic hernia removal. METHODS: Five patients undergoing video-assisted thoracic surgery for spinal fusion were studied. Neurogenic mixed evoked potentials were elicited by electrodes seated into intervertebral discs through thoracoscopy and recorded from peripheral nerves of the lower limbs. Moreover, the study included the case of a patient with a thoracic hernia who underwent video-assisted thoracic surgery with combined thoracoscopic neurogenic mixed evoked potential and standard somatosensory evoked potential monitoring. RESULTS: Neurogenic mixed evoked potentials were recorded consistently after spinal cord stimulation in all patients. For the patient with a thoracic hernia, neurogenic mixed evoked potentials suddenly disappeared, whereas somatosensory evoked potentials were not significantly modified, leading to surgery interruption. Neurogenic mixed evoked potentials progressively reappeared after a 30-minute delay. Postoperation examination revealed a Brown-Sequard's syndrome with incomplete right motor deficit. CONCLUSIONS: Neurogenic mixed evoked potentials evoked by anterior stimulation through thoracoscopy are of interest for spinal cord monitoring when posterior electrical stimulation is impossible, and they provide reliable information regarding spinal motor pathways.

Histological features of large bone allografts.

We performed biopsies during reoperation for minor complications in two active young patients 9 and 19 months after massive bone allograft implantation for bone tumour. The grafts were dead and resorption-apposition activity, when present, was predominantly in subperiosteal areas. Inflammatory infiltration was very seldom found. Features considered as 'microfractures' or 'microcracks' were noted in the cortical ring together with the formation of woven bone, in areas with remodelling. Such cracks are likely to be of mechanical origin and do not inevitably lead to complications.

Efficacy of nerve root versus interspinous injections of glucocorticoids in the treatment of disk-related sciatica. A pilot, prospective, randomized, double-blind study.

STUDY OBJECTIVES: Pilot study comparing the short-term efficacy on pain and functional impairment of nerve root sheath versus interspinous glucocorticoid injections in patients admitted to a French rheumatology department for disk-related sciatica or femoral neuralgia. PATIENTS AND METHODS: Thirty patients with refractory nerve root pain (sciatica, n = 29; femoral neuralgia, n = 1) for a mean of four months were randomized to nerve root injection (n = 17) or interspinous injection (n = 13) of the same mixture of 0.10 g of lidocaine hydrochloride and 3.75 mg of cortivazol. Both injection methods were performed under analgesia and benzodiazepine sedation to maintain double blinding. Each patient was evaluated daily during the first seven days of bed rest in the hospital, then after discharge on postinjection day 28. RESULTS: Prompt pain relief was obtained in both groups. On day 1, the mean pain scale score (0-100) fell from 70 +/- 3.9 to 26 +/- 5.6 in the nerve root group and from 63 +/- 4 to 23 +/- 4.7 in the interspinous group. These results were sustained on D7 and D28. CONCLUSIONS: The unusually high level of efficacy of glucocorticoid injection in our study may be ascribable in part to strong placebo and Hawthorne effects and in part to the intrinsic effects of the injections. Whether nerve root injection is superior over interspinous injection remains unproven.

[Magnetic resonance imaging for lumbar disk pathology. incidence of false negatives]. / Imagerie par résonance magnétique pour pathologie discale lombaire. Fréquence des faux-négatifs.

Magnetic resonance imaging (MRI) has had an impressive impact on evaluation of degenerative diseases of the spine. Nevertheless, false negatives can occur on images involving lumbar discs. Degenerative disc diseases documented on discrography and/or pathology examination of the discs can go unrecognized. Likewise sensitivity for the detection of protruding discal hernias is not totally satisfactory (20% false negatives). Finally, a magnetic resonance image visualizing displacement of the disc is not specific (10 to 15% false positives); images showing protrusion or hernia can be seen in 30% of asymptomatic patients. Although MRI gives slightly more information than other imaging techniques, false images do exist. Moreover, the usefulness of MRI to demonstrate disc disease in case of a negative CT-scan remains to be demonstrated.

[Extensometry and primary anchorage of femur implants. Study of the upper metaphyseal intracortical support of the B.P.R cement-less implant]. / Extensométrie et ancrage primaire d'implants fémoraux. Etude de l'appui endocortical métaphysaire supérieur de l'implant sans ciment B.P.R.

This study uses extensometry to compare the distribution of strain on a fresh femur before and after implantation of various titanium prostheses: one is a cementless implant with metaphyseal endosteal support; the second is a cemented prosthesis with and without calcar collar contact; the last is a titanium implant with fixation by screens. The precision of the measurements have been improved particularly in the proximal metaphyseal area using bidirectional gauges. The system of loading permits comparison of the different implants and the results obtained with the B.P.R. prosthesis compared with the cemented implant without calcar contact are very close. The effect of the collar appears very limited despite the optimal conditions of the in vivo implantation that improve the calcar-collar contact. The screw implant increases the stress shielding of the proximal area of the femur. The different steps of the experiment illustrate the strain distribution in relation to the implantation of the devices and the contact bone prosthesis. The significant endosteal fixation of the B.P.R. prosthesis in the proximal metaphyseal area allows a better primary anchorage which increases distribution of the stress and therefore results in better secondary fixation by bony ingrowth.

[Bone anchorage and surface condition of the implant. Validity of extraction tests]. / Ancrage osseux et état de surface des implants. Validité des tests d'extraction.

The mechanical strength of the bone-implant interface depends on the morphology and the composition of the implant surface. The great variety of coating materials as well as the condition of the surfaces to be covered, makes a comparative and preclinical evaluation of the different materials for prostheses necessary. The results, the validity and the limits of the extraction tests are discussed in this article.

[Neurogenic mixed evoked potential monitoring during scoliosis surgery: retrospective analysis of 149 cases]. / Utilisation des potentiels évoqués mixtes neurogènes durant la chirurgie des scolioses: analyse rétrospective à propos de 149 cas.

INTRODUCTION: We report a retrospective analysis of spinal cord monitoring with neurogenic mixed evoked potentials (NMEPs) combined with somatosensory evoked potentials (SSEPs) in 149 patients undergoing surgery for spinal deformity. MATERIAL AND METHODS: 149 patients (104 females and 45 males), mean age 28 yrs (13-72 yrs) were studied. NMEPs were elicited by electrical spinal cord stimulation in the rostral part of the surgical field, via two needle electrodes set in the epidural space and in the interspinous ligament above. They were recorded from the sciatic nerve at the knee and the sural nerve at the ankle. SSEPs were recorded from the scalp after stimulation of the posterior tibial nerve at the ankle. A decrease in amplitude of more than 50 p. 100 and/or an increase in latency of more than 10 p. 100 were defined as significant warning criteria. RESULTS: No false-negative result was observed. NMEP modifications did not reach critical value in 143 cases. In 6 cases, significant changes were observed. Moving the stimulation electrodes along the spinal cord allowed spinal lesion localization and helped the surgeon to perform the adapted maneuver, clearly avoiding the occurrence of postoperative neurological defect in 5 of the 6 cases. CONCLUSION: NMEP monitoring is a sensitive and specific method useful for detecting an impending lesion of the spinal cord. NMEPs are also helpful in localizing the spinal level of the lesion. They represent a primary choice tool for neuromonitoring during scoliosis surgery.

[Dual-energy X-ray absorptiometry: value in orthopedics]. / L'absorptiométrie biphotonique à rayons: intérêt en orthopédie.

We emphasize the opportunity of an in vivo bone mass measurement with an easy and accurate technique for orthopedic practice. At the present time, Dual Energy X Ray Absorptiometry (DEXA) is the most used technique, and is a safe and short examination. It can assess the quantity of mineral of any region of the body with a remarkable reproducibility (1 to 3 per cent). New machines are improved, and they permit many practical applications beyond the osteoporosis field. Thus, in orthopedics, we can distinguish several interesting topics. Peripheral risk of fracture can be evaluated because of good correlation between bone mineral content and biomechanical properties of bone. Even if a peripheral fracture occurs after a fall, low bone mineral density plays an important role, as in the case of femoral neck fractures in elderly patients. In traumatological practice, a DEXA with a specialized advice has to be requested if the traumatism cannot fully explain the occurrence of the peripheral fracture. Low bone mineral density defines an osteoporotic state, with the possibility of selecting adequate therapy. The good reproducibility of the measurement allows early estimation of bone loss following a period of immobilization. Varying models of osteosynthesis can be compared in vivo, to evaluate a decrease of "stress shielding" bone resorption. The role of stiffness of an implant on regional bone mineral content can be assessed. Likewise, periprosthetic bone mineral content can be measured in various regions, and followed over time. Specific software allows the exclusion of the region where the metallic prosthesis is projected. The reproducibility of this peripheral bone mineral content is 2 to 3 per cent, which individually allows an estimation of variations of more than 5 per cent. It will be possible to evaluate in vivo the influence of various parameters of the prosthesis on bone mineral content in controlled studies, such as the role of the shape, the position, the structure, the coating. Mineral content of biomaterials and bone grafts are taken into account. Focusing the X Ray beam allows ultrahigh resolution. Precise measurements of very small parts of bone such as rodent tibia or vertebra are possible. The good reproducibility (2 per cent) authorizes the evaluation of various parameters which modify bone remodeling, such as immobilization or activity, ovariectomy. Preventive or curative therapeutics which change bone mass can be evaluated in animal pre clinical studies. There are other methods of measurement of bone mineral content. Digitalization of radiographs is not sufficiently accurate and CT Scan generate high levels of radiation. The DEXA is actually the best compromise for an accurate and reproducible measurement of the bone mineral content in vivo. This method will certainly be an important tool in orthopedics for several clinical or animal investigations in the future.

[Filling of bone defects using biphasic macroporous calcium phosphate ceramic. Apropos of 23 cases]. / Comblements osseux par céramique phosphocalcique biphasée macroporeuse. A propos de 23 cas.

PURPOSE OF THE STUDY: The authors report their experience with the use of a biphasic macroporous calcium phosphate bone substitute. MATERIALS AND METHODS: In 23 cases (22 patients) a biphasic macroporous calcium phosphate ceramic was used to fill a pathological bone defect. The ceramic used in this study was a macroporous (400 to 600 mu) component consisting of 60 per cent hydroxyapatite and 40 per cent beta-tricalcium phosphate. It was in the form of granules (2 to 3 mm), sticks (20 x 5 x 5 or 10 x 5 x 5 mm) or custom made blocks. In 6 cases, the ceramic was used alone; in 12 cases with autologous bone marrow and in 5 cases with autologous cancellous bone grafts. In 14 cases, the bone defect was due to conservative treatment of a benign tumor, in 3 cases due to aseptic post-traumatic non union, in 3 cases due to wide resection for malignant tumors of the pelvis and in 3 cases following osteotomy. Post operative assessment was made from clinical, radiographic and histological findings. RESULTS: 2 patients died 6 and 8 months post operatively and 2 were lost to follow up at 2 and 5 months with both having good clinical and radiographic results when last seen. For the remaining 19 cases, the average follow-up was 20 months (from 6 to 62 months). No local, regional or general deleterious effects were noted. Radiologically the bone ceramic junction healed in all cases except 2 within 3 months. In these last two cases, healing required 6 and 7 months. No radiolucent line appeared around the ceramic. No stress fractures occurred in the substitute. Histologically, 3 biopsies showed new bone formation throughout the ceramic with apposition of a well differentiated lamellar bone directly apposed to the ceramic. DISCUSSION: Animal experimentations have proven the interest of similar ceramics: macroporosity enhances bone rehabilitation and the biphasic characteristics associate the advantages of slow resorption of hydroxyapatite and more easily resorbed beta-calcium phosphate. No deleterious clinical, radiographical or histological effects were observed, confirming the biocompatibility of this substitute. Despite the poor mechanical properties of this macroporous ceramic before implantation, good clinical and radiographic results suggest improvement of these properties in the composite new formed bone-ceramic after implantation. CONCLUSION: We believe that macroporous biphasic ceramic is a good substitute for use in bone defects when good primary mechanical stability and contact with the host bone are present. Further clinical and experimental studies are necessary to determine the limits of such a substitute in terms of volume and to control its mechanical properties following implantation.

[In vitro assessment of combining osteogenic cells with macroporous calcium-phosphate ceramics]. / Etude in vitro de l'association de cellules ostéogènes avec une céramique en phosphate de calcium macroporeuse.

PURPOSE OF THE STUDY: Bone grafts or bone substitutes are required to fill bone defects resulting from trauma or surgical resection of tumors. Calcium-phosphate ceramics are synthetic bone substitutes which promote new bone formation by osteoconduction. These ceramics possess osteoconductive properties but have no intrinsic osteoinductive capacity. They are unable to induce new bone formation in extraossesous sites. One solution to develop bone substitutes with osteogenic properties would be to associate biomaterials with osteoprogenitors. MATERIALS AND METHODS: We studied the in vitro osteogenic potential of human bone-marrow cells cultured on macroporous calcium phosphate (CaP) ceramic, examining stromal cell proliferation and differentiation. Osteogenic differentiation was evaluated in terms of alkaline phosphatase activity and immunological characterization of the extracellular fibrillar matrix formed by these cells. The specimens were examined by scanning and transmission electron microscopy. RESULTS: Human bone-marrow cells proliferated on CaP ceramic. The proliferating bone-marrow cells expressed an osteoblastic phenotype as shown by alkaline phosphatase activity and synthesis in ceramic pores of an extracellular matrix composed of fibronectin, osteocalcin and collagen I. In addition, numerous microcrystals of apatite precipitated on the fibrillar matrix, producing a mineralized fibrillar network within the ceramic. CONCLUSION: This study demonstrates that human bone-marrow cells cultured on macroporous CaP ceramic do not lose their osteoblastic phenotype even after 21 days of culture, and that they can induce osteogenesis in a CaP ceramic in vitro. This type of new "hybrid material" appears promising for the future.