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P12 Effects of methylprednisolone and erythropoietin on experimental spinal cord injuries Author(s): Abdurrahman ÇETIN, Kemal NAS, Cahfer GÜLOGLU, Hüseyin BÜYÜKBAYRAM, Adnan CEVIZ Name of ISCoS Member (Author): Kemal NAS Main institution where the work was done: Dicle University, School of Medicine Objectives: to evaluate the effect of methylprednisolone (MPD) and recombinant human erythropoietin (rHu-EPO) on degree of neurological improvement by using a neurological function test and histopathological examination in spinal cord injured rats. Methods: Experimental study was designed to evaluate acute beneficial effects on behavioral (motor) assessments by the systemic administration of rHu-EPO (1000 unit./kg, i.p.) and MPD (30 mg/kg i.p.) in the setting of traumatic spinal cord injury (TSCI). The damaged spinal cord was also evaluated histopathologically. Results: Significant differences were found in neurological function scores between control groups and MPD and rHu-EPO 1000 u and rHu-EPO 1000 u + MPD groups (p<0.001). There was also statistically significant difference between MDP and rHu-EPO 1000 u + MPD groups (p<0.01). Histopathological findings of severe ishcemia were found in control group. There was significant decrease in ischemic injury in rHu-EPO 1000 u and rHu-EPO 1000 u + MPD group compared to the control group (p<0.001). Conclusions: Significant improvements were found by using RHu-EPO 1000 ünite + MPD in neurological function deficits and histopathological findings of spinal cord injuries. P13 The effects of systemically administered of methylprednisolone and recombinant human erythropoietin in rats after spinal cord ischemic injury Author(s): Kemal NAS, Abdurrahman ÇETIN, Hüseyin BÜYÜKBAYRAM, Adnan CEVIZ Name of ISCoS Member (Author): Kemal NAS Main institution where the work was done: Dicle University, School of Medicine Objective: To evaluate whether recombinant human erythropoetin (rHu-EPO) and methylprednisolone (MPD) improves neurological function and histopathological outcome if systemically administered after traumatic spinal cord injury. Methods: Animals constituted a moderate compression of 0.6 N which was produced by application of an aneurysm clip at level T3 for 1 minute. RHu-EPO (1000 and 3000 units per kg of body weight i.p.) and MPD (30 mg/kg) administered 5 minutes after trauma. Results: Statistically significant improvements between the control group and the groups that taken medical treatment have been observed according to the neurological function test scores (p<0.001). When rHu-EPO 3000 units group and rHu-EPO 3000 units + MPD group were compared with each other, the difference was statistically significant (p<0.029). In the control group, histopathologically severe ischemic findings have been observed. A significant decrease in ischemic damage has been detected when MPD + rHu-EPO 3000 units group was compared with the control group (p<0.001). Conclusions: There has been most significant neurological functional and histophatological improvements after systematical administration of rHu-EPO 1000 units and/or MPD and MPD + rHu-EPO 3000 units in the spinal cord injury. Furthermore, the MPD + rHu-EPO 3000 units group provides early neurological function and histopathological recovery. P14 Critical evulation of the modern guidelines for spinal tauma management. Author(s): Pentelényi T., Zsolczai S., Klauber A. Name of ISCoS Member (Author): Pentelényi T., Zsolczai S., Klauber A. Main institution where the work was done: National Institute of Traumatology, Department of Neurosurgery, Budapest , Hungary This is a keynote lecture on up-to-date treatment of severe spinal injuries in the mirror of the latest evidence-based guidelines for spinal trauma management. There are no standards, no guidelines, all modalities are options. We have chosen among them those options by which proper modern treatment-strategy can be constructed. Severe spinal trauma cases must be operated on in 60-80 %. There are emergency, absolute and relative indications for surgery. Emergency operations and neuroprotective treatment must be started in 6-8 hours. Local treatment includes reduction, decompression and stabilization. Their conservative and operative methods as up-to-date options are skeletal traction , halo fixation, odontoid screw fixation, C 1-2 transarticular screw fixation, ventral spondylodesis with plate or cage implants, rarely posterior softwire or long rod fixations in the cervical spine, and transpedicle screw, plate or rod fixation, ventral plate and cage fixation or combined posterior-anterior dynamical long rod stabilization with ventral butressing in the Th-L spine. Titanium implants and dynamical stabilization are preferred. Long lasting neurorehabilitation is compulsory. Surgical decompression must be done always from the side where compression occurs. Conclusion: 1. In spinal trauma all treatment modalities are only options. 2. Neurological improvement after surgery must be at least as good or even better then that after conservative treatment. 3. If surgical decompression is indicated it has to be performed among all conditions on the contrary that no proving prospective randomized clinical trial is available for its statistical effectivity! P15 A New Idea for less Invasive Stabilisation in Spinal cord injury Patients Author(s): Röhl Klaus, Weidt Friedrich, Mall Volker (Halle) Name of ISCoS Member (Author): Röhl, Klaus Main institution where the work was done: Centre for Spinal Injuries and Spinal Trauma / Trauma Centre Berufsgenossenschaftliche Unfallklinik „Bergmannstrost“ Aim: One of the questions we have is the using of the optimesh system comfortable for patient and orthopaedic surgeon and we need some information about the fusion rate in using in 3 cases: osteoporotic burst fractures, intervertebral fusion in cases of spondylolisthesis and A-B types of fractures. Material & methods: Optimesh is a three dimensional knittered system with a polymeric mesh, designed to contain and reinforce bone graft and bone graft substitute materials at an osseous implant. The implantation instrument is designed with a diameter of 6 mm allowed through a small portal a implant a large, expandable mesh in a collapse state to improve stability immediately post op. In this cases of treatment we look for the outcome using a VAS scale prae and post op and the kyphosis angle after 3 month. 12 patients was undergoing this new method with filling the optimesh with allograft granular materials. There are no non fusion and no infect situation after using optimesh. In using the VAS scale there is a increase from 8,7 (prae) to 4,3 (post) operative. Conclusion: The optimesh system is a new alternative for the inter and intrabody fusion of thoracic and lumbar spine using the advantages of granular materials and improve immediately stability post op. P16 The influence of factors associated with deterioration of respiratory function in the Acute Cervical Spinal Cord Injured patients, requiring early intervention Author(s): Dr Juliette M Stander Name of ISCoS Member (Author): Dr Juliette M Stander Main institution where the work was done: Groote Schuur Hospital OBJECTIVES To determine the influence of factors associated with deterioration of respiratory function in the Acute Cervical Spinal Cord Injured patients, requiring various types of early respiratory support and intervention. DESIGN The study comprises Acute Cervical Spinal Cord Injured patients admitted to the ICU requiring early respiratory support and intervention. The following factors were recorded: neurological diagnosis, mode of injury, delay in admission, smoking history, underlying lung pathology, aspiration, distended abdomen, period of inotropic support, timing of surgery, period of non invasive ventilatory support, period of ventilatory support, lung collapse, etc. SETTING Acute Spinal Cord Injury UnitGroote Schuur HospitalSouth Africa SUBJECTS 50 Acute Cervical Spinal Cord Injured patients admitted to the ASCI Unit, Groote Schuur Hospital P17 Five years of experience in the treatment of spasticity in spinal cord injuries with intrathecal baclofen Author(s): Klaus Röhl, Thomas Richter, Volker Mall Name of ISCoS Member (Author): Röhl, Klaus Main institution where the work was done: Centre for Spinal Injuries and Spinal Trauma / Trauma Centre Berufsgenossenschaftliche Unfallklinik „Bergmannstrost“ Aim: In this retrospective study we wanted to evaluated the functional benefit of spaticity before and after continous intrathecal baclofen infusion via a subcutaneously implanted pump. Objektives: To evaluate the effect of continous intrathecal baclofen infusion via a subcutaneously implanted pumps on spasticity of spinal cord injured patients. Settings: Center of spinal cord injuries and clinic for orthopaedic surgery Bergmannstrost Halle Germany. Method: 33 patients resistant to oral medication an with implanted baclofen pump were retrospectively, by phonecall or through examination during the pump refillment, graded using the Ashworth scale. Spasticity of the lower extremities was scored according to the Ashworth Scale. Results: In the patients Ashworth values after pump implantation were significantly lower than before (Wilcoxon`s test: p<0.001). Conclusion: Continuous intrathecal baclofen infusion via a subcutaneously implanted programmable pump significantly reduces spasticity of lower extremities
A handout will be provided with an up-to-date reference list and links to high-quality downloadable educational material. Sample references and links are provided here:
(Another abstract describes a parallel project (Belanger et al) presenting on a CD and web-downloadable resource this information and relevant procedures.) P19 Complications in Early Rehabilitation Period of Patients with Spinal Cord Injuries Author(s): Aleksandras Krisciunas, Tomas Morkevicius Main institution where the work was done: Department of Rehabilitation, Kaunas University of Medicine Aim. To determine most often occurring complications during early rehabilitation period in patients with spinal cord injuries. Method and Material. The study was based on analysis of medical documents of the patients with spinal cord injuries hospitalized in the Subdivision of Neurorehabilitation, Kaunas University of Medicine. The total number of the studied cases was 114: 78 men (68.4 %) and 36 women (31.6 %) at the age from 14 to 94 years (average age, 14 years). Results: There were 36 cases (31.6 %) with spinal cord injury at the level of cervical segments; 37 (32.4 %), at the level of thoracic segments; 40 (35.1 %), at the level of lumbar segments; and 1 (0.9 %), at the level of the sacrum. The most often documented complications were as follows: pains, 85 (74.6 %) cases; uroinfection, 51(44.7 %); spasticity, 36 (31.6 %); mental and psychosomatic problems, 25 (21.9%); decubitus ulcers, 20 (17.5 %). Conclusion. The most often occurring complications during early rehabilitation period, which can influence the duration and efficacy of rehabilitation, are pains, uroinfection, and spasticity. P20 INCOMPLETE SPINAL CORD INJURIES: SOME DATA AND CONSIDERATIONS ON WALKING RECOVERY C. Pistarini, A. Caroli, G. Bertotti, S. Eretti, G.Robbiani Recovery
of the ability to walk after a spinal cord injury, particularly one
that is incomplete, is one of the primary aims of rehabilitation treatment,
even if it is a functional goal that can only be reached in some cases
because of the complexity of the neuromotor skills required. |
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