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1.
J Burn Care Res ; 28(6): 905-8, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17925658

RESUMO

High voltage electrical injuries usually cause devastating consequences for patients, most of which result in permanent disability. Spinal cord injury (SCI) caused by high voltage electrical injury is uncommon in the literature. We present a 29-year-old male patient who was diagnosed as having delayed SCI after high voltage electrical injury. The patient developed muscle weakness in the lower extremities with the loss of pinprick sensation below the fifth cervical spinal segment, 2 days after the high voltage electrical injury. Magnetic resonance imaging of the brain, cervical and thoracic spine was normal. Nerve conduction and needle electromyography studies were normal, except for bilateral tibial and left median somatosensory-evoked potentials. The findings on initial examination and neurophysical investigation showed incomplete cervical SCI at the C5 level. He was able to walk with a pair of canes and bilateral ankle-foot orthosis at the end of the 2-month rehabilitation. Follow-up physical and electrophysiological examination of the patient 15 months after injury showed further improvement. The patient was able to walk with a pair of canes without orthoses. Electrophysiological studies are useful instruments in the diagnosis and follow-up of these patients. Early rehabilitation is essential to obtain a favorable outcome in patients with SCI caused by high voltage electrical injury.


Assuntos
Queimaduras por Corrente Elétrica/complicações , Vértebras Cervicais/lesões , Traumatismos da Medula Espinal/etiologia , Adulto , Vértebras Cervicais/fisiopatologia , Potenciais Somatossensoriais Evocados/fisiologia , Humanos , Masculino , Traumatismos da Medula Espinal/fisiopatologia , Traumatismos da Medula Espinal/reabilitação , Fatores de Tempo
2.
Immunol Lett ; 111(2): 84-91, 2007 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-17618693

RESUMO

Humanized antibody-based treatment modalities represent an active area of investigation. Included in these strategies are passive administrations of monoclonal antibodies, which recognize tumor necrosis factor alpha (TNF-alpha). However, several problems associated with these types of treatment strategies have been reported in the literature. We attempted to address the issue related to unresponsiveness to infliximab that might be induced by anti-idiotype response to the passively administered humanized monoclonal antibody. The characteristics and functional importance of antibodies to infliximab (ATI) were investigated in human sera. We studied the binding characteristics of ATI to infliximab, TNF-alpha Receptor-I (RI, p55) and Receptor-II (RII, p75). In addition, cytotoxicity effect on L929 cells and blocking effects on the binding of TNF-alpha with infliximab and etanercept were also analyzed. On the basis of the results obtained from the experiments, it seems that the target epitope for ATI is related with somewhere else not residing in the region capable of generating "mirror image". The results presented indicate that ATI does not mimic the functional characteristics of TNF-alpha. However, ATI inhibited the binding properties of infliximab to TNF-alpha.


Assuntos
Anticorpos Anti-Idiotípicos/imunologia , Anticorpos Monoclonais/imunologia , Artrite Reumatoide/tratamento farmacológico , Fator de Necrose Tumoral alfa/imunologia , Animais , Anticorpos Anti-Idiotípicos/metabolismo , Anticorpos Monoclonais/metabolismo , Anticorpos Monoclonais/uso terapêutico , Antirreumáticos/imunologia , Antirreumáticos/metabolismo , Humanos , Imunização Passiva , Infliximab , Camundongos , Fator de Necrose Tumoral alfa/metabolismo
3.
Disabil Rehabil ; 29(16): 1271-9, 2007 Aug 30.
Artigo em Inglês | MEDLINE | ID: mdl-17654002

RESUMO

PURPOSE: To investigate the validity and reliability of the Turkish translation of the original Pediatric Evaluation of Disability Inventory (PEDI). METHOD: On May 2003, we received permission from Boston University to translate and use the PEDI for Research purposes. PEDI Functional Skills scale and Caregiver Assistance scale was administered by physiatrists to 573 healthy Turkish children (295 males and 278 females; the age range: 7 months to 7(1/2) years) in two different healthcare centres in Ankara. The Turkish translation of the PEDI was again administered to 102 children after five days in order to assess test-retest reliability. Intraclass correlation coefficients (ICC) and Cronbach's alphas (alpha) were calculated. The test-retest reliability was assessed by Spearman's correlation coefficient. Internal construct validity was assessed by using Rasch unidimensional measurement model. RESULTS: High Cronbach's alpha coefficients (> or =0.98), high ICC values (> or =0.96) and high Spearman correlation coefficients (> or =0.86) were found. The internal construct validity was confirmed by good fit to the Rasch measurement model. The fit statistics conducted in the study was acceptable, except for some items. CONCLUSIONS: The Turkish translation of the PEDI is valid and reliable for the Turkish child population. We believe that PEDI is a detailed and useful instrument for the evaluation of efficiency of pediatric rehabilitation programme.


Assuntos
Atividades Cotidianas , Avaliação da Deficiência , Crianças com Deficiência/classificação , Traduções , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Reprodutibilidade dos Testes , Estatísticas não Paramétricas , Turquia
4.
Am J Phys Med Rehabil ; 86(3): 176-82, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17167346

RESUMO

OBJECTIVE: To evaluate the WeeFIM instrument's reliability and internal construct validity for the Turkish child population. DESIGN: License was taken from UDSmr to use the WeeFIM instrument. For the reliability and validity studies of the Turkish translation of the WeeFIM instrument, 573 Turkish nondisabled children were included in the study. The reliability of the instrument was assessed by Cronbach's alpha coefficient, intraclass correlation coefficient (ICC), and test-retest reliability. Internal construct validity was assessed by both using Rasch unidimensional measurement model and testing for differential item functioning for age and gender. RESULTS: Cronbach alpha value was 0.99 for motor WeeFIM rating and 0.99 for cognitive WeeFIM rating. ICC was 0.81 for motor WeeFIM rating and 0.92 for cognitive WeeFIM rating. The internal construct validity of the Turkish translation of the WeeFIM instrument was confirmed by excellent fit to the Rasch measurement model. Two subscales were found from the principal component analysis of standardized residual correlation for items. Among the items, bowel management, bladder management, eating, and comprehension showed considerable levels of misfit. CONCLUSIONS: The Turkish translation of the WeeFIM instrument is valid, reliable, and practical for the Turkish child population. Further studies are required to determine the cross-cultural validity of the instrument.


Assuntos
Atividades Cotidianas , Proteção da Criança , Indicadores Básicos de Saúde , Criança , Pré-Escolar , Comparação Transcultural , Feminino , Humanos , Lactente , Masculino , Análise de Componente Principal , Reprodutibilidade dos Testes , Turquia
5.
J Spinal Cord Med ; 29(4): 396-401, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17044390

RESUMO

BACKGROUND/OBJECTIVE: This study was performed to evaluate the bone mineral density (BMD) values in patients with spinal cord injury (SCI) and determine the effects of the level, severity, and duration of the neurological lesion and spasticity on BMD values. METHODS: A total of 75 patients with traumatic SCI and a healthy control group of 39 people were included in the study. The BMD values of the lumbar spine and 4 different regions of the hip (femoral neck, Ward's triangle, trochanter, and femoral shaft) of all cases were measured using dual energy x-ray absorptiometry. The biochemical markers were also analyzed. RESULTS: The BMD values in all measured regions were found to be decreased in patients compared with that of controls. The level and severity of the lesion and the spasticity did not significantly affect BMD values in the regions analyzed. The BMD values of the hip decreased as the duration of SCI increased. The levels of plasma phosphorus and alkaline phosphatase, calcium in 24-hour urine samples, and the calcium/creatinine ratio in spot urines were found to be significantly higher in the patient group. CONCLUSION: All patients with SCI had lower BMD values than controls. The level and severity of SCI and spasticity did not significantly affect BMD values. The BMD values of the hip decreased as the duration of SCI increased.


Assuntos
Densidade Óssea , Traumatismos da Medula Espinal/fisiopatologia , Adulto , Idoso , Estudos de Casos e Controles , Feminino , Humanos , Vértebras Lombares , Masculino , Pessoa de Meia-Idade , Espasticidade Muscular/etiologia , Paraplegia/etiologia , Quadriplegia/etiologia , Traumatismos da Medula Espinal/complicações , Fatores de Tempo , Índices de Gravidade do Trauma
6.
Rheumatol Int ; 27(2): 191-6, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16896989

RESUMO

Acute ulnar neuropathy at the wrist is an extremely uncommon condition, at times requiring a high index of suspicion for the diagnosis. Clinical presentations of ulnar nerve lesions at the wrist and hand show variations due to the complex anatomic course of the nerve in distal sites. We report a case of acute ulnar neuropathy at the wrist caused by a ganglion in Guyon's canal, being initially misinterpreted as flexor tenosynovitis. The accurate diagnosis of selective distal motor neuropathy of ulnar nerve was made electrophysiologically. Magnetic resonance imaging revealed a well defined soft tissue mass consistent with a ganglion, compressing the ulnar nerve in Guyon's canal. Entrapment neuropathies are one of the common conditions handled by physiatrists. Ulnar nerve lesions at the wrist should be kept in mind in the differential diagnosis of patients with wrist or hand pain. Magnetic resonance imaging is a useful method in the anatomical evaluation of acute focal neuropathies.


Assuntos
Erros de Diagnóstico , Cistos Glanglionares/complicações , Síndromes de Compressão do Nervo Ulnar/diagnóstico , Síndromes de Compressão do Nervo Ulnar/etiologia , Adulto , Feminino , Cistos Glanglionares/patologia , Cistos Glanglionares/cirurgia , Humanos , Imageamento por Ressonância Magnética , Tenossinovite/diagnóstico , Nervo Ulnar/fisiopatologia , Síndromes de Compressão do Nervo Ulnar/cirurgia
7.
Rheumatol Int ; 26(5): 473-80, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16341700

RESUMO

Therapeutic proteins, such as infliximab, have revolutionized the treatment of many diseases during the last decade and more than 80 therapeutic proteins are currently approved for clinical use. However, all exogenous proteins have the potential to cause antibody formation. In order to ensure patient safety and the efficacy of therapeutic proteins, careful monitoring of the immunogenicity of therapeutic proteins is therefore necessary not only during preclinical trials, but also during the treatment of patients. Here, we report a clear-cut demonstration of the induction of anti-infliximab antibodies during the treatment of a patient with ankylosing spondylitis (AS). Assessment of anti-infliximab antibodies in sera obtained at various time periods were performed using a highly specific double antigen assay system developed in our laboratory. Immunoreactivity was found to be solely specific for infliximab. Because all sera obtained from the patient were found to be negative for the presence of human anti-mouse antibody (HAMA) and anti-human antibodies. The loss of effect of infliximab, as judged by observing the relapse of signs and symptoms of disease in the patient, seemed to be related with the appearance of antibodies. This study clearly demonstrates that monitoring for the induction of specific antibodies during clinical trials is an important issue for therapeutic proteins.


Assuntos
Anticorpos Monoclonais/farmacocinética , Fatores Imunológicos/farmacocinética , Espondilite Anquilosante/tratamento farmacológico , Adulto , Animais , Anticorpos Monoclonais/imunologia , Especificidade de Anticorpos , Humanos , Alótipos de Imunoglobulina/imunologia , Fatores Imunológicos/imunologia , Infliximab , Masculino , Camundongos
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