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3.
J Orthop Trauma ; 26(2): 98-106, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21804410

RESUMO

OBJECTIVE: The objective of the study was to evaluate functional outcome, patient self-assessment, and radiographic outcome at 1 year in displaced three- and four-part proximal humeral fractures (OTA group 11-B2 and 11-C2). DESIGN: Randomized controlled trial. SETTING: Academic medical center. PATIENTS/PARTICIPANTS: Fifty patients aged 60 years or older with displaced three- or four-part proximal humeral fractures and no previous shoulder injuries were randomized either to surgical treatment or to conservative closed treatment. Twenty-five patients were included in each group. Forty-eight patients completed 12-month follow-up. Two surgical patients died within 3 months. INTERVENTION: The surgically treated group had a standardized surgical treatment with open reduction and internal fixation using an angular stable plate and cerclages. Instructed physical therapy started the third postoperative day. The conservative treatment group had a standardized nonoperative treatment that included closed reduction if displacement between the head and metaphyseal shaft fragment exceeded 50% of the diaphyseal diameter. Physical therapy started on the fifteenth postoperative day. MAIN OUTCOME MEASUREMENTS: The main outcome was the mean difference in Constant score between the injured and noninjured shoulder at 12 months. The secondary outcomes were patient self-assessment (American Shoulder and Elbow Surgeons score) and radiographic ratings at 12 months. RESULTS: At 12 months, mean Constant scores favored conservative treatment by 2.4 points (nonsignificant; P = 0.62). There was no significant difference in mean patient self-assessment. However, radiographic outcomes were significantly better for surgically treated patients. CONCLUSION: There is no evidence of a difference in functional outcome at 1-year follow-up between surgical treatment and conservative treatment of displaced proximal humeral fractures in elderly patients.


Assuntos
Placas Ósseas , Fixação Interna de Fraturas/instrumentação , Fixação Interna de Fraturas/métodos , Consolidação da Fratura , Fraturas Mal-Unidas/cirurgia , Fraturas do Ombro/cirurgia , Idoso , Idoso de 80 Anos ou mais , Feminino , Fraturas Mal-Unidas/diagnóstico , Humanos , Masculino , Pessoa de Meia-Idade , Recuperação de Função Fisiológica , Fraturas do Ombro/diagnóstico , Resultado do Tratamento
4.
Tidsskr Nor Laegeforen ; 131(6): 583-6, 2011 Mar 18.
Artigo em Norueguês | MEDLINE | ID: mdl-21423311

RESUMO

BACKGROUND: SOD1 mutations account for less than 25 % of cases with familial amyotrophic lateral sclerosis and may cause atypical phenotypes. CASE REPORT: A young woman developed progressive right ankle paresis that made running difficult after two years. Neurological examination revealed flaccid paresis of the right calf without fasciculations or sensory deficits. Electromyography displayed evidence of denervation restricted to the right calf. Sequencing of the SOD1 gene revealed an A > G mutation in nucleotide position 140, that causes substitution of arginine with histidine in amino acid position 46 (H46R). The patient's father had developed similar symptoms at the age of 60 but was still ambulant 5 years later. The patient's grandmother developed similar symptoms aged 40, and used a wheelchair for several years before she died in her nineties. None of the affected family members developed overt arm or bulbar pareses. CONCLUSION: The H46R SOD1 mutation in this case of familial amyotrophic lateral sclerosis causes a slowly progressive lower motor neuron disease that remains restricted to the legs for years or even decades.


Assuntos
Esclerose Lateral Amiotrófica/genética , Debilidade Muscular/genética , Adulto , Esclerose Lateral Amiotrófica/diagnóstico , Diagnóstico Diferencial , Progressão da Doença , Feminino , Neuropatia Hereditária Motora e Sensorial/diagnóstico , Neuropatia Hereditária Motora e Sensorial/genética , Humanos , Perna (Membro) , Debilidade Muscular/diagnóstico , Exame Neurológico , Doenças Neuromusculares/diagnóstico , Doenças Neuromusculares/genética , Mutação Puntual , Superóxido Dismutase/genética
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