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Pain Med ; 12(1): 27-35, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21040436

RESUMO

OBJECTIVES: Many patients experience pain for a short duration after conventional radiofrequency (CRF) denervation for lumbar facet pain. The aim of the present study was to evaluate the efficacy and cost of administering diclofenac sodium for the relief of pain after CRF denervation. METHODS: After denervation, 66 patients were randomly allocated into three groups to receive either placebo for 7 days (group A), diclofenac sodium for 3 days (group B), or diclofenac sodium for 7 days (Group C). The patients' pain visual analgesia score (VAS) and side effect were recorded at baseline 1, 7, 14, 30, and 60 days after treatment. Oswestry Disability Index (ODI), Patients' Satisfaction Score (PSS), and dosage and cost of the drugs used for pain management were recorded at baseline, 30 and 60 days after treatment. RESULTS: VAS in groups B and C both was less than that in group A at 1 and 7 days after treatment (P<0.05 and 0.01, respectively). PSS in groups B and C was significantly better than in group A at 30 and 60 days after treatment (P<0.05). The rate of side effects was similar among the three groups at all times (P>0.05). The cost of analgesic administration in group B was significantly less than in groups A and C (P<0.05). CONCLUSION: Diclofenac sodium administration improves analgesia and the PSS after CRF denervation. Compared to a 7-day dosage, a 3-day diclofenac sodium therapy has similar efficacy and less cost for the treatment of pain after CRF neurotomy.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Ablação por Cateter/métodos , Denervação/métodos , Diclofenaco/uso terapêutico , Dor Lombar/cirurgia , Dor Pós-Operatória/tratamento farmacológico , Articulação Zigapofisária , Idoso , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/efeitos adversos , Análise Custo-Benefício , Diclofenaco/administração & dosagem , Diclofenaco/efeitos adversos , Avaliação da Deficiência , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Medição da Dor , Satisfação do Paciente , Resultado do Tratamento
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