RESUMO
OBJECTIVE: To evaluate the efficacy and safety of DM/Q (capsules containing dextromethorphan [DM] and quinidine [Q]) compared with placebo, taken twice daily, for the treatment of pseudobulbar affect over a 12-week period in multiple sclerosis patients. METHODS: A total of 150 patients were randomized in a double-blind, placebo-controlled study to assess pseudobulbar affect with the validated Center for Neurologic Study-Lability Scale. Each patient also recorded the number of episodes experienced between visits, estimated quality of life and quality of relationships on visual analog scales, and completed a pain rating scale. RESULTS: Patients receiving DM/Q had greater reductions in Center for Neurologic Study-Lability Scale scores than those receiving placebo (p < 0.0001) at all clinic visits (days 15, 29, 57, and 85). All secondary end points also favored DM/Q, including the number of crying or laughing episodes (p Assuntos
Afeto/efeitos dos fármacos
, Dextrometorfano/uso terapêutico
, Antagonistas de Aminoácidos Excitatórios/uso terapêutico
, Esclerose Múltipla/tratamento farmacológico
, Esclerose Múltipla/psicologia
, Quinidina/uso terapêutico
, Idoso
, Choro
, Dextrometorfano/efeitos adversos
, Dextrometorfano/farmacocinética
, Método Duplo-Cego
, Combinação de Medicamentos
, Antagonistas de Aminoácidos Excitatórios/efeitos adversos
, Antagonistas de Aminoácidos Excitatórios/farmacocinética
, Feminino
, Humanos
, Riso
, Masculino
, Pessoa de Meia-Idade
, Medição da Dor/efeitos dos fármacos
, Qualidade de Vida
, Quinidina/efeitos adversos
, Quinidina/farmacocinética