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1.
Clinics ; 71(1): 5-9, Jan. 2016. tab
Article in English | LILACS | ID: lil-771945

ABSTRACT

OBJECTIVE: To determine the therapeutic effects of two selective GABA-A agonists, zopiclone and eszopiclone, in the treatment of insomnia. METHODS: This study comprised a phase III, single-center, randomized, double-blind, double-dummy, parallel-group, non-inferiority trial. Patients were randomized to receive zopiclone 7.5 mg or eszopiclone 3 mg, both orally, for four weeks. In total, 199 patients were evaluated during two visits and then followed for at least six weeks. The primary endpoint was the Insomnia Severity Index after four weeks of treatment. Secondary endpoints were obtained through polysomnography data, including total sleep time, sleep latency and sleep efficiency. The frequency of adverse events was also analyzed. ClinicalTrials.gov: NCT01100164. RESULTS: The primary efficacy analysis demonstrated the non-inferiority of eszopiclone over zopiclone. Analysis of objective parameters assessed by polysomnography showed that eszopiclone increased total sleep time and also improved sleep efficiency. The safety profile of both study treatments was similar and the most common events reported in both groups were dysgeusia, headache, dizziness, irritability and nausea. Adverse events were observed in 223 patients, 109 (85.2%) in the eszopiclone group and 114 (87.7%) in the zopiclone group. CONCLUSION: Based on the Insomnia Severity Index at the end of four weeks of treatment, eszopiclone demonstrated efficacy comparable to that of zopiclone in the treatment of insomnia, increasing total sleep time as well as sleep efficiency according to polysomnography.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Young Adult , Azabicyclo Compounds/therapeutic use , Eszopiclone/therapeutic use , Hypnotics and Sedatives/therapeutic use , Piperazines/therapeutic use , Sleep Initiation and Maintenance Disorders/drug therapy , Azabicyclo Compounds/adverse effects , Double-Blind Method , Dysgeusia/chemically induced , Eszopiclone/adverse effects , Headache/chemically induced , Hypnotics and Sedatives/adverse effects , Polysomnography , Piperazines/adverse effects , Treatment Outcome
2.
Arq. odontol ; 46(1): 48-55, 2010. ilus
Article in Portuguese | LILACS, BBO | ID: lil-583641

ABSTRACT

É comum, em pacientes oncológicos submetidos à terapia antineoplásica, o desenvolvimento de complicações orais agudas ou tardias. Esses distúrbios na integridade e função da cavidade bucal se devem ao fato de que a radioterapia e quimioterapia não são capazes de destruir as células tumorais sem lesionar células normais. Dentre as complicações orais encontram-se a mucosite, xerostomia, disgeusia, as infecções fúngicas, bacterianas e virais, as cáries de radiação, trismo, osteorradionecrose, neurotoxicidade, e, em pacientes pediátricos, o comprometimento da formação óssea, muscular e dentária. Esses efeitos geralmente variam a cada paciente dependendo de variáveis do tratamento, do paciente e do tumor. O objetivo do presente trabalho foi apresentar as complicações orais decorrentes da terapia antineoplásica bem como a importância da atuação do cirurgião-dentista nesse contexto. Através da literatura pesquisada, foi possível concluir que é imprescindível que os pacientes oncológicos sejam acompanhados antes, durante e após a terapia antineoplásica a fim de que o cirurgião-dentista possa elaborar um plano de tratamento adequado às suas necessidades, de forma a prevenir ou controlar a ocorrência dessas complicações.


Subject(s)
Humans , Male , Female , Dysgeusia/chemically induced , Stomatitis/chemically induced , Antineoplastic Protocols/standards , Xerostomia/chemically induced , Mycoses , Drug Therapy/adverse effects , Radiotherapy/adverse effects
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