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1.
Laryngoscope ; 127(10): E371-E377, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28397271

RESUMO

OBJECTIVE: The aim of this study was to profile and compare the middle ear microbiomes of human subjects with and without chronic otitis media. STUDY DESIGN: Prospective multicenter cohort study. METHODS: All consecutive patients undergoing tympanoplasty surgery for chronic otitis media or ear surgery for conditions other than otitis media were recruited. Sterile swab samples were collected from the middle ear mucosa during surgery. The variable region 4 of the 16S rRNA gene in each sample were amplified using region-specific primers adapted for the Illumina MiSeq sequencer (Illumina, CA, USA)). The sequences were subjected to local blast and classified using Metagenome@KIN (World Fusion, Tokyo, Japan). RESULTS: In total, 155 participants were recruited from seven medical centers. Of these, 88 and 67 had chronic otitis media and normal middle ears, respectively. The most abundant bacterial phyla on the mucosal surfaces of the normal middle ears were Proteobacteria, followed by Actinobacteria, Firmicutes, and Bacteroidetes. The children and adults with normal middle ears differed significantly in terms of middle ear microbiomes. Subjects with chronic otitis media without active inflammation (dry ear) had similar middle ear microbiomes as the normal middle ears group. Subjects with chronic otitis media with active inflammation (wet ear) had a lower prevalence of Proteobacteria and a higher prevalence of Firmicutes than the normal middle ears. CONCLUSION: The human middle ear is inhabited by more diverse microbial communities than was previously thought. Alteration of the middle ear microbiome may contribute to the pathogenesis of chronic otitis media with active inflammation. LEVEL OF EVIDENCE: 2b. Laryngoscope, 127:E371-E377, 2017.


Assuntos
Orelha Média/microbiologia , Microbiota , Otite Média/microbiologia , Actinobacteria/isolamento & purificação , Adolescente , Adulto , Idoso , Bacteroidetes/isolamento & purificação , Criança , Pré-Escolar , Doença Crônica , Feminino , Firmicutes/isolamento & purificação , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Otite Média/cirurgia , Estudos Prospectivos , Proteobactérias/isolamento & purificação , RNA Ribossômico 16S/análise , Timpanoplastia , Adulto Jovem
2.
Asian Pac J Cancer Prev ; 15(22): 9627-30, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25520079

RESUMO

BACKGROUND: Although efficacy of aprepitant for suppressing emesis associated with single-dose cisplatin has been demonstrated, there are limited data on the antiemetic effect of this oral neurokinin-1 receptor antagonist during daily administration of cisplatin. Accordingly, we investigated the efficacy and safety of aprepitant in patients with head and neck cancer (HNC) receiving combination therapy with cisplatin and 5-FU (FP therapy). MATERIALS AND METHODS: Twenty patients with HNC were prospectively studied who received a triple antiemetic regimen comprising granisetron (40 µg/kg on Days 1-4), dexamethasone (8 mg on Days 1-4), and aprepitant (125 mg on day 1 and 80 mg on days 2-5) with FP therapy (cisplatin 20 mg/m2 on days 1-4; 5-FU 400 mg/m2 on days 1-5) (aprepitant group). We also retrospectively studied another 20 HNC patients who received the same regimen except for aprepitant (control group). RESULTS: For efficacy endpoints based on nausea, the aprepitant group showed significantly better results, including a higher rate of complete response (no vomiting and no salvage therapy) for the acute phase (p=0.0342), although there was no marked difference between the two groups with regard to percentage of patients in whom vomiting was suppressed. There were no clinically relevant adverse reactions to aprepitant. CONCLUSIONS: This study suggested that a triple antiemetic regimen containing aprepitant is safe and effective for HNC patients receiving daily cisplatin therapy.


Assuntos
Antieméticos/uso terapêutico , Cisplatino/efeitos adversos , Morfolinas/uso terapêutico , Náusea/tratamento farmacológico , Vômito/tratamento farmacológico , Antineoplásicos/efeitos adversos , Antineoplásicos/uso terapêutico , Aprepitanto , Cisplatino/uso terapêutico , Dexametasona/uso terapêutico , Quimioterapia Combinada , Fluoruracila/efeitos adversos , Fluoruracila/uso terapêutico , Granisetron/uso terapêutico , Neoplasias de Cabeça e Pescoço/tratamento farmacológico , Humanos , Náusea/induzido quimicamente , Antagonistas dos Receptores de Neurocinina-1/uso terapêutico , Estudos Prospectivos , Resultado do Tratamento , Vômito/induzido quimicamente
3.
Hear Res ; 193(1-2): 20-4, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15219316

RESUMO

In this study, we measured human endolymphatic sac potential (ESP) in 8 patients with vestibular schwannoma and in five patients with Ménière's disease during surgery. ESP was measured with a glass electrode filled with 154 mM NaCl and with an outside tip diameter ranging from 2 to 3 microm. The mean value of human ESP in patients with vestibular schwannoma was +13.3+/-1.9 mV. Since electron microscopy showed that the endolymphatic sacs of the eight patients with vestibular schwannoma were normal in the ultrastructures the value can be close to normal human ESP. While in Ménière's disease, three cases showed low potentials and two cases showed almost the same values observed as in the eight patients with vestibular schwannoma. In the two cases with Ménière's disease, the epithelial cells of the endolymphatic sac were preserved. Our study can be considered as the first successful measurement of human ESP and revealed the existence of Ménière's disease having normal endolymphatic sac in function as well as morphology.


Assuntos
Saco Endolinfático/fisiopatologia , Doença de Meniere/fisiopatologia , Neuroma Acústico/fisiopatologia , Adulto , Idoso , Eletrofisiologia , Saco Endolinfático/patologia , Células Epiteliais/patologia , Feminino , Humanos , Masculino , Doença de Meniere/patologia , Microscopia Eletrônica , Microscopia Eletrônica de Varredura , Pessoa de Meia-Idade , Neuroma Acústico/patologia
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