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1.
Braz J Otorhinolaryngol ; 75(2): 280-9, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19575117

RESUMO

UNLABELLED: The ideal adrenaline concentration remains unknown. AIM: Compare topical adrenaline solutions in different concentrations. STUDY DESIGN: Prospective, double blind, randomized trial. PATIENTS AND METHODS: 49 patients divided in 3 groups underwent endoscopic sinus surgery, using only topical solutions of adrenaline in different concentrations (1:2,000, 1:10,000 and 1:50,000). We compared the duration of surgery, intra-operative bleeding, plasmatic levels of catecholamines, hemodynamic parameters and changes in heart rhythm. RESULTS: Surgery time was shorter in the group using adrenaline 1:2,000, which also showed less bleeding in all evaluations (objective and subjective - p < 0.0001). Plasmatic levels of epinephrine rose in all groups, more sharply in the 1:2,000 group. There was a trend towards elevation of blood pressure in the groups using adrenaline 1:2,000 and 1:10,000, with a greater occurrence of hypertensive peaks. DISCUSSION: We found a very significance bleeding difference favoring the 1:2,000. The blood pressure elevation in the 1:2,000 and 1:10,000 groups was progressive but very slow throughout the procedure, which could be associated with the anesthesia technique. CONCLUSION: We favor the use of topical adrenalin 1:2,000 due to a clear superiority in hemostasis. Further investigation is needed to corroborate our findings.


Assuntos
Endoscopia/métodos , Epinefrina/administração & dosagem , Doenças dos Seios Paranasais/cirurgia , Vasoconstritores/administração & dosagem , Administração Tópica , Adolescente , Adulto , Catecolaminas/sangue , Método Duplo-Cego , Feminino , Hemodinâmica , Hemostasia Cirúrgica , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem
2.
Braz J Otorhinolaryngol ; 85(1): 92-98, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29773520

RESUMO

INTRODUCTION: In different parts of the world, mutations in the GJB2 gene are associated with nonsyndromic hearing loss, and the homozygous 35delG mutation (p.Gly12Valfs*2) is a major cause of hereditary hearing loss. However, the 35delG mutation is not equally prevalent across ethnicities, making it important to study other mutations, especially in multiethnic countries such as Brazil. OBJECTIVE: This study aimed to identify different mutations in the GJB2 gene in patients with severe to profound nonsyndromic sensorineural hearing loss of putative genetic origin, and who were negative or heterozygote for the 35delG mutation. METHODS: Observational study that analyzed 100 ethnically characterized Brazilian patients with nonsyndromic severe to profound sensorineural hearing loss, who were negative or heterozygote for the 35delG mutation. GJB2 mutations were detected by DNA-based sequencing in this population. Participants' ethnicities were identified as Latin European, Non-Latin European, Jewish, Native, Turkish, Afro-American, Asian and Others. RESULTS: Sixteen participants were heterozygote for the 35delG mutation; 14 participants, including three 35delG heterozygote's, had nine different alterations in the GJB2 gene. One variant, p.Ser199Glnfs*9, detected in two participants, was previously unreported. Three variants were pathogenic (p.Trp172*, p.Val167Met, and p.Arg75Trp), two were non-pathogenic (p.Val27Ile and p.Ile196Thr), and three variants were indeterminate (p.Met34Thr, p.Arg127Leu, and p.Lys168Arg). Three cases of compound heterozygosity were detected: p.[(Gly12Valfs*2)];[(Trp172*)], p.[(Gly12Valfs*2)](;)[(Met34Thr)], and p.[(Gly12Valfs*2)(;)[(Ser199Glnfs*9)]). CONCLUSION: This study detected previously unclassified variants and one case of previously unreported compound heterozygosity.


Assuntos
Conexinas/genética , Perda Auditiva Neurossensorial/etnologia , Perda Auditiva Neurossensorial/genética , Mutação , Adolescente , Adulto , Brasil/etnologia , Criança , Pré-Escolar , Conexina 26 , Surdez/etnologia , Surdez/genética , Feminino , Frequência do Gene , Perda Auditiva Neurossensorial/congênito , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Adulto Jovem
3.
Int J Pediatr Otorhinolaryngol ; 72(5): 711-4, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18329728

RESUMO

Dubowitz syndrome is a rare, autosomal recessive disorder characterized by intrauterine growth retardation, short stature, microcephaly, distinct facial dysmorphism, and psychomotoric retardation. The hyper-immunoglobulin E (hyper-IgE or Job syndrome) is a primary immunodeficiency characterized by recurrent staphylococcal abscesses, recurrent cyst-forming pneumonia, and an elevated serum IgE level of >2000 IU/ml. We present the first case to our knowledge of an association between Dubowitz syndrome, hyper-IgE syndrome, and nasal polyposis (due to allergic fungal sinusitis) in a 14-year-old girl. Eosinophilic inflammatory reaction is the feature present in all three conditions. Unlike most cases of allergic fungal sinusitis, this case was not treated with an initial booster of oral steroids due to the risk of disseminated invasive fungal infection, reported in other cases of hyper-IgE syndrome. The case and its management is presented and discussed.


Assuntos
Anormalidades Múltiplas , Síndrome de Job/complicações , Pólipos Nasais/complicações , Adolescente , Feminino , Humanos , Micoses/complicações , Pólipos Nasais/imunologia , Pólipos Nasais/microbiologia , Sinusite/complicações
4.
Braz J Otorhinolaryngol ; 74(1): 7-15, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18392495

RESUMO

UNLABELLED: Foreign bodies are one of the most common ENT (Ear, Nose and Throat) urgencies. Serious complications may occur, like tympanic perforations and bronchoaspiration, but they are uncommon. AIM: To analyze a 1356 foreign body series and establish causes for the complications, looking at prevention. MATERIALS AND METHODS: 1356 patients with ear, nose and throat foreign bodies from the ENT Department of Souza Aguiar Hospital, in Rio de Janeiro, between 1992 and 2000, were analyzed in a retrospective study for parameters like age, gender, type and localization of the foreign body, time span between introduction and removal of the foreign body and complications. RESULTS: The most common foreign bodies were beans and the most frequent age was between 1 and 4 years old. Ear foreign bodies were the most common, followed by nasal foreign bodies. Complications were statistically related to time, childs age and practical experience of the physician. CONCLUSION: Most of the situations related to ENT foreign bodies are avoidable. Improvements in Public Health Assistance and otolaryngologists training are essential to avoid serious complications.


Assuntos
Orelha , Corpos Estranhos/complicações , Laringe , Cavidade Nasal , Faringe , Adolescente , Adulto , Idoso , Brasil/epidemiologia , Criança , Pré-Escolar , Feminino , Corpos Estranhos/epidemiologia , Corpos Estranhos/terapia , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos
5.
Braz J Otorhinolaryngol ; 74(4): 613-6, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18852991

RESUMO

Otitis media is one of the most common infectious diseases of infancy; a reduction in its incidence would have a significant economic and social impact. Vaccines may play a role in the prevention of otitis media. This report discusses vaccines against pneumococci and influenza viruses. We reviewed the literature for results of studies examining the role of these vaccines in the prevention of otitis media. The 23-valent polysaccharide anti-pneumococcal vaccine did not modify the incidence of otitis media in children aged 2 years less, the age group with the highest incidence of otitis. The heptavalent anti-pneumococcal vaccine did not significantly reduce the incidence of otitis media overall. This vaccine did, however, reduce the number of episodes of otitis media with effusion and the number of recurrences; it also altered the profile of causative microorganisms by increasing otitis caused by different microorganisms. We found the inactivated anti-influenza virus vaccine to be effective in reducing otitis media during peak incidence periods of influenza. As these new vaccines are currently available in Brazil, otolaryngologists must be aware of their potential role and impact in the reduction of otitis media, to counsel patients appropriately.


Assuntos
Vacinas contra Influenza/uso terapêutico , Otite Média/prevenção & controle , Vacinas Pneumocócicas/uso terapêutico , Pré-Escolar , Humanos , Esquemas de Imunização , Lactente , Vacinação
6.
Braz J Otorhinolaryngol ; 74(6): 912-918, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19582349

RESUMO

UNLABELLED: Occupational and environmental exposure to agricultural pesticides represent an important health care problem in our country. Among the symptoms presented, dizziness stands out, because of a probable toxic action. AIM: The goal of our study was to characterize vestibular test results from rural workers occupationally and environmentally exposed to organophosphates used in agricultural pesticides. MATERIALS AND METHODS: We carried out a cohort cross-sectional study with 18 rural workers from Teresópolis, RJ. Age ranged between 16 and 59 years, with a mean value of 39.6 years, 5 were males and 13 females. We used three questionnaires with questions associated with general and auditory health, and more specific questions about dizziness and its association with work. All workers underwent clinical evaluation, audiometry and vectoelectronystagmography. RESULTS: Results showed that 16 workers had irritative peripheral body balance disorder and 7 workers had sensorineural hearing loss, thus suggesting that agricultural pesticides cause vestibular alterations through a slow and silent intoxication. CONCLUSIONS: Medical care for this population exposed to neurotoxic substances require an interdisciplinary approach, to guarantee efficient preventive and therapeutic measures.


Assuntos
Doenças dos Trabalhadores Agrícolas/induzido quimicamente , Perda Auditiva Neurossensorial/induzido quimicamente , Compostos Organofosforados/toxicidade , Equilíbrio Postural/efeitos dos fármacos , Transtornos de Sensação/induzido quimicamente , Adolescente , Adulto , Doenças dos Trabalhadores Agrícolas/diagnóstico , Audiometria , Estudos de Coortes , Estudos Transversais , Eletronistagmografia , Feminino , Perda Auditiva Neurossensorial/diagnóstico , Humanos , Masculino , Pessoa de Meia-Idade , Exposição Ocupacional , Transtornos de Sensação/diagnóstico , Adulto Jovem
7.
Braz J Otorhinolaryngol ; 74(4): 617-20, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18852992

RESUMO

UNLABELLED: Acute atypical mastoiditis, with temporal and/or facial edema, is called squamozygomatic mastoiditis. There are only a few reports of this occurrence in the literature, which occurs because of an inflammatory process spread to the zygommatic apophysis, when mastoid pneumatization reaches the zygoma or the squamous portion of the temporal bone. Diagnosis is made based on clinical history, physical exam and mastoid CT scan. Treatment is carried out with antibiotic therapy and surgery. AIM: To present a case of squamozygomatic mastoiditis and review the literature. PATIENTS AND METHODS: Report of a case treated in our hospital during the year of 2003 and literature review through the Internet, we also reviewed otolaryngology books from known authors. DISCUSSION: Squamozygomatic mastoiditis is an atypical mastoiditis in which the inflammatory process spreads to the zygomatic apophysis. The infection reaches the temporal bone squamous portion and makes a fistula between this portion and the temporal muscle, shifting the pinna of the ear downwards and it may reach the face, eyes and eyelids. Diagnosis is carried out by clinical history, physical examination and mastoid CT Scan. Treatment is surgical, associated with antibiotic therapy.


Assuntos
Mastoidite/diagnóstico , Infecções Pneumocócicas , Doença Aguda , Feminino , Humanos , Mastoidite/microbiologia , Mastoidite/terapia , Pessoa de Meia-Idade , Infecções Pneumocócicas/microbiologia , Streptococcus pneumoniae/isolamento & purificação , Resultado do Tratamento
8.
Braz J Otorhinolaryngol ; 73(2): 215-25, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17589730

RESUMO

UNLABELLED: Recent studies analyzing audibility thresholds at frequencies over 8 KHz have brought new perspectives on the investigation of auditory damage. These studies, however, have not yet reached a consensus on normal standards for auditory thresholds at these frequencies. AIM: To analyze the results of high frequency auditory thresholds in individuals aged between 18 and 29 years with no otological complaints. TYPE OF STUDY: A prospective, cross-sectional study. METHODS: 60 conventional audiometries were done and 51 of these exams were within normal limits in individuals aged 18 to 29 years. These selected individuals underwent high-frequency audiometry using the AMPLAID 460 device and Sennheiser HD 520 II earphones, and thresholds were obtained in dB HL Results: There was no significant difference in auditory thresholds between males and females. High-frequency auditory thresholds were obtained for individuals with no otological complaint, aged between 18 and 29 years. CONCLUSION: It has been suggested that such data could be used as a normal reference for further studies with similar standard equipment, to analyze auditory alterations presented in young individuals.


Assuntos
Audiometria/métodos , Limiar Auditivo/fisiologia , Adolescente , Adulto , Audiometria de Tons Puros , Estudos Transversais , Feminino , Humanos , Masculino , Estudos Prospectivos , Valores de Referência
9.
J Laryngol Otol ; 120(1): 67-9, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16359155

RESUMO

Disseminated histoplasmosis is a disease with a high case-fatality rate, especially in patients with the acquired immunodeficiency syndrome (AIDS). The disease can occur in various sites, such as the lungs, eyes, oral cavity, larynx, nervous system, gastrointestinal tract and, more rarely, the nasal sinus region. It is a cosmopolitan mycosis with a high prevalence in Brazil. Nasal manifestation of the disease is rare, with only three cases reported in the literature, but it is part of the differential diagnosis for other granulomatous diseases, such as Wegener's granulomatosis, tegumentary leishmaniasis and nasal lymphoma. The authors of this study present a literature review and report a case of nasal histoplasmosis in a patient with AIDS. No record of such an aggressive presentation has been reported previously in the literature.


Assuntos
Síndrome da Imunodeficiência Adquirida/complicações , Histoplasmose/complicações , Doenças Nasais/complicações , Síndrome da Imunodeficiência Adquirida/patologia , Adulto , Anfotericina B/administração & dosagem , Antifúngicos/administração & dosagem , Feminino , Histoplasmose/tratamento farmacológico , Histoplasmose/patologia , Humanos , Injeções Intravenosas , Deformidades Adquiridas Nasais/etiologia , Doenças Nasais/tratamento farmacológico , Doenças Nasais/patologia , Resultado do Tratamento
10.
Braz J Otorhinolaryngol ; 72(2): 252-5, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16951861

RESUMO

UNLABELLED: Tonsillectomy is one of the most commonly performed procedures of the head and neck. It is performed for a wide variety of indications in both adults and children. It is common to send the material achieved in the surgery to routine histopathologic exam, as to analyze suspected material or for a medical-legal documentation. OBJECTIVE: Analyze the utility and cost of routine histopathologic diagnosis for tonsillectomy. METHODOLOGY: retrospective study of the histopathologic result of all tonsillectomies between 1978 and 2004 in a university hospital and analyzed the files of the patients with cancer. RESULTS: 2103 results of histopathologic exams were analyzed. Of these, only four cases presented any case of malignancy, being all of these non-Hodgkin lymphoma and already suspected before the surgery. DISCUSSION: The world literature has encountered similar results and each time more the histopathologic analysis of all cases is questioned. The cost of the exam is high and your results, in the case of malignancy were already knew before the surgery. CONCLUSION: Histopathologic analysis of all tonsillectomies is not indicated. The risks factors established by Beaty should guide the solicitation of the exam, to try to low the costs with unnecessary exams.


Assuntos
Biópsia/economia , Tonsila Palatina/patologia , Tonsilectomia , Análise Custo-Benefício , Humanos , Tonsila Palatina/cirurgia , Estudos Retrospectivos , Fatores de Risco , Neoplasias Tonsilares/diagnóstico , Neoplasias Tonsilares/patologia , Tonsilectomia/economia
11.
Braz J Otorhinolaryngol ; 72(1): 18-23, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16917548

RESUMO

UNLABELLED: Nasal cavities foreign bodies are common accidents in children, sometimes leading, in accordance with the literature, to complications such as epistaxis and bronchoaspiration. Diagnosis is often made with anterior rhinoscopy, but sometimes nasal fibroendoscopy and imaging may be useful. AIM: To evaluate 420 cases of nasal foreign bodies removed in ENT Service of Souza Aguiar Hospital, Rio de Janeiro, as related to sex, age, type of foreign body and complications. MATERIALS AND METHOD: 420 cases of nasal foreign bodies removed in the ENT service of Souza Aguiar Hospital between December 1992 and December 1998 were evaluated according to the parameters related above. RESULTS: We found higher incidence between 0 and 4 years of age, and the most frequently found foreign bodies were foam fragments, plastic pieces of little toys, beans and paper fragments. Complications occurred in 9.05% of the cases, epistaxis and vestibulitis being the commonest. CONCLUSION: Nasal foreign bodies are especially found between the ages of 0 and 4 years. In our study, foam fragments and small plastic objects were the most frequent foreign bodies found. Complications were found in 9.05% of the cases, headed by epistaxis and nasal vestibulitis.


Assuntos
Corpos Estranhos , Cavidade Nasal , Adolescente , Adulto , Distribuição por Idade , Idoso , Brasil/epidemiologia , Criança , Pré-Escolar , Feminino , Corpos Estranhos/complicações , Corpos Estranhos/diagnóstico , Corpos Estranhos/epidemiologia , Humanos , Incidência , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Fatores de Tempo
12.
Braz J Otorhinolaryngol ; 71(3): 274-80, 2005.
Artigo em Português | MEDLINE | ID: mdl-16446929

RESUMO

UNLABELLED: The nitrous oxide is an inhaling gas that can increase intratympanic pressure during the anesthetic act and cause negative pressure after it is discontinued, mainly in patients with Eustachian tube dysfunction. These pressure variations may come up with clinical implications such as tympanic membrane rupture, ossicular system disarticulation, haemotympanum, barotraumas, prosthesis displacement stapaedotomy and tympanic graft lateralization after tympanoplasty, in addition to serous fluid entrance into the middle ear during the negative pressure phase. AIM: To evaluate the nitrous oxide influence on the middle ear pressure in a population without tube malfunction performing pre and postoperative tympanometry. STUDY DESIGN: Transversal cohort. MATERIAL AND METHOD: A prospective study was carried out with Universitário Clementino Fraga Filho Hospital- UFRJ intern patients, subject to general anesthesia with the use of 50% nitrous oxide from April to June 2003. It was also evaluated whether the duration of surgery, associated anesthetics, presence of allergic rhinitis and nasal septal deviation could contribute to the appearing of intratympanic pressure alteration. RESULTS: The sample is made up of 50 patients, in almost half of them (48%), postoperative tympanometry alterations (type C curve) were found, when comparing to the preoperative tympanometric control (type A curve). Neither sex nor age interfered in the appearing of tympanometry alterations during the post operative as well as the surgery timing. The anesthetic type volatile associate, nasal septal deviation and allergic rhinitis were not able to influence during the postoperative middle ear pressure. CONCLUSION: The nitrous oxide modifies intratympanic pressure during the anesthetic act as well as after it was discontinued.


Assuntos
Testes de Impedância Acústica , Anestesia Geral , Orelha Média/efeitos dos fármacos , Óxido Nitroso/farmacologia , Membrana Timpânica/efeitos dos fármacos , Adolescente , Adulto , Fatores Etários , Idoso , Estudos Transversais , Orelha Média/fisiopatologia , Tuba Auditiva/efeitos dos fármacos , Tuba Auditiva/fisiopatologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Septo Nasal/fisiopatologia , Pressão , Estudos Prospectivos , Rinite/fisiopatologia , Fatores Sexuais , Fatores de Tempo
13.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);85(1): 92-98, Jan.-Feb. 2019. tab
Artigo em Inglês | LILACS | ID: biblio-984045

RESUMO

Abstract Introduction: In different parts of the world, mutations in the GJB2 gene are associated with nonsyndromic hearing loss, and the homozygous 35delG mutation (p.Gly12Valfs*2) is a major cause of hereditary hearing loss. However, the 35delG mutation is not equally prevalent across ethnicities, making it important to study other mutations, especially in multiethnic countries such as Brazil. Objective: This study aimed to identify different mutations in the GJB2 gene in patients with severe to profound nonsyndromic sensorineural hearing loss of putative genetic origin, and who were negative or heterozygote for the 35delG mutation. Methods: Observational study that analyzed 100 ethnically characterized Brazilian patients with nonsyndromic severe to profound sensorineural hearing loss, who were negative or heterozygote for the 35delG mutation. GJB2 mutations were detected by DNA-based sequencing in this population. Participants' ethnicities were identified as Latin European, Non-Latin European, Jewish, Native, Turkish, Afro-American, Asian and Others. Results: Sixteen participants were heterozygote for the 35delG mutation; 14 participants, including three 35delG heterozygote's, had nine different alterations in the GJB2 gene. One variant, p.Ser199Glnfs*9, detected in two participants, was previously unreported. Three variants were pathogenic (p.Trp172*, p.Val167Met, and p.Arg75Trp), two were non-pathogenic (p.Val27Ile and p.Ile196Thr), and three variants were indeterminate (p.Met34Thr, p.Arg127Leu, and p.Lys168Arg). Three cases of compound heterozygosity were detected: p.[(Gly12Valfs*2)];[(Trp172*)], p.[(Gly12Valfs*2)](;)[(Met34Thr)], and p.[(Gly12Valfs*2)(;)[(Ser199Glnfs*9)]). Conclusion: This study detected previously unclassified variants and one case of previously unreported compound heterozygosity.


Resumo Introdução: Em diferentes partes do mundo, mutações do gene GJB2 estão associadas a perda auditiva não sindrômica e a mutação homozigótica 35delG (p.Gly12Valfs*2) é uma das principais causas de perda auditiva hereditária. No entanto, a mutação 35delG não é igualmente prevalente em todas as etnias, faz com que seja importante estudar outras mutações, especialmente em países multiétnicos, como o Brasil. Objetivo: Identificar diferentes mutações no gene GJB2 em pacientes com perda auditiva neurossensorial grave ou profunda não sindrômica de origem genética putativa e negativos ou heterozigotos para a mutação 35delG. Método: Estudo observacional que analisou 100 pacientes brasileiros caracterizados etnicamente, com perda auditiva neurossensorial grave ou profunda não sindrômica, negativos ou heterozigotos para a mutação 35delG. As mutações de GJB2 foram detectadas por sequenciamento baseado no DNA nessa população. As etnias dos participantes foram identificadas como latino-europeia, não latino-europeia, judaica, nativa, turca, negra, asiática e outras. Resultados: Dezesseis participantes eram heterozigotos para a mutação 35delG e 14, incluindo três heterozigotos para 35delG, apresentaram nove alterações no gene GJB2. Uma variante, p.Ser199Glnfs*9, detectada em dois participantes, não havia sido relatada anteriormente. Três variantes eram patogênicas (p.Trp172*, p.Val167Met, e p.Arg75Trp), duas não patogênicas (p.Val27Ile e p.Ile196Thr) e três indeterminadas (p.Met34Thr, p.Arg127Leu, e p.Lys168Arg). Três casos de heterozigosidade composta foram detectados: p.[(Gly12Valfs*2)];[(Trp172*)], p.[(Gly12Valfs*2)](;)[(Met34Thr)], e p.[(Gly12Valfs*2)(;)[(Ser199Glnfs*9)]). Conclusão: Este estudo detectou variantes não classificadas anteriormente e um caso de heterozigosidade composta ainda não relatada.


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Adulto , Pessoa de Meia-Idade , Adulto Jovem , Conexinas/genética , Perda Auditiva Neurossensorial/etnologia , Perda Auditiva Neurossensorial/genética , Mutação , Índice de Gravidade de Doença , Brasil/etnologia , Surdez/etnologia , Surdez/genética , Frequência do Gene , Perda Auditiva Neurossensorial/congênito
14.
Braz J Otorhinolaryngol ; 80(4): 305-10, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25183180

RESUMO

INTRODUCTION: Knowledge of the characteristics related to profound hearing loss is a matter of great importance, as it allows for the etiological and prognostic identification and strategic planning for public health interventions. OBJECTIVE: To assess the different etiologies of hearing loss, age at diagnosis of the hearing loss, its relation to language acquisition, and the age at the first consultation in this service for cochlear implant assessment. METHODS: This was a historical cohort, cross-sectional study, using retrospective analysis of the records of 115 patients with confirmed sensorineural hearing loss, who were followed in a university hospital, based on gender, age of hearing loss, age at the first consultation, language, and hearing loss etiology. RESULTS AND CONCLUSION: The majority of patients assessed for cochlear implants attend the first consultation when they are older than one year (an alarming mean of 3.8 years in the prelingual group) in spite of the early diagnosis of hearing loss. This reflects an already deficient health care system, in terms of referral. The idiopathic cause remains the most frequently identified. Among the known causes, the most prevalent are perinatal causes and meningitis.


Assuntos
Implante Coclear , Implantes Cocleares , Perda Auditiva Neurossensorial/cirurgia , Adolescente , Adulto , Criança , Pré-Escolar , Estudos Transversais , Feminino , Perda Auditiva Neurossensorial/etiologia , Humanos , Lactente , Masculino , Estudos Retrospectivos , Adulto Jovem
15.
Int Arch Otorhinolaryngol ; 17(1): 85-91, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25991999

RESUMO

AIM: Antibiotic prophylaxis aims to prevent infection of surgical sites before contamination or infection occurs. Prolonged antibiotic prophylaxis does not enhance the prevention of surgical infection and is associated with higher rates of antibiotic-resistant microorganisms. This review of the literature concerning antibiotic prophylaxis, with an emphasis on otolaryngologic surgery, aims to develop a guide for the use of antibiotic prophylaxis in otolaryngologic surgery in order to reduce the numbers of complications stemming from the indiscriminate use of antibiotics.

19.
Braz J Otorhinolaryngol ; 77(3): 334-40, 2011 Jun.
Artigo em Inglês, Português | MEDLINE | ID: mdl-21739008

RESUMO

UNLABELLED: The harmony of the facial profile is widely influenced by the height and form of the nasal dorsum. A few millimeters can make the lateral view aesthetically more or less pleasing and adequate in a subject's face. Professionals working with facial aesthetics should focus not only on the surgical techniques for proposed outcomes, but also with the subtleties and subjectivity that characterize aesthetic concepts and judgment. MATERIAL AND METHODS: A prospective survey to evaluate the preferences of a group of healthcare professionals working with facial aesthetics, a group of fine artists, and lay people about the best nasal radix height; the survey involved comparing 3 different nasal radix heights using computer-altered photographs of women with measurements close to the Caucasian standard. RESULTS AND CONCLUSION: The lowest position of the nasal radix--close to the height of the pupil--was preferred (53%), followed by the middle position (superior crease of the eye). The highest position, resembling classic Greek statues, was considered the worst. The authors evaluated the effect of age, gender, and educational level on the choice of the best and worst female profiles.


Assuntos
Estética , Nariz/anatomia & histologia , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Brasil , Escolaridade , Face/anatomia & histologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Fatores Sexuais , Cirurgia Plástica , População Branca , Adulto Jovem
20.
Fisioter. Bras ; 17(4): f:366-I: 374, jul.-ago. 2016.
Artigo em Português | LILACS | ID: biblio-882575

RESUMO

Objetivo: Descrever as características clínicas da vestibulopatia e os fatores a ela associados, a partir dos resultados da vectoeletronistagmografia (VENG) na população pediátrica referida para avaliação no Setor de Otoneurologia de um Hospital Universitário. Métodos: Estudo observacional, descritivo, transversal, com coleta retrospectiva de dados de fichas do Setor de Otoneurologia de um Hospital Universitário, contendo a anamnese otoneurológica e os resultados de VENG realizados em crianças e adolescentes com tontura, durante o período de maio de 1998 a dezembro de 2010. Resultados: Foram avaliadas 16 pacientes, com idade entre quatro e 18 anos, com distribuição igualitária de gênero. A maioria apresentava tontura rotatória, acompanhada de zumbido e de náuseas ou vômitos, sem alteração à VENG. A história de traumatismo craniano foi o único fator significativamente associado à presença de alteração à VENG, estando presente nos três pacientes que apresentaram resultados compatíveis com síndrome vestibular periférica. Conclusão: A sintomatologia vestibular periférica predomina na infância. Ainda assim, na maioria das vezes a VENG se apresenta normal, o que sugere uma limitação diagnóstica deste exame. No entanto, quando a sintomatologia vestibular persistente ocorre após quadro de traumatismo craniano, a VENG não só é útil à diferenciação de afecções periféricas de centrais, como auxilia a conduta terapêutica a ser tomada. (AU)


Objective: To describe the clinical features of vestibular disease and factors associated with it, based on the results of vectoelectronystagmography (VENG) in the pediatric population evaluated at the Otoneurology of an University Hospital. Methods: This observational, descriptive, cross-sectional study, with retrospective data collection of registration forms of Otoneurology Department of a University Hospital, containing otoneurologic interviews and the results of VENG, was performed in children and adolescents with dizziness from May 1998 to December 2010. Results: Sixteen patients 4-18 years old were evaluated, with equal gender distribution. Most patients had vertigo accompanied by tinnitus and nausea or vomiting, without changing the VENG. A history of brain damage was the only factor significantly associated with the presence of alterations in the VENG, which was observed in three patients who showed consistent results with peripheral vestibular syndrome. Conclusion: The peripheral vestibular symptomatology predominates in childhood. However, most cases the VENG seems to be normal, which suggests a limitation of this diagnostic testing. But, when persistent vestibular symptoms occur after the episode of brain trauma, VENG is useful to differentiate peripheral from central disorders, and helps in the therapeutic conduct to be adopted. (AU)


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Doenças Vestibulares , Adolescente , Criança , Vertigem
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