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1.
J Neuroophthalmol ; 35(2): 182-4, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25786202

RESUMO

We report central serous chorioretinopathy (CSC) in a patient with Susac syndrome. The diagnosis of Susac syndrome was based on the results of funduscopy, brain magnetic resonance imaging, and audiometric testing. Our case demonstrates that possible choroidal involvement in Susac syndrome may lead to the development of CSC.


Assuntos
Coriorretinopatia Serosa Central/etiologia , Síndrome de Susac/complicações , Adulto , Coriorretinopatia Serosa Central/diagnóstico , Feminino , Angiofluoresceinografia , Humanos , Imageamento por Ressonância Magnética , Tomografia de Coerência Óptica
2.
Eur Arch Otorhinolaryngol ; 272(7): 1687-91, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25182390

RESUMO

We aimed to find out whether snoring relieve with nasal surgery in patients with nasal obstruction. Sixty-four patients who underwent septoplasty under general anesthesia with complaint of nasal obstruction and snoring at Haydarpasa Numune Education and Research Hospital were enrolled in the study. All patients were evaluated by otolaryngological examination. Septal deviation was graded as mild, moderate and severe with endoscopy. Variables examined included age, sex, body mass index. All patients also completed the questionnaires, including Nose Obstruction Symptom Evaluation scale (NOSE), Epworth Sleepiness Scale (ESS), and Snore Symptom Inventory (SSI) before and after septoplasty. NOSE scale, ESS, and SSI scores showed statistically significant improvement after nasal surgery (p < 0.01) but we could not find any statistically significant association between septal deviation grading and improvement in scores of NOSE scale, ESS, and SSI (p > 0.05). Added to this, the association between body mass index (BMI) and improvement in scores of NOSE scale, ESS, and SSI did not reach statistical significance (p > 0.05). Our results demonstrated that septoplasty is effective on the subjective parameters of nasal obstruction in habitual snorers irrespective of the nasal septal deviation and severity of BMI.


Assuntos
Obstrução Nasal , Deformidades Adquiridas Nasais , Rinoplastia/métodos , Ronco , Adulto , Feminino , Humanos , Masculino , Obstrução Nasal/complicações , Obstrução Nasal/cirurgia , Septo Nasal/cirurgia , Deformidades Adquiridas Nasais/complicações , Deformidades Adquiridas Nasais/diagnóstico , Deformidades Adquiridas Nasais/cirurgia , Ronco/etiologia , Ronco/cirurgia , Inquéritos e Questionários , Resultado do Tratamento
3.
Eur Arch Otorhinolaryngol ; 272(2): 345-9, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24874588

RESUMO

Biofilms are sessile communities of bacteria embedded in self-produced extracellular polysaccharide matrix and are considered to be responsible for bacterial infections in humans. Topical surfactant use on silicone nasal splints may have a preventive effect on biofilm formation. The objective of this study is to investigate the effect of surfactant-containing nasal solutions on biofilm formation over the surface of silicone nasal splints. Forty patients were randomized after septoplasty to receive surfactant-containing saline solution (group 1) or saline without surfactant (group 2). At the postoperative 48th, 72th and 96th hours, pieces of splint samples were taken and prepared for scanning electron microscopic evaluation. Biofilm formation was observed in 3, 6 and 14 of 20 samples in group 1 (surfactant used) and 3, 14 and 20 of 20 samples in group 2 (control) at 48th, 72th and 96th hours, respectively. Biofilm formation incidences of groups at 48th hour were similar (p > 0.05), whereas it was significantly lower at group 1 regarding 72th and 96th hours (p < 0.05). Surfactant-containing nasal solutions have an inhibitory effect on biofilm formation over the surface of silicone nasal splints especially after 48 h. Surfactant-containing nasal solutions may have an important role in nasal septal dressing in the future.


Assuntos
Biofilmes/efeitos dos fármacos , Septo Nasal/cirurgia , Rinoplastia , Contenções , Tensoativos/farmacologia , Adulto , Humanos , Microscopia Eletrônica de Varredura , Pessoa de Meia-Idade , Estudos Prospectivos , Silicones , Soluções
4.
Am J Otolaryngol ; 34(5): 530-6, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23890702

RESUMO

OBJECTIVE: The aim of this experimental study was to evaluate the effects of hyperbaric oxygen, methylprednisolone and combined hyperbaric oxygen-methylprednisolone treatments on traumatic facial nerve regeneration in rats. SUBJECTS AND METHODS: After exposure to facial nerve injury, four groups of rats were created with five subjects in each group: Group 1 (hyperbaric oxygen), group 2 (control), group 3 (combined hyperbaric oxygen-methylprednisolone), group 4 (methylprednisolone). Facial nerve specimens from sacrificed animals were examined for axonal degeneration, vascular congestion, macro vacuolization, axon diameter and thickness of myelin sheath. RESULTS: There were significant differences with regard to axonal degeneration, vascular congestion and axon diameter between group 3 and the control group. In addition to lower axonal degeneration and vascular congestion, a larger diameter of axons was observed in group 3. There were significant differences with regard to vascular congestion and axon diameter between group 4 and the control group. We observed thicker myelin and lower axonal degeneration in group 3 compared with group 4. CONCLUSION: The combination therapy with hyperbaric oxygen and methylprednisolone had an additive beneficial effect on regeneration of the facial nerve and may provide better treatment outcomes than methylprednisolone or hyperbaric oxygen therapy alone.


Assuntos
Traumatismos do Nervo Facial/terapia , Nervo Facial/fisiologia , Oxigenoterapia Hiperbárica/métodos , Metilprednisolona/uso terapêutico , Regeneração Nervosa , Animais , Modelos Animais de Doenças , Nervo Facial/efeitos dos fármacos , Traumatismos do Nervo Facial/fisiopatologia , Glucocorticoides/uso terapêutico , Ratos , Ratos Sprague-Dawley
5.
Iran J Otorhinolaryngol ; 34(124): 225-232, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36246199

RESUMO

Introduction: We aimed to compare the effectiveness of wideband absorbance in detecting ossicular chain discontinuity with intraoperative findings. Materials and Methods: In this study, 58 ears from 38 patients with chronic otitis media (COM) were included. Twenty-six ears with perforation and intact ossicular chain were determined as Group 1, 12 ears with perforation and ossicular chain defects were determined as Group 2, and 20 ears with normal hearing and intact tympanic membrane were determined as Group 3. The comparison of the groups was made considering the static (non-pressure) absorbance analysis performed using wideband tympanometry. Results: When perforation sites were evaluated in Group 1 and Group 2; there were 12 anterior perforations, 7 posterior perforations, and 19 subtotal perforations. Air conduction thresholds in Group 2 were significantly (P<0.05) higher than in Group 1, as expected in pure tone audiometry. When wideband absorbance (WBA) measurements were evaluated in all 3 groups, no significant difference (P>0.05) was found between the frequencies 226 to 1000 Hz. WBA measurements at 8 frequencies between 1888-2311 Hz in Group 1 were significantly lower than Group 3 (P<0.05). WBA measurements at 4 frequencies between 3462-3886 Hz frequencies in Group 2 were significantly lower than Group 1 (P<0.05). Conclusions: Our findings concluded that a significant decrease in absorbance values in the narrow frequency range may be valuable in predicting ossicular chain defects.

6.
Eur Arch Otorhinolaryngol ; 267(10): 1523-6, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20480369

RESUMO

The purpose of this study is to investigate the prevalence of Körner's septum (KS) in temporal bones with varying degrees of pneumatization and to evaluate any relationship between the degree of pneumatization and the presence of KS. Data were obtained retrospectively from 356 temporal bone high-resolution computed tomography of 178 patients who underwent tympanoplasty. Mastoid bone pneumatization was classified as aerated, diploic and sclerotic. The presence of Körner's septum was also investigated. The relationship between the presence of Körner's septum and the type of mastoid pneumatization was assessed. KS was encountered in 98 out of total 356 ears. Prevalence of KS was not statistically different between aerated (31%, n = 36), diploic (24.7%, n = 27) and sclerotic mastoids (26.9%, n = 35; p > 0.05). In conclusion, there is no relationship between the presence of KS and the degree of pneumatization. The presence of KS does not necessarily corroborate the presence of poor pneumatization.


Assuntos
Suturas Cranianas/patologia , Processo Mastoide/patologia , Osso Petroso/patologia , Estudos de Coortes , Suturas Cranianas/diagnóstico por imagem , Humanos , Processo Mastoide/diagnóstico por imagem , Osso Petroso/diagnóstico por imagem , Estudos Retrospectivos , Esclerose/diagnóstico por imagem , Tomografia Computadorizada por Raios X , Timpanoplastia
7.
Sisli Etfal Hastan Tip Bul ; 54(1): 29-35, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32377130

RESUMO

OBJECTIVES: This study aims to investigate the effects of empiric lansoprazol therapy on laryngopharyngeal (LPR) and gastroesophageal (GOR) reflux symptoms and laryngological findings. METHODS: Sixty-seven patients with suspected LPR related symptoms were prospectively analyzed in this study. Following eleven symptoms were asked to patients using LPR symptom questionnaire; sore throat, throat burning, throat clearing, globus sensation, cough, halitosis, dysphonia, dysphagia, postnasal dripping, vocal fatigue and sputum. GOR symptoms were evaluated with the Frequency Scale for the Symptoms of Gastroesophageal Reflux Disease (FSSG) questionnaire consist of twelve symptoms. Posterior larynx, arytenoids and interarytenoid area were evaluated with a 70° endoscope. Erythema, edema and nodularity were graded separately using 4 point severity scale to examine laryngeal signs. All patients were treated using 30 mg lansoprazole once daily for four weeks. After the end of medication, symptoms and laryngoscopic signs were evaluated again with the same method. The pretreatment and posttreatment values were compared with statistical analyses. RESULTS: There was a statistically significant decrease in LPR symptom scores and total scores of FSSG. The severity of nodularity in the posterior larynx, arytenoids and interarytenoid area was improved after treatment. There was no statistically significant difference in erythema on each area larynx. Edema in the posterior larynx and interarytenoid area was improved but there was no change on the edema of arytenoids. CONCLUSION: A short period of empiric antireflux treatment has a significant improving effect on all LPR symptoms and most of GOR symptoms. However, it was insufficient on laryngeal signs. Further research is needed to investigate longer times of treatment for the complete resolution of symptoms and signs.

8.
Acta Otolaryngol ; 133(12): 1266-72, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23972320

RESUMO

CONCLUSION: This study demonstrated that treatment with montelukast in combination with levocetirizine may have a beneficial effect on clinical improvement of middle ear fluid in children with otitis media with effusion (OME). OBJECTIVE: To evaluate the effect of the combination of montelukast and levocetirizine on shortening the duration of effusion in successfully treated OME in children. METHODS: This was a randomized, prospective, double-blind, placebo-controlled trial. The study group consisted of 120 children (age range 2-6 years), who were diagnosed with OME of at least 2 months duration. The children were randomized into one of four groups. The treatment packs containing montelukast 4 mg (tablet) and/or levocetirizine 2.5 mg/5 ml as the active drug or placebo were prepared, numbered, and distributed by the second author. RESULTS: The amelioration of bilateral otoscopic sign scores in the combination therapy group was statistically significantly greater than in all the other groups (p < 0.05). Improvement in bilateral tympanometric findings in the combination therapy group and montelukast group was greater than in the other groups. However, this difference was not statistically significant (p > 0.05). When we compared the difference between otoscopic sign scores before and after treatment we found that it was statistically significant in every group (p > 0.05). However, the significant improvement in tympanometric findings occurred in all groups except the levocetirizine group (p > 0.05).


Assuntos
Acetatos/administração & dosagem , Cetirizina/administração & dosagem , Otite Média com Derrame/tratamento farmacológico , Quinolinas/administração & dosagem , Administração Oral , Criança , Pré-Escolar , Ciclopropanos , Relação Dose-Resposta a Droga , Método Duplo-Cego , Quimioterapia Combinada , Seguimentos , Antagonistas não Sedativos dos Receptores H1 da Histamina/administração & dosagem , Humanos , Antagonistas de Leucotrienos/administração & dosagem , Masculino , Otite Média com Derrame/diagnóstico , Otoscopia , Estudos Prospectivos , Sulfetos , Resultado do Tratamento
9.
Laryngoscope ; 123(11): 2610-4, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23918211

RESUMO

OBJECTIVES/HYPOTHESIS: The aim of this study was to investigate the serum levels of montelukast when administered alone or in combination with desloratadine. STUDY DESIGN: A prospective crossover study. METHODS: Twenty-three healthy volunteers were investigated in two sessions. Volunteers were given 10 mg of montelukast orally with 250 mL water in the first session. The same subjects were given 10 mg of montelukast in fixed combination with 5 mg desloratadine 10 days after first session. Blood samples were collected 2, 3, and 4 hours after drug administration, and kept at -80°C after both applications. Plasma samples were analyzed for montelukast concentration. RESULTS: Mean concentration values of both groups were not statistically different (P > .05), but the differences were statistically significant according to time (P < .05). Statistically significant difference was not found between the groups according to the area under curve on the basis of both marginal and cumulative values for all different time intervals (P > .05). CONCLUSIONS: The absorption rate of montelukast was not altered when administered with desloratadine. This study suggested that desloratadine does not influence the bioavailability of montelukast, and their combination therapy can be used safely.


Assuntos
Acetatos/administração & dosagem , Acetatos/sangue , Antagonistas não Sedativos dos Receptores H1 da Histamina/administração & dosagem , Antagonistas de Leucotrienos/administração & dosagem , Antagonistas de Leucotrienos/sangue , Loratadina/análogos & derivados , Quinolinas/administração & dosagem , Quinolinas/sangue , Adulto , Disponibilidade Biológica , Estudos Cross-Over , Ciclopropanos , Interações Medicamentosas , Feminino , Antagonistas não Sedativos dos Receptores H1 da Histamina/farmacologia , Humanos , Loratadina/administração & dosagem , Loratadina/farmacologia , Masculino , Estudos Prospectivos , Sulfetos , Adulto Jovem
10.
Int J Pediatr Otorhinolaryngol ; 74(11): 1316-9, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20828840

RESUMO

OBJECTIVE: The goal of this study is to determine the correlation of clinical symptoms of UAO (upper airway obstruction) with radiographic evaluation of adenoidal obstruction and tonsil size in children with adenotonsillar hypertrophy and to evaluate the usefulness of lateral neck radiography. STUDY DESIGN: Prospective study. SETTING: Haydarpasa Numune Research and Education Hospital, Istanbul, Turkey. SUBJECTS AND METHODS: This study analyses 95 children with one or more of the symptoms of UAO. Clinical symptoms were assessed by a standardized questionnaire evaluating the severity of symptoms. All patients underwent otolaryngologic examination and their tonsil sizes were graded. 74 of 95 patients underwent digital lateral soft tissue radiographs. Assessment of nasopharyngeal obstruction in radiographs was done according to four different methods. RESULTS: We did not find statistically siginificant correlation between symptom scores and radiologic measurements according to Johanneson (r=0.072, p=0.544, p>0.05) and Crepeau (r=0.034, p=0.773, p>0.05). The correlations between OSA score and Cohen and Konak's method and AN ratio were weak and not statistically siginificant (p=0.133, r=0.176; p=0.290, r=0.125 respectively; p>0.05). But, we found a statistically siginificant correlation between the tonsil grade and symptom scores (r=0.216, p=0.036, p<0.05). CONCLUSION: Our results have demonstrated that radiologic measurements of the nasopharyngeal obstruction do not correlate with clinical symptoms of UAO, but clinical assessment of tonsil size does.


Assuntos
Tonsila Faríngea/patologia , Obstrução das Vias Respiratórias/diagnóstico por imagem , Tonsila Palatina/patologia , Adenoidectomia , Tonsila Faríngea/cirurgia , Obstrução das Vias Respiratórias/etiologia , Criança , Pré-Escolar , Tomada de Decisões , Humanos , Hipertrofia/diagnóstico por imagem , Lactente , Radiografia , Índice de Gravidade de Doença
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