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2.
Eur Arch Otorhinolaryngol ; 271(6): 1437-41, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23771322

RESUMO

The objective of the study was to identify important factors in the perioperative management of children undergoing bone anchored hearing device (BAHD) surgery in a paediatric tertiary centre. We also aim to compare current practice and identify any changes in practice with the previous study carried out in the same paediatric tertiary centre in 2000. Children undergoing BAHD surgery between January 2008 and January 2011 were identified on a departmental database. A retrospective case note review was performed and compared with data collected prior to 2000. In the study period, 194 children were identified to have had BAHD surgery. 134 case notes were available for analysis and of these children, 353 anaesthetics were identified. 45.5% of the children had a recognised syndrome or dysmorphism and 17% had a congenital cardiac anomaly. 16% of the children were classified as a grade 3 or 4 laryngoscopy, but 83.3% were managed with a laryngeal mask. 11.9% of the children had an intraoperative complication and 4.8% a postoperative complication. 88.4% of children were managed as day cases. Compared with the previous study in 2000, there was a smaller proportion of syndromic or dysmorphic children and a larger proportion of children were managed with a laryngeal mask. As BAHD surgery has become more common and as its indications have expanded, the perioperative management has evolved. The proportion of children with congenital heart disease has remained constant, but there has been a marked reduction in the number of children with syndromes involving the head and neck. We have found that even in complex craniofacial cases, the laryngeal mask is increasingly being used with good results. However, advanced paediatric airway experience was still required in a small number of cases, heightening the awareness that specialised paediatric support services are necessary for a comprehensive BAHD programme.


Assuntos
Auxiliares de Audição , Perda Auditiva/reabilitação , Complicações Pós-Operatórias , Implantação de Prótese , Adolescente , Anestesia Geral , Criança , Pré-Escolar , Estudos de Coortes , Anormalidades Craniofaciais/complicações , Feminino , Humanos , Intubação Intratraqueal , Máscaras Laríngeas , Masculino , Estudos Retrospectivos , Âncoras de Sutura , Centros de Atenção Terciária
3.
Otol Neurotol ; 45(9): 1037-1044, 2024 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-39186326

RESUMO

OBJECTIVE: To investigate the clinical outcomes of bone-anchored hearing implant surgery using the MONO procedure. STUDY DESIGN: Multicenter, multinational, single-arm, prospective trial with a 12-month follow-up. SETTING: Seven European university hospitals from the United Kingdom, Sweden, Denmark, and The Netherlands. PATIENTS: Fifty-one adult patients requiring surgical intervention for bone conduction hearing. INTERVENTION: Bone-anchored hearing implant surgery using the MONO procedure. MAIN OUTCOME MEASURES: The primary endpoint assessed implant usability 3 months after surgery. Implant status, soft tissue reactions, pain and numbness, postoperative events, and sound processor usage were assessed at all follow-up visits. Hearing-related quality of life was evaluated using the Glasgow Benefit Inventory (GBI). RESULTS: At 3 months, 94.2% of the implant/abutment complexes provided reliable anchorage for sound processor usage. No severe intraoperative complications occurred. Sixty-nine percent of surgeries were performed under local anesthesia, with surgery lasting 10 minutes on average. Four implants were lost due to trauma (n = 2), spontaneous loss of osseointegration (n = 1), or incomplete insertion (n = 1). Adverse soft tissue reactions occurred in 2.6% of visits, with a maximum Holgers grade of 3 (n = 1) and grade 2 (n = 5) across patients. Hearing-related quality of life at 3 months improved in 96% of patients. CONCLUSION: The MONO procedure provides a safe and efficient surgical technique for inserting bone-anchored hearing implants with few and minor intra- and postoperative complications.


Assuntos
Condução Óssea , Procedimentos Cirúrgicos Minimamente Invasivos , Qualidade de Vida , Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Estudos Prospectivos , Adulto , Idoso , Procedimentos Cirúrgicos Minimamente Invasivos/métodos , Resultado do Tratamento , Auxiliares de Audição , Implantação de Prótese/métodos , Perda Auditiva/cirurgia , Idoso de 80 Anos ou mais , Perda Auditiva Condutiva/cirurgia
4.
Ann Otol Rhinol Laryngol ; 122(9): 582-7, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24224402

RESUMO

OBJECTIVES: We sought to determine the outcome of implantation of a bone-anchored hearing device in children with unilateral conductive hearing loss. METHODS: A retrospective case note analysis was used in a tertiary referral pediatric hospital to study 17 consecutive cases of pediatric patients with unilateral conductive hearing loss who were fitted with a bone-anchored hearing device between 2005 and 2010. RESULTS: The average age of the patients at the time of bone-anchored hearing device fitting was 10 years 6 months (range, 6 years 3 months to 16 years). Qualitative subjective outcome measures demonstrated benefit. The vast majority of patients reported improved social and physical functioning and improved quality of life. All 17 patients are currently using their bone-anchored hearing device on a daily basis after a follow-up of 6 months. CONCLUSIONS: This study has shown improved quality of life in children with unilateral hearing loss after implantation of their bone-anchored hearing device. There was a high degree of patient satisfaction and improvement in health status reported by children and/or carers. Bone-anchored hearing devices have an important role in the management of children with symptomatic unilateral hearing loss. Perhaps earlier consideration of a bone-anchored hearing device would be appropriate in selected cases.


Assuntos
Condução Óssea/fisiologia , Cuidadores/normas , Auxiliares de Audição , Perda Auditiva Condutiva/cirurgia , Perda Auditiva Unilateral/cirurgia , Percepção da Fala/fisiologia , Âncoras de Sutura , Criança , Feminino , Seguimentos , Perda Auditiva Condutiva/fisiopatologia , Perda Auditiva Unilateral/fisiopatologia , Humanos , Masculino , Satisfação do Paciente , Estudos Retrospectivos , Inquéritos e Questionários
5.
Otol Neurotol ; 43(2): 236-243, 2022 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-34699403

RESUMO

INTRODUCTION: Superior canal dehiscence syndrome (SCDS) is a rare disorder characterized by an array of audiovestibular symptoms due to a dehiscence of bone overlying the superior semicircular canal (SSC). In the presence of debilitating symptoms, surgical management, to plug or resurface the SCC is performed. Although computed tomography (CT) may overestimate the size or presence of a dehiscence due to a partial volume effect, it remains an invaluable diagnostic tool. OBJECTIVES: To assess for correlation between the arc and length of dehiscence and clinical symptomology. METHOD: A single-center, single-operator retrospective analysis of 42 patients who underwent trans mastoid plugging of SCC with confirmed radiological dehiscence of their SSC between January 2008 and July 2019 was undertaken. Patients were assessed based on seven predefined clinical symptoms. Length and arc of dehiscence's were evaluated by means of high resolution (0.5 mm) CT (HRCT), using multiplanar reconstruction (MPR). Receiver operating characteristics (ROC), and more specifically the area under the ROC curve (AUROC) were used to assess for statistical significance. RESULTS: Our results demonstrate overall very little correlation between the arc and size of the dehiscence and symptoms. The only statistically significant correlation we found was between length of dehiscence and the presence of aural fullness. CONCLUSION: SCDS is a debilitating condition with an array of symptoms on presentation. While dehiscence length demonstrated a correlation with aural fullness, no other symptomology in patients with radiologically evident SCDS demonstrated a statistically significant correlation either against the length or arc of dehiscence.


Assuntos
Processo Mastoide , Canais Semicirculares , Humanos , Estudos Retrospectivos , Canais Semicirculares/diagnóstico por imagem , Canais Semicirculares/cirurgia , Tomografia Computadorizada por Raios X
6.
Otol Neurotol ; 40(10): 1326-1332, 2019 12.
Artigo em Inglês | MEDLINE | ID: mdl-31688616

RESUMO

BACKGROUND: Bone anchored hearing implants (BAHI) are widely used and highly successful, accompanied with a high level of patient satisfaction across most techniques. A large UK teaching hospital switched from the previously used wide diameter titanium fixture and drilling system to the novel minimally invasive technique and laser ablated titanium implant. Before this change the rates of fixture failure and skin problems necessitating abutment change were 1% each. METHODS: Retrospective case note review of consecutive BAHI patients drawn from an electronic database between January 2015 and October 2016. RESULTS: Data from a total of 118 procedures were reviewed, with different combinations of surgical techniques and implant types. Sixty procedures were performed via the novel minimally invasive technique with 21 failures (35%). Fourty-eight modified minimally invasive technique procedures were performed with seven failures. In 64 of the procedures, laser ablated titanium fixtures were placed with 21 failures (32.8%). In 54 procedures wide diameter titanium fixtures were placed with eight failures (5%). CONCLUSION: Initial experience with the novel minimally invasive technique and laser ablated titanium fixture showed significantly higher failure rates than expected. This prompted a change to an open technique and subsequent abandonment of the laser ablated titanium fixture and custom drilling solution in our institution.


Assuntos
Prótese Ancorada no Osso , Auxiliares de Audição , Perda Auditiva Condutiva/cirurgia , Procedimentos Cirúrgicos Minimamente Invasivos , Titânio , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Bases de Dados Factuais , Feminino , Audição , Humanos , Masculino , Pessoa de Meia-Idade , Próteses Neurais , Estudos Retrospectivos , Reino Unido , Adulto Jovem
7.
Otol Neurotol ; 40(2): 200-203, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30624403

RESUMO

OBJECTIVES: This study aims to review the utility and interassessor reliability of Holgers classification by simultaneously testing various professionals of the bone-anchored implant team for their impression of a series of randomized images. STUDY DESIGN: Retrospective review of a randomized series of bone-anchored implant fixture clinical photographs from the database at a tertiary referral university hospital. Raters were blinded to the contemporaneous Holgers grading assigned by the Clinical Nurse Specialist at initial assessment. Multivariate analysis was performed for correlation between scores for assessors and between grades of assessor. SETTING: Queen Elizabeth Hospital, Birmingham, UK a tertiary center for BAHIs. PATIENTS: Patients implanted from May 2012 until November 2014. MAIN OUTCOME MEASURE: Photographs of fixture sites of adult patients were taken following bone-anchored hearing implant surgery using either a tissue reduction (a split skin graft or linear incision technique was used) or tissue preservation approach, at 1 week, 6 months, and 12 months postoperatively. On a single occasion 263 images were reviewed by 10 assessors (2 consultants, 2 higher surgical trainees, 3 junior doctors, and 3 audiologists). Images were displayed at 10-second intervals and were scored by each assessor. Assessors were blinded to patient identity, time points and to each other's scores. Results were then compared against the real-time scoring of Holgers grades done by the BAHI specialist nurse to compare scores. RESULTS: Overall 227 (86.2%) images were with tissue reduction technique of which 110 (41.8%) were with linear incision and 117 (44.4%) were with a split skin graft (SSG); and 36 (13.6%) were with tissue preservation technique. Of these 263 images, 104 were at 1 week (39.5%), 70 were at 6 months (26.6%), and 89 were at 12 months (33.9%). The cumulative scores for each grade scored by blinding the time points were: 0 = 1132 (43.04%), total 1 = 995 (37.83%), total 2 = 346 (13.15%), total 3 = 141 (5.36%), total 4 = 16 (0.6%). 2630 data points had a variance of only 0.6415 for each nominal. Multivariate correlation between all assessors was r =0.7230 (Pearson's R). Correlations between consultants r=0.6317, higher surgical trainees r=0.7351, junior doctors r=0.7599, and audiologists r=0.7981.There is a good correlation (r=0.89) with no statistically significant differences between the SSG and linear incision groups (p>0.05), possibly suggesting Holgers score is comparable within both these tissue reduction techniques.There is a moderate correlation (r=0.58) with statistically significant differences between tissue preservation versus tissue reduction groups (p<0.05), possibly suggesting tissue preservation gives better results with lower Holgers scores than tissue reduction. CONCLUSION: Holgers scoring system is a reliable tool with respect to inter-rater variability across all levels of experience. Correlation was closer with audiologists and lesser experienced assessors.


Assuntos
Prótese Ancorada no Osso/efeitos adversos , Auxiliares de Audição/efeitos adversos , Complicações Pós-Operatórias/diagnóstico , Complicações Pós-Operatórias/patologia , Índice de Gravidade de Doença , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Estudos Retrospectivos
8.
Otol Neurotol ; 38(7): 924-930, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28538469

RESUMO

HYPOTHESIS: Assess the clinical acceptability of direct acoustic cochlear implantation for patients with advanced otosclerosis and the support for conducting a controlled trial of its effectiveness in the United Kingdom. BACKGROUND: Emerging evidence supports the efficacy of direct acoustic cochlear implantation in patients with advanced otosclerosis whose needs cannot be managed using the combination of stapes surgery and hearing aids. A controlled trial would provide evidence for its effectiveness and cost-effectiveness to healthcare commissioners. METHODS: An online survey of clinical professionals was constructed to characterize current standard of care for patients with advanced otosclerosis and to assess whether clinicians would be willing to refer patients into a trial to evaluate direct acoustic cochlear implantation. A consensus process was conducted to define inclusion criteria for the future trial. RESULTS: No survey respondent considered direct acoustic cochlear implantation to be inappropriate with a majority indicating that they would refer patients into a future trial. The consensus was that there is a lack of available treatment options for those patients with bone conduction thresholds worse than 55 dB HL and who did not meet current criteria for cochlear implantation. CONCLUSION: The present study confirms that a controlled trial to evaluate the effectiveness of direct acoustic cochlear implantation would have the support of clinicians in the United Kingdom. A feasibility study would be required to determine whether patients who meet the inclusion criteria could be recruited in a timely manner and in sufficient numbers to conduct a formal evaluation of effectiveness.


Assuntos
Implante Coclear , Otosclerose/terapia , Adulto , Condução Óssea , Implante Coclear/economia , Consenso , Análise Custo-Benefício , Técnica Delphi , Feminino , Pesquisas sobre Atenção à Saúde , Auxiliares de Audição , Humanos , Masculino , Pessoa de Meia-Idade , Otosclerose/economia , Otosclerose/epidemiologia , Aceitação pelo Paciente de Cuidados de Saúde , Cirurgia do Estribo , Falha de Tratamento , Reino Unido/epidemiologia
9.
J Laryngol Otol ; 119(5): 403-4, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15949109

RESUMO

We present the first reported case of a squamous cell carcinoma recurrence on a reconstructed flap in the pharynx treated successfully with topical chemotherapy. The patient, treated for a pharyngeal cancer with resection and reconstruction with a free radial forearm flap, and post-operative radiotherapy, developed a tumour on the flap more than two years after surgery. The recurrence was also squamous carcinoma, but there was only superficial infiltration. This was treated with 5-fluorouracil paste placed in the pharynx, with resolution of the tumour. The patient was alive and well more than 28 months after this treatment, with no sign of disease recurrence. Topical chemotherapy for treatment of oral cancer is well described for early disease, but we show that it may be a useful treatment in recurrent disease in selected patients.


Assuntos
Antimetabólitos Antineoplásicos/administração & dosagem , Carcinoma de Células Escamosas/tratamento farmacológico , Fluoruracila/administração & dosagem , Neoplasias Faríngeas/tratamento farmacológico , Administração Tópica , Idoso , Humanos , Masculino , Recidiva Local de Neoplasia , Resultado do Tratamento
10.
JAMA Otolaryngol Head Neck Surg ; 141(8): 757-60, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25996844

RESUMO

IMPORTANCE: We report a new syndrome, which we are calling head-jolting nystagmus, that expands the differential diagnosis of head movement-induced paroxysmal vertigo. OBSERVATIONS: Two male patients (65 and 58 years old) described rotational vertigo after violent and brief (1- to 2-second) oscillations of the head (head jolting) that triggered intense horizontal nystagmus lasting 45 seconds. Accelerations of the head required to induce these episodes could only be achieved by the patients themselves. In case 1, the episodes gradually disappeared over a 6-year period. In case 2, magnetic resonance imaging (3-T) suggested a filling defect within the left horizontal semicircular canal. He underwent surgical canal plugging in March 2013 that resolved the symptoms. CONCLUSIONS AND RELEVANCE: We attribute head-jolting nystagmus to dislodged material within the horizontal semicircular canal and provide a mechanistic model to explain its origin.


Assuntos
Vertigem Posicional Paroxística Benigna/diagnóstico , Movimentos da Cabeça , Nistagmo Patológico/diagnóstico , Canais Semicirculares , Idoso , Vertigem Posicional Paroxística Benigna/etiologia , Humanos , Masculino , Pessoa de Meia-Idade , Nistagmo Patológico/etiologia , Síndrome
11.
J Neurol Surg Rep ; 75(1): e113-6, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25083369

RESUMO

Introduction Congenital cholesteatomas of the temporal bone are epidermoid cysts of embryologic origin that result in progressive desquamation and trapping of squamous epithelium behind an intact tympanic membrane. They are benign, slowly progressive lesions that can be found in various areas of the temporal bone. We report a case of a patient with a massive cholesteatoma first detected at the age of 64 years, causing significant destruction of the mastoid and petrous temporal bones, and adjacent occipital bone. Methods We reviewed the literature and a case report of a patient seen in our institution recently. The Medline database was used to search multiple terms including "congenital" and "cholesteatoma." Results The patient's congenital cholesteatoma was detected incidentally on a computed tomography scan when the patient's only symptoms were unilateral conductive hearing loss with a family history of hearing loss. It was subsequently successfully operated on with minimal postoperative complications. Conclusions Congenital cholesteatomas of mastoid origin can often exist for many years in a subclinical state and develop into a massive size before causing symptoms. A high index of suspicion is necessary to detect congenital cholesteatomas in patients with unilateral conductive hearing loss who are otherwise asymptomatic and have a normal tympanic membrane.

12.
Otol Neurotol ; 34(1): 100-3, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23187927

RESUMO

OBJECTIVE: To report our experience in a series of children with single-sided sensorineural deafness where a bone-anchored hearing device (BAHD) was used for auditory rehabilitation. STUDY DESIGN: Retrospective case review. SETTING: Tertiary referral centre. PATIENTS: Eight children (4 boys and 4 girls) who had BAHD surgery for single-sided sensorineural deafness between 2007 and 2010. INTERVENTION(S): Bone-anchored hearing device was used for auditory rehabilitation. MAIN OUTCOME MEASURE(S): Glasgow Children's Benefit Inventory (GCBI), Single-sided Deafness (SSD) Questionnaire and change in health benefit scores (visual analogue scale). RESULTS: All but one of the children showed a positive GCBI score; the child that reported a negative score was because of low self confidence and self-esteem issues secondary to bullying at school. The results of the SSD questionnaire were generally positive with a mean satisfaction score of the BAHD as 9/10. All the children had an improvement in heath benefit. CONCLUSION: Our findings add further evidence to support patient perceived benefit of a BAHD in single sided sensorineural deafness in the paediatric population.


Assuntos
Auxiliares de Audição , Perda Auditiva Neurossensorial/cirurgia , Perda Auditiva Unilateral/cirurgia , Qualidade de Vida , Adolescente , Criança , Feminino , Seguimentos , Humanos , Masculino , Satisfação do Paciente , Implantação de Prótese/métodos , Estudos Retrospectivos , Inquéritos e Questionários , Âncoras de Sutura , Resultado do Tratamento
13.
Adv Otorhinolaryngol ; 71: 132-139, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21389713

RESUMO

Hearing amplification technology has been evolving since the 19th century. Currently in most audiology departments, the mainstay of hearing rehabilitation is performed with conventional air and bone conduction aids. These are cost-effective, non-invasive hearing aids but are not without their drawbacks. This chapter explores the advantages and disadvantages of conventional hearing aids compared with the bone-anchored hearing aids. Although the bone-anchored hearing aids are a more expensive invasive option, there is increasing evidence that the benefits outweigh the disadvantages. Users report improved quality of life, health status and audiological rehabilitation.


Assuntos
Condução Óssea/fisiologia , Correção de Deficiência Auditiva/instrumentação , Auxiliares de Audição , Perda Auditiva Condutiva/reabilitação , Indicadores Básicos de Saúde , Perda Auditiva Condutiva/fisiopatologia , Humanos , Osseointegração/fisiologia , Desenho de Prótese , Ajuste de Prótese , Qualidade de Vida , Percepção da Fala/fisiologia , Âncoras de Sutura
15.
Ann R Coll Surg Engl ; 88(2): 157-60, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16551407

RESUMO

INTRODUCTION: With increased cross cover of specialities at night and more direct triaging of casualty patients to ENT wards, there is an increased need to ensure that there is adequate provision of emergency airway management. There are currently no national guidelines on what equipment should be available on ENT wards, and the authors have devised a portable airway box with all equipment deemed necessary to manage an acute airway. We believe that all junior doctors covering ENT should have airway training and access to an airway box. The aim of this study was to determine the provision of on-ward airway equipment and training on ENT wards in England. MATERIALS AND METHODS: A telephone survey of all English hospitals with in-patient ENT services. RESULTS: A total of 103 departments were contacted with 98% response rate. Most wards were covered by a combination of ENT and other specialties. Results indicated that only 18% of departments had an airway box and 28% had some training in airway management. CONCLUSIONS: Results suggest poor provision of emergency airway equipment and training on wards. We recommend the use of an airway box, and list of minimal equipment required.


Assuntos
Serviço Hospitalar de Emergência/normas , Tratamento de Emergência/normas , Equipamentos e Provisões Hospitalares/normas , Transtornos Respiratórios/terapia , Emergências , Medicina de Emergência/educação , Tratamento de Emergência/instrumentação , Inglaterra , Equipamentos e Provisões Hospitalares/provisão & distribuição , Humanos , Corpo Clínico Hospitalar/educação , Quartos de Pacientes/normas , Terapia Respiratória/instrumentação
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