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1.
Otol Neurotol ; 45(2): 150-153, 2024 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-38082465

RESUMO

OBJECTIVE: To compare observation of otologic surgery using a traditional operating microscope (OM) and a three-dimensional exoscope. STUDY DESIGN: Prospective, nonrandomized, noncontrolled study. SETTING: Tertiary care center. METHODS: Senior medical students and otolaryngology trainees observing otologic surgery performed with OM and exoscope were asked to complete a questionnaire comparing the two experiences. The key variables were image clarity, depth perception, observer's level of motion sickness during the surgery, the participant's understanding of middle ear anatomy, and their overall preference between OM and exoscope. RESULTS: Twenty-two observers participated in the study. Subjective clarity of the image was significantly better with the exoscope compared with the OM (9.7 ± 0.6 versus 6.9 ± 1.7, p = 0.0004) as well as the depth perception (9.25 ± 0.87 versus 5 ± 2.69, p = 0.0007). Observers subjectively had an improved understanding of middle ear anatomy after observing an exoscopic surgery, but not a microscopic surgery. All but one observer preferred the exoscope. CONCLUSION: The three-dimensional exoscope may be a valuable educational tool for teaching trainees otologic surgery. More objective studies are needed in the future to assess the degree of improvement.


Assuntos
Procedimentos Neurocirúrgicos , Procedimentos Cirúrgicos Otológicos , Humanos , Procedimentos Neurocirúrgicos/métodos , Estudos Prospectivos , Microscopia , Procedimentos Cirúrgicos Otológicos/métodos , Microcirurgia/métodos
2.
Am J Otolaryngol ; 45(2): 104171, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38101128

RESUMO

OBJECTIVES: The purpose of this study was to determine the incidence of adverse events in the first 48 h (acute) 14 days (subacute) in post supraglottoplasty pediatric patients. A secondary aim was to determine if postoperative hospital admission after supraglottoplasty in pediatric patients is necessary. METHODS: This study was a retrospective review of pediatric patients who underwent supraglottoplasty at a tertiary care center. Data were obtained from January 2017-December 2020, totaling 107 patients. Pediatric patients who underwent supraglottoplasty were included in the study. Information regarding patients' demographics, length of postoperative hospital stay, comorbid conditions, unit of hospital admission, intraoperative and postoperative adverse events, and readmission within the first 14 days was gathered and analyzed. RESULTS: The incidence of postoperative adverse events for all subjects after supraglottoplasty was 5.7 % (N = 6). The most common postoperative complications were respiratory distress (N = 2), followed by substernal retractions, stridor, and decreased oral intake (N = 1). There was no statistically significant increased incidence in any group of patients, regardless of their unit of stay post-operatively (p = 0.39). CONCLUSIONS: Supraglottoplasty is a safe surgical option for patients with severe laryngomalacia. While each patient's care is individualized, we demonstrate that post-operative hospital admission is not necessary for healthy children undergoing supraglottoplasty. LEVEL OF EVIDENCE: III - This is a retrospective chart review.


Assuntos
Laringomalácia , Criança , Humanos , Lactente , Estudos Retrospectivos , Laringomalácia/cirurgia , Hospitalização , Tempo de Internação , Complicações Pós-Operatórias/epidemiologia , Dispneia , Glote/cirurgia , Resultado do Tratamento
3.
Facial Plast Surg Clin North Am ; 31(4): 511-519, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37806684

RESUMO

Neurotoxins are the most popular nonsurgical aesthetic procedure for men and women of all ages. Five botulinum toxin A (BoNTA) products represent the current palette of available BoNTA for cosmetic use. Off-label uses of BoNTA continue to expand and are now used for skin rejuvenation, to treat various skin disorders, and in facial nerve paralysis. Dermal and subdermal injections of dilute BoNTA has grown in popularity and been shown to improve skin texture and quality. Common targets for chemodenervation in facial nerve synkinesis are ipsilateral orbicularis oculi, mentalis, depressor anguli oris, buccinator, corrugator muscles, and the ipsilateral and/or contralateral frontalis.


Assuntos
Toxinas Botulínicas Tipo A , Envelhecimento da Pele , Masculino , Humanos , Feminino , Toxinas Botulínicas Tipo A/uso terapêutico , Neurotoxinas/uso terapêutico , Neurotransmissores , Face
4.
Facial Plast Surg Clin North Am ; 31(4): 557-566, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37806689

RESUMO

Non-surgical services are an important part of many facial plastic surgery practices and can improve patient satisfaction as well as bring new patients to the practice. An aesthetician can help to prepare patients for surgery and non-surgical procedures as well as optimize skin care during the recovery period. The scope of practice of aestheticians varies widely between states. Facial plastic surgeons who are delegating procedures to an aesthetician need to be familiar and comply with the state regulations and be up to date on ongoing changes. The connection between nutrition, skin, aging, and recovery from surgical procedures is a current topic of interest. Multiple studies suggest that nutraceuticals can provide clinically significant benefits for skin, wound healing, and hair.


Assuntos
Procedimentos de Cirurgia Plástica , Cirurgia Plástica , Humanos , Face/cirurgia , Higiene da Pele , Satisfação do Paciente
5.
Int J Pediatr Otorhinolaryngol ; 174: 111734, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37757707

RESUMO

OBJECTIVES: To determine whether late-preterm and full-term neonates in the neonatal intensive care unit (NICU) with diagnosed gastroesophageal reflux (GERD) have an increased incidence of feeding difficulties, dysphagia, and oral aversion. To determine the incidence of reflux medication use in late-preterm and full-term neonates in the NICU. METHODS: Neonates greater than 34 weeks gestational age (GA) diagnosed with reflux, who were hospitalized for at least five days, were included in the study. Neonates with anatomical anomalies that interfere with feeding are excluded. The control group included neonates greater than 34 weeks GA not diagnosed with reflux. The key outcome variables were subjective ease of feeding, oral aversion, and placement on nasogastric (NG), orogastric (OG), or requirement of total parenteral nutrition (TPN). Statistical analysis was performed using chi-squared and t-test to compare incidence of feeding difficulties between the groups. A p-value <0.05 was considered significant. RESULTS: In neonates with a diagnosis of reflux, 42.02% had feeding difficulties (66 patients). In the control group, 30.49% of neonates had feeding difficulties (218 patients). Feeding difficulties in neonates with reflux was 11.55% higher than in the control group (p = 0.001). CONCLUSION: Late-preterm and full-term neonates diagnosed with reflux have a higher incidence of feeding difficulties than those who did not have reflux. Only 0.86% of neonates diagnosed with reflux were treated with anti-reflux medications at this large tertiary care children's hospital.


Assuntos
Transtornos de Deglutição , Refluxo Gastroesofágico , Recém-Nascido , Criança , Humanos , Unidades de Terapia Intensiva Neonatal , Transtornos de Deglutição/epidemiologia , Transtornos de Deglutição/terapia , Incidência , Refluxo Gastroesofágico/epidemiologia , Refluxo Gastroesofágico/terapia , Intubação Gastrointestinal
6.
Ear Nose Throat J ; 100(2): 86-89, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31155943

RESUMO

OBJECTIVES: To analyze the incidence of developing contralateral Ménière's disease (MD) in patients who undergo labyrinthectomy for vestibular dysfunction in unilateral MD. STUDY DESIGN: Retrospective chart review. PARTICIPANTS AND METHODS: Adult patients with a diagnosis of MD who underwent surgical labyrinthectomy with minimum follow-up of 12 months were included. Patients who experienced chemical labyrinthectomy, surgical labyrinthectomy for a diagnosis other than MD, contralateral ear surgery, or bilateral MD before the labyrinthectomy were excluded. The key outcome measure is whether symptoms of MD developed in the contralateral ear post-labyrinthectomy. Statistical analysis was performed using χ2 (Fisher exact) test for discrete variables and the Student t test for continuous variables. A P value < .05 was considered significant. RESULTS: Of the140 patients who underwent labyrinthectomy for intractable vertigo due to unilateral MD, 84 had at least 1 year follow-up appointments. Twelve percent (10/84) of these patients developed contralateral MD, which was diagnosed by a neuro-otologist based on symptoms consistent with MD, including low-frequency sensorineural hearing loss. Average age in years is 63.12 (10.83; mean [SD]) at time of surgery. Average follow-up was 35.57 (15.89) months (range: 12-69 months). CONCLUSION: The incidence of contralateral MD development in patients who underwent labyrinthectomy for unilateral MD is 12%. The current literature states that MD has a 30% bilateral involvement rate. Our incidence is significantly lower when compared to the current literature.


Assuntos
Orelha Interna/cirurgia , Perda Auditiva Neurossensorial/epidemiologia , Doença de Meniere/epidemiologia , Complicações Pós-Operatórias/epidemiologia , Vertigem/cirurgia , Idoso , Feminino , Seguimentos , Perda Auditiva Neurossensorial/etiologia , Humanos , Incidência , Masculino , Doença de Meniere/etiologia , Doença de Meniere/cirurgia , Pessoa de Meia-Idade , Complicações Pós-Operatórias/etiologia , Estudos Retrospectivos , Vertigem/etiologia
7.
J Voice ; 35(6): 886-891, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32362577

RESUMO

INTRODUCTION: The Lombard effect (LE) is a phenomenon in which speakers adjust their vocal production by raising the volume in noisy environments. As a result, the LE can create problems of vocal strain, fatigue and potential injury. OBJECTIVES: This study aims to examine the difference in vocal intensity output in subjects wearing unilateral hearing protection versus no hearing protection in the presence of background noise. METHODS: Each subject was seated inside a sound booth wearing a head-mounted microphone. Subjects were asked to read an excerpt from "The Rainbow Passage" while various levels of background noise were played: 50, 60, 70, and 80 dBA (Multitalker Babble). Each noise level was played while the subject was with and without unilateral ear protection (Optime 98 Earmuff [3M]) in random order. The earmuff has a noise reduction rating of 25 dB. After each reading of the text, subjects were asked to rate communication disturbance, vocal clarity, and discomfort during talking using a 10 cm visual analogue scale. RESULTS: The LE is reduced from 0.38 dB/dB to 0.29 dB/dB with unilateral ear occlusion. However, self-perception of disturbance, clarity and comfort were not affected by unilateral occlusion, only by noise level. CONCLUSIONS: Unilateral hearing protection reduces the LE and may protect against phonotrauma when speaking in an environment with loud background noise.


Assuntos
Ruído , Voz , Dispositivos de Proteção das Orelhas , Audição , Humanos , Ruído/efeitos adversos , Som
8.
Otolaryngol Head Neck Surg ; 165(1): 89-92, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-33320050

RESUMO

This study compares nasopharyngeal and tracheal samples for COVID-19 viral testing in patients with a tracheostomy. This was a prospective cohort study done at 2 academic hospitals between March and June 2020. Patients admitted through the emergency department who had a COVID-19 test and an existing tracheostomy or underwent a tracheostomy during the admission period were included. Patients with a positive initial nasopharyngeal swab were placed in the experimental group (n = 8), while those with a negative swab were the control group (n = 7). Nasopharyngeal and tracheal samples underwent COVID-19 testing using the Abbott RealTime SARS-CoV-2 RNA assay. Fourteen patients underwent tracheostomy, and 1 had an existing tracheostomy. The average duration of viral shedding in nasopharyngeal samples was 20.9 days. One patient (6.7%) tested positive in tracheal secretions after a negative nasopharyngeal swab. In the remaining patients (93.3%), the nasopharyngeal and tracheal specimens correlated.


Assuntos
Secreções Corporais/química , Teste de Ácido Nucleico para COVID-19/métodos , COVID-19/diagnóstico , Nariz , Faringe , RNA Viral/análise , SARS-CoV-2/genética , Traqueia , Adulto , Idoso , COVID-19/terapia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Traqueostomia
9.
Int J Pediatr Otorhinolaryngol ; 111: 80-83, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29958620

RESUMO

INTRODUCTION: The use of honey in wound care is becoming more common due to the proven benefit in all three phases of wound healing, as well as the antibacterial and antibiofilm properties. We present our experience using TheraHoney gel, a medical grade honey, for the successful treatment of cochlear implant associated skin breakdown. OBJECTIVE: To describe the role of TheraHoney gel in the management of cutaneous infection and ulceration associated with cochlear implants. METHODS: Three cases of wounds treated traditionally with antibiotics, plus the addition of TheraHoney, were retrospectively reviewed. The first patient had a superficial 1 × 1 cm ulcer, the second patient had bilateral ulcers: one superficial 1.5 × 1.5 cm ulcer and the other a 1.5 × 2 cm stage III pressure ulcer with an exposed receiver stimulator, and the third patient with a 3 × 3.5 cm stage III ulcer with an exposed receiver stimulator. RESULTS: With the addition of TheraHoney gel, complete wound closure was achieved at all three patients without the need for surgical reconstruction. CONCLUSION: Cutaneous infection with or without skin breakdown is a common delayed complication after cochlear implantation. We demonstrate the efficacy of adding medical grade honey in promoting healing in infected scalp pressure ulcers overlying the cochlear implant site.


Assuntos
Implante Coclear , Mel , Infecção da Ferida Cirúrgica/terapia , Antibacterianos/uso terapêutico , Criança , Pré-Escolar , Implante Coclear/instrumentação , Implantes Cocleares , Terapia Combinada , Feminino , Humanos , Cicatrização
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