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1.
J Laryngol Otol ; 136(12): 1309-1313, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-35698818

RESUMEN

OBJECTIVE: Rhino-orbito-cerebral mucormycosis is a rapidly progressive disease with high mortality rates of about 60 per cent. The increasing incidence of rhino-orbito-cerebral mucormycosis in coronavirus disease 2019 patients in India and worldwide has become a matter of concern owing to the case fatality rate. This study explored the use of low dose aspirin in decreasing the mortality rate of coronavirus disease 2019 associated mucormycosis. METHOD: This was a retrospective observational study. Patients suffering from post-coronavirus disease 2019 mucormycosis were included in the study. Each patient was treated with surgical debridement and systemic amphotericin B. Low dose aspirin was added, and mortality rates were compared with the patients who did not receive aspirin. RESULTS: The demographic data and rhino-orbito-cerebral mucormycosis staging between the two groups were not significantly different. There was a statistically significant difference in mortality outcomes between the two groups (p = 0.029) and a 1.77 times higher risk of dying for patients not receiving aspirin. Kaplan-Meier survival indicated that patients receiving aspirin had better survival rates (p = 0.04). CONCLUSION: Low dose aspirin improves survival rates in coronavirus disease 2019 associated mucormycosis.


Asunto(s)
COVID-19 , Mucormicosis , Enfermedades Orbitales , Humanos , Mucormicosis/tratamiento farmacológico , Estudios Retrospectivos , Aspirina/uso terapéutico , Antifúngicos/uso terapéutico , Desbridamiento
2.
Cochlear Implants Int ; 17(2): 105-8, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26252730

RESUMEN

OBJECTIVES: To present the case histories and management by LASER tympanic neurectomy of two patients who presented with pain as their only symptom after cochlear implantation, avoiding the need for device removal. CLINICAL PRESENTATION: Two of our patients presented with otalgia, which appeared 6 months after cochlear implantation and resulted in their refusing to use the device. The pain was not controlled by repeated remapping or medical management. Neither patient showed evidence of infection or inflammation around their device. X-rays showed that there were no extracochlear electrodes or evidence of extrusion. One patient had current leakage from two electrodes, which were switched off, but the pain persisted. INTERVENTION: Both patients received an intratympanic injection of 1 ml of 0.5% Bupivacaine to anaesthetize the tympanic plexus in the middle ear and were then observed for a day, found to have relief of their pain and were able to use the implant with audiological benefit for this short time, until the effect of the anaesthetic had worn off. Therefore we planned and performed a tympanic neurectomy on both patients using CO2 laser. CONCLUSION: Tympanic neurectomy removed the pain in two cochlear implant patients who presented with pain which was present only when the implant was switched on.


Asunto(s)
Implantación Coclear/efectos adversos , Implantes Cocleares/efectos adversos , Desnervación/métodos , Neuralgia/cirugía , Dolor Postoperatorio/cirugía , Oído Medio/inervación , Oído Medio/cirugía , Femenino , Humanos , Lactante , Terapia por Láser/métodos , Masculino , Neuralgia/etiología , Dolor Postoperatorio/etiología , Adulto Joven
3.
Indian J Otolaryngol Head Neck Surg ; 67(Suppl 1): 40-6, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25621252

RESUMEN

To compare the functional results between posterior cordotomy, cordoplasty and external procedure in managing bilateral vocal cord paralysis in one of the largest published study group. Retrospective and comparative study. 54 patients with bilateral vocal cord paralysis who underwent posterior cordotomy (Group-I), cordoplasty (Group-II) and external procedure (Group-III) from 2001 to 2013 were compared for functional outcomes. Successful decannulation was achieved more in Group-I and II than in Group-III. Voice outcome was better in Group-II patients compared to other groups. Outcomes of cordoplasty was better than posterior cordotomy and external procedures, with acceptable airway and good quality of voice. Posterior cordotomy is preferred in patients without tracheostomy and in pediatric patients. In patients with tracheostomy or who accept temporary tracheostomy, a cordoplasty is preferred for favorable voice. External procedure is preferred for patients not fit for general anesthesia.

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