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العنوان
Role of Intra-Tympanic Injection in Different Otological Disorders /
المؤلف
Abas, Nashwa Mohammed Refat.
هيئة الاعداد
باحث / Nashwa Mohammed Refat Abas
مشرف / Essam Abd El- Wanes Behery
مشرف / Enaas Ahmad Kolkaila
مشرف / Heba Abd El- Rehim Abo El- Naga
الموضوع
Pediatric otology - Popular works. Hearing disorders. Middle ear. Audiology.
تاريخ النشر
2012.
عدد الصفحات
108 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
جراحة
تاريخ الإجازة
1/2/2012
مكان الإجازة
جامعة المنوفية - كلية الطب - Audiology
الفهرس
Only 14 pages are availabe for public view

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from 108

Abstract

Many inner ear disorders such as sudden sensori-neural hearing loss, Ménière’s disease, autoimmune inner ear disease and tinnitus cannot be adequately treated by systemic drug delivery.
The clinical usefulness, however, is limited by undesirable side effects of these drugs arising from the high systemic doses required to achieve therapeutic concentration in the cochlea (Erin et al., 2008).
Several methods are available which include direct intra-tympanic perfusion into the middle ear and Micro-Catheters or Micro-Wicks which are placed against the round window (Plontke et al., 2006). Intra-tympanic delivery can be accomplished via perfusion of the middle ear with the goal of diffusion through the round window membrane into the fluid spaces of the inner ear (Erin et al., 2008).
The main advantages of intra-tympanic therapy are the ease of administration, avoidance of surgery, alternative therapy when systemic route is contra-indicated or poorly tolerated, and possible salvage therapy when systemic therapy fails (Doyle et al., 2004).
Advantages of Intra-tympanic steroid therapy: Intra-tympanic steroid perfusion has the advantages of avoiding the systemic side effects associated with oral corticosteroids and delivering high concentrations to the inner ear end organ. Steroids delivered by the intra-tympanic route demonstrate higher concentrations in the perilymph than those administered intravenously. The best profile has been reported for methylprednisolone (Parnes et al., 1999).