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Sudden onset hearing loss unilateral,was tun gegen pl?tzlichen tinnitus,ringing in ears caused by tylenol overdose,tinnitus one ear tmj pain - Good Point

Author: admin | 07.10.2013 | Category: Treatment For Ear Ringing

Idiopathic sudden sensorineural hearing loss is a medical emergency that requires urgent diagnosis and treatment, and the adaptation of a proper protocol for management is a priority. Idiopathic sudden sensorineural hearing loss (ISSNHL) [1] is a well-known clinical condition characterized by a sudden occurrence in one or both ears of sensorineural hearing loss of more than 30 dB in at least three contiguous audiometric frequencies over a time course of no more than 72 hours.
Hearing impairment is a common problem worldwide and even more problematic in developing countries. Sensorineural hearing loss [4-9] (or nerve-related deafness) involves damage to the ear caused by aging, prenatal and birth-related problems, viral and bacterial infections, heredity, trauma, exposure to loud noise, fluid backup, or tumor in the inner ear. This retrospective study was conducted from January 2002 to December 2003 to identify patients with ISSNHL. We found no age relation or significant side predilection, and the duration of improvement was variable, extending from less than 1 week to up to 6 weeks. The prognosis of tinnitus involved full recovery in all but one of the grade 4 patients; the unrecovered patient had at 8 kHz a dip that did not improve. All but three patients who developed dizziness (those with very severe hearing loss) had fully recovered in a few days; the unrecovered group had dizzy spells that lasted more than a few days. ISSNHL is a symptom of cochlear injury and is characterized by sudden onset; within a few hours, it reaches its maximum peak.
Although called sudden, hearing loss seems unlikely to be abrupt but rather probably evolves over a few hours [6].
Research conducted by the Institute of Audiology in Turin documented that 5,925 cases were diagnosed over a 5-year period (1990-1995) [7]. Many causes can trigger sudden hearing loss [6-10] but, despite extensive evaluation, the majority of cases elude definitive diagnosis and, therefore, remain idiopathic.
Our study revealed that the treatment protocol involving steroid therapy in Qatar resulted in hearing improvement in 57.4% of patients with ISSNHL. Redness, pain in the eyes and extreme sensitivity to bright light or photophobia are some of the other ocular symptoms of Cogan’s syndrome. Hearing loss which is often bilateral in nature progresses to complete deafness, within two years of the initial onset of this condition.
Dysfunction of the vestibuloauditory system due to inflammation of the delicate tissues which line the inner ear is primarily responsible for vertigo. Blood vessel inflammation, which is  common among patients suffering from this rare immune disorder, can also cause vertigo.
Young children are usually diagnosed with Cogan’s syndrome when they experience difficulty in holding their balance.
Photophobia along with severe vertigo can cause individuals suffering form Cogan’s syndrome to experience nausea.
Myalgia, anthralgia, fever and chills are some of the other non specific symptoms of Cogan’s syndrome. Management of Idiopathic Sudden Sensorineural Hearing Loss: Experience in Newly Developing Qatar. A report prepared by the Department of Otolaryngology [3] at University of Texas Medical Branch documented approximately 15,000 reported cases of ISSNHL per year worldwide, with 4,000 of those cases occurring in the United States. Therefore, we have a pressing need to study the causes of ISSNHL and suggest a treatment protocol for ISSNHL. Of the studied subjects, 81% were male and 19% were female (median age, 43 years; range, 24-67 years). Of the seven patients (33.3%) who showed no improvement in their hearing both audiologically and clinically (grade 1), six patients had dizzy spells when first seen, four had audiometric HTLs of 65 dB or no response at 8 kHz, five had high-frequency sloping audiometric curves, and all showed no improvement at 6 weeks' duration. Incidentally that patient developed recurrence of hearing loss 12 week later but in the opposite ear, which was also treated with steroid therapy and showed remarkable improvement.
ISSNHL is the most intractable of hearing loss types, because its fundamental cause is hair cell death.


The researchers concluded that sudden idiopathic hearing loss, often attributed to general vascular causes, was one of the most frequent reasons for monolateral hearing loss. Furthermore, we concluded that results can be improved if the disorder is diagnosed early in patients using proper protocols and if early treatment is undertaken. Department of Medical Statistics and Epidemiology, Hamad General Hospital and Hamad Medical Corporation, Doha, Qatar. This disorder which affects young adults (between the ages of 20 and 30) is typified by vestibuloauditory dysfunction and interstitial keratitis.
Cogan, described for the very first time the specific symptoms of this serious inflammatory disorder. Individuals who suffer from this particular inflammatory disorder may experience progressive loss of vision. Photophobia which is a common symptom of Cogan’s disorder can trigger massive migraine headaches. Initially a person who is suffering from this rare inflammatory disorder may experience mild to moderate loss of hearing. Adopting an aggressive treatment strategy is the best and probably the only way to avoid profound deafness among Cogan’s syndrome patients.
Vertigo, which is different from dizziness, is basically a feeling that objects in an individual’s immediate environment are moving or spinning uncontrollably. Once again the onset of acute nausea among Cogan’s syndrome patients is linked to vestibulo-auditory dysfunction. The aim of this study was to determine and identify as early as possible those factors that play the important role in the prognosis of the condition, to describe the experience, and to suggest a treatment protocol that can be adopted in a tertiary hospital, such as Hamad General Hospital. Because of its various etiological possibilities and its prognostic characteristics, urgent attention and treatment are required, and the condition may be considered as an emergency. One in every 10,000- 15,000 people experience this condition, with the highest incidence occurring between 50 and 60 years of age. The prevalence of hearing loss increases with age; most hearing losses develop over a period of 25-30 years.
The aim of this study was to identify patients with ISSNHL as early as possible, to describe their experience, and to suggest a treatment protocol that can be adopted in a tertiary hospital, such as Hamad General Hospital. Tympanometry showed a type-A curve in all patients, and acoustic reflex results were negative in the affected ear in 13 patients. Spectacular advances have recently been made in our understanding of hair cell physiology and molecular biology, offering new hope of alleviating ISSNHL [10]. Also, we observed in our study that most patients who had ISSNHL ranged in age from 40 to 60 years, although the highest rate was found among men.
Monolateral sensorineural hearing loss, which is not seriously disabling, represents a handicap from the social point of view. The degree of hearing loss may vary from mild to severe and may involve different parts of the hearing frequency range.
Suggested causes of ISSNHL include viral infections, immunologic vascular compromise, and intracochlear membrane breaks. Samson, Department of Epidemiology and Medical Statistics, Hamad Medical Cor poration, for her kind help in preparing and typing the manuscript. Sudden hearing loss due to large vestibular aqueduct syndrome in a child: Should exploratory tympanotomy be performed? The excessive inflammation in the eyes and the ears, which is a hallmark of this disorder, is due to the immune system launching an attack on the delicate tissues that line the inner eyes and the ears.
Besides affecting eyesight and auditory functions, Cogan’s syndrome can also cause major organ damage due to inflammation of the blood vessels.


However, because of controversies regarding etiology and the need for urgent treatment, various diagnosis and treatment protocols were advocated by different centers.
Many hypotheses have been advanced to explain its etiology: viral inflammation, vascular diseases, allergic reaction, rupture of intralabyrinthine membranes, and autoimmune diseases.
Audiological evaluation, including pure-tone audiometry, tympanometry, speech audiometry, and auditory brainstem-evoked response testing results were included.
All patients except one had unilateral ear involvement and revealed almost equal frequency of involvement for both left and right ears. Only three patients had speech audiometry and, for auditory brainstem response, results in nine patients were normal except for decreased HTL.
Six patients of the grade 4 group had flat, basin-shaped or up-turning audiometric curves (Fig. We observed in our study that some of the causes of sudden or fluctuating sensorineural hearing loss were meningitis, multiple sclerosis, or Friedreich's ataxia. People who have started to lose weight all of a sudden should get themselves checked for this dangerous immune disorder. The severity of balance problems in an individual suffering from Cogan’s disorder depends on the extent of the disease condition. It was conducted in the ear, nose, and throat outpatient clinics at Hamad General Hospital and the ear, nose, and throat wards at Rumailah Hospital. Recently, increasing interest is centered on the means of diagnosis and treatment, leading to the emergence of quite a variety of protocols adopted by different treatment centers. With respect to laboratory investigations, results of complete blood cell count, erythrocyte sedimentation rate, blood film for abnormal cells, and coagulation screening were normal in all patients. This lack of co-ordination among patients suffering from Cogan’s syndrome increases their risk of suffering falls.
Many studies have been carried out to assess the histopathology of the labyrinth in cases of ISSNHL and to provide a better understanding of the etiopathogenesis [10]. In ten of the twelve patients who showed improvement, the duration of onset was less than 14 days and was less than 7 days in six of eight patients in grade 4. The incidence of tinnitus compares well with that in the literature [11,12]; however, tinnitus did not assist well in determining which patients would suffer hearing loss.
In all the studied cases, patients had an intact tympanic membrane and revealed no other ear, nose, and throat abnormality.
The treatment protocol that was adopted-consisting of high-dose steroid therapy, full-dose antiviral drug (acyclovir), and a histamine analog, betahistine-resulted in hearing improvement in 57.4% of cases.
Finally, most causes of ISSNHL remain unknown; thus the term idiopathic is applied to these cases. In respect to the duration of illness, 33.3% of the studied patients had the complaint for 2 weeks, and 19% had it for more than 4 weeks. However, a high incidence of associated dizziness may be responsible for poor recovery incidence in our series, so it can be considered to indicate a poor prognosis [13-15]. The results of our study revealed that the steroid therapy protocol practiced in Qatar resulted in hearing improvement in patients with idiopathic sudden sensorineural hearing loss. Good prognostic factors include early diagnosis, marked reduction of symptoms, and improved shape of the audiometric curve.



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