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1.
HNO ; 72(4): 291-302, 2024 Apr.
Article De | MEDLINE | ID: mdl-38351342

Idiopathic sudden sensorineural hearing loss (ISSNHL) is one of the most common diseases in otolaryngology. Its etiology remains unknown. Furthermore, there is only a low level of evidence for the efficacy of established treatment modalities. In addition to systemic glucocorticoids, intratympanic corticosteroid treatment (ICT) has become increasingly important for treatment of ISSNHL. Different application strategies and treatment regimens have been described; however, uniform standards do not yet exist. ICT may be used for primary treatment as well as salvage therapy. Current data from meta-analyses show no benefit of intratympanic versus systemic primary therapy for sudden hearing loss (moderate evidence) but suggest a benefit of intratympanic secondary treatment over no treatment or placebo (high effect size, low evidence). Regarding combination of systemic and local glucocorticoid therapy in primary treatment of hearing loss, there may be a small benefit over systemic treatment alone (low effect size, low evidence).


Hearing Loss, Sensorineural , Hearing Loss, Sudden , Humans , Glucocorticoids , Hearing Loss, Sudden/diagnosis , Hearing Loss, Sudden/drug therapy , Dexamethasone/therapeutic use , Treatment Outcome , Hearing Loss, Sensorineural/diagnosis , Hearing Loss, Sensorineural/drug therapy , Hearing Loss, Sensorineural/etiology , Adrenal Cortex Hormones/therapeutic use , Injection, Intratympanic , Audiometry, Pure-Tone/adverse effects
2.
PLoS One ; 17(11): e0268863, 2022.
Article En | MEDLINE | ID: mdl-36350807

BACKGROUND: The reprocessing of daily used medical devices is often inadequate, making them a potential source of infection. In addition, there are usually no consistent and technically standardized procedures available for this purpose. Hence, the aim of this study is to analyze the bacterial contamination and the effectiveness of Ultraviolet light-based (UV light-based) reprocessing of daily used medical devices. MATERIAL AND METHODS: Six different everyday medical devices (20 each; stethoscopes, tourniquets, bandage scissors, reflex hammers, tuning forks, and nystagmus glasses) were tested for bacterial contamination. All medical devices were then exposed to UV-C light for 25 seconds. Medical devices with a smooth surface were pre-cleaned with a water-based wipe. Contact samples were taken before and after reprocessing. RESULTS: Immediately after clinical use, 104 of 120 contact samples showed an average bacterial contamination of 44.8±64.3 colony forming units (CFU) (0-300 CFU), also including potentially pathogenic bacteria. Two further culture media were completely overgrown with potentially pathogenic bacteria. The stethoscopes were found to have the highest average contamination of 90±91.6 CFU. After reprocessing, 118 of 120 samples were sterile, resulting in an average residual contamination of 0.02±0.1 CFU in two samples, whereby only bacteria of the ordinary skin flora were found. CONCLUSION: The present study shows the potentially clinically relevant bacterial contamination of everyday used medical devices. The reprocessing method tested here using UV light appears to be a suitable method for disinfection, especially for objects that up to now have been difficult to disinfect or cannot be disinfected in a standardized manner.


Equipment Contamination , Ultraviolet Rays , Equipment Contamination/prevention & control , Disinfection/methods , Bacteria , Drug Contamination
3.
Auris Nasus Larynx ; 45(5): 959-965, 2018 Oct.
Article En | MEDLINE | ID: mdl-29571548

OBJECTIVE: Eustachian tube dysfunction (ETD) affects approximately 1% of adults in the general population. Non treated Eustachian tube dysfunction can result in chronic middle ear diseases, which have been shown to significantly affect taste sensitivity. A promising treatment is balloon dilatation of the Eustachian tube. The primary aim of the present study was to investigate whether individuals with ETD had impairment in chemosensory functions, and the changes of the chemosensory function after balloon dilatation of the Eustachian tube. METHODS: 26 patients (17 female, 9 male) (=56 ears) suffering from ETD with a mean age of 39±15years were included in the present study. 20 patients (76%) returned to be evaluated at the follow up (=40 ears) 51±22days after balloon dilatation. For pre- and post operation, gustatory function was measured with a lateralized gustatory test with the taste strips and olfactory function was tested by means of the Sniffin' Sticks test battery (threshold, discrimination and identification (ID)). RESULTS: Patients' baseline taste function (summed taste score 9.8±3.5 (mean±SD)) was significantly impaired compared to normative data (summed taste score 12.4±2.3; p=0.002). After balloon dilatation of the Eustachian tube, the taste function remained stable (summed taste score 9.4±4.3; p=0.814). Olfactory function (odor ID, summed score (TDI)) improved postoperatively (TDI 32.4±3.6) compared to pre-operative scores (TDI 33.6±4.0; p=0.012), but not to a clinically relevant extent. CONCLUSION: This study suggests, that patients suffering from ETD exhibit reduced taste scores. Balloon dilatation of the Eustachian tube does not seem to influence gustatory function, but olfactory function showed improvement.


Ear Diseases/surgery , Eustachian Tube/surgery , Smell/physiology , Taste/physiology , Adult , Dilatation/methods , Ear Diseases/physiopathology , Eustachian Tube/physiopathology , Female , Humans , Male , Middle Aged , Treatment Outcome , Young Adult
4.
Laryngoscope ; 128(3): E86-E90, 2018 03.
Article En | MEDLINE | ID: mdl-28895150

OBJECTIVES/HYPOTHESIS: Olfactory dysfunction is common among the general population, with chronic rhinosinusitis (CRS) as one of the leading causes. Patients affected by CRS often report changes in taste sensations; however, quantitative measurements have not been performed to date. Therefore, the present study aimed to investigate gustatory and olfactory function in CRS patients prior to and after multimodal treatment. STUDY DESIGN: Prospective cohort study. METHODS: Twenty-one patients suffering from CRS with nasal polyps (14 male, seven female) with a mean age of 48 ± 15 years were included in the study. Chemosensory function was assessed prior to and approximately 190 days after multimodal treatment, which included endoscopic sinus surgery, oral antibiotics for 5 days, oral steroids for 12 days, and at least 6 weeks of topical nasal steroids. Olfactory function was tested with the Sniffin' Sticks test battery, whereas gustatory function was measured with taste strips. A clinically relevant change in olfactory function was defined as a change of ≥5 points in the threshold, discrimination, and identification scores. RESULTS: Compared to normative data, patients baseline gustatory and olfactory function was impaired. After multimodal treatment, improvements were seen in olfactory function for eight patients (42%), remained stable in 10 patients (53%), and deteriorated in one patient (5%). Taste function remained unchanged following sinus surgery. CONCLUSIONS: Patients suffering from CRS with polyps exhibit olfactory and taste dysfunctions. Multimodal treatment leads to an improvement in olfactory, but not gustatory functionality. LEVEL OF EVIDENCE: 4. Laryngoscope, 128:E86-E90, 2018.


Rhinitis/physiopathology , Sinusitis/physiopathology , Smell/physiology , Taste/physiology , Administration, Oral , Administration, Topical , Adult , Anti-Bacterial Agents/administration & dosage , Chronic Disease , Combined Modality Therapy , Endoscopy/methods , Female , Humans , Male , Middle Aged , Nasal Surgical Procedures/methods , Nose , Olfaction Disorders/etiology , Olfaction Disorders/physiopathology , Paranasal Sinuses/physiopathology , Prospective Studies , Rhinitis/complications , Rhinitis/therapy , Sinusitis/complications , Sinusitis/therapy , Steroids/administration & dosage , Taste Disorders/etiology , Taste Disorders/physiopathology , Treatment Outcome
5.
Eur Arch Otorhinolaryngol ; 271(6): 1635-9, 2014 Jun.
Article En | MEDLINE | ID: mdl-24398866

The treatment of diseases of the lingual tonsils is still under debate, and surgical interventions are often associated with significant morbidity and complications. The aim of the present study was to evaluate the safety of lingual tonsillectomy using cold ablation (coblation) as a new treatment of lingual tonsil diseases. In this retrospective, bicentric study, we included all patients between 2005 and 2012 who underwent cold ablation (Coblation(®)) of the lingual tonsils. We assessed the frequency of postoperative complications based on the patients' charts. A total of 108 patients (47 ± 13, 6 years) underwent lingual tonsillectomy using coblation. All patients were operated on under general anesthesia as inpatients. Intraoperative complications did not occur. Three patients (2.8%) needed revision surgery due to postoperative hemorrhage, and in one of those cases, three revisions were necessary. There was no postoperative airway compromise and no need for tracheostomy. There was no hypoglossal nerve paralysis, but in the case needing multiple revisions, a weakness of the hypoglossal nerve persisted. In all the cases, oral intake was possible with adequate analgesia. Coblation of the tongue base is a safe procedure with a relatively low rate of postoperative complications. Postoperative hemorrhage is the most relevant complication that occurred in our series of patients. Future studies are needed to evaluate the efficacy of the procedure in the treatment of obstructive sleep apnea.


Ablation Techniques/methods , Palatine Tonsil/surgery , Postoperative Hemorrhage/surgery , Sleep Apnea, Obstructive/surgery , Adult , Cohort Studies , Female , Humans , Hypertrophy/complications , Hypertrophy/surgery , Male , Middle Aged , Palatine Tonsil/pathology , Postoperative Complications , Reoperation , Retrospective Studies , Sleep Apnea, Obstructive/etiology , Tongue , Tonsillectomy/methods , Treatment Outcome
6.
Curr Opin Allergy Clin Immunol ; 3(1): 21-7, 2003 Feb.
Article En | MEDLINE | ID: mdl-12582310

PURPOSE OF REVIEW: The increasing prevalence of allergic rhinitis, its impact on individual quality of life and social costs, as well as its role as a risk factor for asthma, underline the need for improved treatment options for this disorder. We reviewed the recent literature published in English, dealing with relevant and appropriately controlled clinical trials on the treatment of allergic rhinitis. RECENT FINDINGS: In addition to well established pharmacological therapies with antihistamines, corticosteroids, decongestants and mast cell stabilizers, new therapeutic options become increasingly important, including leukotriene modifiers, anti-immunoglobulin E antibodies, phosphodiesterase inhibitors and intranasal heparin; there also exist new developments in appropriate allergen specific immunotherapy. SUMMARY: Promising results, both with established and novel treatment options, are communicated, but further studies are still necessary to confirm these data.


Rhinitis, Allergic, Perennial/drug therapy , Rhinitis, Allergic, Perennial/therapy , Administration, Intranasal , Antibodies/therapeutic use , Desensitization, Immunologic , Heparin/therapeutic use , Humans , Immunoglobulin E/immunology , Leukotriene Antagonists/therapeutic use , Phosphodiesterase Inhibitors/therapeutic use
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