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dc.contributor.authorSapd, Tarik
dc.contributor.authorYazici, Sara
dc.contributor.authorEvcimik, M. Fatih
dc.contributor.authorBozkurt, Ziya
dc.contributor.authorKaravus, Ahmet
dc.contributor.authorUgurlu, Bayram
dc.contributor.authorOzkurt, Emre
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:05:25Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:05:25Z
dc.date.issued2008
dc.identifier.issn0300-0729
dc.identifier.urihttp://hdl.handle.net/11446/3486
dc.descriptionWOS: 000254852800008en_US
dc.descriptionPubMed ID: 18444492en_US
dc.description.abstractIdiopathic rhinitis without eosinophilia is a group of frequently observed diseases, the aetiopathogenesis of which is not yet well known. One of the most disturbing symptoms for patients within this disease group is nasal hypersecretion. Although many different treatments have been tried for hypersecretion, nasal topical drugs form the basis of any such therapy today. Ipratropium bromide (IB) is a drug of first choice in nasal hypersecretion therapy. It displays a parasympatholytic effect in topical use and antagonizes acetylcholine transport in efferent parasympathetic nerves, thus decreasing submucosal gland secretion, which is the cause of hypersecretion. Botulinum toxin type A (BTX-A) is among the alternative treatment choices that is increasingly used in symptomatic treatment of nasal hypersecretion. Our study was planned with the aim of comparing the effect of these two groups of drugs on nasal hypersecretion. Thirty-eight patients who were diagnosed with idiopathic rhinitis without eosinophilia were included in the study and were divided in 3 different groups: In the first group, a total of 10 units of BTX-A were injected into both nasal cavities. In the second group, 3x2 18 was injected into both nasal cavities for 4 weeks. The third group received intranasal physiologic saline as placebo. The patients were evaluated in terms of nasal hypersecretion with visual analogue scale prior to the treatment and at weeks 1, 2, 4, 8, and 12 during the follow-up period. Throughout the 8 weeks follow-up period, the patient complaints displayed a 41.2% decrease in the group that received BTX-A and a 61.4% decrease in the group which received IB, while no change was observed in the control group. Both drug groups were well tolerated by the patients, with no serious adverse or systemic effects. As a result, while IB and BTX-A differ in terms of method of application, they display a similar degree and duration of efficiency in hypersecretion therapy.en_US
dc.language.isoengen_US
dc.publisherINT RHINOLOGIC SOCen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectbotulinum toxinen_US
dc.subjectipratropium bromideen_US
dc.subjectidiopathic rhinitis without eosinophiliaen_US
dc.subjectsecretionen_US
dc.subjecthypersecretionen_US
dc.titleInvestigation of the effects of intranasal botulinum toxin type a and ipratropium bromide nasal spray on nasal hypersecretion in idiopathic rhinitis without eosinophiliaen_US
dc.typearticleen_US
dc.relation.journalRHINOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue1en_US
dc.identifier.volume46en_US
dc.identifier.startpage45en_US
dc.identifier.endpage51en_US
dc.contributor.authorID0000-0003-0606-864Xen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Yazici, Sara -- Evcimik, M. Fatih -- Bozkurt, Ziya -- Karavus, Ahmet -- Ugurlu, Bayram -- Ozkurt, Emre] Fatih Sultan Mehmet Training & Res Hosp, Dept Otorhinolaryngol Head & Neck Surg, TR-34752 Istanbul, Turkey -- [Sapd, Tarik] Istanbul Bilim Univ, Fac Med, Dept Otorhinolaryngol, Istanbul, Turkeyen_US


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