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dc.contributor.authorSoy, Fatih
dc.contributor.authorÖzbay, Can
dc.contributor.authorKulduk, Erkan
dc.contributor.authorDündar, Rıza
dc.contributor.authorYazıcı, Haşmet
dc.contributor.authorSakarya, Engin
dc.date.accessioned2019-10-17T07:55:33Z
dc.date.available2019-10-17T07:55:33Z
dc.date.issued2015en_US
dc.identifier.issn0165-5876
dc.identifier.issn1872-8464
dc.identifier.urihttps://doi.org/10.1016/j.ijporl.2015.04.039
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7779
dc.descriptionYazıcı, Haşmet (Balikesir Author)en_US
dc.description.abstractObjectives: To demonstrate the effects of various cerumenolytic solutions in vivo and in vitro and to measure the change in pain following treatment. Methods: The study was done as a single-centre, prospective and double-blind study. Among 1243 paediatric patients with total or nearly total occlusive plug in 4 years period, those who accepted endoscopic ear examination and cleaning via aspiration after a follow-up period of at least 10 days following treatment were included in the study. Day of total TM visualisation was noted and removal coefficient was calculated. The pre and post-treatment pain levels of the patients were assessed using analogue chromatic continuous scale (ACCS). In the in vitro part, cerumen samples collected at equal amounts from 20 patients were treated at 36400 C in 6 different tubes with the same solutions and their dissolution degrees were assessed over a period of 5 days (Hour 6, Hour 12, Hour 48, Hour 72, Hour 92, Hour 120). Additionally, the degree of resolution in the tube treated with distilled water was considered to be the control reference. Results: In the in vivo part of the study, total TM visualisation was observed in Group 1 at 50.2% (Day 3), in Group at 57.1%, in Group at 62.3%, in Group at 44.3% and in Group Sat 73.5%. The group with the lowest removal co-efficient was Group 5 (removal co-efficient = 1.623). In reference to the ACCS pain scores of the patients, the intra-group change pre-post treatment was found statistically significant for all groups (p = 0.008; p = 0.0222; p = 0.005; p = 0.026; p = 0.018). After statistical analysis between the groups the difference between Group 5 and other groups was found statistically significant (p = 0.002; p = 0.026; p = 0.044; p = 0.034). In the in vitro part of the study, the best dissolution was observed in Group 2. Conclusions: In our study, the best cerumenolytic solutions were identified to be glycerine 10 cc + 3% hydrogen peroxide 10 cc + 10% sodium bicarbonate 10 cc + distilled water 10 cc. Especially the use of this mixture ease in terms of pain for the patient and in terms of time and comfort for the physician during the removal procedure.en_US
dc.language.isoengen_US
dc.publisherElsevier Ireland Ltden_US
dc.relation.isversionof10.1016/j.ijporl.2015.04.039en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectEar Waxen_US
dc.subjectCerumenen_US
dc.subjectCerumenolyticsen_US
dc.subjectAnalogue Chromatic Continuous Scale ACSSen_US
dc.titleA new approach for cerumenolytic treatment in children: In vivo and in vitro studyen_US
dc.typearticleen_US
dc.relation.journalInternational Journal of Pediatric Otorhinolaryngologyen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0002-3469-2653en_US
dc.identifier.volume79en_US
dc.identifier.issue7en_US
dc.identifier.startpage1096en_US
dc.identifier.endpage1100en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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