Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4222
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dc.contributor.authorKapti, Hasan Burhanettin-
dc.contributor.authorKorkmaz, Hakan-
dc.date.accessioned2024-03-15T08:28:58Z-
dc.date.available2024-03-15T08:28:58Z-
dc.date.issued2022-
dc.identifier.citationKapti, HB., Korkmaz, H. (2022). Evaluation of the efficacy of postoperative triamcinolone in endoscopic dacryocystorhinostomy using lacrimal symptom questionnaire. Int. Ophthalmol., 42(8), 2573-2580. https://doi.org/10.1007/s10792-022-02305-6en_US
dc.identifier.issn0165-5701-
dc.identifier.issn1573-2630-
dc.identifier.urihttp://dx.doi.org/10.1007/s10792-022-02305-6-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:000782219600006-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4222-
dc.descriptionWoS Categories: Ophthalmologyen_US
dc.descriptionWeb of Science Index: Science Citation Index Expanded (SCI-EXPANDED)en_US
dc.descriptionResearch Areas: Ophthalmologyen_US
dc.description.abstractPurpose To evaluate the effect of postoperative nasal triamcinolone spray use in primary endoscopic dacryocystorhinostomy using The Lacrimal Symptom Questionnaire. Methods This study included a series of 50 consecutive retrospective cases with primary endoscopic dacryocystorhinostomy and with silicone stent implantation who were followed up for 6 months postoperatively. Patients using nasal triamcinolone spray for 3 months postoperatively were included in the triamcinolone group. Patients not using triamcinolone were included in the control group. Lacrimal stents were removed 3 months postoperatively. The Lacrimal Symptom Questionnaire (Lac-Q) was performed in the preoperative and postoperative 6th month. Anatomical success, functional success, and changes in lacrimal symptom and social impact scores were compared between the two groups 6 months after surgery. Results Results of 48 endoscopic dacryocystorhinostomies performed on 48 patients (23 triamcinolone group, 25 control group) meeting the inclusion criteria were analyzed. The anatomical success rate (95.7% vs. 84.0%, p = 0.350) and the functional success rate (91.3% vs. 76.0%, p = 0.249) were higher in the triamcinolone group, but this difference was not statistically significant. No complications were observed in the triamcinolone group, whereas complications developed in two patients in the control group (p = 0.490). The mean change in total lac-Q score was 11.0 in the triamcinolone group and 9.0 in the control group (p = 0.011). The mean change in social impact score was 4.0 in the triamcinolone group and 3.0 in the control group (p = 0.005). Mean change in lacrimal symptom score was 6.0 in the triamcinolone group and 6.0 in the control group (p = 0.368) Conclusions Our study indicated that postoperative use of triamcinolone spray increases the success rate of endoscopic dacryocystorhinostomy and also revealed that triamcinolone may also lead to greater improvement in quality of life scores than the control group using a validated questionnaire.en_US
dc.language.isoengen_US
dc.publisherSPRINGER-DORDRECHTen_US
dc.relation.isversionof10.1007/s10792-022-02305-6en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectTriamcinolone, Endoscopic, Dacryocystorhinostomy, Lacrimal symptom questionnaireen_US
dc.subjectOSTIUM GRANULOMAS, SINUS SURGERY, DOUBLE-BLIND, OUTCOMES, POLYPOSISen_US
dc.titleEvaluation of the efficacy of postoperative triamcinolone in endoscopic dacryocystorhinostomy using lacrimal symptom questionnaireen_US
dc.typearticleen_US
dc.relation.journalINTERNATIONAL OPHTHALMOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-3960-654Xen_US
dc.identifier.volume42en_US
dc.identifier.issue8en_US
dc.identifier.startpage2573en_US
dc.identifier.endpage2580en_US
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