نمایش مختصر رکورد

dc.contributor.authorJamali, Sen_US
dc.contributor.authorSabermoghaddam, Men_US
dc.contributor.authorSabermoghaddam, AAen_US
dc.contributor.authorKiarudi, MYen_US
dc.contributor.authorBakhtiari, Een_US
dc.date.accessioned1401-12-09T23:22:00Zfa_IR
dc.date.accessioned2023-02-28T23:22:00Z
dc.date.available1401-12-09T23:22:00Zfa_IR
dc.date.available2023-02-28T23:22:00Z
dc.date.issued2023-03-01en_US
dc.date.issued1401-12-10fa_IR
dc.identifier.citation(1401). مجله علمی دانشگاه علوم پزشکی بابل, 25(1), 78-87.fa_IR
dc.identifier.issn1561-4107
dc.identifier.issn2251-7170
dc.identifier.urihttp://jbums.org/article-1-10727-en.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/941218
dc.description.abstractBackground and Objective: It is very important and necessary to use certain methods in order to prevent or reduce the intensity of pain after surgery. Of all known methods, those that avoid the dangerous side effects of opioids or nonsteroidal anti-inflammatory drugs (NSAIDs) can be useful. The present study was conducted with the aim of investigating the effect of topical dexamethasone on postoperative pain intensity in patients undergoing dacryocystorhinostomy (DCR). Methods: This double-blind randomized clinical trial was conducted on 80 patients aged 18-75 who were candidates for DCR and referred to Khatam Al-Anbia Hospital in Mashhad. Patients were randomly divided into control and intervention (dexamethasone) groups. In the intervention group, at the end of the procedure, a tampon impregnated with dexamethasone was placed in the upper part of the middle concha. In the control group, a tampon washed in distilled water was placed in the same place. Pain intensity was recorded on a verbal rating scale (VRS) 0, 3, 6, 12, 18 and 24 hours after the operation. Findings: There was no significant difference in pain intensity at different time points in the two groups of intervention and control; the frequency of severe pain during recovery was equal to 22.5% and 15.7%, within 3 hours after the operation was equal to 17.5% and 10.0%, within 6 hours after the operation was equal to 12.5% and 0.5%, within 12 hours after the operation was equal to 12.5% and 2.5%, within 18 hours after the operation was equal to 0% and 2.5% and within 24 hours after the operation was equal to 0% and 0%, respectively. There was no significant difference in the process of changes in pain intensity during the 24 hours of the study based on the follow-up test. Conclusion: The results of the study showed that topical use of a single dose of dexamethasone (8 mg) could not reduce postoperative pain as well as the need for opioids in DCR surgery.en_US
dc.format.extent434
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherدانشگاه علوم پزشکی بابلfa_IR
dc.relation.ispartofمجله علمی دانشگاه علوم پزشکی بابلfa_IR
dc.relation.ispartofJournal of Babol University Of Medical Sciencesen_US
dc.subjectDacryocystorhinostomyen_US
dc.subjectDexamethasoneen_US
dc.subjectPainen_US
dc.subjectRandomized Clinical Trialen_US
dc.subjectVerbal Rating Scale.en_US
dc.subjectsurgeryen_US
dc.titleThe Effect of Topical Dexamethasone on Postoperative Pain Intensity in Patients Undergoing Dacryocystorhinostomy Procedureen_US
dc.typeTexten_US
dc.typeResearchen_US
dc.contributor.department1.Eye Research Center, Mashhad University of Medical Sciences, Mashhad, I.R.Iran.en_US
dc.contributor.department2.Department of Anesthesiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, I.R.Iran.en_US
dc.contributor.department1.Eye Research Center, Mashhad University of Medical Sciences, Mashhad, I.R.Iran.en_US
dc.contributor.department1.Eye Research Center, Mashhad University of Medical Sciences, Mashhad, I.R.Iran.en_US
dc.contributor.department1.Eye Research Center, Mashhad University of Medical Sciences, Mashhad, I.R.Iran.en_US
dc.citation.volume25
dc.citation.issue1
dc.citation.spage78
dc.citation.epage87


فایل‌های این مورد

Thumbnail

این مورد در مجموعه‌های زیر وجود دارد:

نمایش مختصر رکورد