Publication:
Clinical effectiveness of nebulised budesonide in the treatment of acute asthma attacks

dc.contributor.buuauthorEdiger, Dane
dc.contributor.buuauthorCOŞKUN, NECMİYE FUNDA
dc.contributor.buuauthorEDİGER, DANE
dc.contributor.buuauthorCoskun, Funda
dc.contributor.buuauthorKunt Uzaslan, Esra
dc.contributor.buuauthorGürdal Yüksel, Eser
dc.contributor.buuauthorEge, Ercüment
dc.contributor.buuauthorGözü, Oktay
dc.contributor.buuauthorKaradag, Mehmet
dc.contributor.buuauthorKARADAĞ, MEHMET
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Göğüs Hastalıkları Anabilim Dalı.
dc.contributor.orcid0000-0002-2954-4293
dc.contributor.orcid0000-0003-3604-8826
dc.contributor.orcid0000-0002-9027-1132
dc.contributor.researcheridAAG-8744-2021
dc.contributor.researcheridAAD-1271-2019
dc.contributor.researcheridAAE-9142-2019
dc.date.accessioned2024-10-08T05:25:33Z
dc.date.available2024-10-08T05:25:33Z
dc.date.issued2006-01-01
dc.description.abstractNebulized budesonide (NB) might offer topical anti-inflammatory activity and be an alternative to systemic corticosteroid (SC) in the treatment of acute asthma. The aim of this study was to compare the effect of NB with SC on lung function and clinical findings of adult patients with acute asthma. Thirty patients admitted to clinic with asthma attack (F/M:26/4; mean age: 47.1 +/- 2.1 years) were enrolled to the study. The patients were randomized into three groups; Group I were treated with NB alone (4 mg/day), Group II SC alone (1 mg/kg/day methylprednisolone), Group III NB plus SC. Pulmonary functions and respiratory symptom scores were measured and recorded before and during 7 days of study. Spirometric parameters significantly improved in all groups at 7th day significantly (p< 0.05) without a difference among groups (p> 0.05). FEV 1 % levels increased significantly at the first day of study in Group I and III (p< 0.05), but didn't change in Group II until 5th day of study. The mean symptom scores decreased significantly at the second day in Group I (p< 0.05), and at the 4th day in other groups. NB with or without SC improved successfully airway obstruction and symptoms in patients hospitalized with acute asthma attack as the 1st treatment day in comparison with SC alone and this effect lasted for 7 days. Regarding the superior safety profile and comparable efficacy with SC, NB might be an alternative to the patients with moderate-severe asthma attacks.
dc.identifier.endpage136
dc.identifier.issn0494-1373
dc.identifier.issue2
dc.identifier.startpage128
dc.identifier.urihttps://hdl.handle.net/11452/46014
dc.identifier.volume54
dc.identifier.wos000421208200004
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherTurkish Assoc Tuberculosis & Thorax
dc.relation.journalTuberkuloz Ve Torak-tuberculosis And Thorax
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.subjectInhalation suspension
dc.subjectInhaled budesonide
dc.subjectOral prednisolone
dc.subjectExacerbations
dc.subjectInfants
dc.subjectCorticosteroids
dc.subjectBudesonide
dc.subjectNebulized
dc.subjectSystemic corticosteroid
dc.subjectAsthma attack
dc.subjectEfficacy
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectRespiratory system
dc.titleClinical effectiveness of nebulised budesonide in the treatment of acute asthma attacks
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationea25ddfe-3514-411c-8862-e891b0cd651b
relation.isAuthorOfPublication061153e8-bbd9-4c2a-97f6-dc51171a1143
relation.isAuthorOfPublicationd7720460-3eae-413a-9ffc-16d206d8b896
relation.isAuthorOfPublication.latestForDiscoveryea25ddfe-3514-411c-8862-e891b0cd651b

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