Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/128108
Campo DC | Valor | idioma |
---|---|---|
dc.contributor.author | Bateman, E.D. | en_US |
dc.contributor.author | Britton, M. | en_US |
dc.contributor.author | Carrillo Díaz, Teresa | en_US |
dc.contributor.author | Almeida, A. | en_US |
dc.contributor.author | Wixon, C. | en_US |
dc.date.accessioned | 2023-12-22T15:17:36Z | - |
dc.date.available | 2023-12-22T15:17:36Z | - |
dc.date.issued | 1998 | en_US |
dc.identifier.issn | 1179-1918 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/128108 | - |
dc.description.abstract | Objective: The efficacy and tolerability of a new combination inhaler containing both salmeterol 50μg and fluticasone 100μg in a single device was compared with the delivery of the two drugs via two separate inhalers in a multicentre, double-blind, double-dummy study. Patients: 244 symptomatic asthma patients (age range 12 to 78 years) were randomised to a 12-week treatment period with either salmeterol/fluticasone (50/100μg twice daily) via a single inhaler (combination) and placebo twice daily via another, or salmeterol 50μg twice daily via one inhaler and fluticasone 100μg twice daily via another (concurrent). Results: Morning peak expiratory flow rate (PEFR), symptoms and tolerability were collected throughout the treatment period. Adjusted mean improvements in morning PEFR were 42 and 33 L/min for combination and concurrent therapies, respectively, over the 12-week treatment period. Adjusted mean improvements in forced expiratory volume in 1 second (FEV1) from baseline at week 12 were 0.20 and 0.17L for combination and concurrent therapies, respectively. 60% of patients receiving combination inhaler and 64% of those receiving concurrent therapy had a mean daytime symptom score of zero over the treatment period compared with 17 and 15%, respectively, at baseline. Both treatments were well tolerated. Geometric mean morning serum cortisol levels were similar and no differences in the frequency of abnormal results were noted between the two groups. Conclusion: This was the first study reporting the control of asthma by administration of salmeterol and fluticasone in combination via a single inhaler. The new combination inhaler was as effective and well tolerated as the two drugs administered individually and has potential advantages in terms of convenience. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Clinical Drug Investigation | en_US |
dc.source | Clinical Drug Investigation [1179-1918], v. 16, pp. 193-201 (Septiembre 1998) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.title | A Salmeterol/Fluticasone Combination. A new effective and well tolerated treatment of Asthma | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.type | Article | en_US |
dc.description.lastpage | 201 | en_US |
dc.description.firstpage | 193 | en_US |
dc.relation.volume | 16 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 9 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Septiembre 1998 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.jcr | 0,71 | |
dc.description.jcrq | Q3 | |
dc.description.scie | SCIE | |
item.grantfulltext | open | - |
item.fulltext | Con texto completo | - |
crisitem.author.dept | GIR IUIBS: Patología y Tecnología médica | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0002-3047-8908 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.fullName | Carrillo Díaz, Teresa | - |
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