Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial
Autor(a) principal: | |
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Data de Publicação: | 2001 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S1516-31802001000500004 http://repositorio.unifesp.br/handle/11600/1245 |
Resumo: | CONTEXT: Budesonide is an inhaled corticosteroid with high topical potency and low systemic activity recommended in the treatment of chronic asthma. OBJECTIVE: This study was conducted to determine the efficacy and safety of inhaled budesonide via a breath-activated, multi-dose, dry-powder inhaler. TYPE OF STUDY: Multicenter randomized parallel-group, placebo-controlled, double-blind, clinical trial. SETTING: Multicenter study in the university units. PARTICIPANTS: Adult patients with mild-to-moderate asthma that was not controlled using bronchodilator therapy alone. PROCEDURES: Comparison of budesonide 400 µg administered twice daily via a breath-activated, multi-dose, dry-powder inhaler with placebo, in 43 adult patients (aged 15 to 78 years) with mild-to-moderate asthma (FEV1 71% of predicted normal) that was not controlled using bronchodilator therapy alone. MAIN MEASUREMENTS: Efficacy was assessed by pulmonary function tests and asthma symptom control (as perceived by the patients) and the use of rescue medication. RESULTS: Budesonide 400 µg (bid) was significantly more effective than placebo in improving morning peak expiratory flow (mean difference: 67.9 l/min; P < 0.005) and FEV1 (mean difference: 0.60 l; P < 0.005) over the 8-week treatment period. Onset of action, assessed by morning peak expiratory flow, occurred within the first two weeks of treatment. CONCLUSIONS: Budesonide via a breath-activated, multi-dose, dry-powder inhaler results in a rapid onset of asthma control, which is maintained over time and is well tolerated in adults with mild-to-moderate asthma. |
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Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trialAsthmaInhaled corticosteroidBudesonideAsmaCorticóide inalatórioBudesonidaCONTEXT: Budesonide is an inhaled corticosteroid with high topical potency and low systemic activity recommended in the treatment of chronic asthma. OBJECTIVE: This study was conducted to determine the efficacy and safety of inhaled budesonide via a breath-activated, multi-dose, dry-powder inhaler. TYPE OF STUDY: Multicenter randomized parallel-group, placebo-controlled, double-blind, clinical trial. SETTING: Multicenter study in the university units. PARTICIPANTS: Adult patients with mild-to-moderate asthma that was not controlled using bronchodilator therapy alone. PROCEDURES: Comparison of budesonide 400 µg administered twice daily via a breath-activated, multi-dose, dry-powder inhaler with placebo, in 43 adult patients (aged 15 to 78 years) with mild-to-moderate asthma (FEV1 71% of predicted normal) that was not controlled using bronchodilator therapy alone. MAIN MEASUREMENTS: Efficacy was assessed by pulmonary function tests and asthma symptom control (as perceived by the patients) and the use of rescue medication. RESULTS: Budesonide 400 µg (bid) was significantly more effective than placebo in improving morning peak expiratory flow (mean difference: 67.9 l/min; P < 0.005) and FEV1 (mean difference: 0.60 l; P < 0.005) over the 8-week treatment period. Onset of action, assessed by morning peak expiratory flow, occurred within the first two weeks of treatment. CONCLUSIONS: Budesonide via a breath-activated, multi-dose, dry-powder inhaler results in a rapid onset of asthma control, which is maintained over time and is well tolerated in adults with mild-to-moderate asthma.CONTEXTO: A budesonida é um corticóide inalatório de alta potência tópica e baixa atividade sistêmica recomendado no tratamento da asma crônica. OBJETIVO: Determinar a eficácia e tolerabilidade da budesonida via um inalador em pó com atividade inspiratória e multidose, comparada com placebo, em pacientes adultos portadores de asma leve ou moderada não-controlados com terapia broncodilatadora. TIPO DE ESTUDO: Estudo randomizado com dois grupos paralelos, duplo-cego, placebo controlado. LOCAL: Estudo multicêntrico em centros universitários. PARTICIPANTES: 43 pacientes adultos (idade entre 15 e 78 anos), portadores de asma leve ou moderada (VEF1 71% do normal previsto) não-controlados com terapia broncodilatadora. PROCEDIMENTOS: Para comparar, com placebo, a eficácia e tolerabilidade de 400 µg de budesonida, administradas duas vezes ao dia, via turbuhaler. VARIÁVEIS ESTUDADAS: A eficácia foi determinada através de testes de função pulmonar, controle dos sintomas de asma e uso de medicação de resgate. RESULTADOS: 400 µg de budesonida duas vezes ao dia foram significantemente mais efetivas que placebo em relação ao aumento do peak expiratory flow matutino (67,9 l/min. p < 0,005) e VEF1 (0,60 l/min., p < 0,05) nas oito semanas de tratamento. CONCLUSÃO: O tratamento com budesonida via um inalador em pó com atividade inspiratória e multidose, em pacientes portadores de asma leve e moderada, é bem tolerado e resulta em rápido e duradouro controle da asma.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Hospital São PauloPontifícia Universidade CatólicaHospital do Servidor Público EstadualUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP, EPM, Hospital São PauloSciELOAssociação Paulista de Medicina - APMUniversidade Federal de São Paulo (UNIFESP)Pontifícia Universidade CatólicaHospital do Servidor Público EstadualFernandes, Ana Luisa Godoy [UNIFESP]Faresin, Sonia Maria [UNIFESP]Amorim, Maria Marta Ferreira [UNIFESP]Fritscher, Carlos CézarPereira, Carlos Alberto de Castro [UNIFESP]Jardim, José Roberto [UNIFESP]2015-06-14T13:29:30Z2015-06-14T13:29:30Z2001-09-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion169-174application/pdfhttp://dx.doi.org/10.1590/S1516-31802001000500004São Paulo Medical Journal. Associação Paulista de Medicina - APM, v. 119, n. 5, p. 169-174, 2001.10.1590/S1516-31802001000500004S1516-31802001000500004.pdf1516-3180S1516-31802001000500004http://repositorio.unifesp.br/handle/11600/1245engSão Paulo Medical Journalinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-30T00:32:26Zoai:repositorio.unifesp.br/:11600/1245Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-30T00:32:26Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
title |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
spellingShingle |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial Fernandes, Ana Luisa Godoy [UNIFESP] Asthma Inhaled corticosteroid Budesonide Asma Corticóide inalatório Budesonida |
title_short |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
title_full |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
title_fullStr |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
title_full_unstemmed |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
title_sort |
Inhaled budesonide for adults with mild-to-moderate asthma: a randomized placebo-controlled, double-blind clinical trial |
author |
Fernandes, Ana Luisa Godoy [UNIFESP] |
author_facet |
Fernandes, Ana Luisa Godoy [UNIFESP] Faresin, Sonia Maria [UNIFESP] Amorim, Maria Marta Ferreira [UNIFESP] Fritscher, Carlos Cézar Pereira, Carlos Alberto de Castro [UNIFESP] Jardim, José Roberto [UNIFESP] |
author_role |
author |
author2 |
Faresin, Sonia Maria [UNIFESP] Amorim, Maria Marta Ferreira [UNIFESP] Fritscher, Carlos Cézar Pereira, Carlos Alberto de Castro [UNIFESP] Jardim, José Roberto [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Pontifícia Universidade Católica Hospital do Servidor Público Estadual |
dc.contributor.author.fl_str_mv |
Fernandes, Ana Luisa Godoy [UNIFESP] Faresin, Sonia Maria [UNIFESP] Amorim, Maria Marta Ferreira [UNIFESP] Fritscher, Carlos Cézar Pereira, Carlos Alberto de Castro [UNIFESP] Jardim, José Roberto [UNIFESP] |
dc.subject.por.fl_str_mv |
Asthma Inhaled corticosteroid Budesonide Asma Corticóide inalatório Budesonida |
topic |
Asthma Inhaled corticosteroid Budesonide Asma Corticóide inalatório Budesonida |
description |
CONTEXT: Budesonide is an inhaled corticosteroid with high topical potency and low systemic activity recommended in the treatment of chronic asthma. OBJECTIVE: This study was conducted to determine the efficacy and safety of inhaled budesonide via a breath-activated, multi-dose, dry-powder inhaler. TYPE OF STUDY: Multicenter randomized parallel-group, placebo-controlled, double-blind, clinical trial. SETTING: Multicenter study in the university units. PARTICIPANTS: Adult patients with mild-to-moderate asthma that was not controlled using bronchodilator therapy alone. PROCEDURES: Comparison of budesonide 400 µg administered twice daily via a breath-activated, multi-dose, dry-powder inhaler with placebo, in 43 adult patients (aged 15 to 78 years) with mild-to-moderate asthma (FEV1 71% of predicted normal) that was not controlled using bronchodilator therapy alone. MAIN MEASUREMENTS: Efficacy was assessed by pulmonary function tests and asthma symptom control (as perceived by the patients) and the use of rescue medication. RESULTS: Budesonide 400 µg (bid) was significantly more effective than placebo in improving morning peak expiratory flow (mean difference: 67.9 l/min; P < 0.005) and FEV1 (mean difference: 0.60 l; P < 0.005) over the 8-week treatment period. Onset of action, assessed by morning peak expiratory flow, occurred within the first two weeks of treatment. CONCLUSIONS: Budesonide via a breath-activated, multi-dose, dry-powder inhaler results in a rapid onset of asthma control, which is maintained over time and is well tolerated in adults with mild-to-moderate asthma. |
publishDate |
2001 |
dc.date.none.fl_str_mv |
2001-09-06 2015-06-14T13:29:30Z 2015-06-14T13:29:30Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S1516-31802001000500004 São Paulo Medical Journal. Associação Paulista de Medicina - APM, v. 119, n. 5, p. 169-174, 2001. 10.1590/S1516-31802001000500004 S1516-31802001000500004.pdf 1516-3180 S1516-31802001000500004 http://repositorio.unifesp.br/handle/11600/1245 |
url |
http://dx.doi.org/10.1590/S1516-31802001000500004 http://repositorio.unifesp.br/handle/11600/1245 |
identifier_str_mv |
São Paulo Medical Journal. Associação Paulista de Medicina - APM, v. 119, n. 5, p. 169-174, 2001. 10.1590/S1516-31802001000500004 S1516-31802001000500004.pdf 1516-3180 S1516-31802001000500004 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
São Paulo Medical Journal |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
169-174 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Paulista de Medicina - APM |
publisher.none.fl_str_mv |
Associação Paulista de Medicina - APM |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268324710711296 |