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Short-acting bronchodilators for the management of acute exacerbations of chronic obstructive pulmonary disease in the hospital setting: systematic review.
Kopsaftis, Zoe A; Sulaiman, Nur S; Mountain, Oliver D; Carson-Chahhoud, Kristin V; Phillips, Paddy A; Smith, Brian J.
Afiliación
  • Kopsaftis ZA; Faculty of Health Science, Division of Medicine, The University of Adelaide, Adelaide, South Australia, Australia. zoe.kopsaftis@adelaide.edu.au.
  • Sulaiman NS; Clinical Practice Unit, The Queen Elizabeth Hospital, Adelaide, South Australia, Australia. zoe.kopsaftis@adelaide.edu.au.
  • Mountain OD; Respiratory Medicine Unit, The Queen Elizabeth Hospital, Central Adelaide Local Health Network, Adelaide, South Australia, Australia. zoe.kopsaftis@adelaide.edu.au.
  • Carson-Chahhoud KV; Clinical Practice Unit, The Queen Elizabeth Hospital, Adelaide, South Australia, Australia.
  • Phillips PA; Faculty of Health Science, Division of Medicine, The University of Adelaide, Adelaide, South Australia, Australia.
  • Smith BJ; Faculty of Health Science, Division of Medicine, The University of Adelaide, Adelaide, South Australia, Australia.
Syst Rev ; 7(1): 213, 2018 11 29.
Article en En | MEDLINE | ID: mdl-30497532
BACKGROUND: Currently, there is a lack of guidelines for the use of short-acting bronchodilators (SABD) in people admitted to hospital for acute exacerbation of chronic obstructive pulmonary disease (AECOPD), despite routine use in practice and risk of cardiac adverse events. AIM: To review the evidence that underpins use and optimal dose, in terms of risk versus benefit, of SABD for inpatient management of AECOPD and collate the results for future guidelines. METHODS: Medline, Embase, the Cochrane Central Register of Controlled Trials, clinicaltrials.gov and International Clinical Trials Registry Platform were searched (inception to November 2017) for published and ongoing studies. Included studies were randomised controlled trials or controlled clinical trials investigating the effect of SABD (ß2-agonist and/or ipratropium) on inpatients with a diagnosis of AECOPD. This review was undertaken in accordance with PRISMA guidelines and a pre-defined protocol. Due to heterogeneous methodologies, meta-analysis was not possible so the results were synthesised qualitatively. RESULTS: Of 1378 studies identified, 10 met inclusion criteria. Narrative synthesis of 10 studies revealed no significant differences in most outcomes of interest relative to dose, delivery via inhaler or nebuliser, and type of ß2-agonist used. However, some evidence demonstrated significantly increased cardiac side effects with increased dosage of ß2-agonist (45% versus 24%), P<0.05). CONCLUSION: This review identified a paucity of methodologically rigorous evidence evaluating use of SABD among AECOPD. The available evidence did not identify any additional benefits for participants receiving higher doses of short-acting ß2-agonists compared to lower doses, or based on type of delivery method or ß2-agonists used. However, there was a small increase in some adverse events for participants using higher doses of ß2-agonists.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adhesión a Directriz / Enfermedad Pulmonar Obstructiva Crónica / Quimioterapia Combinada / Agonistas de Receptores Adrenérgicos beta 2 / Hospitalización Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Syst Rev Año: 2018 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adhesión a Directriz / Enfermedad Pulmonar Obstructiva Crónica / Quimioterapia Combinada / Agonistas de Receptores Adrenérgicos beta 2 / Hospitalización Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Syst Rev Año: 2018 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido