Long-Acting Beta2-Agonist and Inhaled Corticosteroid Combination Therapy for Adult Persistent Asthma: Systematic Review of Clinical Outcomes and Economic Evaluation

Aim: To evaluate the clinical efficacy, safety, and cost effectiveness of long-acting beta2-agonist and inhaled corticosteroid (LABA-ICS) combination therapy for adults (12 years of age or older) diagnosed with persistent asthma.

Conclusions and results: For most patients with persistent asthma, the initial and only therapy needed is inhaled corticosteroid (ICS). The clinical review found statistically important, but not clinically meaningful, benefits from switching to combination therapy in managing most asthma not controlled by ICS. A primary economic analysis from a Canadian perspective found that the later a long-acting beta2-agonist (LABA) is introduced into therapy, the more cost effective the treatment strategy becomes. The analysis suggests that introducing LABA before patients have tried high-dose ICS therapy is not justified.

Recommendations: Not applicable.

Methods: Clinical and economic analyses were conducted. For the clinical analysis, RCTs comparing LABA-ICS with ICS monotherapy or another LABA-ICS combination therapy for managing persistent adult asthma were identified, and meta-analyses were performed when appropriate. For the economic analysis, we conducted a systematic review of economic evaluations comparing the use of LABA-ICS combination therapy with ICS monotherapy in patients (12 years of age or older) with asthma. A Markov model was created to estimate the long-term costs and quality-adjusted life-years (QALYs) associated with four strategies relating to the optimum time to introduce LABA: in combination with ICS as initial therapy; after lack of control on low-dose ICS; after lack of control on medium-dose ICS; or after lack of control on high-dose IC.

Further research/reviews required: More comparative research seems warranted, eg, to provide evidence on potential clinical benefits after using fixed versus variable dosing.

Written by: Bond K, Coyle D, O’Gorman K, Coyle K, Spooner C, Lemière C, Vandermeer B, Tjosvold L, and Rowe BH, CADTH, Canada

INAHTA Brief issue: 2010/001

Agency: CADTH, Canadian Agency for Drugs and Technologies in Health
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Reference:

CADTH Health Technology Report, Issue 122, November 2009. ISBN 978-926680-24-8 (print), ISBN 978-1-926680-25-5 (online)


Other publications:
on Immunologic Diseases
on Respiratory Tract Diseases
from CADTH


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