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Review Article |

Long-Acting β2-Agonist Step-off in Patients With Controlled Asthma:  Systematic Review With Meta-analysis

Jan L. Brozek, MD, PhD; Monica Kraft, MD; Jerry A. Krishnan, MD, PhD; Michelle M. Cloutier, MD; Stephen C. Lazarus, MD; James T. Li, MD, PhD; Nancy Santesso, RD, MLIS; Robert C. Strunk, MD; Thomas B. Casale, MD
Arch Intern Med. 2012;172(18):1365-1375. doi:10.1001/archinternmed.2012.3250.
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Background  Because of concerns about the safety of long-acting β2-agonist (LABA) use in patients with asthma, withdrawal of the LABA is recommended by the US Food and Drug Administration once asthma is controlled by combination therapy with a LABA and inhaled corticosteroid (ICS).

Objective  To perform a systematic review and meta-analysis assessing evidence supporting the discontinuation of LABA therapy once asthma control has been achieved with a combination of ICS and LABA.

Data Sources  MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials databases were searched (through August 2010), references of identified studies and selected narrative review articles were evaluated, registries of clinical trials were reviewed, and manufacturers of LABAs were contacted.

Study Selection  Randomized controlled trials of discontinuation of LABA therapy in patients with asthma controlled with a combination of ICS and LABA.

Data Extraction  Two reviewers independently screened each title and abstract in the initial searches and then the full text of each nominated article to extract data for analyses.

Results  Of 1492 screened articles, only 5 trials involving patients aged 15 years or older fulfilled a priori–specified inclusion criteria. Results did not favor the LABA step-off approach compared with no change in treatment. The LABA step-off regimen increased asthma impairment, with worse Asthma Quality of Life Questionnaire score (mean difference [95% CI], 0.32 [0.14-0.51] points lower); worse Asthma Control Questionnaire score (0.24 [0.13-0.35] points higher); fewer symptom-free days (9.15% [1.62%-16.69%] less); and greater risk of withdrawal from study resulting from lack of efficacy or loss of asthma control (risk ratio, 3.27 [2.16-4.96]). Risk of exacerbations and deaths after LABA step-off were not evaluable because of the small number of events and short duration of follow-up.

Conclusions  Evidence suggests that discontinuing LABA therapy in adults and older children with asthma controlled with a combination of ICSs and LABAs results in increased asthma-associated impairment. Additional trials measuring all long-term patient-important outcomes are needed.

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Figures

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Figure 1. Flow of information through the different stages of the systematic review (for details about the excluded studies, see eAppendix 2). CENTRAL indicates Cochrane Central Register of Controlled Trials.

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Figure 2. Forest plots of the effects of continuing long-acting β2-agonist (LABA) therapy vs stepping off with regard to any use of systemic corticosteroids, asthma control, and quality of life. ACQ indicates Asthma Control Questionnaire; RR, risk ratio. The size of the data marker corresponds to the relative weight assigned in the analysis. *Risk ratio. Mantel-Haenszel method; random effects analysis model. †Data obtained directly from the study sponsor. ‡Inverse variance method; random effects analysis model. §Asthma Quality of Life Questionnaire (AQLQ) (data obtained directly from the study sponsor); higher values indicate better quality of life. Sign of change score was changed to allow same direction of change in both studies. Results favored combination of inhaled corticosteroid plus LABA. ∥Marks AQLQ; higher values indicate better quality of life.

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Grahic Jump Location

Figure 3. Forest plots of the effects of continuing long-acting β2-agonist (LABA) therapy vs stepping off with regard to deterioration of symptoms, night-waking due to asthma, and any serious adverse effect. OR indicates odds ratio; RR, risk ratio. The size of the data marker corresponds to the relative weight assigned in the analysis. *Inverse variance method; random effects analysis model. †Change from baseline. ‡Variability obtained directly from the study sponsor. §Final score. ∥Control group: breast cancer in situ, traffic accident, musculoskeletal chest pain; experimental group: tension headache; none was deemed related to study medication. ¶Control group: loss of consciousness, car crash, breast cancer, chest pain; experimental group: pulmonary embolism. #Control group: gallstones, severe respiratory tract infection; experimental group: bleeding hemorrhoids, esophageal narrowing, and a cerebral arteriovenous malformation thought to have been congenital. **Control group: cholecystitis; experimental group: herniated lumbar disc, breast cancer.

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