Table 1.
Summary of primary outcome: risk of exacerbation.
| Study, country | Age, years, mean (range) | Diagnosis | N of Patients | Intervention | Details of treatment | Timepoints of outcomes | Significant key results |
| Maspero 2008[7], Latin America and Turkey | 9.3 (6–14) | Persistent asthma | 548 | SFC vs. MON | SFC: Inhaled 50 μg/100 μg BID vs. MON: Oral 5 mg QD for 12 weeks | 12 weeks | SFC treatment decreased risk of asthma exacerbation (10.3% vs. 23.2%, P < 0.001) |
| Ma 2016[6], China | 4.4 (NR) | Mild to moderate asthma | 80 | SFC vs. MON | SFC: Inhaled 50 μg/100 μg BID (reduced 1/4 dosage for patients’ condition and pulmonary functions after 6 months and 12 months) vs. MON: Oral 4 mg (<6 years) or 5 mg (≥6 years) QD for 1 year | 6 months, 12 months, and 18 months | SFC treatment significantly decreased the risk of emergency entering at 18 months (7.5% vs. 17.5%, P < 0.05). No significant differences of mild asthma exacerbation at any time |
| Zhang 2009[21], China | 8.6 (6–13) | Moderate persistent asthma | 75 | SFC vs. MFC | SFC: Inhaled 50 μg/100 μg BID vs. MFC: Oral 5 mg QD/125 μg BID for 12 weeks | 12 weeks | No significant differences |
| Lenney 2013[29], UK | 10.39 (6.5–14.67) | Uncontrolled asthma | 63 | SFC vs. MFC | SFC: Inhaled 50 μg/100 μg BID vs. MFC: Oral 5 mg QD/100 μg BID for 48 weeks | 24 weeks and 48 weeks | No significant differences |
BID: Twice daily; QD: Once daily; MFC: Montelukast/fluticasone; MON: Montelukast sodium; NA: Not applicable; NR: Not reported; SCF: Combination salmeterol/fluticasone; SFC: Salmeterol/fluticasone.