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- W2375569759 abstract "AIM: To evaluate the clinical efficacy and safety of salmeterol xinafoate and fluticasone propionate in the treatment of moderate and severe asthma children. METHODS: Eighty sick children with moderate and severe asthma were randomly divided into two groups. These children in the treatment group (n=50) were given salmeterol xinafoate and fluticasone propionate, 50 μg/ 100 μg, bid in the patients aged 5 to 11 a and 50 μg/ 250 μg, bid in those aged 12 to 14 a, respectively. These children in the control group (n=30) were given fluticasone propionate (flixotide) 125 μg, bid in the patients aged 5 to 11 a and 250 μg in those aged 12 to 14 a, respectively. RESULTS: There was significant difference in PEFam, PEFpm and the days of using salbutamol after 8 wk treatment in two groups (P 0.05). Self-assessment in two groups had also significant difference after 4 wk treatment (P 0.05). Asthma symptom scores were improved significantly after 3 mo treatment (P 0.05). Each group had one patient suffering pharynx malaise who recovered quickly after proper treatments. CONCLUSION: Salmeterol xinafoate and fluticasone propionate possesses good effectiveness, safety and well tolerance in the treatment of moderate and severe asthma children." @default.
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- W2375569759 date "2004-01-01" @default.
- W2375569759 modified "2023-09-26" @default.
- W2375569759 title "Therapeutic effect of salmeterol xinafoate and fluticasone propionate powder for inhalation in treatment of 50 moderate and severe asthma children" @default.
- W2375569759 hasPublicationYear "2004" @default.
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