TY - JOUR
T1 - Prednisolone oral solution plus inhaled procaterol for acute asthma in children: A double-blind randomized controlled trial
AU - Huang, Li-Hsin
AU - Shyur, Shyh-Dar
AU - Wen, Da-Chin
AU - Chang, Yi-Chi
AU - Ma, Yi-Chun
AU - Lin, Sheng-Chieh
AU - Wu, Wen-Chiu
AU - Wu, Jiunn-Yi
N1 - Export Date: 7 April 2016
CODEN: TEYZF
通訊地址: Shyur, S.-D.; Allergy and Immunology Section, Department of Pediatrics, Mackay Memorial Hospital, 92, Chungshan North Road, Taipei, Taiwan; 電子郵件: [email protected]
化學物質/CAS: prednisolone, 50-24-8; procaterol, 62929-91-3, 72332-33-3; Prednisolone, 50-24-8; Procaterol, 72332-33-3
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PY - 2007
Y1 - 2007
N2 - Background: To evaluate the efficacy of prednisolone sodium phosphate oral solution plus inhaled procaterol in the treatment of acute asthma in children. Methods: Forty-three patients aged 6 to 12 years with an acute exacerbation of asthma were double-blind randomized into one of two treatment groups in a 1:1 ratio:1) prednisolone oral solution +placebo tablets + procaterol MDI or 2) prednisolone tablets +placebo oral solution + procaterol MDI, all given three times daily for 7 days. Peak expiratory flow rate (PEFR), 24-hour reflective asthma symptom scores, spirometry and pulmonary index score (PIS) were recorded before and after treatment. Net changes in PEFR, symptom score, PIS, Forced Expiratory Volume in the first second (FEV1), FEV1/forced vital capacity (FVC), forced expiratory flow between 25 and 75 percent of the forced vital capacity (FEF25-75%) (before and after treatment) and global assessment by the investigator and the subjects or their parents were analyzed. Results: The two groups were statistically similar at baseline values of these parameters. After a 7-day course of treatment, the net change of PEFR before and after treatment was significantly improved in both groups, but there was no significant difference in the net change of PEFR between the two groups (57.27 ± 31.44 L/min vs. 54.29 ± 30.04 L/min, difference 2.99 ± 30.76L/min, mean ± SD, P=0.752). The net change in PIS and total symptom score did not differ between the two groups (P=0.091 and 0.827, respectively). Similarly, the FEV1, FEV1/FVC and FEF25-75% all improved with either treatment, and neither group was significantly superior to the other group (P=0.162, 0.48 and 0.081, respectively). Global assessment by the investigator and the subjects or their parents at the end of study indicated an essentially comparable result. Conclusions: Prednisolone sodium phosphate oral solution plus inhaled procaterol is as efficacious as prednisolone tablets plus inhaled procaterol in the management of acute asthma in children.
AB - Background: To evaluate the efficacy of prednisolone sodium phosphate oral solution plus inhaled procaterol in the treatment of acute asthma in children. Methods: Forty-three patients aged 6 to 12 years with an acute exacerbation of asthma were double-blind randomized into one of two treatment groups in a 1:1 ratio:1) prednisolone oral solution +placebo tablets + procaterol MDI or 2) prednisolone tablets +placebo oral solution + procaterol MDI, all given three times daily for 7 days. Peak expiratory flow rate (PEFR), 24-hour reflective asthma symptom scores, spirometry and pulmonary index score (PIS) were recorded before and after treatment. Net changes in PEFR, symptom score, PIS, Forced Expiratory Volume in the first second (FEV1), FEV1/forced vital capacity (FVC), forced expiratory flow between 25 and 75 percent of the forced vital capacity (FEF25-75%) (before and after treatment) and global assessment by the investigator and the subjects or their parents were analyzed. Results: The two groups were statistically similar at baseline values of these parameters. After a 7-day course of treatment, the net change of PEFR before and after treatment was significantly improved in both groups, but there was no significant difference in the net change of PEFR between the two groups (57.27 ± 31.44 L/min vs. 54.29 ± 30.04 L/min, difference 2.99 ± 30.76L/min, mean ± SD, P=0.752). The net change in PIS and total symptom score did not differ between the two groups (P=0.091 and 0.827, respectively). Similarly, the FEV1, FEV1/FVC and FEF25-75% all improved with either treatment, and neither group was significantly superior to the other group (P=0.162, 0.48 and 0.081, respectively). Global assessment by the investigator and the subjects or their parents at the end of study indicated an essentially comparable result. Conclusions: Prednisolone sodium phosphate oral solution plus inhaled procaterol is as efficacious as prednisolone tablets plus inhaled procaterol in the management of acute asthma in children.
KW - Acute asthma
KW - Prednisolone
KW - Solution
KW - Tablet
KW - placebo
KW - prednisolone
KW - procaterol
KW - abdominal pain
KW - allergic reaction
KW - article
KW - asthma
KW - breathing rate
KW - child
KW - clinical article
KW - clinical trial
KW - combination chemotherapy
KW - controlled clinical trial
KW - controlled study
KW - disease severity
KW - double blind procedure
KW - drug efficacy
KW - expiratory flow rate
KW - forced expiratory volume
KW - human
KW - randomized controlled trial
KW - spirometry
KW - tremor
KW - Acute Disease
KW - Administration, Inhalation
KW - Administration, Oral
KW - Asthma
KW - Child
KW - Child, Preschool
KW - Double-Blind Method
KW - Female
KW - Forced Expiratory Volume
KW - Humans
KW - Male
KW - Procaterol
M3 - Article
SN - 1608-8115
VL - 48
SP - 257
JO - Acta Paediatrica Taiwanica
JF - Acta Paediatrica Taiwanica
IS - 5
ER -