TY - JOUR
T1 - Randomized controlled trial to improve care for urban children with asthma: Results of the school-based asthma therapy trial
AU - Halterman, Jill S.
AU - Szilagyi, Peter G.
AU - Fisher, Susan G.
AU - Fagnano, Maria
AU - Tremblay, Paul
AU - Conn, Kelly M.
AU - Wang, Hongyue
AU - Borrelli, Belinda
PY - 2011/3
Y1 - 2011/3
N2 - Objective: To evaluate the impact of the School-Based Asthma Therapy trial on asthma symptoms among urban children with persistent asthma. Design: Randomized trial, with children stratified by smoke exposure in the home and randomized to a school-based care group or a usual care control group. Setting: Rochester, New York. Participants: Children aged 3 to 10 years with persistent asthma. Interventions: Directly observed administration of daily preventive asthma medications by school nurses (with dose adjustments according to National Heart, Lung, and Blood Institute Expert Panel guidelines) and a home-based environmental tobacco smoke reduction program for smokeexposed children, using motivational interviewing. Main Outcome Measure: Mean number of symptomfree days per 2 weeks during the peak winter season (November-February), assessed by blinded interviews. Results: We enrolled 530 children (74% participation rate). During the peak winter season, children receiving preventive medications through school had significantly more symptom-free days compared with children in the control group (adjusted difference = 0.92 days per 2 weeks; 95% confidence interval, 0.50-1.33) and also had fewer nighttime symptoms, less rescue medication use, and fewer days with limited activity (all P <.01). Children in the treatment group also were less likely than those in the control group to have an exacerbation requiring treatment with prednisone (12% vs 18%, respectively; relative risk = 0.64; 95% confidence interval, 0.41-1.00). Stratified analyses showed positive intervention effects even for children with smoke exposure (n = 285; mean symptom-free days per 2 weeks: 11.6 for children in the treatment group vs 10.9 for those in the control group; difference = 0.96 days per 2 weeks; 95% confidence interval, 0.39-1.52). Conclusions: The School-Based Asthma Therapy intervention significantly improved symptomsamongurban children with persistent asthma. This program could serve as a model for improved asthma care in urban communities. Trial Registration: clinicaltrials.gov Identifier: NCT00296998. ©2011 American Medical Association. All rights reserved.
AB - Objective: To evaluate the impact of the School-Based Asthma Therapy trial on asthma symptoms among urban children with persistent asthma. Design: Randomized trial, with children stratified by smoke exposure in the home and randomized to a school-based care group or a usual care control group. Setting: Rochester, New York. Participants: Children aged 3 to 10 years with persistent asthma. Interventions: Directly observed administration of daily preventive asthma medications by school nurses (with dose adjustments according to National Heart, Lung, and Blood Institute Expert Panel guidelines) and a home-based environmental tobacco smoke reduction program for smokeexposed children, using motivational interviewing. Main Outcome Measure: Mean number of symptomfree days per 2 weeks during the peak winter season (November-February), assessed by blinded interviews. Results: We enrolled 530 children (74% participation rate). During the peak winter season, children receiving preventive medications through school had significantly more symptom-free days compared with children in the control group (adjusted difference = 0.92 days per 2 weeks; 95% confidence interval, 0.50-1.33) and also had fewer nighttime symptoms, less rescue medication use, and fewer days with limited activity (all P <.01). Children in the treatment group also were less likely than those in the control group to have an exacerbation requiring treatment with prednisone (12% vs 18%, respectively; relative risk = 0.64; 95% confidence interval, 0.41-1.00). Stratified analyses showed positive intervention effects even for children with smoke exposure (n = 285; mean symptom-free days per 2 weeks: 11.6 for children in the treatment group vs 10.9 for those in the control group; difference = 0.96 days per 2 weeks; 95% confidence interval, 0.39-1.52). Conclusions: The School-Based Asthma Therapy intervention significantly improved symptomsamongurban children with persistent asthma. This program could serve as a model for improved asthma care in urban communities. Trial Registration: clinicaltrials.gov Identifier: NCT00296998. ©2011 American Medical Association. All rights reserved.
U2 - 10.1001/archpediatrics.2011.1
DO - 10.1001/archpediatrics.2011.1
M3 - Article
SN - 1072-4710
VL - 165
SP - 262
EP - 268
JO - Archives of Pediatrics and Adolescent Medicine
JF - Archives of Pediatrics and Adolescent Medicine
IS - 3
ER -