Nguyen William T, Stewart Charles, Fisher Kimberley, Tolley Elizabeth, Lew Dukhee Betty, Self Timothy H
University of Tennessee and LeBonheur Children's Medical Center, 910 Madison Avenue, Memphis, TN 38163, USA.
Allergy Asthma Proc. 2005 Mar-Apr;26(2):129-34.
Although current national guidelines suggest combination inhaled corticosteroid/long-acting inhaled beta2-agonist as the preferred treatment in moderate and severe persistent asthma for children, trials aimed at reducing emergency department (ED) visits and hospitalizations in minority inner-city children have not been conducted with the combination product of fluticasone/salmeterol via Diskus (Advair). This study assessed the effect of fluticasone/salmeterol combination via Diskus therapy on hospitalizations and ED visits in children with asthma. We conducted a prospective 1-year study with an intervention group compared with a usual care control group. This study took place at an inner-city university-affiliated children's medical center allergy clinic. Inner-city patients with asthma aged 4-17 years with a history of frequent ED visits and hospitalizations for the 2 previous years were enrolled beginning in July 2001. A control group of inner-city asthmatic patients was identified via hospital medical records. Patients were prescribed fluticasone/salmeterol combination via Diskus (n = 39) for 1 year and were compared with a usual care control group (n = 39). Although the investigators did not intervene in the control patients, review of their records revealed that all control patients had inhaled corticosteroids prescribed during the intervention period. Outcome measures included ED visits and hospitalizations for 1 year after enrollment versus the mean for acute care visits for 2 years before enrollment in the study. The intervention group had a 20% reduction in ED visits, which was significant compared with the control group (p = 0.017); both groups had significant reductions in hospitalizations. The risk of experiencing an asthma exacerbation (ED visit or hospitalization) was reduced by 33% in the intervention group compared with the control group (risk ratio, 0.67; 95% confidence interval, 0.49-0.90; p = 0.005). Our results suggest that fluticasone/salmeterol combination via Diskus is associated with a reduction in risk of acute exacerbations of asthma in inner-city children, including ED visits and hospitalizations.
尽管当前国家指南建议吸入性糖皮质激素/长效吸入性β2受体激动剂联合使用是中重度持续性哮喘患儿的首选治疗方法,但尚未针对使用氟替卡松/沙美特罗联合制剂(舒利迭)减少少数族裔市中心儿童急诊就诊和住院情况进行试验。本研究评估了使用舒利迭治疗的氟替卡松/沙美特罗联合制剂对哮喘患儿住院和急诊就诊的影响。我们进行了一项为期1年的前瞻性研究,将干预组与常规护理对照组进行比较。本研究在一所市中心大学附属医院的儿童医疗中心过敏门诊进行。从2001年7月开始,招募了年龄在4至17岁、过去两年有频繁急诊就诊和住院病史的市中心哮喘患者。通过医院病历确定了一组市中心哮喘患者作为对照组。患者接受了为期1年的舒利迭氟替卡松/沙美特罗联合制剂治疗(n = 39),并与常规护理对照组(n = 39)进行比较。尽管研究人员未对对照患者进行干预,但对他们记录的审查显示,所有对照患者在干预期间都接受了吸入性糖皮质激素治疗。观察指标包括入组后1年的急诊就诊和住院情况,与入组研究前2年急性护理就诊的平均值进行比较。干预组的急诊就诊次数减少了20%,与对照组相比具有显著性差异(p = 0.017);两组的住院次数均显著减少。与对照组相比,干预组哮喘急性发作(急诊就诊或住院)的风险降低了33%(风险比,0.67;95%置信区间,0.49 - 0.90;p = 0.005)。我们的结果表明,使用舒利迭的氟替卡松/沙美特罗联合制剂与降低市中心儿童哮喘急性发作的风险相关,包括急诊就诊和住院情况。