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首页> 外文期刊>The Journal of pediatrics >Long-term budesonide or nedocromil treatment, once discontinued, does not alter the course of mild to moderate asthma in children and adolescents.
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Long-term budesonide or nedocromil treatment, once discontinued, does not alter the course of mild to moderate asthma in children and adolescents.

机译:长期停用布地奈德或奈多克罗米治疗,不会改变儿童和青少年的轻度至中度哮喘病程。

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OBJECTIVES: To determine whether long-term, continuous use of inhaled anti-inflammatory medications affects asthma outcomes in children with mild to moderate asthma after use is discontinued. STUDY DESIGN: Of the 1041 participants in the Childhood Asthma Management Program randomized clinical trial, 941 (90%) were followed to determine whether 4.3 years of twice-daily budesonide or nedocromil administration (each compared with placebo) affected subsequent asthma outcomes during a 4.8-year posttrial period in which treatment was managed by the participants' physicians. RESULTS: The groups treated continuously during the trial with either budesonide or nedocromil did not differ from the group given placebo in terms of lung function, control of asthma, or psychological status at the end of 4.8 years of posttrial follow-up. However, the decreased mean height in the budesonide group relative to the placebo group at the end of the trial (1.1 cm; P = .005) remained statistically significant (0.9 cm; P = .01) after an additional 4.8 years and was more pronounced in girls (1.7 cm; P = .001) than in boys (0.3 cm; P = .49). Participants in all groups used inhaled corticosteroids during 30% of the posttrial period. CONCLUSIONS: Clinically meaningful improvements in the control of asthma and in airway responsiveness achieved during continuous treatment with inhaled corticosteroids do not persist after continuous treatment is discontinued.
机译:目的:确定长期停用吸入抗炎药是否会影响停用后轻度至中度哮喘儿童的哮喘结局。研究设计:在“儿童哮喘管理计划”的1041名参与者中,进行了941次(90%)随访,以确定4.8岁的布地奈德或奈多克罗米每天两次服用(与安慰剂相比)是否在4.8期间影响了随后的哮喘结果参与者的医师管理治疗的三年后阶段。结果:在试验后连续4.8年结束时,在试验期间连续用布地奈德或奈多克罗米治疗的组与安慰剂组在肺功能,哮喘控制或心理状况方面无差异。然而,在试验结束时,布地奈德组相对于安慰剂组的平均身高降低(1.1 cm; P = .005),在再过4.8年后仍保持统计学显着性(0.9 cm; P = .01),且该下降幅度更大女孩(1.7 cm; P = .001)比男孩(0.3 cm; P = .49)明显。所有组的参与者在审判后的30%期间均使用吸入性糖皮质激素。结论:在连续治疗中止后,在持续使用吸入糖皮质激素治疗期间,哮喘控制和气道反应性的临床意义改善并未持续。

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