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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Establishing a therapeutic index for the inhaled corticosteroids: part II. Comparisons of systemic activity and safety among different inhaled corticosteroids.
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Establishing a therapeutic index for the inhaled corticosteroids: part II. Comparisons of systemic activity and safety among different inhaled corticosteroids.

机译:建立吸入性糖皮质激素的治疗​​指数:第二部分。不同吸入性糖皮质激素的全身活性和安全性比较。

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摘要

The systemic activity and safety of inhaled corticosteroids are best studied in randomized, controlled, long-term trials with clinically relevant doses in subjects. These studies require large numbers of enrolled subjects and are difficult to conduct. Potential confounders to safety analyses must be controlled. The occurrence and magnitude of adrenal suppression has been the most extensively evaluated systemic effect of inhaled corticosteroids. The significance of these findings in relation to relevant clinical outcomes must be evaluated. At low to medium inhaled corticosteroid dosages, the hypothalamic-pituitary-adrenal axis is minimally and only partially suppressed. Statistically significant changes occur at high inhaled corticosteroid dosages; the magnitude of this effect is less than with prednisone, > or = 10 mg/day. Standards for the design of growth studies in children with asthma have been recommended and recently implemented. Four randomized, controlled, clinical trials have reported reductions in growth rates of > 1 cm/yr with beclomethasone < or = 400 microg/day. By comparison, 2 randomized controlled clinical trials with fluticasone, 50 to 100 microg twice daily via dry powder inhaler, could not detect differences in height velocity in prepubertal children treated with cromolyn sodium or placebo. Trials with low to medium doses of beclomethasone, fluticasone, and budesonide document little to no effect on bone mineral density and bone metabolism. Population-based and limited randomized controlled trials suggest that low to medium doses of inhaled corticosteroids do not cause cataracts or glaucoma. Patients requiring high-dose inhaled corticosteroids should be monitored for adverse effects, with appropriate lifestyle changes and pharmacologic strategies implemented.
机译:吸入皮质类固醇的全身活性和安全性最好在具有临床相关剂量的受试者的随机,对照,长期试验中进行研究。这些研究需要大量的注册受试者,并且难以进行。安全分析的潜在混杂因素必须加以控制。肾上腺抑制的发生和程度是吸入皮质类固醇的最广泛评估的全身作用。必须评估这些发现相对于相关临床结果的重要性。在低至中度吸入皮质类固醇剂量下,下丘脑-垂体-肾上腺轴被最小化并且仅被部分抑制。大量吸入皮质类固醇激素会引起统计学上的显着变化。这种作用的幅度小于泼尼松≥10 mg /天。已推荐并最近实施了哮喘儿童生长研究设计标准。四个随机对照临床试验报告说,倍氯米松<或= 400 microg / day可使生长速率降低> 1 cm / yr。相比之下,两项每日两次通过干粉吸入器使用氟替卡松(50至100微克)的随机对照临床试验未能检测到使用克罗莫林钠或安慰剂治疗的青春期前儿童身高速度的差异。低至中等剂量倍氯米松,氟替卡松和布地奈德的试验对骨矿物质密度和骨代谢影响很小甚至没有影响。基于人群的有限随机对照试验表明,吸入中低剂量的皮质类固醇不会引起白内障或青光眼。需要监测需要大剂量吸入糖皮质激素的患者的不良反应,并适当改变生活方式和实施药理学策略。

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