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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Efficacy and tolerability of systemic methylprednisolone in children and adolescents with chronic rhinosinusitis: a double-blind, placebo-controlled randomized trial.
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Efficacy and tolerability of systemic methylprednisolone in children and adolescents with chronic rhinosinusitis: a double-blind, placebo-controlled randomized trial.

机译:全身性甲基泼尼松龙在患有慢性鼻鼻窦炎的儿童和青少年中的疗效和耐受性:一项双盲,安慰剂对照的随机试验。

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BACKGROUND: The place of systemic corticosteroids in the treatment of children with chronic rhinosinusitis (CRS) remains unclear. OBJECTIVE: We sought to assess the effectiveness and tolerability of oral methylprednisolone as an anti-inflammatory adjunct in the treatment of CRS in children. METHODS: Forty-eight children (age, 6-17 years) with clinically and radiologically proved CRS were included. Patients were randomly assigned to either oral amoxicillin/clavulanate (AMX/C) and methylprednisolone or AMX/C and placebo twice daily for 30 days. Oral methylprednisolone was administered for the first 15 days with a tapering schedule. Primary parameters were mean change in symptom and sinus computed tomographic (CT) scan scores after treatment. Secondary study parameters were mean changes in individual symptom scores after treatment, relapse rate, and tolerability. RESULTS: Forty-five patients completed the study: 22 received AMX/C and methylprednisolone, and 23 received AMX/C and placebo. Both groups demonstrated significant improvements in symptom and sinus CT scores when comparing baseline values with end-of-treatment values (P < .001). Methylprednisolone as an adjunct was significantly more effective than placebo in reducing CT scores (P = .004), total rhinosinusitis symptoms (P = .001), and individual symptoms of nasal obstruction (P = .001), postnasal discharge (P = .007), and cough (P = .009). At the end of treatment, 48% of the children in the placebo group still had abnormal findings on CT scans versus 14% in the methylprednisolone group (P = .013). Therapy-related adverse events were not different between groups. Although insignificant, the incidence of clinical relapses was also less in the methylprednisolone group (25%) compared with that in the placebo group (43%, P = .137). CONCLUSION: Oral methylprednisolone is well tolerated and provides added benefit to treatment with antibiotics for children with CRS.
机译:背景:全身性激素治疗儿童慢性鼻-鼻窦炎(CRS)的位置尚不清楚。目的:我们试图评估口服甲基强的松龙作为抗炎辅助剂治疗儿童CRS的有效性和耐受性。方法:纳入了经临床和放射学证实为CRS的48例儿童(6-17岁)。患者随机分为口服阿莫西林/克拉维酸盐(AMX / C)和甲基泼尼松龙或AMX / C和安慰剂,每天两次,共30天。口服甲基泼尼松龙的头15天的给药时间表逐渐减少。主要参数是治疗后症状的平均变化和鼻窦计算机断层扫描(CT)扫描得分。二级研究参数是治疗后个体症状评分的平均变化,复发率和耐受性。结果:45位患者完成了研究:22位接受AMX / C和甲基泼尼松龙,23位接受AMX / C和安慰剂。当将基线值与治疗结束值进行比较时,两组均表现出症状和鼻窦CT评分的显着改善(P <.001)。甲基强的松龙作为佐剂在降低CT评分(P = .004),总鼻-鼻窦炎症状(P = .001)和鼻塞的个别症状(P = .001),鼻后分泌物(P =。 007)和咳嗽(P = 0.009)。在治疗结束时,安慰剂组48%的儿童在CT扫描中仍发现异常,而甲基强的松龙组则为14%(P = .013)。两组之间与治疗相关的不良事件没有差异。尽管微不足道,但甲基泼尼松龙组(25%)的临床复发率也低于安慰剂组(43%,P = .137)。结论:口服甲基泼尼松龙具有良好的耐受性,并且为患有CRS的儿童提供了更多的抗生素治疗益处。

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