Zhang Linjie, Mendoza-Sassi Raúl A, César Juraci A, Chadha Neil K
Department of Maternal and Child Health, Federal University of Rio Grande, Rua Visconde Paranaguá 102, Centro, Rio Grande, RS, Brazil, 96201-900.
Cochrane Database Syst Rev. 2008 Jul 16;2008(3):CD006286. doi: 10.1002/14651858.CD006286.pub2.
Adenoidal hypertrophy is generally considered a common condition of childhood. When obstructive sleep apnoea or cardio-respiratory syndrome occurs, adenoidectomy is generally indicated. In less severe cases, non-surgical interventions may be considered, however few medical alternatives are currently available. Intranasal steroids may be used to reduce nasal airway obstruction.
To assess the effectiveness of intranasal corticosteroids for improving nasal airway obstruction in children with moderate to severe adenoidal hypertrophy.
Our search included the Cochrane Ear, Nose and Throat Disorders Group Trials Register, the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 2, 2007), MEDLINE (1951 to 2007) and EMBASE (1974 to 2007). All searches were initially performed in May 2007 and updated in April 2008.
Randomised controlled trials comparing intranasal corticosteroids with placebo or no intervention or other treatment in children aged 0-12 years with moderate to severe adenoidal hypertrophy.
Data from the included trials were extracted and trial quality was assessed by two authors independently. Meta-analysis was not applicable and data were summarised in a narrative format.
Five randomised trials, including a total of 349 patients, met the inclusion criteria of the review. All trials except one showed significant efficacy of intranasal corticosteroids in improving nasal obstruction symptoms and in reducing adenoid size. The first eight-week cross-over study showed that treatment with beclomethasone (336 micrograms/day) yielded a greater improvement in mean symptom scores than placebo (-18.5 vs. -8.5, P < 0.05) and a larger reduction in mean adenoid/choana ratio than placebo (right, -14% vs. +0.4%, p=0.002; left, -15% vs. -2.0%, p=0.0006) between week 0 and week 4. The second four-week cross-over study demonstrated that the nasal obstruction index decreased by at least 50% from baseline in 38% of patients treated with beclomethasone (400 micrograms/day) between week 0 and week 2, whereas none of the patients treated with placebo had such improvement (p<0.01). The third randomized, parallel-group trial showed that 77.7% of patients treated with mometasone (100 micrograms/day) for 40 days demonstrated an improvement in nasal obstruction symptoms and a decrease in adenoid size, such that adenoidectomy could be avoided, whereas no significant improvement was observed in the placebo group. The fourth randomized, parallel-group trial showed that eight-weeks of treatment with flunisolide (500 micrograms/day) was associated with a lager reduction in adenoid size than isotonic saline solution (p<0.05). In contrast, one randomised, parallel-group trial did not find significant improvement in nasal obstruction symptoms and adenoid size after eight weeks of treatment with beclomethasone (200 micrograms/day).
AUTHORS' CONCLUSIONS: Limited evidence suggests that intranasal corticosteroids may significantly improve nasal obstruction symptoms in children with moderate to severe adenoidal hypertrophy, and this improvement may be associated with a reduction of adenoid size. The long-term effect of intranasal corticosteroids in these patients remains to be defined.
腺样体肥大通常被认为是儿童的常见病症。当发生阻塞性睡眠呼吸暂停或心肺综合征时,一般建议进行腺样体切除术。在不太严重的情况下,可考虑非手术干预措施,然而目前几乎没有其他医学替代方法。鼻内类固醇可用于减轻鼻气道阻塞。
评估鼻内皮质类固醇对改善中重度腺样体肥大儿童鼻气道阻塞的有效性。
我们的检索包括Cochrane耳、鼻和咽喉疾病组试验注册库、Cochrane对照试验中央注册库(CENTRAL)(Cochrane图书馆2007年第2期)、MEDLINE(1951年至2007年)和EMBASE(1974年至2007年)。所有检索最初于2007年5月进行,并于2008年4月更新。
比较鼻内皮质类固醇与安慰剂、无干预措施或其他治疗方法对0至12岁中重度腺样体肥大儿童影响的随机对照试验。
提取纳入试验的数据,由两位作者独立评估试验质量。不适用荟萃分析,数据以叙述形式汇总。
五项随机试验,共349例患者,符合本综述的纳入标准。除一项试验外,所有试验均显示鼻内皮质类固醇在改善鼻塞症状和缩小腺样体大小方面具有显著疗效。第一项为期八周的交叉试验表明,在第0周和第4周之间,使用倍氯米松(336微克/天)治疗的患者平均症状评分改善程度大于安慰剂组(-18.5对-8.5,P<0.05),平均腺样体/后鼻孔比值缩小幅度大于安慰剂组(右侧,-14%对+0.4%,p=0.002;左侧,-15%对-2.0%,p=0.0006)。第二项为期四周的交叉试验表明,在第0周和第2周之间,使用倍氯米松(400微克/天)治疗的患者中,38%的患者鼻塞指数从基线至少降低了50%,而使用安慰剂治疗的患者无一有此改善(p<0.01)。第三项随机平行组试验表明,使用莫米松(100微克/天)治疗40天的患者中,77.7%的患者鼻塞症状得到改善,腺样体大小减小,从而可避免进行腺样体切除术,而安慰剂组未观察到显著改善。第四项随机平行组试验表明,使用氟尼缩松(500微克/天)治疗八周后,腺样体大小缩小幅度大于等渗盐溶液(p<0.05)。相比之下,一项随机平行组试验未发现使用倍氯米松(200微克/天)治疗八周后鼻塞症状和腺样体大小有显著改善。
有限的证据表明,鼻内皮质类固醇可能显著改善中重度腺样体肥大儿童的鼻塞症状,且这种改善可能与腺样体大小缩小有关。鼻内皮质类固醇对这些患者的长期影响仍有待确定。