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产前倍他米松对肺功能的长期影响:一项随机对照试验的30年随访

Long term effects of antenatal betamethasone on lung function: 30 year follow up of a randomised controlled trial.

作者信息

Dalziel S R, Rea H H, Walker N K, Parag V, Mantell C, Rodgers A, Harding J E

机构信息

Clinical Trials Research Unit, The University of Auckland, Auckland, New Zealand.

出版信息

Thorax. 2006 Aug;61(8):678-83. doi: 10.1136/thx.2005.051763. Epub 2006 Apr 6.

Abstract

BACKGROUND

Antenatal betamethasone is routinely used for the prevention of neonatal respiratory distress syndrome in preterm infants. However, little is known of the long term effects of exposure to antenatal betamethasone on lung function in adulthood.

METHODS

Five hundred and thirty four 30 year olds whose mothers had participated in the first and largest randomised controlled trial of antenatal betamethasone were followed. Lung function was assessed by portable spirometric testing. The prevalence of asthma symptoms was assessed using the European Community Respiratory Health Survey questionnaire.

RESULTS

Fifty (20%) betamethasone exposed and 53 (19%) placebo exposed participants met the criteria for current asthma (relative risk 0.98 (95% CI 0.74 to 1.30), p = 0.89). 181 betamethasone exposed and 202 placebo exposed participants had acceptable spirometric data. There were no differences in lung function between betamethasone and placebo exposed groups (mean (SD) forced vital capacity in the betamethasone and placebo groups 105.9 (12.0) v 106.6 (12.6)% predicted, difference = -0.7 (95% CI -3.2 to 1.8), p = 0.59; mean (SD) forced expiratory volume in 1 second in the betamethasone and placebo groups 98.9 (13.4) v 98.5 (13.6)% predicted, difference = 0.3 (95% CI -2.4 to 3.1, p = 0.80)).

CONCLUSIONS

Antenatal exposure to a single course of betamethasone does not alter lung function or the prevalence of wheeze and asthma at age 30.

摘要

背景

产前使用倍他米松常用于预防早产儿的新生儿呼吸窘迫综合征。然而,产前接触倍他米松对成年后肺功能的长期影响却知之甚少。

方法

对534名30岁的成年人进行随访,他们的母亲曾参与了第一项也是最大规模的产前倍他米松随机对照试验。通过便携式肺量计测试评估肺功能。使用欧洲共同体呼吸健康调查问卷评估哮喘症状的患病率。

结果

50名(20%)接触倍他米松和53名(19%)接触安慰剂的参与者符合当前哮喘的标准(相对风险0.98(95%可信区间0.74至1.30),p = 0.89)。181名接触倍他米松和202名接触安慰剂的参与者有可接受的肺量计数据。接触倍他米松组和接触安慰剂组之间的肺功能没有差异(倍他米松组和安慰剂组的平均(标准差)用力肺活量分别为预测值的105.9(12.0)%和106.6(12.6)%,差异=-0.7(95%可信区间-3.2至1.8),p = 0.59;倍他米松组和安慰剂组的平均(标准差)第1秒用力呼气量分别为预测值的98.9(13.4)%和98.5(13.6)%,差异=0.3(95%可信区间-2.4至3.1),p = 0.80)。

结论

产前单次接触倍他米松不会改变30岁时的肺功能或喘息和哮喘的患病率。

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