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极微量地塞米松促进机械通气早产儿拔管。

Extremely low-dose dexamethasone to facilitate extubation in mechanically ventilated preterm babies.

机构信息

Regional Neonatal Unit, Royal Maternity Hospital, Queen's University Belfast, Belfast, UK.

出版信息

Neonatology. 2011;100(3):285-9. doi: 10.1159/000326273. Epub 2011 Jun 23.

DOI:10.1159/000326273
PMID:21701221
Abstract

BACKGROUND

Bronchopulmonary dysplasia (BPD) is a major respiratory complication of extreme prematurity. Dexamethasone is effective in reducing ventilation requirements in babies with BPD, but follow-up studies have raised concerns about long-term neurological sequelae. Few studies have investigated the lowest dose effective for weaning from mechanical ventilation.

OBJECTIVES

Between January 2004 and December 2008 the practice in a tertiary neonatal unit was to use extremely low doses of dexamethasone for severe BPD, commencing at 0.05 mg/kg/day and decreasing over 9 days, with a cumulative dose of 0.24 mg/kg. The objective of this observational study was to assess the effectiveness of the extremely low-dose course in facilitating extubation.

METHODS

The babies who had received extremely low-dose dexamethasone to facilitate weaning from mechanical ventilation were identified. Details of treatment and respiratory support were recorded. Serial oxygenation indices (OI) during the dexamethasone course were calculated, and these were analysed to assess the effect of treatment on ventilation requirements.

RESULTS

One hundred and ninety extremely preterm babies were admitted during this 5-year period. Sixteen babies received extremely low-dose dexamethasone. The median gestation was 25 weeks and the median birth weight was 644 g. Before starting dexamethasone, the median OI was 10.6, but by day 7 of treatment it had fallen to 5.4. By the end of the course, 12 of the 16 babies had been successfully extubated.

CONCLUSIONS

This short dexamethasone course appears effective in facilitating extubation. Randomised trials with long-term follow-up are needed to determine the role of extremely low-dose dexamethasone in preterm babies with evolving BPD.

摘要

背景

支气管肺发育不良(BPD)是极早产儿的主要呼吸并发症。地塞米松可有效降低 BPD 患儿的通气需求,但后续研究对其长期神经后遗症提出了担忧。很少有研究调查过可有效实现从机械通气撤机的最低剂量。

目的

在 2004 年 1 月至 2008 年 12 月期间,三级新生儿病房的治疗实践是使用极低剂量的地塞米松治疗严重 BPD,起始剂量为 0.05 mg/kg/天,持续 9 天,累积剂量为 0.24 mg/kg。本观察性研究的目的是评估极低剂量疗程在促进撤机方面的有效性。

方法

确定了接受极低剂量地塞米松以促进从机械通气撤机的婴儿。记录了治疗和呼吸支持的详细信息。计算了地塞米松疗程期间的氧合指数(OI)系列,并对其进行分析,以评估治疗对通气需求的影响。

结果

在 5 年期间,有 190 名极早产儿入住。16 名婴儿接受了极低剂量地塞米松治疗。中位胎龄为 25 周,中位出生体重为 644 克。开始地塞米松治疗前,OI 中位数为 10.6,但治疗第 7 天时已降至 5.4。疗程结束时,16 名婴儿中有 12 名成功撤机。

结论

该短期地塞米松疗程似乎可有效促进撤机。需要进行长期随访的随机试验,以确定极低剂量地塞米松在患有进展性 BPD 的早产儿中的作用。

相似文献

1
Extremely low-dose dexamethasone to facilitate extubation in mechanically ventilated preterm babies.极微量地塞米松促进机械通气早产儿拔管。
Neonatology. 2011;100(3):285-9. doi: 10.1159/000326273. Epub 2011 Jun 23.
2
Randomized, double-blinded trial of low-dose dexamethasone: II. Functional residual capacity and pulmonary outcome in very low birth weight infants at risk for bronchopulmonary dysplasia.低剂量地塞米松的随机双盲试验:II. 支气管肺发育不良高危极低出生体重儿的功能残气量和肺部转归
Pediatr Pulmonol. 2004 Jul;38(1):55-63. doi: 10.1002/ppul.20037.
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Three-year experience with neonatal ventilation from a tertiary care hospital in Delhi.德里一家三级护理医院的新生儿通气三年经验。
Indian Pediatr. 1993 Jun;30(6):783-9.
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A controlled trial of dexamethasone to prevent bronchopulmonary dysplasia in surfactant-treated infants.地塞米松预防接受表面活性剂治疗婴儿支气管肺发育不良的对照试验。
Pediatrics. 1996 Aug;98(2 Pt 1):204-10.
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Outcome at 2 years of age of infants from the DART study: a multicenter, international, randomized, controlled trial of low-dose dexamethasone.DART研究中2岁婴儿的结局:一项低剂量地塞米松的多中心、国际、随机对照试验
Pediatrics. 2007 Apr;119(4):716-21. doi: 10.1542/peds.2006-2806.
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Low-dose dexamethasone facilitates extubation among chronically ventilator-dependent infants: a multicenter, international, randomized, controlled trial.低剂量地塞米松有助于长期依赖呼吸机的婴儿脱机:一项多中心、国际、随机、对照试验。
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9
Factors associated with successful extubation following the first course of systemic dexamethasone in ventilator-dependent preterm infants with or at risk of developing bronchopulmonary dysplasia.在患有支气管肺发育不良或有患支气管肺发育不良风险的依赖呼吸机的早产儿中,与首次全身应用地塞米松疗程后成功拔管相关的因素。
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10
[Dexamethasone therapy in bronchopulmonary dysplasia].
Klin Padiatr. 1989 Jan-Feb;201(1):11-5. doi: 10.1055/s-2007-1025268.

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