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新生儿晚发性败血症的预防:一项随机对照试验。

Prevention of neonatal late-onset sepsis: a randomised controlled trial.

作者信息

Alcock Gary, Liley Helen G, Cooke Lucy, Gray Peter H

机构信息

Newborn Services, Mater Mothers' Hospital, Raymond Tce, South Brisbane, QLD, 4101, Australia.

Present address: The Townsville Hospital, 100 Angus Smith Drive, Douglas, 4814, Australia.

出版信息

BMC Pediatr. 2017 Apr 4;17(1):98. doi: 10.1186/s12887-017-0855-3.

Abstract

BACKGROUND

Late-onset sepsis (LOS), defined as sepsis occurring after 48 h of age causes substantial mortality and morbidity in very low birth weight infants. Risk factors for LOS include immaturity, intravascular catheters, mechanical ventilation, and prolonged parenteral nutrition (PN). Little attention has been paid to studying the effects of PN administration methods. The aim of the study was to compare a bundle of measures for PN line management incorporating a strict aseptic technique with standard line management on LOS in very low birth weight infants.

METHODS

Infants <1500 g birth weight who required PN were randomised to either a bundle of a strict aseptic technique for line management together with single use intravascular catheter for PN or a standard technique. The primary outcome was the incidence of LOS in the first 28 days of life. Secondary outcomes were mortality, neonatal morbidities and developmental outcome at 12 months of age.

RESULTS

There were 126 infants in the aseptic technique group and 123 in the standard technique group. Forty (31.8%) infants in the aseptic technique group and 36 (29.3%) in the standard technique group had an episode of sepsis (p = 0.77). This corresponds to incidences of 15.8 and 14.2 episodes of sepsis per 1000 patient days respectively. Subgroup analyses for infants <1000 g also revealed no difference in the rate of sepsis between the intervention and control groups. (p = 0.43). There were no significant differences in secondary outcomes and development between the groups.

CONCLUSION

A bundle of measures including strict aseptic technique for parenteral nutrition line management did not result in a reduction in LOS when compared to a standard technique. There is no evidence to recommend this as routine practice.

TRIAL REGISTRATION

Interdisciplinary Maternal Perinatal Australasian Collaborative Trials (IMPACT) Network, TRN registration number: PT0363. Date: 06/03/2001; Australian New Zealand Clinical Trials Registry (ANZCTR), TRN registration number: ACTRN12617000455369 . Date: 28/03/2017 (retrospectively registered).

摘要

背景

迟发性败血症(LOS)定义为出生48小时后发生的败血症,在极低出生体重儿中会导致相当高的死亡率和发病率。LOS的风险因素包括不成熟、血管内导管、机械通气和长期肠外营养(PN)。很少有人关注研究PN给药方法的影响。本研究的目的是比较采用严格无菌技术的PN管路管理措施与标准管路管理措施对极低出生体重儿LOS的影响。

方法

出生体重<1500g且需要PN的婴儿被随机分为两组,一组采用严格无菌技术进行管路管理并使用一次性血管内导管进行PN,另一组采用标准技术。主要结局是出生后28天内LOS的发生率。次要结局是死亡率、新生儿发病率和12个月龄时的发育结局。

结果

无菌技术组有126例婴儿,标准技术组有123例婴儿。无菌技术组40例(31.8%)婴儿和标准技术组36例(29.3%)婴儿发生了败血症(p = 0.77)。这分别相当于每1000个患者日败血症发生率为15.8例和14.2例。对出生体重<1000g的婴儿进行亚组分析也显示,干预组和对照组之间败血症发生率没有差异(p = 0.43)。两组之间的次要结局和发育情况没有显著差异。

结论

与标准技术相比,包括严格无菌技术进行肠外营养管路管理的一系列措施并未降低LOS。没有证据推荐将此作为常规做法。

试验注册

跨学科母婴澳大利亚协作试验(IMPACT)网络,试验注册号:PT0363。日期:20(此处原文可能有误,推测为2001)年3月6日;澳大利亚新西兰临床试验注册中心(ANZCTR),试验注册号:ACTRN12617000455369。日期:2017年3月28日(追溯注册)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f97/5381090/b20101375180/12887_2017_855_Fig1_HTML.jpg

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