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Azithromycin for Eradication of and Prevention of Bronchopulmonary Dysplasia in Preterm Neonates in the Neonatal Intensive Care Unit.阿奇霉素用于新生儿重症监护病房中早产儿支气管肺发育不良的根除和预防
J Pediatr Pharmacol Ther. 2023;28(1):10-19. doi: 10.5863/1551-6776-28.1.10. Epub 2023 Feb 3.
2
Azithromycin to prevent bronchopulmonary dysplasia in ureaplasma-infected preterm infants: pharmacokinetics, safety, microbial response, and clinical outcomes with a 20-milligram-per-kilogram single intravenous dose.阿奇霉素预防解脲脲原体感染早产儿支气管肺发育不良的研究:20 毫克/千克单次静脉注射的药代动力学、安全性、微生物反应和临床结局。
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3
Ureaplasma, bronchopulmonary dysplasia, and azithromycin in European neonatal intensive care units: a survey.欧洲新生儿重症监护病房中的脲原体、支气管肺发育不良与阿奇霉素:一项调查
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Use of azithromycin for the prevention of bronchopulmonary dysplasia in preterm infants: a randomized, double-blind, placebo controlled trial.阿奇霉素预防早产儿支气管肺发育不良的随机、双盲、安慰剂对照试验。
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Association of Ureaplasma infection pattern and azithromycin treatment effect with bronchopulmonary dysplasia in Ureaplasma positive infants: a cohort study.解脲脲原体感染模式及阿奇霉素治疗效果与解脲脲原体阳性婴儿支气管肺发育不良的相关性:一项队列研究。
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Azithromycin for preventing bronchopulmonary dysplasia in preterm infants: A systematic review and meta-analysis.阿奇霉素预防早产儿支气管肺发育不良的系统评价和荟萃分析。
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Effect of antenatal azithromycin for Ureaplasma spp. on neonatal outcome at ≤30 weeks' gestational age.产前阿奇霉素治疗解脲脲原体对孕周≤30周新生儿结局的影响。
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Azithromycin and other macrolides for prevention of bronchopulmonary dysplasia: a systematic review and meta-analysis.阿奇霉素及其他大环内酯类药物预防支气管肺发育不良:一项系统评价与荟萃分析
Neonatology. 2014;106(4):337-47. doi: 10.1159/000363493. Epub 2014 Oct 1.

引用本文的文献

1
Neonatal central nervous system infection by Ureaplasma species is rare, but relevant: results from a multicenter nationwide surveillance study.脲原体属引起的新生儿中枢神经系统感染罕见,但值得关注:一项全国多中心监测研究的结果
Infection. 2024 Nov 25. doi: 10.1007/s15010-024-02435-2.
2
[Clinical characteristics of infection and colonization in extremely preterm infants].[极早产儿感染与定植的临床特征]
Zhongguo Dang Dai Er Ke Za Zhi. 2024 Aug 15;26(8):811-816. doi: 10.7499/j.issn.1008-8830.2403002.

本文引用的文献

1
Maternal Vaginal spp. Colonization in Early Pregnancy Is Associated with Adverse Short- and Long-Term Outcome of Very Preterm Infants.孕早期母体阴道微生物定植与极早早产儿不良短期和长期结局相关。
Children (Basel). 2021 Apr 3;8(4):276. doi: 10.3390/children8040276.
2
Randomized trial of azithromycin to eradicate Ureaplasma respiratory colonization in preterm infants: 2-year outcomes.随机试验阿奇霉素根除早产儿脲原体呼吸道定植:2 年结局。
Pediatr Res. 2022 Jan;91(1):178-187. doi: 10.1038/s41390-021-01437-2. Epub 2021 Mar 3.
3
Azithromycin for preventing bronchopulmonary dysplasia in preterm infants: A systematic review and meta-analysis.阿奇霉素预防早产儿支气管肺发育不良的系统评价和荟萃分析。
Pediatr Pulmonol. 2021 May;56(5):957-966. doi: 10.1002/ppul.25230. Epub 2020 Dec 31.
4
Study protocol: azithromycin therapy for chronic lung disease of prematurity (AZTEC) - a randomised, placebo-controlled trial of azithromycin for the prevention of chronic lung disease of prematurity in preterm infants.研究方案:阿奇霉素治疗早产儿慢性肺病(AZTEC)-阿奇霉素预防早产儿慢性肺病的随机、安慰剂对照试验。
BMJ Open. 2020 Oct 6;10(10):e041528. doi: 10.1136/bmjopen-2020-041528.
5
Use of Azithromycin for the Prevention of Lung Injury in Mechanically Ventilated Preterm Neonates: A Randomized Controlled Trial.阿奇霉素预防机械通气早产儿肺损伤的随机对照试验。
Neonatology. 2020;117(4):522-528. doi: 10.1159/000509462. Epub 2020 Sep 7.
6
Randomised trial of azithromycin to eradicate in preterm infants.随机试验阿奇霉素根除早产儿。
Arch Dis Child Fetal Neonatal Ed. 2020 Nov;105(6):615-622. doi: 10.1136/archdischild-2019-318122. Epub 2020 Mar 13.
7
The association of prenatal and postnatal macrolide exposure with subsequent development of infantile hypertrophic pyloric stenosis: a systematic review and meta-analysis.产前和产后大环内酯类暴露与婴儿肥厚性幽门狭窄发展的关联:系统评价和荟萃分析。
Ital J Pediatr. 2019 Feb 4;45(1):20. doi: 10.1186/s13052-019-0613-2.
8
Association of prematurity with the development of infantile hypertrophic pyloric stenosis.早产与婴儿肥厚性幽门狭窄发展的关联。
Pediatr Res. 2015 Aug;78(2):218-22. doi: 10.1038/pr.2015.92. Epub 2015 May 7.
9
Azithromycin in early infancy and pyloric stenosis.婴儿早期阿奇霉素与幽门狭窄
Pediatrics. 2015 Mar;135(3):483-8. doi: 10.1542/peds.2014-2026.
10
Pharmacokinetics, microbial response, and pulmonary outcomes of multidose intravenous azithromycin in preterm infants at risk for Ureaplasma respiratory colonization.多剂量静脉注射阿奇霉素在有脲原体呼吸道定植风险的早产儿中的药代动力学、微生物反应及肺部转归
Antimicrob Agents Chemother. 2015 Jan;59(1):570-8. doi: 10.1128/AAC.03951-14. Epub 2014 Nov 10.

阿奇霉素用于新生儿重症监护病房中早产儿支气管肺发育不良的根除和预防

Azithromycin for Eradication of and Prevention of Bronchopulmonary Dysplasia in Preterm Neonates in the Neonatal Intensive Care Unit.

作者信息

Chang Eugenie, Ballard Kaci E, Johnson Peter N, Nandyal Raja, Miller Jamie L

机构信息

Department of Pharmacy: Clinical and Administrative Sciences (EC, KEB, PNJ, JLM), University of Oklahoma College of Pharmacy, Oklahoma City, Oklahoma.

Section of Neonatology (RN), Department of Pediatrics, University of Oklahoma College of Medicine, Oklahoma City, Oklahoma.

出版信息

J Pediatr Pharmacol Ther. 2023;28(1):10-19. doi: 10.5863/1551-6776-28.1.10. Epub 2023 Feb 3.

DOI:10.5863/1551-6776-28.1.10
PMID:36777984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9901312/
Abstract

Azithromycin has been explored as a treatment option for eradication of and prevention of bronchopulmonary dysplasia (BPD) in preterm neonates. However, there is debate about the need for eradication of and whether azithromycin is safe and efficacious for this indication. This literature review provides an overview of the evidence for use of azithromycin for eradication of and prevention of BPD, including dosing and duration of azithromycin used in these studies. The literature search included articles published in the English language in Medline and PubMed from 1946 to January 2022. Relevant citations within identified articles were also reviewed. A total of 9 studies representing 388 neonates were included. The percentage of neonates that tested positive for in these studies ranged from 18.6% to 57.1%. Azithromycin was initiated at <3 days of life in 8 studies (88.9%). Dosing was variable and ranged from 5 to 20 mg/kg/dose administered once daily, and the duration of treatment ranged from 1 to 35 days. Most studies used intravenous azithromycin. Overall, azithromycin was more efficacious than placebo at eradication; however, most of these studies did not find a difference in the incidence of BPD between patients receiving azithromycin versus placebo. No adverse effects, specifically pyloric stenosis or QT interval prolongation, were noted in these studies.

摘要

阿奇霉素已被探索作为根除和预防早产儿支气管肺发育不良(BPD)的一种治疗选择。然而,对于是否需要根除以及阿奇霉素用于该适应症是否安全有效存在争议。这篇文献综述概述了使用阿奇霉素根除和预防BPD的证据,包括这些研究中使用的阿奇霉素剂量和疗程。文献检索包括1946年至2022年1月在Medline和PubMed上发表的英文文章。对已识别文章中的相关引用也进行了审查。总共纳入了9项研究,涉及388名新生儿。这些研究中检测呈阳性的新生儿百分比在18.6%至57.1%之间。8项研究(88.9%)在出生后<3天开始使用阿奇霉素。剂量各不相同,每日一次给药剂量为5至20mg/kg,治疗疗程为1至35天。大多数研究使用静脉注射阿奇霉素。总体而言,在根除方面阿奇霉素比安慰剂更有效;然而,这些研究中的大多数未发现接受阿奇霉素治疗的患者与接受安慰剂治疗的患者在BPD发生率上存在差异。这些研究中未观察到不良反应,特别是幽门狭窄或QT间期延长。