• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Evaluation of aztreonam and ampicillin vs. amikacin and ampicillin for treatment of neonatal bacterial infections.

作者信息

Umaña M A, Odio C M, Castro E, Salas J L, McCracken G H

机构信息

National Children's Hospital, San José, Costa Rica.

出版信息

Pediatr Infect Dis J. 1990 Mar;9(3):175-80. doi: 10.1097/00006454-199003000-00006.

DOI:10.1097/00006454-199003000-00006
PMID:2186351
Abstract

In a prospective randomized, open study we evaluated aztreonam (AZ) for treatment of neonatal bacterial infections. There were 147 patients enrolled in the study; 75 received AZ and ampicillin (AMP) and 72 amikacin (AM) and AMP (conventional therapy). Twenty-eight AZ/AMP-treated patients and 32 conventionally treated patients had bacteriologically documented infections caused by gram-negative enteric bacilli or Pseudomonas species. Treatment groups were comparable in age, clinical status, and type and severity of underlying disease at the time of enrollment. Bronchopneumonia and infections caused by Pseudomonas species occurred significantly more often in AM/AMP-treated patients compared with patients given AZ/AMP. Sepsis was documented in 83% of patients in each treatment group and Gram-negative enteric bacilli and Pseudomonas species were the principal pathogens. Median peak serum bactericidal titers against the etiologic agent were 1:64 for the AZ/AMP and 1:16 for AM/AMP-treated patients. Case fatality rates resulting from the primary infection were 7 and 22% (P = 0.011), superinfection occurred in 39% and 34% and treatment failure occurred in 7 and 28% (P = 0.036) of the AZ/AMP and AM/AMP-treated patients, respectively. No clinical adverse reactions were observed in either group. Based on these results aztreonam appears to be at least as effective as and possibly more effective than amikacin when used initially with ampicillin for empiric treatment of neonatal bacterial infections.

摘要

相似文献

1
Evaluation of aztreonam and ampicillin vs. amikacin and ampicillin for treatment of neonatal bacterial infections.
Pediatr Infect Dis J. 1990 Mar;9(3):175-80. doi: 10.1097/00006454-199003000-00006.
2
A comparative analysis of aztreonam + clindamycin versus tobramycin + clindamycin or amikacin + mezlocillin in the treatment of gram-negative lower respiratory tract infections.
Chemotherapy. 1989;35 Suppl 1:89-100. doi: 10.1159/000238726.
3
Clindamycin plus amikacin versus clindamycin plus aztreonam in established intraabdominal infections.
Surgery. 1994 Jul;116(1):28-35.
4
Randomized trial using piperacillin versus ampicillin and amikacin for treatment of premature neonates with risk factors for sepsis.使用哌拉西林与氨苄西林和阿米卡星治疗有败血症危险因素的早产儿的随机试验。
Eur J Clin Microbiol Infect Dis. 1989 Mar;8(3):241-4. doi: 10.1007/BF01965268.
5
Clinical experience with aztreonam for treatment of infections in children.氨曲南治疗儿童感染的临床经验。
Rev Infect Dis. 1991 May-Jun;13 Suppl 7:S582-5. doi: 10.1093/clinids/13.supplement_7.s582.
6
Moxalactam therapy for neonatal meningitis due to gram-negative enteric bacilli. A prospective controlled evaluation.羟羧氧酰胺菌素治疗革兰阴性肠道杆菌所致新生儿脑膜炎。一项前瞻性对照评估。
JAMA. 1984 Sep 21;252(11):1427-32.
7
Therapeutic efficacy of the combination of aztreonam with cefotaxime in the treatment of severe nosocomial pneumonia. Comparative study against amikacin combined with cefotaxime.氨曲南与头孢噻肟联合治疗重症医院获得性肺炎的疗效。与阿米卡星联合头孢噻肟的对比研究。
Chemotherapy. 1989;35 Suppl 1:15-24. doi: 10.1159/000238716.
8
Aztreonam therapy in neutropenic patients with cancer.
Am J Med. 1986 Aug;81(2):243-8. doi: 10.1016/0002-9343(86)90258-5.
9
Randomized clinical trial of aztreonam and aminoglycoside antibiotics in the treatment of serious infections caused by gram-negative bacilli.氨曲南与氨基糖苷类抗生素治疗革兰氏阴性杆菌所致严重感染的随机临床试验。
Antimicrob Agents Chemother. 1989 Aug;33(8):1137-43. doi: 10.1128/AAC.33.8.1137.
10
A comparative study on aztreonam, ceftazidime and amikacin in the treatment of complicated urinary tract infections.氨曲南、头孢他啶和阿米卡星治疗复杂性尿路感染的对比研究。
J Chemother. 1991 Dec;3(6):376-82. doi: 10.1080/1120009x.1991.11739124.

引用本文的文献

1
Transfer learning predicts species-specific drug interactions in emerging pathogens.迁移学习可预测新兴病原体中的物种特异性药物相互作用。
bioRxiv. 2024 Jun 6:2024.06.04.597386. doi: 10.1101/2024.06.04.597386.
2
A flux-based machine learning model to simulate the impact of pathogen metabolic heterogeneity on drug interactions.一种基于通量的机器学习模型,用于模拟病原体代谢异质性对药物相互作用的影响。
PNAS Nexus. 2022 Jul 22;1(3):pgac132. doi: 10.1093/pnasnexus/pgac132. eCollection 2022 Jul.
3
Neonatal sepsis: a systematic review of core outcomes from randomised clinical trials.
新生儿败血症:随机临床试验核心结局的系统评价。
Pediatr Res. 2022 Mar;91(4):735-742. doi: 10.1038/s41390-021-01883-y. Epub 2022 Jan 7.
4
Antibiotic regimens for early-onset neonatal sepsis.新生儿早发性败血症的抗生素治疗方案。
Cochrane Database Syst Rev. 2021 May 17;5(5):CD013837. doi: 10.1002/14651858.CD013837.pub2.
5
Antibiotic regimens for late-onset neonatal sepsis.晚发型新生儿败血症的抗生素治疗方案。
Cochrane Database Syst Rev. 2021 May 8;5(5):CD013836. doi: 10.1002/14651858.CD013836.pub2.
6
Meropenem vs standard of care for treatment of late onset sepsis in children of less than 90 days of age: study protocol for a randomised controlled trial.美罗培南对比常规护理治疗<90 天的儿童晚发性败血症:一项随机对照试验的研究方案。
Trials. 2011 Sep 30;12:215. doi: 10.1186/1745-6215-12-215.
7
Antibiotic regimens for suspected late onset sepsis in newborn infants.新生儿疑似晚发型败血症的抗生素治疗方案。
Cochrane Database Syst Rev. 2005 Jul 20;2005(3):CD004501. doi: 10.1002/14651858.CD004501.pub2.
8
Antibiotic regimens for suspected early neonatal sepsis.疑似早发型新生儿败血症的抗生素治疗方案。
Cochrane Database Syst Rev. 2004 Oct 18;2004(4):CD004495. doi: 10.1002/14651858.CD004495.pub2.
9
Antibiotics in neonatal infections: a review.新生儿感染中的抗生素:综述
Drugs. 1999 Sep;58(3):405-27. doi: 10.2165/00003495-199958030-00003.
10
Antibacterial-induced nephrotoxicity in the newborn.新生儿抗菌药物诱导的肾毒性
Drug Saf. 1999 Mar;20(3):245-67. doi: 10.2165/00002018-199920030-00005.