Pediatric Sepsis - Part I: "Children are not small adults!"

Derek S Wheeler, Hector R Wong, Basilia Zingarelli
{"title":"Pediatric Sepsis - Part I: \"Children are not small adults!\"","authors":"Derek S Wheeler, Hector R Wong, Basilia Zingarelli","doi":"10.2174/1875041901104010004","DOIUrl":null,"url":null,"abstract":"<p><p>The recognition, diagnosis, and management of sepsis remain among the greatest challenges in pediatric critical care medicine. Sepsis remains among the leading causes of death in both developed and underdeveloped countries and has an incidence that is predicted to increase each year. Unfortunately, promising therapies derived from preclinical models have universally failed to significantly reduce the substantial mortality and morbidity associated with sepsis. There are several key developmental differences in the host response to infection and therapy that clearly delineate pediatric sepsis as a separate, albeit related, entity from adult sepsis. Thus, there remains a critical need for well-designed epidemiologic and mechanistic studies of pediatric sepsis in order to gain a better understanding of these unique developmental differences so that we may provide the appropriate treatment. Herein, we will review the important differences in the pediatric host response to sepsis, highlighting key differences at the whole-organism level, organ system level, and cellular and molecular level.</p>","PeriodicalId":89637,"journal":{"name":"The open inflammation journal","volume":"4 ","pages":"4-15"},"PeriodicalIF":0.0000,"publicationDate":"2011-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3665507/pdf/nihms352209.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The open inflammation journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1875041901104010004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The recognition, diagnosis, and management of sepsis remain among the greatest challenges in pediatric critical care medicine. Sepsis remains among the leading causes of death in both developed and underdeveloped countries and has an incidence that is predicted to increase each year. Unfortunately, promising therapies derived from preclinical models have universally failed to significantly reduce the substantial mortality and morbidity associated with sepsis. There are several key developmental differences in the host response to infection and therapy that clearly delineate pediatric sepsis as a separate, albeit related, entity from adult sepsis. Thus, there remains a critical need for well-designed epidemiologic and mechanistic studies of pediatric sepsis in order to gain a better understanding of these unique developmental differences so that we may provide the appropriate treatment. Herein, we will review the important differences in the pediatric host response to sepsis, highlighting key differences at the whole-organism level, organ system level, and cellular and molecular level.

儿童败血症-第一部分:“儿童不是小大人!”
脓毒症的识别、诊断和管理仍然是儿科重症医学面临的最大挑战之一。败血症仍然是发达国家和不发达国家的主要死亡原因之一,预计其发病率每年都会增加。不幸的是,来自临床前模型的有希望的治疗方法普遍未能显著降低与败血症相关的大量死亡率和发病率。宿主对感染和治疗的反应有几个关键的发育差异,这些差异清楚地将儿童败血症与成人败血症区分开来,尽管两者相关。因此,为了更好地了解这些独特的发育差异,我们仍然迫切需要对儿童败血症进行精心设计的流行病学和机制研究,以便我们可以提供适当的治疗。在此,我们将回顾儿童宿主对败血症反应的重要差异,强调在整体水平、器官系统水平、细胞和分子水平上的关键差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信