凤凰城小儿败血症和脓毒性休克新标准:全面视角的优势与未来

Vanessa Soares Lanziotti, Andrea Ventura, S. Kache, Jaime Fernández-Sarmiento
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引用次数: 0

摘要

在希腊神话中,凤凰鸟象征着战胜死亡的生命和伴随转变的力量。因此,凤凰城是新的儿科脓毒症评分标准的恰当名称,这既与神话有关,也与该评分标准首次发布的地点有关(美国亚利桑那州凤凰城召开的重症医学会(Society of Critical Care Medicine - SCCM))。(1)凤凰城儿科败血症(PPS)败血症和脓毒性休克标准旨在识别因感染导致器官功能障碍而危及生命的儿童(1 个月至小于 18 岁),该评分是基于 300 多万次儿科电子健康会诊制定的,(2)考虑到儿科和成人败血症研究,这是一项了不起的成就。之前的儿科败血症标准由国际儿科败血症共识会议(IPSCC)于 2005 年发布,败血症被定义为存在全身炎症反应综合征(SIRS)的疑似或确诊感染(图 1)。(3)尽管这些标准在日常实践中得到了广泛应用,但自该定义提出以来,已发现了其局限性。(4)值得关注的具体局限性包括:缺乏对全球背景的考虑,导致这些标准在资源有限的环境中的适用性面临挑战,而这些环境正是败血症负担最重的地方;床旁应用的可变性,导致患者诊断的延迟;以及无法在全球范围内使用这些标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Phoenix criteria for pediatric sepsis and septic shock: the strengths and the future of a comprehensive perspective
In Greek mythology, the phoenix bird symbolizes life that overcomes death and the strength that accompanies transformation. Therefore, Phoenix is an appropriate name for the new Pediatric Sepsis Score owing to both the mythological reference and the location where it was first presented (Society of Critical Care Medicine – SCCM - Conference in Phoenix, Arizona). (1) The Phoenix Pediatric Sepsis (PPS) criteria for sepsis and septic shock are intended to identify children (1 month to <18 years) with life-threatening organ dysfunction due to infection, and the score was developed based on more than three million pediatric electronic health encounters, (2) which is a remarkable achievement considering pediatric and adult sepsis studies. The previous pediatric sepsis criteria were published in 2005 by the International Pediatric Sepsis Consensus Conference (IPSCC), and sepsis was defined as a suspected or confirmed infection in the presence of systemic inflammatory response syndrome (SIRS) (Figure 1). (3) Although these criteria are broadly used in daily practice, limitations to this definition have been identified since its inception. (4) Specific limitations of concern include a lack of consideration of a global context, leading to challenges in the applicabiblity of these criteria in limited-resource settings where the highest sepsis burden lies; variability in application at the bedside, which leads to delay in patient diagnosis; and the inability to
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