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新生儿脓毒性休克的病理生理学和治疗。

Pathophysiology and treatment of septic shock in neonates.

机构信息

Division of Neonatal-Perinatal Medicine, Department of Pediatrics, Duke University, 2424 Hock Plaza, Suite 504, DUMC Box 2739, Durham, NC 27710, USA.

出版信息

Clin Perinatol. 2010 Jun;37(2):439-79. doi: 10.1016/j.clp.2010.04.002.

Abstract

Neonatal septic shock is a devastating condition associated with high morbidity and mortality. Definitions for the sepsis continuum and treatment algorithms specific for premature neonates are needed to improve studies of septic shock and assess benefit from clinical interventions. Unique features of the immature immune system and pathophysiologic responses to sepsis, particularly those of extremely preterm infants, necessitate that clinical trials consider them as a separate group. Keen clinical suspicion and knowledge of risk factors will help to identify those neonates at greatest risk for development of septic shock. Genomic and proteomic approaches, particularly those that use very small sample volumes, will increase our understanding of the pathophysiology and direct the development of novel agents for prevention and treatment of severe sepsis and shock in the neonate. Although at present antimicrobial therapy and supportive care remain the foundation of treatment, in the future immunomodulatory agents are likely to improve outcomes for this vulnerable population.

摘要

新生儿败血症性休克是一种严重的疾病,与高发病率和死亡率相关。需要为败血症连续统定义和早产儿专用的治疗算法,以改善败血症性休克的研究并评估临床干预的获益。不成熟的免疫系统的独特特征和对败血症的病理生理反应,特别是极早产儿的反应,需要临床试验将其视为一个单独的组别。敏锐的临床怀疑和对危险因素的了解将有助于识别那些发生败血症性休克风险最大的新生儿。基因组和蛋白质组学方法,特别是那些使用非常小样本量的方法,将增加我们对病理生理学的理解,并指导为新生儿严重败血症和休克开发新的预防和治疗药物。尽管目前抗菌治疗和支持性护理仍然是治疗的基础,但在未来,免疫调节剂可能会改善这一脆弱人群的结局。

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