Bernstein Hilton M, Calhoun Darlene A, Christensen Robert D
University of South Florida Children's Research Institute, All Children's Hospital, St. Petersburg, Florida 33701, USA.
Curr Opin Pediatr. 2002 Feb;14(1):91-4. doi: 10.1097/00008480-200202000-00016.
Bacterial sepsis is a major cause of neonatal morbidity and mortality. Successful management of neonatal sepsis requires early diagnosis, appropriate antimicrobial treatment, and aggressive intensive care. However, even when steps are taken appropriately, mortality rates can be high, particularly among certain subgroups, such as extremely preterm neonates and neonates with neutropenia. Multiple factors contribute to the increased susceptibility of neonates to infection, including developmental quantitative and qualitative neutrophil defects. Studies of infected animal and human neonates suggest that the use of recombinant human granulocyte colony stimulating factor (rhG-CSF) or recombinant human granulocyte macrophage colony stimulating factor (rhGM-CSF) can partially counterbalance these defects and thereby reduce morbidity and mortality. However, the body of clinical evidence is currently not sufficient to recommend rhG-CSF or rhGM-CSF administration confidently as routine adjunctive treatment for neonates with sepsis.
细菌性败血症是新生儿发病和死亡的主要原因。成功管理新生儿败血症需要早期诊断、适当的抗菌治疗以及积极的重症监护。然而,即使采取了适当的措施,死亡率仍可能很高,尤其是在某些亚组中,如极早产儿和中性粒细胞减少的新生儿。多种因素导致新生儿对感染的易感性增加,包括发育性定量和定性中性粒细胞缺陷。对受感染的动物和人类新生儿的研究表明,使用重组人粒细胞集落刺激因子(rhG-CSF)或重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)可以部分抵消这些缺陷,从而降低发病率和死亡率。然而,目前的临床证据不足以自信地推荐将rhG-CSF或rhGM-CSF作为败血症新生儿的常规辅助治疗。