Teng R-J, Wu T-J, Garrison R D, Sharma R, Hudak M L
Division of Neonatology, Department of Pediatrics, University of Florida Health Science Center at Jacksonville, Jacksonville, FL, USA.
J Perinatol. 2009 Mar;29(3):219-24. doi: 10.1038/jp.2008.202. Epub 2008 Dec 11.
Evidence is contradictory whether very low-birth-weight (VLBW, birth weight <1500 g) infants with early neutropenia (NP), especially those born to mothers with preeclampsia experience a greater incidence of nosocomial infection (NI).
To investigate whether NP within the first 7 days of life is a risk factor for NI in VLBW infants.
Over a 42-month period, we identified all VLBW infants born at <or=34 weeks gestation who survived for more than 72 h. Infants who had no evidence of early infection, who had at least one complete blood count performed in the first week of life, and who were not given prophylactic recombinant human granulocyte colony-stimulating factor (rhG-CSF) were included in this retrospective study. Early NP was defined as an absolute neutrophil count less than 1500 per microl at any time during the first week of life. NI was defined as the culture of a bacterial or fungal pathogen from a sterile body fluid that was obtained after 72 h of life in an infant with one or more clinical signs of infection.
A total of 338 VLBW infants were reviewed. Of those, 51 infants were excluded because of death or onset of an infection before 72 h of age, lack of a complete blood count in the first week of life or treatment with rhG-CSF. Of the remaining 287 infants, NI occurred in 11 of 77 (14.3%) infants with early NP compared to 42 of 210 (20.0%) infants without early NP (P=0.31). Infants who developed NI were smaller and less mature, had lower Apgar scores, were more frequently instrumented with central lines and required a longer duration of parenteral nutrition compared to infants without NI. Infants with NI also had a higher mortality and a greater incidence of necrotizing enterocolitis, severe intraventricular hemorrhage and threshold retinopathy of prematurity. However, using stepwise multivariate logistic regression analysis, only the duration of parenteral nutrition and gestational age were significant risk factors for NI.
Our data do not support the hypothesis that early NP increases the risk for NI in VLBW infants.
关于极低出生体重(VLBW,出生体重<1500g)且伴有早期中性粒细胞减少(NP)的婴儿,尤其是母亲患有先兆子痫的此类婴儿,其医院感染(NI)发生率是否更高,证据存在矛盾。
调查出生后7天内的NP是否是VLBW婴儿发生NI的危险因素。
在42个月的时间里,我们确定了所有孕周≤34周且存活超过72小时的VLBW婴儿。本回顾性研究纳入了无早期感染证据、出生后第一周至少进行过一次全血细胞计数且未接受预防性重组人粒细胞集落刺激因子(rhG-CSF)治疗的婴儿。早期NP定义为出生后第一周内任何时间绝对中性粒细胞计数低于每微升1500个。NI定义为在出生72小时后从无菌体液中培养出细菌或真菌病原体,且婴儿有一个或多个感染临床体征。
共审查了338例VLBW婴儿。其中,51例婴儿因在72小时前死亡或感染、出生后第一周缺乏全血细胞计数或接受rhG-CSF治疗而被排除。在其余287例婴儿中,77例有早期NP的婴儿中有11例(14.3%)发生NI,而210例无早期NP的婴儿中有42例(20.0%)发生NI(P=0.31)。与未发生NI的婴儿相比,发生NI的婴儿体型更小、成熟度更低、阿氏评分更低,更频繁地使用中心静脉导管,且需要更长时间的肠外营养。发生NI的婴儿死亡率更高,坏死性小肠结肠炎、重度脑室内出血和阈值性早产儿视网膜病变的发生率也更高。然而,通过逐步多因素逻辑回归分析,只有肠外营养时间和孕周是NI的显著危险因素。
我们的数据不支持早期NP会增加VLBW婴儿发生NI风险这一假说。