Ottolini Mary C, Lundgren Kathleen, Mirkinson Laura J, Cason Sheila, Ottolini Martin G
Hospitalist Division, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USA.
Pediatr Infect Dis J. 2003 May;22(5):430-4. doi: 10.1097/01.inf.0000068206.11303.dd.
In May 1996, the CDC recommended obtaining a complete blood count and blood culture (BC) from all asymptomatic "at risk" newborns; those > or =35 weeks gestation born to mothers with group B streptococcal vaginal colonization or those with maternal fever, premature rupture of membranes or previous infant with group B streptococcal disease; who did not receive adequate intrapartum antibiotic prophylaxis.
DESIGN/METHODS: During the study period (May 1996 to July 1999), a complete blood count and BC were obtained within 4 h from all asymptomatic at risk newborns of > or =35 weeks gestation. White blood cell count (WBC) and BC results and prevalence of clinical or culture-proven sepsis were obtained by chart review. We determined the sensitivity/specificity and likelihood ratios of an abnormal WBC (total >30 000 or <5000/mm3; absolute neutrophil count <1500/mm3, or a band form-polymorphonuclear cell ratio of >0.2) to distinguish between clinically septic vs. nonseptic term at risk newborns.
Of 20 554 deliveries 1665 were initially asymptomatic at risk newborns; 17 (1.0%) developed early onset sepsis, all within 48 h. WBC was abnormal in 7 of 17 (41%) and in 447 of 1648 (27%) who remained nonseptic. None of the 1665 term at risk newborns had a positive BC. The sensitivity and specificity of an abnormal WBC in predicting which at risk newborns would develop sepsis were 41 and 73%, respectively. The positive likelihood ratio was 1.52, whereas the negative likelihood ratio was 0.81, with an odds ratio of 1.88.
Since the implementation of the CDC guidelines for maternal intrapartum antibiotic prophylaxis, culture-proved sepsis has become rare at our institution. Although BC did not aid in the diagnosis of sepsis among asymptomatic at risk newborns, close observation in the first 24 h remained critically important.
1996年5月,美国疾病控制与预防中心(CDC)建议对所有无症状的“高危”新生儿进行全血细胞计数和血培养(BC);这些新生儿指孕周≥35周、母亲有B族链球菌阴道定植的新生儿,或母亲有发热、胎膜早破或之前有婴儿患B族链球菌病的新生儿;且这些新生儿未接受充分的产时抗生素预防。
设计/方法:在研究期间(1996年5月至1999年7月),对所有孕周≥35周的无症状高危新生儿在4小时内进行全血细胞计数和血培养。通过查阅病历获取白细胞计数(WBC)、血培养结果以及临床或培养证实的败血症患病率。我们确定了异常白细胞(总数>30000或<5000/mm³;绝对中性粒细胞计数<1500/mm³,或杆状核-多形核细胞比例>0.2)区分临床败血症与非败血症足月高危新生儿的敏感性/特异性和似然比。
在20554例分娩中,1665例最初为无症状高危新生儿;17例(1.0%)发生早发性败血症,均在48小时内。17例中有7例(41%)白细胞异常,1648例未发生败血症的新生儿中有447例(27%)白细胞异常。1665例足月高危新生儿血培养均为阴性。异常白细胞预测高危新生儿发生败血症的敏感性和特异性分别为41%和73%。阳性似然比为1.52,阴性似然比为0.81,比值比为1.88。
自实施CDC关于产妇产时抗生素预防的指南以来,在我们机构培养证实的败血症已变得罕见。虽然血培养无助于无症状高危新生儿败血症的诊断,但在最初24小时内密切观察仍然至关重要。