Division of High Risk Pregnancy, Mackay Memorial Hospital, Taipei, Taiwan.
Taiwan J Obstet Gynecol. 2012 Mar;51(1):26-30. doi: 10.1016/j.tjog.2012.01.006.
This study was conducted to document the perinatal risk factors associated with early-onset neonatal Escherichia coli sepsis and adverse neonatal outcomes.
A case-control study of early-onset E coli sepsis compared with that of non-E coli sepsis was conducted by a retrospective data review of all infants with a diagnosis of sepsis during the first 7 days of life from the pediatric unit of Mackay Memorial Hospital from January 2004 to October 2008. After adjustment for gestational age, each patient with E coli early-onset sepsis was further compared with two gestational age-matched uninfected controls.
Compared with infants with non-E coli sepsis (n = 27), infants with E coli sepsis (n = 19) were more likely to have preterm birth, especially at less than 30 weeks of gestation (47% vs. 4%, p < 0.01), very low birth weights (<1500 g; 47% vs. 4%, p < 0.01), intrapartum fever (26% vs. 4%, p = 0.036), preterm premature rupture of membranes (PPROM; 74% vs. 11%, p < 0.01), prolonged rupture of membranes (>24 hours; 47% vs. 0%, p < 0.01), antibiotic use (63% vs. 15%, p < 0.01), and sepsis onset on the first day of life (63% vs. 15%, p < 0.01). After adjusting for gestational age, intrapartum fever (26% vs. 5%, p = 0.035) and PPROM (74% vs. 39%, p = 0.015) were more common in infants with E coli sepsis. Fifteen of the 19 E coli isolates (79%) were ampicillin-resistant, and three (16%) were gentamicin-resistant. Antepartum and intrapartum antibiotic exposure was associated with ampicillin-resistant E coli sepsis (100% vs. 43%, p < 0.01).
Early-onset E coli sepsis is more common in premature and very low birth weight infants and is more likely associated with intrapartum fever, PPROM, and sepsis onset on the first day of life than non-E coli sepsis. Broad-spectrum, multiple antibiotics or longer duration of antibiotic exposure may be associated with antibiotic-resistant pathogen infection.
本研究旨在记录与早发型新生儿大肠埃希菌败血症及不良新生儿结局相关的围产期危险因素。
本病例对照研究通过回顾性分析 2004 年 1 月至 2008 年 10 月期间在麦吉尔纪念医院儿科病房确诊为生后 7 天内败血症的所有婴儿的资料,比较早发型大肠埃希菌败血症与非大肠埃希菌败血症。将胎龄校正后,每位早发型大肠埃希菌败血症患儿均与 2 名胎龄相匹配的未感染对照进一步比较。
与非大肠埃希菌败血症患儿(n=27)相比,大肠埃希菌败血症患儿(n=19)更易发生早产,尤其是胎龄<30 周(47% vs. 4%,p<0.01)、极低出生体重儿(<1500g;47% vs. 4%,p<0.01)、产时发热(26% vs. 4%,p=0.036)、胎膜早破(PPROM;74% vs. 11%,p<0.01)、胎膜早破时间延长(>24 小时;47% vs. 0%,p<0.01)、抗生素使用(63% vs. 15%,p<0.01)、生后第 1 天发病(63% vs. 15%,p<0.01)。校正胎龄后,产时发热(26% vs. 5%,p=0.035)和 PPROM(74% vs. 39%,p=0.015)在大肠埃希菌败血症患儿中更为常见。19 株大肠埃希菌分离株中,15 株(79%)对氨苄西林耐药,3 株(16%)对庆大霉素耐药。产前和产时使用抗生素与氨苄西林耐药大肠埃希菌败血症相关(100% vs. 43%,p<0.01)。
早发型大肠埃希菌败血症更常见于早产儿和极低出生体重儿,且与产时发热、PPROM 及生后第 1 天发病相关,而非大肠埃希菌败血症。广谱、多种抗生素或更长时间的抗生素暴露可能与抗生素耐药病原体感染相关。