Timing of intrapartum ampicillin and prevention of vertical transmission of group B Streptococcus

被引:103
作者
De Cueto, M
Sanchez, MJ
Sampedro, A
Miranda, JA
Herruzo, AJ
Rosa-Fraile, M
机构
[1] Hosp Virgen Nieves, Microbiol Serv, Granada 18014, Spain
[2] Hosp Virgen Nieves, Dept Obstet & Gynaecol, Granada 18014, Spain
关键词
D O I
10.1016/S0029-7844(97)00587-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To evaluate the relationship between the time elapsed from the administration of ampicillin prophylaxis to delivery and its efficacy in interrupting intrapartum transmission of group B streptococcus. Methods: During the 12-month study period, all women who came to the Virgen de las Nieves Hospital (Granada, Spain) for delivery were screened for group B streptococcus vaginal carriage by a pigment-detection culture-based procedure. Colonized women were treated with ampicillin (2 g intravenously), and the interval between ampicillin administration and delivery was recorded. Newborns from colonized mothers also were screened to detect group B streptococcus colonization. Results: During the study period, 4525 women were admitted to the hospital for delivery and screened for group B streptococcus vaginal colonization. Group B streptococcus was detected in 543 women (12%), of whom 454 gave birth vaginally to 454 liveborn infants. Intrapartum ampicillin was given to 201 of these 454 women (44%), and 10% of the newborns from mothers who received intrapartum ampicillin prophylaxis were colonized by group B streptococcus. The relationship between timing of ampicillin administration and rate of neonatal group B streptococcal transmission was as follows: less than 1 hour before delivery, 46%; 1-2 hours, 29%; 2-4 hours, 2.9%; and more than 4 hours, 1.2%. Among the 253 mothers who received no intrapartum prophylaxis, colonization was found in 120 of their newborns (47%). Conclusion: When the time between the start of ampicillin prophylaxis and delivery is at least 2 hours, vertical transmission of group B streptococcus is minimized.
引用
收藏
页码:112 / 114
页数:3
相关论文
共 12 条
[1]  
[Anonymous], 1996, MMWR Recomm Rep, V45, P1
[2]  
Ascher D P, 1993, J Perinatol, V13, P212
[3]  
Baker C.J., 1995, INFECT DIS FETUS NEW, V37, P980
[4]   Inadequacy of rapid immunoassays for intrapartum detection of group B streptococcal carriers [J].
Baker, CJ .
OBSTETRICS AND GYNECOLOGY, 1996, 88 (01) :51-55
[5]   PREVENTION OF EARLY-ONSET NEONATAL GROUP-B STREPTOCOCCAL DISEASE WITH SELECTIVE INTRAPARTUM CHEMOPROPHYLAXIS [J].
BOYER, KM ;
GOTOFF, SP .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (26) :1665-1669
[6]  
DECUETO M, 1995, EUR J CLIN MICROBIOL, V14, P810
[7]   GROUP-B STREPTOCOCCUS (GBS) AND NEONATAL INFECTIONS - THE CASE FOR INTRAPARTUM CHEMOPROPHYLAXIS [J].
GARLAND, SM ;
FLIEGNER, JR .
AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 1991, 31 (02) :119-122
[8]  
GIBBS RS, 1994, OBSTET GYNECOL, V84, P496
[9]  
PYLIPOW M, 1994, PEDIATRICS, V93, P631
[10]  
ROSA M, 1992, J CLIN MICROBIOL, V30, P1019