Horváth B, Grasselly M, Lakatos F, Kneffel P
Vas Megyei Markusovszky Kórház, Szombathely, Szülészet-Nögyógyászati Osztály.
Orv Hetil. 1998 Nov 29;139(48):2899-901.
This study was performed prospectively. Between 1. January 1995 and 31 December 1997, a modification of the screening-based strategy protocol was implemented. Antenatal screening cultures for GBS were performed at approximately 30-32 weeks of gestation. The protocol recommends the use of antibiotic prophylaxis to GBS positive women with any of the obstetric risk factors for early-onset of GBS disease. Our regiment for prophylaxis for patients in labor was ampicillin 2 g. intravenously then 1 g. i.v. every 4 hours until delivery. Before this study had started (1984-1994), there were 149 serious neonatal GBS infection (149/15,040 pregnancy, among them were 97 premature infants. Thirty-one infants suffered from connatal sepsis. We observed 29 lethal infection. Between January 01, 1995, and December 31, 1997, 4150 women participated in this investigation. The incidence of positive group B Streptococcus cultures from the vaginal samples was 11.6% (481/4150). During the study period (3 years), serious GBS infection was detected in 46 infants (1.1%). There were 9 cases of neonatal sepsis (0.2%), two of them suffered lethal infections (0.05%). There was no late onset of GBS disease and lethal outcome in the last two years. Our investigations bears clinical importance because we confirmed that group B streptococcal colonization is an important risk factor for neonatal infection. The selective intrapartum chemoprophylaxis is a safe and effective intervention to prevent early-onset severe GBS disease.
本研究为前瞻性研究。在1995年1月1日至1997年12月31日期间,实施了基于筛查策略方案的修改。在妊娠约30 - 32周时进行B族链球菌(GBS)的产前筛查培养。该方案建议对有任何早发性GBS疾病产科危险因素的GBS阳性女性使用抗生素预防。我们对分娩患者的预防方案是静脉注射氨苄西林2克,然后每4小时静脉注射1克直至分娩。在本研究开始之前(1984 - 1994年),有149例严重的新生儿GBS感染(149/15040次妊娠,其中97例为早产儿。31例婴儿患有先天性败血症。我们观察到29例致命感染。在1995年1月1日至1997年12月31日期间,4150名女性参与了这项调查。阴道样本中B族链球菌培养阳性的发生率为11.6%(481/4150)。在研究期间(3年),在46例婴儿中检测到严重的GBS感染(1.1%)。有9例新生儿败血症(0.2%),其中2例患有致命感染(0.05%)。在最后两年中没有GBS疾病的迟发性发作和致命结局。我们的研究具有临床重要性,因为我们证实B族链球菌定植是新生儿感染的重要危险因素。选择性产时化学预防是预防早发性严重GBS疾病的一种安全有效的干预措施。