Grable I A, Garcia P M, Perry D, Socol M L
Department of Obstetrics and Gynecology, Northwestern University Medical School, Chicago, Illinois, USA.
Am J Obstet Gynecol. 1996 Oct;175(4 Pt 1):1036-42. doi: 10.1016/s0002-9378(96)80049-4.
Our purpose was to determine whether ampicillin prolongs the latency period after preterm premature rupture of membranes in patients colonized with group B Streptococcus.
Sixty patients presenting at < or = 35 weeks' gestation with preterm premature rupture of membranes were included in the study. Cervical, vaginal, and perianal cultures for group B premature rupture were obtained. The participants then were randomized to receive either ampicillin or placebo intravenously for 24 hours and then orally until hospital discharge or delivery. All patients were treated without the use of tocolytic drugs. The chi(2) test, Fisher exact test, Student t test, and Wilcoxon signed-rank test were used for statistical analysis when appropriate.
Fifteen patients had cultures positive for group B Streptococcus. Patients with cultures positive for group B Streptococcus who received ampicillin (n = 8) were more likely not to have been delivered of their infants 48 hours after preterm premature rupture of membranes than patients who received placebo (n = 7), a statistically significant difference (100% vs 43%; p = 0.01; relative risk 2.3; 95% confidence interval 1.2 to 4.5). Seven days after preterm premature rupture of membranes, however, there was no significant difference in percentage of patients with cultures positive for group B Streptococcus who remained undelivered (63% vs 29%; p = 0.19; relative risk, 2.2; 95% confidence interval 0.7 to 7.1). Among patients with cultures negative for group B Streptococcus, there was a trend for patients who received ampicillin to remain undelivered 48 hours after preterm premature rupture of membranes compared with those who received placebo, but the difference was not statistically significant (87% vs 64%; p = 0.07; relative risk, 1.4; 95% confidence interval 1.0 to 1.9). There also was no difference in percentage of patients with cultures negative for group B Streptococcus who remained undelivered 7 days after preterm premature rupture of membranes 39% vs 27%; p = 0.40; relative risk, 1.4; 95% confidence interval 0.61 to 3.3). There were no differences between the treatment and placebo arms of the group B Streptococcus positive and negative cohorts in incidence of cesarean section, chorioamnionitis, postpartum endometritis, or neonatal infectious morbidity.
Use of antibiotics increases the percentage of patients with cultures positive for group B Streptococcus who remain undelivered 48 hours after preterm premature rupture of membranes. Antibiotic therapy may provide a window of opportunity for maternal treatment with corticosteroids to decrease the risk for neonatal morbidity among these preterm gestations.
我们的目的是确定氨苄西林是否能延长B族链球菌定植患者胎膜早破后的潜伏期。
本研究纳入了60例妊娠小于或等于35周且胎膜早破的患者。获取宫颈、阴道和肛周B族链球菌培养物。然后将参与者随机分为静脉注射氨苄西林或安慰剂24小时,之后口服直至出院或分娩。所有患者均未使用宫缩抑制剂进行治疗。在适当情况下,使用卡方检验、Fisher精确检验、Student t检验和Wilcoxon符号秩检验进行统计分析。
15例患者的B族链球菌培养呈阳性。与接受安慰剂的患者(n = 7)相比,接受氨苄西林治疗的B族链球菌培养阳性患者(n = 8)在胎膜早破后48小时内分娩婴儿的可能性较小,差异有统计学意义(100% 对43%;p = 0.01;相对风险2.3;95%置信区间1.2至4.5)。然而,在胎膜早破7天后,B族链球菌培养阳性且未分娩的患者百分比无显著差异(63% 对29%;p = 0.19;相对风险2.2;95%置信区间0.7至7.1)。在B族链球菌培养阴性的患者中,与接受安慰剂的患者相比,接受氨苄西林治疗的患者在胎膜早破后48小时内未分娩有一定趋势,但差异无统计学意义(87% 对64%;p = 0.07;相对风险1.4;95%置信区间1.0至1.9)。在胎膜早破7天后,B族链球菌培养阴性且未分娩的患者百分比也无差异(39% 对27%;p = 0.40;相对风险1.4;95%置信区间0.61至3.3)。B族链球菌阳性和阴性队列的治疗组与安慰剂组在剖宫产、绒毛膜羊膜炎、产后子宫内膜炎或新生儿感染发病率方面无差异。
使用抗生素可增加胎膜早破后48小时内B族链球菌培养阳性且未分娩患者的百分比。抗生素治疗可能为母体使用皮质类固醇治疗提供一个机会窗口,以降低这些早产妊娠中新生儿发病的风险。