Antibiotic Prevention for Maternal Group B Streptococcal Colonization on Neonatal GBS-Related Adverse Outcomes: A Meta-Analysis
- School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China
Maternal colonization with group B Streptococcus (GBS) during pregnancy increases the risk of neonatal infection by vertical transmission. However, it remains unclear whether treating all colonized women during labor exposes a large number of their neonates to possible adverse effects without benefit. We performed a meta-analysis to assess the effect of intrapartum antibiotic prophylaxis on neonatal adverse outcomes. We identified studies by searching several English and Chinese electronic databases and reviewing relevant articles. Data were pooled using fixed-effects or random-effects meta-analysis, and for each outcome both risk ratio (RR) and 95% confidence intervals (95% CIs) were calculated. Fourteen studies (2,051 pregnant women and 2,063 neonates) were included, comprising 13 randomized clinical trials and 1 cohort study. Antibiotic prophylaxis is associated with a significant reduced risk of all cause infections (RR = 0.28, 95% CI = 0.18–0.42), GBS infection (RR = 0.24, 95% CI = 0.13–0.44), early-onset GBS infection (RR = 0.24, 95% CI = 0.13–0.45), non-GBS infections (RR = 0.34, 95% CI = 0.20–0.59), and GBS colonization (RR = 0.10, 95% CI = 0.06–0.16). But no significant reduction was observed in late-onset GBS infection, mortality from early-onset GBS infection or from non-GBS infections. Notably, no significant differences were found between ampicillin and penicillin prevention for neonatal adverse outcomes. Our findings suggest that antibiotic prophylaxis is effective in reducing neonatal GBS colonization and infection.
Group B Streptococcus (GBS) is a significant cause of neonatal sepsis and meningitis and of severe infections in pregnant women (Murayama et al., 2009). GBS is also a commensal that colonizes the gastrointestinal and genitourinary tracts, resulting significant maternal and perinatal morbidity, and can be transmitted from a GBS-colonized mother to her newborn via the ascending route during labor and delivery, causing neonatal severe invasive diseases such as an early-onset GBS (EOGBS) disease occurring within the first week and a late-onset GBS (LOGBS) disease occurring between 1 week and 3 months of life (Borchardt et al., 2006; Huber et al., 2011; Stoll et al., 2011; Okike et al., 2014). American Centers for Disease Control (CDC) had published three guidelines in the past 20 years (1996, 2002, and 2010) that recommend the use of a risk-based or screening-based approach to identify candidates for intrapartum antibiotic prophylaxis (IAP; Centers for Disease Control and Prevention (CDC), 1996; Schrag et al., 2002; Verani et al., 2010).
It is important to know if IAP does more good than harm in trying to reduce mortality and morbidity from neonatal GBS infection. However, the potential efficacy of IAP is not clear. A few studies reported a significant inverse association between IAP and neonatal GBS-related adverse outcomes (including GBS infection and early-onset GBS infection), while other studies found no significant association between the two (Matorras et al., 1991; Gervasio et al., 2001; EI Helali et al., 2009; Li and Meng, 2010). In addition, there were a few quantitative reviews evaluated the efficacy of IAP for women with specific diseases [preterm premature rupture of membranes (PROM) or chorioamnionitis; (Egarter et al., 1996; Benitz et al., 1999)], but the potential preventive effect for healthy women is still unclear. Therefore, we systematically identified RCT and cohort studies on the issue published up to April 2016, and carried out a meta-analysis to explore the potential effect of intrapartum antibiotics for maternal GBS colonization on neonatal adverse outcomes (including GBS colonization, infection, and mortality).
The meta-analysis was conducted following the PRISMA guidelines (Moher et al., 2010). Studies were identified through a systematic search of MEDLIINE, PUBMED, WANGFANG, and CNKI, from January 1979 to April 2016, using the following searching terms: (“group B streptococcus” or “streptococcus agalactiae”) and (“antibiotic” or “anti-bacterial agents” or “intrapartum antibiotic prophylaxis”) and (“perinatal period” or “pregnant women”). In addition, reference lists of all retrieved articles and previous systematic reviews were checked for further eligible publications. We restricted our search to studies performed in human studies and published in English or Chinese.
Inclusion and Exclusion Criteria
Two investigators (SM Li and JY Huang) independently reviewed and assessed the eligibility of identified studies using the following inclusion and exclusion criteria. The inclusion criteria required studies to: (1) include original data from RCT or cohort studies; (2) be based on pregnant women known to be colonized with GBS in the vaginal/ intestinal tract and/or the urinary tract at any time during the pregnancy; (3) provide information on intrapartum use of antibiotics; (4) assess the impact of antibiotics on clinical outcomes of neonates; and (5) apply treatment or placebo explicitly and equally to both treatment and control participants. Studies were excluded if they: (1) were case reports, letters, abstracts, reviews, or meta-analyses; (2) did not mention how many participants were allocated to treatment or control group; and (3) administered intrapartum treatment to both treatment group and control group. When multiple articles reported the same study population, only the most recent and informative study that met inclusion criteria was included.
Outcomes of Interest
The outcomes of interest included: (1) neonatal mortality (including all cause mortality, mortality from EOGBS infection or infections caused by bacteria other than GBS); (2) neonatal infection [including all cause infections, GBS infection, EOGBS infection (symptoms and signs of sepsis or pneumonia in a neonate born to a GBS positive mother, and positive GBS bacterial cultures which from normally sterile body fluids obtained from the neonate), LOGBS infection (infection due to GBS in an infant at least seven days old), and infections caused by bacteria other than GBS]; and (3) neonatal GBS colonization (swabs sampled in external ear, nose, throat, umbilicus, and rectum within 24 h of birth were cultured GBS positive).
Data extracted from each study included the name of the first author, publication year, country, study design, population source, number of participants, antibiotic use, and adverse outcomes of neonates. Detailed information is shown in Table 1 and Table S1. Two investigators (SM Li and JY Huang) independently reviewed and cross-checked the data, and disagreements were resolved by consensus.
For each study retained for the meta-analysis, we assessed methodological quality based on following criteria: (1) Randomized controlled trials were assessed using the Jadad scale; and (2) non-RCTs were assessed using the Newcastle-Ottawa quality assessment scale (NOS; Jadad et al., 1996; Wells et al., 2011). The Jadad scale awards 1–5 points and RCTs with ≥3 points are considered high-quality studies. The NOS is categorized into three dimensions (including the selection populations, comparability of groups, and outcome/exposure of interest), and non-RCTs with ≥5 points indicate high-quality studies.
All statistical analyses were performed by using Stata statistical software version 14.0 (Stata Corporation LP, College Station, Texas, USA). All summary estimates of the relative ratio (RR) were pooled by either fixed-effects model (P for heterogeneity > 0.1) or random-effects model (P for heterogeneity ≤ 0.1; Mantel and Haenszel, 1959; DerSimonian and Laird, 1986). Heterogeneity among studies was tested by the chi-squared test with the Cochrane Q statistic (significant at P ≤ 0.1) and quantified by I2 statistic (Higgins and Thompson, 2002; Higgins et al., 2003). The subgroup analysis was performed according to maternal conditions (without infectious symptoms vs. with probable infectious symptoms), study quality (high-quality vs. low-quality), gestational ages (35–37 vs. 17–43 weeks) and antibiotic prevention (ampicillin vs. penicillin), using χ2-tests (significant at P ≤ 0.05).
Characteristics of Eligible Studies
The flowchart of literature search for meta-analysis was shown in Figure 1. By reading the abstracts and using our criteria, 41 studies were selected for detailed evaluation; 30 studies were excluded for the reasons noted in Figure 1. Three studies were included through manual searches of the relevant systematic reviews and reference list (Egarter et al., 1996; Benitz et al., 1999; Ohlsson and Shah, 2014). Finally, 14 studies were included in the final analysis (Yow et al., 1979; Easmon et al., 1983; Boyer and Gotoff, 1986; Lim et al., 1986; Tuppurainen and Hallman, 1989; Matorras et al., 1991; Gervasio et al., 2001; EI Helali et al., 2009; Li and Meng, 2010; Shen et al., 2012; Bai, 2014; Ma et al., 2014; Yang, 2015; Zhang et al., 2015). The main characteristics of eligible studies are given in Table 1 and the main characteristics of participants are given in Table S1. There were 13 RCT studies and one cohort study with a total of 2051 pregnant women and 2063 neonates. Six of these studies were conducted in China, four were in USA and the rest were in Europe.
Thirteen manuscripts were RCTs. The maximum score in the Jadad scale was three because it is difficult to have a double-blind study in this field. Two studies received Jadad scores of 3, four studies received 2, and seven studies received 1. The only non-RCT study received NOS score of 7 (Table 1).
Antibiotic Prevention for Neonatal Mortality
The overall RRs of neonatal mortality for IAP were presented in Figure 2. No statistically significant reduction was observed in the incidence of all cause mortality (RR = 0.35, 95% CI = 0.05–2.78), mortality from EOGBS infection (RR = 0.51, 95% CI = 0.06–4.55) or from non-GBS infections (RR = 0.31, 95% CI = 0.01–7.50). There was no evidence of heterogeneity among studies on all cause mortality (P = 0.469, I2 = 0%) and mortality from EOGBS infection (P = 0.633, I2 = 0%).
Figure 2. Summary relative risk of neonatal mortality for antibiotic prophylaxis. The combined relative risk was achieved using fixed-effects model. (GBS, group B Streptococcus; EOGBS, early-onset group B streptococcal).
Antibiotic Prevention for Neonatal Infection
The overall RRs of neonatal infection for IAP were presented in Figure 3. Overall, there was a significant reduction in the incidence of all cause infections (RR = 0.28, 95% CI = 0.18–0.42), GBS infection (RR = 0.24, 95% CI = 0.13–0.44), EOGBS infection (RR = 0.24, 95% CI = 0.13–0.45), and non-GBS infections (RR = 0.34, 95% CI = 0.20–0.59) for antibiotic prophylaxis. However, no statistically significant reduction was observed in LOGBS infection (RR = 0.36, 95% CI = 0.01–8.69). There was no evidence of heterogeneity among studies on all cause infections (P = 0.892, I2 = 0%), GBS infection (P = 0.723, I2 = 0%), EOGBS infection (P = 0.747, I2 = 0%), and non-GBS infections (P = 0.840, I2 = 0%).
Figure 3. Summary relative risk of neonatal infections cause by GBS or bacteria other than GBS for antibiotic prophylaxis. The combined relative risk was achieved using fixed-effects model. (GBS, group B Streptococcus; EOGBS, early-onset group B streptococcal; LOGBS, late-onset group B streptococcal).
Antibiotic Prevention for Neonatal GBS Colonization
The overall RRs of neonatal GBS colonization for IAP were presented in Figure 4. There was a significant reduction in the incidence of neonatal GBS colonization for antibiotic prophylaxis (RR = 0.10, 95% CI = 0.06–0.16), with no evidence of heterogeneity among studies (P = 0.184, I2 = 32.0%).
Figure 4. Summary relative risk of neonatal group B streptococcal colonization for antibiotic prophylaxis. The combined relative risk was achieved using fixed-effects model.
Comparison of Efficacy of Ampicillin and Penicillin
In subgroup analysis by antibiotic prevention (ampicillin vs. penicillin) for neonatal adverse outcomes (Table 2), we found a similar efficacy in prevention of all cause mortality (RR = 0.19, 95% CI = 0.01–3.82, for ampicillin; RR = 0.93, 95% CI = 0.04–22.61, for penicillin; P for difference = 0.474), all cause infections (RR = 0.15, 95% CI = 0.04–0.48, for ampicillin; RR = 0.32, 95% CI = 0.21–0.50, for penicillin; P for difference = 0.272), and GBS colonization (RR = 0.08, 95% CI = 0.02–0.27, for ampicillin; RR = 0.13, 95% CI = 95% CI = 0.05–0.33, for penicillin; P for difference = 0.670) between two groups. When differentiating adverse outcomes in GBS-related and other bacteria related, there was still evidence of similar risks of mortality from EOGBS infection (P for difference = 0.634), GBS infection (P for difference = 0.199), EOGBS infection (P for difference = 0.233), and non-GBS infections (P for difference = 0.916) between two groups. The number of studies on other outcomes was too small to perform subgroup analysis on.
Impact of Study Quality, Maternal Condition, and Gestational Ages
In subgroup analysis by study quality (Table 3), we found a similar efficacy in prevention of all cause infections (P for difference = 0.789), GBS infection (P for difference = 0.474), EOGBS infection (P for difference = 0.464), non-GBS infections (P for difference = 0.349), and GBS colonization (P for difference = 0.258) between two groups. The number of studies on other outcomes was too small to perform subgroup analysis on. In subgroup analysis by maternal conditions (Table 4), we found a similar efficacy in prevention of all cause mortality (P for difference = 0.474), mortality from EOGBS infection (P for difference = 0.634), all cause infections (P for difference = 0.703), GBS infection (P for difference = 0.566), EOGBS infection (P for difference = 0.624), non-GBS infections (P for difference = 0.488), and GBS colonization (P for difference = 0.465) between two groups. In subgroup analysis by gestational ages (Table 5), we found a similar efficacy in prevention of all cause infections (P for difference = 0.179), GBS infection (P for difference = 0.351), EOGBS infection (P for difference = 0.390), non-GBS infections (P for difference = 0.279), and GBS colonization (P for difference = 0.502) between two groups.
We contributed additionally to the literature by including more new trials to explore the potential role of antibiotic prophylaxis and differentiating neonatal adverse outcomes in GBS and non-GBS related diseases to make neonatal adverse outcomes clearer. This updated meta-analysis confirms that antibiotic prophylaxis appears to significantly reduce the risk of neonatal adverse outcomes, including all cause infections, GBS infection, EOGBS infection, non-GBS infections, and GBS colonization.
There are two types of interventions that may reduce the risk of neonatal GBS infection by vertical transmission, including for high-risk (PROM, chorioamnionitis and so on) and moderate-risk (vaginal GBS colonization, maternal fever, prematurity, and low birth weight) mothers. Although evidence from two previous meta-analyses indicated that antibiotic therapy significantly reduced the risk of sepsis in infants born to women with PROM and chorioamnionitis (Egarter et al., 1996; Benitz et al., 1999), but the potential effect for moderate-risk women is still unclear. A few available studies have explored the potential association between intrapartum antibiotics for GBS-colonized women and neonatal GBS-related infections, but current evidence is inconsistent (Boyer and Gotoff, 1986; Tuppurainen and Hallman, 1989; Shen et al., 2012; Ma et al., 2014). The only meta-analysis (four trials) on intrapartum antibiotics for maternal GBS colonization published so far indicated that incidence of EOGBS infection was reduced with intrapartum antibiotics compared to no treatment (Ohlsson and Shah, 2014). Our meta-analysis based on 14 studies provides more reliable evidence that prophylactic antibiotics for GBS-colonized women significantly reduce the risk of all cause infections, GBS infection, EOGBS infection, and non-GBS infections, indicating that antibiotic prophylaxis may reduce the risk of bacteria vertical transmission (including GBS isolates). Notably, only two RCTs conducted more than 20 years ago and enrolling a total of 289 women have been published, and as a result we found no significant reduction in LOGBS infection in our meta-analysis study. These findings highlight the need for further well designed and conducted RCTs to better understand the potential effect of antibiotic prophylaxis on LOGBS infection.
The potential effect of antibiotic prophylaxis for GBS colonized women on neonatal mortality remains unclear. It is remarkable that previous evidence on the topic has been so poorly studied, and only two studies enrolling a total of 615 women have been published (Boyer and Gotoff, 1986; Gervasio et al., 2001). Our meta-analysis on these two studies revealed that the use of intrapartum antibiotics did not significantly reduce the incidence of mortality from EOGBS infection and mortality from all causes. It is possible that the sample size was insufficient for effective assessment of intrapartum antibiotics on such low neonatal mortality (0.23% in treatment group, 1.08% in control group, for all cause mortality; 0.23% in treatment group, 0.54% in control group, for mortality from EOGBS infection; Gervasio et al., 2001; Boyer and Gotoff, 1986). With a type I error of 0.05 and power of 80% and the above incidences, 1,640 women per group and 6,894 women per group were required to detect a significant difference in mortality from all causes and mortality from EOGBS infection, respectively.
Neonatal GBS colonization is an important risk factor for the morbidity and mortality of early-onset GBS disease. Prevention of neonatal GBS colonization has been examined in several previous studies, with reduced risk ranging from 0.01 to 0.22 (Yow et al., 1979; Easmon et al., 1983; Boyer and Gotoff, 1986; Lim et al., 1986; Matorras et al., 1991; EI Helali et al., 2009; Li and Meng, 2010). Our study additionally contributes to the literature by combining these inconsistent findings and indicated that intrapartum antibiotics can prevent GBS vertical transmission from colonized mothers to their infants (RR = 0.10 for neonatal GBS colonization). Note that there are at least two mechanisms by which neonatal colonization is prevented. First, numbers of organisms in the mother's vagina and rectum are reduced temporarily so that the infant is delivered though a field that is less contaminated by GBS. Second, the level of antibiotic (ampicillin or penicillin) in the amniotic fluid remains high, so the baby is bathed in a solution of antibiotic and he swallows the fluid.
Information on whether intrapartum ampicillin is preferable to penicillin for GBS colonized women is lacking. This study compared the efficacy of ampicillin and penicillin prevention, and found that ampicillin and penicillin are similarly effective in prevention for neonatal GBS-related outcomes (including GBS colonization, GBS infection, EOGBS infection, and mortality from EOGBS infection), indicating that ampicillin may be an acceptable alternative to penicillin for the prevention of neonatal GBS-related diseases. As penicillin had a narrower spectrum of antimicrobial activity and GBS continued to be susceptible to it, penicillin was the chief choice for IAP, with ampicillin as an acceptable alternative for the prevention of maternal infections. Notably, the ORACLE trial revealed that the prescription of amoxicillin–clavulanate or erythromycin for preterm labor (SPL) women was associated with an increased risk of cerebral palsy among their children at 7 years of age, supporting the opinion that antibiotics are not advisable in SPL without clinical signs of infection (Kenyon et al., 2008). Therefore, future studies must direct more attention to exploring the long-term effect of intrapartum antibiotics for neonatal adverse outcomes.
However, the increased use of intrapartum antibiotics to prevent GBS diseases has raised public health concerns over the emergence of antibiotic resistance among GBS strains. Several studies have reported that erythromycin and clindamycin resistance were the most common phenotypes (Jannati et al., 2012; Bolukaoto et al., 2015; Goudarzi et al., 2015; Kuang et al., 2015; Malek-Jafarian et al., 2015; Suhaimi et al., 2016). Since the first CDC guideline had been published in 1996, the frequency of erythromycin-resistant strains increased after a year (Lin et al., 2000). Although previous studies had not reported resistance to penicillin or ampicillin which was the first-line beta-lactam antibiotics, GBS with reduced penicillin susceptibility had been reported (Kimura et al., 2008; Jannati et al., 2012; Seki et al., 2015; Suhaimi et al., 2016). On the other hand, the increasing resistance to the macrolides and clindamycin which used as alternative drugs for penicillin allergic patients should be paid attention, and guideline for these patients need to be further study (Bolukaoto et al., 2015).
There are several potential limitations to this meta-analysis. First, we did not attempt to search for unpublished studies, believing that the rigor of the peer-review process guarantees the quality of a published trial, which could bring the publication bias. However, because not all trials are registered in public databases, a reliable estimate of the publication bias is not yet possible. Second, although statistical homogeneity did not exist for all outcomes, the question of clinical homogeneity is difficult to answer. There were differences in study design, population source, gestational ages, maternal conditions, study quality, and therapeutic regimens. However, the likelihood should be small, because no significant heterogeneity was observed in the subgroup analysis for gestational ages, maternal conditions, and study quality. Third, only 2 (15.4%, 2/13) RCTs are considered high-quality studies since it was difficult to conduct a double blind RCT study in this field. Finally, pooling of the English and Chinese literature together to extract the relevant studies may bring language selection bias and increase the heterogeneity of study participants. However, it brings more eligible studies and thus more information for evaluating the efficacy of IAP for neonatal GBS diseases, and there was no evidence of heterogeneity among studies on neonatal outcomes.
In conclusion, this meta-analysis shows that antibiotic prophylaxis is effective in interrupting vertical transmission of GBS and in reducing the incidence of GBS infections (including EOGBS infection). However, the potential preventive effectiveness of antibiotic prophylaxis to reduce neonatal LOGBS infection and mortality from GBS infection is inconclusive, given lack of evidence from well designed and conducted trials.
SL and JH contributed equally to this work; conception and design of the study, XY, ZY, and SL; collection of data, SL and JH; analysis and interpretation of data, XY, SL, JH, ZC, and DG; drafting of the manuscript, XY, SL, and JH; all co-authors participated in the writing of the manuscript and approved the version submitted for publication.
This work was supported by the Science and Technology Planning Project of Guangdong province (No. 2014A020212306).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fmicb.2017.00374/full#supplementary-material
Benitz, W. E., Gould, J. B., and Druzin, M. L. (1999). Antimicrobial prevention of early-onset group B streptococcal sepsis: estimates of risk reduction based on a critical literature review. Pediatrics 103:e78. doi: 10.1542/peds.103.6.e78
Bolukaoto, J. Y., Monyama, C. M., Chukwu, M. O., Lekala, A. M., Nchabeleng, M., Maloba, M. R. B., et al. (2015). Antibiotic resistance of Streptococcus agalactiae isolated from pregnant women in Garankuwa, South Africa. BMC Res. Notes 8:364. doi: 10.1186/s13104-015-1328-0
Borchardt, S. M., DeBusscher, J. H., Tallman, P. A., Manning, S. D., Marrs, C. F., Kurzynski, T. A., et al. (2006). Frequency of antimicrobial resistance among invasive and colonizing Group B streptococcal isolates. BMC Infect. Dis. 6:57. doi: 10.1186/1471-2334-6-57
Boyer, K. M., and Gotoff, S. P. (1986). Prevention of early-onset neonatal group B streptococcal disease with selective intrapartum chemoprophylaxis. New Eng. J. Med. 314, 1665–1669. doi: 10.1056/NEJM198606263142603
Centers for Disease Control Prevention (CDC) (1996). Prevention of perinatal group B streptococcal disease: a public health perspective. MMWR Recomm. Rep. 45, 1–24. Available online at: https://www.cdc.gov/mmwr/preview/mmwrhtml/00043277.htm
Easmon, C. S., Hastings, M. J., Deeley, J., Bloxham, B., Rivers, R. P., and Marwood, R. (1983). The effect of intrapartum chemoprophylaxis on the vertical transmission of group B streptococci. Br. J. Obstet. Gynaecol. 90, 633–635. doi: 10.1111/j.1471-0528.1983.tb09280.x
Egarter, C., Leitich, H., Karas, H., Wieser, F., Husslein, P., Kaider, A., et al. (1996). Antibiotic treatment in preterm premature rupture of membranes and neonatal morbidity: a metaanalysis. Am. J. Obstet. Gynecol. 174, 589–597. doi: 10.1016/S0002-9378(96)70433-7
EI Helali, N., Nguyen, J. C., Ly, A., Giovangrandi, Y., and Trinquart, L. (2009). Diagnostic accuracy of a rapid real-time polymerase chain reaction assay for universal intrapartum group B streptococcus screening. Clin. Infect. Dis. 49, 417–423. doi: 10.1086/600303
Gervasio, C. T., Mantaring, B. S., Alankar, S., and Shankaran, S. (2001). Early-onset neonatal group B streptococcal sepsis: intrapartum antibiotic prophylaxis in the clinical setting. J. Perinatol. 21, 9–14. doi: 10.1038/sj.jp.7200476
Goudarzi, G., Ghafarzadeh, M., Shakib, P., and Anbari, K. (2015). Culture and real-time PCR based maternal screening and antibiotic susceptibility for group B Streptococcus: an Iranian experience. Glob. J. Health Sci. 7, 233–239. doi: 10.5539/gjhs.v7n6p233
Huber, C. A., McOdimba, F., Pflueger, V., Daubenberger, C. A., and Revathi, G. (2011). Characterization of invasive and colonizing isolates of Streptococcus agalactiae in East African adults. J. Clin. Microbiol. 49, 3652–3655. doi: 10.1128/JCM.01288-11
Jadad, A. R., Moore, R. A., Carroll, D., Jenkinson, C., Reynolds, D. J. M., Gavaghan, D. J., et al. (1996). Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control. Clin. Trials 17, 1–12. doi: 10.1016/0197-2456(95)00134-4
Jannati, E., Roshani, M., Arzanlou, M., Habibzadeh, S., Rahimi, G., and Shapuri, R. (2012). Capsular serotype and antibiotic resistance of group B streptococci isolated from pregnant women in Ardabil, Iran. Iran. J. Microbiol. 4, 130–135.
Kenyon, S., Pike, K., Jones, D. R., Brocklehurst, P., Marlow, N., Salt, A., et al. (2008). Childhood outcomes after prescription of antibiotics to pregnant women with spontaneous preterm labour: 7-year follow-up of the ORACLE II trial. Lancet 372, 1319–1327. doi: 10.1016/S0140-6736(08)61203-9
Kimura, K., Suzuki, S., Wachino, J.-i., Kurokawa, H., Yamane, K., Shibata, N., et al. (2008). First molecular characterization of group B streptococci with reduced penicillin susceptibility. Antimicrob. Agents Chemother. 52, 2890–2897. doi: 10.1128/AAC.00185-08
Kuang, L. H., Mu, L. Y., Su, M., Zhou, W., and Jiang, Y. M. (2015). Epidemiology and resistance mechanisms of group B Streptococci in Late-pregnant maternal birth canal. Sichuan Da Xue Xue Bao Yi Xue Ban 46, 692–696. doi: 10.13464/j.scuxbyxb.2015.05.009
Li, H. M., and Meng, W. L. (2010). Infection surveillance of group B streptococcus and infection studies of meternal-infant vertical transmission in pregnant women of migrant population. Mod. Hosp. 10, 28–30. doi: 10.3969/j.issn.1671-332X.2010.04.012
Lim, D. V., Morales, W. J., Walsh, A. F., and Kazanis, D. (1986). Reduction of morbidity and mortality rates for neonatal group B streptococcal disease through early diagnosis and chemoprophylaxis. J. Clin. Microbiol. 23, 489–492.
Lin, F.-Y. C., Azimi, P. H., Weisman, L. E., Philips, J. B. III, Regan, J., Clark, P., et al. (2000). Antibiotic susceptibility profiles for group B streptococci isolated from neonates, 1995–1998. Clin. Infect. Dis. 31, 76–79. doi: 10.1086/313936
Malek-Jafarian, M., Hosseini, F. S., and Ahmadi, A. R. (2015). Pattern of infection and antibiotic activity among Streptococcus agalactiae isolates from adults in Mashhad, Iran. Rep. Biochem. Mol. Biol. 3, 692–696.
Matorras, R., García-Perea, A., Omeñaca, F., Diez-Enciso, M., Madero, R., and Usandizaga, J. A. (1991). Intrapartum chemoprophylaxis of early-onset group B streptococcal disease. Eur. J. Obst. Gynecol. Reprod. Biol. 40, 57–62. doi: 10.1016/0028-2243(91)90045-M
Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., and Group, P. (2010). Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int. J. Surg. 8, 336–341. doi: 10.1016/j.ijsu.2010.02.007
Murayama, S. Y., Seki, C., Sakata, H., Sunaoshi, K., Nakayama, E., Iwata, S., et al. (2009). Capsular type and antibiotic resistance in Streptococcus agalactiae isolates from patients, ranging from newborns to the elderly, with invasive infections. Antimicrob. Agents Chemother. 53, 2650–2653. doi: 10.1128/AAC.01716-08
Okike, I. O., Ribeiro, S., Ramsay, M. E., Heath, P. T., Sharland, M., and Ladhani, S. N. (2014). Trends in bacterial, mycobacterial, and fungal meningitis in England and Wales 2004–11: an observational study. Lancet Infect. Dis. 14, 301–307. doi: 10.1016/S1473-3099(13)70332-3
Schrag, S., Gorwitz, R., Fultz-Butts, K., and Schuchat, A. (2002). Prevention of perinatal group B streptococcal disease. revised guidelines from CDC. MMWR Recomm. Rep. 51, 1–22. Available online at: https://www.cdc.gov/mmwr/preview/mmwrhtml/rr5111a1.htm
Seki, T., Kimura, K., Reid, M. E., Miyazaki, A., Banno, H., Jin, W., et al. (2015). High isolation rate of MDR group B streptococci with reduced penicillin susceptibility in Japan. J. Antimicrob. Chemother. 70, 2725–2728. doi: 10.1093/jac/dkv203
Shen, W., Liu, Q., and Zhang, J. Z. (2012). Clinical observation of intervention of group B streptococcus infection in gestation period. Chin. J. Postgrad. Med. 35, 12–14. doi: 10.3760/cma.j.issn.1673-4904.2012.12.005
Stoll, B. J., Hansen, N. I., Sánchez, P. J., Faix, R. G., Poindexter, B. B., Van Meurs, K. P., et al. (2011). Early onset neonatal sepsis: the burden of group B Streptococcal and E. coli disease continues. Pediatrics 127, 817–826. doi: 10.1542/peds.2010-2217
Suhaimi, M. E. S., Desa, M. N. M., Eskandarian, N., Pillayc, S. G., Ismaild, Z., Neela, V. K, et al. (2016). Characterization of a group B Streptococcus infection based on the demographics, serotypes, antimicrobial susceptibility and genotypes of selected isolates from sterile and non-sterile isolation sites in three major hospitals in Malaysia. J. Infect. Public Health. 10, 14–21. doi: 10.1016/j.jiph.2016.01.009
Tuppurainen, N., and Hallman, M. (1989). Prevention of neonatal group B streptococcal disease: intrapartum detection and chemoprophylaxis of heavily colonized parturients. Obstet. Sgynecol. 73, 583–587.
Verani, J. R., McGee, L., and Schrag, S. J. (2010). Prevention of perinatal group B streptococcal disease–revised guidelines from CDC, 2010. MMWR Recomm. Rep. 59, 1–36. Available online at: https://www.cdc.gov/mmwr/preview/mmwrhtml/rr5910a1.htm
Wells, G. A., Shea, B., O'Connell, D., et al. (2011). The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Nonrandomized Studies in Meta-Analyses. Available online at: http://wwwohrica/programs/clinical_epidemiology/oxfordasp
Yow, M. D., Mason, E. O., Leeds, L. J., Thompson, P. K., Clark, D. J., and Gardner, S. E. (1979). Ampicillin prevents intrapartum transmission of group B streptococcus. JAMA 241, 1245–1247. doi: 10.1001/jama.1979.03290380021019
Keywords: group B Streptococcus, infection, intrapartum antibiotic prophylaxis, clinical adverse outcomes, meta-analysis
Citation: Li S, Huang J, Chen Z, Guo D, Yao Z and Ye X (2017) Antibiotic Prevention for Maternal Group B Streptococcal Colonization on Neonatal GBS-Related Adverse Outcomes: A Meta-Analysis. Front. Microbiol. 8:374. doi: 10.3389/fmicb.2017.00374
Received: 16 November 2016; Accepted: 23 February 2017;
Published: 17 March 2017.
Edited by:Miguel Cacho Teixeira, Universidade de Lisboa, Portugal
Reviewed by:Zhe-Sheng Chen, St. John's University, USA
Jinma Ren, University of Illinois College Of Medicine at Peoria, USA
Guillaume Sébire, McGill University, Canada
Copyright © 2017 Li, Huang, Chen, Guo, Yao and Ye. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiaohua Ye, firstname.lastname@example.org
†These authors have contributed equally to this work.