切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2021, Vol. 17 ›› Issue (03) : 347 -354. doi: 10.3877/cma.j.issn.1673-5250.2021.03.017

论著

晚孕期孕妇生殖道B族链球菌感染对母儿结局的影响
东蓓, 周素芳(), 张璇   
  • 收稿日期:2020-10-09 修回日期:2021-05-07 出版日期:2021-06-01
  • 通信作者: 周素芳

Effect of group B Streptococcus infection in genital tract of pregnant women in third trimester on maternal and infant outcomes

Bei Dong, Sufang Zhou(), Xuan Zhang   

  • Received:2020-10-09 Revised:2021-05-07 Published:2021-06-01
  • Corresponding author: Sufang Zhou
  • Supported by:
    Maternal and Child Health Research Project of Jiangsu Province(F201668)
引用本文:

东蓓, 周素芳, 张璇. 晚孕期孕妇生殖道B族链球菌感染对母儿结局的影响[J/OL]. 中华妇幼临床医学杂志(电子版), 2021, 17(03): 347-354.

Bei Dong, Sufang Zhou, Xuan Zhang. Effect of group B Streptococcus infection in genital tract of pregnant women in third trimester on maternal and infant outcomes[J/OL]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2021, 17(03): 347-354.

目的

探讨晚孕期孕妇生殖道B族链球菌(GBS)感染的影响因素及其对母儿结局的影响。

方法

选择2016年8月至2018年8月,在苏州高新区人民医院进行产前检查,并于35~37孕周时采取荧光定量PCR进行GBS DNA检测的1 149例晚孕期孕妇为研究对象。采用回顾性分析方法,将其分为研究组(n=81,GBS DNA呈阳性)与对照组(n=1 068,GBS DNA呈阴性)。对研究组GBS感染孕妇,采取产时抗菌药物预防(IAP)措施。收集2组受试者年龄、受教育程度、孕次、产次、流产史、分娩方式,分娩孕龄与人体质量指数(BMI)、血清维生素D含量,妊娠期糖尿病(GDM)、胎膜早破与产后出血发生情况,以及研究组新生儿出生后第4周GBS感染随访结果,并采用成组t检验、Mann-Whitney U检验、χ2检验等进行统计学比较。采用多因素非条件logistic回归分析,对晚孕期孕妇GBS感染影响因素进行分析。本研究遵循的程序符合2013年新修订的《世界医学协会赫尔辛基宣言》要求,并通过苏州高新区人民医院伦理委员会审批(审批文号:[2016]伦审批第001号)。

结果

①2组孕妇中,初产妇与经产妇构成比、流产史、GDM发生率、血清维生素D含量比较,差异均无统计学意义(P>0.05),而2组孕妇年龄、受教育程度构成比与分娩时BMI分别比较,差异均有统计学意义(t=-2.004、P=0.045,χ2=69.972、P<0.001,t=7.054、P<0.001)。②晚孕期孕妇GBS感染影响因素的多因素非条件logistic回归分析结果显示,分娩时BMI≥25 kg/m2与受教育程度为高中及以下,均为晚孕期孕妇GBS感染的独立危险因素(OR=2.901、6.137,95%CI:1.782~4.722、3.737~10.078,均为P<0.001)。③研究组孕妇产褥期感染、新生儿肺炎发生率分别为3.7%(3/81)与4.9%(4/81),分别显著高于对照组的0.8%(9/1 068)与1.0%(11/1 068),并且差异均有统计学意义(P=0.047,χ2=6.150、P=0.013)。④研究组孕妇分娩的81例新生儿的出生后1周GBS阳性率为53.1 %(43/81),早发型GBS肺炎发生率为2.5%(2/81)。

结论

分娩时孕妇BMI≥25 kg/m2与受教育程度为高中及以下,均为其GBS感染的独立危险因素。晚孕期孕妇GBS感染可导致其产褥期感染及新生儿肺炎发生率增高。

Objective

To explore influencing factors of group B Streptococcus (GBS) in genital tract of pregnant women in third trimester and its effects on outcomes of pregnant women and infants.

Methods

From August 2016 to August 2018, a total of 1 149 pregnant women in third trimester who received prenatal examination in People′s Hospital of Suzhou High-tech Zone and detection of GBS DNA by fluorescence quantitative PCR at gestational age of 35-37 weeks were selected as research subjects. By retrospective analysis method, they were divided into study group (n=81, GBS DNA+ in genital tract), and control group (n=1 068, GBS DNA- in genital tract). Measures of intrapartum antibiotic prophylaxis (IAP) was taken to subjects in study group. Clinical data of 2 groups such as age, educational background, gravidity, parity, history of abortion, mode of delivery, gestational age and body mass index (BMI) at delivery, serum vitamin D levels, rates of gestational diabetes mellitus (GDM), premature rupture of membranes, postpartum hemorrhage, and follow-up of GBS infection of neonates in study group at 4 weeks after birth were collected. Independent-samples t test, Mann-Whitney U test and chi-square test were used for statistical comparisons. Multivariate unconditional logistic regression analysis was used to analyze influencing factors of GBS infection in genital tract of pregnant women in third trimester. The procedure in this study was in line with the requirements of Helsinki Declaration of the World Medical Association revised in 2013, and has been approved by the Ethics Committee of People′s Hospital of Suzhou High-tech Zone (Approval No. 2016-001).

Results

①There were no statistically significant differences in composition ratio of primipara and multipara, history of abortion, incidence of GDM and serum vitamin D levels between two groups (P>0.05). While there were statistically significant differences in age, composition ratio of educational background and BMI at delivery between two groups (t=-2.004, P=0.045; χ2=69.972, P<0.001; t=7.054, P<0.001). ②Multivariate unconditional logistic regression analysis showed that BMI≥25 kg/m2 at delivery and high school education level or below were independent risk factors for GBS infection in genital tract of pregnant women in third trimester (OR=2.901, 6.137, 95%CI: 1.782-4.722, 3.737-10.078, all P<0.001). ③The incidence of puerperium infection and neonatal pneumonia in study group were 3.7% (3/81) and 4.9% (4/81), which were significantly higher than those in control group 0.8% (9/1 068) and 1.0% (11/1 068), respectively, and both differences were statistically significant (P=0.047; χ2=6.150, P=0.013). ④Among 81 neonates of study group, positive rate of GBS at 1 week after birth was 53.1% (43/81). The incidence of early onset GBS pneumonia in neonates was 2.5% (2/81).

Conclusions

BMI≥25 kg/m2 at delivery and high school education level or below are independent risk factors for GBS infection in genital tract of pregnant women in third trimester, and may lead to increased incidence of puerperium infection and neonatal pneumonia.

表1 晚孕期孕妇发生生殖道GBS感染影响因素的单因素分析
表2 晚孕期孕妇发生生殖道GBS感染影响因素的多因素非条件logistic回归分析变量的含义及其赋值情况
表3 晚孕期孕妇发生生殖道GBS感染影响因素的多因素非条件logistic回归分析
表4 2组孕妇及其分娩新生儿结局比较[例数(%)]
[1]
曲业敏,马淑青,李彬彬. 围生期B族链球菌感染及预防的研究进展[J]. 中国微生态学杂志2014, 26(11): 1356-1358. DOI: 10.13381/j.cnki.cjm.201411032.
[2]
Tien N, Ho CM, Lin HJ, et al. Multilocus sequence typing of invasive group B Streptococcus in central area of Taiwan[J]. J Microbiol Immunol Infect, 2011, 44(6): 430-434. DOI: org/10.1016/j.jmii.2011.04.013.
[3]
Chen IL, Chiu NC, Chi H, et al. Changing of bloodstream infections in a medical center neonatal intensive care unit[J]. J Microbiol Immunol Infect, 2017, 50(4): 514-520.DOI: 10.1016/j.jmii.2015.08.023.
[4]
Lin MC, Chiu NC, Chi H, et al. Evolving trends of neonatal and childhood bacterial meningitis in northern Taiwan[J]. J Microbiol Immunol Infect, 2015, 48(3): 296-301. DOI: 10.1016/j.jmii.2013.08.012.
[5]
臧玉琴,王辰,田文艳,等. B族链球菌感染致不良妊娠结局机制的研究进展[J]. 中华微生物学和免疫学杂志2018, 38(9): 716-720. DOI: 10.3760/cma.j.issn.0254-5101.2018.09.012.
[6]
Verani JR, McGee L, Schrag SJ, et al. Prevention of perinatal group B streptococcal disease--revised guidelines from CDC, 2010[J]. MMWR Recomm Rep, 2010, 59(RR-10): 1-36.
[7]
Baker CJ. The spectrum of perinatal group B streptococcal disease[J]. Vaccine, 2013, 31(Suppl 4): D3-D6. DOI: 10.1016/j.vaccine.2013.02.030.
[8]
Guan X, Mu X, Ji W, et al. Epidemiology of invasive group B streptococcal disease in infants from urban area of South China, 2011-2014[J]. BMC Infect Dis, 2018, 18(1): 14. DOI: 10.1186/s12879-017-2811-0.
[9]
华春珍,俞蕙,庄捷秋,等. 2011至2015年181例儿童无乳链球菌血流感染多中心研究[J].中华儿科杂志2016, 54(8): 577-581. DOI: 10.3760/cma.j.issn.0578-1310.2016.08.004.
[10]
林新祝,吴健宁,张雪芹,等. 晚孕期阴道B族链球菌定植与新生儿感染的关系[J]. 中华围产医学杂志2016, 19(7): 491-496. DOI: 10.3760/cma.j.issn.1007-9408.2016.07.003.
[11]
Madrid L, Seale AC, Kohli-Lynch M, et al. Infant group B streptococcal disease incidence and serotypes worldwide: systematic review and Meta-analyses[J]. Clin Infect Dis, 2017, 65(suppl_2): S160-S172. DOI: 10.1093/cid/cix656.
[12]
Wollheim C, Sperhacke RD, Fontana SKR, et al. Group B Streptococcus detection in pregnant women via culture and PCR methods[J]. Rev Soc Bras Med Trop, 2017, 50(2): 179-183. DOI: 10.1590/0037-8682-0454-2016.
[13]
李东,张树琛,时琰丽,等. 北京地区孕晚期妇女定植B族链球菌耐药状况与血清型分布情况分析[J]. 首都医科大学学报2018, 39(4): 591-595. DOI: 10.3969/j.issn.1006-7795.2018.04.021.
[14]
容莉莉,关小珊,刘海英,等. 广州地区GBS阳性孕妇GBS致病菌株的基因分型及分子流行病学调查[J]. 现代检验医学杂志2017, 32(1): 87-90. DOI: 10.3969/j.issn.1671-7414.2017.01.024.
[15]
Ji W, Zhang L, Guo Z, et al. Colonization prevalence and antibiotic susceptibility of group B Streptococcus in pregnant woman over a 6-year period in Dongguan, China[J]. PLoS One, 2017, 12(8): e0183083. DOI: 10.1371/journal.pone.0183083.
[16]
宋海燕,郑旭,由晓颜,等. 青岛孕晚期妇女B族链球菌定植、药敏及血清型分析[J]. 中国实验诊断学2019, 23(11): 1937-1939. DOI: 10.3969/j.issn.1007-4287.2019.11.018.
[17]
高晶,汪雅萍,蒋南燕,等. 克林霉素诱导耐药B族链球菌同源性分析及耐药基因研究[J]. 中华检验医学杂志2018, 41(1): 24-28. DOI: 10.3760/cma.j.issn.1009-9158.2018.01.007.
[18]
Kim EJ, Oh KY, Kim MY, et al. Risk factors for group B Streptococcus colonization among pregnant women in Korea[J]. Epidemiol Health, 201 1, 33: e2011010. DOI: 10.4178/epih/e2011010.
[19]
Rick AM, Aguilar A, Cortes R, et al. Group B Streptococci colonization in pregnant Guatemalan women: prevalence, risk factors, and vaginal microbiome[J]. Open Forum Infect Dis, 2017, 4(1): ofx020. DOI: 10.1093/ofid/ofx020.
[20]
Helmig RB, Gertsen JB. Diagnostic accuracy of polymerase chain reaction for intrapartum detection of group B Streptococcus colonization[J]. Acta Obstet Gynecol Scand, 2017, 96(9): 1070-1074. DOI: 10.1111/aogs.13169.
[21]
杨梦楠,花晓琳,金敏菲,等. 妊娠期B族链球菌感染现状及对母儿结局的影响[J]. 现代妇产科进展2019, 28(3): 173-177. DOI: 10.13283/j.cnki.xdfckjz.2019.03.002.
[22]
孟婵,周洁琼,钟媛媛. 妊娠晚期B族链球菌感染的流行病学研究[J]. 重庆医学2019, 48(23): 4067-4070. DOI: 10.3969/j.issn.1671-8348.2019.23.027.
[23]
Namugongo A, Bazira J, Fajardot Y, et al. Group B Streptococcus colonization among pregnant women attending Antenatal Care at Tertiary Hospital in rural Southwestern Uganda[J]. Int J Microbiol, 2016, 2016: 3816184. DOI: 10.1155/2016/3816184.
[24]
Najminajmi N, Jehan I, Sikandar R, et al. Maternal genital tract colonisation by group B Streptococcus: a hospital based study[J]. J Pak Med Assoc, 2013, 63(9): 1103-1107.
[25]
Maxwell C, Gaudet L, Cassir G, et al. Guideline No. 391-pregnancy and maternal obesity part 1: pre-conception and prenatal care[J]. J Obstet Gynaecol Can, 2019, 41(11): 1623-1640. DOI: 10.1016/j.jogc.2019.03.026PlumXMetrics.
[26]
Maxwell C, Gaudet L, Cassir G, et al. Guideline No. 392-pregnancy and maternal obesity part 2: team planning for delivery and postpartum care[J]. J Obstet Gynaecol Can, 2019, 41(11): 1660-1675. DOI: 10.1016/j.jogc.2019.03.027.
[27]
赵丽娟,李合欣,张彦玲. 围产期孕妇B族链球菌感染及妊娠结局的相关研究[J]. 中国药物与临床2018, 18(12): 2186-2187. DOI: 10.11655/zgywylc2018.12.050.
[28]
周卫萍. 晚孕期孕妇阴道B族链球菌定植与新生儿感染的相关性分析[J]. 中国医药指南2019, 17(23): 141-142. DOI: 10.15912/j.cnki.gocm.2019.23.116.
[29]
廖宗琳,陈丽霞,沈宏志,等. 围产期孕妇生殖道B族链球菌感染的影响因素分析及对妊娠结局的影响[J]. 中华医院感染学杂志2018, 28(2): 247-249, 253. DOI: 10.11816/cn.ni.2018-173073.
[30]
梅艳,张萍,金敏菲,等. 妊娠相关B族链球菌感染的研究进展[J]. 中华围产医学杂志2017, 20(12): 895-898. DOI: 10.3760/cma.j.issn.1007-9408.2017.12.011.
[31]
Kobayashi M, Schrag SJ, Alderson MR, et al. WHO consultation on group B Streptococcus vaccine development: report from a meeting held on 27-28 April 2016[J]. Vaccine, 2019, 50(37): 7307-7314. DOI: 10.1016/j.vaccine.2016.12.029.
[32]
林新祝,祝垚,林雅茵,等. B族链球菌不同侵袭性感染类型临床特征及药敏试验的多中心研究[J]. 中华围产医学杂志2019, 22(8): 597-603. DOI: 10.3760/cma.j.issn.1007-9408.2019.08.012.
[33]
罗力冰,周镇邦,劳锦辉,等. 孕晚期B族链球菌筛查及分娩期预防性抗生素治疗效果的临床分析[J]. 中华围产医学杂志2018, 21(8): 537-540. DOI: 10.3760/cma.j.issn.1007-9408.2018.08.006.
[1] 明昊, 肖迎聪, 巨艳, 宋宏萍. 乳腺癌风险预测模型的研究现状[J/OL]. 中华乳腺病杂志(电子版), 2024, 18(05): 287-291.
[2] 庄燕, 戴林峰, 张海东, 陈秋华, 聂清芳. 脓毒症患者早期生存影响因素及Cox 风险预测模型构建[J/OL]. 中华危重症医学杂志(电子版), 2024, 17(05): 372-378.
[3] 钱警语, 郑明明. 《2024意大利妇产科学会非侵入性和侵入性产前诊断指南》解读[J/OL]. 中华妇幼临床医学杂志(电子版), 2024, 20(05): 486-492.
[4] 黄蓉, 梁自毓, 祁文瑾. NLRP3炎症小体在胎膜早破孕妇血清中的表达及其意义[J/OL]. 中华妇幼临床医学杂志(电子版), 2024, 20(05): 540-548.
[5] 何霞, 黄蓉, 祁文瑾. 胎膜早破孕妇胎盘与胎膜菌群丰度的高通量测序研究[J/OL]. 中华妇幼临床医学杂志(电子版), 2024, 20(05): 549-555.
[6] 谢江燕, 王亚菲, 贺芳. 妊娠合并血栓性血小板减少性紫癜2例并文献复习[J/OL]. 中华妇幼临床医学杂志(电子版), 2024, 20(05): 556-563.
[7] 黄鸿初, 黄美容, 温丽红. 血液系统恶性肿瘤患者化疗后粒细胞缺乏感染的危险因素和风险预测模型[J/OL]. 中华实验和临床感染病杂志(电子版), 2024, 18(05): 285-292.
[8] 罗文斌, 韩玮. 胰腺癌患者首次化疗后中重度骨髓抑制的相关危险因素分析及预测模型构建[J/OL]. 中华普通外科学文献(电子版), 2024, 18(05): 357-362.
[9] 贺斌, 马晋峰. 胃癌脾门淋巴结转移危险因素[J/OL]. 中华普外科手术学杂志(电子版), 2024, 18(06): 694-699.
[10] 林凯, 潘勇, 赵高平, 杨春. 造口还纳术后切口疝的危险因素分析与预防策略[J/OL]. 中华疝和腹壁外科杂志(电子版), 2024, 18(06): 634-638.
[11] 杨闯, 马雪. 腹壁疝术后感染的危险因素分析[J/OL]. 中华疝和腹壁外科杂志(电子版), 2024, 18(06): 693-696.
[12] 周艳, 李盈, 周小兵, 程发辉, 何恒正. 不同类型补片联合Nissen 胃底折叠术修补食管裂孔疝的疗效及复发潜在危险因素[J/OL]. 中华疝和腹壁外科杂志(电子版), 2024, 18(05): 528-533.
[13] 张伟伟, 陈启, 翁和语, 黄亮. 随机森林模型预测T1 期结直肠癌淋巴结转移的初步研究[J/OL]. 中华结直肠疾病电子杂志, 2024, 13(05): 389-393.
[14] 颜世锐, 熊辉. 感染性心内膜炎合并急性肾损伤患者的危险因素探索及死亡风险预测[J/OL]. 中华临床医师杂志(电子版), 2024, 18(07): 618-624.
[15] 李文哲, 王毅, 崔建, 郑启航, 王靖彦, 于湘友. 新疆维吾尔自治区重症患者急性肾功能异常的危险因素分析[J/OL]. 中华卫生应急电子杂志, 2024, 10(05): 269-276.
阅读次数
全文


摘要


AI


AI小编
你好!我是《中华医学电子期刊资源库》AI小编,有什么可以帮您的吗?