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临床试验/NCT02511444
NCT02511444已完成不适用

Intrapartum Rapid GBS Testing in Patients Presenting With Threatened Preterm Labor

MemorialCare Health System2 个研究点 分布在 1 个国家目标入组 342 人开始时间: 2015年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
342
试验地点
2
主要终点
Negative predictive value of GBS real time PCR performed intrapartum

研究概览

简要总结

The purpose of this study is to evaluate the test characteristics of a rapid intrapartum real- time polymerase chain reaction (RT-PCR) compared to the intrapartum GBS culture as the standard in preterm patients presenting with threatened preterm labor or with obstetric indications for preterm delivery.

详细描述

Group B streptococcus (GBS) or Streptococcus agalactiae is a gram-positive bacterium that colonizes 10-40% of maternal gastrointestinal and urogenital tract sites. Maternal colonization remains the primary risk factor and the leading cause of early onset GBS disease in infants in the United States. Transmission of GBS to the neonate in early onset GBS cases occurs at the time of labor and delivery, with a transmission rate of 52.5% if no intrapartum antibiotics are used. Of those neonates, 1-2% term infants and 8% of preterm infants will develop early onset disease.

The Centers for Disease Control (CDC) recommends universal screening at 35-37 weeks via culture of the vagina and rectum. If this is performed ≤5 weeks before delivery, it has a sensitivity of 85% and a negative predictive value of 95-98%. There is a downside to screening remote from delivery however; vaginal GBS colonization fluctuates in the same woman over time, thus rendering possibly inaccurate GBS results. It has been reported that at least 10% of antenatal GBS negative women turned positive at the time of labor. This may suggest that screening at the time of delivery is a more accurate method of predicting actual GBS colonization status. In fact, a majority of neonatal GBS sepsis occurs in infants born to mothers with a negative antepartum screening culture.

Currently, a standard GBS culture may take up to 3 days to obtain results. A rapid diagnostic test has more recently been studied as a possible method of GBS screening - real-time polymerase chain reaction (RT-PCR). Prior studies of RT-PCR, specifically the Cepheid GeneXpert GBS assay used at Miller's Children's and Women's Hospital, have reported sensitivity from 85-98.5% and specificity of 96-99.6% using data from term gestations. The CDC currently permits the use of RT-PCR as a rapid screening test for those with unknown status at term.

Several reports demonstrate that RT-PCR is a rapid, more sensitive method than standard culture for determining the intrapartum GBS colonization status. Some studies have also demonstrated the ability of RT-PCR to identify patients who would otherwise be missed by traditional GBS culture. A study by Mueller et al demonstrated that out of 64 patients with positive RT-PCR results, 10 were actually negative on culture. A cost-effectiveness analysis has demonstrated that PCR intrapartum screening strategy is not any less cost-effective than traditional culture and confers a significant decrease in early onset GBS disease in term gestations.

Preterm infants suffer the highest rate of mortality from GBS infection, with up to 30% mortality in those < 33 weeks affected by GBS sepsis. Identifying GBS colonization is thus imperative in the 7-11% of all pregnancies affected by preterm labor, given that they will not have undergone universal screening yet (which typically occurs at 35-37 weeks). While the CDC recommends giving antibiotics to patients with unknown GBS status at substantial risk for preterm delivery, implementation of this recommendation is poor.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Pregnant women presenting for unplanned obstetrical care at a participating clinical study site
  • Gestational age between 21 6/7 and 36 6/7 weeks
  • Subject has not participated in the study before
  • Subject agrees to complete all aspects of the study and provide informed consent in accordance with applicable regulations
  • Signs and/or symptoms suggestive of preterm labor, whereby the managing clinician suspects preterm labor
  • Uterine contractions (with or without pain)
  • Intermittent lower abdominal pain, dull backache, pelvic pressure
  • Vaginal bleeding during the second and third trimester
  • Menstrual-like intestinal cramping (with or without diarrhea)
  • Change in vaginal discharge (amount, color, or consistency)
  • Vague sense of discomfort characterized as "not feeling right"
  • Change in cervical exam (cervical dilation, effacement, or consistency)
  • Signs and symptoms necessitating preterm delivery (i.e abruption, preeclampsia, hemolysis elevated liver enzymes, low platelet (HELLP) syndrome, ruptured membranes, chorioamnionitis, fetal indications)

排除标准

  • Exposure to antibiotics within 1 week prior to enrollment (15)
  • Known GBS bacteriuria at the time of enrollment
  • Prior history of neonatal GBS sepsis

结局指标

主要结局

Negative predictive value of GBS real time PCR performed intrapartum

时间窗: up to one and a half year

Specificity of intrapartum GBS real time PCR compared to intrapartum GBS

时间窗: up to one and a half year

Sensitivity of intrapartum GBS real time PCR compared to intrapartum GBS culture

时间窗: up to one and a half year

Positive predictive value of GBS Real time PCR performed intrapartum

时间窗: up to one and a half year

次要结局

  • Neonatal GBS septicemia(up to one and a half year)
  • Composite neonatal morbidity(up to one and a half year)
  • Maternal intrapartum chorioamnionitis(up to one and a half year)
  • Neonatal respiratory distress(up to one and half year)
  • number of neonatal intensive care unit days(up to one and a half year)
  • necrotizing enterocolitis(up to one and a half year)
  • Gestational age at delivery(up to one and a half year)
  • Neonatal mortality rate(up to one and a half year)
  • vaginal delivery(up to one and a half year)
  • Postpartum hemorrhage(up to one and a half year)
  • Maternal postpartum endometritis(up to one and a half year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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