Multimodales Monitoring Des Fetalen Inflammationsrisikos Bei frühem Vorzeitigen Blasensprung (PPROM)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Preterm Premature Rupture of Membranes
- Sponsor
- Martin-Luther-Universität Halle-Wittenberg
- Enrollment
- 57
- Locations
- 4
- Primary Endpoint
- Odds ratio for severe fetal/early onset neonatal Infection
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
The purpose of this study is to examine whether the value of vaginal fluid cytokine levels as well as computerized fetal ECG analysis are suitable clinical parameters to detect an imminent intra-amniotic inflammation with a high risk of fetal inflammatory response syndrome (FIRS) or a neonatal early onset sepsis (EOS) and whether these parameters can be determined on a daily basis in the clinical monitoring of pregnancies complicated by PPROM.
Detailed Description
Preterm premature rupture of membranes (PPROM) is one of the leading causes for preterm birth and adverse neonatal outcome. Between 24 0/7 and 34 0/7 weeks of gestation the prolongation of pregnancy is the recommended course of action to reduce the risks of prematurity in most countries. An intra-amniotic infection resulting in fetal inflammatory response syndrome (FIRS) or early onset neonatal sepsis (EOS) is often associated with high morbidity and mortality. Standard monitoring includes the maternal response to inflammation (i.e. maternal serum parameters) as well as fetal signs of acute FIRS (i.e. fetal tachycardia, high cytokine level in amniotic fluid obtained by amniocentesis). Changes of fetal ECG-parameters are also a sign of an acute FIRS. Currently, there is no adequate parameter for the surveillance of a possible ongoing intra-amniotic infection. Other studies have reported a correlation between vaginal fluid interleukine 6 (IL6) collected noninvasively and the risk of FIRS and EOS. Information obtained by computerized fetal ECG analysis might be suitable to detect early signs of fetal infection before the manifestation of FIRS. With the implementation of a vaginal fluid collector it is possible to detect the vaginal fluid cytokine in clinical everyday routine. With the improvement of fetal ECG monitoring it is possible to record the fetal ECG daily. This study examines the correlation between these new parameters and the onset of fetal infection before the manifestation of a severe systemic fetal inflammation.
Investigators
Gregor Seliger
Dr. med.; chief resident
Martin-Luther-Universität Halle-Wittenberg
Eligibility Criteria
Inclusion Criteria
- •Clinical diagnosis of preterm rupture of the fetal membranes
- •Pregnancy between 24 0/7 and 34 0/7 weeks of gestation
- •Ability to give informed consent in german or english
Exclusion Criteria
- •Sign of acute amniotic infection syndrome
- •independent indication for urgent delivery
- •Active labor
- •Missing informed consent
Outcomes
Primary Outcomes
Odds ratio for severe fetal/early onset neonatal Infection
Time Frame: postpartum one point assessment/ first three days post partum
combined outcome - rate of: early onset neonatal sepsis, elevated IL6 concentration in cord blood sample, histological signs of funisitis
Secondary Outcomes
- necrotizing enterocolitis(28 days)
- Severe neonatal cerebral hemorrhage(28 days)
- combined neonatal adverse outcome(28 days)
- late onset neonatal sepsis(28 days)
- umbilical cord blood IL 6 concentration(first day after delivery)
- neonatal early onset sepsis(3 days)
- histological funisitis(first day after delivery)