Skip to main content
OpenTrials
Completed

NCT Number: NCT02590198

Diagnostic Performance Comparison Between Procalcitonin-based vs. ANAES-based Guidelines

Neonatal bacterial infection remains a serious pathology in industrialized countries despite the use of prophylaxis measures for group B streptococcus (GBS) (peri-partum antibiotic in women with GBS colonization), which was implemented in the United States in 1996 and in France in 2001 and has led to a dramatic decrease in the incidence of neonatal bacterial infections. However, early onset neonatal infection (EONI), which is defined as an infection occurring during the first 6 days after birth (as opposed to late onset neonatal infections (LONI) occurring between days 7-89), is still one of the leading causes of neonatal morbidity and mortality. Physicians consider EONI a significant diagnostic and therapeutic emergency due to the potential for sudden onset and rapid evolution of sepsis in newborns with immature immune systems. Currently, in France, detection of EONI is based on national consensus guidelines published in 2002 (ANAES recommendations). There are broad indications to provide empirical antibiotic treatment pending diagnostic confirmation through different complementary exams. To ensure that every infected newborn is diagnosed, biological assessments are often repeated and result in the use of invasive and painful procedures, anemia and financial concerns. Moreover, in cases of abnormal biological results, many newborns are subjected to intravenous (IV) antibiotic treatments requiring hospitalization and separation from their mother. However recent studies have shown that antibiotics can have a potentially deleterious effect on the neonatal digestive microbiota and result in the appearance of antibiotic-resistant bacteria, with possible long-term consequences on the health of the child.

Procalcitonin (PCT) is a calcitonin prohormone secreted from the parenchymal tissues. This marker of inflammation has been shown to be a valuable diagnostic marker for bacterial infection in adults and in children. It also seems to be a reliable marker for neonatal bacterial infection, which would make it useful in the detection of EONI. Because physiological levels of PCT vary during the first days of life, possibly due to postnatal intestinal bacterial colonization, levels of this marker are difficult to interpret in the early neonatal period. However, in a study of 2151 newborns with suspected EONI, Nicolas Joram et al. found that PCT obtained from the umbilical blood cord, prior to newborn intestinal colonization, bypasses this postnatal physiological peak of PCT and effectively constitutes a discriminant marker to distinguish between infected and healthy infants using a cutoff value of 0.6 ng/ml.

Subsequent to this pilot study, several studies on PCT in umbilical blood cord confirmed its good diagnostic performance for EONI, particularly when included in a diagnostic algorithm. This marker could contribute to a better estimation of EONI risk in order to limit the use of unnecessary complementary exams and prescription of antibiotics and their associated short- and long-term side effects in healthy newborns.

Therefore, in this study, the investigators propose to test the diagnostic value of a PCT-based algorithm in newborns suspected of having EONI. The investigators hypothesize that this algorithm is as efficient as those currently used (ANAES), but will limit coinciding biological exams and exposure to antibiotics during the neonatal period.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Angers University Hospital, Angers, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All children born at > 36 weeks gestation in one of the 15 participating maternity or neonatology units and suspected having EONI according to the ANAES recommendations (clinical suspicion of chorioamnionitis, intrapartum maternal fever > 38°C, infected twin, spontaneous premature delivery at < 37 gestational weeks, prolonged rupture of membrane for > 12 hours, maternal group B Streptococcus colonization without full prophylactic antibiotic treatment, or signs of fetal asphyxia) will be included in the study.
  • Oral Consent (Non Opposition).

Exclusion criteria

  • Newborns will be considered ineligible if:
  • Parental non opposition is not obtained, if the parents do not speak French, present severe dementia and/or cannot be reached on day 6.
  • Nosocomial neonatal infection, severe congenital malformation or obstetrically explained neonatal asphyxia are diagnosed.
  • Secondary parental opposition.

Treatment and study plan

ANAES algorithm

Other

care as recommended by ANAES, with ANAES algorithm

PCT algorithm

Other

care based on PCT algorithm

Primary outcomes

  1. Primary outcome is a composite outcome including: death from any cause, intensive care unit admission for any reason, disease-specific complications, diagnosis of EONI after maternity discharge, need for antibiotics with hospital readmission

    Time frame: 6 days after birth

    The primary noninferiority endpoint is a composite of overall adverse outcomes induced by EONI occuring within 6 days following birth. It includes death, Neonatal Intensive care Unit (NICU) admission, or hospital readmission. The investigators chose this primary endpoint because the French definition of EONI diagnostic is subjective, specifically in case of possible EONI in case of gastric fluid positivity, and is finally rarely objectivated. Moreover, the new PCT-based algorithm do not require any gastric fluid analysis and modify the usual French definition of possible EONI, impossible to use in this context. Focusing on serious adverse event outcomes seems a very pragmatic and efficient methodologic strategy.

Secondary outcomes

  1. death

    Time frame: Day 6 and Day 90

    components of the primary outcome (death/NICU/rehospitalisation + antibiotics) will be considered independently, as is advised for a composite outcome.

  2. NICU admission

    Time frame: Day 6 and Day 90

    components of the primary outcome (death/NICU/rehospitalisation + antibiotics) will be considered independently, as is advised for a composite outcome.

  3. rehospitalisation in connection with antibiotic treatment

    Time frame: Day 6 and Day 90

    components of the primary outcome (death/NICU/rehospitalisation + antibiotics) will be considered independently, as is advised for a composite outcome.

  4. Inter-period frequency comparison of secondary adverse effect (SAE) and adverse effect (AE) related to antibiotics.

    Time frame: Day 6 and Day 90

  5. Number of blood samples induced by the 2 algorithms

    Time frame: Day 6 and Day 90

    EONI diagnostic exams frequency for EONI induced by the 2 algorithms (number of blood samples)

  6. Number of newborns investigated by the 2 algorithms

    Time frame: Day 6 and Day 90

    EONI diagnostic exams frequency for EONI induced by the 2 algorithms ( number of newborns investigated).

  7. Inter-period cumulated hospital stay length (including maternity stay)

    Time frame: Day 90

  8. clinical and biological description of EONI and LONI

    Time frame: 12 months

    Description of EONI and LONI bacteriological epidemiology (No recent data in France and Europe): frequency, typology...

Sponsors and collaborators

Lead sponsor

Nantes University Hospital

Other

Collaborators

  • Centre Hospitalier de Bretagne Sud
  • Créteil Hospital
  • Nantes Polyclinic
  • Poitiers University Hospital
  • Rennes University Hospital
  • University Hospital, Angers
  • University Hospital, Bordeaux
  • University Hospital, Brest
  • University Hospital, Paris
  • University Hospital, Tours

Registry information

Official study title

Diagnostic Performance Comparison Between Procalcitonin-based vs. ANAES-based Guidelines; Impact on Antibiotic Use in Newborns With Suspected Early-onset Neonatal Infection (EONI)

Acronym: DIACORD

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Oct 28, 2015
Registry last updated
Sep 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.