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Catheter Biofilm Microbiome in Infected Neonatal Catheters.

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Baylor College of Medicine

Status

Completed

Conditions

Catheter-associated Bloodstream Infections (CLABSI)

Treatments

Other: Sample collection

Study type

Observational

Funder types

Other

Identifiers

NCT01985737
Blood Stream Infections
H-33004

Details and patient eligibility

About

Percutaneously Inserted Central Catheters (PICCs) are special tubes that are inserted into blood vessels of premature babies (neonates) to give them nutrition and medications. Sometimes these tubes get infected and they need to be removed. Also, the babies need to be given medications to treat these infections (antibiotics). PICC infections in neonates are a serious problem and we need to find new ways of detecting infections early so that we can treat them promptly to avoid complications.

The purpose of this study is to understand what causes tube infections in neonates and to develop a test to detect tube infections early to avoid complications.

Full description

Catheter-associated bloodstream infections (CLABSIs) are a significant component of healthcare-associated infections (HAI),which are associated with significant mortality, morbidity and healthcare costs. Neonates are at higher risk for CLABSIs than children or adults and CLABSIs are seen more commonly in neonatal than pediatric or adult intensive care units. Neonates, who develop CLABSIs, are not only at serious risk for mortality but also long term neurodevelopmental impairment. CLABSIs are often caused by organisms colonizing the skin and the most frequently isolated organisms are CONS, S. aureus and Candida.

The catheter biofilm microbiome, to our knowledge has not been investigated before. Evaluation of biofilm microbial signatures and microbial DNA load is a novel strategy that may permit earlier diagnosis of CLABSIs. Earlier detection may enable earlier targeted therapy such as antimicrobial lock solutions and may facilitate preservation of catheters in this vulnerable population. Catheter microbial DNA signatures or load may be useful biomarkers to not only predict or diagnose infections but to monitor antibiotic therapy and to confirm resolution of infection.

We will study 15 percutaneously inserted central catheters (PICC) each from neonates with CLABSIs and those without. We will evaluate the bacterial microbiome by profiling V3-5 region of the 16S rDNA, by PCR and pyrosequencing. We will correlate the catheter biofilm microbiome with catheter tip cultures and the skin microbiome at the catheter entry site. We aim to identify microbial signatures that predispose to dissemination of infection from catheter biofilms leading to CLABSIs. Further, we will quantify microbial DNA load in blood from the catheters at the time of removal, by real-time PCR of the bacterial 16S rDNA.

Enrollment

144 patients

Sex

All

Ages

1 day to 3 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Neonates with a percutaneously inserted central catheters (Neo PICC) who may or may not develop CLABSIs

Exclusion criteria

  • Infants with known Immunodeficiency Syndrome

Trial design

144 participants in 2 patient groups

Infants with infected PICC line
Description:
After informed consent the subjects that develop a PICC line infection in the NICU will serve as the cases.
Treatment:
Other: Sample collection
Infants without infected PICC line
Description:
After informed consent the subjects that do not develop a PICC line infection in the NICU will serve as the controls.
Treatment:
Other: Sample collection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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