Safety and Efficacy Study of Ethanol Locking to Prevent Central Line Infection in Premature Neonates
Primary Purpose
Infection Associated With Catheter, Bacteremia, Sepsis
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ethanol lock
Heparinized saline
Sponsored by
About this trial
This is an interventional prevention trial for Infection Associated With Catheter focused on measuring Central line associated infection, PICC associated infection, Neonatal central line associated sepsis, Central line colonization, Ethanol Lock
Eligibility Criteria
Inclusion Criteria:
- Preterm infants < 32 weeks gestation at birth who require a PICC
Exclusion Criteria:
- Any baby with a positive blood culture less than 48 hours prior to PICC placement; any infant who requires pressors in excess of >5 mcg/kg/min
Sites / Locations
- East Carolina University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Ethanol
Heparinized saline
Arm Description
Assigned intervention is a 70% ethanol lock, placed every 72 hours for 15 minutes, for the duration of the PICC line.
Intervention is to place a heparinized saline lock every 72 hours for 15 minutes, for the duration of the line.
Outcomes
Primary Outcome Measures
Incidence of PICC-related sepsis in infants with ethanol-treated vs. Placebo treated lines
Primary endpoint of the study is to compare the incidence of PICC-related sepsis in infants with ethanol treated vs. Placebo treated lines by study day 28. PICC-related sepsis is defined by any 2 clinical signs or symptoms plus one positive peripheral blood culture for a recognized pathogen in this population other than coagulase-negative staphylococcus, or 2 positive peripheral blood cultures for coagulase-negative staphylococcus within 48 hours.
Secondary Outcome Measures
Evaluation of PICC colonization following ethanol locking
PICC colonization is reflected by growth of >15 CFU from a 5-cm segement of the PICC tip by semiquantitative (roll-plate) culture, or growoth of >100 CFU by quantitative (sonication) broth culture in an otherwise asymptomatic patient.
Whether the primary and secondary endpoints differ by birthweight strata
Birthweight stratification will use a 3-tiered subset (<1000g, 1000-1250g, and >1250g) consistent with existing neonatal literature.
To determine whether ethanol lock treatment impacts incidence of clinical evaluations for suspected sepsis
Other evaluations for suspected sepsis are those not defined by the primary endpoint but meeting criteria for infection of some other sterile body fluid (urine or CSF).
To determine whether antibiotic use for any indication (including non-bacteremia) alters the incidence of PICC-related infection or colonization as defined in the primary and secondary endpoints
See above
Determine side effects of ethanol locking in premature babies
To determine the side effects of flushing ethanol locks into premature infants following lock therapy, if any
To determine effect of ethanol locking on neonatal PICC lines
To determine how ethanol locking affects central line function and integrity in vivo, if at all.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01365312
Brief Title
Safety and Efficacy Study of Ethanol Locking to Prevent Central Line Infection in Premature Neonates
Official Title
A Prospective, Randomized, Blinded, Placebo-Controlled Trial of Periodic, Brief Ethanol Locks to Prevent Peripherally-Inserted Central Catheter (PICC) Infections in Preterm Infants in the Neonatal Intensive Care Unit
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Terminated
Why Stopped
Primary investigator relocated
Study Start Date
February 2010 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
East Carolina University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Appropriate delivery of adequate nutrition and medications in premature infants often requires central venous access in the form of a special IV called a PICC (peripherally inserted central catheter). While a necessary feature of neonatal intensive care, PICCs pose significant risk: among the most serious of these is infection. One common, successful infection control practice used in older children and adults involves the use of a lock, in which a fluid-filled syringe is attached to the end of an IV when it is not in use in order to prevent and/or treat clotting or infection. The solution is left for some period of time and is then either withdrawn from the line or flushed into the patient. The solution could be saline, antibiotics, other antiseptics, or any combination of these. However in the premature infant, use of antibiotics as a locking compound risks leaving behind organisms resistant to treatment; antiseptics can irritate vessels and cause breakage to sensitive premature skin; saline has neither sterilization nor anti-infective properties. By contrast, ethanol neutralizes or kills most bacteria, viruses, and fungi without the risk of resistance, and because it is not externally applied there is no risk to baby skin. Ethanol-based lock protocols have been used safely and effectively in both adult and pediatric populations without adverse effects, but this has not been tested in premature babies because fluids and medication are delivered continuously: placement of a lock traditionally requires an extended pause (hours or days) in fluid and medication administration.
To overcome these key limitations, a periodic, brief ethanol lock protocol was designed such that both infant exposure and interruptions to fluid and medication delivery would be minimized. The lock is practical, cheap, easy to place, and takes advantage of an existing daily pause during which IV tubing and fluids hooked up to the PICC are changed. The objective of this study is to test the hypothesis that use of a 70% ethanol lock, every 3rd day, for 15 minutes, will safely and effectively reduce PICC infection in our unit.
Detailed Description
PICC infection is of particular concern in the NICU because of the need for long term intravenous access in many very-low and the majority of extremely-low birthweight infants, the very populations at highest risk for infection in the first place. Central lines are a mainstay of treatment in these babies because of the need for extended parenteral nutrition, which itself has been associated with blood stream infection, not to mention the increased use of anti-infectives, added hospitalization costs, longer length of stay, and negative impact upon nutrition delivery when infectious complications occur.
Existing infection control practices differ by unit and region, and include hand washing, sterile precautions at insertion and dressing changes, elimination of mandatory scheduled dressing changes, minimizing port access to the extent permitted by clinical care, prophylactic antibiotics, and closed medication systems. Success is variable: there is no standard highly effective, safe approach to infection control, and central line infection remains a leading cause of morbidity and mortality in the NICU.
A standard practice to maintain central line patency when it is not in use is to lock it with a syringe containing a heparinized solution. Locks containing antibiotics have been used to prevent infection of central lines and to treat already-infected lines, but this approach confers risk of development of organisms resistant to treatment. External chlorhexidine-impregnated dressings have been used but can harm premature skin and do not achieve sterilization of the lumen or hub, where most infections originate.
Medical grade ethyl alcohol (ethanol) is a widely used compound with uses as a disinfectant, preservative, antidote to ingested ethylene glycol (anti-freeze), and anti-microbial. The FDA lists no specific approval or indication though it's use is widely recognized. Multiple studies have been conducted in sheep, children and adults, using 0.5-2 mL 70% ethanol locks to successfully prevent and/or treat catheter related infection without development of resistant organisms, adverse side effects to patients, or disruptions in catheter integrity. Though the ethanol lock approach has not yet been applied to premature neonates, safe and successful precedent in humans as young as 3 months is established; ours is the first trial of ethanol locking in a NICU setting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection Associated With Catheter, Bacteremia, Sepsis
Keywords
Central line associated infection, PICC associated infection, Neonatal central line associated sepsis, Central line colonization, Ethanol Lock
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ethanol
Arm Type
Experimental
Arm Description
Assigned intervention is a 70% ethanol lock, placed every 72 hours for 15 minutes, for the duration of the PICC line.
Arm Title
Heparinized saline
Arm Type
Placebo Comparator
Arm Description
Intervention is to place a heparinized saline lock every 72 hours for 15 minutes, for the duration of the line.
Intervention Type
Drug
Intervention Name(s)
Ethanol lock
Intervention Description
Placement of 0.5 cc 70% ethanol, every 72 hours, for 15 minutes, into PICC lines randomized to ethanol intervention
Intervention Type
Drug
Intervention Name(s)
Heparinized saline
Intervention Description
0.5 cc heparinized saline to be placed once every 72 hours for 15 minutes, in PICC lines randomized to placebo
Primary Outcome Measure Information:
Title
Incidence of PICC-related sepsis in infants with ethanol-treated vs. Placebo treated lines
Description
Primary endpoint of the study is to compare the incidence of PICC-related sepsis in infants with ethanol treated vs. Placebo treated lines by study day 28. PICC-related sepsis is defined by any 2 clinical signs or symptoms plus one positive peripheral blood culture for a recognized pathogen in this population other than coagulase-negative staphylococcus, or 2 positive peripheral blood cultures for coagulase-negative staphylococcus within 48 hours.
Time Frame
Study Day #28 or sooner if PICC is discontinued before day #28
Secondary Outcome Measure Information:
Title
Evaluation of PICC colonization following ethanol locking
Description
PICC colonization is reflected by growth of >15 CFU from a 5-cm segement of the PICC tip by semiquantitative (roll-plate) culture, or growoth of >100 CFU by quantitative (sonication) broth culture in an otherwise asymptomatic patient.
Time Frame
Duration of PICC use, average of 3 weeks
Title
Whether the primary and secondary endpoints differ by birthweight strata
Description
Birthweight stratification will use a 3-tiered subset (<1000g, 1000-1250g, and >1250g) consistent with existing neonatal literature.
Time Frame
Duration of PICC use, average of 3 weeks
Title
To determine whether ethanol lock treatment impacts incidence of clinical evaluations for suspected sepsis
Description
Other evaluations for suspected sepsis are those not defined by the primary endpoint but meeting criteria for infection of some other sterile body fluid (urine or CSF).
Time Frame
Duration of PICC use, average of 3 weeks
Title
To determine whether antibiotic use for any indication (including non-bacteremia) alters the incidence of PICC-related infection or colonization as defined in the primary and secondary endpoints
Description
See above
Time Frame
Duration of PICC use, average of 3 weeks
Title
Determine side effects of ethanol locking in premature babies
Description
To determine the side effects of flushing ethanol locks into premature infants following lock therapy, if any
Time Frame
Duration of PICC use, average of 3 weeks
Title
To determine effect of ethanol locking on neonatal PICC lines
Description
To determine how ethanol locking affects central line function and integrity in vivo, if at all.
Time Frame
Duration of PICC use, average of 3 weeks
10. Eligibility
Sex
All
Maximum Age & Unit of Time
32 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Preterm infants < 32 weeks gestation at birth who require a PICC
Exclusion Criteria:
Any baby with a positive blood culture less than 48 hours prior to PICC placement; any infant who requires pressors in excess of >5 mcg/kg/min
Facility Information:
Facility Name
East Carolina University
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States
12. IPD Sharing Statement
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Safety and Efficacy Study of Ethanol Locking to Prevent Central Line Infection in Premature Neonates
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