Evaluation of the Clinical Practice of Using of a 70% Ethanol Lock Solution for the Prevention of Catheter Related Blood Stream Infections in Pediatric Patients Undergoing Intestinal Rehabilitation

This study has been withdrawn prior to enrollment.
(PI decided to withdraw study)
Sponsor:
Information provided by:
University of Nebraska
ClinicalTrials.gov Identifier:
NCT01409772
First received: May 22, 2009
Last updated: June 15, 2012
Last verified: June 2012

May 22, 2009
June 15, 2012
December 2009
June 2011   (final data collection date for primary outcome measure)
To determine the 90 day infection rate in eligible subjects for the term immediately prior to enrollment in the study protocol. [ Time Frame: 90 days ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01409772 on ClinicalTrials.gov Archive Site
  • 90 day CRBSI rate in enrolled subjects. [ Time Frame: 90 days ] [ Designated as safety issue: No ]
  • Type of organism involved in CRBSI, and the treatment strategy used for each infection. [ Time Frame: 90 days ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Evaluation of the Clinical Practice of Using of a 70% Ethanol Lock Solution for the Prevention of Catheter Related Blood Stream Infections in Pediatric Patients Undergoing Intestinal Rehabilitation
Evaluation of the Clinical Practice of Using of a 70 % Ethanol Lock Solution for the Prevention of Catheter Related Blood Stream Infections in Pediatric Patients Undergoing Intestinal Rehabilitation

The purpose of this study is to evaluate the clinical practice of the prophylactic use of ethanol locks for the prevention of catheter related blood stream infections in pediatric intestinal rehabilitation program patients requiring total parenteral nutrition.

Catheter- related blood stream infections are a serious complication for pediatric patients receiving parenteral nutrition. The leading causes of death in infants with short bowel syndrome (SBS) who are being treated with parenteral nutrition are central line sepsis and liver failure associated with the prolonged use of parenteral nutrition. (Cuffari, 2006) Incidence of infection ranges from 3% to 60% over the life span of each catheter. (Fratino, 2002) Interruption of nutritional support, antibiotic resistance and septic complications resulting from frequent infections can be life threatening to this fragile patient population. This patient population is dependent upon maintenance of central venous access for survival. Frequent hospitalizations, loss of work, and financial complications result in decreased quality of life for these patients and their caretakers. The cost of hospital treatment of catheter related bloodstream infections (CRBSI) has been estimated to range from $4000 to $56,000 for each occurrence. (MMWR 2002)

Vascular access sites are also limited in the pediatric population, and removal of central access for infection may diminish future ability to provide vital parenteral nutrition.(MMWR, 2002) Therefore, improvements in the ability to prevent infection are of utmost importance in this patient population.

The concept of antibiotic lock technique was developed in the late 1980s and was derived from various heparin lock protocols. Antibiotic locks have been used for both management and prevention of infection in vascular access devices. Antimicrobial choices for use in the antibiotic lock technique are dependent on the different pathogens suspected to infect the catheter lumen, characteristics of the organisms, and the pharmacodynamic properties of the antimicrobial agent. There is a risk of selection for multi-drug resistant organisms when antibiotic locks are utilized. In addition, heparin must be added to an antibiotic lock solution to maintain catheter patency.

More recently, ethanol locks have been utilized as a treatment option for children with CRBSIs. Ethanol is not only bactericidal and fungicidal in nature but also reveals thrombolytic properties. (Mouw, 2008) The thrombolytic properties eliminate the need for heparin addition to maintain catheter patency. Although utilized as treatment, ethanol is not currently being used for CRBSI prevention at our institution. Along with decreasing the risk of emerging antibiotic resistance, the investigators are attempting to determine if using ethanol as a lock solution will diminish the number of infections in the Intestinal Rehabilitation Program population, leading to decreased patient complications and costs. UNMC has the largest population of Intestinal Rehabilitation Program participants in the country making this a uniquely well-suited clinic in which to gather data surrounding this emerging infection-prevention strategy.

Observational
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Short Bowel Syndrome

  • Blood Stream Infections
  • Short Bowel Syndrome
Drug: Ethanol Lock
Ethanol Lock
Intestinal Rehab
Intervention: Drug: Ethanol Lock
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
December 2011
June 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Signed informed consent/assent and willingness to adhere to protocol
  • Intestinal rehabilitation patients with documented short bowel syndrome
  • Age: newborn to 19 years of age
  • Indwelling tunneled venous catheter placed for the purpose of total parenteral nutrition/IV fluids, with a 2 hour or longer window out of 24 hours for ethanol lock instillation
  • No history of alcohol abuse
  • No history of hypersensitivity to ethanol
  • No history or documented active seizure disorder

Exclusion Criteria:

  • Parent/guardian unwilling to sign consent
  • Active bacterial infection
  • Non-tunneled, non-permanent catheter (triple lumen or PICC)
  • Pre-existing condition that would prevent enrollment as determined by each patients' physician
  • Inability to adhere to protocol
Both
up to 25 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01409772
156-09-FB
No
Kari Simonsen, MD, University of Nebraska Medical Center
University of Nebraska
Not Provided
Principal Investigator: Kari A Simonsen, MD UNMC
University of Nebraska
June 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP