Pediatric Central Venous Access Device Lock Solutions: A Network Meta-analysis

Mari Takashima1,2,3, Yukiko Ezure4, Luis Furuya-Kanamori4

  • 1School of Nursing, Midwifery and Social Work, The University of Queensland, St Lucia, Queensland, Australia.

Pediatrics
|January 30, 2024
PubMed

Insights

Chelating agents and antibiotic locks may prevent central venous access device (CVAD)-associated bloodstream infections in children. Thrombolytic agents can prevent CVAD occlusion, but ethanol may increase risks.

Area of Science:

  • Pediatric critical care medicine
  • Pharmacology
  • Infectious disease prevention

Background:

  • Central venous access devices (CVADs) are crucial in pediatric care but prone to complications.
  • Lock solutions are routinely used to prevent and treat CVAD-related issues like infection, thrombosis, and occlusion.

Purpose of the Study:

  • To systematically review and rank various lock solutions for preventing or treating CVAD complications in pediatric patients.
  • To provide evidence-based recommendations for optimal lock solution selection.

Main Methods:

  • A systematic review and network meta-analysis of randomized controlled trials (RCTs) was conducted.
  • Searched five databases and two clinical trial registries for relevant studies.
  • Extracted data on CVAD-associated bloodstream infection (BSI), thrombosis, occlusion, failure, and mortality.

Main Results:

  • Chelating agents and antibiotic locks showed potential in preventing CVAD-associated BSI compared to heparinized saline.
  • Preventative thrombolytic agents were associated with reduced odds of CVAD occlusion.
  • Ethanol demonstrated increased odds of CVAD occlusion, while no solutions impacted thrombosis, CVAD failure, or mortality.

Conclusions:

  • Chelating agents and antibiotic locks may be effective for preventing pediatric CVAD-associated BSI.
  • Thrombolytic agents are a viable option for preventing CVAD occlusion.
  • Ethanol is not recommended for CVAD lock solutions due to increased occlusion risk.
Abstract