Pediatric home-based central venous access device dressings: Medical liquid adhesive versus standard care to reduce dressing disruption: The STICKY-kids RCT protocol - Summary - MDSpire

Pediatric home-based central venous access device dressings: Medical liquid adhesive versus standard care to reduce dressing disruption: The STICKY-kids RCT protocol

  • By

  • Tricia M. Kleidon

  • Mari Takashima

  • Victoria Gibson

  • Robert S. Ware

  • R. N. Nicole Marsh

  • Amanda J Ullman

  • July 16, 2026

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Objective:

To determine whether the use of medical liquid adhesive (MLA) in conjunction with standard dressing practices reduces dressing disruption and decreases central venous access device (CVAD) complications in children receiving in-home care.

Approach:
  • Study Design: A two-arm, parallel-group, superiority randomized controlled trial (RCT) comparing MLA plus standard care with standard care alone.
  • Population: Children aged 0-18 years requiring a CVAD for 7 days or more, receiving intravenous therapy through the Hospital-At-Home program.
  • Eligibility Criteria: Excludes children receiving end-of-life care, with hypersensitivity to MLA, significant skin compromise, or prior participation in the trial.
Key Findings:
  • MLA reduced initial central venous catheter dressing failure from 50% to 28% in adults.
  • MLA prolonged time to first dressing failure and reduced dressing changes without increasing medical adhesive-related skin injury (MARSI).
Interpretation:

Limitations:
  • The study is limited to a specific population within the Hospital-At-Home program.
  • Potential variability in home environments may affect outcomes.
Conclusion:

The STICKY Kids trial seeks to provide high-quality evidence on improving CVAD dressing durability in pediatric patients receiving home-based intravenous therapies.

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