Incidence, severity and outcome of central line related complications in pediatric oncology patients; A single center study

J Pediatr Surg. 2019 Sep;54(9):1894-1900. doi: 10.1016/j.jpedsurg.2018.10.054. Epub 2018 Oct 30.

Abstract

Background: Central venous access device (CVAD)-related complications are associated with high morbidity rates. This study was performed to underline the importance of CVAD-complication prevention and treatment.

Methods: An audit of practice of CVAD-related complications in pediatric oncology patients receiving a CVAD between January 2015 and June 2017 was performed. CVADs included were totally implantable venous access ports (TIVAPs), Hickman-Broviac® (HB), nontunneled, and peripherally inserted CVADs.

Results: A total of 201 children, with 307 CVADs, were analyzed. The incidence rates per 1000 CVAD-days for the most common complications were 1.66 for malfunctions, and 1.51 for central line-associated bloodstream infections (CLABSIs). Of all CVADs inserted, 37.1% were removed owing to complications, of which 45.6% were owing to CLABSIs. In 42% of the CLABSIs, the CLABSI could be successfully cured with systemic antibiotic treatment only. Of all included patients, 5.0% were admitted to the intensive care unit owing to CLABSI. The HB-CVAD compared to the TIVAP was a risk factor for CVAD-related complications, CLABSIs and dislocations in particular.

Conclusions: The incidence of CVAD-related complications is high. Research on the prevention and treatment of CVAD-related complications in pediatric oncology patients should be a high priority for all health care professionals.

Type of study: Prognosis study (retrospective).

Level of evidence: Level II.

Keywords: CLABSI; Central line complications; Pediatric oncology.

MeSH terms

  • Catheter-Related Infections / epidemiology*
  • Catheterization, Central Venous* / adverse effects
  • Catheterization, Central Venous* / statistics & numerical data
  • Central Venous Catheters / adverse effects*
  • Child
  • Humans
  • Incidence
  • Neoplasms* / epidemiology
  • Neoplasms* / therapy
  • Retrospective Studies