A microbiological survey of bicarbonate-based replacement circuits in continuous veno-venous hemofiltration

Iain Moore1, Rammohan Bhat, Nicholas A Hoenich

  • 1Department of Renal Medicine, Freeman Hospital, Newcastle-upon-Tyne, United Kingdom.

Critical Care Medicine
|December 31, 2008
PubMed
Abstract

Insights

Microbial contamination is common in continuous veno-venous hemofiltration (CVVH) replacement fluid circuits, posing risks to critically ill patients. This study highlights frequent breaches in microbial integrity in standard CVVH equipment.

Area of Science:

  • Nephrology
  • Critical Care Medicine
  • Microbiology

Background:

  • Clinically significant pyrogen transfer in dialysate and substitution fluids is a known risk in hemodialysis.
  • Strict microbiological purity standards are established for chronic hemodialysis and hemodiafiltration.
  • Preliminary evidence suggests fluid contamination potential in continuous renal replacement therapy (CRRT).

Purpose of the Study:

  • To define the microbial integrity of modern continuous veno-venous hemofiltration (CVVH) replacement fluid circuitry.
  • To assess the extent of microbial contamination in industry-standard CVVH equipment.
  • To identify potential risks associated with fluid contamination in CRRT.

Main Methods:

  • Studied 24 CVVH replacement fluid circuits at the completion of therapy.
  • Conducted culture and endotoxin assays of replacement fluid.
  • Performed endoluminal swab cultures and electron microscopy of tubing samples.

Main Results:

  • Nine of 24 replacement fluid cultures exceeded European Pharmacopoeia standards for ultrapure water.
  • One of 24 endotoxin measurements breached European Pharmacopoeia standards.
  • Electron microscopy revealed biofilm contamination in 13 of 24 tubing samples; only 7 circuits were free from microbial contamination.

Conclusions:

  • Frequent breaches of microbial integrity were confirmed in industry-standard, bicarbonate-based CVVH circuits.
  • This contamination indicates a potential added risk to vulnerable, critically ill patients receiving systemic fluid infusion.
  • Discusses measures to reduce contamination levels and their impact in CVVH therapy.

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