Browse by author
Lookup NU author(s): Dr Andrew Kilner, Dr Katherine Orr, Dr Suren Kanagasundaram
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Objective: The potential for clinically significant transfer of pyrogen-inducing material in dialysate and substitution fluids is well recognized in the setting of chronic hemodialysis and hemodiafiltration and has led to the establishment of strict standards for microbiological purity. Preliminary evidence has indicated the potential for fluid contamination in continuous renal replacement therapy, and although the scale of the problem in contemporary, industry-standard equipment is unclear. We aimed to define the microbial integrity of modern continuous veno-venous hemofiltration (CVVH) replacement fluid circuitry. Design: Twenty-four CVVH replacement fluid circuits (mean lifespan, 34.2 hours; range, 4-86) were studied at completion of therapy. Setting: The integrated critical care unit and cardiothoracic intensive care unit of the Freeman Hospital, Newcastle upon Tyne, United Kingdom, between January and August 2007. Subjects. Patents with renal failure receiving treatment with CVVH. Interventions. Nil. Measurements: Culture and endotoxin assays of replacement fluid, culture of endoluminal swabs, and electron microscopy of harvested tubing. Main Results: Of the 24 replacement fluid cultures, nine (mean lifespan 32.8 hours, range 5-79) breached European Pharmacopoeia standards for ultrapure water (
Author(s): Moore I, Bhat R, Hoenich NA, Kilner AJ, Prabhu M, Orr KE, Kanagasundaram NS
Publication type: Article
Publication status: Published
Journal: Critical Care Medicine
Year: 2009
Volume: 37
Issue: 2
Pages: 496-500
ISSN (print): 0090-3493
ISSN (electronic): 1530-0293
Publisher: Lippincott Williams & Wilkins
URL: http://dx.doi.org/10.1097/CCM.0b013e3181957987
DOI: 10.1097/CCM.0b013e3181957987
Altmetrics provided by Altmetric