Original Article

Investigations into the Sterility of Manually Assembled Extracorporeal Circuits with Vented Reservoirs

¹ State University of New York Upstate Medical University, Department of Cardiovascular Perfusion, College of Health Professions
² State University of New York Upstate Medical University, Department of Anesthesiology, College of Health Professions
³ State University of New York Upstate Medical University, Department of Clinical Pathology, College of Health Professions
⁴ State University of New York Upstate Medical University, Department of Surgery, College of Health Professions

^* Address correspondence to: Bruce Searles, BS, CCP Assistant Professor and Department Chair Department of Cardiovascular Perfusion College of Health Professions SUNY Upstate Medical University 750 East Adams St. Syracuse, NY 13210

Abstract

This study was designed to investigate the ability of an extracorporeal circuit (ECC) with a vented hard shell reservoir to remain sterile for a period of 72 h under dry conditions. The study was conducted in three phases. In Phase One: Two previously published methods for detecting contamination of the ECC were compared. A group of positive controls was collected by contaminating identical circuits with a known level of Enterobacter cloacae (ATTC: 13047) before initiating a regimen of “sample–dilute–sample” culturing. Negative controls for this phase were conducted by randomly sampling 1 L per manufacturer’s lot of lactated ringers with each detection method. Culture results suggest that large volume filtration, but not small aliquot sampling, is sensitive to extremely low levels of contamination. No growth was detected in any negative control samples.

In Phase Two: 19 ECC consisting of a membrane oxygenator, vented hardshell reservoir, arterial filter, and PVC tubing were removed from their sterile packages, assembled, and left unprotected in the moderate traffic environment of a research laboratory. The circuits were then primed with Lactated Ringer’s solution. The prime solution was sampled for aerobic contamination by large volume filtration. None of the 19 samples detected contamination.

In Phase Three: 43 ECC identical to the Phase Two circuits were assembled and left unprotected in the substerile pump room. The circuits were then primed, circulated, and cultured as in Phase Two. One of the 43 samples was discarded because of a recognized break in aseptic technique during sample collection. None of the remaining samples detected contamination. Mathematical calculations of binomial probabilities suggest that the chance of an open ECC developing a detectable level of contamination within 72 h of its dry assembly is insignificant.