Evaluation of swirling, pH, and glucose tests for the detection of bacterial contamination in platelet concentrates
- 12 November 1996
- journal article
- research article
- Published by Wiley in Transfusion
- Vol. 36 (11-12) , 989-993
- https://doi.org/10.1046/j.1537-2995.1996.36111297091744.x
Abstract
Although infrequent, episodes of transfusion-associated bacterial sepsis may lead to serious outcomes or death and therefore are of concern. This study evaluates the sensitivity of three surrogate tests for the presence of bacteria in platelet concentrates: cessation of swirling, low extracellular pH, and low plasma glucose levels. Day 0 platelet concentrates were inoculated with low levels of one of seven bacterial strains and stored with agitation at 20 to 24 degrees C for up to 5 days. In the morning and afternoon of each day of storage, bacterial levels were ascertained by quantitative plate culture, and platelet concentrates were tested for platelet pH, plasma glucose, and swirling. Quantitative and semiquantitative dipstick techniques were used to determine pH and glucose levels. Platelet concentrates had attained stationary phase growth of Streptococcus pyogenes, Staphylococcus aureus, Escherichia coli, Bacillus cereus, Enterobacter cloacae, Streptococcus mitis, or Staphylococcus epidermidis (> or = 10(7) -10(8) colony-forming units [CFU]/mL) before either the swirling or dipstick methods suggested the presence of bacteria. The sensitivity of swirling and glucose tests for detecting bacterial contamination in platelet concentrates was generally comparable. Although the sensitivity of the pH test was generally similar to that of swirling and glucose tests for most bacteria, platelet concentrates contaminated with E. cloacae had normal pH despite the presence of high levels of bacteria (> or = 10(7)-10(8) CFU/mL). The sensitivity in detection of bacteria in platelet concentrates by the swirling technique or by measuring extracellular pH or plasma glucose is less than the sensitivity reported for microscopy with Gram stain (10(5)-10(6) CFU/mL), fluorescence microscopy with acridine orange stain (10(4)-10(5) CFU/mL), chemiluminescence detection of ribosomal RNA (10(3)-10(4) CFU/mL), and automated bacterial culture (1 CFU/sample volume).Keywords
This publication has 23 references indexed in Scilit:
- Buffy‐Coat‐Derived Platelet Concentrates Prepared from Half‐Strength Citrate CPD and CPD Whole‐Blood Units: Comparison between Three Additive Solutions: In vitro StudiesVox Sanguinis, 1995
- A prospective study of symptomatic bacteremia following platelet transfusion and of its managementTransfusion, 1994
- A prospective microbiologic surveillance program to detect and prevent the transfusion of bacterially contaminated plateletsTransfusion, 1993
- A Novel Screening Method for the Detection of Microbial Contamination of Platelet ConcentratesVox Sanguinis, 1993
- The use of a chemiluminescence‐linked universal bacterial ribosomal RNA gene probe and blood gas analysis for the rapid detection of bacterial contamination in white cell‐reduced and nonreduced plateletsTransfusion, 1993
- Storage of platelets in additive solutions: the effect of citrate and acetate in in vitro studiesTransfusion, 1993
- Strategies for the avoidance of bacterial contamination of blood componentsTransfusion, 1993
- Prestorage removal of Yersinia enterocolitica from red cells with white cell‐reduction filtersTransfusion, 1992
- Evaluation of two instruments for noninvasive platelet concentrate quality assessmentTransfusion, 1989
- Evaluation of the buffy-coat smear for rapid detection of bacteremiaPublished by American Medical Association (AMA) ,1981