Abstracts
Comparative efficacy of bacterial culture versus pathogen inactivation to reduce the risk of transfusion-associated sepsis.
Presented at: 22nd Congress of the Society of French Transfusion Sanguine (SFTS) 2005, 6/27/05 - 6/30/05
Objective: This study compared the efficacy of bacterial screening using a culture method (BacT/Alert System, Biomerieux) with pathogen inactivation (INTERCEPT Blood System, Baxter Healthcare) to prevent the transfusion of platelet components contaminated with bacteria.
Methods: Seven strains of bacteria associated with transfusion-associated sepsis, including Gram-positive, Gram-negative and the anaerobes were studied. Paired (Control and Test) platelet concentrates (PC) containing approximately 3 x10E11 platelets in 300 mL of 35% plasma and 65% InterSol® were contaminated with each strain of bacteria at 10, 100, and 1,000 cfu per unit. After an overnight storage, the Test PC was treated with INTERCEPT (150 µM amotosalen and 3 J/sq cm UVA). The Control PC was not treated. Both units were assayed for aerobic and anaerobic bacteria using the BacT/Alert System at the time of bacterial inoculation and on days 1, 2 and 5 of storage. A platelet sample was considered contaminated with bacteria if a positive signal was registered within 120 hrs of culture.
Results: For Control PC, cultures failed to detect low-dose inocula (Table 1). In contrast, all Test PC treated with INTERCEPT remained negative by BacT/Alert cultures throughout the entire 5-day observation period regardless of the strain and the contamination level.
Conclusions: Bacterial detection using cultures may fail to detect low levels of bacteria. Failure to detect bacteria will result in the release of contaminated platelet products with “test negative-to-date” status. In contrast, inactivation of bacteria is capable of preventing release of contaminated platelet components.
Table 1 |
Time (h=hours) to Positive Culture* |
|
10 cfu/unit |
100 cfu/unit |
1,000 cfu/unit |
|
aerobe |
anaerobe |
aerobe |
anaerobe |
aerobe |
anaerobe |
|
Inoculated Control PC (Untreated) |
|
|
|
|
|
|
|
Staphylococcus aureus |
13.9h |
16.1h |
11 h |
12 h |
7h |
7h |
|
Staphylococcus epidermidis |
Neg |
Neg |
50 h |
35 h |
16h |
16h |
|
Propionibacterium acnes |
Neg |
50 h |
Neg |
D5 +50h |
Neg |
D5 +50h |
|
Escherichia coli |
Neg |
Neg |
Neg |
Neg |
4h |
4h |
|
Clostridium perfringens |
n.a. |
n.a. |
n.a. |
n.a. |
11.3 h |
Neg |
|
Streptococcus agalactiae |
Neg |
Neg |
D2 +8.4h |
12.7 h |
8h |
8h |
|
Klebsiella pneumonia |
D2 +8h |
D2 +8h |
D2 +7.4h |
D2 +7.4h |
8h |
8h |
|
Inoculated Test PC (treated with INTERCEPT) |
|
|
|
|
|
|
|
All 7 strains studied |
Neg |
Neg |
Neg |
Neg |
Neg |
Neg |
|
* D=day sampled, where not indicated, samples were withdrawn on day 1. |
Key words: Bacterial screening; bacterial inactivation; amotosalen; UVA
|