Prevention of transfusion of platelet components contaminated with low levels of bacteria: a comparison of bacteria culture and pathogen inactivation methods
Abstract
BACKGROUND: This study compared the efficacy of bacterial detection with inactivation for reducing the risk associated with transfusion of platelet (PLT) components contaminated with low levels of bacteria. STUDY DESIGN AND METHODS: Twenty‐one double‐dose PLTs were spiked with seven species of bacteria at three levels (0.003‐0.03, 0.03‐0.3, 0.3‐3 colony‐forming units [CFUs]/mL). After split, each PLT unit contained 1 to 10, 10 to 100, and 100 to 1000 CFUs. One unit was photochemically treated (PCT; 150 µmol/L amotosalen and 3 J/cm 2 ultraviolet A). The other unit was untreated. All units were stored and sampled on Days 1, 2, and 5 of storage for aerobic and anaerobic culture in the BacT/ALERT system (bioMérieux). PLTs were classified as sterile when no bacterial growth was detected after 120 hours of culture. RESULTS: In all PCT PLTs, no bacteria were detected throughout 5 days of storage regardless of species, level of contamination, and sampling time. In untreated PLTs, Staphylococcus aureus was consistently detected by culturing. Growth of 1 to 10 CFUs per unit Staphylococcus epidermidis, 1 to 100 CFUs per unit of Klebsiella pneumoniae, and 1 to 1000 CFUs per unit Propionibacterium acnes was delayed and only detectable after 5, 2, and 5 days of storage, respectively. Low levels of Streptococcus agalactiae (1‐10 CFUs/unit), Escherichia coli (1‐100 CFUs/unit), and Clostridium perfringens (1‐100 CFUs/unit) were not detected during 5 days of storage, although bacterial outgrowth was detected at higher levels of contamination. CONCLUSIONS: For the seven bacterial species examined, contaminated PLTs may be released for transfusion on test‐negative‐to‐date status. In contrast, bacterial inactivation by PCT could reduce the risk associated with transfusion of PLTs contaminated with low levels of these bacteria.
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Furan- and pyrone-side monoadducts of both 8-MOP and S59 are formed upon UVA irradiation in a much lower yield (close to 1%) than ICLs.
“It was found that furan-and pyrone-side monoadducts of both 8-MOP and S59, a recently developed psoralen derivative for pathogen inactivation in blood products (171,172), are formed upon UVA irradiation in a much lower yield (close to 1%) than ICLs.”
From Photoinduced Damage to Cellular DNA: Direct and Photosensitized Reactions<sup>†</sup> (2012) · cites this paper as [172]
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Photoinduced Damage to Cellular DNA: Direct and Photosensitized Reactions<sup>†</sup>
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- Authors
- Nussbaumer, W., Allersdorfer, D., Grabmer, C., Rheinschmidt, M., Lin, L., Schönitzer, D., & Lass‐Flörl, C.
- Affiliations
- Innsbruck Medical University (AT)
- Universität Innsbruck (AT)
- Corresponding author
- Nussbaumer, Walter
- ORCID
- Lass‐Flörl, Cornelia
- Venue
- Transfusion
- Publisher
- Wiley
- Published
- 2007-06-16
- Volume
- 47
- Issue
- 7
- Pages
- 1125-1133
- ISSN
- 0041-1132 (ISSN-L)
- 1537-2995
- OpenAlex
- W2124338926
- Cited by
- 51
- References
- 41
- Citations by year
- 2026: 1 · 2025: 1 · 2020: 1 · 2019: 1 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 5 · 2013: 2 · 2012: 5
- FWCI
- 3.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Transfusion (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Biochemistry › Blood transfusion and management
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Microbial Inactivation Methods
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Photodynamic Therapy Research Studies
- Keywords
- platelet transfusion, bacterial contamination, pathogen inactivation, photochemical treatment, amotosalen, bacterial culture, bacterial detection, Staphylococcus aureus, Staphylococcus epidermidis, Klebsiella pneumoniae, Propionibacterium acnes, Streptococcus agalactiae, Escherichia coli, Clostridium perfringens, transfusion safety, transfusion-transmitted infections
- MeSH terms
- Bacteria, Bacterial Infections, Bacteriological Techniques, Humans, Methods, Platelet Transfusion, Microbial Viability
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