Processing of peripheral blood progenitor cell components in improved clean areas does not reduce the rate of microbial contamination
Autor: | Petra Krakowitzky, Uwe Cassens, Henk S.P. Garritsen, Rudolf-Josef Fischer, Christoph Ahlke, Georg Peters, Jörg Wüllenweber, Walter Sibrowski |
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Rok vydání: | 2002 |
Předmět: |
Adult
Catheterization Central Venous medicine.medical_specialty Sterility testing Immunology Group ii Bacteremia Microbial contamination Gram-Positive Bacteria Toxicology Catheterization Peripheral Gram-Negative Bacteria medicine Humans Immunology and Allergy Leukapheresis Progenitor cell Child Gram-Positive Bacterial Infections Cryopreservation Risk Management business.industry Sterilization Transfusion medicine Hematology Contamination Environment Controlled Peripheral blood Surgery Blood Blood donor Blood Preservation Equipment Contamination Gram-Negative Bacterial Infections business Follow-Up Studies |
Zdroj: | Transfusion. 42:10-17 |
ISSN: | 1537-2995 0041-1132 |
DOI: | 10.1046/j.1537-2995.2002.00013.x |
Popis: | BACKGROUND: Microbial contamination of peripheral blood progenitor cell components (PBPCs) may cause severe complications in immunosuppressed recipients. Therefore, principles of Good Manufacturing Practice (GMP) are applicable for processing of PBPC components to reduce potential risks of contamination. STUDY DESIGN AND METHODS: It was investigated in a retrospective study whether the microbial contamination of PBPC components could be reduced after processing in improved clean areas according to the “Manufacture of Sterile Medicinal Products.” Starting in 1994, a total of 1478 autologous and allogeneic PBPC components have been collected and processed into 3149 cryopreservation bags at the Department of Transfusion Medicine. Sterility testing was performed for all bags. Until December 1998, 783 PBPC components were processed at a clean bench only (group I). Thereafter, 695 PBPC components have been processed at a clean bench located in a clean area with an airlock system for personnel and equipment (group II). RESULTS: In group I, 16 of 1555 bags (1.03%) showed positive results in the first sterility testing. In group II, 21 of 1594 bags (1.32%) were positive (p = NS). The clinical follow-up was inconspicuous. CONCLUSION: Microbial contamination of PBPC components could not be reduced by installation of improved clean area conditions. |
Databáze: | OpenAIRE |
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