Bacterial contamination of platelets for transfusion: strategies for prevention

被引:118
作者
Levy, Jerrold H. [1 ]
Neal, Matthew D. [2 ]
Herman, Jay H. [3 ]
机构
[1] Duke Univ Hosp, 2301 Erwin Rd, Durham, NC 27710 USA
[2] Univ Pittsburgh, Med Ctr, 200 Lothrop St, Pittsburgh, PA 15213 USA
[3] Thomas Jefferson Univ Hosp, 111 S 11th St, Philadelphia, PA 19107 USA
来源
CRITICAL CARE | 2018年 / 22卷
关键词
Bacterial contamination; Bacterial detection; Hemovigilance; Pathogen reduction/inactivation; Platelets; Prevention strategies; Septic transfusion reaction (STR); Transfusion; Transfusion-transmitted bacterial infection (TTBI); PATHOGEN-REDUCTION TECHNOLOGY; WAVELENGTH ULTRAVIOLET-LIGHT; CRITICALLY-ILL PATIENTS; BLOOD COMPONENTS; PHOTOCHEMICAL TREATMENT; THERAPEUTIC-EFFICACY; APHERESIS PLATELETS; CLINICAL-TRIAL; UNITED-STATES; SPRINT TRIAL;
D O I
10.1186/s13054-018-2212-9
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Platelet transfusions carry greater risks of infection, sepsis, and death than any other blood product, owing primarily to bacterial contamination. Many patients may be at particular risk, including critically ill patients in the intensive care unit. This narrative review provides an overview of the problem and an update on strategies for the prevention, detection, and reduction/inactivation of bacterial contaminants in platelets. Bacterial contamination and septic transfusion reactions are major sources of morbidity and mortality. Between 1:1000 and 1:2500 platelet units are bacterially contaminated. The skin bacterial microflora is a primary source of contamination, and enteric contaminants are rare but may be clinically devastating, while platelet storage conditions can support bacterial growth. Donor selection, blood diversion, and hemovigilance are effective but have limitations. Biofilm-producing species can adhere to biological and non-biological surfaces and evade detection. Primary bacterial culture testing of apheresis platelets is in routine use in the US. Pathogen reduction/inactivation technologies compatible with platelets use ultraviolet light-based mechanisms to target nucleic acids of contaminating bacteria and other pathogens. These methods have demonstrated safety and efficacy and represent a proactive approach for inactivating contaminants before transfusion to prevent transfusion-transmitted infections. One system, which combines ultraviolet A and amotosalen for broad-spectrum pathogen inactivation, is approved in both the US and Europe. Current US Food and Drug Administration recommendations advocate enhanced bacterial testing or pathogen reduction/inactivation strategies (or both) to further improve platelet safety. Risks of bacterial contamination of platelets and transfusion-transmitted infections have been significantly mitigated, but not eliminated, by improvements in prevention and detection strategies. Regulatory-approved technologies for pathogen reduction/inactivation have further enhanced the safety of platelet transfusions. Ongoing development of these technologies holds great promise.
引用
收藏
页数:8
相关论文
共 68 条
[31]   Pathogen Inactivation of Platelet and Plasma Blood Components for Transfusion Using the INTERCEPT Blood System™ [J].
Irsch, Johannes ;
Lin, Lily .
TRANSFUSION MEDICINE AND HEMOTHERAPY, 2011, 38 (01) :19-31
[32]   Detection of bacterial contamination in prestorage culture-negative apheresis platelets on day of issue with the Pan Genera Detection test [J].
Jacobs, Michael R. ;
Smith, Daniel ;
Heaton, W. Andrew ;
Zantek, Nicole D. ;
Good, Caryn E. .
TRANSFUSION, 2011, 51 (12) :2573-2582
[33]   Costs and benefits of bacterial culturing and pathogen reduction in the Netherlands [J].
Janssen, Mart P. ;
van der Poel, Cees L. ;
Buskens, Erik ;
Bonneux, Luc ;
Bonsel, Gouke J. ;
van Hout, Ben A. .
TRANSFUSION, 2006, 46 (06) :956-965
[34]   Treatment of Platelet Concentrates with the Mirasol Pathogen Inactivation System Modulates Platelet Oxidative Stress and NF-κB Activation [J].
Johnson, Lacey ;
Marks, Denese .
TRANSFUSION MEDICINE AND HEMOTHERAPY, 2015, 42 (03) :169-175
[35]   Improved yield of minimal proportional sample volume platelet bacterial culture [J].
Kamel, Hany ;
Townsend, Mary ;
Bravo, Marjorie ;
Vassallo, Ralph R. .
TRANSFUSION, 2017, 57 (10) :2413-2419
[36]   A patient-oriented risk-benefit analysis of pathogen-inactivated blood components: application to apheresis platelets in the United States [J].
Kleinman, Steven ;
Reed, William ;
Stassinopoulos, Adonis .
TRANSFUSION, 2013, 53 (07) :1603-1618
[37]   A prospective, active haemovigilance study with combined cohort analysis of 19 175 transfusions of platelet components prepared with amotosalen-UVA photochemical treatment [J].
Knutson, F. ;
Osselaer, J. ;
Pierelli, L. ;
Lozano, M. ;
Cid, J. ;
Tardivel, R. ;
Garraud, O. ;
Hervig, T. ;
Domanovic, D. ;
Cukjati, M. ;
Gudmundson, S. ;
Hjalmarsdottir, I. B. ;
Castrillo, A. ;
Gonzalez, R. ;
Brihante, D. ;
Santos, M. ;
Schlenke, P. ;
Elliott, A. ;
Lin, J. -S. ;
Tappe, D. ;
Stassinopoulos, A. ;
Green, J. ;
Corash, L. .
VOX SANGUINIS, 2015, 109 (04) :343-352
[38]   Addressing the risk of bacterial contamination in platelets: a hospital economic perspective [J].
Li, Justin W. ;
Brecher, Mark E. ;
Jacobson, Jessica L. ;
Harm, Sarah K. ;
Chen, Dorothy ;
El-Gamil, Audrey ;
Dobson, Al ;
Mintz, Paul D. .
TRANSFUSION, 2017, 57 (10) :2321-2328
[39]   Platelet transfusions for critically ill patients with thrombocytopenia [J].
Lieberman, Lani ;
Bercovitz, Rachel S. ;
Sholapur, Naushin S. ;
Heddle, Nancy M. ;
Stanworth, Simon J. ;
Arnold, Donald M. .
BLOOD, 2014, 123 (08) :1146-1151
[40]   Photochemical treatment of platelet concentrates with amotosalen and long-wavelength ultraviolet light inactivates a broad spectrum of pathogenic bacteria [J].
Lin, L ;
Dikeman, R ;
Molini, B ;
Lukehart, SA ;
Lane, R ;
Dupuis, K ;
Metzel, P ;
Corash, L .
TRANSFUSION, 2004, 44 (10) :1496-1504