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Transfusion transmitted infectious agents, excluding hepatitis and human immunodeficiency viruses
1Finnish Red Cross Blood Transfusion Service, Helsinki.
Acta Anaesthesiologica Scandinavica. Supplementum
|January 1, 1988
Summary
Transfusion-transmitted infections pose risks, including cytomegalovirus (CMV) and human T-lymphotropic virus type 1 (HTLV-1). Bacterial contamination in stored platelets is also a concern for blood safety.
Area of Science:
- Infectious disease transmission
- Hematology
- Transfusion medicine
Background:
- Blood transfusion carries risks of transmitting various infectious agents, including viruses, parasites, and bacteria.
- Cytomegalovirus (CMV) infection prevention in immunocompromised patients, such as bone marrow recipients, is crucial.
- Emerging and re-emerging infectious agents necessitate ongoing vigilance in blood safety protocols.
Purpose of the Study:
- To review the spectrum of transfusion-transmitted infections.
- To highlight key pathogens and their associated risks in blood products.
- To discuss current strategies and considerations for mitigating transfusion-related infectious risks.
Main Methods:
- Literature review of transfusion-transmitted pathogens.
- Analysis of clinical implications and prevention strategies for viral, parasitic, and bacterial infections.
- Discussion of blood bank screening and product storage considerations.
Main Results:
- Cytomegalovirus (CMV) seronegative blood effectively prevents CMV infection in susceptible recipients.
- Human T-lymphotropic virus type 1 (HTLV-1) transmission is a concern, prompting donor screening in endemic areas.
- Bacterial contamination of platelet products during prolonged storage remains a significant risk.
Conclusions:
- Implementing pathogen-reducti on strategies and appropriate donor screening are vital for blood safety.
- Careful management of blood products, including storage conditions, is essential to minimize infectious complications.
- Continuous monitoring and adaptation of transfusion practices are necessary to address evolving transfusion-transmitted infection risks.