Survey of current practice for prevention of transfusion-transmitted cytomegalovirus in the United States: leucoreduction vs. cytomegalovirus-seronegative
- PMID: 19695013
- DOI: 10.1111/j.1423-0410.2009.01228.x
Survey of current practice for prevention of transfusion-transmitted cytomegalovirus in the United States: leucoreduction vs. cytomegalovirus-seronegative
Abstract
Background and objectives: Cytomegalovirus (CMV) is a significant pathogen transmissible through blood transfusion that can have devastating effects on immunocompromised patients. Current transfusion practice provides two choices for transfusion of cellular blood components that reduce the risk of transfusion-transmitted CMV (TT-CMV): blood components collected from CMV seronegative donors and leucocyte-reduced (LR) blood components.
Materials and methods: A web-based survey was designed and administered to AABB physician members in April 2007 to collect information regarding current blood banking and clinical practices for prevention of TT-CMV in the United States.
Results: Individuals representing 183 different institutions completed the entire survey (an institutional response rate of 32.5%). Sixty-five percent of respondents indicated that their institution considered that CMV-seronegative and LR products are equally effective in preventing TT-CMV. When analyzed by institutional type, academic institutions and community hospitals were more likely to subscribe to the premise that LR blood components are equally effective at preventing TT-CMV, than were community blood centres and government institutions. However, reported practices for specific patient populations did not match this view of equivalence between CMV-seronegative and LR products with many patient populations preferentially receiving CMV-seronegative components. Fetal and neonatal populations were more likely than other patient populations to receive CMV-seronegative products to reduce the risk of TT-CMV.
Conclusion: There is wide variability in transfusion practices to reduce the risk of TT-CMV. Lack of a consensus approach may reflect the conflicting data that exist in the literature as well as adherence to longstanding practice.
Similar articles
-
High prevalence of cytomegalovirus DNA in plasma samples of blood donors in connection with seroconversion.Transfusion. 2007 Nov;47(11):1972-83. doi: 10.1111/j.1537-2995.2007.01420.x. Transfusion. 2007. PMID: 17958525
-
Survey of Institutional Policies for Provision of "CMV-Safe" Blood in Ontario.Am J Clin Pathol. 2016 Nov 1;146(5):578-584. doi: 10.1093/ajcp/aqw181. Am J Clin Pathol. 2016. PMID: 28430958
-
CMV and blood transfusions.Rev Med Virol. 2002 Jul-Aug;12(4):211-9. doi: 10.1002/rmv.353. Rev Med Virol. 2002. PMID: 12125013 Review.
-
Survey on Transfusion-Transmitted Cytomegalovirus and Cytomegalovirus Disease Mitigation.Arch Pathol Lab Med. 2017 Dec;141(12):1705-1711. doi: 10.5858/arpa.2016-0461-OA. Epub 2017 Aug 29. Arch Pathol Lab Med. 2017. PMID: 28849943
-
Transfusion-transmitted cytomegalovirus infection.Hematol Oncol Clin North Am. 1995 Feb;9(1):155-66. Hematol Oncol Clin North Am. 1995. PMID: 7737939 Review.
Cited by
-
Postnatal cytomegalovirus infection: a pilot comparative effectiveness study of transfusion safety using leukoreduced-only transfusion strategy.Transfusion. 2016 Aug;56(8):1945-50. doi: 10.1111/trf.13605. Epub 2016 Apr 15. Transfusion. 2016. PMID: 27080192 Free PMC article.
-
Prevention of maternal cytomegalovirus infection: current status and future prospects.Int J Womens Health. 2010 Aug 9;2:23-35. doi: 10.2147/ijwh.s5782. Int J Womens Health. 2010. PMID: 21072294 Free PMC article.
-
Leucoreduction of blood components: an effective way to increase blood safety?Blood Transfus. 2016 May;14(2):214-27. doi: 10.2450/2015.0154-15. Epub 2015 Dec 16. Blood Transfus. 2016. PMID: 26710353 Free PMC article. Review.
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous