Impact of donor arm skin disinfection on the bacterial contamination rate of platelet concentrates
Article first published online: 4 OCT 2002
Volume 83, Issue 3, pages 204–208, October 2002
How to Cite
Lee, C. K., Ho, P. L., Chan, N. K., Mak, A., Hong, J. and Lin, C. K. (2002), Impact of donor arm skin disinfection on the bacterial contamination rate of platelet concentrates. Vox Sanguinis, 83: 204–208. doi: 10.1046/j.1423-0410.2002.00219.x
- Issue published online: 4 OCT 2002
- Article first published online: 4 OCT 2002
- Received: 18 February 2002, revised 6 May 2002, accepted 11 May 2002
- bacterial contamination;
- blood transfusion;
- platelet concentrates;
Background and Objectives Despite improved methods for detecting bacterial contamination of blood products, bacterial sepsis remains a significant risk in blood transfusion. This study was undertaken to investigate whether adopting a different skin disinfection protocol could reduce the rate of bacterial contamination of platelet concentrates.
Materials and Methods Two skin disinfection protocols were consecutively used in the routine blood collection setting during two 10-month periods: 0·5% cetrimide/0·05% chlorhexidine solution followed by 70% isopropyl alcohol (first 10-month time-period); and 10% povidone-iodine followed by 70% isopropyl alcohol (second 10-month time-period). The rates of bacterial contamination of platelet concentrates were monitored by using a surveillance programme described previously.
Results The overall bacterial contamination rate in the first time-period was 0·072%. After introduction of the povidone-iodine and isopropyl alcohol protocol, the bacterial contamination rate decreased to 0·042% (relative risk reduction: −0·42; 95% confidence interval, −0·12 to −0·61, P= 0·009). There were no differences in the types of micro-organisms identified (P = 0·7).
Conclusions Skin disinfection by povidone-iodine and isopropyl alcohol is more effective than that by cetrimide/chorhexidine and isopropyl alcohol in reducing venepuncture-associated contamination of platelet concentrates by skin flora. Our data indicate that the disinfection protocol should be used on a routine basis and such implementation should translate into a significant improvement in blood safety to patients receiving platelet transfusion.