S. Zaza et al., BACTERIAL-CONTAMINATION OF PLATELETS AT A UNIVERSITY HOSPITAL - INCREASED IDENTIFICATION DUE TO INTENSIFIED SURVEILLANCE, Infection control and hospital epidemiology, 15(2), 1994, pp. 82-87
BACKGROUND: A cluster of bacterial contamination of platelets occurred
at a university hospital in a one-month period. This unusual clusteri
ng allowed us to examine the likely mechanism of contamination and cli
nical sequelae. METHODS: We reviewed medical records of patients recei
ving random donor platelet transfusions to determine numbers of platel
ets transfused, reactions reported, and episodes of bacterial contamin
ation. We also reviewed procedures at the collecting blood agencies an
d the hospital blood bank. RESULTS: Four patients received bacterially
contaminated platelets during June and July 1991. The rates of report
ed platelet transfusion reactions increased significantly (P<0.001) fr
om September 1989 through July 1991 (study period); in addition, the r
ate of contamination of platelets during June and July 1991 was 23-fol
d higher than during die previous 21 months (P<0.001). Surveillance me
thodology changed dramatically during the study period, contributing t
o the recognition of the current cluster. Pathogens isolated from the
contaminated platelet pools were Bacillus cereus, Staphylococcus epide
rmidis, or Pseudomonas aeruginosa in titers ranging from 10(6) to 10(8
) colony forming units/mL. Four constituent individual platelet units
identified as the probable cause of the outbreak (including one postep
idemic episode) were significantly older (mean age, 4.8 days) than 106
randomly selected individual platelet units (mean age, 3.7 days; P =
0.04). Platelet pools were transfused an average of 2.5 hours after po
oling. Review of blood collection and platelet preparation practices d
id not identify breaks in procedure or technique that could have cause
d contamination. CONCLUSIONS: Increased awareness of platelet transfus
ion reactions by clinical staff and routine culturing of all platelets
associated with tranfusion reactions will identify contaminated plate
lets. Identification of contaminated platelets is necessary to treat a
ffected patients appropriately and to determine the prevalence of and
risk factors for contaminated platelets (Infect Control Hosp Epidemiol
1994;15:82-87).