R. Patel et al., OPTIMIZATION OF DETECTION OF CYTOMEGALOVIRUS VIREMIA IN TRANSPLANTATION RECIPIENTS BY SHELL VIAL ASSAY, Journal of clinical microbiology, 33(11), 1995, pp. 2984-2986
Cytomegalovirus (CMV) viremia is a widely used laboratory marker of CM
V disease following transplantation and is additionally used to trigge
r preemptive antiviral therapy, Despite this, the optimal method for d
iagnosing CMV viremia in transplantation recipients remains unknown. T
o determine the sampling frequency and blood volume required for the o
ptimal diagnosis of viremia by shell vial assay, a prospective study o
f 46 viremic transplantation recipients was conducted, Blood specimens
(2.5 and 5 ml) were collected twice, 3 h apart, at a median of 1.4 da
ys (range, 1 to 3 days) after the triggering shell vial positive blood
had been collected. Considering a single 2.5-ml specimen, an average
of only 40% of previously viremic patients had documented CMV in their
blood; this increased to 50% when a second 2.5-ml sample of blood was
collected 3 h later, The yields of two 2.5-ml versus two 5-ml samples
were 50 versus 61%, respectively, Viremia as detected by shell vial a
ssay is intermittent, and increasing the frequency and volume of blood
sampling increases its diagnosis. These results have implications in
diagnosis of CMV infection and its preemptive therapy.