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Journal of Clinical Microbiology, September 1998, p. 2554-2556, Vol. 36, No. 9
Departments of Clinical
Virology,1
Nephrology,2 and
Haematology,3 Royal Hospitals NHS
Trust, London, United Kingdom
Received 3 March 1998/Returned for modification 9 April
1998/Accepted 14 June 1998
We evaluated a cytomegalovirus (CMV) 24-hour shell vial assay
(SVA), the Murex Hybrid Capture CMV DNA assay (HCA), and a CMV plasma
PCR for the detection of CMV viremia in renal and bone marrow
transplant recipients and human immunodeficiency virus-infected patients. CMV viremia was detected by at least one method in 125 of 317 evaluable samples (39.4%) from 78 patients and was detected in 19.8%
of samples by SVA, 26.8% by HCA, and 32.2% by plasma PCR. There was
moderate to substantial agreement between the results of the different
tests (kappa coefficient = 0.415 to 0.631). However, HCA and
plasma PCR were significantly more sensitive than SVA (P = 0.001 and P < 0.0001, respectively; McNemar's test), and plasma PCR was more sensitive than
HCA (P = 0.031; McNemar's test). HCA and plasma PCR were
more consistently positive than SVA during viremic episodes
(P = 0.0002 and P < 0.0001, respectively; McNemar's test). The use of HCA or plasma PCR may
therefore improve the diagnosis and management of CMV disease in
susceptible patient groups.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Evaluation of the Murex Hybrid Capture Cytomegalovirus DNA Assay
versus Plasma PCR and Shell Vial Assay for Diagnosis of Human
Cytomegalovirus Viremia in Immunocompromised Patients
*
Corresponding author. Mailing address: Department of
Clinical Virology, Royal Hospitals NHS Trust, Whitechapel, London E1 1BB, United Kingdom. Phone: 44 171 377 7141. Fax: 44 171 377 5784. E-mail: W.Y.Barrett-Muir{at}mds.qmw.ac.uk.
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