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Journal of Clinical Microbiology, November 2003, p. 5159-5166, Vol. 41, No. 11
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.11.5159-5166.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Division of Virology, Children's Hospital of Eastern Ontario,1 Divisions of Hematology and Oncology and the Canadian Blood and Bone Marrow Transplant Program, University of Ottawa,2 Health Canada, Ottawa, Ontario, Canada3
Received 1 October 2002/ Returned for modification 5 May 2003/ Accepted 12 July 2003
A total of 676 specimens from 63 recipients of bone marrow allografts were tested for cytomegalovirus (CMV) by the following assays: CMV pp67 NucliSens (NS), AMPLICOR CMV MONITOR (RA), and the Digene CMV DNA test (DG). In a consensus analysis, the sensitivities and specificities were 60 and 99% (NS), 96 and 98% (RA), and 90 and 76% (DG), respectively; for detection of symptomatic CMV infection, they were 60 and 97% (NS), 65 and 97% (RA), and 95 and 77% (DG), respectively. In multivariate analysis, the major risk factor for symptomatic CMV infection was an increase in the viral load in the DG assay; in univariate analyses, maximum viral loads in both DG and RA assays and a rising viral load in the RA assay were also significant. The earliest detection of CMV replication was provided by the RA assay (mean, 39 days posttransplantation), followed by the DG assay (mean, 48 days) and the NS assay (mean, 58 days).
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