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Predictive value of cytomegalovirus (CMV) antigenemia and digene hybrid capture DNA assays for CMV disease in human immunodeficiency virus-infected patients
被引:13
|作者:
Walmsley, S
O'Rourke, K
Mortimer, C
Rachlis, A
Fong, I
Mazzulli, T
机构:
[1] Toronto Gen Hosp, Dept Med, Toronto, ON M5G 2C4, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON, Canada
[4] Univ Toronto, Dept Ophthalmol, Toronto, ON, Canada
[5] Univ Toronto, Dept Pathobiol & Lab Med, Toronto, ON, Canada
[6] St Michaels Hosp, Toronto, ON M5B 1W8, Canada
[7] Sunnybrook Hlth Sci Ctr, Toronto, ON M4N 3M5, Canada
[8] Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
关键词:
D O I:
10.1086/514703
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Oral ganciclovir prophylaxis decreases the incidence of cytomegalovirus (CMV) disease among persons infected with the human immunodeficiency virus (HN), but universal prophylaxis is not cost-effective. We evaluated urine and peripheral brood mononuclear cell cultures, a qualitative and quantitative antigenemia assay, and a commercially available CMV DNA hybridization assay for their ability to predict CMV disease in 138 HIV-infected patients. During a median follow-up of 10 months, 23 patients (17%) developed CMV disease. The sensitivity, specificity, positive predictive value, negative predictive value, and mean lead times for the antigenemia assay (with use of a threshold of 8 positive cells per 10(5) peripheral blood mononuclear cells as a positive) were 74%, 91%, 63%, 95%, and 95 days, respectively. Corresponding figures for the DNA hybridization assay were 91%, 64%, 34%, 97%, and 152 days. These assays can identify patients at increased risk of CMV disease and should allow a strategy of preemptive therapy to be tested.
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页码:573 / 581
页数:9
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