Effective Use of PCR for the Detection of Cytomegalovirus Viremia and Monitoring Therapy in Immunocompromised Patients

被引:6
作者
Bieniek, Radoslaw [3 ]
Kirby, James E. [1 ,2 ]
Cheng, Annie [1 ,2 ]
Eichelberger, Karen [1 ,2 ]
Qian, Qinfang [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Pathol & Lab Med, Memphis, TN 38163 USA
来源
LABMEDICINE | 2011年 / 42卷 / 06期
关键词
cytomegalovirus; CMV; viral load; PCR; Molecular Diagnostics; Microbiology; Virology; Clinical Pathology; ACTIVE ANTIRETROVIRAL THERAPY; END-ORGAN-DISEASE; TRANSPLANT RECIPIENTS; LIVER-TRANSPLANTATION; CMV DISEASE; INFECTION; PLASMA; GANCICLOVIR;
D O I
10.1309/LMP4IL3XGU6MQJCE
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective: To establish criteria for the most productive use of quantitative cytomegalovirus (CMV) polymerase chain reaction (PCR) in transplant and HIV patients, both for diagnosis and monitoring infections. Method: We evaluated the medical records of 108 HIV, bone marrow transplant (BMT), and solid organ transplant (SOT) patients who had positive CMV viral load tests. Results: Cytomegalovirus was detected at median of 47 and 183.5 days after BMT and SOT, respectively. All HIV patients who had positive CMV viremia had CD4 cell counts <175 cells/mu L, and all HIV patients with end-organ disease had CD4 cell counts <75 cells/mu L. The median time for CMV to become undetectable after treatment was 22, 21, and 31 days for HIV, BMT, and SOT patients, respectively. Conclusion: Cytomegalovirus viral load screening focusing on high-risk periods may be cost effective. A CMV viral load does not decrease rapidly with treatment. The CMV PCR for monitoring therapy should not be performed more than once a week.
引用
收藏
页码:339 / 343
页数:5
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