Clinical utility of cytomegalovirus viral load testing for predicting CMV disease in D+/R- solid organ transplant recipients

被引:80
作者
Humar, A [1 ]
Paya, C
Pescovitz, MD
Dominguez, E
Washburn, K
Blumberg, E
Alexander, B
Freeman, R
Heaton, N
Mueller, B
机构
[1] Toronto Gen Hosp, Univ Hlth Network, Toronto, ON, Canada
[2] Mayo Clin, Rochester, MN USA
[3] Indiana Univ, Dept Surg & Microbiol Immunol, Indianapolis, IN 46204 USA
[4] Univ Nebraska, Med Ctr, Univ Med Associates, Omaha, NE USA
[5] Univ Texas, Ctr Hlth, San Antonio, TX 78285 USA
[6] Hosp Univ Penn, Philadelphia, PA 19104 USA
[7] Duke Univ, Med Ctr & Hlth Syst, Durham, NC USA
[8] New England Med Ctr Transplant Surg, Boston, MA USA
[9] Kings Coll Hosp London, Liver Transplant Dept, London, England
[10] Roche Prod Ltd, Basel, Switzerland
关键词
cytomegalovirus; ganciclovir; solid organ transplant; valganciclovir; viral load;
D O I
10.1111/j.1600-6143.2004.00391.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Despite prophylaxis, cytomegalovirus (CMV) disease is common in donor seropositive (D+)/recipient seronegative (R-) transplant patients after cessation of prophylaxis. Early detection of CMV may allow for pre-emptive therapy to prevent active disease. The clinical utility of quantitative plasma viral load measurements for predicting CMV disease was determined in 364 D+/R- organ transplant patients receiving prophylaxis (100 d of valganciclovir or oral ganciclovir). Measurements were performed every 2 weeks until day 100 and at months 4, 4.5, 5, 6, 8 and 12 post-transplant. CMV disease occurred in 64 (17.6%) patients by 12 months. Using a positive cut-off value of > 400 copies/mL, sensitivity was 38%, specificity 60%, positive predictive value 17%, and negative predictive value 82% for prediction of CMV disease. Therefore, routine monitoring would have predicted disease in only 24/64 (38%) patients. The test characteristics were not improved by changing the viral load cut-off point for defining a positive result. Similarly, single time point measures at the end of prophylaxis or month 4 had low sensitivity for disease prediction. Overall, regular CMV plasma viral load measurements were only of modest value in predicting CMV disease.
引用
收藏
页码:644 / 649
页数:6
相关论文
共 20 条
[1]   The role of PCR in the diagnosis and management of CMV in solid organ recipients - What is the predictive value for the development of disease and should PCR be used to guide antiviral therapy? [J].
Abecassis, MM ;
Koffron, AJ ;
Kaplan, B ;
Buckingham, M ;
Muldoon, JP ;
Cribbins, AJ ;
Kaufman, DB ;
Fryer, JP ;
Stuart, J ;
Stuart, FP .
TRANSPLANTATION, 1997, 63 (02) :275-279
[2]   Prognostic significance and risk factors of untreated cytomegalovirus viremia in liver transplant recipients [J].
Badley, AD ;
Patel, R ;
Portela, DF ;
Harmsen, WS ;
Smith, TF ;
Ilstrup, DM ;
Steers, JL ;
Wiesner, RH ;
Paya, CV .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (02) :446-449
[3]   Surveillance cultures of blood, urine, and throat specimens are not valuable for predicting cytomegalovirus disease in liver transplant recipients [J].
Falagas, ME ;
Snydman, DR ;
Ruthazer, R ;
Werner, BG ;
Griffith, J ;
Rohrer, R ;
Freeman, R ;
Fawaz, K ;
Hoffman, MA ;
Kaplan, M ;
Gill, M ;
Rubin, RH ;
Dienstag, JL ;
Doran, M ;
ORourke, E ;
Vacanti, J ;
Jenkins, R ;
Lewis, WD ;
Hammer, S ;
Martin, M ;
Fairchild, R ;
Werner, BG ;
Grady, GF ;
Leszczynski, J ;
Dougherty, N ;
Katz, A ;
Fausett, G ;
Platt, R ;
Cheeseman, SH ;
Pasternack, M ;
Gorbach, SL .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (05) :824-829
[4]   Infection in organ-transplant recipients [J].
Fishman, JA ;
Rubin, RH .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (24) :1741-1751
[5]   Randomised trial of efficacy and safety of oral ganciclovir in the prevention of cytomegalovirus disease in liver-transplant recipients [J].
Gane, E ;
Saliba, F ;
Valdecasas, GJC ;
OGrady, J ;
Pescovitz, MD ;
Lyman, S ;
Robinson, CA .
LANCET, 1997, 350 (9093) :1729-1733
[6]   The independent role of cytomegalovirus as a risk factor for invasive fungal disease in orthotopic liver transplant recipients [J].
George, MJ ;
Snydman, DR ;
Werner, BG ;
Griffith, J ;
Falagas, ME ;
Dougherty, NN ;
Rubin, RH .
AMERICAN JOURNAL OF MEDICINE, 1997, 103 (02) :106-113
[7]   Clinical utility of quantitative cytomegalovirus viral load determination for predicting cytomegalovirus disease in liver transplant recipients [J].
Humar, A ;
Gregson, D ;
Caliendo, AM ;
McGeer, A ;
Malkan, G ;
Krajden, M ;
Corey, P ;
Greig, P ;
Walmsley, S ;
Levy, G ;
Mazzulli, T .
TRANSPLANTATION, 1999, 68 (09) :1305-1311
[8]   Definitions of cytomegalovirus infection and disease in transplant recipients [J].
Ljungman, P ;
Griffiths, P ;
Paya, C .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (08) :1094-1097
[9]   Posttransplant lymphoproliferative disease in primary Epstein-Barr virus infection after liver transplantation: The role of cytomegalovirus disease [J].
Manez, R ;
Breinig, MC ;
Linden, P ;
Wilson, J ;
TorreCisneros, J ;
Kusne, S ;
Dummer, S ;
Ho, M .
JOURNAL OF INFECTIOUS DISEASES, 1997, 176 (06) :1462-1467
[10]   Cytomegalovirus infection after liver transplantation: Viral load as a guide to treating clinical infection [J].
Norris, S ;
Kosar, Y ;
Donaldson, N ;
Smith, HM ;
Zolfino, T ;
O'Grady, JG ;
Muiesan, P ;
Rela, M ;
Heaton, N .
TRANSPLANTATION, 2002, 74 (04) :527-531