Surveillance of cytomegalovirus infection in haematopoietic stem cell transplantation patients

被引:15
作者
Bonon, SHA
Menoni, SMF
Rossi, CL
De Souza, CA
Vigorito, AC
Costa, DB
Costa, SCB
机构
[1] Univ Estadual Campinas, Fac Med Sci, Dept Internal Med, BR-13081970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Fac Med Sci, Dept Clin Pathol, BR-13081970 Campinas, SP, Brazil
[3] Univ Estadual Campinas, Fac Med Sci, Bone Marrow Transplant Unit, Hemoctr, BR-13081970 Campinas, SP, Brazil
[4] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06510 USA
关键词
cytomegalovirus infection; PCR; bone marrow transplantation;
D O I
10.1016/j.jinf.2003.11.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives. The aim of this study was to describe our experience in the Cytomegalovirus control of active CMV infection following HSCT using two strategies of CMV infection treatment: ganciclovir universal prophylaxis at low doses and pre-emptive therapy with ganciclovir. Methods. The surveillance was based on the monitoring of antigenaemia (AGM) and on a nested potymerase chain reaction (N-PCR) for the detection of CMV in both strategies. Forty-five recipients with malignant diseases and with a risk for CMV disease received universal prophylaxis (Group A). The non-treated group consisted of 24 patients, most of them with non-malignant diseases who did not receive universal prophylaxis (Group B). Results. In Group A, the incidence of positive AGM was 51%, with a positive PCR of 68.9%. In Group B, the AGM positivity was 66.7% and that of N-PCR was 66.7%. CMV disease occurred in 6/55 patients (10.9%), with 2/36 (5.5%) from Group A and 4/19 (21%) from Group B. Two of these six patients (33.3%) died of CMV disease. Conclusions. Our result suggests that AGM and N-PCR can be used as markers for assessing the monitoring and the introduction pre-emptive therapy. This approach could prove to be more cost-effective than ganciclovir universal prophylaxis for treating CMV infection. (C) 2003 The British Infection Society. Published by Elsevier Ltd. ALL rights reserved.
引用
收藏
页码:130 / 137
页数:8
相关论文
共 40 条
[1]  
ALTMAN DG, 1991, PRACTICAL STAT MED R, V14, P410
[2]  
Azevedo A. M., 1996, British Journal of Haematology, V93, P250
[3]  
BOECKH M, 1992, BLOOD, V80, P1358
[4]   Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity [J].
Boeckh, M ;
Leisenring, W ;
Riddell, SR ;
Bowden, RA ;
Huang, ML ;
Myerson, D ;
Stevens-Ayers, T ;
Flowers, MED ;
Cunningham, T ;
Corey, L .
BLOOD, 2003, 101 (02) :407-414
[5]   Cytomegalovirus pp65 antigenemia-guided early treatment with ganciclovir versus ganciclovir at engraftment after allogeneic marrow transplantation: A randomized double-blind study [J].
Boeckh, M ;
Gooley, TA ;
Myerson, D ;
Cunningham, T ;
Schoch, G ;
Bowden, RA .
BLOOD, 1996, 88 (10) :4063-4071
[6]   Quantitation of cytomegalovirus: Methodologic aspects and clinical applications [J].
Boeckh, M ;
Boivin, G .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (03) :533-+
[7]   High incidence of cytomegalovirus infection after nonmyeloablative stem cell transplantation: potential role of Campath-1H in delaying immune reconstitution [J].
Chakrabarti, S ;
Mackinnon, S ;
Chopra, R ;
Kottaridis, PD ;
Peggs, K ;
O'Gorman, P ;
Chakraverty, R ;
Marshall, T ;
Osman, H ;
Mahendra, P ;
Craddock, C ;
Waldmann, H ;
Hale, G ;
Fegan, CD ;
Yong, K ;
Goldstone, AH ;
Linch, DC ;
Milligan, DW .
BLOOD, 2002, 99 (12) :4357-4363
[8]   Detection of cytomegalovirus infections by PCR in renal transplant patients [J].
Costa, SCB ;
Miranda, SRP ;
Alves, G ;
Rossi, CL ;
Figueiredo, LTM ;
Costa, FF .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1999, 32 (08) :953-959
[9]   DETECTION OF CYTOMEGALO-VIRUS IN URINE FROM NEWBORNS BY USING POLYMERASE CHAIN-REACTION DNA AMPLIFICATION [J].
DEMMLER, GJ ;
BUFFONE, GJ ;
SCHIMBOR, CM ;
MAY, RA .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (06) :1177-1184
[10]  
Eid K, 2002, BONE MARROW TRANSPL, V29, pS238