Does Cytomegalovirus Serology Impact Outcome After Pediatric Heart Transplantation?

被引:35
作者
Mahle, William T. [1 ]
Fourshee, Margaret T. [2 ]
Naftel, David M. [2 ]
Alejos, Juan C. [3 ]
Caldwell, Randall L. [4 ]
Uzark, Karen [5 ,6 ]
Berg, Alexandria [1 ]
Kanter, Kirk R. [7 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA 30322 USA
[2] Univ Alabama Birmingham, Dept Cardiothorac Surg, Birmingham, AL USA
[3] Univ Calif Los Angeles, Sch Med, Dept Pediat, Los Angeles, CA 90024 USA
[4] Riley Childrens Hosp, Dept Pediat, Indianapolis, IN USA
[5] Dept Pediat, Cincinnati, OH USA
[6] Cincinnati Childrens Med Ctr, Cincinnati, OH USA
[7] Emory Univ, Dept Cardiothorac Surg, Atlanta, GA 30322 USA
关键词
CORONARY-ARTERY-DISEASE; LUNG-TRANSPLANTATION; INFECTION; REGISTRY;
D O I
10.1016/j.healun.2009.07.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Cytomegalovirus (CMV) infection has been implicated in a number of complications after heart transplantation. A recent study suggested that children with positive CMV serology (CMV+) before transplantation are at increased risk of developing coronary allograft vasculopathy (CAV) and death when compared with CMV- recipients. We analyzed data from the Pediatric Heart Transplant Study Group to determine the impact of recipient CMV status and CMV mismatching on outcome. In addition, the use and efficacy of CMV prophylaxis were studied. Methods: Subjects <18 years of age who underwent heart transplantation during the period from 1993 to 2007 were analyzed. Those transplants in which either the recipient or donor were <6 months of age were excluded due to the confounding effects of maternal antibody. The primary outcome variable was freedom from CAV (mild or greater). Secondary outcomes included freedom from death and freedom from clinical CMV infection. Risk factors were assessed using parametric hazard regression. Results: Of the 1,598 subjects included in the analysis, 637 (40%) were CMV+ at the time, of transplantation. Some form of CMV prophylaxis was administered to 67% of all recipients, most commonly with a CMV mismatch (donor CMV+/recipient CMV-). Freedom from clinical CMV infection at 5 years was 91%. Pre-transplant CMV serology was not associated with mortality (p = 0.40) or risk of developing CAV (p = 0.10). CMV mismatch was associated with increased risk of clinical CMV disease (P < 0.001). The use of CMV prophylaxis had no association with mortality or development of CAV. There was also no significant association between CMV prophylaxis and the development of clinical CMV infection. Conclusions: CMV+ serology at time of pediatric heart transplantation had no demonstrable association with death or development of CAV. CMV- recipients who receive a CMV+ organ are at increased risk of clinical CMV disease. CMV prophylaxis was commonly used, although further studies are needed to establish an optimal approach for prevention of CMV disease in this population. J Heart Lung Transplant 2009;28: 1299-305. Copyright (C) 2009 by the International Society for Heart and Lung Transplantation.
引用
收藏
页码:1299 / 1305
页数:7
相关论文
共 20 条
[11]   Positive pretransplantation cytomegalovirus serology is a risk factor for cardiac allograft vasculopathy in children [J].
Hussain, Tarique ;
Burch, Michael ;
Fenton, Matthew J. ;
Whitmore, Pauline M. ;
Rees, Philip ;
Elliott, Martin ;
Aurora, Paul .
CIRCULATION, 2007, 115 (13) :1798-1805
[12]  
KOSKINEN P, 1995, TRANSPLANT P, V27, P574
[13]   The impact and outcome of transplant coronary artery disease in a pediatric population: A 9-year multi-institutional study [J].
Pahl, E ;
Naftel, DC ;
Kuhn, MA ;
Shaddy, RE ;
Morrow, WR ;
Canter, CE ;
Kirklin, J .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2005, 24 (06) :645-651
[14]   Relevance of cytomegalovirus infection and coronary-artery remodeling in the first year after heart transplantation: A prospective three-dimensional intravascular ultrasound study [J].
Potena, L ;
Grigioni, F ;
Ortolani, P ;
Magnani, G ;
Marrozzini, C ;
Falchetti, E ;
Barbieri, A ;
Bacchi-Reggiani, L ;
Lazzarotto, T ;
Marzocchi, A ;
Magelli, C ;
Landini, MP ;
Branzi, A .
TRANSPLANTATION, 2003, 75 (06) :839-843
[15]   CMV and transplant-related coronary atherosclerosis:: An immunohistochemical, in situ hybridization, and polymerase chain reaction in situ study [J].
Sambiase, NV ;
Higuchi, MD ;
Nuovo, G ;
Gutierrez, PS ;
Fiorelli, AI ;
Uip, DE ;
Ramires, JA .
MODERN PATHOLOGY, 2000, 13 (02) :173-179
[16]   Endothelial dysfunction and cytomegalovirus replication in pediatric heart transplantation [J].
Simmonds, Jacob ;
Fenton, Matthew ;
Dewar, Catherine ;
Ellins, Elizabeth ;
Storry, Clare ;
Cubitt, David ;
Deanfield, John ;
Klein, Nigel ;
Halcox, Julian ;
Burch, Michael .
CIRCULATION, 2008, 117 (20) :2657-2661
[17]   Registry of the International Society for Heart and Lung Transplantation: Twenty-fourth official adult heart transplant report - 2007 [J].
Taylor, David O. ;
Edwards, Leah B. ;
Boucek, Mark M. ;
Trulock, Elbert P. ;
Aurora, Paul ;
Christie, Jason ;
Dobbels, Fabienne ;
Rahmel, Axel O. ;
Keck, Berkeley M. ;
Hertz, Marshall I. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2007, 26 (08) :769-781
[18]  
Valantine H A, 1999, Transpl Infect Dis, V1 Suppl 1, P25
[19]  
Vozarova L, 2003, Bratisl Lek Listy, V104, P317
[20]  
Weill D, 2001, Transpl Infect Dis, V3 Suppl 2, P44