Cytomegalovirus infections following renal transplantation - effects of antiviral prophylaxis: a report of the North American Pediatric Renal Transplant Cooperative Study

被引:34
作者
Bock, GH [1 ]
Sullivan, EK [1 ]
Miller, D [1 ]
Gimon, D [1 ]
Alexander, S [1 ]
Ellis, E [1 ]
Elshihabi, I [1 ]
机构
[1] Fairfax Hosp, Ctr Childrens Kidney, Annandale, VA 22003 USA
关键词
renal transplantation; infectious complications; cytomegalovirus; viral prophylaxis; risk analysis;
D O I
10.1007/s004670050361
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Post-transplant cytomegalovirus (CMV) infections are a source of significant morbidity. However, the extent of the problem and the benefits of various antiviral prophylactic therapies remain incompletely understood. The North American Pediatric Renal Transplant Cooperative Study registry was screened to identify patients hospitalized for CMV infections during the Ist post-renal transplant year between 1987 and 1993. Using a control group of transplant recipients, we performed a retrospective analysis of risk factors for CMV disease among these hospitalized patients and studied the effects of various viral prophylactic strategies on CMV risk, clinical manifestations, and outcome. We identified 142 patients hospitalized with CMV infections, the majority of which included major organ involvement. A CMV-positive kidney donor was the most significant risk factor for hospitalization [odds ratio (OR) = 5.2, P < 0.0001] irrespective of recipient age or CMV immune status. As opposed to antiviral agents (acyclovir, ganciclovir) or pooled IgG, prophylaxis with enriched anti-CMV IgG significantly reduced the risk of CMV hospitalization (OR = 0.31, P = 0.03). The prophylactic use of antiviral agents was associated with a decreased risk of major organ involvement during the CMV infection (OR = 0.34, P < 0.005). Among the patients with CMV, the 3-year graft survival was significantly better for those who received any form of prophylaxis compared with those who received none (88% vs, 52%, P < 0.001). Our findings suggest a role for combined CMV-enriched IgG and antiviral agent prophylaxis for post-transplant CMV disease. Such an approach could diminish the incidence and severity of CMV infection and appears to have an independent favorable effect on graft outcome.
引用
收藏
页码:665 / 671
页数:7
相关论文
共 34 条
  • [1] A RANDOMIZED, PLACEBO-CONTROLLED TRIAL OF ORAL ACYCLOVIR FOR THE PREVENTION OF CYTOMEGALO-VIRUS DISEASE IN RECIPIENTS OF RENAL-ALLOGRAFTS
    BALFOUR, HH
    CHACE, BA
    STAPLETON, JT
    SIMMONS, RL
    FRYD, DS
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (21) : 1381 - 1387
  • [2] BOSCH FH, 1989, TRANSPLANT INT, V2, P92, DOI 10.1111/j.1432-2277.1989.tb01846.x
  • [3] THE EFFECT OF CYTOMEGALO-VIRUS INFECTION ON RENAL-ALLOGRAFT FUNCTION AND REJECTION IN A RAT MODEL
    BRUNING, JH
    BRUGGEMAN, CA
    VRIESMAN, PJV
    [J]. TRANSPLANTATION, 1989, 47 (04) : 742 - 744
  • [4] CYTOMEGALOVIRUS-INFECTION AS A COMPLICATION OF OKT3 THERAPY IN KIDNEY-TRANSPLANT RECIPIENTS
    CONLON, PJ
    CARMODY, M
    DONOHOE, J
    SPENCER, S
    SMYTH, E
    WALSHE, JJ
    [J]. IRISH JOURNAL OF MEDICAL SCIENCE, 1992, 161 (11) : 630 - 632
  • [5] GANCICLOVIR EFFECTIVELY TREATS CYTOMEGALOVIRUS DISEASE AFTER SOLID-ORGAN TRANSPLANTATION, EVEN DURING REJECTION TREATMENT
    DEKONING, J
    VANDORP, WT
    VANES, LA
    VANTWOUT, JW
    VANDERWOUDE, FJ
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 1992, 7 (04) : 350 - 356
  • [6] A PROSPECTIVE RANDOMIZED STUDY OF ACYCLOVIR VERSUS GANCICLOVIR PLUS HUMAN IMMUNE GLOBULIN PROPHYLAXIS OF CYTOMEGALOVIRUS-INFECTION AFTER SOLID-ORGAN TRANSPLANTATION
    DUNN, DL
    GILLINGHAM, KJ
    KRAMER, MA
    SCHMIDT, WJ
    ERICE, A
    BALFOUR, HH
    GORES, PF
    GRUESSNER, RWG
    MATAS, AJ
    PAYNE, WD
    SUTHERLAND, DER
    NAJARIAN, JS
    [J]. TRANSPLANTATION, 1994, 57 (06) : 876 - 884
  • [7] NEW APPROACHES TO THE DIAGNOSIS, PREVENTION, AND TREATMENT OF CYTOMEGALOVIRUS-INFECTION AFTER TRANSPLANTATION
    DUNN, DL
    NAJARIAN, JS
    [J]. AMERICAN JOURNAL OF SURGERY, 1991, 161 (02) : 250 - 255
  • [8] DUNN DL, 1989, INFECT SURG, V8, P164
  • [9] Ellis E. N., 1996, Journal of the American Society of Nephrology, V7, P1931
  • [10] FISCHER L, 1993, TRANSPLANT INT, V6, P201, DOI 10.1007/BF00337099