ERADICATION OF CYTOMEGALOVIRUS REACTIVATION DISEASE USING HIGH-DOSE ACYCLOVIR AND TARGETED INTRAVENOUS GANCICLOVIR IN KIDNEY AND KIDNEY PANCREAS TRANSPLANTATION/
Gk. Shen et al., ERADICATION OF CYTOMEGALOVIRUS REACTIVATION DISEASE USING HIGH-DOSE ACYCLOVIR AND TARGETED INTRAVENOUS GANCICLOVIR IN KIDNEY AND KIDNEY PANCREAS TRANSPLANTATION/, Transplantation, 64(6), 1997, pp. 931-933
Background. The attack rate of cytomegalovirus (CMV) is over 50% in so
lid organ transplant recipients at risk for primary CMV infection and
in those receiving antilymphocyte antibody therapy. Various CMV prophy
laxis regimens over the last few years have reduced the attack rate to
around 20% overall. Methods. We report our results using high-dose ac
yclovir for 3 months after transplant, with targeted intravenous ganci
clovir for the duration of any antilymphocyte antibody therapy, in our
kidney and simultaneous pancreas/kidney transplant recipients. Record
s of 109 consecutive patients over a 2-year period were reviewed. Resu
lts. Six cases of CMV disease were identified. Five cases occurred in
21 patients at risk for primary CMV disease (24%), whereas only one ca
se occurred in 73 patients at risk for CMV reactivation (1.4%). Conclu
sion. We conclude that high-dose acyclovir and targeted ganciclovir is
excellent prophylaxis against CMV reactivation in kidney and simultan
eous pancreas/kidney transplantation.