%0 Journal Article %1 Mitsani2010 %A Mitsani, Dimitra %A Nguyen, M Hong %A Kwak, Eun J. %A Silveira, Fernanda P. %A Vadnerkar, Aniket %A Pilewski, Joseph %A Crespo, Maria %A Toyoda, Yoshiya %A Bermudez, Christian %A Clancy, Cornelius J. %D 2010 %J J Heart Lung Transplant %K cmv transplantation virus prophylaxis %N 9 %P 1014--1020 %R 10.1016/j.healun.2010.04.022 %T Cytomegalovirus disease among donor-positive/recipient-negative lung transplant recipients in the era of valganciclovir prophylaxis. %U http://dx.doi.org/10.1016/j.healun.2010.04.022 %V 29 %X Valganciclovir prophylaxis is advocated for lung transplant recipients, but its efficacy is unknown.Retrospective review was done of 109 donor-positive/recipient-negative lung transplant patients who received alemtuzumab induction and valganciclovir for cytomegalovirus prophylaxis.Median duration of follow-up after transplant was 27 months. Valganciclovir dose reductions (< 900 mg/day or renal-equivalent) were required for 18 patients (17\%) due to toxicity, most commonly for neutropenia (n = 15) or gastrointestinal symptoms (n = 2). Of the 109 patients, 34 (31\%) had no CMV infections, 45 (41\%) had asymptomatic viremia, and 30 (27\%) had CMV disease. CMV disease developed off prophylaxis in 10 patients (18\%) at a median of 8.7 months after transplant and 2 months after valganciclovir discontinuation. Breakthrough disease occurred during prophylaxis in 10 patients (9\%) at a median of 6.7 months. Patients with asymptomatic viremia or no CMV infection received prophylaxis for median 8.6 and 8.7 months, respectively. Risk factors for CMV disease by univariate analysis were increased age (p = 0.01), single-lung transplant (p = 0.03), chronic obstructive pulmonary disease (p = 0.05), reduced-dose valganciclovir (p = 0.001), and less than 6 months of prophylaxis (p = 0.005). By multivariate analysis, advanced age (p = 0.01) and reduced-dose valganciclovir (p = 0.0006) were independent risk factors for CMV disease. CMV disease developed in 4 patients (4\%) due to ganciclovir-resistant viruses. CMV-attributable mortality was 5\% (5 of 109), including 100\% (4 of 4) with ganciclovir-resistant disease.Valganciclovir prophylaxis among donor-positive/recipient-negative lung transplant recipients delayed but did not eliminate CMV disease or CMV-related deaths and was limited by toxicity and ganciclovir-resistance. Our experience suggests that valganciclovir at reduced-doses or for less than 6 months is sub-optimal in preventing CMV disease.

@article{Mitsani2010, abstract = {Valganciclovir prophylaxis is advocated for lung transplant recipients, but its efficacy is unknown.Retrospective review was done of 109 donor-positive/recipient-negative lung transplant patients who received alemtuzumab induction and valganciclovir for cytomegalovirus prophylaxis.Median duration of follow-up after transplant was 27 months. Valganciclovir dose reductions (< 900 mg/day or renal-equivalent) were required for 18 patients (17\%) due to toxicity, most commonly for neutropenia (n = 15) or gastrointestinal symptoms (n = 2). Of the 109 patients, 34 (31\%) had no CMV infections, 45 (41\%) had asymptomatic viremia, and 30 (27\%) had CMV disease. CMV disease developed off prophylaxis in 10 patients (18\%) at a median of 8.7 months after transplant and 2 months after valganciclovir discontinuation. Breakthrough disease occurred during prophylaxis in 10 patients (9\%) at a median of 6.7 months. Patients with asymptomatic viremia or no CMV infection received prophylaxis for median 8.6 and 8.7 months, respectively. Risk factors for CMV disease by univariate analysis were increased age (p = 0.01), single-lung transplant (p = 0.03), chronic obstructive pulmonary disease (p = 0.05), reduced-dose valganciclovir (p = 0.001), and less than 6 months of prophylaxis (p = 0.005). By multivariate analysis, advanced age (p = 0.01) and reduced-dose valganciclovir (p = 0.0006) were independent risk factors for CMV disease. CMV disease developed in 4 patients (4\%) due to ganciclovir-resistant viruses. CMV-attributable mortality was 5\% (5 of 109), including 100\% (4 of 4) with ganciclovir-resistant disease.Valganciclovir prophylaxis among donor-positive/recipient-negative lung transplant recipients delayed but did not eliminate CMV disease or CMV-related deaths and was limited by toxicity and ganciclovir-resistance. Our experience suggests that valganciclovir at reduced-doses or for less than 6 months is sub-optimal in preventing CMV disease.}, added-at = {2012-06-20T05:08:49.000+0200}, author = {Mitsani, Dimitra and Nguyen, M Hong and Kwak, Eun J. and Silveira, Fernanda P. and Vadnerkar, Aniket and Pilewski, Joseph and Crespo, Maria and Toyoda, Yoshiya and Bermudez, Christian and Clancy, Cornelius J.}, biburl = {https://www.bibsonomy.org/bibtex/2769f86e847c0f4db53c6de1cce05fc4c/aorchid}, description = {resistant CMV is bad. Alemtuzumab for CMV mismatches is probably not a good idea.}, doi = {10.1016/j.healun.2010.04.022}, file = {:ID_General/TransplantClinical/JHeartLungTransplant.29.1014.pdf:PDF}, groups = {public}, institution = {Department of Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.}, interhash = {53bd7d565c0e4084292e4aed15729a5b}, intrahash = {769f86e847c0f4db53c6de1cce05fc4c}, journal = {J Heart Lung Transplant}, keywords = {cmv transplantation virus prophylaxis}, language = {eng}, medline-pst = {ppublish}, month = Sep, number = 9, pages = {1014--1020}, pii = {S1053-2498(10)00279-2}, pmid = {20598582}, timestamp = {2012-06-20T05:08:49.000+0200}, title = {Cytomegalovirus disease among donor-positive/recipient-negative lung transplant recipients in the era of valganciclovir prophylaxis.}, url = {http://dx.doi.org/10.1016/j.healun.2010.04.022}, username = {aorchid}, volume = 29, year = 2010 }