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Ganciclovir-resistant (GanR) cytomegalovirus (CMV) is an emerging clinical problem in organ transplant recipients, particularly recipients of kidney and pancreas and lung transplants. GanR CMV, a late posttransplantation complication, is observed predominantly among CMV-seronegative recipients of organs from seropositive donors, especially among recipients receiving intensive immunosuppression and having prolonged exposure to ganciclovir. Given the limitations of current diagnostic methods, if GanR CMV is clinically suspected, empirical treatment with intravenously administered foscarnet should be used in conjunction with reductions in immunosuppressive therapy and possibly CMV hyperimmune globulin. Better diagnostic tools and newer, less-toxic antiviral agents with different mechanisms of action are urgently needed to decrease the morbidity associated with this complication in organ transplant recipients.
 

Cytomegalovirus (CMV) remains an important pathogen in organ transplant recipients, and ganciclovir has been the antiviral agent of choice both for prevention and treatment of CMV disease. Shortly after the introduction of ganciclovir in the late 1980s, sporadic cases of ganciclovir-resistant (GanR) CMV were reported in severely immunocompromised patients, usually after prolonged exposure to ganciclovir . During the AIDS epidemic, the development of ganciclovir resistance was reported among patients with AIDS who were receiving prolonged ganciclovir therapy for CMV retinitis. Furthermore, studies demonstrated that in vitro resistance to ganciclovir was associated with clinical progression of CMV disease .

In contrast, during this same period, only isolated cases of GanR CMV were reported among solid-organ transplant (SOT) recipients. However, more recently, with the advent of more widespread use of oral ganciclovir and use of more-intensive immunosuppressive strategies, there has been increased recognition of ganciclovir resistance as a clinical problem in organ transplant recipients.

In the present article, I summarize the current understanding of the pathogenesis, clinical manifestations, diagnosis, and management of GanR CMV in SOT recipients. My goal is to provide to clinicians who care for SOT recipients the information necessary to promptly recognize and appropriately treat patients with suspected or documented GanR CMV. I refer readers to other sources for more-detailed discussions of the molecular virologic aspects of GanR CMV
 

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