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Cytomegalovirus infection and disease after liver transplantation
Authors:Dr. Robert J. Stratta MD  Mark S. Shaeffer PharmD  Rodney S. Markin MD  PhD  R. Patrick Wood MD  Alan N. Langnas DO  Elizabeth C. Reed MD  Jeremiah P. Donovan MD  Gail L. Woods MD  Kathleen A. Bradshaw RN  Todd J. Pillen PA  Byers W. Shaw Jr. MD
Affiliation:(1) Department of Surgery, University of Nebraska Medical Center, 600 South 42nd Street, 68198-3280 Omaha, Nebraska;(2) Department of Pharmacy Practice, University of Nebraska Medical Center, 600 South 42nd Street, 68198-3280 Omaha, Nebraska;(3) Department of Pathology and Microbiology, University of Nebraska Medical Center, 600 South 42nd Street, 68198-3280 Omaha, Nebraska;(4) Department of Internal Medicine, University of Nebraska Medical Center, 600 South 42nd Street, 68198-3280 Omaha, Nebraska
Abstract:Cytomegalovirus is the single most important pathogen in clinical transplantation. Although much progress has been made in our understanding of the molecular biology and epidemiology of CMV infection and in our ability to diagnosis and treat CMV disease, it remains a major cause of morbidity but is no longer a major cause of mortality after liver transplantation. Risk factors for CMV disease after liver transplantation include donor and recipient serologic status, the use of antilymphocyte therapy, and retransplantation. CMV disease occurs early after transplantation, and the most frequent site of disease is the hepatic allograft. We have treated 79 patients with intravenous ganciclovir, with ultimate control of disease achieved in 69 patients (87.3%). Preliminary results using intravenous immunoglobulin and oral acyclovir for CMV prophylaxis in high-risk patients have been encouraging. In addition to producing clinical syndromes, CMV may have direct immunologic effects and is a marker of the net state of immunosuppression.
Keywords:acyclovir  cytomegalovirus  ganciclovir  immunoglobulin  immunosuppression  liver transplantation  OKT3
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