Prevention of Cytomegalovirus Disease in Moderate-Risk (D+/R+ and D-/R+) Renal Transplant Recipients Receiving Basiliximab Induction Therapy: an Efficacy and Safety Evaluation of 3 vs. 6 Months of Low-Dose Valganciclovir
Steven Gabardi, PharmD1, Rosemary Cross, PharmD2, Kelly DePiero, PharmD3, Travis B. Dick, PharmD, BCPS4, Pamela R. Maxwell, Pharm.D., BCPS5, Joelle Nelson, Pharm.D.6, Erin N. Newkirk, Pharm.D.7, Kathleen Nguyen, PharmD8, Jeong M. Park, M.S., Pharm.D.9, Eric M. Tichy, Pharm.D., BCPS10, Kimi Ueda, Pharm.D.11, Renee Weng, Pharm.D.12 and Angela Q. Maldonado, Pharm, D, BCPS13
1Department of Pharmacy & Renal Divison, Brigham & Women's Hospital; Department of Medicine, Harvard Medical School, Boston, MA
2Piedmont Hospital, Atlanta, GA
3Lahey Clinic Medical Center, Burlington, MA
4Intermountain Medical Center, Murray, UT
5University Transplant Center, The University of Texas Health Science Center at San Antonio, San Antonio, TX
6University Health System, San Antonio, TX
7Froedtert & the Medical College of Wisconsin, Milwaukee, WI
8University of California Irvine Medical Center, Orange, CA
9University of Michigan, Ann Arbor, MI
10Yale-New Haven Hospital, New Haven, CT
11California Pacific Medical Center, San Francisco, CA
12UC-Irvine, Orange, CA
13Sacred Heart Medical Center, Spokane, WA