| Literature DB >> 27321569 |
R W King1, M J Baca1, V T Armenti1,2, B Kaplan3,4.
Abstract
In 2012, the U.S. Food and Drug Administration issued guidelines advising kidney transplant recipients (KTRs) to discontinue mycophenolate (MPA) in preparation for pregnancy. Little is known about how this guidance has affected pregnancy and graft outcomes. The purpose of this retrospective cohort study was to investigate any association between the discontinuation of MPA and KTR pregnancy and graft outcomes. Data from the National Transplantation Pregnancy Registry included 382 cases in which KTRs managed on MPA became pregnant. Overall, 22 variables, including the time in which a KTR discontinued MPA, were assessed across four end points: miscarriages, birth defects, and 2- and 5-year postpartum graft loss. Birth defects and miscarriages were similar among KTRs who discontinued MPA >6 and <6 weeks prior to pregnancy and during the first trimester. In contrast, discontinuing MPA during the second trimester or later significantly increased the risk of miscarriages (odds ratio [OR] 9.35, 95% confidence interval [CI] 4.31-20.00, p < 0.001) and birth defects (OR 6.06, 95% CI 1.96-18.87, p = 0.002). Discontinuing MPA <6 weeks prior to pregnancy was associated with an increased risk of 5-year graft loss. For the fetus, there is value to discontinuing MPA anytime prior to the second trimester. Adhering to current guidelines does not negatively affect graft survival. © Copyright 2016 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: antiproliferative agent: mycophenolate mofetil (MMF); antiproliferative agent: mycophenolate sodium; clinical research/practice; drug toxicity; enteric coated; graft survival; immunosuppressant; kidney transplantation/nephrology; obstetrics and gynecology; pharmacology; pregnancy
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Year: 2016 PMID: 27321569 DOI: 10.1111/ajt.13928
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086