Pharmacologic Considerations for Solid Organ Transplant Recipients Who Become Pregnant

被引:11
作者
Casale, Jillian P. [1 ]
Doligalski, Christina T. [1 ]
机构
[1] Tampa Gen Hosp, Dept Pharm, Tampa, FL 33606 USA
来源
PHARMACOTHERAPY | 2016年 / 36卷 / 09期
关键词
pregnancy; solid organ transplantation; immunosuppression; BIRTH-WEIGHT; IMMUNOLOGICAL EVALUATION; PHYSIOLOGICAL-CHANGES; IMMUNE-SYSTEM; INFANTS BORN; IN-UTERO; EXPOSURE; OUTCOMES; WOMEN; RISK;
D O I
10.1002/phar.1800
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Females of childbearing age represent a large population of solid organ transplant recipients. With fertility commonly restored after transplantation, the possibility of pregnancy becomes a reality for many patients. Since the first published report of a successful pregnancy after solid organ transplantation in 1963, the number of pregnancies reported for female organ recipients has continued to increase. Despite this, information on the management of immunosuppression during pregnancy is limited, and a summary of these data is lacking in the literature. In addition to the many pharmacotherapeutic challenges in this unique patient population, physiologic changes in the peripartum period significantly affect the pharmacokinetics and pharmacodynamics of commonly used immunosuppressive agents. These changes, as well as the adverse effects and safety concerns of medications, must all be taken in to consideration to optimize outcomes for both mother and baby. In this review, we provide clinicians caring for female solid organ transplant recipients who wish to become pregnant or who are currently pregnant with a comprehensive review of maternal and fetal risks of pregnancy after transplantation. In addition, pharmacokinetic and pharmacodynamic changes of pregnancy will be discussed, and a summary of data regarding optimal immunosuppression management during pregnancy will be presented.
引用
收藏
页码:971 / 982
页数:12
相关论文
共 63 条
[1]   Pregnancy-induced changes in pharmacokinetics - A mechanistic-based approach [J].
Anderson, GD .
CLINICAL PHARMACOKINETICS, 2005, 44 (10) :989-1008
[2]  
[Anonymous], FED REG
[3]  
[Anonymous], 2016, AM J TRANSPLANT, V16, P4
[4]  
ARMENTI VT, 1995, TRANSPLANTATION, V59, P476
[5]   Immunosuppression in pregnancy - Choices for infant and maternal health [J].
Armenti, VT ;
Moritz, MJ ;
Cardonick, EH ;
Davison, JM .
DRUGS, 2002, 62 (16) :2361-2375
[6]   Morbidity and mortality among very-low-birth-weight neonates with intrauterine growth restriction [J].
Bernstein, IM ;
Horbar, JD ;
Badger, GJ ;
Ohlsson, A ;
Golan, L .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2000, 182 (01) :198-206
[7]  
BIESENBACH G, 1989, NEPHROL DIAL TRANSPL, V4, P667
[8]   INVITRO METABOLISM OF PREDNISOLONE, DEXAMETHASONE, BETAMETHASONE, AND CORTISOL BY HUMAN PLACENTA [J].
BLANFORD, AT ;
MURPHY, BEP .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1977, 127 (03) :264-267
[9]  
Briggs G G., 2015, Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk
[10]  
Bristol-Myers Squibb Company, 2014, NUL BEL PACK INS