Immunosuppressant therapy during gestation
Identifieur interne : 002938 ( Main/Exploration ); précédent : 002937; suivant : 002939Immunosuppressant therapy during gestation
Auteurs : Bertis B. Little [États-Unis]Source :
- Seminars in Perinatology [ 0146-0005 ] ; 1997.
English descriptors
- Teeft :
- Alkylating agents, Animal studies, Anomaly, Arthritis, Arthritis rheum, Autoimmune diseases, Azathioprine, Birth defects, Birth weight, Breast milk, Case report, Chloroquine, Cleft palate, Congenital, Congenital anomalies, Cyclosporine, Fetal, Fetal development, Fetal growth restriction, First trimester, Gold salts, Gold therapy, Gravid patients, Gynecol, Heart transplant recipients, Immune system, Immunosuppressant, Immunosuppressive agents, Inflammatory bowel disease, Maternal side effects, Medical center, Obstet, Obstet gynecol, Prednisone, Pregnancy, Pregnancy outcome, Pregnant women, Renal, Renal allograft recipients, Renal transplant mothers, Renal transplant patients, Renal transplant recipients, Renal transplantation, Rheumatoid arthritis, Steroid, Transplant, Transplantation, Ulcerative colitis.
Abstract
Use of immunosuppressants during pregnancy is indicated for anti-rejection therapy in transplantation patients and treatment of autoimmune diseases. Maternal side effects include nephrotoxocity and hepatotoxicity. All immunosuppressant drugs cross the placenta. Immunosuppressant use during the first trimester is not strongly associated with an increased risk of congenital anomalies, although some agents (eg, azathioprine) may be associated with slightly increased frequencies of birth defects. Effects of exposure to this class of drugs during the second and third trimesters affect the fetus' immune system. The result is an infant with a transiently compromised immune system at an increased risk of slightly lower birth weight. Other direct toxic effects of the drugs on the infant's pancreas, liver, and lymphocytes are reported. Certain agents (eg, penicillamine, chloroquine) should be avoided during pregnancy, if possible. However, their use cannot be discontinued during pregnancy given the life-threatening nature of the indication for use of immunosuppressants.
Url:
DOI: 10.1016/S0146-0005(97)80057-2
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Use of immunosuppressants during pregnancy is indicated for anti-rejection therapy in transplantation patients and treatment of autoimmune diseases. Maternal side effects include nephrotoxocity and hepatotoxicity. All immunosuppressant drugs cross the placenta. Immunosuppressant use during the first trimester is not strongly associated with an increased risk of congenital anomalies, although some agents (eg, azathioprine) may be associated with slightly increased frequencies of birth defects. Effects of exposure to this class of drugs during the second and third trimesters affect the fetus' immune system. The result is an infant with a transiently compromised immune system at an increased risk of slightly lower birth weight. Other direct toxic effects of the drugs on the infant's pancreas, liver, and lymphocytes are reported. Certain agents (eg, penicillamine, chloroquine) should be avoided during pregnancy, if possible. However, their use cannot be discontinued during pregnancy given the life-threatening nature of the indication for use of immunosuppressants.</div>
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