Geneviève Genest1,2, Karen A Spitzer3,4, Carl A Laskin3,4. 1. From the Department of Allergy and Immunology, McGill University, Montreal, Quebec; TRIO Fertility; Department of Obstetrics and Gynaecology, University of Toronto; Division of Rheumatology, Department of Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada. genevieve.genest@mail.mcgill.ca. 2. G. Genest, MD, FRCPC, Department of Allergy and Immunology, McGill University; K.A. Spitzer, MSc, TRIO Fertility; C.A. Laskin, MD, FRCPC, TRIO Fertility; Division of Rheumatology, Department of Medicine, Mount Sinai Hospital; Division of Reproductive Endocrinology, Department of Obstetrics and Gynaecology, University of Toronto. genevieve.genest@mail.mcgill.ca. 3. From the Department of Allergy and Immunology, McGill University, Montreal, Quebec; TRIO Fertility; Department of Obstetrics and Gynaecology, University of Toronto; Division of Rheumatology, Department of Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada. 4. G. Genest, MD, FRCPC, Department of Allergy and Immunology, McGill University; K.A. Spitzer, MSc, TRIO Fertility; C.A. Laskin, MD, FRCPC, TRIO Fertility; Division of Rheumatology, Department of Medicine, Mount Sinai Hospital; Division of Reproductive Endocrinology, Department of Obstetrics and Gynaecology, University of Toronto.
Abstract
OBJECTIVE: Tumor necrosis factor inhibitors (TNFi) are increasingly used in pregnancy but are frequently withheld in the second or third trimesters. We evaluated the maternal and fetal outcomes of women who continued their TNFi throughout pregnancy compared to women who interrupted TNFi during pregnancy. METHODS: We retrospectively analyzed the outcomes of women seen in clinic with rheumatoid arthritis (RA), psoriatic arthritis, juvenile idiopathic arthritis (JIA), or ankylosing spondylitis, who were exposed to TNFi during pregnancy. We separated pregnancies into 2 groups based on the level of TNFi exposure and compared outcomes. RESULTS: In Group 1 (TNFi exposure in first trimester only), 11 women had 14 pregnancies and 12 live births. There were 2 first-trimester losses (2/14, 14%), one in the setting of active RA. Five pregnancies (5/14, 35.7%) were complicated by a disease flare. Eight patients (8/12, 66%) flared postpartum. In Group 2 (TNFi exposure throughout pregnancy), 29 women had 32 pregnancies and 34 live births. Three (3/28, 10.7%) adverse pregnancy outcomes were reported in 2 patients. One patient had a twin pregnancy and delivered at 33 weeks after developing preterm premature rupture of membranes at 32 weeks in the setting of a JIA flare. Her second pregnancy was complicated by active JIA before and throughout gestation, and hemolysis, elevated liver enzyme levels, and low platelet levels (HELLP) syndrome at 39 weeks. Another patient with comorbid antiphospholipid syndrome underwent a cesarean birth at 36 weeks for suspicion of HELLP syndrome. Six (6/32, 18.7%) postpartum flares occurred. CONCLUSION: Women who discontinued their TNFi during pregnancy had a higher risk of peri- or postpartum flare compared to those who continued their TNFi throughout pregnancy.
OBJECTIVE: Tumor necrosis factor inhibitors (TNFi) are increasingly used in pregnancy but are frequently withheld in the second or third trimesters. We evaluated the maternal and fetal outcomes of women who continued their TNFi throughout pregnancy compared to women who interrupted TNFi during pregnancy. METHODS: We retrospectively analyzed the outcomes of women seen in clinic with rheumatoid arthritis (RA), psoriatic arthritis, juvenile idiopathic arthritis (JIA), or ankylosing spondylitis, who were exposed to TNFi during pregnancy. We separated pregnancies into 2 groups based on the level of TNFi exposure and compared outcomes. RESULTS: In Group 1 (TNFi exposure in first trimester only), 11 women had 14 pregnancies and 12 live births. There were 2 first-trimester losses (2/14, 14%), one in the setting of active RA. Five pregnancies (5/14, 35.7%) were complicated by a disease flare. Eight patients (8/12, 66%) flared postpartum. In Group 2 (TNFi exposure throughout pregnancy), 29 women had 32 pregnancies and 34 live births. Three (3/28, 10.7%) adverse pregnancy outcomes were reported in 2 patients. One patient had a twin pregnancy and delivered at 33 weeks after developing preterm premature rupture of membranes at 32 weeks in the setting of a JIA flare. Her second pregnancy was complicated by active JIA before and throughout gestation, and hemolysis, elevated liver enzyme levels, and low platelet levels (HELLP) syndrome at 39 weeks. Another patient with comorbid antiphospholipid syndrome underwent a cesarean birth at 36 weeks for suspicion of HELLP syndrome. Six (6/32, 18.7%) postpartum flares occurred. CONCLUSION:Women who discontinued their TNFi during pregnancy had a higher risk of peri- or postpartum flare compared to those who continued their TNFi throughout pregnancy.
Authors: Laura J O'Byrne; Safi G Alqatari; Gillian M Maher; Aoife M O'Sullivan; Ali S Khashan; Grainne P Murphy; Fergus P McCarthy Journal: BJOG Date: 2022-02-16 Impact factor: 7.331