2019
DOI: 10.1177/1753495x19841799
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The use of biologics for autoimmune rheumatic diseases in fertility and pregnancy

Abstract: In an age where autoimmune rheumatic diseases are successfully managed with biologics, their discontinuation in pregnancy is inadvisable without careful forethought; maternal disease activity is associated with adverse pregnancy outcomes, which has long-term implications for both mother and offspring. We aim to provide clinicians with the necessary tools to facilitate decision-making – when a biologic should be used, when it can be discontinued in pregnancy if appropriate. The pathophysiology of these biologic… Show more

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Cited by 10 publications
(10 citation statements)
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References 92 publications
(102 reference statements)
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“…Almost 50% of the patients continued the medication during the third trimester of pregnancy and a third of them until the time of delivery, and there was no increased risk of neonatal infection or infections during the first year of life [ 133 ]. Live vaccines are contraindicated in the first six months of life, especially BCG vaccine (Bacillus Calmette–Guérin) [ 134 ].…”
Section: Pathological Transfer Of Igg—biological Therapy In Pregnamentioning
confidence: 99%
“…Almost 50% of the patients continued the medication during the third trimester of pregnancy and a third of them until the time of delivery, and there was no increased risk of neonatal infection or infections during the first year of life [ 133 ]. Live vaccines are contraindicated in the first six months of life, especially BCG vaccine (Bacillus Calmette–Guérin) [ 134 ].…”
Section: Pathological Transfer Of Igg—biological Therapy In Pregnamentioning
confidence: 99%
“…Before week 14 of pregnancy, biological drug molecules enter the foetus through passive diffusion and only insignificant volumes reach the foetus during embryogenesis (first 12 weeks of pregnancy). However, from the second trimester, the crossing of biological drugs is facilitated by an increased expression of trophoblast Fc receptors, and IgG transport is most intense in the third trimester of pregnancy, as a result of which neonatal IgG1 levels are often higher than maternal levels [32][33][34]. TNF-α inhibitors (etanercept, infliximab, adalimumab, golimumab and certolizumab pegol) are the most researched biological agents in terms of use by pregnant women.…”
Section: Discussionmentioning
confidence: 99%
“…All rights reserved. Case series and registry data suggest no increased rate of congenital abnormalities [84][85][86][87] Case series and registry data suggests no increased rate of spontaneous abortions [84][85][86][87] NA Animal studies suggest no increased risk of malformation in survivors and one human case report showed no adverse neonatal outcome 91 Animal studies suggest a non-dose-related increase in spontaneous miscarriages and neonatal death 91 NA IMMUNO MODULATORS Anakinra Animal studies and human case reports suggest no increased risk of structural defects [92][93][94] Case series suggests no increased risk of fetal loss or preterm birth NA No human data in lactation. Probably compatible based on large molecular weight.…”
Section: Namentioning
confidence: 99%