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Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades

OBJECTIVE: Using a large, de‐identified electronic health record database with over 3.2 million patients, we aimed to identify trends of systemic lupus erythematosus (SLE) medication use during pregnancy and birth outcomes from 1989 to 2020. METHODS: Using a previously validated algorithm for SLE de...

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Autores principales: Barnado, April, Hubbard, Janie, Green, Sarah, Camai, Alex, Wheless, Lee, Osmundson, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374054/
https://www.ncbi.nlm.nih.gov/pubmed/35670028
http://dx.doi.org/10.1002/acr2.11447
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author Barnado, April
Hubbard, Janie
Green, Sarah
Camai, Alex
Wheless, Lee
Osmundson, Sarah
author_facet Barnado, April
Hubbard, Janie
Green, Sarah
Camai, Alex
Wheless, Lee
Osmundson, Sarah
author_sort Barnado, April
collection PubMed
description OBJECTIVE: Using a large, de‐identified electronic health record database with over 3.2 million patients, we aimed to identify trends of systemic lupus erythematosus (SLE) medication use during pregnancy and birth outcomes from 1989 to 2020. METHODS: Using a previously validated algorithm for SLE deliveries, we identified 255 pregnancies in patients with SLE and 604 pregnancies in controls with no known autoimmune diseases. We examined demographics, medications, SLE comorbidities, and maternal and fetal outcomes in SLE and control deliveries. RESULTS: Compared with control deliveries, SLE deliveries were more likely to be complicated by preterm delivery (odds ratio [OR]: 6.71; 95% confidence interval [CI]: 4.31‐10.55; P < 0.001) and preeclampsia (OR: 3.22; 95% CI: 1.83‐5.66; P < 0.001) after adjusting for age at delivery, race, and parity. In a longitudinal analysis, medication use during SLE pregnancies remained relatively stable, with some increased use of hydroxychloroquine over time but no increase in aspirin use. For SLE deliveries, preterm delivery and preeclampsia rates remained stable. CONCLUSION: We observed rates of preeclampsia and preterm delivery in SLE that were five times higher than the general population and higher compared with other prospective SLE cohorts. Furthermore, we did not observe improved outcomes over time with preeclampsia and preterm delivery. Despite increasing evidence for universal use of hydroxychloroquine and aspirin, we did not observe substantially higher use of these medications over time, particularly for aspirin. Our results demonstrate the continued need to prioritize educational and implementation efforts to improve adverse pregnancy outcomes in SLE.
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spelling pubmed-93740542022-08-16 Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades Barnado, April Hubbard, Janie Green, Sarah Camai, Alex Wheless, Lee Osmundson, Sarah ACR Open Rheumatol Original Articles OBJECTIVE: Using a large, de‐identified electronic health record database with over 3.2 million patients, we aimed to identify trends of systemic lupus erythematosus (SLE) medication use during pregnancy and birth outcomes from 1989 to 2020. METHODS: Using a previously validated algorithm for SLE deliveries, we identified 255 pregnancies in patients with SLE and 604 pregnancies in controls with no known autoimmune diseases. We examined demographics, medications, SLE comorbidities, and maternal and fetal outcomes in SLE and control deliveries. RESULTS: Compared with control deliveries, SLE deliveries were more likely to be complicated by preterm delivery (odds ratio [OR]: 6.71; 95% confidence interval [CI]: 4.31‐10.55; P < 0.001) and preeclampsia (OR: 3.22; 95% CI: 1.83‐5.66; P < 0.001) after adjusting for age at delivery, race, and parity. In a longitudinal analysis, medication use during SLE pregnancies remained relatively stable, with some increased use of hydroxychloroquine over time but no increase in aspirin use. For SLE deliveries, preterm delivery and preeclampsia rates remained stable. CONCLUSION: We observed rates of preeclampsia and preterm delivery in SLE that were five times higher than the general population and higher compared with other prospective SLE cohorts. Furthermore, we did not observe improved outcomes over time with preeclampsia and preterm delivery. Despite increasing evidence for universal use of hydroxychloroquine and aspirin, we did not observe substantially higher use of these medications over time, particularly for aspirin. Our results demonstrate the continued need to prioritize educational and implementation efforts to improve adverse pregnancy outcomes in SLE. Wiley Periodicals, Inc. 2022-06-06 /pmc/articles/PMC9374054/ /pubmed/35670028 http://dx.doi.org/10.1002/acr2.11447 Text en © 2022 The Authors. ACR Open Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Barnado, April
Hubbard, Janie
Green, Sarah
Camai, Alex
Wheless, Lee
Osmundson, Sarah
Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title_full Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title_fullStr Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title_full_unstemmed Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title_short Systemic Lupus Erythematosus Delivery Outcomes Are Unchanged Across Three Decades
title_sort systemic lupus erythematosus delivery outcomes are unchanged across three decades
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374054/
https://www.ncbi.nlm.nih.gov/pubmed/35670028
http://dx.doi.org/10.1002/acr2.11447
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