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Early versus late onset of hypertensive disorders in twins—The placental perspective

OBJECTIVES: Early and late hypertensive disorders in pregnancy (HDP) are different entities in singleton gestations, with earlier onset associated with higher rates of placental maternal vascular malperfusion lesions (MVMs). It is still not known if this distinction apply for twin gestations as well...

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Autores principales: Aviram, Amir, Barrett, Jon, Zaltz, Arthur, Sherman, Christopher, Melamed, Nir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217648/
http://dx.doi.org/10.1016/j.jogc.2020.02.013
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author Aviram, Amir
Barrett, Jon
Zaltz, Arthur
Sherman, Christopher
Melamed, Nir
author_facet Aviram, Amir
Barrett, Jon
Zaltz, Arthur
Sherman, Christopher
Melamed, Nir
author_sort Aviram, Amir
collection PubMed
description OBJECTIVES: Early and late hypertensive disorders in pregnancy (HDP) are different entities in singleton gestations, with earlier onset associated with higher rates of placental maternal vascular malperfusion lesions (MVMs). It is still not known if this distinction apply for twin gestations as well. METHODS: Retrospective study of women with DCDA twin gestations and HDP (2001–2015), with a placental pathology evaluation. Placental lesions were classified according to the Amsterdam criteria. Pregnancies with early onset HDP (≤34 weeks) were compared with pregnancies with late onset HDP (>34 weeks). RESULTS: Out of 1655 twin deliveries, 161 (9.7%) were complicated by HDP: 77 (47.8%) had preeclampsia, and 84 (52.2%) had gestational hypertension. Forty patients (24.8%) had early onset HDP. Early HDP was associated with a higher rate of 1 MVMs (p=0.01), ≥2 MVMs (p=0.009) and with a lower rate of chronic villitis (p=0.02). In multivariable analysis, using late HDP as reference, early HDP was associated with a higher prevalence of ≥1 MVMs (aOR 1.9, 95% CI 1.1–3.5, p=0.03) and ≥2 MVMs (aOR 2.6, 95% CI 1.05–6.3, p=0.04). Early HDP was also less associated with chronic villitis (aOR 0.2, 95% CI 0.05–0.9), as chronic villitis is usually associated with a more advanced gestational age. CONCLUSIONS: While the mechanism underlying HDP in singleton and twins’ gestations may be different, similar to singleton pregnancies, early onset (≤34 weeks gestation) of HDP in twins’ gestation is associated with a higher prevalence of MVM's, suggesting of reduced placental perfusion in early onset HDP in twins.
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spelling pubmed-72176482020-05-13 Early versus late onset of hypertensive disorders in twins—The placental perspective Aviram, Amir Barrett, Jon Zaltz, Arthur Sherman, Christopher Melamed, Nir J Obstet Gynaecol Can Article OBJECTIVES: Early and late hypertensive disorders in pregnancy (HDP) are different entities in singleton gestations, with earlier onset associated with higher rates of placental maternal vascular malperfusion lesions (MVMs). It is still not known if this distinction apply for twin gestations as well. METHODS: Retrospective study of women with DCDA twin gestations and HDP (2001–2015), with a placental pathology evaluation. Placental lesions were classified according to the Amsterdam criteria. Pregnancies with early onset HDP (≤34 weeks) were compared with pregnancies with late onset HDP (>34 weeks). RESULTS: Out of 1655 twin deliveries, 161 (9.7%) were complicated by HDP: 77 (47.8%) had preeclampsia, and 84 (52.2%) had gestational hypertension. Forty patients (24.8%) had early onset HDP. Early HDP was associated with a higher rate of 1 MVMs (p=0.01), ≥2 MVMs (p=0.009) and with a lower rate of chronic villitis (p=0.02). In multivariable analysis, using late HDP as reference, early HDP was associated with a higher prevalence of ≥1 MVMs (aOR 1.9, 95% CI 1.1–3.5, p=0.03) and ≥2 MVMs (aOR 2.6, 95% CI 1.05–6.3, p=0.04). Early HDP was also less associated with chronic villitis (aOR 0.2, 95% CI 0.05–0.9), as chronic villitis is usually associated with a more advanced gestational age. CONCLUSIONS: While the mechanism underlying HDP in singleton and twins’ gestations may be different, similar to singleton pregnancies, early onset (≤34 weeks gestation) of HDP in twins’ gestation is associated with a higher prevalence of MVM's, suggesting of reduced placental perfusion in early onset HDP in twins. Published by Elsevier Inc. 2020-05 2020-05-12 /pmc/articles/PMC7217648/ http://dx.doi.org/10.1016/j.jogc.2020.02.013 Text en Copyright © 2020 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Aviram, Amir
Barrett, Jon
Zaltz, Arthur
Sherman, Christopher
Melamed, Nir
Early versus late onset of hypertensive disorders in twins—The placental perspective
title Early versus late onset of hypertensive disorders in twins—The placental perspective
title_full Early versus late onset of hypertensive disorders in twins—The placental perspective
title_fullStr Early versus late onset of hypertensive disorders in twins—The placental perspective
title_full_unstemmed Early versus late onset of hypertensive disorders in twins—The placental perspective
title_short Early versus late onset of hypertensive disorders in twins—The placental perspective
title_sort early versus late onset of hypertensive disorders in twins—the placental perspective
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217648/
http://dx.doi.org/10.1016/j.jogc.2020.02.013
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