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Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism

Amniotic fluid embolism (AFE) is one of the leading causes of maternal mortality and morbidity in developed countries. Current thinking about pathophysiology has shifted away from embolism toward a maternal immune response to the fetus. Two immunologic mechanisms have been studied to date. Anaphylax...

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Autor principal: Benson, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182579/
https://www.ncbi.nlm.nih.gov/pubmed/21969840
http://dx.doi.org/10.1155/2012/946576
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author Benson, Michael D.
author_facet Benson, Michael D.
author_sort Benson, Michael D.
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description Amniotic fluid embolism (AFE) is one of the leading causes of maternal mortality and morbidity in developed countries. Current thinking about pathophysiology has shifted away from embolism toward a maternal immune response to the fetus. Two immunologic mechanisms have been studied to date. Anaphylaxis appears to be doubtful while the available evidence supports a role for complement activation. With the mechanism remaining to be elucidated, AFE remains a clinical diagnosis. It is diagnosed based on one or more of four key signs/symptoms: cardiovascular collapse, respiratory distress, coagulopathy, and/or coma/seizures. The only laboratory test that reliably supports the diagnosis is the finding of fetal material in the maternal pulmonary circulation at autopsy. Perhaps the most compelling mystery surrounding AFE is not why one in 20,000 parturients are afflicted, but rather how the vast majority of women can tolerate the foreign antigenic presence of their fetus both within their uterus and circulation?
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spelling pubmed-31825792011-10-03 Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism Benson, Michael D. Clin Dev Immunol Review Article Amniotic fluid embolism (AFE) is one of the leading causes of maternal mortality and morbidity in developed countries. Current thinking about pathophysiology has shifted away from embolism toward a maternal immune response to the fetus. Two immunologic mechanisms have been studied to date. Anaphylaxis appears to be doubtful while the available evidence supports a role for complement activation. With the mechanism remaining to be elucidated, AFE remains a clinical diagnosis. It is diagnosed based on one or more of four key signs/symptoms: cardiovascular collapse, respiratory distress, coagulopathy, and/or coma/seizures. The only laboratory test that reliably supports the diagnosis is the finding of fetal material in the maternal pulmonary circulation at autopsy. Perhaps the most compelling mystery surrounding AFE is not why one in 20,000 parturients are afflicted, but rather how the vast majority of women can tolerate the foreign antigenic presence of their fetus both within their uterus and circulation? Hindawi Publishing Corporation 2012 2011-09-29 /pmc/articles/PMC3182579/ /pubmed/21969840 http://dx.doi.org/10.1155/2012/946576 Text en Copyright © 2012 Michael D. Benson. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Benson, Michael D.
Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title_full Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title_fullStr Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title_full_unstemmed Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title_short Current Concepts of Immunology and Diagnosis in Amniotic Fluid Embolism
title_sort current concepts of immunology and diagnosis in amniotic fluid embolism
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182579/
https://www.ncbi.nlm.nih.gov/pubmed/21969840
http://dx.doi.org/10.1155/2012/946576
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