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Common pathway coagulopathy and hemorrhagic edema of infancy

When screening tests of haemostasis are abnormal, it is important to identify at which point in the coagulation cascade dysfunction may be occurring. This may assist to identify a specific deficiency/dysfunction, the type of bleeding to be anticipated, and replacement therapy if required. Unmasking...

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Detalles Bibliográficos
Autores principales: Gard, Jye, Armiento, Raffaela, Cartwright, Anna, Bell, Shelley, Greenway, Anthea, O'Reilly, Erin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585055/
https://www.ncbi.nlm.nih.gov/pubmed/37867536
http://dx.doi.org/10.1002/ccr3.8060
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author Gard, Jye
Armiento, Raffaela
Cartwright, Anna
Bell, Shelley
Greenway, Anthea
O'Reilly, Erin
author_facet Gard, Jye
Armiento, Raffaela
Cartwright, Anna
Bell, Shelley
Greenway, Anthea
O'Reilly, Erin
author_sort Gard, Jye
collection PubMed
description When screening tests of haemostasis are abnormal, it is important to identify at which point in the coagulation cascade dysfunction may be occurring. This may assist to identify a specific deficiency/dysfunction, the type of bleeding to be anticipated, and replacement therapy if required. Unmasking of an inherited coagulopathy or the development of an acquired coagulopathy may occur in the setting of a second (febrile) illness. Differentiating between inherited and acquired coagulopathies will rely on clinicians taking a thorough personal and family bleeding history, and correlating these findings with the haemostasis screening results.
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spelling pubmed-105850552023-10-20 Common pathway coagulopathy and hemorrhagic edema of infancy Gard, Jye Armiento, Raffaela Cartwright, Anna Bell, Shelley Greenway, Anthea O'Reilly, Erin Clin Case Rep Case Report When screening tests of haemostasis are abnormal, it is important to identify at which point in the coagulation cascade dysfunction may be occurring. This may assist to identify a specific deficiency/dysfunction, the type of bleeding to be anticipated, and replacement therapy if required. Unmasking of an inherited coagulopathy or the development of an acquired coagulopathy may occur in the setting of a second (febrile) illness. Differentiating between inherited and acquired coagulopathies will rely on clinicians taking a thorough personal and family bleeding history, and correlating these findings with the haemostasis screening results. John Wiley and Sons Inc. 2023-10-18 /pmc/articles/PMC10585055/ /pubmed/37867536 http://dx.doi.org/10.1002/ccr3.8060 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. 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 Case Report
Gard, Jye
Armiento, Raffaela
Cartwright, Anna
Bell, Shelley
Greenway, Anthea
O'Reilly, Erin
Common pathway coagulopathy and hemorrhagic edema of infancy
title Common pathway coagulopathy and hemorrhagic edema of infancy
title_full Common pathway coagulopathy and hemorrhagic edema of infancy
title_fullStr Common pathway coagulopathy and hemorrhagic edema of infancy
title_full_unstemmed Common pathway coagulopathy and hemorrhagic edema of infancy
title_short Common pathway coagulopathy and hemorrhagic edema of infancy
title_sort common pathway coagulopathy and hemorrhagic edema of infancy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585055/
https://www.ncbi.nlm.nih.gov/pubmed/37867536
http://dx.doi.org/10.1002/ccr3.8060
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