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Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report

BACKGROUND: Emicizumab is a novel prophylactic medication used to treat patients with hemophilia A. It is indicated to minimize the frequency of bleeding episodes and the severity of serious bleeding in patients with hemophilia A utilizing inhibitors. However, some cases of bleeding episodes have be...

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Autores principales: Albattat, Sami, Alabdultaif, Abbas, Albattat, Fatimah, Albattat, Batla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948523/
https://www.ncbi.nlm.nih.gov/pubmed/36814352
http://dx.doi.org/10.1186/s13256-023-03783-7
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author Albattat, Sami
Alabdultaif, Abbas
Albattat, Fatimah
Albattat, Batla
author_facet Albattat, Sami
Alabdultaif, Abbas
Albattat, Fatimah
Albattat, Batla
author_sort Albattat, Sami
collection PubMed
description BACKGROUND: Emicizumab is a novel prophylactic medication used to treat patients with hemophilia A. It is indicated to minimize the frequency of bleeding episodes and the severity of serious bleeding in patients with hemophilia A utilizing inhibitors. However, some cases of bleeding episodes have been reported, and more data are needed regarding their management and expected outcomes. CASE PRESENTATION: We report a case of a 4-year-old Saudi Arabian boy with severe hemophilia A who presented with a post-traumatic cerebral hemorrhage. The patient, with high titer inhibitors, was on emicizumab prophylaxis therapy. On hospital admission, he received tranexamic acid (10 mg intravenously, every 6 hours), and recombinant activated factor VII 120 µg/kg every 2 hours for 2 days then every 4 hours for 4 days. On follow-up, the patient showed no signs of neurological deficit. There was no need for emergency neurosurgical intervention since the bleeding had been controlled throughout the first 2 days. There were no recorded thrombotic sequelae or neurological complications, with complete resolution within 10 days. CONCLUSIONS: This case implies that low-dose recombinant activated factor VII might be used safely and effectively with patients with hemophilia A on emicizumab prophylaxis, to reduce the risk of cerebral hemorrhage or another episode of serious bleeding along with its long-term complications.
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spelling pubmed-99485232023-02-24 Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report Albattat, Sami Alabdultaif, Abbas Albattat, Fatimah Albattat, Batla J Med Case Rep Case Report BACKGROUND: Emicizumab is a novel prophylactic medication used to treat patients with hemophilia A. It is indicated to minimize the frequency of bleeding episodes and the severity of serious bleeding in patients with hemophilia A utilizing inhibitors. However, some cases of bleeding episodes have been reported, and more data are needed regarding their management and expected outcomes. CASE PRESENTATION: We report a case of a 4-year-old Saudi Arabian boy with severe hemophilia A who presented with a post-traumatic cerebral hemorrhage. The patient, with high titer inhibitors, was on emicizumab prophylaxis therapy. On hospital admission, he received tranexamic acid (10 mg intravenously, every 6 hours), and recombinant activated factor VII 120 µg/kg every 2 hours for 2 days then every 4 hours for 4 days. On follow-up, the patient showed no signs of neurological deficit. There was no need for emergency neurosurgical intervention since the bleeding had been controlled throughout the first 2 days. There were no recorded thrombotic sequelae or neurological complications, with complete resolution within 10 days. CONCLUSIONS: This case implies that low-dose recombinant activated factor VII might be used safely and effectively with patients with hemophilia A on emicizumab prophylaxis, to reduce the risk of cerebral hemorrhage or another episode of serious bleeding along with its long-term complications. BioMed Central 2023-02-23 /pmc/articles/PMC9948523/ /pubmed/36814352 http://dx.doi.org/10.1186/s13256-023-03783-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Albattat, Sami
Alabdultaif, Abbas
Albattat, Fatimah
Albattat, Batla
Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title_full Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title_fullStr Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title_full_unstemmed Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title_short Cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
title_sort cerebellar hematoma in severe hemophilia with inhibitor on emicizumab prophylaxis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948523/
https://www.ncbi.nlm.nih.gov/pubmed/36814352
http://dx.doi.org/10.1186/s13256-023-03783-7
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