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Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement
In typical hemolytic uremic syndrome (HUS) approximately 25% of patients show central nervous system (CNS) involvement often leading to serious long-term disabilities. We used the C5-complement inhibitor Eculizumab as rescue therapy. From 2011 to 2014, 11 children (median age 22 months, range 11–175...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616562/ https://www.ncbi.nlm.nih.gov/pubmed/26091445 http://dx.doi.org/10.1097/MD.0000000000001000 |
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author | Pape, Lars Hartmann, Hans Bange, Franz Christoph Suerbaum, Sebastian Bueltmann, Eva Ahlenstiel-Grunow, Thurid |
author_facet | Pape, Lars Hartmann, Hans Bange, Franz Christoph Suerbaum, Sebastian Bueltmann, Eva Ahlenstiel-Grunow, Thurid |
author_sort | Pape, Lars |
collection | PubMed |
description | In typical hemolytic uremic syndrome (HUS) approximately 25% of patients show central nervous system (CNS) involvement often leading to serious long-term disabilities. We used the C5-complement inhibitor Eculizumab as rescue therapy. From 2011 to 2014, 11 children (median age 22 months, range 11–175) with enterohemorrhagic Escherichia coli-positive HUS requiring dialysis who had seizures (11/11) and/or were in a stupor or coma (10/11) were treated with Eculizumab. Two patients enrolled on the Safety and Efficacy Study of Eculizumab in Shiga-Toxin Producing E coli Hemolytic-Uremic Syndrome (STEC-HUS) each received 6 doses of Eculizumab, 3 patients 2 doses, and 6 patients 1 dose. Laboratory diagnostics of blood samples and magnetic resonance imaging (MRI) were performed as per center practice. Data were analyzed retrospectively. Cranial MRI was abnormal in 8 of 10 patients with findings in the basal ganglia and/or white matter. A 2-year-old boy with severe cardiac involvement and status epilepticus needed repeated cardio-pulmonary resuscitation and extracorporeal membrane oxygenation. He died 8 days after start of Eculizumab treatment. Two patients with hemorrhagic colitis and repeated seizures required artificial ventilation for 6 and 16 days, respectively. At the time of discharge, 1 patient showed severe neurological impairment and 1 mild neurological impairment. The 8 surviving patients experienced no further seizures after the first dose of Eculizumab. Three patients showed mild neurological impairment at discharge, whilst the remaining 5 showed no impairment. The platelets normalized 4 days (median) after the first dose of Eculizumab (range 0–20 days). The mean duration of dialysis after the first dose of Eculizumab was 14.1 ± 6.1 days. In children with typical HUS and CNS involvement early use of Eculizumab appears to improve neurological outcome. In severe HUS cases which progress rapidly with multiple organ involvement, late treatment with Eculizumab seems to show less benefit. We speculate that prophylactic Eculizumab therapy before development of neurological symptoms could be advantageous. |
format | Online Article Text |
id | pubmed-4616562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-46165622015-10-27 Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement Pape, Lars Hartmann, Hans Bange, Franz Christoph Suerbaum, Sebastian Bueltmann, Eva Ahlenstiel-Grunow, Thurid Medicine (Baltimore) 6200 In typical hemolytic uremic syndrome (HUS) approximately 25% of patients show central nervous system (CNS) involvement often leading to serious long-term disabilities. We used the C5-complement inhibitor Eculizumab as rescue therapy. From 2011 to 2014, 11 children (median age 22 months, range 11–175) with enterohemorrhagic Escherichia coli-positive HUS requiring dialysis who had seizures (11/11) and/or were in a stupor or coma (10/11) were treated with Eculizumab. Two patients enrolled on the Safety and Efficacy Study of Eculizumab in Shiga-Toxin Producing E coli Hemolytic-Uremic Syndrome (STEC-HUS) each received 6 doses of Eculizumab, 3 patients 2 doses, and 6 patients 1 dose. Laboratory diagnostics of blood samples and magnetic resonance imaging (MRI) were performed as per center practice. Data were analyzed retrospectively. Cranial MRI was abnormal in 8 of 10 patients with findings in the basal ganglia and/or white matter. A 2-year-old boy with severe cardiac involvement and status epilepticus needed repeated cardio-pulmonary resuscitation and extracorporeal membrane oxygenation. He died 8 days after start of Eculizumab treatment. Two patients with hemorrhagic colitis and repeated seizures required artificial ventilation for 6 and 16 days, respectively. At the time of discharge, 1 patient showed severe neurological impairment and 1 mild neurological impairment. The 8 surviving patients experienced no further seizures after the first dose of Eculizumab. Three patients showed mild neurological impairment at discharge, whilst the remaining 5 showed no impairment. The platelets normalized 4 days (median) after the first dose of Eculizumab (range 0–20 days). The mean duration of dialysis after the first dose of Eculizumab was 14.1 ± 6.1 days. In children with typical HUS and CNS involvement early use of Eculizumab appears to improve neurological outcome. In severe HUS cases which progress rapidly with multiple organ involvement, late treatment with Eculizumab seems to show less benefit. We speculate that prophylactic Eculizumab therapy before development of neurological symptoms could be advantageous. Wolters Kluwer Health 2016-06-19 /pmc/articles/PMC4616562/ /pubmed/26091445 http://dx.doi.org/10.1097/MD.0000000000001000 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 6200 Pape, Lars Hartmann, Hans Bange, Franz Christoph Suerbaum, Sebastian Bueltmann, Eva Ahlenstiel-Grunow, Thurid Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title | Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title_full | Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title_fullStr | Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title_full_unstemmed | Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title_short | Eculizumab in Typical Hemolytic Uremic Syndrome (HUS) With Neurological Involvement |
title_sort | eculizumab in typical hemolytic uremic syndrome (hus) with neurological involvement |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616562/ https://www.ncbi.nlm.nih.gov/pubmed/26091445 http://dx.doi.org/10.1097/MD.0000000000001000 |
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