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ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give?
BACKGROUND: Immune thrombocytopenia (ITP) is an autoimmune disease associated with isolated thrombocytopenia, which is caused by an imbalance between platelet production and platelet destruction. Petechial and mucous membrane hemorrhages are characteristic of ITP, but life-threatening bleeding rarel...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419130/ https://www.ncbi.nlm.nih.gov/pubmed/34486084 http://dx.doi.org/10.1186/s40348-021-00121-z |
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author | von Lukowicz, Hannah Schlegel, Paul-Gerhardt Härtel, Christoph Morbach, Henner Haubitz, Imme Wiegering, Verena |
author_facet | von Lukowicz, Hannah Schlegel, Paul-Gerhardt Härtel, Christoph Morbach, Henner Haubitz, Imme Wiegering, Verena |
author_sort | von Lukowicz, Hannah |
collection | PubMed |
description | BACKGROUND: Immune thrombocytopenia (ITP) is an autoimmune disease associated with isolated thrombocytopenia, which is caused by an imbalance between platelet production and platelet destruction. Petechial and mucous membrane hemorrhages are characteristic of ITP, but life-threatening bleeding rarely occurs. Depending on the bleeding symptoms, ITP can be treated with glucocorticoids (GC), intravenous immunoglobulins (IVIG), or in severe cases, platelet transfusions. Mild bleeding does not necessarily require therapy. Using the German Surveillance Unit for rare Pediatric Diseases (ESPED) we conducted a prospective survey on ITP patients in all German Children's Hospitals between September 2018 and August 2019. We collected data on ITP, including the clinical course, therapy implementation recommendations (according to the Association of German Scientific Medical Societies guidelines), outcome, and influence of treatment regimens depending on the treating physician´s experience with ITP patients. RESULTS: Of the 287 recorded cases of children with ITP, 268 questionnaires were sent to the authors. Two hundred seventeen of the questionnaires fulfilled the inclusion criteria. ITP affected boys and girls similarly, and the median age of manifestation was 3.5 years. The main reasons for hospitalization were thrombocytopenia, bleeding signs, hematomas, and/or petechiae. Bleeding scores were ≤ 3 in 96% of children, which corresponded to a low-to-moderately low risk of bleeding. No life-threatening bleeding was documented. The most common therapies were IVIG (n = 59), GC (n = 33), or a combination of these (n = 17). Blood products (i.e., red blood cells, platelet concentrate, and fresh frozen plasma) were given to 13 patients. Compared to the established guidelines, 67 patients were over-treated, and 2 patients were under-treated. CONCLUSIONS: Adherence to German ITP treatment guidelines is currently limited. To improve patient safety and medical care, better medical training and dissemination of the guidelines are required in line with targeted analyses of patients with serious bleeding events to identify potential risk constellations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40348-021-00121-z. |
format | Online Article Text |
id | pubmed-8419130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-84191302021-09-22 ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? von Lukowicz, Hannah Schlegel, Paul-Gerhardt Härtel, Christoph Morbach, Henner Haubitz, Imme Wiegering, Verena Mol Cell Pediatr Research BACKGROUND: Immune thrombocytopenia (ITP) is an autoimmune disease associated with isolated thrombocytopenia, which is caused by an imbalance between platelet production and platelet destruction. Petechial and mucous membrane hemorrhages are characteristic of ITP, but life-threatening bleeding rarely occurs. Depending on the bleeding symptoms, ITP can be treated with glucocorticoids (GC), intravenous immunoglobulins (IVIG), or in severe cases, platelet transfusions. Mild bleeding does not necessarily require therapy. Using the German Surveillance Unit for rare Pediatric Diseases (ESPED) we conducted a prospective survey on ITP patients in all German Children's Hospitals between September 2018 and August 2019. We collected data on ITP, including the clinical course, therapy implementation recommendations (according to the Association of German Scientific Medical Societies guidelines), outcome, and influence of treatment regimens depending on the treating physician´s experience with ITP patients. RESULTS: Of the 287 recorded cases of children with ITP, 268 questionnaires were sent to the authors. Two hundred seventeen of the questionnaires fulfilled the inclusion criteria. ITP affected boys and girls similarly, and the median age of manifestation was 3.5 years. The main reasons for hospitalization were thrombocytopenia, bleeding signs, hematomas, and/or petechiae. Bleeding scores were ≤ 3 in 96% of children, which corresponded to a low-to-moderately low risk of bleeding. No life-threatening bleeding was documented. The most common therapies were IVIG (n = 59), GC (n = 33), or a combination of these (n = 17). Blood products (i.e., red blood cells, platelet concentrate, and fresh frozen plasma) were given to 13 patients. Compared to the established guidelines, 67 patients were over-treated, and 2 patients were under-treated. CONCLUSIONS: Adherence to German ITP treatment guidelines is currently limited. To improve patient safety and medical care, better medical training and dissemination of the guidelines are required in line with targeted analyses of patients with serious bleeding events to identify potential risk constellations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40348-021-00121-z. Springer Berlin Heidelberg 2021-09-05 /pmc/articles/PMC8419130/ /pubmed/34486084 http://dx.doi.org/10.1186/s40348-021-00121-z Text en © The Author(s) 2021 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/) . |
spellingShingle | Research von Lukowicz, Hannah Schlegel, Paul-Gerhardt Härtel, Christoph Morbach, Henner Haubitz, Imme Wiegering, Verena ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title | ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title_full | ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title_fullStr | ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title_full_unstemmed | ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title_short | ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
title_sort | esped survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419130/ https://www.ncbi.nlm.nih.gov/pubmed/34486084 http://dx.doi.org/10.1186/s40348-021-00121-z |
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