Skip to main content
Top
Published in: Molecular and Cellular Pediatrics 1/2021

Open Access 01-12-2021 | Petechiae | Research

ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give?

Authors: Hannah von Lukowicz, Paul-Gerhardt Schlegel, Christoph Härtel, Henner Morbach, Imme Haubitz, Verena Wiegering

Published in: Molecular and Cellular Pediatrics | Issue 1/2021

Login to get access

Abstract

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.
Appendix
Available only for authorised users
Literature
6.
go back to reference Schoettler ML, Graham D, Tao W, Stack M, Shu E, Kerr L, Neufeld EJ, Grace RF (2017) Increasing observation rates in low risk pediatric immune thrombocytopenia using a Standardized Clinical Assessment and Management Plan (SCAMP®). Pediatr Blood Cancer. 64(5):e26303 https://doi.org/10.1002/pbc.26303CrossRef Schoettler ML, Graham D, Tao W, Stack M, Shu E, Kerr L, Neufeld EJ, Grace RF (2017) Increasing observation rates in low risk pediatric immune thrombocytopenia using a Standardized Clinical Assessment and Management Plan (SCAMP®). Pediatr Blood Cancer. 64(5):e26303 https://​doi.​org/​10.​1002/​pbc.​26303CrossRef
8.
go back to reference Kühne T, Imbach P, Bolton-Maggs PH, Berchtold W, Blanchette V, Buchanan GR (2001) Newly diagnosed idiopathic thrombocytopenic purpura in childhood: an observational study. Lancet 358:2122–2125CrossRef Kühne T, Imbach P, Bolton-Maggs PH, Berchtold W, Blanchette V, Buchanan GR (2001) Newly diagnosed idiopathic thrombocytopenic purpura in childhood: an observational study. Lancet 358:2122–2125CrossRef
13.
go back to reference British Committee for Standards in Haematology General Haematology Task Force (2003) Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. Br J Haematol 120:574–596CrossRef British Committee for Standards in Haematology General Haematology Task Force (2003) Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. Br J Haematol 120:574–596CrossRef
16.
go back to reference Friedman JN, Beck CE (2019) Diagnosis and management of typical, newly diagnosed primary immune thrombocytopenia (ITP) of childhood. Paediatr Child Health 24:54CrossRef Friedman JN, Beck CE (2019) Diagnosis and management of typical, newly diagnosed primary immune thrombocytopenia (ITP) of childhood. Paediatr Child Health 24:54CrossRef
17.
go back to reference Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, Chong BH, Cines DB, Gernsheimer TB, Godeau B, Grainger J, Greer I, Hunt BJ, Imbach PA, Lyons G, McMillan R, Rodeghiero F, Sanz MA, Tarantino M, Watson S, Young J, Kuter DJ (2010) International consensus report on the investigation and management of primary immune thrombocytopenia. Blood 115(2):168–186. https://doi.org/10.1182/blood-2009-06-225565CrossRefPubMed Provan D, Stasi R, Newland AC, Blanchette VS, Bolton-Maggs P, Bussel JB, Chong BH, Cines DB, Gernsheimer TB, Godeau B, Grainger J, Greer I, Hunt BJ, Imbach PA, Lyons G, McMillan R, Rodeghiero F, Sanz MA, Tarantino M, Watson S, Young J, Kuter DJ (2010) International consensus report on the investigation and management of primary immune thrombocytopenia. Blood 115(2):168–186. https://​doi.​org/​10.​1182/​blood-2009-06-225565CrossRefPubMed
19.
go back to reference Heitink-Pollé KMJ, Uiterwaal CSPM, Porcelijn L, Tamminga RYJ, Smiers FJ, van Woerden N, Wesseling J, Vidarsson G, Laarhoven AG, de Haas M, Bruin MCA, TIKI Investigators (2018) Intravenous immunoglobulin vs observation in childhood immune thrombocytopenia: a randomized controlled trial. Blood 132(9):883–891. https://doi.org/10.1182/blood-2018-02-830844CrossRefPubMed Heitink-Pollé KMJ, Uiterwaal CSPM, Porcelijn L, Tamminga RYJ, Smiers FJ, van Woerden N, Wesseling J, Vidarsson G, Laarhoven AG, de Haas M, Bruin MCA, TIKI Investigators (2018) Intravenous immunoglobulin vs observation in childhood immune thrombocytopenia: a randomized controlled trial. Blood 132(9):883–891. https://​doi.​org/​10.​1182/​blood-2018-02-830844CrossRefPubMed
Metadata
Title
ESPED survey on newly diagnosed immune thrombocytopenia in childhood: how much treatment do we give?
Authors
Hannah von Lukowicz
Paul-Gerhardt Schlegel
Christoph Härtel
Henner Morbach
Imme Haubitz
Verena Wiegering
Publication date
01-12-2021
Publisher
Springer Berlin Heidelberg
Published in
Molecular and Cellular Pediatrics / Issue 1/2021
Electronic ISSN: 2194-7791
DOI
https://doi.org/10.1186/s40348-021-00121-z

Other articles of this Issue 1/2021

Molecular and Cellular Pediatrics 1/2021 Go to the issue