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„Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik

BACKGROUND: Since the beginning of the SARS-CoV‑2 pandemic, cases of the hyperinflammatory syndrome pediatric inflammatory multisystem syndrome (PIMS) have been accumulating. The clinical presentation is variable and it occurs 2–6 weeks after infection with SARS-CoV‑2. As of today, immunoglobulins a...

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Autores principales: Boeckelmann, Moritz, Glaser, Nicola, Dejas, F., Östreicher, I., Grüner, J., Höche, A., Akanbi, S., Thiemig, D., Rossi, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773388/
https://www.ncbi.nlm.nih.gov/pubmed/35079175
http://dx.doi.org/10.1007/s00112-021-01394-4
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author Boeckelmann, Moritz
Glaser, Nicola
Dejas, F.
Östreicher, I.
Grüner, J.
Höche, A.
Akanbi, S.
Thiemig, D.
Rossi, R.
author_facet Boeckelmann, Moritz
Glaser, Nicola
Dejas, F.
Östreicher, I.
Grüner, J.
Höche, A.
Akanbi, S.
Thiemig, D.
Rossi, R.
author_sort Boeckelmann, Moritz
collection PubMed
description BACKGROUND: Since the beginning of the SARS-CoV‑2 pandemic, cases of the hyperinflammatory syndrome pediatric inflammatory multisystem syndrome (PIMS) have been accumulating. The clinical presentation is variable and it occurs 2–6 weeks after infection with SARS-CoV‑2. As of today, immunoglobulins and/or steroids as well as ASS are used for medication. METHOD: In our clinic 11 patients presented with PIMS between 06/2020 and 06/2021, whose data were retrospectively collected and analyzed. RESULTS: Of the 11 patients 6 were male, the age distribution ranged from 4–18 years and 7 were overweight or obese. Almost all patients showed gastrointestinal and cardiovascular involvement, 4 had respiratory symptoms, 6 showed signs of nephritis. All showed blood count changes with anemia or leukocytosis and coagulopathy. CRP, ferritin, and soluble IL2 receptor were highly elevated in all patients. Only 2 patients had neither troponin‑T nor NT-pro-BNP elevation and 7 patients had impaired left ventricular function. Positive SARS-CoV‑2 serology was found in 10, and positive SARS-CoV‑2 PCR via nasopharyngeal swabs in 2. All were initially treated with antibiotics, 3 patients required O(2) supplementation, 6 required intensive care and 5 required vasoactive agents. All but one patient received immunoglobulins and ASS, 5 received prednisolone. Length of stay ranged from 4–51 days. CONCLUSION: PIMS is a severe acute hyperinflammatory disease, which was secured in 11 patients in our clinic. In some cases, there was a need for intensive care. Under anti-inflammatory therapy there was a good response without exception.
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spelling pubmed-87733882022-01-21 „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik Boeckelmann, Moritz Glaser, Nicola Dejas, F. Östreicher, I. Grüner, J. Höche, A. Akanbi, S. Thiemig, D. Rossi, R. Monatsschr Kinderheilkd Originalien BACKGROUND: Since the beginning of the SARS-CoV‑2 pandemic, cases of the hyperinflammatory syndrome pediatric inflammatory multisystem syndrome (PIMS) have been accumulating. The clinical presentation is variable and it occurs 2–6 weeks after infection with SARS-CoV‑2. As of today, immunoglobulins and/or steroids as well as ASS are used for medication. METHOD: In our clinic 11 patients presented with PIMS between 06/2020 and 06/2021, whose data were retrospectively collected and analyzed. RESULTS: Of the 11 patients 6 were male, the age distribution ranged from 4–18 years and 7 were overweight or obese. Almost all patients showed gastrointestinal and cardiovascular involvement, 4 had respiratory symptoms, 6 showed signs of nephritis. All showed blood count changes with anemia or leukocytosis and coagulopathy. CRP, ferritin, and soluble IL2 receptor were highly elevated in all patients. Only 2 patients had neither troponin‑T nor NT-pro-BNP elevation and 7 patients had impaired left ventricular function. Positive SARS-CoV‑2 serology was found in 10, and positive SARS-CoV‑2 PCR via nasopharyngeal swabs in 2. All were initially treated with antibiotics, 3 patients required O(2) supplementation, 6 required intensive care and 5 required vasoactive agents. All but one patient received immunoglobulins and ASS, 5 received prednisolone. Length of stay ranged from 4–51 days. CONCLUSION: PIMS is a severe acute hyperinflammatory disease, which was secured in 11 patients in our clinic. In some cases, there was a need for intensive care. Under anti-inflammatory therapy there was a good response without exception. Springer Medizin 2022-01-20 2022 /pmc/articles/PMC8773388/ /pubmed/35079175 http://dx.doi.org/10.1007/s00112-021-01394-4 Text en © The Author(s), under exclusive licence to Springer Medizin Verlag GmbH, ein Teil von Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Originalien
Boeckelmann, Moritz
Glaser, Nicola
Dejas, F.
Östreicher, I.
Grüner, J.
Höche, A.
Akanbi, S.
Thiemig, D.
Rossi, R.
„Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title_full „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title_fullStr „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title_full_unstemmed „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title_short „Pediatric inflammatory multisystem syndrome“ – Erfahrungen aus einer Berliner Kinderklinik
title_sort „pediatric inflammatory multisystem syndrome“ – erfahrungen aus einer berliner kinderklinik
topic Originalien
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773388/
https://www.ncbi.nlm.nih.gov/pubmed/35079175
http://dx.doi.org/10.1007/s00112-021-01394-4
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