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Methylprednisolone versus intravenous immunoglobulins in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS): an open-label, multicentre, randomised trial

Methylprednisolone versus intravenous immunoglobulins in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS): an open-label, multicentre, randomised trial
Methylprednisolone versus intravenous immunoglobulins in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS): an open-label, multicentre, randomised trial

Background: the emergence of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) led to the widespread use of anti-inflammatory treatments in the absence of evidence from randomised controlled trials (RCTs). We aimed to assess the effectiveness of intravenous methylprednisolone compared with intravenous immunoglobulins. 

Methods: this is an open-label, multicentre, two-arm RCT done at ten hospitals in Switzerland in children younger than 18 years hospitalised with PIMS-TS (defined as age <18 years; fever and biochemical evidence of inflammation, and single or multiorgan dysfunction; microbiologically proven or putative contact with SARS-CoV-2; and exclusion of any other probable disease). Patients were randomly assigned 1:1 to intravenous methylprednisolone (10 mg/kg per day for 3 days) or intravenous immunoglobulins (2 g/kg as a single dose). The primary outcome was length of hospital stay censored at day 28, death, or discharge. Secondary outcomes included proportion and duration of organ support. Analyses were done by intention-to-treat. The study was registered with Swiss National Clinical Trials Portal (SNCTP000004720) and ClinicalTrials.gov (NCT04826588). 

Findings: between May 21, 2021, and April 15, 2022, 75 patients with a median age of 9·1 years (IQR 6·2–12·2) were included in the intention-to-treat population (37 in the methylprednisolone group and 38 in the intravenous immunoglobulins group). The median length of hospital stay was 6·0 days (IQR 4·0–8·0) in the methylprednisolone group and 6·0 days (IQR 5·0–8·8) in the intravenous immunoglobulins group (estimated effect size –0·037 of the log10 transformed times, 95% CI –0·13 to 0·065, p=0·42). Fewer patients in the methylprednisolone group (ten [27%] of 37) required respiratory support compared with the intravenous immunoglobulin group (21 [55%] of 38, p=0·025). Need and duration of inotropes, admission to intensive care units, cardiac events after baseline, and major bleeding and thrombotic events were not significantly different between the study groups. 

Interpretation: in this RCT, treatment with methylprednisolone in children with PIMS-TS did not significantly affect the length of hospital stay compared with intravenous immunoglobulins. Intravenous methylprednisolone could be an acceptable first-line treatment in children with PIMS-TS. 

Funding: NOMIS Foundation, Vontobel Foundation, and Gaydoul Foundation.

Adolescent, COVID-19, Child, Humans, Immunoglobulins, Intravenous/therapeutic use, Methylprednisolone/therapeutic use, Randomized Controlled Trials as Topic, SARS-CoV-2
2352-4650
238-248
Welzel, Tatjana
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Atkinson, Andrew
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Schöbi, Nina
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Bailey, Douggl G.N.
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Blanchard-Rohner, Geraldine
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Buettcher, Michael
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Grazioli, Serge
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Koehler, Henrik
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Perez, Marie Helene
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Trück, Johannes
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Vanoni, Federica
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Zimmermann, Petra
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Sanchez, Carlos
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Bielicki, Julia A.
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Schlapbach, Luregn J.
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Hammer, Jürg
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Kohns Vasconcelos, Malte
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Mettauer, Nicole
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Meyer, Alexandra
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Trachsel, Daniel
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von Kalckreuth, Clemens
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Woerner, Andreas
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Zutter, Andreas
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Kottanattu, Lisa
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Mazzara, Calogero
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Severi Conti, Alessia
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Aebi, Christoph
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Glöckler, Martin
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Pallivathukal, Sabine
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Riedel, Thomas
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Cudré-Cung, Hong Phuc
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Pavlovic, Mladen
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Bordessoule, Alice
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L'Huillier, Arnaud G.
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Martin, Anne Laure
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Polito, Angelo
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Rohr, Marie
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Rodriguez, Maria Isabel
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Faust, Saul N.
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Swissped RECOVERY Trial Group
Welzel, Tatjana
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Atkinson, Andrew
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Schöbi, Nina
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Andre, Maya C.
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Bailey, Douggl G.N.
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Blanchard-Rohner, Geraldine
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Buettcher, Michael
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Grazioli, Serge
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Koehler, Henrik
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Perez, Marie Helene
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Trück, Johannes
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Vanoni, Federica
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Zimmermann, Petra
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Sanchez, Carlos
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Bielicki, Julia A.
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Schlapbach, Luregn J.
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Donner, Birgit
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Hammer, Jürg
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Heininger, Ulrich
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Kohns Vasconcelos, Malte
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Mettauer, Nicole
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Schlaeppi, Chloé
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Trachsel, Daniel
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Vaezipour, Nina
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von Kalckreuth, Clemens
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Woerner, Andreas
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Zutter, Andreas
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Kottanattu, Lisa
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Mazzara, Calogero
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Severi Conti, Alessia
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Aebi, Christoph
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Duppenthaler, Andrea
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Glöckler, Martin
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Pallivathukal, Sabine
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Riedel, Thomas
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Cudré-Cung, Hong Phuc
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Pavlovic, Mladen
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Bordessoule, Alice
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L'Huillier, Arnaud G.
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Martin, Anne Laure
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Polito, Angelo
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Rohr, Marie
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Rodriguez, Maria Isabel
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Faust, Saul N.
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Welzel, Tatjana, Atkinson, Andrew, Schöbi, Nina, Andre, Maya C., Bailey, Douggl G.N. and Blanchard-Rohner, Geraldine , Swissped RECOVERY Trial Group (2023) Methylprednisolone versus intravenous immunoglobulins in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS): an open-label, multicentre, randomised trial. The Lancet Child and Adolescent Health, 7 (4), 238-248. (doi:10.1016/S2352-4642(23)00020-2).

Record type: Article

Abstract

Background: the emergence of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) led to the widespread use of anti-inflammatory treatments in the absence of evidence from randomised controlled trials (RCTs). We aimed to assess the effectiveness of intravenous methylprednisolone compared with intravenous immunoglobulins. 

Methods: this is an open-label, multicentre, two-arm RCT done at ten hospitals in Switzerland in children younger than 18 years hospitalised with PIMS-TS (defined as age <18 years; fever and biochemical evidence of inflammation, and single or multiorgan dysfunction; microbiologically proven or putative contact with SARS-CoV-2; and exclusion of any other probable disease). Patients were randomly assigned 1:1 to intravenous methylprednisolone (10 mg/kg per day for 3 days) or intravenous immunoglobulins (2 g/kg as a single dose). The primary outcome was length of hospital stay censored at day 28, death, or discharge. Secondary outcomes included proportion and duration of organ support. Analyses were done by intention-to-treat. The study was registered with Swiss National Clinical Trials Portal (SNCTP000004720) and ClinicalTrials.gov (NCT04826588). 

Findings: between May 21, 2021, and April 15, 2022, 75 patients with a median age of 9·1 years (IQR 6·2–12·2) were included in the intention-to-treat population (37 in the methylprednisolone group and 38 in the intravenous immunoglobulins group). The median length of hospital stay was 6·0 days (IQR 4·0–8·0) in the methylprednisolone group and 6·0 days (IQR 5·0–8·8) in the intravenous immunoglobulins group (estimated effect size –0·037 of the log10 transformed times, 95% CI –0·13 to 0·065, p=0·42). Fewer patients in the methylprednisolone group (ten [27%] of 37) required respiratory support compared with the intravenous immunoglobulin group (21 [55%] of 38, p=0·025). Need and duration of inotropes, admission to intensive care units, cardiac events after baseline, and major bleeding and thrombotic events were not significantly different between the study groups. 

Interpretation: in this RCT, treatment with methylprednisolone in children with PIMS-TS did not significantly affect the length of hospital stay compared with intravenous immunoglobulins. Intravenous methylprednisolone could be an acceptable first-line treatment in children with PIMS-TS. 

Funding: NOMIS Foundation, Vontobel Foundation, and Gaydoul Foundation.

This record has no associated files available for download.

More information

e-pub ahead of print date: 3 February 2023
Published date: 20 March 2023
Additional Information: Funding Information: The study design originated from the publicly available UK RECOVERY trial protocol, which was conceived by lead investigators Martin Landray and Peter Horby (University of Oxford). We want to thank the parents and patients for participating in the Swissped RECOVERY trial. Furthermore, we thank all study team members involved in patient care and recruitment, SwissPedNet for the support of recruitments and study conduct at all sites, and Regina Santoro for the central data monitoring. In addition, we thank Thomas Jaki (Faculty of Informatics and Data Science, University Regensburg, Germany) for discussion around the Bayesian approach. We thank Michelle Clements (MRC Clinical Trials Unit, UCL, London, UK), Carlo Giaquinto (Department of Mother and Child Health, University of Padova, Padova, Italy), and Robin Kobbe (University Medical Centre Hamburg-Eppendorf, Institute for Infection Research and Vaccine Development, and Bernhard Nocht Institute for Tropical Medicine, Infectious Disease Epidemiology, Hamburg, Germany) for the independent data monitoring and agreeing to be part of the independent data monitoring committee. Furthermore, we thank Alasdair Bamford (Department of Pediatric Infectious Diseases, Great Ormond Street Hospital for Children NHS Foundation Trust, MRC Clinical Trials Unit at UCL, and UCL Great Ormond Street Institute of Child Health, London, UK), Pablo Rojo Conejo (Pediatric Infectious Disease Unit, Fundación para la Investigación Biomédica del Hospital 12 de Octubre, Madrid, Spain), Adriana H Tremoulet (University of California San Diego and the Rady Children's Hospital, San Diego, California, USA), and Kate Webb (Red Cross War Memorial Children's Hospital, University of Cape Town, and Francis Crick Institute, Cape Town, South Africa), for the independent endpoint evaluation and agreeing to be part of the blinded Endpoint Review Committee. Publisher Copyright: © 2023 Elsevier Ltd
Keywords: Adolescent, COVID-19, Child, Humans, Immunoglobulins, Intravenous/therapeutic use, Methylprednisolone/therapeutic use, Randomized Controlled Trials as Topic, SARS-CoV-2

Identifiers

Local EPrints ID: 477455
URI: http://eprints.soton.ac.uk/id/eprint/477455
ISSN: 2352-4650
PURE UUID: 4c50b6da-e915-4139-a07d-8d6aaea41f43
ORCID for Saul N. Faust: ORCID iD orcid.org/0000-0003-3410-7642

Catalogue record

Date deposited: 06 Jun 2023 17:07
Last modified: 18 Mar 2024 03:04

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Contributors

Author: Tatjana Welzel
Author: Andrew Atkinson
Author: Nina Schöbi
Author: Maya C. Andre
Author: Douggl G.N. Bailey
Author: Geraldine Blanchard-Rohner
Author: Michael Buettcher
Author: Serge Grazioli
Author: Henrik Koehler
Author: Marie Helene Perez
Author: Johannes Trück
Author: Federica Vanoni
Author: Petra Zimmermann
Author: Carlos Sanchez
Author: Julia A. Bielicki
Author: Luregn J. Schlapbach
Author: Andreas Bieri
Author: Spyridoula Gysi
Author: Indra Janz
Author: Birgit Donner
Author: Jürg Hammer
Author: Ulrich Heininger
Author: Malte Kohns Vasconcelos
Author: Nicole Mettauer
Author: Alexandra Meyer
Author: Diana Reppucci
Author: Chloé Schlaeppi
Author: Daniel Trachsel
Author: Nina Vaezipour
Author: Clemens von Kalckreuth
Author: Andreas Woerner
Author: Andreas Zutter
Author: Lisa Kottanattu
Author: Calogero Mazzara
Author: Alessia Severi Conti
Author: Christoph Aebi
Author: Philipp K.A. Agyeman
Author: Andrea Duppenthaler
Author: Martin Glöckler
Author: Sabine Pallivathukal
Author: Thomas Riedel
Author: Hong Phuc Cudré-Cung
Author: Mladen Pavlovic
Author: Alice Bordessoule
Author: Arnaud G. L'Huillier
Author: Anne Laure Martin
Author: Angelo Polito
Author: Marie Rohr
Author: Maria Isabel Rodriguez
Author: Saul N. Faust ORCID iD
Corporate Author: Swissped RECOVERY Trial Group

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