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Multicenter Randomized Trial of Methylprednisolone vs. Intravenous Immunoglobulins to Treat the Pediatric Inflammatory Multisystem Syndrome-Temporally Associated With SARS-CoV-2 (PIMS-TS): Protocol of the Swissped RECOVERY Trial.

Welzel, T; Schöbi, N; André, MC; Bailey, DGN; Blanchard-Rohner, G; Buettcher, M; Grazioli, S; Koehler, H; Perez, M-H; Trück, J; et al. Welzel, T; Schöbi, N; André, MC; Bailey, DGN; Blanchard-Rohner, G; Buettcher, M; Grazioli, S; Koehler, H; Perez, M-H; Trück, J; Vanoni, F; Zimmermann, P; Atkinson, A; Sanchez, C; Whittaker, E; Faust, SN; Bielicki, JA; Schlapbach, LJ; Swissped Recovery Trial (2022) Multicenter Randomized Trial of Methylprednisolone vs. Intravenous Immunoglobulins to Treat the Pediatric Inflammatory Multisystem Syndrome-Temporally Associated With SARS-CoV-2 (PIMS-TS): Protocol of the Swissped RECOVERY Trial. Front Pediatr, 10. p. 905046. ISSN 2296-2360 https://doi.org/10.3389/fped.2022.905046
SGUL Authors: Bielicki, Julia Anna

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Abstract

Introduction: In 2020, a new disease entitled Pediatric Inflammatory Multisystem Syndrome temporally associated with COVID-19 (PIMS-TS), or Multisystem Inflammatory Syndrome in Children (MIS-C), emerged, with thousands of children affected globally. There is no available evidence based on randomized controlled trials (RCT) to date on the two most commonly used immunomodulatory treatments, intravenous immunoglobulins (IVIG) and corticosteroids. Therefore, the Swissped RECOVERY trial was conducted to assess whether intravenous (IV) methylprednisolone shortens hospital length of stay compared with IVIG. Methods and Analysis: Swissped RECOVERY is an ongoing investigator-initiated, open-label, multicenter two-arm RCT in children and adolescents <18 years hospitalized with a diagnosis of PIMS-TS. The trial is recruiting at 10 sites across Switzerland. Patients diagnosed with PIMS-TS are randomized 1:1 to methylprednisolone IV (10 mg/kg/day for 3 days) or IVIG (2 g/kg as a single dose). The primary outcome is hospital length of stay censored at day 28, death, or discharge (whichever is first). The target total sample size is ~80 patients 1:1 randomized to each study arm. Ancillary and exploratory studies on inflammation, vaccination acceptance and coverage, long-term outcomes, and healthcare costs are pre-planned. Significance: Currently, robust trial evidence for the treatment of PIMS-TS is lacking, with a controversy surrounding the use of corticosteroids vs. IVIG. This trial will provide evidence for the effectiveness and safety of these two treatments. Ethics and Dissemination: The study protocol, which was designed based on the U.K. RECOVERY trial, the patient information and consent forms, and other study-specific study documents were approved by the local ethics committees (Project ID: 2021-00362). Registration Details: The study is registered on the Swiss National Clinical Trials Portal (SNCTP000004720) and Clinicaltrials.gov (NCT04826588).

Item Type: Article
Additional Information: Copyright © 2022 Welzel, Schöbi, André, Bailey, Blanchard-Rohner, Buettcher, Grazioli, Koehler, Perez, Trück, Vanoni, Zimmermann, Atkinson, Sanchez, Whittaker, Faust, Bielicki, Schlapbach and the Swissped Recovery Trial. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Keywords: COVID-19, MIS-C, SARS-CoV-2, children, mortality, quality of life, treatment, trial, Swissped Recovery Trial
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Front Pediatr
ISSN: 2296-2360
Language: eng
Dates:
DateEvent
20 May 2022Published
18 April 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
PubMed ID: 35669398
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114417
Publisher's version: https://doi.org/10.3389/fped.2022.905046

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