Evidence map›Paper›PMID 32956615›Full record

ReviewThe Lancet. Child & adolescent health2021

A national consensus management pathway for paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS): results of a national Delphi process.

Rachel Harwood, Benjamin Allin, Christine E Jones, Elizabeth Whittaker, Padmanabhan Ramnarayan, Athimalaipet V Ramanan, Musa Kaleem, Robert Tulloh, Mark J Peters, Sarah Almond and 7 more

Erratum issued Registry-linked trialOpen access · bronzeAbstract readReviewConsensus Statement
In one paragraph

Review in The Lancet. Child & adolescent health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05560906 (Study of Virus-specific Lymphocytic Cell Populations in Non-invasive Nasal Mucosa Samples of MIS-C Patients, and Intra-population Shifts in Inflammatory Tissues in the Acute Phase of MIS-C and in Health), which is not on this map. Cited by 170 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed, 9 pooled it
55.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05560906 unknown statusnot on this map

Study of Virus-specific Lymphocytic Cell Populations in Non-invasive Nasal Mucosa Samples of MIS-C Patients, and Intra-population Shifts in Inflammatory Tissues in the Acute Phase of MIS-C and in Health

Typeobservational_patient_registrySponsorMedical University of WarsawRan2021 to 2022Enrolled20ConditionsMIS-C Associated With COVID-19, COVID-19
3 · Its place in the literature

Who cites it

170 citing papers in PubMed, 9 syntheses or guidelines pooled it, 327 citations in OpenAlex.

  1. Pooled it
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  17. MIS-C: Diagnosis, Management, and Outcomes.Open forum infectious diseases · 2026
    Review
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110 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 11 institutions in 1 country.

Rachel HarwoodDepartment of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK. Electronic address: Rachel.Harwood@liverpool.ac.uk.
Benjamin AllinNational Perinatal Epidemiology Unit, Nuffield Department of Health, University of Oxford, Oxford, UK; Department of Paediatric Surgery, Ozxford Children's Hospital, Oxford, UK.
Christine E JonesNIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton Foundation NHS Trust and Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, UK.
Elizabeth WhittakerDepartment of Paediatrics, Imperial College Healthcare NHS Trust, London, UK; Section of Paediatric Infectious Disease, Department of Infectious Disease, Imperial College London, London, UK.
Padmanabhan RamnarayanChildren's Acute Transport Service, Great Ormond Street Hospital for Children, London, UK.
Athimalaipet V RamananDepartment of Paediatric Rheumatology, Bristol Royal Hospital for Children, Bristol, UK; Royal National Hospital for Rheumatic Diseases, Bath, UK; University of Bristol, Bristol, UK.
Musa KaleemDepartment of Paediatric Radiology, Alder Hey Children's Hospital, Liverpool, UK.
Robert TullohDepartment of Paediatric Cardiology, Bristol Royal Hospital for Children, Bristol, UK; University of Bristol, Bristol, UK.
Mark J PetersUniversity College London Great Ormond Street Institute of Child Health and Great Ormond Street Hospital NHS Trust, NIHR Biomedical Research Centre, London, UK.
Sarah AlmondDepartment of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK.
Peter J DavisPaediatric Intensive Care Unit, Bristol Royal Hospital for Children, Bristol, UK.
Michael LevinDepartment of Paediatrics, Imperial College Healthcare NHS Trust, London, UK; Section of Paediatric Infectious Disease, Department of Infectious Disease, Imperial College London, London, UK.
Andrew TometzkiDepartment of Paediatric Cardiology, Bristol Royal Hospital for Children, Bristol, UK.
Saul N FaustNIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton Foundation NHS Trust and Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, UK.
Marian KnightNational Perinatal Epidemiology Unit, Nuffield Department of Health, University of Oxford, Oxford, UK.
Simon KennyDepartment of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK; NHS England/Improvement, Redditch, UK.
PIMS-TS National Consensus Management Study Group
Bristol Royal Hospital for Children · GBAlder Hey Children's Hospital · GBUniversity of Liverpool · GBUniversity of Oxford · GBGreat Ormond Street Hospital · GBImperial College Healthcare NHS Trust · GBImperial College London · GBNHS EnglandNIHR Southampton Biomedical Research Centre · GBUniversity of Bristol · GBUniversity of Southampton · GB

Funding

Department of Health CS-2015-15-016
6 · The paper itself

Abstract

Paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS) is a novel condition that was first reported in April, 2020. We aimed to develop a national consensus management pathway for the UK to provide guidance for clinicians caring for children with PIMS-TS. A three-phase online Delphi process and virtual consensus meeting sought consensus over the investigation, management, and research priorities from multidisciplinary clinicians caring for children with PIMS-TS. We used 140 consensus statements to derive a consensus management pathway that describes the initial investigation of children with suspected PIMS-TS, including blood markers to help determine the severity of disease, an echocardiogram, and a viral and septic screen to exclude other infectious causes of illness. The importance of a multidisciplinary team in decision making for children with PIMS-TS is highlighted throughout the guidance, along with the recommended treatment options, including supportive care, intravenous immunoglobulin, methylprednisolone, and biological therapies. These include IL-1 antagonists (eg, anakinra), IL-6 receptor blockers (eg, tocilizumab), and anti-TNF agents (eg, infliximab) for children with Kawasaki disease-like phenotype and non-specific presentations. Use of a rapid online Delphi process has made it possible to generate a national consensus pathway in a timely and cost-efficient manner in the middle of a global pandemic. The consensus statements represent the views of UK clinicians and are applicable to children in the UK suspected of having PIMS-TS. Future evidence will inform updates to this guidance, which in the interim provides a solid framework to support clinicians caring for children with PIMS-TS. This process has directly informed new PIMS-TS specific treatment groups as part of the adaptive UK RECOVERY trial protocol, which is the first formal randomised controlled trial of therapies for PIMS-TS globally.

Indexed as

COVID-19Critical PathwaysDisease ManagementSystemic Inflammatory Response SyndromeChildHumansInterdisciplinary CommunicationUnited Kingdom

Identifiers

PMID32956615
PMCPMC7500943
OpenAlexW3087378474

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.