Evidence map›Paper›PMID 36703139›Full record

ArticleTrials2023

Multi-centre, randomised, open-label, blinded endpoint assessed, trial of corticosteroids plus intravenous immunoglobulin (IVIG) and aspirin, versus IVIG and aspirin for prevention of coronary artery aneurysms (CAA) in Kawasaki disease (KD): the KD CAA prevention (KD-CAAP) trial protocol.

Despina Eleftheriou, Yolanda Collaco Moraes, Cara Purvis, Molly Pursell, Marta Merida Morillas, Robin Kahn, Maria Mossberg, Filip Kucera, Robert Tulloh, Joseph F Standing and 9 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.5field-weighted citation impact, top 8% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 3 countries.

Despina EleftheriouUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK. d.eleftheriou@ucl.ac.uk.ORCID http://orcid.org/0000-0002-5312-2269
Yolanda Collaco MoraesMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Cara PurvisMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Molly PursellMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Marta Merida MorillasMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Robin KahnDepartment of Paediatrics, Lund University, Clinical Sciences, Lund, Sweden.
Maria MossbergDepartment of Paediatrics, Lund University, Clinical Sciences, Lund, Sweden.
Filip KuceraGreat Ormond Street Hospital, London, UK.
Robert TullohBristol Heart Institute, Bristol, UK.
Joseph F StandingUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Veronica SwallowSheffield Hallam University, Sheffield, UK.
Rachael McCormackSocieti Foundation CIO, The UK Foundation for Kawasaki Disease, Newark, UK.
Jethro HerbergSection of Paediatric Infectious Diseases, Imperial College London, London, UK.
Michael LevinSection of Paediatric Infectious Diseases, Imperial College London, London, UK.
Mandy WanPharmacy Department, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Nigel KleinUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
Roisin ConnonMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Ann Sarah WalkerMedical Research Council (MRC) Clinical Trials Unit (CTU) at University College London (UCL), London, UK.
Paul BroganUCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK.
MRC Clinical Trials Unit at UCL · GBGreat Ormond Street Hospital · GBImperial College London · GBLund University · SEKing's College London · GBNIHR Bristol Cardiovascular Biomedical Research Unit · GBSheffield Hallam University · GB

Funding

Medical Research Council MC_UU_00004/05Medical Research Council MR/M008665/1Versus Arthritis 21791
6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is an acute self-limiting inflammatory vasculitis affecting predominantly medium-sized arteries, particularly the coronary arteries. A number of recent studies conducted in different European countries have demonstrated alarmingly high coronary complications despite treatment with intravenous immunoglobulin (IVIG). These high complication rates now emphasize the need for an urgent reappraisal of IVIG as the sole primary therapeutic agent for KD. The Kawasaki disease CAA prevention (KD-CAAP) trial will test the hypothesis that immediate adjunctive corticosteroid treatment to standard of care IVIG and aspirin will reduce coronary artery aneurysm (CAA) rates in unselected KD patients across Europe.

methodsKD-CAAP is a multicentre, randomised, controlled, open-label, blinded endpoint assessed trial that will be conducted across Europe supported by the conect4children pan-European clinical trials network. Patients with KD who satisfy the eligibility criteria will be randomised (1:1) to receive either oral prednisolone 2 mg/kg/day plus standard of care therapy IVIG (2 g/kg) and aspirin (40 mg/kg/day); or IVIG and aspirin alone. Further management is dictated by temperature and C-reactive protein (CRP) responses. Co-primary outcomes are as follows: (i) any CAA within the 3 months of trial follow-up; (ii) average estimate of maximum coronary Z-score at weeks 1, 2 and 6 adjusting for rescue treatment. Additional outcomes will be assessed including cost effectiveness, quality of life, corticosteroid toxicity and other safety outcomes. DISCUSSION: Several recent studies have indicated that coronary complications associated with KD across Europe are much higher than early trials of IVIG had initially suggested. KD-CAAP directly addresses this issue by exploring the therapeutic benefit of adjunctive corticosteroids in unselected KD cases. If we find that corticosteroids prevent CAA and are safe, this is a cheap and widely available intervention that could be implemented immediately for the benefit of children.

trial registrationISRCTN71987471- March 31, 2020; Eudract 2019-004433-17.

Indexed as

Adrenal Cortex HormonesAneurysmAspirinImmunoglobulins, IntravenousMucocutaneous Lymph Node SyndromeAdolescentChildChild, PreschoolCoronary VesselsHumansInfantMulticenter Studies as TopicQuality of LifeRandomized Controlled Trials as TopicAdrenal Cortex HormonesAspirinImmunoglobulins, IntravenousCoronary artery aneurysmsCorticosteroidsKawasaki disease

Identifiers

PMID36703139
PMCPMC9879235
OpenAlexW4318069641

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.