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Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study.
Channon-Wells, Samuel; Vito, Ortensia; McArdle, Andrew J; Seaby, Eleanor G; Patel, Harsita; Shah, Priyen; Pazukhina, Ekaterina; Wilson, Clare; Broderick, Claire; D'Souza, Giselle; Keren, Ilana; Nijman, Ruud G; Tremoulet, Adriana; Munblit, Daniel; Ulloa-Gutierrez, Rolando; Carter, Michael J; Ramnarayan, Padmanabhan; De, Tisham; Hoggart, Clive; Whittaker, Elizabeth; Herberg, Jethro A; Kaforou, Myrsini; Cunnington, Aubrey J; Blyuss, Oleg; Levin, Michael.
  • Channon-Wells S; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Vito O; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • McArdle AJ; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Seaby EG; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Patel H; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Shah P; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Pazukhina E; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Wilson C; Genomic Informatics Group, University of Southampton, Southampton, UK.
  • Broderick C; Translational Genomics Group, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • D'Souza G; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Keren I; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Nijman RG; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Tremoulet A; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Munblit D; Istanbul, Türkiye.
  • Ulloa-Gutierrez R; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Carter MJ; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Ramnarayan P; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • De T; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Hoggart C; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Whittaker E; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Herberg JA; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Kaforou M; Centre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
  • Cunnington AJ; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
  • Blyuss O; Department of Paediatric Emergency Medicine, Division of Medicine, St Mary's hospital-Imperial College NHS Healthcare Trust, London, London, UK.
  • Levin M; Department of Paediatrics, University of California San Diego-Rady Children's Hospital San Diego, San Diego, CA, USA.
Lancet Rheumatol ; 5(4): e184-e199, 2023 Apr.
Статья в английский | MEDLINE | ID: covidwho-2239656
ABSTRACT

Background:

Multisystem inflammatory syndrome in children (MIS-C), a hyperinflammatory condition associated with SARS-CoV-2 infection, has emerged as a serious illness in children worldwide. Immunoglobulin or glucocorticoids, or both, are currently recommended treatments.

Methods:

The Best Available Treatment Study evaluated immunomodulatory treatments for MIS-C in an international observational cohort. Analysis of the first 614 patients was previously reported. In this propensity-weighted cohort study, clinical and outcome data from children with suspected or proven MIS-C were collected onto a web-based Research Electronic Data Capture database. After excluding neonates and incomplete or duplicate records, inverse probability weighting was used to compare primary treatments with intravenous immunoglobulin, intravenous immunoglobulin plus glucocorticoids, or glucocorticoids alone, using intravenous immunoglobulin as the reference treatment. Primary outcomes were a composite of inotropic or ventilator support from the second day after treatment initiation, or death, and time to improvement on an ordinal clinical severity scale. Secondary outcomes included treatment escalation, clinical deterioration, fever, and coronary artery aneurysm occurrence and resolution. This study is registered with the ISRCTN registry, ISRCTN69546370.

Findings:

We enrolled 2101 children (aged 0 months to 19 years) with clinically diagnosed MIS-C from 39 countries between June 14, 2020, and April 25, 2022, and, following exclusions, 2009 patients were included for analysis (median age 8·0 years [IQR 4·2-11·4], 1191 [59·3%] male and 818 [40·7%] female, and 825 [41·1%] White). 680 (33·8%) patients received primary treatment with intravenous immunoglobulin, 698 (34·7%) with intravenous immunoglobulin plus glucocorticoids, 487 (24·2%) with glucocorticoids alone; 59 (2·9%) patients received other combinations, including biologicals, and 85 (4·2%) patients received no immunomodulators. There were no significant differences between treatments for primary outcomes for the 1586 patients with complete baseline and outcome data that were considered for primary analysis. Adjusted odds ratios for ventilation, inotropic support, or death were 1·09 (95% CI 0·75-1·58; corrected p value=1·00) for intravenous immunoglobulin plus glucocorticoids and 0·93 (0·58-1·47; corrected p value=1·00) for glucocorticoids alone, versus intravenous immunoglobulin alone. Adjusted average hazard ratios for time to improvement were 1·04 (95% CI 0·91-1·20; corrected p value=1·00) for intravenous immunoglobulin plus glucocorticoids, and 0·84 (0·70-1·00; corrected p value=0·22) for glucocorticoids alone, versus intravenous immunoglobulin alone. Treatment escalation was less frequent for intravenous immunoglobulin plus glucocorticoids (OR 0·15 [95% CI 0·11-0·20]; p<0·0001) and glucocorticoids alone (0·68 [0·50-0·93]; p=0·014) versus intravenous immunoglobulin alone. Persistent fever (from day 2 onward) was less common with intravenous immunoglobulin plus glucocorticoids compared with either intravenous immunoglobulin alone (OR 0·50 [95% CI 0·38-0·67]; p<0·0001) or glucocorticoids alone (0·63 [0·45-0·88]; p=0·0058). Coronary artery aneurysm occurrence and resolution did not differ significantly between treatment groups.

Interpretation:

Recovery rates, including occurrence and resolution of coronary artery aneurysms, were similar for primary treatment with intravenous immunoglobulin when compared to glucocorticoids or intravenous immunoglobulin plus glucocorticoids. Initial treatment with glucocorticoids appears to be a safe alternative to immunoglobulin or combined therapy, and might be advantageous in view of the cost and limited availability of intravenous immunoglobulin in many countries.

Funding:

Imperial College London, the European Union's Horizon 2020, Wellcome Trust, the Medical Research Foundation, UK National Institute for Health and Care Research, and National Institutes of Health.

Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Тип исследования: Когортное исследование / Экспериментальные исследования / Наблюдательное исследование / Прогностическое исследование / Рандомизированные контролируемые испытания Язык: английский Журнал: Lancet Rheumatol Год: 2023 Тип: Статья Аффилированная страна: S2665-9913(23)00029-2

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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Тип исследования: Когортное исследование / Экспериментальные исследования / Наблюдательное исследование / Прогностическое исследование / Рандомизированные контролируемые испытания Язык: английский Журнал: Lancet Rheumatol Год: 2023 Тип: Статья Аффилированная страна: S2665-9913(23)00029-2