Cargando…

Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949883/
https://www.ncbi.nlm.nih.gov/pubmed/36855438
http://dx.doi.org/10.1016/S2665-9913(23)00029-2
_version_ 1784893044511735808
author 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
author_facet 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
author_sort Channon-Wells, Samuel
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9949883
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Author(s). Published by Elsevier Ltd.
record_format MEDLINE/PubMed
spelling pubmed-99498832023-02-24 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 Lancet Rheumatol Articles 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. The Author(s). Published by Elsevier Ltd. 2023-04 2023-02-14 /pmc/articles/PMC9949883/ /pubmed/36855438 http://dx.doi.org/10.1016/S2665-9913(23)00029-2 Text en © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Articles
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
Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title_full Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title_fullStr Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title_full_unstemmed Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title_short Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
title_sort immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949883/
https://www.ncbi.nlm.nih.gov/pubmed/36855438
http://dx.doi.org/10.1016/S2665-9913(23)00029-2
work_keys_str_mv AT channonwellssamuel immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT vitoortensia immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT mcardleandrewj immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT seabyeleanorg immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT patelharsita immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT shahpriyen immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT pazukhinaekaterina immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT wilsonclare immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT broderickclaire immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT dsouzagiselle immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT kerenilana immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT nijmanruudg immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT tremouletadriana immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT munblitdaniel immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT ulloagutierrezrolando immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT cartermichaelj immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT ramnarayanpadmanabhan immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT detisham immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT hoggartclive immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT whittakerelizabeth immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT herbergjethroa immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT kaforoumyrsini immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT cunningtonaubreyj immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT blyussoleg immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT levinmichael immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy
AT immunoglobulinglucocorticoidorcombinationtherapyformultisysteminflammatorysyndromeinchildrenapropensityweightedcohortstudy