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Clinical presentation, diagnosis and management of multisystem inflammatory syndrome in children (MIS-C): a systematic review

BackgroundKnowledge about multisystem inflammatory syndrome in children (MIS-C) is evolving, and evidence-based standardised diagnostic and management protocols are lacking. Our review aims to summarise the clinical and diagnostic features, management strategies and outcomes of MIS-C and evaluate th...

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Published in:BMJ paediatrics open 2024-06, Vol.8 (1), p.e002344
Main Authors: Abbas, Qalab, Ali, Haider, Amjad, Fatima, Hussain, Muhammad Zaid Hamid, Rahman, Abdu R, Khan, Maryam Hameed, Padhani, Zahra A, Abbas, Fatima, Imam, Danyal, Alikhan, Zuviya, Belgaumi, Sameer M., Mohsin, Shazia, Sattar, Faiza, Siddiqui, Arsalan, Lassi, Zohra S, Das, Jai K
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container_title BMJ paediatrics open
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creator Abbas, Qalab
Ali, Haider
Amjad, Fatima
Hussain, Muhammad Zaid Hamid
Rahman, Abdu R
Khan, Maryam Hameed
Padhani, Zahra A
Abbas, Fatima
Imam, Danyal
Alikhan, Zuviya
Belgaumi, Sameer M.
Mohsin, Shazia
Sattar, Faiza
Siddiqui, Arsalan
Lassi, Zohra S
Das, Jai K
description BackgroundKnowledge about multisystem inflammatory syndrome in children (MIS-C) is evolving, and evidence-based standardised diagnostic and management protocols are lacking. Our review aims to summarise the clinical and diagnostic features, management strategies and outcomes of MIS-C and evaluate the variances in disease parameters and outcomes between high-income countries (HIC) and middle-income countries (MIC).MethodsWe searched four databases from December 2019 to March 2023. Observational studies with a sample size of 10 or more patients were included. Mean and prevalence ratios for various variables were pooled by random effects model using R. A mixed generalised linear model was employed to account for the heterogeneity, and publication bias was assessed via funnel and Doi plots. The primary outcome was pooled mean mortality among patients with MIS-C. Subgroup analysis was conducted based on the income status of the country of study.ResultsA total of 120 studies (20 881 cases) were included in the review. The most common clinical presentations were fever (99%; 95% CI 99.6% to 100%), gastrointestinal symptoms (76.7%; 95% CI 73.1% to 79.9%) and dermatological symptoms (63.3%; 95% CI 58.7% to 67.7%). Laboratory investigations suggested raised inflammatory, coagulation and cardiac markers. The most common management strategies were intravenous immunoglobulins (87.5%; 95% CI 82.9% to 91%) and steroids (74.7%; 95% CI 68.7% to 79.9%). Around 53.1% (95% CI 47.3% to 58.9%) required paediatric intensive care unit admissions, and overall mortality was 3.9% (95% CI 2.7% to 5.6%). Patients in MIC were younger, had a higher frequency of respiratory distress and evidence of cardiac dysfunction, with a longer hospital and intensive care unit stay and had a higher mortality rate than patients in HIC.ConclusionMIS-C is a severe multisystem disease with better mortality outcomes in HIC as compared with MIC. The findings emphasise the need for standardised protocols and further research to optimise patient care and address disparities between HIC and MIC.PROSPERO registration numberCRD42020195823.
doi_str_mv 10.1136/bmjpo-2023-002344
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Our review aims to summarise the clinical and diagnostic features, management strategies and outcomes of MIS-C and evaluate the variances in disease parameters and outcomes between high-income countries (HIC) and middle-income countries (MIC).MethodsWe searched four databases from December 2019 to March 2023. Observational studies with a sample size of 10 or more patients were included. Mean and prevalence ratios for various variables were pooled by random effects model using R. A mixed generalised linear model was employed to account for the heterogeneity, and publication bias was assessed via funnel and Doi plots. The primary outcome was pooled mean mortality among patients with MIS-C. Subgroup analysis was conducted based on the income status of the country of study.ResultsA total of 120 studies (20 881 cases) were included in the review. The most common clinical presentations were fever (99%; 95% CI 99.6% to 100%), gastrointestinal symptoms (76.7%; 95% CI 73.1% to 79.9%) and dermatological symptoms (63.3%; 95% CI 58.7% to 67.7%). Laboratory investigations suggested raised inflammatory, coagulation and cardiac markers. The most common management strategies were intravenous immunoglobulins (87.5%; 95% CI 82.9% to 91%) and steroids (74.7%; 95% CI 68.7% to 79.9%). Around 53.1% (95% CI 47.3% to 58.9%) required paediatric intensive care unit admissions, and overall mortality was 3.9% (95% CI 2.7% to 5.6%). Patients in MIC were younger, had a higher frequency of respiratory distress and evidence of cardiac dysfunction, with a longer hospital and intensive care unit stay and had a higher mortality rate than patients in HIC.ConclusionMIS-C is a severe multisystem disease with better mortality outcomes in HIC as compared with MIC. The findings emphasise the need for standardised protocols and further research to optimise patient care and address disparities between HIC and MIC.PROSPERO registration numberCRD42020195823.</description><identifier>ISSN: 2399-9772</identifier><identifier>EISSN: 2399-9772</identifier><identifier>DOI: 10.1136/bmjpo-2023-002344</identifier><identifier>PMID: 38844384</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>Child ; COVID-19 ; COVID-19 - complications ; COVID-19 - diagnosis ; COVID-19 - mortality ; COVID-19 - therapy ; Cross-sectional studies ; Data collection ; Disease ; Hospitals ; Humans ; Industrialized nations ; Infectious Diseases ; Intensive care ; Medical diagnosis ; Medical laboratories ; Mortality ; Multisystem inflammatory syndrome in children ; Patients ; Pediatrics ; Severe acute respiratory syndrome coronavirus 2 ; Systematic review ; Systemic Inflammatory Response Syndrome - diagnosis ; Systemic Inflammatory Response Syndrome - mortality ; Systemic Inflammatory Response Syndrome - therapy</subject><ispartof>BMJ paediatrics open, 2024-06, Vol.8 (1), p.e002344</ispartof><rights>Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-b441t-ca65d1eb1e7f3c4e023c85ba036d3c28fcce9899689d80c7cb97668c0040b3af3</cites><orcidid>0000-0001-7845-6065</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bmjpaedsopen.bmj.com/content/8/1/e002344.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://bmjpaedsopen.bmj.com/content/8/1/e002344.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27907,27908,53774,53776,55333,77411,77437</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38844384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abbas, Qalab</creatorcontrib><creatorcontrib>Ali, Haider</creatorcontrib><creatorcontrib>Amjad, Fatima</creatorcontrib><creatorcontrib>Hussain, Muhammad Zaid Hamid</creatorcontrib><creatorcontrib>Rahman, Abdu R</creatorcontrib><creatorcontrib>Khan, Maryam Hameed</creatorcontrib><creatorcontrib>Padhani, Zahra A</creatorcontrib><creatorcontrib>Abbas, Fatima</creatorcontrib><creatorcontrib>Imam, Danyal</creatorcontrib><creatorcontrib>Alikhan, Zuviya</creatorcontrib><creatorcontrib>Belgaumi, Sameer M.</creatorcontrib><creatorcontrib>Mohsin, Shazia</creatorcontrib><creatorcontrib>Sattar, Faiza</creatorcontrib><creatorcontrib>Siddiqui, Arsalan</creatorcontrib><creatorcontrib>Lassi, Zohra S</creatorcontrib><creatorcontrib>Das, Jai K</creatorcontrib><title>Clinical presentation, diagnosis and management of multisystem inflammatory syndrome in children (MIS-C): a systematic review</title><title>BMJ paediatrics open</title><addtitle>bmjpo</addtitle><addtitle>BMJ Paediatrics Open</addtitle><addtitle>BMJ Paediatr Open</addtitle><description>BackgroundKnowledge about multisystem inflammatory syndrome in children (MIS-C) is evolving, and evidence-based standardised diagnostic and management protocols are lacking. Our review aims to summarise the clinical and diagnostic features, management strategies and outcomes of MIS-C and evaluate the variances in disease parameters and outcomes between high-income countries (HIC) and middle-income countries (MIC).MethodsWe searched four databases from December 2019 to March 2023. Observational studies with a sample size of 10 or more patients were included. Mean and prevalence ratios for various variables were pooled by random effects model using R. A mixed generalised linear model was employed to account for the heterogeneity, and publication bias was assessed via funnel and Doi plots. The primary outcome was pooled mean mortality among patients with MIS-C. Subgroup analysis was conducted based on the income status of the country of study.ResultsA total of 120 studies (20 881 cases) were included in the review. The most common clinical presentations were fever (99%; 95% CI 99.6% to 100%), gastrointestinal symptoms (76.7%; 95% CI 73.1% to 79.9%) and dermatological symptoms (63.3%; 95% CI 58.7% to 67.7%). Laboratory investigations suggested raised inflammatory, coagulation and cardiac markers. The most common management strategies were intravenous immunoglobulins (87.5%; 95% CI 82.9% to 91%) and steroids (74.7%; 95% CI 68.7% to 79.9%). Around 53.1% (95% CI 47.3% to 58.9%) required paediatric intensive care unit admissions, and overall mortality was 3.9% (95% CI 2.7% to 5.6%). Patients in MIC were younger, had a higher frequency of respiratory distress and evidence of cardiac dysfunction, with a longer hospital and intensive care unit stay and had a higher mortality rate than patients in HIC.ConclusionMIS-C is a severe multisystem disease with better mortality outcomes in HIC as compared with MIC. The findings emphasise the need for standardised protocols and further research to optimise patient care and address disparities between HIC and MIC.PROSPERO registration numberCRD42020195823.</description><subject>Child</subject><subject>COVID-19</subject><subject>COVID-19 - complications</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 - mortality</subject><subject>COVID-19 - therapy</subject><subject>Cross-sectional studies</subject><subject>Data collection</subject><subject>Disease</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Industrialized nations</subject><subject>Infectious Diseases</subject><subject>Intensive care</subject><subject>Medical diagnosis</subject><subject>Medical laboratories</subject><subject>Mortality</subject><subject>Multisystem inflammatory syndrome in children</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Systematic review</subject><subject>Systemic Inflammatory Response Syndrome - diagnosis</subject><subject>Systemic Inflammatory Response Syndrome - mortality</subject><subject>Systemic Inflammatory Response Syndrome - therapy</subject><issn>2399-9772</issn><issn>2399-9772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>DOA</sourceid><recordid>eNp1Uk1v1DAQjRCIVqU_gAuyxKVIBOyM49hcEFrxsVIRB-BsObaz9Sq2Fzsp2gP_He-mlBaJi8eaee_Nh15VPSX4FSHAXvd-u4t1gxuocXkofVCdNiBELbqueXjnf1Kd57zFGBPBBW2bx9UJcE4pcHpa_VqNLjitRrRLNtswqcnF8BIZpzYhZpeRCgZ5FdTG-lJGcUB-HieX93myHrkwjMp7NcW0R3kfTIrelizSV240yQZ08Xn9tV69eIMUWjilg0bJXjv780n1aFBjtuc38az6_uH9t9Wn-vLLx_Xq3WXdU0qmWivWGmJ7YrsBNLVlXc3bXmFgBnTDB61t2U0wLgzHutO96BjjGmOKe1ADnFXrRddEtZW75LxKexmVk8dETBupUhlrtJKyDgSA6VljKIOel67MUMspYA5EFK23i9Zu7r01uhwlqfGe6P1KcFdyE68lIYQBAygKFzcKKf6YbZ6kd1nbcVTBxjlLwKwVvGXNAfr8H-g2zimUWx1RmLOuZQVFFpROMedkh9tpCJYHs8ijWeTBLHIxS-E8u7vGLeOPNQqgXgCF-7fr_wV_AwCkyws</recordid><startdate>20240606</startdate><enddate>20240606</enddate><creator>Abbas, Qalab</creator><creator>Ali, Haider</creator><creator>Amjad, Fatima</creator><creator>Hussain, Muhammad Zaid Hamid</creator><creator>Rahman, Abdu R</creator><creator>Khan, Maryam Hameed</creator><creator>Padhani, Zahra A</creator><creator>Abbas, Fatima</creator><creator>Imam, Danyal</creator><creator>Alikhan, Zuviya</creator><creator>Belgaumi, Sameer M.</creator><creator>Mohsin, Shazia</creator><creator>Sattar, Faiza</creator><creator>Siddiqui, Arsalan</creator><creator>Lassi, Zohra S</creator><creator>Das, Jai K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7845-6065</orcidid></search><sort><creationdate>20240606</creationdate><title>Clinical presentation, diagnosis and management of multisystem inflammatory syndrome in children (MIS-C): a systematic review</title><author>Abbas, Qalab ; Ali, Haider ; Amjad, Fatima ; Hussain, Muhammad Zaid Hamid ; Rahman, Abdu R ; Khan, Maryam Hameed ; Padhani, Zahra A ; Abbas, Fatima ; Imam, Danyal ; Alikhan, Zuviya ; Belgaumi, Sameer M. ; Mohsin, Shazia ; Sattar, Faiza ; Siddiqui, Arsalan ; Lassi, Zohra S ; Das, Jai K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b441t-ca65d1eb1e7f3c4e023c85ba036d3c28fcce9899689d80c7cb97668c0040b3af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Child</topic><topic>COVID-19</topic><topic>COVID-19 - complications</topic><topic>COVID-19 - diagnosis</topic><topic>COVID-19 - mortality</topic><topic>COVID-19 - therapy</topic><topic>Cross-sectional studies</topic><topic>Data collection</topic><topic>Disease</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Industrialized nations</topic><topic>Infectious Diseases</topic><topic>Intensive care</topic><topic>Medical diagnosis</topic><topic>Medical laboratories</topic><topic>Mortality</topic><topic>Multisystem inflammatory syndrome in children</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Systematic review</topic><topic>Systemic Inflammatory Response Syndrome - diagnosis</topic><topic>Systemic Inflammatory Response Syndrome - mortality</topic><topic>Systemic Inflammatory Response Syndrome - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abbas, Qalab</creatorcontrib><creatorcontrib>Ali, Haider</creatorcontrib><creatorcontrib>Amjad, Fatima</creatorcontrib><creatorcontrib>Hussain, Muhammad Zaid Hamid</creatorcontrib><creatorcontrib>Rahman, Abdu R</creatorcontrib><creatorcontrib>Khan, Maryam Hameed</creatorcontrib><creatorcontrib>Padhani, Zahra A</creatorcontrib><creatorcontrib>Abbas, Fatima</creatorcontrib><creatorcontrib>Imam, Danyal</creatorcontrib><creatorcontrib>Alikhan, Zuviya</creatorcontrib><creatorcontrib>Belgaumi, Sameer M.</creatorcontrib><creatorcontrib>Mohsin, Shazia</creatorcontrib><creatorcontrib>Sattar, Faiza</creatorcontrib><creatorcontrib>Siddiqui, Arsalan</creatorcontrib><creatorcontrib>Lassi, Zohra S</creatorcontrib><creatorcontrib>Das, Jai K</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>ProQuest_Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMJ paediatrics open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abbas, Qalab</au><au>Ali, Haider</au><au>Amjad, Fatima</au><au>Hussain, Muhammad Zaid Hamid</au><au>Rahman, Abdu R</au><au>Khan, Maryam Hameed</au><au>Padhani, Zahra A</au><au>Abbas, Fatima</au><au>Imam, Danyal</au><au>Alikhan, Zuviya</au><au>Belgaumi, Sameer M.</au><au>Mohsin, Shazia</au><au>Sattar, Faiza</au><au>Siddiqui, Arsalan</au><au>Lassi, Zohra S</au><au>Das, Jai K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical presentation, diagnosis and management of multisystem inflammatory syndrome in children (MIS-C): a systematic review</atitle><jtitle>BMJ paediatrics open</jtitle><stitle>bmjpo</stitle><stitle>BMJ Paediatrics Open</stitle><addtitle>BMJ Paediatr Open</addtitle><date>2024-06-06</date><risdate>2024</risdate><volume>8</volume><issue>1</issue><spage>e002344</spage><pages>e002344-</pages><issn>2399-9772</issn><eissn>2399-9772</eissn><abstract>BackgroundKnowledge about multisystem inflammatory syndrome in children (MIS-C) is evolving, and evidence-based standardised diagnostic and management protocols are lacking. Our review aims to summarise the clinical and diagnostic features, management strategies and outcomes of MIS-C and evaluate the variances in disease parameters and outcomes between high-income countries (HIC) and middle-income countries (MIC).MethodsWe searched four databases from December 2019 to March 2023. Observational studies with a sample size of 10 or more patients were included. Mean and prevalence ratios for various variables were pooled by random effects model using R. A mixed generalised linear model was employed to account for the heterogeneity, and publication bias was assessed via funnel and Doi plots. The primary outcome was pooled mean mortality among patients with MIS-C. Subgroup analysis was conducted based on the income status of the country of study.ResultsA total of 120 studies (20 881 cases) were included in the review. The most common clinical presentations were fever (99%; 95% CI 99.6% to 100%), gastrointestinal symptoms (76.7%; 95% CI 73.1% to 79.9%) and dermatological symptoms (63.3%; 95% CI 58.7% to 67.7%). Laboratory investigations suggested raised inflammatory, coagulation and cardiac markers. The most common management strategies were intravenous immunoglobulins (87.5%; 95% CI 82.9% to 91%) and steroids (74.7%; 95% CI 68.7% to 79.9%). Around 53.1% (95% CI 47.3% to 58.9%) required paediatric intensive care unit admissions, and overall mortality was 3.9% (95% CI 2.7% to 5.6%). Patients in MIC were younger, had a higher frequency of respiratory distress and evidence of cardiac dysfunction, with a longer hospital and intensive care unit stay and had a higher mortality rate than patients in HIC.ConclusionMIS-C is a severe multisystem disease with better mortality outcomes in HIC as compared with MIC. The findings emphasise the need for standardised protocols and further research to optimise patient care and address disparities between HIC and MIC.PROSPERO registration numberCRD42020195823.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>38844384</pmid><doi>10.1136/bmjpo-2023-002344</doi><orcidid>https://orcid.org/0000-0001-7845-6065</orcidid><oa>free_for_read</oa></addata></record>
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source BMJ Open Access Journals; PubMed Central
subjects Child
COVID-19
COVID-19 - complications
COVID-19 - diagnosis
COVID-19 - mortality
COVID-19 - therapy
Cross-sectional studies
Data collection
Disease
Hospitals
Humans
Industrialized nations
Infectious Diseases
Intensive care
Medical diagnosis
Medical laboratories
Mortality
Multisystem inflammatory syndrome in children
Patients
Pediatrics
Severe acute respiratory syndrome coronavirus 2
Systematic review
Systemic Inflammatory Response Syndrome - diagnosis
Systemic Inflammatory Response Syndrome - mortality
Systemic Inflammatory Response Syndrome - therapy
title Clinical presentation, diagnosis and management of multisystem inflammatory syndrome in children (MIS-C): a systematic review
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