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Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?

OBJECTIVE: To assess macrophage activation syndrome (MAS) in septic shock leading to multiorgan dysfunction syndrome (MODS). METHODS: A prospective observational study was conducted at a tertiary care hospital to evaluate the MAS criteria in different stages of sepsis. Children aged 6 months to 12 y...

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Autores principales: Nandy, Arnab, Mondal, Tanushree, Sarkar, Mihir, Nag, Shankha Subhra, Chel, Soumita, Ivan, Divyoshanu M., Hazra, Avijit, Mondal, Rakesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical Research and Education Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133880/
https://www.ncbi.nlm.nih.gov/pubmed/33226328
http://dx.doi.org/10.5152/eurjrheum.2020.20081
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author Nandy, Arnab
Mondal, Tanushree
Sarkar, Mihir
Nag, Shankha Subhra
Chel, Soumita
Ivan, Divyoshanu M.
Hazra, Avijit
Mondal, Rakesh
author_facet Nandy, Arnab
Mondal, Tanushree
Sarkar, Mihir
Nag, Shankha Subhra
Chel, Soumita
Ivan, Divyoshanu M.
Hazra, Avijit
Mondal, Rakesh
author_sort Nandy, Arnab
collection PubMed
description OBJECTIVE: To assess macrophage activation syndrome (MAS) in septic shock leading to multiorgan dysfunction syndrome (MODS). METHODS: A prospective observational study was conducted at a tertiary care hospital to evaluate the MAS criteria in different stages of sepsis. Children aged 6 months to 12 years in different stages of septic shock were recruited. The Paediatric Rheumatology International Trials Organisation Collaborative Initiative (PRINTO) criteria of MAS were applied initially at the stage of septic shock and subsequently at the stage of MODS (MODS cohort) or following recovery from septic shock without going through MODS (non-MODS cohort). RESULTS: A total of 127 subjects were studied, with 53 comprising the MODS cohort and the rest 74 the non-MODS cohort. At the initial assessment, a comparable proportion of subjects in the MODS and non-MODS groups satisfied the MAS criteria (20.75% and 25.68%, respectively; p=0.529). However, by the time of progression to MODS, 81.13% of the subjects satisfied the MAS criteria in the MODS group, whereas only 16.18% subjects in the non-MODS group continued to satisfy the MAS criteria (p<0.001). Thus, there was a definite increase in the proportion of subjects showing MAS by the time they progressed to multiorgan dysfunction (p<0.001). In contrast, the proportion declined significantly (25.68% to 16.18%; p=0.008) in the subjects who had recovered. CONCLUSION: The findings bear out the hypothesis that MODS in sepsis is a reflection of MAS secondary to sepsis. However, studies in larger cohorts are needed to validate these findings and explore the therapeutic implications.
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spelling pubmed-81338802021-05-24 Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection? Nandy, Arnab Mondal, Tanushree Sarkar, Mihir Nag, Shankha Subhra Chel, Soumita Ivan, Divyoshanu M. Hazra, Avijit Mondal, Rakesh Eur J Rheumatol Original Article OBJECTIVE: To assess macrophage activation syndrome (MAS) in septic shock leading to multiorgan dysfunction syndrome (MODS). METHODS: A prospective observational study was conducted at a tertiary care hospital to evaluate the MAS criteria in different stages of sepsis. Children aged 6 months to 12 years in different stages of septic shock were recruited. The Paediatric Rheumatology International Trials Organisation Collaborative Initiative (PRINTO) criteria of MAS were applied initially at the stage of septic shock and subsequently at the stage of MODS (MODS cohort) or following recovery from septic shock without going through MODS (non-MODS cohort). RESULTS: A total of 127 subjects were studied, with 53 comprising the MODS cohort and the rest 74 the non-MODS cohort. At the initial assessment, a comparable proportion of subjects in the MODS and non-MODS groups satisfied the MAS criteria (20.75% and 25.68%, respectively; p=0.529). However, by the time of progression to MODS, 81.13% of the subjects satisfied the MAS criteria in the MODS group, whereas only 16.18% subjects in the non-MODS group continued to satisfy the MAS criteria (p<0.001). Thus, there was a definite increase in the proportion of subjects showing MAS by the time they progressed to multiorgan dysfunction (p<0.001). In contrast, the proportion declined significantly (25.68% to 16.18%; p=0.008) in the subjects who had recovered. CONCLUSION: The findings bear out the hypothesis that MODS in sepsis is a reflection of MAS secondary to sepsis. However, studies in larger cohorts are needed to validate these findings and explore the therapeutic implications. Medical Research and Education Association 2021-04 2020-11-19 /pmc/articles/PMC8133880/ /pubmed/33226328 http://dx.doi.org/10.5152/eurjrheum.2020.20081 Text en Copyright © 2021 European Journal of Rheumatology https://creativecommons.org/licenses/by-nc/4.0/Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Original Article
Nandy, Arnab
Mondal, Tanushree
Sarkar, Mihir
Nag, Shankha Subhra
Chel, Soumita
Ivan, Divyoshanu M.
Hazra, Avijit
Mondal, Rakesh
Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title_full Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title_fullStr Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title_full_unstemmed Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title_short Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
title_sort multiorgan dysfunction syndrome in sepsis: is macrophage activation syndrome secondary to infection?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133880/
https://www.ncbi.nlm.nih.gov/pubmed/33226328
http://dx.doi.org/10.5152/eurjrheum.2020.20081
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