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Hyperferritinemia in children hospitalized with scrub typhus

BACKGROUND: Hyperferritinemia is increasingly associated with mortality in sepsis. Studies estimating the prevalence of hyperferritinemia in pediatric scrub typhus are limited. METHODS: This was a secondary analysis of a prospective observational study (FERRIS) from a tertiary care teaching hospital...

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Autores principales: Williams, Vijai, Menon, Nisha, Bhatia, Prateek, Biswal, Manisha, Sreedharanunni, Sreejesh, Jayashree, Muralidharan, Nallasamy, Karthi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890859/
https://www.ncbi.nlm.nih.gov/pubmed/33597024
http://dx.doi.org/10.1186/s41182-021-00304-4
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author Williams, Vijai
Menon, Nisha
Bhatia, Prateek
Biswal, Manisha
Sreedharanunni, Sreejesh
Jayashree, Muralidharan
Nallasamy, Karthi
author_facet Williams, Vijai
Menon, Nisha
Bhatia, Prateek
Biswal, Manisha
Sreedharanunni, Sreejesh
Jayashree, Muralidharan
Nallasamy, Karthi
author_sort Williams, Vijai
collection PubMed
description BACKGROUND: Hyperferritinemia is increasingly associated with mortality in sepsis. Studies estimating the prevalence of hyperferritinemia in pediatric scrub typhus are limited. METHODS: This was a secondary analysis of a prospective observational study (FERRIS) from a tertiary care teaching hospital in North India where 72 children with confirmed scrub typhus, 4 (5.5%) PCR positive, 55 (76.4%)-IgM ELISA positive, and 13 (18.1%)-both PCR and ELISA positive, were analyzed. Serum ferritin was measured in 62 children to identify the prevalence of hyperferritinemia and determine its association with mortality. RESULTS: Hyperferritinemia (> 500 μg/L) was seen in 72.6% [n = 45] children; 26 (41.9%) were mild (500–2000 μg/L), 13 (21%) were moderate (2000–10,000 μg/L), and 6 (9.7%) were severe (> 10,000 μg/L). Early presentation to hospital (≤ 7 days of febrile illness) had more survivors than late presentation (> 7 days). Non-survivors had significantly higher PRISM III, PELOD-2, hyperlactatemia, hypoalbuminemia, organ dysfunction, need for mechanical ventilation, and need of RRT. Ferritin had poor sensitivity and specificity in predicting survival with AUC of 0.56. Organ dysfunction and risk scores as PRISM III, PELOD 2, and VIS at admission were better predictors with AUC (95% CI) of 0.72 (0.56, 0.89), 0.77 (0.63, 0.92), and 0.90 (0.78, 1.0) respectively. CONCLUSIONS: Hyperferritinemia is common in scrub typhus but it did not predict survival. Organ dysfunction and risk scores were better predictors of mortality than ferritin.
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spelling pubmed-78908592021-02-22 Hyperferritinemia in children hospitalized with scrub typhus Williams, Vijai Menon, Nisha Bhatia, Prateek Biswal, Manisha Sreedharanunni, Sreejesh Jayashree, Muralidharan Nallasamy, Karthi Trop Med Health Research BACKGROUND: Hyperferritinemia is increasingly associated with mortality in sepsis. Studies estimating the prevalence of hyperferritinemia in pediatric scrub typhus are limited. METHODS: This was a secondary analysis of a prospective observational study (FERRIS) from a tertiary care teaching hospital in North India where 72 children with confirmed scrub typhus, 4 (5.5%) PCR positive, 55 (76.4%)-IgM ELISA positive, and 13 (18.1%)-both PCR and ELISA positive, were analyzed. Serum ferritin was measured in 62 children to identify the prevalence of hyperferritinemia and determine its association with mortality. RESULTS: Hyperferritinemia (> 500 μg/L) was seen in 72.6% [n = 45] children; 26 (41.9%) were mild (500–2000 μg/L), 13 (21%) were moderate (2000–10,000 μg/L), and 6 (9.7%) were severe (> 10,000 μg/L). Early presentation to hospital (≤ 7 days of febrile illness) had more survivors than late presentation (> 7 days). Non-survivors had significantly higher PRISM III, PELOD-2, hyperlactatemia, hypoalbuminemia, organ dysfunction, need for mechanical ventilation, and need of RRT. Ferritin had poor sensitivity and specificity in predicting survival with AUC of 0.56. Organ dysfunction and risk scores as PRISM III, PELOD 2, and VIS at admission were better predictors with AUC (95% CI) of 0.72 (0.56, 0.89), 0.77 (0.63, 0.92), and 0.90 (0.78, 1.0) respectively. CONCLUSIONS: Hyperferritinemia is common in scrub typhus but it did not predict survival. Organ dysfunction and risk scores were better predictors of mortality than ferritin. BioMed Central 2021-02-17 /pmc/articles/PMC7890859/ /pubmed/33597024 http://dx.doi.org/10.1186/s41182-021-00304-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Williams, Vijai
Menon, Nisha
Bhatia, Prateek
Biswal, Manisha
Sreedharanunni, Sreejesh
Jayashree, Muralidharan
Nallasamy, Karthi
Hyperferritinemia in children hospitalized with scrub typhus
title Hyperferritinemia in children hospitalized with scrub typhus
title_full Hyperferritinemia in children hospitalized with scrub typhus
title_fullStr Hyperferritinemia in children hospitalized with scrub typhus
title_full_unstemmed Hyperferritinemia in children hospitalized with scrub typhus
title_short Hyperferritinemia in children hospitalized with scrub typhus
title_sort hyperferritinemia in children hospitalized with scrub typhus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890859/
https://www.ncbi.nlm.nih.gov/pubmed/33597024
http://dx.doi.org/10.1186/s41182-021-00304-4
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