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Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study
OBJECTIVE: To determine the concordance of mortality risk classification through the use of the Pediatric Index of Mortality (PIM) 2 and 3. METHODS: Through a retrospective cohort, we evaluated patients admitted to the pediatric intensive care unit between April 2016 and December 2018. We calculated...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Medicina Intensiva Brasileira - AMIB
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7853689/ https://www.ncbi.nlm.nih.gov/pubmed/33470360 http://dx.doi.org/10.5935/0103-507X.20200096 |
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author | Patino-Hernandez, Daniela López, Alba Deyanira Quiñonez Zuluaga, César Augusto García, Ángel Alberto Muñoz-Velandia, Oscar Mauricio |
author_facet | Patino-Hernandez, Daniela López, Alba Deyanira Quiñonez Zuluaga, César Augusto García, Ángel Alberto Muñoz-Velandia, Oscar Mauricio |
author_sort | Patino-Hernandez, Daniela |
collection | PubMed |
description | OBJECTIVE: To determine the concordance of mortality risk classification through the use of the Pediatric Index of Mortality (PIM) 2 and 3. METHODS: Through a retrospective cohort, we evaluated patients admitted to the pediatric intensive care unit between April 2016 and December 2018. We calculated the mortality risk with the PIM 2 and 3. Analyses were carried out to determine the concordance between the risk classification obtained with both scales using unweighted and linearly weighted kappa. RESULTS: A total of 722 subjects were included, and 66.6% had a chronic condition. The overall mortality was 3.7%. The global kappa concordance coefficient for classifying patients according to risk with the PIM 2 and 3 was moderate at 0.48 (95%CI 0.43 - 0.53). After linear weighting, concordance was substantial at 0.64 (95%CI 0.59 - 0.69). For cardiac surgery patients, concordance for risk classification was fair at 0.30 (95%CI 0.21 - 0.39), and after linear weighting, concordance was only moderate at 0.49 (95%CI 0.39 - 0.59). The PIM 3 assigned a lower risk than the PIM 2 in 44.8% of patients in this subgroup. CONCLUSION: Our study proves that the PIM 2 and 3 are not clinically equivalent and should not be used interchangeably for quality evaluation across pediatric intensive care units. Validation studies must be performed before using the PIM 2 or PIM 3 in specific settings. |
format | Online Article Text |
id | pubmed-7853689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Associação de Medicina Intensiva Brasileira - AMIB |
record_format | MEDLINE/PubMed |
spelling | pubmed-78536892021-02-04 Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study Patino-Hernandez, Daniela López, Alba Deyanira Quiñonez Zuluaga, César Augusto García, Ángel Alberto Muñoz-Velandia, Oscar Mauricio Rev Bras Ter Intensiva Original Article OBJECTIVE: To determine the concordance of mortality risk classification through the use of the Pediatric Index of Mortality (PIM) 2 and 3. METHODS: Through a retrospective cohort, we evaluated patients admitted to the pediatric intensive care unit between April 2016 and December 2018. We calculated the mortality risk with the PIM 2 and 3. Analyses were carried out to determine the concordance between the risk classification obtained with both scales using unweighted and linearly weighted kappa. RESULTS: A total of 722 subjects were included, and 66.6% had a chronic condition. The overall mortality was 3.7%. The global kappa concordance coefficient for classifying patients according to risk with the PIM 2 and 3 was moderate at 0.48 (95%CI 0.43 - 0.53). After linear weighting, concordance was substantial at 0.64 (95%CI 0.59 - 0.69). For cardiac surgery patients, concordance for risk classification was fair at 0.30 (95%CI 0.21 - 0.39), and after linear weighting, concordance was only moderate at 0.49 (95%CI 0.39 - 0.59). The PIM 3 assigned a lower risk than the PIM 2 in 44.8% of patients in this subgroup. CONCLUSION: Our study proves that the PIM 2 and 3 are not clinically equivalent and should not be used interchangeably for quality evaluation across pediatric intensive care units. Validation studies must be performed before using the PIM 2 or PIM 3 in specific settings. Associação de Medicina Intensiva Brasileira - AMIB 2020 /pmc/articles/PMC7853689/ /pubmed/33470360 http://dx.doi.org/10.5935/0103-507X.20200096 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Patino-Hernandez, Daniela López, Alba Deyanira Quiñonez Zuluaga, César Augusto García, Ángel Alberto Muñoz-Velandia, Oscar Mauricio Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title | Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title_full | Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title_fullStr | Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title_full_unstemmed | Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title_short | Are the Pediatric Index of Mortality 2 and 3 equal predictors of mortality? An intensive care unit-based concordance study |
title_sort | are the pediatric index of mortality 2 and 3 equal predictors of mortality? an intensive care unit-based concordance study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7853689/ https://www.ncbi.nlm.nih.gov/pubmed/33470360 http://dx.doi.org/10.5935/0103-507X.20200096 |
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