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Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether
A competing risk is an event (for example, death in the ICU) that hinders the occurrence of an event of interest (for example, nosocomial infection in the ICU) and it is a common issue in many critical care studies. Not accounting for a competing event may affect how results related to a primary eve...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057054/ https://www.ncbi.nlm.nih.gov/pubmed/25042281 http://dx.doi.org/10.1186/cc13892 |
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author | Muñoz, Alvaro Mongilardi, Nicole Checkley, William |
author_facet | Muñoz, Alvaro Mongilardi, Nicole Checkley, William |
author_sort | Muñoz, Alvaro |
collection | PubMed |
description | A competing risk is an event (for example, death in the ICU) that hinders the occurrence of an event of interest (for example, nosocomial infection in the ICU) and it is a common issue in many critical care studies. Not accounting for a competing event may affect how results related to a primary event of interest are interpreted. In the previous issue of Critical Care, Wolkewitz and colleagues extended traditional models for competing risks to include random effects as a means to quantify heterogeneity among ICUs. Reported results from their analyses based on cause-specific hazards and on sub-hazards of the cumulative incidence function were indicative of lack of proportionality of these hazards over time. Here, we argue that proportionality of hazards can be problematic in competing-risk problems and analyses must consider time by covariate interactions as a default. Moreover, since hazards in competing risks make it difficult to disentangle the effects of frequency and timing of the competing events, their interpretation can be murky. Use of mixtures of flexible and succinct parametric time-to-event models for competing risks permits disentanglement of the frequency and timing at the price of requiring stronger data and a higher number of parameters. We used data from a clinical trial on fluid management strategies for patients with acute respiratory distress syndrome to support our recommendations. |
format | Online Article Text |
id | pubmed-4057054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40570542014-06-14 Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether Muñoz, Alvaro Mongilardi, Nicole Checkley, William Crit Care Commentary A competing risk is an event (for example, death in the ICU) that hinders the occurrence of an event of interest (for example, nosocomial infection in the ICU) and it is a common issue in many critical care studies. Not accounting for a competing event may affect how results related to a primary event of interest are interpreted. In the previous issue of Critical Care, Wolkewitz and colleagues extended traditional models for competing risks to include random effects as a means to quantify heterogeneity among ICUs. Reported results from their analyses based on cause-specific hazards and on sub-hazards of the cumulative incidence function were indicative of lack of proportionality of these hazards over time. Here, we argue that proportionality of hazards can be problematic in competing-risk problems and analyses must consider time by covariate interactions as a default. Moreover, since hazards in competing risks make it difficult to disentangle the effects of frequency and timing of the competing events, their interpretation can be murky. Use of mixtures of flexible and succinct parametric time-to-event models for competing risks permits disentanglement of the frequency and timing at the price of requiring stronger data and a higher number of parameters. We used data from a clinical trial on fluid management strategies for patients with acute respiratory distress syndrome to support our recommendations. BioMed Central 2014 2014-05-27 /pmc/articles/PMC4057054/ /pubmed/25042281 http://dx.doi.org/10.1186/cc13892 Text en Copyright © 2014 Muñoz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 The licensee has exclusive rights to distribute this article, in any medium, for 6 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Muñoz, Alvaro Mongilardi, Nicole Checkley, William Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title | Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title_full | Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title_fullStr | Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title_full_unstemmed | Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title_short | Multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
title_sort | multilevel competing risks in the evaluation of nosocomial infections: time to move on from proportional hazards and even from hazards altogether |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057054/ https://www.ncbi.nlm.nih.gov/pubmed/25042281 http://dx.doi.org/10.1186/cc13892 |
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