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Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology
BACKGROUND: Multi-state models are being increasingly used to capture complex disease pathways. The convenient formula of the exponential multi-state model can facilitate a quick and accessible understanding of the data. However, assuming time constant transition rates is not always plausible. On th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798316/ https://www.ncbi.nlm.nih.gov/pubmed/33430778 http://dx.doi.org/10.1186/s12874-020-01192-8 |
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author | Hill, Micki Lambert, Paul C. Crowther, Michael J. |
author_facet | Hill, Micki Lambert, Paul C. Crowther, Michael J. |
author_sort | Hill, Micki |
collection | PubMed |
description | BACKGROUND: Multi-state models are being increasingly used to capture complex disease pathways. The convenient formula of the exponential multi-state model can facilitate a quick and accessible understanding of the data. However, assuming time constant transition rates is not always plausible. On the other hand, obtaining predictions from a fitted model with time-dependent transitions can be challenging. One proposed solution is to utilise a general simulation algorithm to calculate predictions from a fitted multi-state model. METHODS: Predictions obtained from an exponential multi-state model were compared to those obtained from two different parametric models and to non-parametric Aalen-Johansen estimates. The first comparative approach fitted a multi-state model with transition-specific distributions, chosen separately based on the Akaike Information Criterion. The second approach was a Royston-Parmar multi-state model with 4 degrees of freedom, which was chosen as a reference model flexible enough to capture complex hazard shapes. All quantities were obtained analytically for the exponential and Aalen-Johansen approaches. The transition rates for the two comparative approaches were also obtained analytically, while all other quantities were obtained from the fitted models via a general simulation algorithm. Metrics investigated were: transition probabilities, attributable mortality (AM), population attributable fraction (PAF) and expected length of stay. This work was performed on previously analysed hospital acquired infection (HAI) data. By definition, a HAI takes three days to develop and therefore selected metrics were also predicted from time 3 (delayed entry). RESULTS: Despite clear deviations from the constant transition rates assumption, the empirical estimates of the transition probabilities were approximated reasonably well by the exponential model. However, functions of the transition probabilities, e.g. AM and PAF, were not well approximated and the comparative models offered considerable improvements for these metrics. They also provided consistent predictions with the empirical estimates in the case of delayed entry time, unlike the exponential model. CONCLUSION: We conclude that methods and software are readily available for obtaining predictions from multi-state models that do not assume constant transition rates. The multistate package in Stata facilitates a range of predictions with confidence intervals, which can provide a more comprehensive understanding of the data. User-friendly code is provided. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12874-020-01192-8). |
format | Online Article Text |
id | pubmed-7798316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77983162021-01-12 Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology Hill, Micki Lambert, Paul C. Crowther, Michael J. BMC Med Res Methodol Research Article BACKGROUND: Multi-state models are being increasingly used to capture complex disease pathways. The convenient formula of the exponential multi-state model can facilitate a quick and accessible understanding of the data. However, assuming time constant transition rates is not always plausible. On the other hand, obtaining predictions from a fitted model with time-dependent transitions can be challenging. One proposed solution is to utilise a general simulation algorithm to calculate predictions from a fitted multi-state model. METHODS: Predictions obtained from an exponential multi-state model were compared to those obtained from two different parametric models and to non-parametric Aalen-Johansen estimates. The first comparative approach fitted a multi-state model with transition-specific distributions, chosen separately based on the Akaike Information Criterion. The second approach was a Royston-Parmar multi-state model with 4 degrees of freedom, which was chosen as a reference model flexible enough to capture complex hazard shapes. All quantities were obtained analytically for the exponential and Aalen-Johansen approaches. The transition rates for the two comparative approaches were also obtained analytically, while all other quantities were obtained from the fitted models via a general simulation algorithm. Metrics investigated were: transition probabilities, attributable mortality (AM), population attributable fraction (PAF) and expected length of stay. This work was performed on previously analysed hospital acquired infection (HAI) data. By definition, a HAI takes three days to develop and therefore selected metrics were also predicted from time 3 (delayed entry). RESULTS: Despite clear deviations from the constant transition rates assumption, the empirical estimates of the transition probabilities were approximated reasonably well by the exponential model. However, functions of the transition probabilities, e.g. AM and PAF, were not well approximated and the comparative models offered considerable improvements for these metrics. They also provided consistent predictions with the empirical estimates in the case of delayed entry time, unlike the exponential model. CONCLUSION: We conclude that methods and software are readily available for obtaining predictions from multi-state models that do not assume constant transition rates. The multistate package in Stata facilitates a range of predictions with confidence intervals, which can provide a more comprehensive understanding of the data. User-friendly code is provided. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12874-020-01192-8). BioMed Central 2021-01-11 /pmc/articles/PMC7798316/ /pubmed/33430778 http://dx.doi.org/10.1186/s12874-020-01192-8 Text en © The Author(s) 2021 Open Access This 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, visithttp://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Hill, Micki Lambert, Paul C. Crowther, Michael J. Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title | Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title_full | Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title_fullStr | Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title_full_unstemmed | Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title_short | Relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
title_sort | relaxing the assumption of constant transition rates in a multi-state model in hospital epidemiology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798316/ https://www.ncbi.nlm.nih.gov/pubmed/33430778 http://dx.doi.org/10.1186/s12874-020-01192-8 |
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