TY - JOUR
T1 - A Two-stage Dynamic Model to Enable Updating of Clinical Risk Prediction from Longitudinal Health Record Data: Illustrated with Kidney Function.
AU - Akbarov, Artur
AU - Williams, Richard
AU - Brown, Benjamin
AU - Mamas, Mamas
AU - Peek, Niels
AU - Buchan, Iain
AU - Sperrin, Matthew
N1 - MR/K006665/1, Medical Research Council, United Kingdom
PY - 2015/1
Y1 - 2015/1
N2 - We demonstrate the use of electronic records and repeated measures of risk factors therein, to enable deeper understanding of the relationship between the full longitudinal trajectory of risk factors and outcomes. To illustrate, dynamic mixed effect modelling is used to summarise the level, trend and monitoring intensity of kidney function. The output from this model then forms covariates for a recurrent event Cox proportional hazards model for predicting adverse events (AE). Using data from Salford, UK, our multivariate model finds that steeper declines in kidney function raise the hazard of AE (HR: 1.13, 95% CI (1.05, 1.22)). There is a non-proportional relationship between the hazard of AE and the monitoring intensity of kidney function. Neither of these variables would be present in a classical risk prediction model.. This work illustrates the potential of using the full longitudinal profile of risk factors, rather than just their level. There is an opportunity for deep statistical learning leading to rich clinical insight using longitudinal signals in electronic data.
AB - We demonstrate the use of electronic records and repeated measures of risk factors therein, to enable deeper understanding of the relationship between the full longitudinal trajectory of risk factors and outcomes. To illustrate, dynamic mixed effect modelling is used to summarise the level, trend and monitoring intensity of kidney function. The output from this model then forms covariates for a recurrent event Cox proportional hazards model for predicting adverse events (AE). Using data from Salford, UK, our multivariate model finds that steeper declines in kidney function raise the hazard of AE (HR: 1.13, 95% CI (1.05, 1.22)). There is a non-proportional relationship between the hazard of AE and the monitoring intensity of kidney function. Neither of these variables would be present in a classical risk prediction model.. This work illustrates the potential of using the full longitudinal profile of risk factors, rather than just their level. There is an opportunity for deep statistical learning leading to rich clinical insight using longitudinal signals in electronic data.
U2 - 10.3233/978-1-61499-564-7-696
DO - 10.3233/978-1-61499-564-7-696
M3 - Article
C2 - 26262141
SN - 0926-9630
VL - 216
SP - 696
EP - 700
JO - Studies in Health Technology and Informatics
JF - Studies in Health Technology and Informatics
ER -