A novel methodological framework for multimodality, trajectory model-based prognostication.

introductionPrognostic tools typically combine several time-invariant clinical predictors using regression models that yield a single, time-invariant outcome prediction. This results in considerable information loss as repeatedly or continuously sampled data are aggregated into single summary measures. We describe a method for real-time multivariate outcome prediction that accommodates both longitudinal data and time-invariant clinical characteristics.

methodsWe included comatose patients treated after resuscitation from cardiac arrest who underwent ≥6 h of electroencephalographic (EEG) monitoring. We used Persyst v13 (Persyst Development Corp, Prescott AZ) to generate quantitative EEG (qEEG) features and calculated hourly summaries of whole brain suppression ratio and amplitude-integrated EEG. We randomly selected half of subjects as a training sample and used the other half as a test sample. We applied group-based trajectory modeling (GBTM) to the training sample to group patients based on qEEG evolution, then estimated the relationship of group membership and clinical covariates with awakening from coma and surviving to hospital discharge using logistic regression. We used these parameters to calculate posterior probabilities of group membership (PPGMs) in the test sample, and built three prognostic models: adjusted logistic regression (no GBTM), unadjusted GBTM (no clinical covariates) and adjusted GBTM (all data). We compared these models performance characteristics.

resultsWe included 723 patients. Group-specific outcome estimates from a 7-group GBTM ranged from 0 to 75%. Compared to unadjusted GBTM, adjusted GBTM calibration was significantly improved at 6 and 12 h, and time to an outcome estimate <10% and <5% were significantly shortened. Compared to simple logistic regression, adjusted GBTM identified a substantially larger proportion of subjects with outcome probability <1%.

conclusionsWe describe a novel methodology for combining GBTM output and clinical covariates to estimate patient-specific prognosis over time. Refinement of such methods should form the basis for new avenues of prognostication research that minimize loss of clinically important information.