Predicting Imminent Health Outcomes from Common Lab Results

Abstract

In recent years, most hospitals have implemented Electronic Health Records to manage and integrate a wide range of medical information, including diagnostics, medication admission and laboratory test results. Certain laboratory variables may serve as indicators of a patient's clinical deterioration, making laboratory data a valuable tool for identifying high-risk patients. This work introduces a framework for predicting imminent health outcomes (IHO) of multimorbidity patients using laboratory test data. Our cohort includes 322,316 multimorbidity patients that performed laboratory tests in a large teaching hospital between January 2007 and August 2021. Two Imminent Health Outcomes predictive tools were developed. The first considers all patients in the dataset. The second was developed using a subset of patients with Heart Failure (HF) as the main comorbidity (5% of the entire dataset), considering that HF is a highly prevalent syndrome in multimorbidity patients. This predictive model achieved a reasonable predictive performance (AUROC = 0.718, 95% CI 0.708-0.756, and AUPRC = 0.663, 95% CI 0.630-0.701). C-reactive protein and NT-proBNP are the lab tests that most positively contribute to the prediction of IHO. The IHO predictive tool has the potential to help the medical team identify patients at high-risk of an imminent adverse event, highlighting the laboratory variables that are most contributing to the deterioration of the patient.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This work was developed by the IntelligentCare project LISBOA-01-0247-FEDER-045948 that is co-financed by the ERDF/LISBOA2020 and by FCT under CMU-Portugal and by FCT under projects UIDB/50021/2020, UIDB/00408/2020, UIDP/00408/2020.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee/IRB of Hospital da Luz Lisboa gave ethical approval for this work

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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