Heterogenous Effect of Automated Alerts on Mortality

ABSTRACT

We analyzed data from 13,483 hospitalized patients with acute kidney injury (AKI) from three randomized controlled trials to assess the heterogenous effects of automated electronic alerts on 14-day mortality. We modeled and predicted individualized alert effects on a subset of the ELAIA-1 patients and validated it internally on ELAIA-1 holdout patients and externally on ELAIA-2 and UPenn trial patients. Patients predicted to benefit from alerts had significantly lower mortality compared to those predicted to be harmed (p-interaction<0.05). In external cohorts, 43 deaths may have been preventable if alerts were restricted to likely beneficiaries. Machine-learning based meta-analysis identified reduced mortality with alerts among patients with higher blood pressures and lower predicted risk, but increased mortality in non-urban and non-teaching hospitals. Provider responses to alerts varied across subgroups. These findings suggest that tailoring alerts to patient phenotypes may improve outcomes and support the need for a prospective trial of individualized alert strategies.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This work was partially supported by a grant from the National Institutes of Health (F31 NS115447) to Benjamin Wissel.

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:

The institutional review board of Duke University Health System gave ethical approval for this work (#00115914), and all trials data utilized were previously approved. All patient data was obtained from other groups, retrospectivley reviewed, and analyzed. No patients were prospectivley assigned nor treatment altered from our findings.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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

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

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Data availability

All of the data used in these analyses are publicly available on DRYAD.

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