Key result
Cluster-randomized ACT-HF trial tests whether EHR-integrated AI tool improves GDMT adherence in HFrEF.
Why the study?
Guidelines recommend GDMT to manage progressive and pervasive HFrEF, yet adherence remains low.
Does an AI-enabled clinical decision support software integrated into the EHR improve the total number of prescribed GDMT medications for adults with HFrEF?
RCT (n=2,148)
Cluster-randomized
Yes
Does an AI-enabled clinical decision support software integrated into the EHR improve the total number of prescribed GDMT medications for adults with HFrEF?
Answers are grounded in this paper and cite their sources.
The ACT-HF trial is designed to evaluate whether an AI-enabled, EHR-integrated clinical decision support system can increase guideline-directed medical therapy prescribing rates in outpatients with heart failure with reduced ejection fraction.
Background: Heart failure with reduced ejection fraction (HFrEF) is progressive and pervasive. Guidelines provide evidence-based recommendations to manage HFrEF, yet adherence to Guideline Directed Medical Therapy (GDMT) is low. An opportunity exists to improve adherence by delivering actionable data, reducing clinician information overload, and enhancing patient care. A Pragmatic Trial Evaluating the Impact of the Anumana Clinical Decision Support Tool for Guideline-Directed Management of Heart Failure (ACT-HF) will evaluate a clinical decision support software (CDSS) that integrates in electronic health records (EHR), automates chart review, and identifies care gaps. Methods: Anumana's Guideline Navigator is an innovative, multi-module AI-enabled CDSS with automated chart review to rapidly analyze EHR data, detect care gaps, and provide alerts for eligible patients not receiving optimal GDMT. ACT-HF, a multi-center cluster pragmatic trial, will recruit and randomize clinician participants (≤250) from 2 health systems to receive intervention software or provide usual care. The trial will evaluate outpatient care for adults with documented HFrEF and not on optimal GDMT (>2148). Outcomes will be evaluated at 90 days. Clinician participants may discuss results with patients, but patients will not have access to the CDSS. Results: Primary outcome is change in GDMT medications; exploratory endpoints include clinical outcomes, resource utilization, and usability. Subgroup analyses include health system, clinician, and patient-level characteristics associated with outcomes. Conclusion: Building on efforts to improve GDMT adherence, ACT-HF will test Anumana's Guideline Navigator in a multicenter study to evaluate outcomes and further refine the CDSS EHR integration EHR for improved clinical utility, workflow integration, and patient outcomes.
No takes yet. Share an insight, caveat, or question.
Lopez‐Jimenez et al. (2025) conducted an RCT in Heart failure with reduced ejection fraction (HFrEF) (n=2,148). Anumana's Guideline Navigator (Clinical Decision Support Tool) vs. Usual care was evaluated on Total number of GDMT-HF-recommended HFrEF medications prescribed at 90-days post clinical encounter, per patient. The ACT-HF study is an ongoing pragmatic trial designed to evaluate whether a novel EHR-integrated clinical decision support tool improves adherence to guideline-directed medical therapy in patients with HFrEF, with primary results expected in late 2025.
Synapse has enriched 10 related papers. Consider them for comparative context: