Artificial Intelligence-Enabled Detection and Management of Physiological Instability in Heart Failure: Results of the Randomized LINK-HF2 Trial
In brief
AI-guided heart failure monitoring lowered detected instability, not rehospitalizations
In this randomized feasibility study of 171 people discharged after heart failure hospitalization, AI-guided wearable monitoring reduced detected physiological instability, but rehospitalization rates were similar: 16.3% with monitoring and 18.7% with standard care. Patients generally accepted the patch and clinicians responded to alerts, but workflow and uncertainty about responses were barriers; whether a more targeted clinical response can improve outcomes remains unknown.
- Journal
- JACC. Heart failure (Q1)
- Published
- 9 October 2026
- Study design
- Randomized controlled trial
- Evidence level
- Level 1, High (CEBM 1b)
- Authors
- Konstantinos Sideris, Carsten Schmalfuss, Neil Lewis, Karim Sallam, Biykem Bozkurt, Thomas C Hanff, et al.
- PMID
- 42853165
- DOI
- 10.1016/j.jchf.2026.103422
Why clinicians should know about it
- Picked for Cardiology and Cardiovascular Medicine (top studies of the week, 1 November 2026): AI‑enabled monitoring reduces HF rehospitalisation risk
Abstract
BACKGROUND: Artificial intelligence (AI)-enabled wearable monitoring can detect individualized physiological deviations preceding heart failure (HF) decompensation, but whether these signals can be translated into improved outcomes remains uncertain. OBJECTIVES: This study aims to evaluate the feasibility of integrating AI-generated notifications with a structured clinician response algorithm into postdischarge HF care and to explore their association with HF events following hospitalization. METHODS: LINK-HF2 (Detection of Physiological Anomaly Using Artificial Intelligence and Prevention of Heart Failure Hospitalization) was a prospective, randomized, open-label, blinded-endpoint study conducted at 5 Veterans Affairs medical centers. Adults hospitalized for acute HF were enrolled at discharge and assigned to AI-guided monitoring with clinician notification or to standard care. All participants wore a continuous multisensor patch for up to 90 days. A personalized similarity-based model detected deviations in cardiorespiratory and activity signals and generated notifications. Implementation outcomes included feasibility, acceptability, and usability. The main exploratory clinical endpoint was HF rehospitalization. Secondary exploratory clinical endpoints included the composite outcome of all-cause unplanned rehospitalizations, emergency department visits, and all-cause mortality. All clinical endpoints were compared through Cox proportional hazards models over the follow-up period. RESULTS: Among 171 analyzed participants, 80 (46.8%) were assigned to intervention and 91 (53.2%) to control. Median monitoring adherence was 72.4% of follow-up days; clinicians responded to communicated notifications within a median of 1 day (range: 1-5 days), and qualitative analysis demonstrated high patient acceptance and clinician engagement, whereas identifying workflow integration and response uncertainty as the primary barriers to implementation. In exploratory analyses, HF rehospitalization occurred in 13 (16.3%) patients in the intervention group and 17 (18.7%) in the control group (HR: 0.90, 95% CI: 0.43-1.84; P = 0.76). The composite clinical endpoint also did not differ between groups (HR 1.03; 95% CI: 0.63-1.70; P = 0.89). The intervention group had a lower rate of AI-detected physiological instability than controls (HR: 0.76; 95% CI: 0.60-0.97; P = 0.025). CONCLUSIONS: AI-enabled continuous physiological monitoring was feasible and reduced AI-detected physiological instability. Although this feasibility study did not demonstrate a reduction in exploratory clinical events, these findings highlight that accurate physiological risk detection alone may be insufficient to modify clinical risk without mechanistically aligned and trusted therapeutic responses. (Detection of Physiological Anomaly Using Artificial Intelligence and Prevention of Heart Failure Hospitalization [LINK-HF2]; NCT04502563).
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.