ArticleCJC open2025
Device Therapy in Patients with Heart Failure: Is Medication Use Optimized and Are We Targeting Those Patients Most Likely to Benefit?
Article in CJC open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: To determine what proportion of device-eligible patients with heart failure treated in a specialized clinic are on optimal guideline-directed medical therapy (GDMT) at the time of device referral and their benefit-risk status. Methods: A cohort study was conducted of all patients seen between January 2013 and August 2024. We characterized GDMT by the modified Heart Function Collaboratory score at the time of device referral and grouped patients by Multicenter Automatic Defibrillator Implantation Trial-II (MADIT-ICD) benefit-risk score. Results: Of 250 patients potentially eligible for a primary prophylaxis implantable cardioverter defibrillator (ICD), 136 (54.4%) were referred within 6 months of GDMT initiation-34 (25%) were in the lowest MADIT-ICD benefit-risk group and 6 (9.7%) of those not referred were in the highest benefit-risk group. No differences occurred in ICD referral based on sex ( Conclusions: Within 6 months of initiating GDMT, more than half of eligible patients with heart failure had been referred for a device, but one quarter were in the group least likely to benefit from a device, and not all were on optimal GDMT.
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Registered trials
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