Evidence map›Paper›PMID 39395594›Full record

ArticleThe American journal of cardiology2024

Implementation of a Cardiovascular Implantable Electronic Device Heart Failure Prediction Tool-Guided Management Pathway.

Allison Kratka, Gregory Rohrbach, Carrie Puckett, Thomas L Rotering, Merritt H Raitt, Mary A Whooley, Sanket S Dhruva

Abstract read
In one paragraph

Article in The American journal of cardiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Allison KratkaSection of Cardiology, Department of Medicine, San Francisco Veterans Affairs Health Care System, San Francisco, California; University of California San Francisco School of Medicine, San Francisco, California.
Gregory RohrbachSection of Cardiology, Department of Medicine, San Francisco Veterans Affairs Health Care System, San Francisco, California.
Carrie PuckettSection of Cardiology, Department of Medicine, Veterans Affairs Portland Health Care System, Portland, Oregon.
Thomas L RoteringSection of Cardiology, Department of Medicine, San Francisco Veterans Affairs Health Care System, San Francisco, California.
Merritt H RaittSection of Cardiology, Department of Medicine, Veterans Affairs Portland Health Care System, Portland, Oregon; Knight Cardiovascular Institute, Oregon Health and Sciences University, Portland, Oregon.
Mary A WhooleyUniversity of California San Francisco School of Medicine, San Francisco, California; Section of General Internal Medicine, Department of Medicine, San Francisco Veterans Affairs Health Care System, San Francisco, California.
Sanket S DhruvaSection of Cardiology, Department of Medicine, San Francisco Veterans Affairs Health Care System, San Francisco, California; University of California San Francisco School of Medicine, San Francisco, California. Electronic address: sanket.dhruva@ucsf.edu.

Funding

Measurement Science QUERII50HX003266 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI COHEN, BETH, KALTENBACH, TONYA R · 2021 to 2021
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Improving Safety of Cardiovascular Implantable Electronic Devices in VeteransIK2HX003357 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI Sanket S Dhruva · 2022 to 2026
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HSRD VA I50 HX003266HSRD VA IK2 HX003357
6 · The paper itself

Abstract

Cardiovascular implantable electronic devices (CIEDs) monitor physiologic variables that could identify subacute heart failure (HF) decompensation and impending HF hospitalization. One such algorithm uses measurements from the previous 30 days of CIED remote monitoring data to predict low-, medium-, or high-probability of HF hospitalization in the next 30 days. We sought to understand how to prospectively implement the use of such algorithms in routine HF care. From January 18, 2024 to April 19, 2024, HF risk categories were predicted from scheduled remote transmissions every 30 days and from unscheduled transmissions for all patients at 2 distinct cardiology clinics. Clinicians contacted and assessed patients at high risk regarding symptoms and then provided an empiric 3-day diuretic intervention (initiation or dose augmentation), adjusted guideline-directed medical therapy, or performed other clinical action as appropriate. Among 358 patients with 1,140 remote transmissions, 72 (20%) had ≥1 transmission categorized as high-risk. The mean patient age was 72.8 years, 346 (97%) were male, and 221 (62%) had a pre-existing diagnosis of HF. Of these 72 patients, 67 (93%) were successfully contacted, 34 (51%) had no HF symptoms, 24 (36%) had mild to moderate symptoms, and 2 (3%) had severe symptoms. A total of 46 patients (69%) had clinical action taken, including 28 (42%) with a diuretic intervention and 12 (18%) with guideline-directed medical therapy augmented. In this implementation study, clinicians contacted and assessed nearly all patients at high risk for HF decompensation based on CIED remote monitoring data and intervened in more than 2/3s. A randomized clinical trial is needed to determine whether this algorithm and subsequent intervention improves clinical outcomes.

Indexed as

AlgorithmsDefibrillators, ImplantableHeart FailureAgedAged, 80 and overCardiac Resynchronization Therapy DevicesDiureticsFemaleHospitalizationHumansMaleMiddle AgedProspective StudiesRemote Sensing TechnologyRisk AssessmentDiureticscardiovascular implantable electronic deviceheart failureheart failure hospitalizationimplementation

Identifiers

PMID39395594
PMCPMC11645256

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.