Evidence map›Paper›PMID 36713022›Full record

ArticleEuropean heart journal. Digital health2022

Daily ambulatory remote monitoring system for drug escalation in chronic heart failure with reduced ejection fraction: pilot phase of DAVID-HF study.

Chun Ka Wong, Ka Chun Un, Mi Zhou, Yangyang Cheng, Yuk Ming Lau, Puigi Catherine Shea, Hin Wai Lui, Ming Liang Zuo, Li Xue Yin, Esther W Chan and 12 more

2 registry-linked trialsAbstract read
In one paragraph

Article in European heart journal. Digital health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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.

NCT06671171 completednot on this mapstarted 2025, after this paper: background citation

Wearable Assessment of Thoracic, Cardiac Health and Exercise Performance Trial

TypeobservationalSponsorThe University of Hong KongRan2025 to 2026Enrolled50ConditionsCongenital Heart Disease, Pulmonary Hypertension, Heart Failure, Coronary Artery DiseaseArmsApple Watch Series 9
NCT07663799 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Wearable Assessment of Thoracic, Cardiac Health and Exercise Performance Trial Prospective (WATCH-XP)

TypeobservationalSponsorThe University of Hong KongRan2026 to 2028Enrolled20ConditionsCongenital Heart Disease, Pulmonary Hypertension, Heart Failure, Coronary Heart Disease (CHD)ArmsApple Watch Series 9
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

22 authors.

Chun Ka WongDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-5205-9440
Ka Chun UnDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Mi ZhouDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Yangyang ChengDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Yuk Ming LauDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Puigi Catherine SheaDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Hin Wai LuiDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Ming Liang ZuoDepartment of Echocardiography & Non-invasive Cardiology Laboratory, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.
Li Xue YinDepartment of Echocardiography & Non-invasive Cardiology Laboratory, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.
Esther W ChanCentre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Ian C K WongCentre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Simon Wai Ching SinRespiratory Division, Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Pauline Pui Ning YeungRespiratory Division, Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Hao ChenBiofourmis Singapore Pte Ltd, Singapore, Singapore.
Sandi WibowoBiofourmis Singapore Pte Ltd, Singapore, Singapore.
Tong Li Nikki WeiBiofourmis Singapore Pte Ltd, Singapore, Singapore.
Sze Ming LeeHarmony Medical Inc., Hong Kong SAR, China.
Augustine ChowHarmony Medical Inc., Hong Kong SAR, China.
Raymond Cheuk Fung TongHarmony Medical Inc., Hong Kong SAR, China.
Jojo HaiDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Frankie Chor Cheung TamDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Chung Wah SiuDivision of Cardiology, Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: Underutilization of guideline-directed heart failure with reduced ejection fraction (HFrEF) medications contributes to poor outcomes. Methods and results: A pilot study to evaluate the safety and efficacy of a home-based remote monitoring system for HFrEF management was performed. The system included wearable armband monitors paired with the smartphone application. An HFrEF medication titration algorithm was used to adjust medication daily. The primary endpoint was HFrEF medication utilization at 120 days. Twenty patients (60.5 ± 8.2 years, men: 85%) with HFrEF were recruited. All received angiotensin-converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB)/angiotensin receptor-neprilysin inhibitor (ARNI) at recruitment; 45% received ≥50% maximal targeted dose (MTD) with % MTD of 44.4 ± 31.7%. At baseline, 90 and 70% received beta-adrenergic blocker and mineralocorticoid receptor antagonist (MRA), 35% received ≥50% MTD beta-adrenergic blocker with % MTD of 34.1 ± 29.6%, and 25% received ≥50% MTD MRA with % MTD of 25.0 ± 19.9%. At 120 days, 70% received ≥50% MTD ACEI/ARB/ARNI ( Conclusion: Heart failure with reduced ejection fraction medication escalation with remote monitoring appeared feasible.

Indexed as

Drug escalationHeart failureTelemonitoring

Identifiers

PMID36713022
PMCPMC9708020

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Registered trials

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.