# Remote Management of Patients With Heart Failure in Medically Underserved Areas

**Authors:** Jeremy Florence, Sylvain Ploux, Clément Riocreux, F. Daniel Ramirez, Solenn Toupin, Théo Pezel, Guillaume Clerfond, Romain Eschalier

PMC · DOI: 10.1016/j.jacadv.2026.102676 · 2026-03-19

## TL;DR

A remote management program for heart failure patients in underserved areas showed similar outcomes to those in non-underserved areas.

## Contribution

Demonstrates effectiveness of remote heart failure management in medically underserved areas in Europe.

## Key findings

- No significant difference in hospitalization or mortality rates between patients in underserved and non-underserved areas.
- Remote monitoring outcomes were consistent across medically underserved and non-underserved regions.
- MUAs were not associated with the primary outcome after adjusting for covariates.

## Abstract

Medically underserved areas (MUAs) are associated with higher rates of hospitalizations and mortality. Although structured remote management (RM) programs demonstrated clinical benefits, their effectiveness in MUAs in Europe remains scarcely investigated.

The objective of the study was to assess whether heart failure (HF) patients derive similar outcomes from a structured, multiparametric, RM program irrespective of MUA designation.

Consecutive patients enrolled in a standardized, multiparametric, HF RM program between April 2020 and December 2022 in 2 French regions (Auvergne Rhône-Alpes and Nouvelle-Aquitaine) at 2 French university hospitals were included in the study. Inclusion criteria were chronic HF with ≥1 episode of HF hospitalization within the last year or NYHA functional class ≥II associated with an elevated B-type natriuretic peptide. Patient assessments were performed remotely with body weight, blood pressure, heart rate, symptoms, biology, and data from cardiac implantable electronic devices. The primary outcome was the composite of unplanned HF hospitalization or all-cause mortality.

Among 1,040 patients (mean age 72 ± 12 years, 70% male), 32% lived in MUAs. The median follow-up was 20 (IQR: 10-24) months. The annualized rate of the primary outcome was 13.7% (95% CI: 11.9-15.9) in the overall population, with no significant difference between MUAs and no MUAs patients (13.5% [95% CI: 10.3-17.4] vs 13.9% [95% CI: 11.6-16.5]; P = 0.876). MUAs were not associated with the primary outcome (adjusted HR: 0.93; 95% CI: 0.68-1.27; P = 0.84). Using Kaplan-Meier analysis, survival curves showed no difference between MUA and non-MUA patients (P = 0.83).

Our study showed no difference in primary outcome among HF patients enrolled in a structured, multiparametric RM program, irrespective of MUAs.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}
- **Diseases:** impaired quality of (MESH:D060825), atrial fibrillation (MESH:D001281), Deaths (MESH:D003643), malnutrition (MESH:D044342), MUA (MESH:D000069279), dilated cardiomyopathy (MESH:D002311), pulmonary edema (MESH:D011654), anemia (MESH:D000740), cardiogenic shock (MESH:D012770), HF (MESH:D006333), hypertension (MESH:D006973), diabetes (MESH:D003920), ischemic cardiomyopathy (MESH:D009202), COVID-19 (MESH:D000086382), N (MESH:C536108), chronic kidney disease (MESH:D051436)
- **Chemicals:** ACEi (-), digoxin (MESH:D004077), creatinine (MESH:D003404), sacubitril (MESH:C000717211), sodium (MESH:D012964), furosemide (MESH:D005665), urea (MESH:D014508), valsartan (MESH:D000068756), potassium (MESH:D011188)
- **Species:** HF [taxon 2008765], Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019588/full.md

---
Source: https://tomesphere.com/paper/PMC13019588