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Frontiers in Cardiovascular Medicine logoLink to Frontiers in Cardiovascular Medicine
. 2026 May 29;13:1734567. doi: 10.3389/fcvm.2026.1734567

Integrating remote CIED monitoring into heart failure care: evidence, challenges, and opportunities

Raimondo Calvanese 1,*, Carmen D'Amore 1, Claudio Capobianco 1, Francesco Di Fraia 2, Michelangelo Canciello 1, Bernardino Tuccillo 1
PMCID: PMC13260272  PMID: 42291565

Abstract

Remote monitoring (RM) of cardiac implantable electronic devices (CIEDs) has evolved from simple device integrity checks to a cornerstone of personalized heart failure (HF) management. By enabling early detection of subclinical deterioration, CIED-based RM supports proactive clinical interventions, potentially reducing hospitalizations and improving outcomes. Multiparametric algorithms such as HeartLogic, TriageHF, and HeartInsight integrate hemodynamic and arrhythmic parameters to predict HF events with good sensitivity. However, despite increasing evidence of clinical and economic benefits, RM implementation remains inconsistent due to heterogeneous protocols, data latency, and inadequate reimbursement structures. This review summarizes current evidence, operational challenges, and future opportunities for integrating remote CIED monitoring into comprehensive HF care pathways, highlighting the role of artificial intelligence and the need for standardized workflows and reimbursement models.

Keywords: cardiac implantable electronic devices, heart failure, HeartInsight, HeartLogic, remote monitoring, telemedicine, TriageHF

Introduction

Heart failure (HF) is a clinical syndrome associated with substantial morbidity and mortality and remains one of the leading causes of hospitalization worldwide. Rates of rehospitalization are high: approximately 25%–30% of patients are readmitted within one year after discharge, and up to 50% within three years (1–3). According to data from clinical registries and recent trials, an estimated 10%–15% of patients with severe or advanced HF in the United States and Europe carry a cardiac implantable electronic device (CIED); in the most recent trials in HF with reduced ejection fraction (HFrEF), this prevalence reaches ∼30% (4, 5). In recent years, multiparametric monitoring of patients with CIEDs has enabled both verification of device functional status and early detection of subclinical pathophysiological changes that precede HF worsening.

Purpose of the review

The objective of this narrative review is to evaluate the current state of the art in remote monitoring for heart failure via Cardiac Implantable Electronic Devices (CIEDs), highlighting the primary distinctions among commercially available algorithms regarding their underlying technology and clinical evidence. Furthermore, this work provides an in-depth analysis of the organizational frameworks and the prevailing barriers to their implementation within the Italian healthcare system. We conducted a research of the Medline database via PubMed, and of the Coachrane Library for studies published between 2010 and 2025, focusing on remote monitoring of heart failure through implantable devices. The search strategy employed a combination of keywords and MeSH terms, including ‘remote monitoring’, ‘heart failure’, and ‘implantable devices’. In addition, a search of the ClinicalTrials.gov registry was performed to identify primary ongoing trials on the subject.

Management of alerts in patients with CIEDs

Remote monitoring (RM) programs for patients with CIEDs require predefined alert hierarchies and response times. Most alerts involve findings that do not require immediate action (e.g., atrial fibrillation detection), whereas alerts related to device integrity or clinically relevant arrhythmias (e.g., ventricular arrhythmias) necessitate prompt intervention (6). Arrhythmic alerts—including delivered shocks or anti-tachycardia pacing (ATP)—not only indicate increased risk of further arrhythmias but may also signal lead integrity problems.

Each RM center should, based on its local resources, establish and disseminate clear protocols that define: (i) time allocation for daily/weekly alert review, (ii) criteria for patient contact and escalation, and (iii) division of responsibilities within the multidisciplinary team.

Alerts are commonly categorized into two priority levels (Figure 1): (i) red alerts, generated by warnings concerning device function (e.g., low battery, abrupt impedance changes, shocks), which require rapid intervention; and (ii) yellow alerts, indicating conditions that warrant attention (e.g., gradual increase in capture threshold) and typically allow deferred intervention (Table 1).

Figure 1.

Infographic categorizing pacemaker and ICD alerts into red and yellow levels, listing device integrity and clinical alarms for each. Red alerts indicate critical issues like low battery, safety mode, therapy delivery, or out-of-range impedance, while yellow alerts suggest conditions like replacement recommendations, arrhythmia detection, or pacing abnormalities. Each section specifies criteria for both device and catheter concerns, with additional pacing and arrhythmia details included for yellow alerts.

Red (high-priority) and yellow alerts related to clinical events and device integrity in patients with pacemakers and defibrillators. AF, atrial fibrillation; ATP, anti-tachycardia pacing; LV/RV/RA, left/right ventricle/right atrium; NSVT, non-sustained ventricular tachycardia; PM, pacemaker; VF, ventricular fibrillation.

Table 1.

Examples of red and yellow alerts and suggested actions for patients with pacemakers and defibrillators. (See source file for full operational details.).

PACEMAKER
Red Alerts Actions to take
Low battery Voltage
  • Intensify remote controls

  • Schedule PM replacement

PM in Safety Mode (Reset)
  • In-person check for exit from safety mode

Pacing Impedance out of range
  • in-person control

Signs of catheter breakage (Noise) In -person Control
  • Check for EMI (Electromagnetic Interference)

  • EC Breakage: consider implanting a new catheter

Yellow Alerts Actions to take
Battery replacement Schedule replacement in adequate time
MRI Mode Check exit from MRI mode
Non-PM dependent patients
  • Low voltage battery

  • Reset mode

  • Intensify checks/schedule Substitution

  • In-person checks

  • Pacing impedance RA/RV/LV out of range

  • Check the impedance trend/Possible EC replacement

  • RA/RV/LV Pacing thresholds out of range

  • Check pacing threshold trends/Change polarity pacing

  • Noise episode

  • Check Impedances/Correlations with EMI/Break/Change polarity pacing

  • AF burden greater of threshold value

  • OAT evaluation/ Antiarrhythmic therapy evaluation/ Cardioversion

  • NON-sustained Ventricular Tachycardia

  • Clinical evaluation

  • RV pacing percentage greater than the threshold value

  • Clinical evaluation

  • A-V delay modification

  • Upgrading to CRT

  • CRT pacing less than programmed value

  • Clinical Evaluation

  • Atrial Fibrillation: AV Node Ablation

  • AV Delay Modification

  • High PVC Burden: Antiarrhythmic Therapy/Ablation

DEFIBRILLATORS
Red Alerts Recommended Actions
VT-FV detection OFF
  • In-person visit in a short time

End of Life/Low Energy
  • Schedule replacement quickly

Long charging times
  • Intensify checks/Plan replacement

Shock impedance out of range
  • Check trends/Intensify checks/Visit in person

RV lead impedance out of range
  • In-person control:

Noise Episode In person visit:
  • Check for EMI (Electromagnetic Interference)

  • lead fracture

Yellow Alerts Recommended Actions
Replacement recommended
  • Plan replacement

MRI mode
  • Check

RA/RV/LV Pacing thresholds out of range
  • Check trends/Possible EC replacement

Pacing thresholds out of range
  • Check trends/Programming changes/EC replacement

Single shock delivered
  • Contact patient/Intensify checks

ATP delivered
  • Contact patient/Intensify checks

AF burden greater than programmed value
  • Check OAC indication

Ventricular rate in Atrial Arrhythmia greater than programmed value
  • Contact patient/Check adherence to therapy/Clinical evaluation

NSVT in selected patients
  • Intensify checks in relation to the patient

Percentage of RV pacing greater than programmed value
  • Clinical evaluation (upgrading to CRT/programming changes)

Percentage of biventricular pacing less than programmed value
  • Clinical evaluation

  • Atrial fibrillation: Antiarrhythmic therapy/PV ablation/AV node ablation

  • PVC: Antiarrhythmic therapy/ablation

Typical responses to device alerts include:

  • Calling the patient for a rapid in-clinic evaluation (e.g., repeated shocks, battery depletion, suspected lead fracture);

  • Advancing a scheduled outpatient visit according to alert urgency;

  • Intensifying remote checks when parameter changes do not require immediate action;

  • Tailoring alert programming to the individual patient to avoid unnecessary workload (e.g., disabling atrial fibrillation alerts in patients with permanent AF).

For pacemakers, routine remote transmissions are recommended every 3–12 months; for implantable cardioverter–defibrillators (ICDs), every 3–6 months. As the device approaches elective replacement, transmission frequency should increase to every 1–3 months (6). While RM systems share common principles, they differ substantially in philosophy and practical implementation, including the type and number of programmable alerts.

Rationale for remote monitoring in heart failure

CIED-based RM in HF supports early detection of clinical and subclinical deterioration, enables proactive and individualized care, may reduce healthcare utilization and costs, and enhances patient engagement. HF is characterized by progressive worsening, increasing hospitalizations, and declining quality of life (7, 8). Each acute decompensation worsens prognosis and is associated with markedly increased short-term mortality and the risk of rehospitalization (9, 10). Given the high rehospitalization burden and the substantial proportion of patients with HFrEF who carry CIEDs (4, 5), a structured CIED-based RM program is an attractive strategy to mitigate risk.

Parameters derived from CIEDs—such as surrogates of fluid status and arrhythmia burden—help clinicians identify trajectories suggestive of impending decompensation, as well as conditions that could precipitate inappropriate shocks or compromise therapies that modify prognosis (e.g., suboptimal biventricular pacing). By detecting changes early, healthcare teams can adjust therapy promptly, potentially preventing hospitalization and improving outcomes.

RM also facilitates more precise, up-to-date assessments of day-to-day status than periodic in-person visits, allowing clinicians to optimize medications, advise on lifestyle, and consider additional interventions based on objective data trends. From an economic perspective, the growing HF burden is straining health systems: in the United States, total HF-related medical costs were projected to rise from US$20.9 billion in 2012 to US$53.1 billion by 2030 (11). In Italy, the average cost per HF admission is ∼€3,200, with an annual burden of ∼€550 million for acute HF admissions (12). By enabling timely interventions and reducing avoidable hospital encounters, CIED-based RM can contribute to cost containment (13).

Algorithms for remote monitoring of heart failure

Early experiences with CIED-based remote monitoring for HF were largely based on single-parameter strategies, most notably intrathoracic impedance monitoring. The OPTILINK HF trial (14) was one of t the first studies that investigated whether impedance-guided remote monitoring could improve outcomes in patients with chronic HF implanted with ICD or CRT-D devices. In this multicenter, randomized trial, automatic alerts were generated when predefined impedance thresholds were crossed, prompting clinical review and potential therapeutic intervention. However the study didn't show a significant reduction in the primary composite endpoint of all-cause mortality or cardiovascular hospitalization compared with standard care. These neutral results were likely influenced by the limited specificity of impedance as a standalone marker of congestion, variability in alert-driven clinical responses across centers, and the multifactorial pathophysiology of HF decompensation, which cannot be adequately captured by a single physiological signal. Importantly, the OPTILINK experience highlighted the limitations of single-sensor monitoring strategies and provided the basis for the development of contemporary multiparametric algorithms, by integrating congestion surrogates with autonomic, arrhythmic, and activity-related parameters. These new systems allow to improve predictive accuracy, reduce false-positive alerts, and enhance clinical interpretability, thereby enabling more timely and targeted interventions.

Three commonly used multiparametric algorithms support early detection of HF events: HeartLogic (15, 16), TriageHF (17, 18), and HeartInsight (derived from SELENE-HF) (19–21). These tools integrate multiple device-derived signals into a composite index that correlates with short-term HF risk, enabling proactive outreach (Figure 2). Patients in an alert state have higher risk of HF events, atrial fibrillation events (19), and mortality (20).

Figure 2.

Flowchart illustrating the sequence from alerts to assessment to actions in a clinical setting. Blue boxes show alert transmission, alert evaluation, patient contact, therapy compliance, ongoing monitoring, and resulting clinical actions such as heart failure management.

Suggested algorithm for the management of an HF alert generated by CIED-based remote monitoring.

Typical sensing inputs include first and third heart sounds (S1/S3), respiration rate and rapid shallow breathing index, thoracic impedance, day- and night-time heart rate, patient activity, ventricular ectopy, and atrial tachyarrhythmia burden. These sensors can capture HF pathophysiology before patients perceive symptoms.

Operationally, when a composite index exceeds a programmed threshold, an alert is sent to the RM team (e.g., via email/SMS). Clinicians review the dashboard to identify the dominant contributors and, after clinical triage, contact the patient to assess symptoms, adherence, and potential triggers, and to adjust therapy or behaviors as appropriate.

Subsequent remote checks allow rapid assessment of the response to the intervention without an excessive workload increase.

Physiological and device-derived inputs include first and third heart sound (S1/S3), respiratory rate, day and night heart rate trends, patient activity, atrial arrhythmia burden, and thoracic impedance. These sensors can capture HF pathophysiology before patient perceive symptoms.

Depending on the system, they may generate a clinical alert, when the composite index exceeds a programmed threshold, or classify patients into predefined risk stratification to indicate potential clinical worsening.

  • HeartLogic (Boston Scientific): combines S3/S1 heart sounds, thoracic impedance, activity level, night heart rate, and respiratory rate into a single index. A nominal threshold of 16 is commonly used to balance sensitivity and specificity; crossing the threshold indicates elevated risk of an HF event within ∼34 days, with ∼70% sensitivity (16, 19). When the heartLogic index crosses the threshold, an alert was notify to the center. Alert review provides transparency on sensor contributions to guide targeted actions (e.g., optimizing decongestive therapy when thoracic impedance trends suggest fluid accumulation).

  • HeartInsight (Biotronik; implementation following SELENE-HF): the score integrates baseline clinical parameters with temporal trends in seven monitored variables (24-hr and nocturnal mean heart rate, atrial fibrillation burden, daily activity, heart rate variability, ventricular extrasystoles, and thoracic impedance). An automatic alert is generated when three consecutive transmissions yield a score ≥ the nominal threshold (NT = 45). The alert resets when the score falls below a recovery threshold (NT−10). An NT of 45 is recommended as the default (21).

Triage-HF (Medtronic): combines several physiological and device-derived signals, including nocturnal heart rate, patient physical activity, burden of atrial tachyarrhythmias, heart rate trends, and thoracic impedance to generate a stratified risk score (low, medium, or high) to identify early signs of clinical worsening

Management of the HF alert: are we aligned?

Despite the promise of RM, real-world implementation remains heterogeneous, and evidence-based, scalable follow-up protocols are limited. Programs differ in timing and modality of patient contact, criteria for remote therapy adjustment, use of natriuretic peptide testing, and scheduling of in-person assessments. While BNP/NT-proBNP have established roles in HF prognostic stratification and dyspnea evaluation, their role in longitudinal monitoring is debated due to conflicting data: in HFrEF, rapid BNP increases may not predict exacerbations as reliably as in HF with preserved EF (HFpEF). Nevertheless, changes in natriuretic peptides can complement CIED alerts and enhance positive predictive value (16, 22, 23). When feasible, obtaining NT-proBNP in association with specific HF alerts and comparing to baseline may increase protocol sensitivity, recognizing that device-based indices can change well before symptoms.

Importantly, recent evidence suggests that the clinical benefit of RM depends less on the monitoring technology itself and more on the presence of timely, structured clinical reactions to alerts. As showed in a post hoc analysis of OPTILINK study (24), remote monitoring was associated with improved outcomes only when alerts triggered appropriate medical action, including therapy optimization and clinical reassessment. In that study, patients who were appropriately contacted following an alert experienced a significant reduction in the primary endpoint of cardiovascular death or first hospitalization [hazard ratio, 0.61 (95% CI, 0.39–0.95); P = 0.027] compared with those receiving usual care o not appropriate responce. Thus, passive monitoring without organized reaction pathways appears to provide limited benefit. In this context, two studies have specifically explored alert-triggered therapy adjustments.

These studies have explored remote, alert-triggered therapy adjustments. In the MANAGE-HF study (25), 200 patients with hFrEF and cardiac resynchronization therapy or/and implantable cardioverter implants were followed up using the HeartLogic algorithm (Boston Scientific). Early intervention, triggered by alerts, led to a rapid reduction in the HeartLogic index and a decrease in NTproBNP values (1316 pg/mL baseline vs. 1316 pg/mL 12-month visit, p < 0.001). Although the early intervention consisted of a medication augmentation (primarily increased diuretic doses) in 74% of cases, the study highlighted the high heterogeneity of intervention protocols, which varied by center and patient. This procative intervention was associated with a 67% reduction in hHF compared to prestudy rates (Hernandez AF, Albert NM, Allen LA et al. Multiple cardiac sensors for management of heart failure (MANAGE-HF) Phase I results. Abstract presented/published at: ESC-HF 2021. June 29-July 1, 2021. Virtual.).

In INTERVENE-HF (18), TriageHF-guided outreach prompted brief diuretic uptitrations with frequent normalization of thoracic impedance. Across studies, diuretic optimization is the most common immediate intervention. Although the search for robust scientific evidence remains ongoing, it is essential to acknowledge that the significant pathophysiological heterogeneity underlying acute heart failure—coupled with the diverse clinical profiles of patients with varying cardiac etiologies—makes it challenging to standardize a universal therapeutic protocol.

The widespread adoption of remote monitoring for heart failure via CIEDs faces significant challenges that, at present, remain unresolved. The implementation of organizational algorithms, their reimbursement, and subsequent clinical application are contingent upon health policies rooted in robust scientific evidence. Currently, such evidence remains elusive, particularly regarding ‘hard' endpoints—such as mortality reduction—which are difficult to demonstrate due to the extensive heterogeneity of both available technological tools and the structural organization of individual healthcare facilities. Organizational gaps further limit impact. Community-based care integration is often lacking, despite its potential to improve adherence and relieve central RM teams.

Variability across regions and countries complicates standardization and, critically, reimbursement policies remain inconsistent and often inadequate, impeding comprehensive RM adoption.

Obstacles to the diffusion of RM in Italy

RM is considered standard of care for CIED follow-up in many contemporary recommendations (26). However, rapid growth in RM enrollment—accelerated during the COVID-19 pandemic—has strained staffing and workflows without commensurate reimbursement in many European jurisdictions and Italian regions (27–29). Even where expert consensus provides pragmatic recommendations (6), gaps persist in enrollment coordination, maintenance of connectivity, and device programming for optimal RM (30). Alert interpretation models—particularly for HF alerts—are not standardized, and inconsistent response strategies have yielded conflicting outcomes (31, 32). Data latency introduces further bias: availability at the monitoring center may lag device detection due to connectivity issues or delays in review and escalation (33). Late RM activation and suboptimal connectivity exacerbate the problem and perpetuate reliance on in-person visits (29, 34). A structured workflow—preferably a centralized monitoring unit with trained staff operating a hub-and-spoke model—can improve outcomes (33, 35). Despite heterogeneous use (more frequent in ICD/CRT recipients) and uneven reimbursement (e.g., Germany), RM is generally cost-saving compared with exclusive in-clinic follow-up (36). In Europe, lack of adequate reimbursement remains the principal barrier—reported by up to 40% of centers post-COVID-19 and by up to 73% in Italy—while only 10 of 20 Italian regions currently provide tariffs for remote CIED management [(26, 34); Table 2].

Table 2.

Overview of reimbursement for RM across European countries, including tariffs for in-clinic checks, remote CIED management, dedicated hardware/services, and HF disease management.

Country Reimbursement tariff for in-clinic device check Reimbursement tariff for remote CIED management Reimbursement specific for hardware and services for remote monitoring Reimbursement tariff for HF disease management
Austria Y N N Y
Belgium Y N N N
Bulgaria N N N N
Czech Republic Y Y Y N
Denmark Y Y N N
Finland Y Y Y N
France Y Y Y N
Germany Y Y (only ICDs and CRTs) Y (for some health ensurances) N
Hungary Y Y N N
Italy Y Y (in 10 out of 20 regions) N N
Norway Y Y N N
Poland N N N N
Portugal Y Y N Y
Russia N N N N
Slovakia N N N N
Spain Funded, no tariff Funded, no tariff N/A N
Sweden Y Y N N
Switzerland Y Y Y Y
The Netherlands Y Y N Y
UK Y Depending on Clinical Commissioning Groups and NHS Trusts Ordered by NHS Trusts N

Toward a new era in the management of HF

Over the past two decades, RM of CIEDs has evolved from intermittent device integrity checks to continuous, AI-enabled analysis of arrhythmic and hemodynamic parameters. Multiparametric scores predict short-term risk of HF events with reasonable sensitivity (e.g., ∼70%), but unexplained alert rates remain non-trivial (15). Augmenting baseline risk stratification (e.g., Seattle HF Model) and applying AI-based post-processing may reduce false alerts (19). At the same time, optimal clinical response strategies are still being defined. In MANAGE-HF (25), clinicians assessed triggers within three days and escalated therapy as needed—most commonly diuretic intensification, but also guideline-directed medical therapy (GDMT) optimization (e.g., ARNI, ACEi/ARB, MRA, SGLT2i) when appropriate (37). Early decongestive escalation shortened alert duration, whereas systematic GDMT uptitration was less consistently implemented.

Given the robust benefits of disease-modifying agents—often evident within 10–20 days (38, 39)—clinicians should consider prioritizing GDMT optimization when alerts occur in the absence of overt congestion. A recent meta-analysis reported that device-guided, congestion-based management reduced the composite of all-cause mortality and HF hospitalization vs. standard care (40).

Importantly, RM represents an opportunity in elderly patients management (41). In fact RM is associated with high adherence rates, reduced need for in-person visit and allows an early detection on actionable events. However, specific challenges emerged including cognitive impairment, caregiver dependence e higher comorbidity burden, factors that may influence alert transmission and interpretation and therapeutic responsiveness. Thus, it is crucial to develop strategies to enhance the use of RM in this vulnerable group, implementing these approaches in individuals with neurocognitive disorders and visual or hearing impairments continues to present significant challenges. All these challenges could potentially be easly addressed with the support of artificial intelligence.

Economic evaluations, including the randomized EVOLVO trial (42) and subsequent studies (43, 44), showed that RM reduces urgent visits and overall in-hospital encounters, with shorter decision delays after device-detected events—likely contributing to fewer visits and lower costs. According to a recent systematic review of clinical, cost-effectiveness quality of life and cost outcomes, an advantage in terms of cost-effectiveness has been proved for HeartLogic and TriageHF, compared to the respective cardiac implantable electronic device without these algorithms, though available evidence was often of low quality (45).

Future research should focus on pragmatic trials that test standardized, alert-driven care pathways; quantify the incremental value of AI vs. clinician-led triage; and rigorously evaluate cost-effectiveness and reimbursement models, particularly in the rapid growing very elderly HF population.

Acknowledgments

The authors thank the staff of Ospedale del Mare and Azienda Ospedaliero Universitaria San Giovanni di Dio Ruggi d'Aragona for their contribution to patient care and support of the remote monitoring program. The authors also acknowledge the editorial assistance provided for language revision.

Funding Statement

The author(s) declared that financial support was not received for this work and/or its publication.

Footnotes

Edited by: Matteo Cameli, University of Siena, Italy

Reviewed by: Roberto Scacciavillani, Agostino Gemelli University Polyclinic (IRCCS), Italy

Marialuisa Sveva Marozzi, University of Bari Aldo Moro, Italy

Abbreviations AI, artificial intelligence; AF, atrial fibrillation; ARB, angiotensin receptor blocker; ACEi, angiotensin-converting enzyme inhibitor; ARNI, angiotensin receptor–neprilysin inhibitor; ATP, anti-tachycardia pacing; CIED, cardiac implantable electronic device; CRT, cardiac resynchronization therapy; CRT-D, cardiac resynchronization therapy defibrillator; GDMT, guideline-directed medical therapy; HF, heart failure; HFrEF, heart failure with reduced ejection fraction; HFpEF, heart failure with preserved ejection fraction; ICD, implantable cardioverter–defibrillator; NT, nominal threshold; NT-proBNP, N-terminal pro-B-type natriuretic peptide; RM, remote monitoring.

Author contributions

RC: Funding acquisition, Visualization, Project administration, Writing – original draft, Resources, Validation, Formal analysis, Supervision, Writing – review & editing, Conceptualization, Software, Data curation, Methodology, Investigation. CD: Writing – original draft. CC: Conceptualization, Methodology, Writing – review & editing. FD: Data curation, Investigation, Writing – review & editing. MC: Writing – review & editing, Investigation. BT: Investigation, Writing – review & editing.

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that generative AI was not used in the creation of this manuscript.

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