Preventing avoidable readmissions after transcatheter aortic valve implantation matters clinically and operationally. Patients with aortic stenosis undergoing transcatheter aortic valve implantation often have complex comorbidities, procedural risks, and fragile recoveries. Intensified follow-up aims to identify complications early, streamline care transitions, and reduce unplanned utilization without adding undue burden to patients or teams.
Feasibility findings from PREMISS, a randomized trial assessing intensified follow-up after TAVI, indicate this approach can be delivered safely and consistently, with signals relevant to readmission prevention and patient experience. This article situates those signals within service design, reimbursement strategy, and value-based care priorities, outlining a path to scale, measure, and govern an intensified model across diverse cardiac programs.
In this article
Why readmissions after TAVI matter for programs
Readmissions after TAVI complicate recovery, strain program capacity, and expose systems to avoidable costs and penalties. Beyond procedural success, what follows in the first 30 to 90 days is shaped by comorbidity, discharge readiness, symptom recognition, and access to urgent review. Early complications such as conduction abnormalities, bleeding, vascular issues, or heart failure decompensation can emerge subtly and then escalate quickly. A structured follow-up sequence is designed to close this gap, moving surveillance earlier and closer to home. In this context, feasibility is not a trivial box to tick; it is the operational proof that the model can run, be adhered to, and escalate safely.
The burden of 30-day readmission and drivers
Readmissions are multifactorial, but several drivers are consistent across TAVI cohorts. Clinical contributors include conduction disturbance requiring pacing, vascular access complications, bleeding, and early valve-related issues. Patient and system contributors include multimorbidity, social determinants, fragmented transitions, and variability in symptom triage outside of specialist teams. Programs often rely on a first clinic review weeks after discharge, which can miss early deterioration windows. An intensified, protocolized follow-up model brings timeline discipline and clear escalation pathways to address these drivers.
Where intensified follow-up can intervene
Intensified follow-up targets three windows: the immediate post-discharge period, the early ambulatory phase, and the transition to routine care. In each window, scheduled touchpoints aim to verify symptom trajectories, medication use, wound status, hemodynamics, and rhythm. When signals of risk are detected, timely escalation to a procedural team or local service can prevent a cascade toward admission. The approach also addresses nonclinical frictions, such as pharmacy access or transportation barriers, which are frequent triggers of unplanned care. In sum, the model works because time, frequency, and escalation are standardized rather than left to chance.
Feasibility markers in PREMISS
The PREMISS randomized trial assessed whether frequent, protocolized follow-up is deliverable and safe after TAVI. Feasibility markers typically include patient enrollment and retention, completion of scheduled contacts, timeliness of escalation, and the absence of intervention-related harms. Signals that suggest potential readmission reduction should be interpreted cautiously, because feasibility work is not powered for definitive outcomes. Nevertheless, consistent delivery with high adherence and early detection of issues provides the necessary platform for a scale-up trial anchored in utilization and cost. Details of the trial protocol and feasibility outcomes are available via PubMed.
Designing an intensified follow-up model that scales
Scaling an intensified follow-up service requires standardizing components without sacrificing clinical nuance. Programs should specify minimum contact cadence, escalation rules, and handoffs between procedural teams and community services. A reliable documentation framework must ensure that information is visible where decisions happen, not siloed in call notes. For diverse populations, accessibility and health literacy considerations are integral to engagement, not a downstream add-on. The feasibility signal is the starting line for embedding the model across varied site resources and payer environments.
Core components: frequency, modality, escalation
An intensified model usually combines structured calls, prompt clinic reviews when indicated, and home-based checks. Programs can blend telehealth, nurse-led telephone outreach, and device or symptom monitoring into a single pathway. The cadence should be highest in the first two weeks, then taper as risk falls and routines stabilize. Clear escalation triggers for rhythm change, dyspnea, hypotension, wound concerns, or medication issues reduce decision variability. Documented plans enable any team member to escalate consistently and reduce delays when a signal appears.
Workforce and workflow design
Delivering intensified follow-up depends on well-defined roles and right-skilled staff. Nurse coordinators can manage routine contacts and perform algorithm-based assessments; advanced practitioners can resolve medication or symptom questions; cardiologists can adjudicate complex issues or new-onset complications. A shared workflow and centralized task list help manage volume and avoid duplication. Programs should forecast call volumes and escalation rates to align staffing with throughput. Training must emphasize clinical red flags, communication skills, and the importance of closing every loop.
Data, risk stratification, and digital tools
Risk-tuned intensity improves efficiency by focusing resources where they have the greatest impact. Baseline variables such as conduction disease, anemia, renal function, and access-site complexity can inform risk tiers. Applying risk stratification at discharge helps decide cadence and the threshold for in-person review. Integrating remote monitoring for blood pressure, weight, and rhythm can surface silent deterioration when patients feel well. The data layer should support a live dashboard with alerts, trend views, and a concise narrative of recent contacts to support rapid clinical decisions.
Safety, equity, and patient experience
Safety needs explicit guardrails. Escalation within hours for concerning symptoms, same- or next-day procedural team access, and clear emergency instructions are nonnegotiables. To ensure equity, outreach should accommodate language, sensory, cognitive, and social barriers, with options for caregivers to participate. Intentional scheduling reduces no-shows, and backup channels, such as text reminders or community nurse visits, improve reach. Measuring the patient voice through satisfaction, burden of contact, and perceived coordination informs pathway refinements. When intensified models work, patients feel connected rather than surveilled.
Interface with transitional care and primary care
Intensified follow-up sits alongside, not instead of, existing transitions support. Linking with transitional care teams ensures that medication, wound, and rehabilitation needs do not fall between services. Timely communication with primary care clinicians safeguards continuity once the early risk window closes. Shared care plans, visible in the electronic record, clarify who handles what after discharge. Because TAVI patients often live with frailty, functional goals and caregiver support should be included in every plan. Smoother interfaces reduce friction that otherwise drives unplanned utilization.
Financing, metrics, and policy levers
Feasibility opens the door to implementation science, financing models, and measurement frameworks. Systems need to decide how to fund outreach staff, technology, and same-day escalation capacity. Payers and providers will ask whether reduced unplanned care offsets program costs and whether total cost of care moves in the right direction. Early planning for billing, contracting, and performance reporting shortens the time from pilot to standard of care. Aligning these elements with existing policy levers increases the odds of durability.
Aligning with value-based care and readmission penalties
Intensified follow-up is naturally compatible with performance programs focused on utilization and outcomes. In shared savings, bundled payment, or accountable care constructs, lower readmissions and emergency visits strengthen the financial case. Where readmission penalties or public reporting apply, a reliable pathway reduces variability in post-acute care. Standardized follow-up also supports quality domains such as safety, coordination, and patient experience. Programs pursuing quality improvement accreditation can anchor improvement cycles around pathway adherence and escalation timeliness.
Reimbursement pathways and coding
Funding options depend on jurisdiction and payer mix. In many systems, combinations of transitional care management, chronic care management, remote physiologic monitoring, and tele-visit codes can support pieces of the model. Institutional support often covers coordinator time when pathway value is demonstrated via reduced bed-days or avoided readmissions. Bundles that include the procedural episode can build outreach and escalation into the expected cost. Documenting services precisely and capturing time-based codes where allowed are critical to sustainability.
Capacity management and hospital operations
Intensified follow-up can positively influence capacity if it reduces unscheduled returns and lengths of stay. However, programs must plan for the counterfactual: identified issues often trigger earlier planned care, same-day clinics, or device checks. By diverting what would have been overnight admissions into ambulatory care, operations can net a capacity gain. Short-notice procedural time, rapid access slots, and a small pool of observation beds help absorb escalations safely. Coordination with inpatient and catheterization lab leaders prevents new bottlenecks as the ambulatory pathway grows.
Governance, data sharing, and accountability
Governance should define ownership, escalation authority, and data-sharing rules across sites. Since TAVI programs often span networks, consistent documentation and registries allow benchmarking of adherence and outcomes. An operational dashboard that displays pathway fidelity, time-to-escalation, and unplanned utilization supports continuous oversight. Regular case reviews surface near misses and learning opportunities before they become patterns. Transparency with stakeholders builds trust that the model improves safety and utilization, not just metrics.
Measuring what matters
The core utilization outcomes are 30-day and 90-day readmissions, emergency department visits, and observation stays. Safety outcomes include mortality, serious adverse events, and delays in care following triage. Process outcomes include reach and response rates, time-to-escalation, and completion of planned contacts. Patient-reported outcomes and experience measures align the model with person-centered care. Economically, total cost of care, episode cost, and net savings per 100 patients frame budget impact and payer negotiations.
Equity, access, and digital divide
Intensified models risk widening disparities if they assume device access, stable housing, or always-available caregivers. Designing for low-bandwidth channels, multilingual materials, and alternative contact methods reduces exclusion. Offering in-person or home-visit options ensures those with limited technology are not left behind. Programs should monitor outcome and process metrics by sociodemographic strata to detect inequalities early. Equity-focused refinements are not ancillary; they are central to safety and effectiveness.
Implementation road map and change management
Successful adoption begins with a pilot that stress-tests cadence, staffing, and escalation. Clearly define inclusion criteria, contact scripts, and decision trees, then run iterative plan-do-study-act cycles. Parallel workstreams should finalize billing pathways, operations agreements, and data dashboards before scale-up. Leadership sponsorship and clinical champions are essential to sustain momentum during the first quarters. As the model stabilizes, formalize training, competency checks, and audit-feedback to maintain fidelity.
Research priorities after a feasibility signal
Following feasibility, the next step is a powered effectiveness evaluation anchored in utilization and patient-centered outcomes. Randomized or pragmatic designs can test reductions in readmissions, emergency visits, and total cost, while tracking safety and mortality. Subgroup analyses should examine higher-risk strata, including those with conduction disease, renal impairment, or complex access management. Incorporating patient preference and burden measures clarifies how much contact is enough and for whom. Health economic analyses will be central to informing payers and policymakers on reimbursement and adoption.
Contextualizing PREMISS within TAVI evidence
PREMISS adds to a growing body of work suggesting that structured post-procedural surveillance can be delivered safely and consistently. While feasibility does not prove outcome effectiveness, it validates the operational backbone needed for scale-up trials. The focus on early detection, standardized escalation, and multidisciplinary communication aligns with best-practice transition models. Programs with mature pathways in other cardiovascular areas can adapt governance and tooling to the TAVI context. The trial report, accessible on PubMed, provides the protocol foundation for replication.
Stakeholder communication and training
Care teams need clarity on objectives, evidence, and the practicalities of the pathway. Training should include scenario-based exercises for triage and escalation, with feedback loops that close learning gaps. Patients and caregivers benefit from simple, consistent messages on when to call, what to watch, and where to go. Publishing performance dashboards internally builds confidence and invites constructive input. External reporting to leadership or payers should couple utilization gains with patient experience and safety outcomes.
Interoperability and information flow
Information must move at the speed of clinical risk. Interoperability across electronic records, telehealth platforms, and monitoring tools reduces delays and duplication. Brief, structured notes that include red flags, actions, and follow-up create a readable clinical narrative. Standardized handoffs between coordinators, advanced practitioners, and physicians reduce the risk of missed cues. As data maturity grows, teams can analyze pathway bottlenecks and refine cadence and escalation rules.
Linking to program-level quality and certification
Many TAVI programs participate in specialty certification or registry-driven quality initiatives. Embedding intensified follow-up into these frameworks aligns operational effort with recognized standards. Pathway adherence, escalation timeliness, and unplanned care outcomes can be included in scorecards and morbidity reviews. External benchmarking helps identify outliers and best practices for rapid spread. Over time, the pathway becomes a standing element of program quality, not a project.
Building the digital front door
A seamless digital entry point reduces friction for patients and staff. Secure messaging, simple symptom checkers, and one-click scheduling under a single number or portal improve accessibility. Automating reminders and providing human backup reduces missed contacts while maintaining a personal touch. Interfacing with community pharmacists and home-health agencies widens the safety net. As the front door matures, streamlined triage can conserve clinician time while maintaining high reliability.
From feasibility to sustainability
Feasibility signals are necessary but not sufficient for lasting change. Sustainability depends on financing, workforce stabilization, continuous measurement, and a culture that values early detection. As programs iterate, they should guard against contact creep that adds burden without benefit. Balanced dashboards that include safety, utilization, patient experience, and staff well-being guide right-sizing over time. With these elements, intensified follow-up after TAVI can become a durable pillar of post-procedural care.
Outlook
PREMISS demonstrates that an intensified follow-up pathway after TAVI is deliverable and safe, providing the operational scaffolding for outcome-focused evaluations. The strategic opportunity now lies in aligning cadence, staffing, data, and financing to capture value while protecting equity and experience. Policy levers and reimbursement pathways can accelerate adoption if programs demonstrate reductions in unplanned care and total cost. As the field moves from feasibility to effectiveness, implementation science and health economics will be decisive. Done well, intensified follow-up can improve recovery quality for older adults while strengthening the performance and resilience of TAVI programs.
LSF-5284057388 | October 2025
How to cite this article
Team E. Intensified follow-up after tavi: feasibility and system impact. The Life Science Feed. Published November 7, 2025. Updated November 7, 2025. Accessed December 6, 2025. .
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References
- Prevention of readmission by intensified follow-up after transcatheter aortic valve implantation: Feasibility results of the PREMISS randomised controlled trial. https://pubmed.ncbi.nlm.nih.gov/40957461/.
