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SEOUL VALVES 2026

‘Mitral Valve Therapy at the Crossroads: Will TMVR Really Be a Game Changer?’

At SEOUL VALVES 2026, Eberhard Grube, MD (University Hospital Bonn, Germany) presented the evolving landscape of transcatheter mitral valve therapy, focusing on whether transcatheter mitral valve replacement (TMVR) could overcome the remaining limitations of mitral transcatheter edge-to-edge repair (M-TEER). M-TEER has become an established treatment for mitral regurgitation (MR), supported by randomized trials demonstrating clinical benefits, particularly in secondary MR. However, its effectiveness remains anatomy-dependent. In challenging “amber-” and “red-zone” anatomies, residual MR is more frequent and is associated with worse survival and increased heart failure hospitalization. TMVR therefore offers two potential advantages: more complete elimination of MR and treatment of anatomies unsuitable for M-TEER. Early TMVR experience, however, revealed important limitations. The transapical Tendyne system achieved MR ≤1+ in approximately 98% of patients, but substantial peri-procedural mortality of approximately 10% limited its impact on survival. In addition, TMVR studies have reported high screen-failure rates, reflecting the difficulty of accommodating diverse mitral anatomies. The emergence of transfemoral transseptal TMVR may represent an important turning point. He highlighted recent clinical data with the SAPIEN M3 system, which achieved MR ≤1+ in 96% of patients at 1 year, with no peri-procedural deaths, surgical conversions, or LVOT obstruction. These findings suggest that transseptal TMVR may combine effective MR elimination with improved procedural safety. Nevertheless, important challenges remain, including a screen-failure rate of approximately 72%, the need for oral anticoagulation with associated bleeding, and the complexity of the current two-step procedure. Continued device innovation will therefore be required to improve anatomical suitability and simplify implantation. In closing, he emphasized that M-TEER remains the established, RCT-supported backbone of transcatheter MR therapy. Transseptal TMVR may emerge as a complementary strategy, particularly for patients with challenging anatomies unsuitable for M-TEER. Future trials in these “red-zone” patients will be crucial in determining whether TMVR can truly become a game changer in mitral valve therapy. The Evolving Landscape of Mitral Valve Intervention Friday, August 7, 1:00 PM ~ 2:00 PM Presentation Room, Level 2 Check the Session

September 9, 2026 4991

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SEOUL VALVES 2026

TEER in Atrial Functional Mitral Regurgitation: Evidence and Lessons from Real-World Practice

At SEOUL VALVES 2026, Jung-Sun Kim, MD, PhD (Severance Hospital, Korea) reviewed transcatheter edge-to-edge repair (TEER) for atrial functional mitral regurgitation (AFMR). The presentation placed AFMR within the evolving landscape of mitral valve intervention and focused on the gap between a growing clinical need and the limited randomized evidence available for this distinct disease mechanism. AFMR was described as a form of secondary mitral regurgitation driven primarily by atrial and mitral annular remodeling rather than left ventricular disease. In contrast to ventricular functional mitral regurgitation, AFMR commonly occurred in patients with preserved left ventricular ejection fraction, marked left atrial enlargement, Carpentier type I leaflet motion, and no regional wall-motion abnormality. Annular dilatation and atriogenic tethering, particularly of the posterior mitral leaflet, reduced leaflet coaptation and created clinically important regurgitation despite relatively preserved ventricular function. Despite no randomized trial had yet established the role of TEER specifically in AFMR, several multicenter registries and observational analyses had generated a converging signal of benefit. Data from the EuroSMR registry and other contemporary studies suggested that TEER achieved effective mitral regurgitation reduction and that outcomes in appropriately selected patients with AFMR could be comparable to those observed in ventricular functional mitral regurgitation. A recent comparison of TEER with medical therapy also suggested a prognostic association favoring intervention, although the observational nature of the evidence required cautious interpretation. Mechanistic imaging supported the feasibility of the procedure. Three-dimensional mitral valve analyses had shown that TEER increased leaflet coaptation and reduced the anteroposterior annular diameter and mitral annular area. These favorable changes appeared most evident in patients who had annular dilatation without substantial posterior leaflet tethering. The findings reinforced the importance of defining valve geometry before intervention rather than treating AFMR as a uniform diagnosis. Durability remained an important concern because leaflet tension could persist after TEER in AFMR. A separate long-term example presented during the session showed a well-positioned device with mild residual mitral regurgitation at both one year and 2.5 years. The mean diastolic pressure gradient remained low, tricuspid regurgitation improved, pulmonary pressure decreased, and left ventricular ejection fraction rose from the mid-30% range to approximately 50%. Although an individual case could not establish long-term efficacy, it demonstrated that a stable result was achievable when anatomy and procedural execution were favorable. The presentation also identified five practical issues. First, transseptal puncture could be difficult in patients with very large left and right atria. Achieving an adequate inferior and posterior puncture height sometimes required substantial reshaping of the Brockenbrough needle to reach the septum. Second, concomitant tricuspid regurgitation required systematic assessment because right-sided disease and pulmonary hypertension could influence symptoms and prognosis even after successful mitral repair. Third, rhythm control remained an essential component of treatment. Many patients could benefit from rhythm-control strategies before mitral intervention, and the optimal sequence of TEER, atrial fibrillation treatment, and heart-failure-with-preserved-ejection-fraction-directed therapy remained uncertain. Fourth, AFMR itself was heterogeneous. The presentation distinguished an isolated annular-dilatation phenotype from a more advanced atriogenic-hamstringing phenotype. The latter appeared to represent either a late stage of annular disease or a distinct entity and was associated with less favorable procedural and clinical outcomes, suggesting that alternative catheter-based therapies might sometimes be needed. Fifth, the balance between residual mitral regurgitation and transmitral pressure gradient required particular attention. Registry data presented during the session indicated that a post-procedural mean pressure gradient of at least 5 mmHg was associated with worse outcomes in AFMR even when residual regurgitation was mild. Because these patients already had enlarged and dysfunctional left atria, excessive transmitral obstruction could be especially poorly tolerated. Device selection and the number of clips therefore had to achieve meaningful regurgitation reduction without creating an unfavorable gradient. In summary, the session showed that TEER had effectively reduced mitral regurgitation in selected patients with AFMR and that recent observational studies had reported outcomes comparable to those in ventricular functional mitral regurgitation. However, benefit had remained variable and depended on left atrial compliance, leaflet tethering, tricuspid regurgitation, rhythm control, and the post-procedural transmitral gradient. He concluded that AFMR should be approached as a distinct and heterogeneous disease, with careful imaging, staged management of contributing conditions, and individualized procedural planning. Randomized studies were still needed to define the relative roles and optimal timing of TEER, rhythm control, and medical therapy.

September 9, 2026 399

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SEOUL VALVES 2026

Current Status of Tricuspid Valve Interventions in Asia Pacific

At SEOUL VALVES 2026, in the session "Advancing Tricuspid Valve Intervention in 2026," Kent, Chak Yu So, MD (Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong, China) reviewed the current status of tricuspid valve intervention across the Asia-Pacific region, describing a decade of remarkable technical progress now constrained by two problems: uneven device access, and the unresolved question of when and how to treat. He framed tricuspid regurgitation (TR) as no longer the "forgotten valve": common, associated with increased morbidity and mortality, yet rarely operated on because isolated TR surgery carried 8-10% operative mortality, and with no medical therapy shown to alter heart failure hospitalization or death. The 2025 ESC/EACTS guideline update recommended transcatheter tricuspid treatment (Class IIa, Level A) for high-risk patients with symptomatic severe TR despite optimal medical therapy. The device pipeline had expanded quickly, but access had not kept pace: the devices a patient could actually receive still varied sharply from one country to the next, a disparity he described as a "big access gap between regions." The region had begun to generate its own data. An initial four-center T-TEER series from Hong Kong, Taiwan and Thailand (n=106) achieved TR ≤2+ in 74% and NYHA class I/II in 92.2% at 30 days, with major adverse events in 1.9%. In TRAVEL, a prospective study of the transjugular Lux-Valve Plus (n=126), one-year all-cause mortality was 10.3% with a pacemaker rate of 1.6%; in TriStar, focal annuloplasty with the K-Clip (n=96) reduced TR by at least one grade in 94.2% of patients; and a first-in-human series of the Pivot-TR spacer (n=7) showed TR reduction in every case. Randomized evidence matured through 2026. TRILUMINATE Pivotal (n=350) reduced TR to ≤moderate in 87% of the T-TEER arm versus 4.8% of controls at one year, with fewer annualized recurrent heart failure hospitalizations at two years (0.19 vs. 0.26 per patient-year, p=0.02). Tri.FR (n=300) showed an improved composite score in 74.1% versus 40.6% at one year and a 40% relative reduction in heart failure hospitalization at two years. In TRISCEND II (n=400, 2:1 to EVOQUE TTVR vs. medical therapy), the modified intention-to-treat analysis was neutral for death or heart failure hospitalization; a cross-over-status analysis at ACC 2026 favored TTVR (36.0% vs. 57.4%, p=0.004, driven by mortality 19.1% vs. 44.9%, p

September 9, 2026 451

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SEOUL VALVES 2026

Treating the Valve Was Not Enough: A Surgeon’s Case for Addressing AF and the Left Atrial Appendage...

At the 15th SEOUL VALVES 2026 meeting on August 6, Joon Bum Kim, MD, PhD (Asan Medical Center, Korea) presented “T-TEER in AF-Associated Atrial Functional TR: Surgeon’s Perspective” during the session “Advancing Tricuspid Valve Intervention in 2026.” He argued that tricuspid transcatheter edge-to-edge repair (T-TEER) had an important role for inoperable or very high-risk patients, but that treatment of atrial functional, or atrial secondary, tricuspid regurgitation (TR) had to extend beyond the valve itself. He first revisited why isolated tricuspid valve surgery had acquired a high-risk reputation. In a Society of Thoracic Surgeons Adult Cardiac Surgery Database analysis of 6,507 isolated operations (Chen et al, Ann Thorac Surg 2023), operative mortality was 7.3% and new permanent pacemaker implantation occurred in 10.8%. Mortality was associated with New York Heart Association class III or IV symptoms, nonelective surgery, valve replacement, low annual center volume, and higher Model for End-Stage Liver Disease scores; without these risk factors, operative mortality was 1.7%. He used the contrast to argue for earlier referral and for repair whenever feasible. German nationwide data showed how quickly practice had shifted. Annual transcatheter tricuspid valve interventions rose from 394 in 2018 to 3,763 in 2023 while surgical procedures fell from 1,371 to 868, with transcatheter volume overtaking surgery in 2021. He characterized atrial functional TR as a phenotype driven predominantly by right atrial and tricuspid annular dilatation, with less leaflet tethering than ventricular secondary TR. By the time severe TR had developed, however, atrial fibrillation (AF) was typically longstanding and persistent, with markedly enlarged atria and diffuse atrial fibrosis rather than a focal trigger-features that made many patients poor candidates for catheter ablation. He therefore positioned surgery as an opportunity to treat three related targets: the tricuspid valve, AF, and the left atrial appendage (LAA). In a Korean nationwide cohort of 17,247 patients with preoperative AF undergoing aortic or mitral valve surgery (Kim et al, J Thorac Cardiovasc Surg 2024), concomitant surgical ablation was associated, after inverse probability of treatment weighting, with lower risks of all-cause death (hazard ratio [HR] 0.86; 95% confidence interval [CI] 0.80-0.92), ischemic stroke or systemic embolism (HR 0.62; 95% CI 0.55-0.71), and heart failure hospitalization (HR 0.87; 95% CI 0.79-0.96). The cohort excluded concomitant tricuspid procedures but supported the broader value of addressing AF during valve surgery. Among 100 patients who underwent surgery for AF-associated functional mitral or tricuspid insufficiency, postoperative AF recurred in 48.1% at 1 year and 60.2% at 5 years despite ablation in 92%, and recurrence carried more than a threefold higher risk of death, valve reoperation, heart failure rehospitalization, or stroke (adjusted HR 3.33; 95% CI 1.50-7.40; P=.003). LAA exclusion, in contrast, was associated with a lower risk of the same composite outcome (adjusted HR 0.35; P=.010). Asan Medical Center’s 2003-2025 experience then addressed severe TR and AF directly in 162 consecutive patients. In a nonrandomized, multivariable-adjusted comparison, ablation alone did not differ from no ablation, whereas ablation combined with LAA exclusion showed a favorable trend that fell short of statistical significance. Table 1. Multivariable-adjusted primary outcome in the Asan Medical Center severe TR and AF cohort, 2003-2025 Surgical strategy Patients, n Adjusted HR vs no ablation(95% CI) P value No ablation 32 Reference - Surgical ablation only 38 0.98 (0.49-1.99) .97 Surgical ablation plus LAA exclusion 92 0.52 (0.27-1.02) .06 Primary composite outcome: death, stroke, congestive heart failure, or tricuspid valve reoperation. CI, confidence interval; HR, hazard ratio; LAA, left atrial appendage. A companion analysis suggested where that difference may have originated. No stroke occurred after LAA exclusion during follow-up, whereas events accrued steadily with preservation (adjusted subdistribution HR 0.012; 95% CI 0.0004-0.40; P=.013), while all-cause mortality did not differ significantly (adjusted HR 0.46; 95% CI 0.09-2.26; P=.34). He concluded that the evidence did not argue against T-TEER, which remained appropriate for inoperable or very high-risk candidates. Operable patients with AF-associated atrial functional TR, however, deserved a broader discussion of what surgery could accomplish. His final message was that the root cause-AF-should be addressed, and that the potential roles of concomitant AF ablation and LAA treatment had to be clearly explained to patients. Advancing Tricuspid Valve Intervention in 2026 Thursday, August 6, 1:00 PM ~ 2:00 PM Presentation Room, Level 2 Check the Session

September 9, 2026 414

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SEOUL VALVES 2026

Phenotype, Calcium Burden, and the Aorta in Bicuspid AS

At the 15th SEOUL VALVES 2026, Alan C. Yeung, MD (Stanford University School of Medicine, USA) presented “Do’s and Don’ts in Bicuspid TAVR” on August 7, combining a cautionary case, morphology-based evidence, new calcium-score data, and a preview of upcoming randomized trials into a structured approach to transcatheter aortic valve replacement (TAVR) for bicuspid aortic valve (BAV) stenosis. He opened with a case: a 73-year-old man at low surgical risk (STS 0.9%) with severe symptomatic aortic stenosis (aortic valve area 0.6 cm², mean gradient 64 mmHg), a type 1 BAV with right–non-coronary fusion, and a borderline 4.0-cm ascending aorta. Although the heart team had advised surgery, the patient chose TAVR after a long discussion about cardiopulmonary bypass. Crossing the valve proved difficult, requiring a Lunderquist wire, contralateral access, and a sliding balloon technique before a 29-mm SAPIEN 3 Ultra RESILIA was deployed with good valve function. A type A dissection—an intimal tear above the non-coronary cusp extending into the innominate artery—was then identified, mandating conversion to open root replacement; the patient survived after a long hospital stay. Whether the dissection arose from valve-edge injury after deployment or from aortic injury from pushing remained unresolved, and this uncertainty motivated his four-domain BAV-TAVR evaluation routine: age (lifetime management), phenotyping (raphe risk, valve centrality, paravalvular leak [PVL]), calcification (annular injury, expansion/gradient, PVL), and aortic size (dissection risk during TAVR and lifetime risk). Reviewing the Sievers and CT-based Jilaihawi classifications, he recalled that mid-term outcomes after bicuspid TAVR differed by morphology, with a calcified raphe plus excess leaflet calcification portending worse survival (Yoon et al., JACC 2020); in a cohort analysis he presented, survival over 8 years of follow-up likewise differed across commissural phenotypes (p = 0.033), with tricommissural (raphe-type) valves faring worst. He then showed a retrospective analysis (2012–2024) of 276 BAV TAVR patients stratified by CT aortic valve calcium (AVC) score. The 26 patients with an extreme calcium score (>6,000 AU) had higher all-cause mortality over follow-up (46.2% vs. 27.2%; p = 0.042) and at 1 year (19.2% vs. 7.2%; p = 0.035) than the remaining 250, with numerically higher 1-year stroke (7.7% vs. 3.2%) and MACE (23.1% vs. 11.2%). Notably, low-calcium valves (

September 3, 2026 462

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SEOUL VALVES 2026

Bicuspid TAVR: Asan Medical Center Data and a Contemporary Meta-Analysis

At SEOUL VALVES 2026, Jung-Min Ahn, MD, PhD (Asan Medical Center, Korea), delivered a keynote lecture titled “Bicuspid TAVR – AMC Data and Meta-Analysis” in the session Advancing TAVR in 2026. He opened by noting that, although a pooled analysis of six low-risk randomized trials (N = 5,341) showed TAVR to be at least as safe as SAVR for death and disabling stroke, the bicuspid population remained conspicuously under-represented in that evidence: in NOTION-2, which enrolled patients ≤ 75 years of age, the bicuspid cohort showed numerically higher rates of death or disabling stroke after TAVR than after SAVR (6.1% vs. 2.0%; HR 3.1, 95% CI 0.3–30.0). This signal prompted the two analyses he presented. The Asan TAVR Registry analysis included 1,879 patients treated with a balloon-expandable SAPIEN-series valve for native aortic stenosis, of whom 268 (14.2%) had a bicuspid aortic valve (BAV). The proportion of BAV rose steeply as age fell — from 5.6% in patients older than 85 years to 42.7% in those aged 70 years or younger (P for trend < 0.001) — a reminder that any strategy to extend TAVR into younger populations must first solve bicuspid anatomy (Figure 1). Figure 1. Age distribution of the Asan TAVR Registry cohort. The proportion of bicuspid aortic valve rose from 5.6% in patients >85 years to 42.7% in those ≤70 years (P for trend < 0.001). Compared with tricuspid patients, BAV patients were younger (77.0 ± 6.2 vs. 80.8 ± 5.6 years), more often male (67.9% vs. 43.4%), and at lower surgical risk (STS-PROM 2.7 vs. 3.7; all P < 0.001). Aortic stenosis was more severe (peak velocity 5.0 vs. 4.7 m/s; mean gradient 58 vs. 52 mmHg), and CT demonstrated a consistently larger and more complex aortic valve complex: annulus area 510.8 ± 96.5 vs. 434.0 ± 76.0 mm², LVOT area 506 vs. 419 mm², sinus of Valsalva area 992 vs. 812 mm², and higher coronary ostia. The most striking difference was leaflet calcification, roughly twice as heavy in BAV (median 744 [364–1176] vs. 371 [198–634] mm³) and characteristically asymmetric along the raphe (Figure 2). Figure 2. Leaflet calcification volume in bicuspid versus tricuspid aortic stenosis (median 744 vs. 371 mm³). These anatomical features translated directly into procedural differences. Larger prostheses were implanted more often (29 mm THV in 27.6% vs. 10.3%), device-to-annulus area oversizing was lower (104.2 ± 6.5% vs. 110.1 ± 6.0%), and balloon pre-dilation was performed far more frequently (76.5% vs. 45.3%). Notably, less oversizing was applied in BAV across every calcium volume stratum, not only in the most heavily calcified valves. At 30 days, BAV patients experienced more paravalvular aortic regurgitation greater than mild (9.3% vs. 2.7%), more aortic annular or root injury (2.2% vs. 0.8%) and more cardiac tamponade (1.9% vs. 0.4%), yielding a higher composite procedural endpoint (11.9% vs. 4.3%; P < 0.001). Mortality at 30 days was nevertheless identical (0.7% vs. 0.8%), and new permanent pacemaker implantation (7.1% vs. 7.1%), major vascular complications (3.4% vs. 3.4%) and severe prosthesis–patient mismatch (6.4% vs. 4.1%) did not differ (Figure 3). He summarized this pattern as “more complications in bicuspid, without excess mortality.” Figure 3. Thirty-day procedural outcomes: more complications in bicuspid anatomy, without excess mortality. Hemodynamic performance was reassuring. Indexed effective orifice area was comparable between BAV and tricuspid patients through two years, and this held true across all calcification strata, including valves with more than 1,000 mm³ of leaflet calcium. In a propensity-matched cohort of 259 pairs, two-year death was numerically lower in BAV patients (6.9% vs. 13.4%; P = 0.42), attributed largely to their younger age, while stroke was slightly but not significantly higher (3.7% vs. 2.4%; P = 0.20) (Figure 4). Figure 4. Two-year death and stroke in the propensity-matched cohort (259 pairs). To place these single-center findings in a broader context, he presented a meta-analysis of 52 studies (Kumar S, Ahn JM, et al. JACC Advances, in press) addressing two questions. For TAVR in bicuspid versus tricuspid anatomy (39 studies), BAV was associated with higher early risk: moderate or greater paravalvular leak (RR 1.44), aortic root injury (RR 1.83), 30-day stroke (RR 1.27) and 30-day mortality (RR 1.25). By one year, however, mortality (RR 0.84) and stroke (RR 1.00) no longer differed, and STS score rather than valve morphology predicted one-year death. Meta-regression further showed that outcomes of bicuspid TAVR improved progressively with publication year (RR 0.93 per year; P for trend = 0.048), consistent with iterative gains in device technology and implantation technique (Figure 5). Figure 5. Central illustration of the meta-analysis of 52 studies: TAVR in bicuspid versus tricuspid anatomy, and TAVR versus SAVR in bicuspid stenosis. For the second question — TAVR versus SAVR in bicuspid stenosis (13 studies) — the evidence was limited and described a trade-off rather than a clear winner. TAVR carried more moderate or greater paravalvular leak (RR 7.08) and more permanent pacemaker implantation (RR 2.13), whereas major bleeding was substantially less frequent with TAVR (RR 0.27). Thirty-day stroke and mortality did not differ, and there were no data supporting a categorical preference for surgery in bicuspid anatomy. He concluded that carefully selected patients with BAV could undergo TAVR with current-generation devices, and offered several guiding principles: Procedural complications remained more frequent in BAV, so meticulous patient selection and pre-procedural CT planning were essential. Sizing should incorporate calcification volume and its distribution; less oversizing combined with liberal pre-dilation was the strategy adopted at Asan Medical Center. Post-procedural optimization mattered increasingly as the treated population became younger and lifetime management came into play. Not all bicuspid anatomies were suitable for TAVR. Just as the echocardiographic score guides balloon valvuloplasty in rheumatic mitral stenosis, a BAV-specific scoring system should be developed to guide the choice between TAVR and SAVR. His lecture underscored that bicuspid anatomy remained one of the most demanding frontiers in transcatheter therapy — technically manageable today, but still awaiting the dedicated selection tools and long-term durability data needed to treat the younger patients in whom bicuspid disease predominates. Keynote Session: Advancing TAVR in 2026 Thursday, August 6, 1:00 PM ~ 2:00 PM Main Arena, Level 2 Watch Session Video

September 3, 2026 458

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SEOUL VALVES 2026

Transcarotid TAVR: Practical Tips and Early Asan Experience

At the 15th SEOUL VALVES 2026 meeting, Ho Jin Kim, MD, PhD (Asan Medical Center, Korea), delivered a practical lecture titled “Transcarotid TAVR: Practical Tips and Tricks for Non-Transfemoral Access.” His lecture walked through why alternative access is still needed in the contemporary TAVR era, how to decide whether the carotid route is suitable, how to choose a side and prepare the vessel, and which procedural details protect the brain — closing with the early transcarotid experience at his own institution. Transfemoral access remains the standard approach and now accounts for the overwhelming majority of TAVR procedures. In the STS/ACC TVT Registry, femoral access was used in roughly 96% of cases through 2022, while axillary, subclavian, iliac, or carotid access accounted for approximately 3% and transapical, transaortic, or transcaval access for less than 1% (Figure 1). A small but persistent group of patients, however, cannot be treated transfemorally because of peripheral arterial disease, severe calcification, or small and tortuous iliofemoral arteries — and these patients still need a safe alternative route. Planning begins with confirming that transfemoral access is truly unsuitable, then assessing the carotid on CT: a minimal lumen diameter compatible with the planned system, no severe circumferential calcification, and acceptable tortuosity (Figure 1). Per the 2025 JSCAI expert consensus, the approach should be avoided when the common carotid diameter is inadequate — usually below 5 mm — or when there is severe tortuosity, heavy plaque, dissection, or aneurysm. Figure 1. CT-based planning: confirming transfemoral unsuitability and evaluating carotid access anatomy. Side selection should be anatomy-driven rather than habitual — adequate diameter, less tortuosity and calcified plaque, a favorable delivery angle, and no prohibitive prior neck surgery. The left carotid is often preferred, but the right is equally acceptable when its anatomy is better (Figure 2). Figure 2. Anatomy-driven selection between right and left common carotid access. Technically, a 4 cm longitudinal incision parallel to the sternocleidomastoid with at least 3 cm of circumferential dissection leaves room for a proximal umbilical tape and distal clamping, while the vagus nerve is carefully protected. A clean-cut transverse arteriotomy allows atraumatic insertion of the 14-16 Fr sheath and flushing of debris before cerebral flow is restored. Cerebral safety rests on test clamping with bilateral oximetry, systolic blood pressure above 140 mmHg to support collateral perfusion, and careful de-airing before reperfusion (Figure 3). Figure 3. Cerebral protection strategy during transcarotid TAVR. The most common concern — stroke from temporary carotid occlusion — is not supported by comparative data. In an STS/ACC TVT Registry analysis of Evolut recipients (transcarotid n=576 vs. transaxillary n=2,602, propensity-matched), mortality was comparable while stroke was higher with transaxillary access at both 1 month (5.9% vs. 3.1%, p=0.017) and 12 months (7.2% vs. 3.4%, p=0.003). At Asan Medical Center, 12 transcarotid procedures have been performed since December 2023 (mean age 82.2 ± 5.5 years) with no deaths and no disabling strokes (Figure 4). Figure 4. Non-transfemoral TAVR at Asan Medical Center by year and access route, with early transcarotid outcomes. He concluded that transcarotid TAVR should be regarded as a planned alternative rather than a bailout strategy, and summarized three take-home principles: Trandcarotid TAVR is a valuable alternative when transfemoral access is unsuitable — best suited to patients with favorable carotid anatomy. Success starts with CT-based planning and anatomy-driven side selection — choose the safer carotid route, not simply the left or right side. Cerebral safety requires a meticulous strategy — test clamping, systolic blood pressure ≥ 140 mmHg, and de-airing before reperfusion. The Heart Team in Action: Managing Complex TAVR Scenarios Friday, August 7, 1:00 PM ~ 2:00 PM Main Arena, Level 2 Watch Session Video

September 3, 2026 450

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SEOUL VALVES 2026

Seventeen Years of TAVR at AMC: From High-Risk Therapy to Broader Clinical Practice

Transcatheter aortic valve replacement (TAVR) had evolved from a treatment for inoperable or high-risk patients into a mainstream option for severe symptomatic aortic stenosis. Reviewing the 17-year TAVR experience at Asan Medical Center (AMC), Seung-Jung Park, MD, PhD (Asan Medical Center, Korea) showed how randomized trials, guideline changes, device development, and accumulated institutional experience had progressively expanded TAVR toward younger and lower-risk patients. The clinical shift had been driven by a series of trials that moved from high-risk to low-risk populations. The DEDICATE trial, which enrolled 1,414 low- to intermediate-risk patients with a mean age of 74 years and an STS score of 1.8%, had shown a lower 1-year rate of death or fatal or nonfatal stroke with TAVR than with surgical aortic valve replacement (SAVR). A meta-analysis of six low-risk randomized trials had also favored TAVR for individual patient-level all-cause mortality and for death or disabling stroke, reinforcing the move toward lower-risk practice. As TAVR had expanded to younger patients, long-term durability had become a central issue. In the PARTNER 3 trial, low-risk patients had shown comparable 7-year outcomes after SAPIEN 3 TAVR and surgery, including the composite of death, stroke, or rehospitalization. Bioprosthetic valve failure and aortic valve reintervention had also remained similar. Intermediate-risk data had likewise shown comparable long-term mortality between SAPIEN 3 TAVR and SAVR out to 10 years. Self-expanding valve data had provided a somewhat different perspective. In the Evolut Low Risk trial, all-cause death or disabling stroke had remained comparable between TAVR and surgery at six years, but aortic valve reintervention had been more frequent after TAVR at longer follow-up. The presentation linked this difference largely to aortic regurgitation and emphasized that long-term outcomes could vary according to valve design and mechanism. Device selection had therefore remained critical. Balloon-expandable valves had provided stronger radial force, whereas self-expanding valves had been more susceptible to annular constraints and underexpansion. In the ACURATE IDE trial, valve underexpansion had occurred in 21.6% of patients and had been associated with a higher 1-year risk of death, stroke, or rehospitalization. Severe annular and leaflet calcification had been identified as an important contributor. AMC's TAVR program had begun in March 2010 and had grown to more than 300 procedures annually. By 2026, the center had increasingly treated younger and lower-risk patients; 55% had been younger than 75 years and 68% had had an STS score below 4%. Procedural success had reached 99.3%. The center had attributed these results to three principles: Heart Team collaboration, a minimalist procedural strategy, and detailed pre-procedural computed tomography (CT) assessment. The minimalist approach had generally avoided general anesthesia and transesophageal echocardiography, shortened uncomplicated procedures, and facilitated early recovery. CT evaluation had been used to assess vascular access, annular dimensions, the sinus of Valsalva, sinotubular junction, left ventricular outflow tract, coronary height, calcium burden and distribution, bicuspid morphology, and aortopathy. This information had guided valve selection and sizing rather than relying solely on nominal annular measurements. AMC had predominantly used balloon-expandable valves, which accounted for 88% of approximately 2,200 TAVR procedures presented. Calcium burden and distribution had been considered particularly important because they had influenced paravalvular leakage, pacemaker implantation, valve expansion, and other complications. Long-term registry data had shown low overall reintervention rates, while also identifying distinct failure patterns: small annular anatomy had been associated with reintervention for aortic stenosis, whereas self-expanding valves had been associated with a higher risk of reintervention for aortic regurgitation. The program had also extended TAVR to bicuspid aortic stenosis. In the ASAN TAVR Registry, 219 of 2,119 patients had undergone TAVR for bicuspid anatomy. Matched comparisons had shown no significant difference in mortality or stroke between bicuspid and tricuspid TAVR cohorts, although careful assessment of calcium morphology, aortic dimensions, and aortopathy had remained essential. Overall, AMC's 17-year experience had illustrated how TAVR had become a standardized treatment across a broader range of patients. The evidence had supported expansion into low-risk populations, while longer follow-up had shifted attention toward durability, reintervention, and device-specific failure modes. The presentation concluded that durable outcomes had depended not only on valve technology, but also on Heart Team selection, procedural simplification, and meticulous CT-based planning. Opening, Live Case & Lecture 1: TAVR Thursday, August 6, 10:00 AM ~ 11:52 AM Main Arena, Level 2 Watch Session Video

August 27, 2026 471

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SEOUL VALVES 2026

TAVR Durability in 2026: Long-Term Data Reassured, but Lifetime Planning Remained Essential

Durability had remained one of the key concerns surrounding transcatheter aortic valve replacement (TAVR), particularly as the procedure expanded to younger and lower-risk patients. At SEOUL VALVES 2026, David J. Cohen, MD, MSc (Cardiovascular Research Foundation, USA), reviewed long-term clinical evidence and strategies that could further improve transcatheter heart valve durability. He noted that the central question had shifted from whether TAVR could match surgery over five to 10 years to whether it could remain a reliable first treatment for patients expected to live 15 to 20 years or longer. This issue had become more relevant as TAVR use increased among younger patients. U.S. data from 2015 to 2021 showed a progressive rise in TAVR across age groups, including patients younger than 65 years. He cautioned that durability could not be judged by early hemodynamic performance alone, because historical surgical data had shown that clinically meaningful differences in valve durability might not appear until about eight years after implantation. He also emphasized that structural valve deterioration should be distinguished from other causes of bioprosthetic valve dysfunction, including non-structural dysfunction, thrombosis, and endocarditis. Early reintervention after TAVR therefore did not necessarily indicate structural degeneration. Advances in CT imaging, device sizing, sealing skirts, and operator experience had already reduced several mechanisms of early valve dysfunction seen with earlier-generation devices. Long-term randomized data had been reassuring for balloon-expandable TAVR. In PARTNER 3, seven-year aortic valve reintervention rates were similar with SAPIEN 3 TAVR and surgical aortic valve replacement (6.7% vs. 6.0%; HR 1.11, 95% CI 0.63-1.94). Bioprosthetic valve failure was also comparable (6.9% vs. 7.5%; HR 0.90, 95% CI 0.55-1.49), suggesting no meaningful durability disadvantage for SAPIEN 3 through seven years. The Evolut Low Risk trial, however, had raised a signal requiring further surveillance. By seven years, reintervention occurred in 9.8% of TAVR patients versus 6.0% after surgery, largely because of reintervention for aortic regurgitation rather than stenosis. An exploratory analysis suggested a possible association with post-dilation outside recommended guidance, although this had not been consistently reproduced. He therefore advised against overinterpreting the finding but considered avoidance of unnecessary or off-guidance post-dilation prudent, particularly in younger patients. Several strategies to improve durability had emerged. RESILIA anti-calcification technology had shown encouraging evidence for improved tissue preservation, while polymer-based leaflet platforms such as TRIA represented another potential approach, although long-term human data remained limited. Implantation quality could also matter: four-dimensional CT studies had linked hypoattenuated leaflet thickening (HALT) with valve-frame deformation, supporting the concept that more circular and complete valve expansion might reduce leaflet stress and thrombosis. He concluded that evidence through 2026 had been reassuring for contemporary balloon-expandable TAVR, with no meaningful difference from surgery in valve reintervention through seven years. The Evolut signal required continued follow-up, while newer tissue technologies, novel leaflet materials, and optimized implantation offered potential paths toward longer valve life. Until reliable 15- to 20-year durability was established, however, lifetime management remained essential, especially for younger patients who might later require coronary access, redo TAVR, or surgery. Keynote Session: Advancing TAVR in 2026 Thursday, August 6, 1:00 PM ~ 2:00 PM Main Arena, Level 2 Watch Session Video

August 27, 2026 497

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SEOUL VALVES 2026

TAVR in Transition: Ongoing Trials and the Future Landscape

On Thursday, August 6, during the "Keynote Session: Advancing TAVR in 2026" held in the Main Arena, Duk-Woo Park, MD, PhD (Asan Medical Center, Korea) presented a comprehensive overview of the upcoming phase of transcatheter aortic valve replacement (TAVR) clinical trials. He outlined how the field had successfully transitioned from treating extreme and high-risk patients to intermediate and low-risk populations, driven by major randomized clinical trials (RCTs). Moving forward, he identified five unmet clinical needs that shaped the next generation of TAVR trials. Unmet Neede Target Population Key Clinical Trials 1. Earlier Intervention Moderate AS ◆ PROGRESS ◆ EXPAND TAVR II 2. Broader Anatomy Bicuspid AS, Native AR ◆ NAVIGATE ◆ BELIEVERS ◆ ARTIST 3. New-generation Devices Low/Intermediate-risk Severe AS ◆ ENVISION IDE 4. Integrated CAD Care Severe AS with Concomitant CAD ◆ COMPLETE TAVR ◆ TAVI PCI ◆ FAITAVI 5. Optimal Medical Therapy Post-TAVR with HFpEF ◆ ENAVO-TAVR Table 1. Five Unmet Clinical Needs Shaping the Next Generation of TAVR Trials. This table outlines the five primary domains of ongoing research in transcatheter aortic valve replacement (TAVR), detailing the target clinical populations, anatomical focuses, and the major randomized clinical trials (RCTs) currently designed to address these evidentiary gaps. First, he discussed the rationale for earlier intervention in patients with moderate AS. He noted that myocardial damage from pressure overload began well before symptoms appeared and was only partly reversible after aortic valve replacement. Trials such as PROGRESS and EXPAND TAVR II were designed to determine if intervening with TAVR before AS progressed to a severe state outweighed the procedural risks. Second, he addressed the expansion of TAVR into broader anatomical challenges, specifically focusing on bicuspid aortic valve disease and native aortic regurgitation (AR). He highlighted the investigator-initiated NAVIGATE and BELIEVERS trials, which tested TAVR against surgical aortic valve replacement (SAVR) in bicuspid anatomy. Furthermore, the ARTIST trial evaluated the JenaValve Trilogy, a purpose-built device for non-calcified AR anatomy, which had the potential to open up the last major native-valve indication for transcatheter approaches. Third, the lecture covered the impact of new-generation devices and lifetime management strategies. He emphasized that for younger, low-risk patients, factors such as coronary re-access, valve durability, and redo-TAVR feasibility outweighed standard 30-day outcomes. The ENVISION IDE trial was highlighted for its head-to-head comparison of the next-generation Navitor valve against commercial transcatheter heart valves in a large patient cohort. Fourth, he explored the integration of coronary artery disease (CAD) care. With multiple ongoing trials, including COMPLETE TAVR, TAVI PCI, and FAITAVI, investigators aimed to clarify whether, when, and how to optimally revascularize concomitant coronary disease in TAVR candidates. These studies evaluated complex strategies, such as complete percutaneous coronary intervention (PCI) versus medical therapy, the optimal timing of PCI (before versus after TAVR), and physiology-guided versus angiography-guided lesion selection. Finally, the presentation focused on the necessity of optimal medical therapy post-TAVR. He pointed out that up to one in four patients were re-hospitalized for heart failure within two years of an otherwise successful procedure, indicating a persistent residual cardiovascular risk. He introduced the Korean investigator-initiated ENAVO-TAVR trial, which randomized 1,040 post-TAVR patients with heart failure with preserved ejection fraction (HFpEF) across 43 centers to receive either the SGLT2 inhibitor enavogliflozin or a placebo. Figure 1. ENAVO-TAVR Trial Design and Endpoints. Study design of the ENAVO-TAVR trial, a Korean investigator-initiated, placebo-controlled randomized clinical trial. The study evaluates the efficacy of the SGLT2 inhibitor enavogliflozin (0.3 mg once daily) versus placebo in 1,040 patients with severe aortic stenosis and heart failure with preserved ejection fraction (HFpEF) following a successful TAVR procedure. The primary endpoint assesses a composite of major adverse cardiovascular events (all-cause death, myocardial infarction, or stroke) or hospitalization for heart failure at 1 year. In conclusion, he summarized that the next decade of TAVR RCTs focused heavily on precision medicine. The overarching goal of the future landscape was the personalized selection of patients, devices, and treatment timing to optimize lifetime management for individuals with valvular heart disease. Keynote Session: Advancing TAVR in 2026 Thursday, August 6, 1:00 PM ~ 2:00 PM Main Arena, Level 2 Watch Session Video

August 27, 2026 7112

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