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2025 ACC Expert Consensus Decision Pathway: Tricuspid Regurgitation

Clinical Quick Reference — Evaluation and Management

Published: Journal of the American College of Cardiology (2026)
Society: American College of Cardiology
DOI: 10.1016/j.jacc.2025.07.002
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Clinical Recognition of Tricuspid Regurgitation

Tricuspid regurgitation affects 4% of individuals aged ≥75 years. TR is usually secondary to RV/RA enlargement rather than primary valve pathology. Clinical recognition is the first step in the pathway—findings may include elevated JVP, hepatosplenomegaly, peripheral edema, and elevated RV pressures.

Pearl: Most TR in clinical practice is secondary to left-sided heart disease, AF, or RV dysfunction. Early screening in at-risk populations (HF, AF, PH) improves outcomes through earlier intervention when appropriate.

DO: Assess for TR Early

  • Screen for TR in all patients with left-sided HF, AF, or pulmonary hypertension
  • Obtain transthoracic echocardiography (TTE) as first-line imaging modality

Tricuspid Regurgitation Etiology and Classification

Three primary etiologic categories: (1) primary TR, (2) secondary TR (atrial or ventricular), and (3) CIED-related TR. Each has distinct pathophysiology and management implications.

ClassificationSubtypePrimary Etiologies
Primary TRDegenerative, Endocarditis, Trauma, Eisstein anomaly, Carcinoid, Rheumatic, Congenital
Secondary TRVentricular (V-STR)RV dilatation, LV dysfunction, Pulmonary hypertension, Chronic lung/PE disease, IVC shunt
Atrial (A-STR)Atrial arrhythmias, HFpEF
CIED-relatedCausativeLead-TV leaflet interaction
IncidentalCIED present but not direct cause

Tricuspid Regurgitation Severity Assessment

TTE is the imaging modality of first choice. Guidelines recommend assessing TR severity with a combination of structural, qualitative, semi-quantitative, and quantitative measures.

Severity Grading by Echo Parameters

Step 1: Obtain continuous-wave Doppler of TR jet. Grade qualitatively as probable mild, moderate, or severe based on specific signs.
SeverityVC Width (mm)PISA EROA (mm²)RVol (mL)RF (%)
Mild<3<20<30<15
Moderate3–6.920–3930–4415–49
Severe≥7≥40≥45≥50
Pearl: EROA by PISA is the recommended parameter for severity classification. CMR and CT are valuable for complex anatomy and preprocedural planning.

Right Ventricular Assessment

RV function assessment is critical to guide intervention timing and predict outcomes. RV dysfunction portends worse prognosis.

ParameterMild DysfxModerate DysfxSevere Dysfx
TAPSE (mm)14–1710–13<10
RV S' (cm/s)9–116–8<6
RV GLS (%)18–2114–17<14
RV FAC (%)34–4730–33<30
3D RV EF (%)45–5035–45<35

Natural History and Prognosis

TR is independently associated with excess mortality. Two risk models predict outcomes: TRIO score (1–3 year) and TRIO-RV score (3-year). Use MAGGIC HF Survival Calculator for HF cohorts.

Pearl: High-risk TR patients warrant earlier intervention and aggressive GDMT. Risk stratification guides patient counseling and shared decision-making.

Medical Management

No guideline Class I medical therapies exist specifically for TR. Optimization of left-sided HF and comorbidities is foundational.

Therapy Components

DO: Optimize Medical Therapy

  • Initiate evidence-based GDMT for underlying HF and comorbidities
  • Manage AF with rhythm or rate control
  • Aggressively manage BP and CKD

Atrial Fibrillation Management in TR

AF is present in 18–45% of moderate-to-severe TR and is a risk factor for TR progression. Restoring sinus rhythm has been associated with TA remodeling reduction and TR improvement.

AF Management Framework

Tier 1 - Rhythm Control: Direct cardioversion in symptomatic AF. Restoration of sinus rhythm associated with RV reverse remodeling.
Tier 2 - Antiarrhythmic Therapy: Beta-blockers first-line; Class I/III agents for failures.
Tier 3 - Ablation: Consider catheter ablation in recurrent/persistent AF despite antiarrhythmic therapy.

Anticoagulation: Use CHA₂DS₂-VASc for stroke risk and HAS-BLED for bleeding risk assessment.

When to Refer for TV Intervention

Referral to advanced HF/valvular specialist should be considered for severe isolated TR with symptoms, moderate TR with progressive RV dysfunction, or CIED-related causative TR.

I NEED HELP Referral Criteria

LetterDefinitionDescription
IInotropesPrevious/current inotropic support requirement
NNYHAPersistent Class III–IV despite GDMT
EEnd-organ dysfxWorsening renal or hepatic dysfunction
DDefibrillator shocksRecurrent appropriate ICD shocks
HHospitalizations≥1 HF admission in 12 months
EEdema/escalating diureticsPersistent fluid overload
LLow BPSBP <90 mm Hg
PPrognostic medsInability to uptitrate GDMT

Surgical Treatment of TR

Optimal timing for isolated TV surgery is undefined. Surgery is often performed concomitant with left-sided valve disease. Use EuroSCORE II for surgical risk assessment.

Risk FactorPoints
Age ≥70 years1
NYHA Class III–IV1
Right-sided HF signs2
Daily furosemide ≥125 mg2
GFR <30 mL/min2
Elevated bilirubin2
LVEF <60%1
Moderate/severe RV dysfx1
Pearl: Early surgical intervention before progressive RV dysfunction improves outcomes. Early mortality 8–10%; late referral associated with higher perioperative risk.

Transcatheter Tricuspid Valve Intervention

Four main platforms available: (1) T-TEER (MitraClip/TriClip), (2) annuloplasty devices, (3) TTVR, (4) heterotopic CAVI. Choice depends on anatomy, function, and patient candidacy.

T-TEER vs TTVR Comparison

ApproachT-TEERTTVR
MechanismLeaflet approximation (repair)Valve replacement (prosthetic)
Advantages• Wide anatomy applicability
• Less invasive
• Native valve preserved
• Lower thromboembolism
• Most effective TR reduction
• Suitable for severe pathology
• CIED-TR capable
• High-risk surgery alternative
Limitations• Requires excellent imaging
• Less effective with severe tethering
• Modest TR reduction in some
• Limited device sizes
• RV dysfunction concerns
• Leaflet thrombosis risk
• Lifelong anticoagulation

Key Trial Results

TRILUMINATE (T-TEER): 350 patients; KCCQ improved 12.3 vs 0.6 in control (P < 0.001). 87% achieved ≥30% TR reduction.

TRISCEND II (TTVR): Multi-center RCT comparing device therapy vs OMT alone; favorable QoL trends, FDA approval in 2024 for symptomatic severe TR on OMT.

Post-TTVI Risk (TRIVALVE Model)

Predicts in-hospital mortality after TTVI based on AF, GFR <30, elevated GGT/bilirubin, RV HF signs, LVEF <50%. Cut-off 2.5 differentiates high vs low risk.

Management After TV Intervention

Continue GDMT post-intervention; monitor volume status closely. Euvolemia assessment guides safe discharge.

ParameterEuvolemicMild CongestionModerateSevere
OrthopneaNoneMildPresent>2 pillows
JVP<8 cm<10 or HJR+8–10>10
HepatomegalyAbsentLiver edgeModerateMassive/tender
EdemaNone+1+2+3/+4
6MWT>400 m300–400200–300<100 m
BNP/NT-proBNP<100/<400100–299/400–1500300–500/1500–3000>500/>3000

Follow-up: TTE at 6–12 weeks post-TTVI, repeat annually. Continue GDMT; manage AF; monitor for device-specific complications.

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