Managing Valvular Heart Disease
Guides valve disease severity assessment with intervention criteria and surveillance schedules.
Why This Skill Exists
Valvular heart disease affects approximately 2.5% of the US population, with prevalence increasing with age. The 2020 ACC/AHA Guideline for the Management of Patients with Valvular Heart Disease established evidence-based criteria for severity grading, intervention timing, and surveillance. The critical challenge is identifying the optimal window for intervention — too early exposes patients to unnecessary procedural risk, too late results in irreversible ventricular dysfunction.
The emergence of transcatheter therapies (TAVR, MitraClip, TEER) has transformed the treatment landscape, but appropriate patient selection requires precise severity assessment and multidisciplinary Heart Team evaluation. Failure to apply guideline-concordant criteria for intervention leads to both undertreatment and overtreatment.
Checkpoint A: Pre-Draft Intake (Mandatory)
- Which valve(s) are affected and what is the lesion — stenosis, regurgitation, or mixed? (default: "Valve not specified")
- What is the current severity — mild, moderate, or severe? (default: "Severity not graded")
- Is the patient symptomatic (dyspnea, angina, syncope, exercise intolerance)? (default: "Symptom status not documented")
- What is the LVEF and LV dimensions? (default: "Echo data not provided")
- What are the echocardiographic parameters used for grading (velocity, gradient, valve area, regurgitant volume)? (default: "Parameters not listed")
- Has a prior echo been performed for comparison? (default: "No prior study")
- Has the patient been evaluated by a Heart Valve Team? (default: "Not yet evaluated")
- Are there comorbidities affecting surgical risk (STS score, frailty, age)? (default: "Surgical risk not calculated")
Documents to Request
- Current echocardiogram with Doppler assessment
- Prior echocardiograms for trend analysis
- Cardiac catheterization (if hemodynamic confirmation needed)
- Cardiac CT (for TAVR planning or annular sizing)
- STS risk score calculation
- Exercise stress test (for asymptomatic severe disease)
- BNP/NT-proBNP
- Dental clearance (pre-surgery infection risk)
- Coronary angiography (pre-surgical evaluation)
Step 1: Aortic Stenosis Assessment and Management
Severity Grading (ACC/AHA 2020):
| Parameter |
Mild |
Moderate |
Severe |
| Peak velocity (m/s) |
2.0–2.9 |
3.0–3.9 |
≥ 4.0 |
| Mean gradient (mmHg) |
< 20 |
20–39 |
≥ 40 |
| AVA (cm²) |
> 1.5 |
1.0–1.5 |
≤ 1.0 |
| AVAi (cm²/m²) |
— |
— |
≤ 0.6 |
Low-Flow, Low-Gradient AS Subtypes:
- Classical (reduced EF): LVEF < 50%, AVA ≤ 1.0, mean gradient < 40 → dobutamine stress echo to differentiate true-severe from pseudo-severe
- Paradoxical (preserved EF): LVEF ≥ 50%, SVi < 35 mL/m², AVA ≤ 1.0, mean gradient < 40 → often elderly, hypertensive, small LV cavity
Intervention Criteria (Class I):
- Symptomatic severe AS → SAVR or TAVR
- Asymptomatic severe AS with LVEF < 50% → intervention
- Asymptomatic severe AS undergoing other cardiac surgery → concomitant AVR
TAVR vs. SAVR Selection:
- Low surgical risk (STS < 3%): SAVR preferred; TAVR acceptable (ACC/AHA 2020)
- Intermediate risk (STS 3–8%): shared decision-making; both acceptable
- High risk (STS > 8%) or prohibitive: TAVR preferred
- Age < 65: SAVR generally preferred (long-term valve durability)
- Age ≥ 80: TAVR generally preferred
Step 2: Mitral Regurgitation Assessment and Management
Primary (Degenerative) MR Severity — ASE Integrated Approach:
| Parameter |
Mild |
Moderate |
Severe |
| Vena contracta (cm) |
< 0.3 |
0.3–0.69 |
≥ 0.7 |
| EROA (cm²) |
< 0.2 |
0.2–0.39 |
≥ 0.4 |
| Regurgitant volume (mL) |
< 30 |
30–59 |
≥ 60 |
Intervention Criteria for Primary Severe MR (Class I):
- Symptomatic severe MR → surgery (repair preferred over replacement)
- Asymptomatic severe MR with LV dysfunction (LVEF 30–60% or LVESD ≥ 40 mm) → surgery
Secondary (Functional) MR:
- Due to LV dilation and tethering in HFrEF or ischemic cardiomyopathy
- Optimize GDMT first (medical therapy improves functional MR)
- COAPT trial: transcatheter edge-to-edge repair (TEER, MitraClip) for severe secondary MR with LVEF 20–50%, LVESD ≤ 70 mm, on maximal GDMT
- MITRA-FR: no benefit when LV dilation is disproportionately large relative to MR severity
Step 3: Aortic Regurgitation and Right-Sided Valve Disease
Chronic Severe Aortic Regurgitation Intervention Criteria:
- Symptomatic severe AR → surgery (Class I)
- Asymptomatic severe AR with LVEF < 55% → surgery (Class I)
- Asymptomatic severe AR with LVEF ≥ 55% but LV severely dilated (LVESD > 50 mm or indexed > 25 mm/m²) → surgery (Class IIa)
Tricuspid Regurgitation:
- Functional TR (most common): secondary to RV dilation, pulmonary hypertension, or AF
- Severe TR intervention at time of left-sided valve surgery (Class I)
- Isolated severe TR with progressive RV dilation/dysfunction: emerging transcatheter therapies (TVTR)
- Medical management: diuretics, treat underlying cause (PH, left heart disease)
Tricuspid Stenosis (rare):
- Usually rheumatic; mean gradient > 5 mmHg = severe
- Surgical intervention when symptomatic or at time of other valve surgery
Step 4: Surveillance Schedules
Recommended Echo Surveillance Intervals:
| Valve Lesion |
Mild |
Moderate |
Severe (Asymptomatic) |
| Aortic stenosis |
Every 3–5 years |
Every 1–2 years |
Every 6–12 months |
| Aortic regurgitation |
Every 3–5 years |
Every 1–2 years |
Every 6–12 months |
| Mitral regurgitation |
Every 3–5 years |
Every 1–2 years |
Every 6–12 months |
| Mitral stenosis |
Every 3–5 years |
Every 1–2 years |
Every year |
Triggering Earlier Reassessment:
- New or worsening symptoms
- Change in exercise tolerance
- Decline in LVEF or increase in LV dimensions
- New atrial fibrillation
- Rising BNP/NT-proBNP trend
Step 5: Prosthetic Valve Management
Prosthetic Valve Types and Anticoagulation:
| Valve Type |
Anticoagulation |
Target INR |
| Mechanical (aortic) |
Warfarin lifelong |
2.0–3.0 (with aspirin 75–100 mg) |
| Mechanical (mitral) |
Warfarin lifelong |
2.5–3.5 (with aspirin 75–100 mg) |
| Bioprosthetic (surgical) |
Aspirin; consider warfarin × 3–6 months |
2.0–3.0 if warfarin used |
| TAVR |
DAPT × 3–6 months → aspirin alone |
— (DOACs contraindicated post-TAVR per 2020 guideline) |
Prosthetic Valve Dysfunction Surveillance:
- Annual echo with Doppler assessment of gradients and regurgitation
- Rising transvalvular gradient → suspect valve thrombosis, pannus, or patient-prosthesis mismatch
- New paravalvular leak → may require percutaneous closure or reoperation
Checkpoint B: Post-Draft Alignment (Mandatory)
- Is valve disease severity graded with specific echocardiographic parameters?
- Are intervention criteria applied correctly per ACC/AHA 2020 guidelines?
- Is the Heart Team evaluation documented or recommended for intervention candidates?
- Is the surveillance interval appropriate for the severity and symptom status?
- Is prosthetic valve anticoagulation correctly specified if applicable?
Quality Audit
Guidelines
- Never intervene on moderate valve disease based solely on symptoms — confirm severity with quantitative echocardiographic criteria first.
- For severe aortic stenosis, LVEF < 50% is an indication for intervention even in asymptomatic patients — do not wait for symptoms.
- In mitral regurgitation, repair is superior to replacement when feasible — refer to high-volume surgical centers with > 95% repair rates.
- Low-flow, low-gradient aortic stenosis requires dobutamine stress echo or calcium scoring to distinguish true-severe from pseudo-severe — never operate based on a single resting echo.
- TEER (MitraClip) for secondary MR requires strict COAPT trial criteria — patients must be on maximal GDMT and meet anatomic and functional criteria.
- DOACs are currently contraindicated for mechanical heart valves — warfarin is the only acceptable anticoagulant (REALIGN trial harm).
- Endocarditis prophylaxis is indicated for prosthetic valves, prior endocarditis, unrepaired cyanotic CHD, and repaired CHD with residual defects — for dental procedures involving gingival manipulation or periapical region.
- All patients with moderate or greater valve disease should receive annual clinical assessment even between scheduled echo surveillance intervals.
1---2name: managing-valvular-heart-disease3description: Guides valve disease severity assessment with intervention criteria and surveillance schedules. Use when evaluating valve disease, assessing surgical/interventional timing, or monitoring valve function.4---5
6# Managing Valvular Heart Disease
7
8Guides valve disease severity assessment with intervention criteria and surveillance schedules.
9
10## Why This Skill Exists
11
12Valvular heart disease affects approximately 2.5% of the US population, with prevalence increasing with age. The 2020 ACC/AHA Guideline for the Management of Patients with Valvular Heart Disease established evidence-based criteria for severity grading, intervention timing, and surveillance. The critical challenge is identifying the optimal window for intervention — too early exposes patients to unnecessary procedural risk, too late results in irreversible ventricular dysfunction.
13
14The emergence of transcatheter therapies (TAVR, MitraClip, TEER) has transformed the treatment landscape, but appropriate patient selection requires precise severity assessment and multidisciplinary Heart Team evaluation. Failure to apply guideline-concordant criteria for intervention leads to both undertreatment and overtreatment.
15
16---
17
18## Checkpoint A: Pre-Draft Intake (Mandatory)
19
201. Which valve(s) are affected and what is the lesion — stenosis, regurgitation, or mixed? (default: "Valve not specified")
212. What is the current severity — mild, moderate, or severe? (default: "Severity not graded")
223. Is the patient symptomatic (dyspnea, angina, syncope, exercise intolerance)? (default: "Symptom status not documented")
234. What is the LVEF and LV dimensions? (default: "Echo data not provided")
245. What are the echocardiographic parameters used for grading (velocity, gradient, valve area, regurgitant volume)? (default: "Parameters not listed")
256. Has a prior echo been performed for comparison? (default: "No prior study")
267. Has the patient been evaluated by a Heart Valve Team? (default: "Not yet evaluated")
278. Are there comorbidities affecting surgical risk (STS score, frailty, age)? (default: "Surgical risk not calculated")
28
29### Documents to Request
30
31- Current echocardiogram with Doppler assessment
32- Prior echocardiograms for trend analysis
33- Cardiac catheterization (if hemodynamic confirmation needed)
34- Cardiac CT (for TAVR planning or annular sizing)
35- STS risk score calculation
36- Exercise stress test (for asymptomatic severe disease)
37- BNP/NT-proBNP
38- Dental clearance (pre-surgery infection risk)
39- Coronary angiography (pre-surgical evaluation)
40
41---
42
43## Step 1: Aortic Stenosis Assessment and Management
44
45**Severity Grading (ACC/AHA 2020):**
46
47| Parameter | Mild | Moderate | Severe |
48|-----------|------|----------|--------|
49| Peak velocity (m/s) | 2.0–2.9 | 3.0–3.9 | ≥ 4.0 |
50| Mean gradient (mmHg) | < 20 | 20–39 | ≥ 40 |
51| AVA (cm²) | > 1.5 | 1.0–1.5 | ≤ 1.0 |
52| AVAi (cm²/m²) | — | — | ≤ 0.6 |
53
54**Low-Flow, Low-Gradient AS Subtypes:**
55- Classical (reduced EF): LVEF < 50%, AVA ≤ 1.0, mean gradient < 40 → dobutamine stress echo to differentiate true-severe from pseudo-severe
56- Paradoxical (preserved EF): LVEF ≥ 50%, SVi < 35 mL/m², AVA ≤ 1.0, mean gradient < 40 → often elderly, hypertensive, small LV cavity
57
58**Intervention Criteria (Class I):**
59- Symptomatic severe AS → SAVR or TAVR
60- Asymptomatic severe AS with LVEF < 50% → intervention
61- Asymptomatic severe AS undergoing other cardiac surgery → concomitant AVR
62
63**TAVR vs. SAVR Selection:**
64- Low surgical risk (STS < 3%): SAVR preferred; TAVR acceptable (ACC/AHA 2020)
65- Intermediate risk (STS 3–8%): shared decision-making; both acceptable
66- High risk (STS > 8%) or prohibitive: TAVR preferred
67- Age < 65: SAVR generally preferred (long-term valve durability)
68- Age ≥ 80: TAVR generally preferred
69
70---
71
72## Step 2: Mitral Regurgitation Assessment and Management
73
74**Primary (Degenerative) MR Severity — ASE Integrated Approach:**
75
76| Parameter | Mild | Moderate | Severe |
77|-----------|------|----------|--------|
78| Vena contracta (cm) | < 0.3 | 0.3–0.69 | ≥ 0.7 |
79| EROA (cm²) | < 0.2 | 0.2–0.39 | ≥ 0.4 |
80| Regurgitant volume (mL) | < 30 | 30–59 | ≥ 60 |
81
82**Intervention Criteria for Primary Severe MR (Class I):**
83- Symptomatic severe MR → surgery (repair preferred over replacement)
84- Asymptomatic severe MR with LV dysfunction (LVEF 30–60% or LVESD ≥ 40 mm) → surgery
85
86**Secondary (Functional) MR:**
87- Due to LV dilation and tethering in HFrEF or ischemic cardiomyopathy
88- Optimize GDMT first (medical therapy improves functional MR)
89- COAPT trial: transcatheter edge-to-edge repair (TEER, MitraClip) for severe secondary MR with LVEF 20–50%, LVESD ≤ 70 mm, on maximal GDMT
90- MITRA-FR: no benefit when LV dilation is disproportionately large relative to MR severity
91
92---
93
94## Step 3: Aortic Regurgitation and Right-Sided Valve Disease
95
96**Chronic Severe Aortic Regurgitation Intervention Criteria:**
97- Symptomatic severe AR → surgery (Class I)
98- Asymptomatic severe AR with LVEF < 55% → surgery (Class I)
99- Asymptomatic severe AR with LVEF ≥ 55% but LV severely dilated (LVESD > 50 mm or indexed > 25 mm/m²) → surgery (Class IIa)
100
101**Tricuspid Regurgitation:**
102- Functional TR (most common): secondary to RV dilation, pulmonary hypertension, or AF
103- Severe TR intervention at time of left-sided valve surgery (Class I)
104- Isolated severe TR with progressive RV dilation/dysfunction: emerging transcatheter therapies (TVTR)
105- Medical management: diuretics, treat underlying cause (PH, left heart disease)
106
107**Tricuspid Stenosis (rare):**
108- Usually rheumatic; mean gradient > 5 mmHg = severe
109- Surgical intervention when symptomatic or at time of other valve surgery
110
111---
112
113## Step 4: Surveillance Schedules
114
115**Recommended Echo Surveillance Intervals:**
116
117| Valve Lesion | Mild | Moderate | Severe (Asymptomatic) |
118|-------------|------|----------|----------------------|
119| Aortic stenosis | Every 3–5 years | Every 1–2 years | Every 6–12 months |
120| Aortic regurgitation | Every 3–5 years | Every 1–2 years | Every 6–12 months |
121| Mitral regurgitation | Every 3–5 years | Every 1–2 years | Every 6–12 months |
122| Mitral stenosis | Every 3–5 years | Every 1–2 years | Every year |
123
124**Triggering Earlier Reassessment:**
125- New or worsening symptoms
126- Change in exercise tolerance
127- Decline in LVEF or increase in LV dimensions
128- New atrial fibrillation
129- Rising BNP/NT-proBNP trend
130
131---
132
133## Step 5: Prosthetic Valve Management
134
135**Prosthetic Valve Types and Anticoagulation:**
136
137| Valve Type | Anticoagulation | Target INR |
138|-----------|----------------|------------|
139| Mechanical (aortic) | Warfarin lifelong | 2.0–3.0 (with aspirin 75–100 mg) |
140| Mechanical (mitral) | Warfarin lifelong | 2.5–3.5 (with aspirin 75–100 mg) |
141| Bioprosthetic (surgical) | Aspirin; consider warfarin × 3–6 months | 2.0–3.0 if warfarin used |
142| TAVR | DAPT × 3–6 months → aspirin alone | — (DOACs contraindicated post-TAVR per 2020 guideline) |
143
144**Prosthetic Valve Dysfunction Surveillance:**
145- Annual echo with Doppler assessment of gradients and regurgitation
146- Rising transvalvular gradient → suspect valve thrombosis, pannus, or patient-prosthesis mismatch
147- New paravalvular leak → may require percutaneous closure or reoperation
148
149---
150
151## Checkpoint B: Post-Draft Alignment (Mandatory)
152
1531. Is valve disease severity graded with specific echocardiographic parameters?
1542. Are intervention criteria applied correctly per ACC/AHA 2020 guidelines?
1553. Is the Heart Team evaluation documented or recommended for intervention candidates?
1564. Is the surveillance interval appropriate for the severity and symptom status?
1575. Is prosthetic valve anticoagulation correctly specified if applicable?
158
159---
160
161## Quality Audit
162
163- [ ] Each valve lesion identified and severity graded
164- [ ] At least three quantitative echo parameters documented for severe disease
165- [ ] Discordant parameters addressed (low-flow AS, echo vs. cath correlation)
166- [ ] Symptom status documented and correlated with severity
167- [ ] LVEF and LV dimensions assessed for intervention thresholds
168- [ ] ACC/AHA intervention criteria applied with class of recommendation cited
169- [ ] STS risk score calculated for surgical candidates
170- [ ] TAVR vs. SAVR discussion documented with rationale
171- [ ] Heart Team evaluation documented or recommended
172- [ ] Surveillance interval assigned with next echo date
173- [ ] Endocarditis prophylaxis indications reviewed
174- [ ] Prosthetic valve patients: anticoagulation regimen specified
175- [ ] Exercise testing considered for asymptomatic severe disease
176
177---
178
179## Guidelines
180
1811. Never intervene on moderate valve disease based solely on symptoms — confirm severity with quantitative echocardiographic criteria first.
1822. For severe aortic stenosis, LVEF < 50% is an indication for intervention even in asymptomatic patients — do not wait for symptoms.
1833. In mitral regurgitation, repair is superior to replacement when feasible — refer to high-volume surgical centers with > 95% repair rates.
1844. Low-flow, low-gradient aortic stenosis requires dobutamine stress echo or calcium scoring to distinguish true-severe from pseudo-severe — never operate based on a single resting echo.
1855. TEER (MitraClip) for secondary MR requires strict COAPT trial criteria — patients must be on maximal GDMT and meet anatomic and functional criteria.
1866. DOACs are currently contraindicated for mechanical heart valves — warfarin is the only acceptable anticoagulant (REALIGN trial harm).
1877. Endocarditis prophylaxis is indicated for prosthetic valves, prior endocarditis, unrepaired cyanotic CHD, and repaired CHD with residual defects — for dental procedures involving gingival manipulation or periapical region.
1888. All patients with moderate or greater valve disease should receive annual clinical assessment even between scheduled echo surveillance intervals.