2.2 Heart Failure & Cardiac Arrhythmias
Key Takeaways
- Heart failure is categorized by ejection fraction into HFrEF (LVEF ≤40%), HFmrEF (LVEF 41-49%), and HFpEF (LVEF ≥50%), with B-type Natriuretic Peptide (BNP >100 pg/mL or NT-proBNP >300 pg/mL) serving as the primary diagnostic biomarker.
- Guideline-Directed Medical Therapy (GDMT) for HFrEF mandates four foundational pillars proven to improve survival: ARNI (Sacubitril/Valsartan) or ACEi/ARB, Beta-blockers (Carvedilol, Bisoprolol, Metoprolol Succinate), Mineralocorticoid Receptor Antagonists (Spironolactone/Eplerenone), and SGLT2 inhibitors (Dapagliflozin/Empagliflozin).
- Atrial Fibrillation stroke risk is quantified using the CHA2DS2-VASc score (score ≥2 in men or ≥3 in women indicates oral anticoagulation with DOACs), while rate control (target resting HR <110 bpm) is achieved using Beta-blockers or Non-dihydropyridine CCBs.
- Acute narrow-complex SVT in hemodynamically stable patients is managed sequentially with vagal maneuvers followed by rapid IV push Adenosine (6 mg then 12 mg), whereas ANY hemodynamically unstable tachyarrhythmia demands immediate Synchronized Direct Current Cardioversion.
Heart Failure & Cardiac Arrhythmias
1. Heart Failure Definitions & Classification
Heart Failure (HF) is a complex clinical syndrome resulting from structural or functional impairment of ventricular filling or ejection. It is characterized by elevated intracardiac pressures and inadequate cardiac output at rest or during exercise.
Ejection Fraction Categories (ESC / ACC / AHA Guidelines)
- Heart Failure with Reduced Ejection Fraction (HFrEF): $LVEF \le 40%$. Characterized by impaired myocardial contractility (systolic dysfunction), most commonly secondary to CAD, MI, or dilated cardiomyopathy.
- Heart Failure with Mildly Reduced Ejection Fraction (HFmrEF): $LVEF \text{ 41–49%}$. Represents a middle spectrum requiring mild systolic dysfunction management.
- Heart Failure with Preserved Ejection Fraction (HFpEF): $LVEF \ge 50%$. Driven by impaired ventricular relaxation and compliance (diastolic dysfunction), strongly linked to long-standing hypertension, aging, obesity, and diabetes mellitus.
Functional & Staging Systems
| NYHA Functional Class | Symptomatic Limitation | ACC/AHA Stage | Structural Heart Disease Status |
|---|---|---|---|
| Class I | No limitation of physical activity. Ordinary activity does not cause fatigue or dyspnea. | Stage A | High risk for HF (HTN, CAD, DM) without structural heart disease or symptoms. |
| Class II | Slight limitation of physical activity. Comfortable at rest; ordinary activity results in fatigue/palpitations. | Stage B | Structural heart disease present (e.g., prior MI, LV hypertrophy) without HF symptoms. |
| Class III | Marked limitation of physical activity. Comfortable at rest; less than ordinary activity causes symptoms. | Stage C | Structural heart disease with prior or current clinical symptoms of HF. |
| Class IV | Inability to carry on any physical activity without discomfort. Symptoms present even at rest. | Stage D | Refractory end-stage HF requiring specialized interventions (LVAD, transplant). |
2. Diagnostic Workup & Biomarkers
- Natriuretic Peptides (BNP & NT-proBNP): Ventricular myocytes release B-type natriuretic peptide in response to wall stress and volume overload.
- BNP: $<100 \text{ pg/mL}$ rule-out value in acute dyspnea; $>400 \text{ pg/mL}$ strongly indicates acute HF.
- NT-proBNP: $<300 \text{ pg/mL}$ rule-out value; age-adjusted cutoffs for rule-in: $>450 \text{ (<50 yrs)}$, $>900 \text{ (50-75 yrs)}$, $>1800 \text{ (>75 yrs)}$.
- Note: Patients taking Sacubitril/Valsartan (ARNI) will have artificially elevated BNP levels (because Sacubitril inhibits neprilysin which degrades BNP), but NT-proBNP is not degraded by neprilysin and remains accurate.
- Transthoracic Echocardiogram (TTE): Essential initial test to measure LVEF, assess valvular structure, wall motion abnormalities, and estimate pulmonary artery systolic pressure (PASP).
- Chest X-Ray (ABCDE Criteria):
- Alveolar edema (bat-wing appearance)
- Berley (Kerley) B lines (interlobular septal fluid)
- Cardiomegaly (Cardiothoracic ratio >0.50)
- Dilated upper lobe vessels (cephalization)
- Effusions (pleural, blunting of costophrenic angles)
3. Guideline-Directed Medical Therapy (GDMT) for HFrEF
All patients with HFrEF ($LVEF \le 40%$) must be established on the Four Foundational Pillars of GDMT unless contraindications exist, as each class independently reduces all-cause mortality:
| Drug Class | Key Mechanisms & Representatives | Clinical Pearls & Monitoring |
|---|---|---|
| 1. ARNI / ACEi / ARB | ARNI: Sacubitril/Valsartan (Neprilysin inhibitor + ARB). ACEi: Enalapril, Ramipril, Lisinopril. ARB: Valsartan, Candesartan. | ARNI is preferred over ACEi/ARB. Must allow a 36-hour washout period when switching from an ACEi to ARNI to prevent severe angioedema. Monitor Serum $K^+$ and Creatinine. |
| 2. Beta-Blockers | Carvedilol, Bisoprolol, Metoprolol Succinate (sustained-release). | Reduces SNS toxicity and cardiac remodeling. Do not initiate during acute decompensation; start at low doses when patient is euvolemic. |
| 3. MRAs | Spironolactone, Eplerenone (Mineralocorticoid Receptor Antagonists). | Blocks aldosterone remodeling. Indicated if $LVEF \le 40%$. Avoid if Serum $K^+ > 5.0 \text{ mEq/L}$ or Serum Creatinine $>2.5 \text{ mg/dL}$. |
| 4. SGLT2 Inhibitors | Dapagliflozin, Empagliflozin (Sodium-Glucose Cotransporter 2 inhibitors). | Reduces HF hospitalizations and cardiovascular mortality regardless of diabetes status. Risk of euglycemic DKA and UTIs. |
Additional Therapies & Device Indications
- Loop Diuretics (Furosemide, Torsemide): Symptom relief of congestion; does NOT confer mortality benefit, adjust to maintain euvolemia.
- Ivabradine: Inhibits funny ($I_f$) channels in SA node. Indicated if patient is in sinus rhythm with resting heart rate $\ge 70 \text{ bpm}$ despite maximal tolerated beta-blocker dose.
- Hydralazine + Isosorbide Dinitrate: Indicated in self-identified Black patients with persistent NYHA Class III-IV HFrEF despite GDMT, or in patients intolerant to ACEi/ARB/ARNI due to severe renal impairment or hyperkalemia.
- Implantable Cardioverter-Defibrillator (ICD): Primary prevention of sudden cardiac death if $LVEF \le 35%$ despite $\ge 3$ months of optimal GDMT and NYHA Class II-III.
- Cardiac Resynchronization Therapy (CRT-D): Indicated if $LVEF \le 35%$, Sinus Rhythm, and Left Bundle Branch Block (LBBB) with $QRS \ge 150 \text{ ms}$.
4. Acute Decompensated Heart Failure (ADHF)
Clinical presentation is categorized based on Hemodynamic Profiles (Forrester Classification):
- Warm & Wet (Most Common ~80%): Adequate perfusion, severe congestion. Treated with IV Loop Diuretics (Furosemide IV dose $\ge 1-2.5\times$ oral home dose) + IV Vasodilators (Nitroglycerin / Nitroprusside if $SBP > 110 \text{ mmHg}$).
- Cold & Wet (Cardiogenic Shock with Congestion): Poor perfusion ($SBP <90 \text{ mmHg}$, cold extremities, oliguria, altered sensorium) + congestion. Treated with IV Inotropes (Dobutamine, Milrinone) $\pm$ Vasopressors (Norepinephrine) to restore organ perfusion before cautious diuresis.
5. Cardiac Arrhythmias
Atrial Fibrillation (AF)
- ECG Characteristics: Irregularly irregular ventricular response, absence of distinct P waves, fibrillatory waves (rate 350-600 bpm).
- Stroke Risk Stratification (CHA2DS2-VASc Score):
- Congestive heart failure (+1)
- Hypertension (+1)
- A2ge $\ge 75$ years (+2)
- Diabetes mellitus (+1)
- S2troke / TIA / Thromboembolism (+2)
- Vascular disease (prior MI, PAD, aortic plaque) (+1)
- Age 65–74 years (+1)
- Scex category (Female) (+1)
- Recommendation: Score $\ge 2$ in men or $\ge 3$ in women mandates oral anticoagulation with Direct Oral Anticoagulants (DOACs: Apixaban, Rivaroxaban, Dabigatran) preferred over Warfarin.
- Rate Control vs Rhythm Control:
- Rate Control: Target resting HR <110 bpm using Beta-blockers (Metoprolol), Non-dihydropyridine CCBs (Diltiazem, Verapamil - avoid CCBs in HFrEF!), or Digoxin.
- Rhythm Control: Electrical cardioversion or antiarrhythmic drugs (Amiodarone, Flecainide, Propafenone). If AF duration $>48 \text{ hours}$, anticoagulation for at least 3 weeks prior and 4 weeks after cardioversion is required (or TTE/TEE to exclude LA appendage thrombus).
Supraventricular Tachycardia (SVT / AVNRT)
- ECG: Regular, narrow QRS complex (<120 ms), rate 150-250 bpm, P waves hidden or retrogradely buried in QRS.
- Management Algorithm:
- Hemodynamically Unstable $\rightarrow$ Immediate Synchronized Cardioversion (50-100 J).
- Hemodynamically Stable $\rightarrow$ Vagal Maneuvers (modified Valsalva or carotid sinus massage).
- Pharmacotherapy $\rightarrow$ Adenosine $6 \text{ mg}$ rapid IV push followed by $20 \text{ mL}$ saline flush. If no conversion within 1-2 min, give $12 \text{ mg}$ rapid IV push. (Side effects: flushing, bronchospasm, transient cardiac arrest/asystole).
- Second-line: IV Beta-blockers or IV Diltiazem/Verapamil.
Ventricular Tachycardia (VT) vs Wide-Complex Tachycardia
- ECG: Broad QRS complex ($\ge 120 \text{ ms}$), rate >100 bpm. Assume ANY wide-complex tachycardia is VT until proven otherwise.
- Brugada Criteria for VT: Absence of RS complex in all precordial leads, RS interval >100 ms, AV dissociation, fusion or capture beats.
- Management:
- Pulseless VT or VF: Immediate unsynchronized high-energy shock (Defibrillation 200J biphasic) + CPR.
- Unstable VT with Pulse: Immediate Synchronized Cardioversion (100J).
- Stable Monomorphic VT: IV Amiodarone ($150 \text{ mg}$ over 10 min followed by infusion) or IV Procainamide.
Atrioventricular (AV) Heart Blocks
| Type of AV Block | ECG Characteristic | Clinical Features & Management |
|---|---|---|
| First-Degree | Prolonged PR interval ($>200 \text{ ms}$), constant, 1:1 AV conduction | Usually benign, asymptomatic. No treatment required. |
| Second-Degree Mobitz I (Wenckebach) | Progressive prolongation of PR interval until a QRS complex is dropped | AV nodal block. Often transient/benign (vagal tone, inferior MI). Monitor. |
| Second-Degree Mobitz II | Constant PR interval followed by intermittent sudden dropped QRS | Infranodal block (His-Purkinje system). High risk of progression to complete heart block. Requires Permanent Pacemaker. |
| Third-Degree (Complete) | Complete AV dissociation; P waves and QRS complexes occur independently | Severe bradycardia, syncope (Stokes-Adams attacks). Emergency Transcutaneous/Transvenous Pacing followed by Permanent Pacemaker. |
A 65-year-old male with long-standing hypertension presents with exertional dyspnea and bilateral ankle edema. Echocardiogram demonstrates a Left Ventricular Ejection Fraction (LVEF) of 32%. Which combination of drug classes represents the mandatory four foundational pillars of Guideline-Directed Medical Therapy (GDMT) to reduce all-cause mortality in this patient?
A 72-year-old female with a history of hypertension and type 2 diabetes mellitus is newly diagnosed with non-valvular atrial fibrillation. She has no history of stroke, vascular disease, or heart failure. What is her CHA2DS2-VASc score, and what is the recommended stroke prevention strategy?
A 28-year-old male presents to the emergency department with sudden-onset rapid palpitations and lightheadedness. ECG shows a regular narrow-complex tachycardia at a rate of 190 beats/min. His blood pressure is 118/76 mmHg, and systemic physical examination is entirely normal. Modified Valsalva maneuver fails to convert the rhythm. What is the most appropriate first-line pharmacotherapy?
An 80-year-old male presents with recurrent episodes of dizziness and presyncope. Electrocardiogram reveals P waves occurring regularly at a rate of 84 bpm and QRS complexes occurring independently at a regular rate of 34 bpm, with no constant PR interval or relationship between P waves and QRS complexes. What is the diagnosis and definitive management for this patient?