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2021 ESC Guidelines on Cardiac Pacing and CRT

Clinical Quick Reference — Pacing Indications & Cardiac Resynchronization Therapy

Published: European Heart Journal 2021; 42(35): 3427-3520
DOI: 10.1093/eurheartj/ehab364
Chairs: Michael Glikson, Jens Cosedis Nielsen | EHRA Contribution
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What's New in 2021

Major updates from the 2013 ESC guidelines include:

Sinus Node Dysfunction (SND) Pacing

Definition & Diagnosis

Symptomatic SND requires documented bradycardia on ambulatory ECG monitoring (≥2-second pause in sinus rhythm or heart rate <40 bpm during wake hours) in patients with specific symptoms: syncope, presyncope, dyspnea, chest discomfort, or fatigue temporally related to bradycardia.

SND Subtype COR Evidence Indication Details
Symptomatic SND with documented bradycardia Class I A DDD pacing preferred; VVI if AF present/anticipated
Bradycardia-tachycardia syndrome Class I B DDD with rate control or VVI if AF develops
SND without documented bradycardia Class IIb C Limited evidence; consider EP study results

DO: SND Best Practices

  • Document bradycardia (≥2-second pause, HR <40) on ambulatory ECG before pacing decision
  • Use DDD pacing mode in SND without AF to minimize unnecessary RV pacing
  • Program shorter AV delay to optimize LV filling and reduce apical RV pacing burden
  • Monitor patients with PM for new AF development; upgrade to CRT-D if HF develops
  • Avoid VVI pacing in SND unless AF present; DDD preserves AV synchrony

DON'T: Common SND Pitfalls

  • Pace asymptomatic bradycardia or sinus pauses without symptoms
  • Implant VVI pacer for SND without AF documented
  • Place RV lead in apical position if mid-septal alternative available
  • Forget frequent AF screening in SND patients post-implant

Atrioventricular Block Indications

AVB Type COR Evidence Pacing Recommendation
First-degree AVB Class III C No pacing needed unless AV delay >200 ms with symptoms
Second-degree Type I (Wenckebach) Class IIb C Pacing only if symptomatic; rarely needed if HR >40 at rest
Second-degree Type II (Mobitz II) Class I B Permanent pacing indicated (progresses to 3° AVB)
High-degree AVB Class I B Permanent pacing indicated
Third-degree AVB (complete) Class I A Permanent pacing; DDD preferred if AV dissociation

AVB in Special Contexts

Acute Myocardial Infarction: Persistent 3° AVB after anterior MI → permanent pacing (Class I, Evidence C). Inferior MI AVB often transient; observe 5 days before implanting.
Post-Cardiac Surgery: Complete AVB observed for ≥5 days post-op before permanent pacing (Class I). If HPS injury suspected, implant earlier (Class IIa).
Pearl: In Mobitz II, the blocked P wave appears without PR prolongation—QRS is wide and infranodal block. Wenckebach (Type I) shows progressive PR lengthening with eventual dropped beat. Mobitz II is more dangerous and requires pacing.

CRT Indications for Heart Failure

CRT candidacy hinges on three parameters: LVEF ≤35%, QRS morphology & duration, and medical optimization. The 2021 update significantly strengthens LBBB ≥150ms recommendations.

Class I Indications (Recommended)

LVEF ≤35% + LBBB QRS ≥150ms + Symptomatic HF (NYHA II-IV) on OMT
Class I, Evidence B. This is the strongest indication. LBBB morphology (broad notching, prolonged upstroke in V1-V2) predicts best response (>70% response rate).
LVEF ≤35% + LBBB QRS 120-149ms + Symptomatic HF on OMT
Class IIa, Evidence A. Smaller QRS benefit; consider if patient highly symptomatic or recurrent hospitalizations.

Class IIa Indications (Should Be Considered)

LVEF ≤35% + Non-LBBB QRS ≥150ms + Symptomatic HF on OMT
Class IIa, Evidence B. Right bundle branch block (RBBB) or non-specific morphology with wide QRS can benefit; response rates lower (~40-50%) than LBBB.
Upgrade from conventional PM to CRT
Class IIa, Evidence B. Consider in patients with systolic dysfunction (<35%), HF symptoms, and >40% RV pacing burden on conventional pacemaker.

Class IIb Indications (May Be Considered)

LVEF ≤35% + Non-LBBB QRS 120-149ms + Symptomatic HF
Class IIb, Evidence C. Limited data; response unpredictable.
LVEF 35-40% + LBBB QRS ≥120ms with reduced functional capacity
Class IIb, Evidence C. Mildly reduced EF; selectiveuse if significant symptoms.

AF and CRT

Patients with AF eligible for CRT should undergo AV nodal ablation to ensure ≥90-95% biventricular pacing capture. Intrinsic QRS must be ≥120ms LBBB morphology for CRT benefit if native rhythm preserved.

DO: CRT Selection Best Practices

  • Confirm LVEF ≤35% on recent echo (within 3 months preferred)
  • Optimize ACE/ARB, beta-blocker, aldosterone antagonist ≥3-6 weeks before CRT decision
  • Measure QRS duration on 12-lead ECG; assess LBBB morphology carefully (notching V1-V2 indicates LBBB)
  • For AF + CRT: AV ablation with biventricular pacing >95% target
  • Consider CRT-D if LVEF ≤35% + NYHA II-IV despite optimized OMT

DON'T: CRT Pitfalls

  • Implant CRT for non-LBBB QRS <120ms (limited benefit, Class III)
  • Use CRT for LVEF >40% without compelling HF symptoms/HF hospitalization
  • Delay CRT in eligible patient due to borderline EF (35-40%); ICD + CRT can be beneficial if NYHA II-III
  • Forget RV-LV optimization window closes; reassess at 4 weeks post-implant

Conduction System Pacing (CSP)

CSP techniques (His-bundle pacing, left bundle branch pacing) aim to maintain intrinsic ventricular conduction, narrowing QRS and potentially improving outcomes versus RV apical pacing.

His-Bundle Pacing (HBP)

Class IIa, Evidence B: HBP considered for patients requiring RV pacing (SND, AVB, high-degree block) in centers with expertise. Maintains narrow QRS (<120 ms) by capturing His bundle directly.

Advantages

Challenges

Left Bundle Branch Pacing (LBBP)

Class IIb, Evidence C: LBBP is emerging technique with promising early data but limited RCT evidence. Recommendations not yet standardized due to small patient series.

Direct LBB capture may offer superior resynchronization in HF patients vs RV apical pacing. However, procedural complexity, lead positioning challenges, and need for specialized training limit current use.

Pearl: CSP achieves narrower QRS (≈100-120 ms) vs RV apical (~140-160 ms), potentially reducing adverse ventricular remodeling. However, long-term HF outcomes vs CRT-D unclear. Reserve for specialized centers pending larger trials.

Pacemaker Mode Selection & Programming

DDD vs VVI Comparison

Feature DDD Mode VVI Mode
AV Synchrony Maintained (synchronized atrial-ventricular pacing) Lost (ventricular pacing only)
Hemodynamics Preserved atrial "kick"; better CO & BP Loss of synchrony; reduced CO 10-20%
AF Incidence Lower in SND (~30% at 5 years) Higher (~40-50%); retrograde conduction triggers arrhythmia
RV Pacing Burden Can minimize with short AV delay programming 100% RV pacing if no intrinsic conduction
Indication Class I for SND without AF Class I only if AF present/anticipated

Rate-Responsive Pacing

Class I, Evidence A Indicated in patients with chronotropic incompetence (inability to increase HR appropriately during exertion). Used in DDDR or VVIR modes to sensor-mediate rate response when intrinsic AV node cannot accommodate increased metabolic demand.

RV Pacing Minimization Strategies

DO: Device Programming Best Practices

  • Use DDD in SND without AF; program short AV delay (50-100 ms) to minimize RV pacing
  • Assess for chronotropic incompetence in active patients; add rate-response sensor if needed
  • Monitor AF burden regularly; if persistent AF develops, consider VVI mode conversion
  • Program appropriate lower rate limit (60-70 bpm in awake, higher during sleep if needed)
  • Avoid unnecessary ventricular pacing; use threshold testing to confirm lead capture

CIED Complications & Management

Lead-Related Complications

Complication Incidence Risk Factors Management
Lead dislodgement 2.4% (most common) Inexperienced operator, active patient, young age Percutaneous repositioning or replacement; monitor for pacing loss
Lead perforation 0.3-0.7% Thin RV wall, active motion, stiff leads Urgent pericardiocentesis if tamponade; lead removal/replacement
Lead fracture 1-2% Subclavian approach, crush injury, lead age >10 years New lead placement; remove broken lead if high risk
Insulation breakdown 0.5-1% Manufacturing defect, extrinsic damage, age >7 years Lead replacement; monitor for device recall

Infection

Class I, Evidence A Antibiotic prophylaxis required within 1 hour of skin incision (cefazolin 1-2g IV preferred). Device-related bacteremia/endocarditis necessitates early device removal (Class I, Evidence A) with consideration for reimplantation after IV antibiotic course (typically 2-4 weeks).

Incidence: 1.4-1.9% of CIED implants. Risk factors: immunosuppression, diabetes, renal dysfunction, prior device infection, skin integrity issues.

Pocket Hematoma

Frequency: 2.1-9.5% (usually manageable). Most hematomas resolve with pressure and immobilization. Consider reversal of anticoagulation if INR >2 or consider bridging strategy pre-implant. Evacuation needed if hematoma expands or signs of infection.

Tricuspid Regurgitation (TR)

CIED leads may induce or worsen TR, especially with apical RV lead placement. RV pacing duration and lead type associated. No preventive lead selection established. Monitor TR progression on serial echos if hemodynamically significant.

Pitfall: Delayed recognition of lead dislodgement—patient may develop loss of capture or sensing acutely. Always assess 12-lead ECG post-implant for QRS morphology baseline and compare at follow-up visits.

MRI-Conditional Devices & Imaging Safety

MRI-Conditional Pacemakers & ICDs

Class I, Evidence A MRI-conditional devices (labeled as such by manufacturer) are safe during 1.5T or 3T MRI scanning if manufacturer-specific programming conditions are followed (e.g., programmer in-room, specific coil selection, pacemaker-dependent patients require monitoring).

Non-MRI-Conditional Devices

Class IIa, Evidence B If MRI necessary in non-conditional device patients, consider alternatives first (ultrasound, CT). If MRI unavoidable, high-risk protocol with cardiology/EP monitoring, magnet deactivation, and post-procedure interrogation required.

Alternative Imaging

Class IIa, Evidence B Epicardial leads present contraindication to MRI (ferromagnetic heating risk). Consider CT angiography or ultrasound as alternatives.

Leadless pacing: Class IIb, Evidence C. Leadless pacers (no transvenous lead) eliminate ferromagnetic lead concerns, making MRI safer; however, limited long-term data on device longevity and specific MRI protocols still emerging.

Radiation Therapy

Device relocation/shielding strategies required for patients undergoing radiation. Cumulative dose >10 Gy carries higher malfunction risk. Pacemaker-dependent patients require special precautions (temporary pacing backup available).

Special Populations

Elderly Patients

Age alone not contraindication to pacing. Symptomatic bradycardia in octogenarians with adequate functional status warrants pacing (Class I). Dual-chamber preferred over single-chamber for SND preservation of AV synchrony. Minimize unnecessary interventions; shared decision-making essential.

Congenital Heart Disease (CHD)

Class I, Evidence C Pacing indicated if anatomic/congenital abnormalities warrant (e.g., 3° AVB post-surgical repair, complex Tetralogy of Fallot). Lead positioning challenging; epicardial leads often required. Multidisciplinary team approach recommended.

Neuromuscular Diseases

Pregnancy

Pacing may be necessary or deferred based on maternal/fetal risk assessment. No routine indication changes but timing/approach differs. Device implantation preferred in second trimester if urgent. Remote monitoring recommended to minimize fluoroscopy during pregnancy.

Hypertrophic Cardiomyopathy (HCM)

Class IIb, Evidence B AV sequential pacing with short AV delay (70-100 ms) may reduce LV outflow tract gradient in select symptomatic HCM patients refractory to medical therapy. ICD preferred if high sudden death risk.

Long QT Syndrome (LQTS)

ICD generally preferred over pacemaker for primary prevention. High-dose beta-blocker + genetic counseling essential. Pacing may reduce torsades burden in select cases but insufficient evidence for Class I recommendation.

Pearl: Neuromuscular disease patients often have conduction system disease progression. Baseline ECG + periodic ECG monitoring recommended; escalate to ICD if LVEF declines or arrhythmias develop despite pacing.

Device Management & Follow-up Protocols

Pre-Implantation Assessment

Anticoagulation & Antiplatelet Perioperative Management

Continue warfarin (target INR 2-3); delay bridging anticoagulation if INR >2. Continue DOAC without interruption if possible (if not, restart immediately post-implant). Continue aspirin monotherapy without interruption. Heparin bridging use limited unless high-risk (mechanical valve, recent VTE).

In-Office Follow-up Schedule

Device Type First Follow-up Routine Interval
Single/dual-chamber PM 2-12 weeks post-implant ≥12 months (Class IIa, Evidence A)
CRT-P/HBP 2-4 weeks post-implant Every 6 months (Class I, Evidence C)
ICD 2-12 weeks post-implant 3-6 months (device/clinical factors)

Remote Device Monitoring

Class I, Evidence A Recommended for patients with difficulty attending in-office visits or device recalls. Enables real-time transmission of arrhythmia detection, lead/battery status, and alerts.

Battery End-of-Life (EOL) Assessment

DO: Device Management Best Practices

  • Complete comprehensive pre-implant eval; document indication thoroughly in medical record
  • Interrogate device at first post-implant visit (72 hours); assess lead parameters, thresholds, impedances
  • Optimize device programming based on patient symptoms and pacing burden
  • Schedule CRT optimization at 4 weeks post-implant: AV/VV delays programmed to maximize resynchronization
  • Educate patient on device, activity restrictions, MRI precautions, and when to seek care

DON'T: Device Management Pitfalls

  • Implant device without documented indication (e.g., asymptomatic bradycardia)
  • Neglect antibiotic prophylaxis (<1 hour pre-incision) or post-operative wound care
  • Ignore battery EOL; ensure elective change, not emergency
  • Forget post-operative X-ray to confirm lead position; dislodgement must be detected early

Clinical Do's & Don'ts (Summary)

DO

  • Perform comprehensive pre-implantation evaluation for every patient
  • Document bradycardia indication on ambulatory ECG monitoring
  • Minimize RV pacing through AV delay programming strategies (DDD, short AV delays)
  • Use DDD mode in SND; upgrade to CRT if HF develops
  • Assess QRS morphology carefully (LBBB notching in V1-V2 vs RBBB)
  • Optimize medical therapy ≥6 weeks before CRT decision
  • Monitor AF burden regularly; adjust device mode if persistent AF develops
  • Ensure antibiotic prophylaxis (<1 hour pre-incision, cefazolin preferred)
  • Schedule CRT optimization at 4 weeks post-implant
  • Use ambulatory ECG monitoring for bradycardia evaluation (Holter, event monitor)

DON'T

  • Pace asymptomatic bradycardia without documented indication
  • Implant VVI pacemaker for SND without AF documented
  • Use single-chamber VVI when dual-chamber DDD indicated
  • Implant CRT for non-LBBB QRS <120 ms (Class III, Evidence B)
  • Perform permanent pacing for transient AVB without 5-day observation period (post-op/MI context)
  • Place RV lead in apical position if mid-septal alternative available
  • Implant pacemaker before TAVI in RBBB without clear bradycardia indication
  • Recommend routine pacing for mechanical tricuspid valve without other indication
  • Forget frequent AF screening in SND patients post-implant
  • Neglect device interrogation post-implant; must verify lead capture & sensing

Clinical Decision Support Calculators

Use these tools to assess risk, predict outcomes, and support clinical decision-making: