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Comprehensive history
and physical examination Sleep apnea?
(Class I)
Echocardiography
SND Diagnostic AV Block Conduction disorder
if structural heart
algorithm Diagnostic algorithmÁ Diagnostic algorithm§
disease suspected
Exercise-related
symptoms
Yes
No Infrequent
Exercise ECG testing Symptoms ICM
(Class IIa) (>30 days) (Class IIa)
Abnormal Normal
Ambulatory ECG
monitoringŒ
(Class I)
Significant arrythmias
No significant
arrhythmias
Conduction disorder
SND AV Block with 1:1 AV conduction Observation
Continued
SND Diagnostic AV Block Conduction disorder concern for
algorithm Diagnostic algorithmÁ Diagnostic algorithm§ bradycardia?
Figure 2. Initial Evaluation of Suspected
or Documented SND Algorithm
Evidence for sinus
node dysfunction*
Reversible or
Yes
Can we make these lines
No
this arrow?
(Class I)
even?
Treatment
effective or
unnecessary
Suspicion for
Yes No structural heart
disease
Observe
Yes
Transthoracic
echocardiography
(Class IIa)
No
Suspicion
for infitrative CM,
endocarditis,
ACHD
Yes
No
Advanced imaging
(Class IIa)
Treat identified
abnormalities
Symptoms
No Observe
Yes
Exercise
related
Yes No
If not already performed:
Exercise ECG testing
(Class IIa)
Diagnostic
If not already performed:
No Ambulatory ECG monitoring
(Class I)
Yes
Electrophysiology study
(if performed for other reasons)
(Class IIb)
Reversible or
Physiologic cause
Yes No
Treat underlying cause as
needed, e.g., sleep apnea
(Class I)
Treatment
effective or not
necessary
Mobitz
type II 2° AV Block,
No Advanced AV Block,
Yes complete heart
block
Observe
Yes No
Transthoracic
echocardiography Suspicion for
(Class I) structural heart
disease
Suspicion Yes
for infiltrative CM,
endocarditis, ACHD,
etc. Suspicion
for infiltrative CM, No
Yes endocarditis, ACHD,
Advanced No etc.
imaging*
(Class IIa) Yes No
AV block
treatment Advanced Transthoracic
algorithm imaging echocardiography
(Class IIa) (Class IIa)
Treat identified
abnormalities
Determine
site of AV
AV nodeΐ Block
Unclear
Infranodal (Mobitz Type I)
e.g. 2:1 AV Block
Symptoms Symptoms
Exercise testing
Yes No Infranodal No
(Class IIa) Yes
Electrophysiology
study Infranodal
(Class IIb)
Noninvasive Evaluation
Resting ECG
External loop recorder (patient or • Frequent, spontaneous symptoms potentially related to bradycardia or conduction
auto triggered) disorder, likely to recur within 2–6 wk
Mobile cardiac outpatient • Spontaneous symptoms, potentially related to bradycardia or conduction disorder, that are too brief,
telemetry too subtle, or too infrequent to be readily documented with patient activated monitors
• In high-risk patients whose rhythm requires real-time monitoring
Implantable cardiac monitor • Recurrent, infrequent, unexplained symptoms, potentially related to bradycardia or conduction
disorder after a nondiagnostic initial workup, with or without structural heart disease
Cardiac Imaging
Recommendations for Cardiac Imaging in Bradycardia or Conduction Disorders
Invasive Testing
Implantable Cardiac Monitor
Yes
Atropine*
(Class IIa)
Drug
Type? Yes
Toxicity?†
Yes
No
MI with Aminophylline
Yes
AV Block? (COR IIb)
No
Beta-agonists
(COR IIb)
Yes
Continued
symptoms?
Yes
Acute Pacing
Algorithm‡
Acute Management of Reversible Causes of SND
Drugs or toxins*
Toluene, organophosphates, tetrodotoxin, cocaine
Electrolyte abnormality
Hyperkalemia, hypokalemia, hypoglycemia
Hypothyroidism
Hypovolemic shock
Hypoxemia, hypercarbia, acidosis
Sleep apnea, respiratory insufficiency (suffocation, drowning, stroke, drug overdose)
Infection
Lyme disease, legionella, psittacosis, typhoid fever, typhus, listeria, malaria, leptospirosis, Dengue fever, viral
hemorrhagic fevers, Guillain-Barre
Medications*
Beta blockers, non-dihydropyridine calcium channel blockers, digoxin, antiarrhythmic drugs, lithium,
methyldopa, risperidone, cisplatin, interferon
*Incomplete list
Acute Medical Therapy
Recommendations for Atropine and Beta-Agonists for Bradycardia Attributable to
SND
Atropine 0.5-1 mg IV (may be repeated every 3-5 min to a maximum dose of 3 mg)
Dopamine 5 to 20 mcg/kg/min IV, starting at 5 mcg/kg/min and increasing by 5 mcg/kg/min every 2 min
Isoproterenol 20-60 mcg IV bolus followed doses of 10-20 mcg, or infusion of 1-20 mcg/min based on heart rate response
10% calcium chloride 1-2 g IV every 10-20 min or an infusion of 0.2-0.4 mL/kg/h
10% calcium gluconate 3-6 g IV every 10-20 min or an infusion at 0.6-1.2 mL/kg/h
High dose insulin therapy IV bolus of 1 unit/kg followed by an infusion of 0.5 units/kg/h
Digoxin overdose
Digoxin antibody fragment Dosage is dependent on amount ingested or known digoxin concentration
Table 8. Acute Medical Management with
Theophylline or Aminophylline for Bradycardia
Attributable to SND or Atrioventricular Block
Theophylline 300 mg IV, followed by oral dose of 5-10 mg/kg/d titrated to effect
Spinal cord injury
Critically
ill due to
bradycardia
Yes No
Permanent
Transcutaneous pacemaker indicated and
pacing (Class IIb) capability immediately
available
Yes No
Yes No
Externalized Temporary
permanent transvenous
pacing lead pacing wire
(Class IIa) (Class IIa)
General Principles of Chronic
Therapy/Management of Bradycardia due to SND
Recommendations for General Principles of Chronic Therapy/Management of
Bradycardia Attributable to SND
Confirm symptoms
Rule out reversible
causes
Due
to required GDMT
(no reasonable
alternative)
Symptoms
No correlate with
bradycardia
Yes
Response
Infrequent
suggests symptomatic
pacing? Significant
sinus node
comorbidities?
dysfunction?
No
Yes No
Yes
Single chamber
Willing to
ventricular pacing
have a PPM?
(Class IIa)
Normal
AV conduction Yes No
and reason to
avoid an RV Oral theophylline
lead? (Class IIb)
Yes No
Bradycardia Attributable to
Atrioventricular Block
Table 9. Etiology of Atrioventricular Block
Congenital/genetic Vagotonic-associated with increased vagal tone
Congenital AV block (associated with maternal Sleep, obstructive sleep apnea
systemic lupus erythematosus) High-level athletic conditioning
Congenital heart defects (e.g., L-TGA) Neurocardiogenic
Genetic (e.g., SCN5A mutations)
Infectious Metabolic/endocrine
Lyme carditis Acid-base disorders
Bacterial endocarditis with perivalvar abscess Poisoning/overdose (e.g., mercury, cyanide, carbon
Acute rheumatic fever monoxide, mad honey)
Chagas disease Thyroid disease (both hypothyroidism and
Toxoplasmosis hyperthyroidism)
Adrenal disease (e.g., pheochromocytoma,
hypoaldosteronism)
Ischemic Iatrogenic
Acute MI Medication related
Coronary ischemia without infarction—unstable o Beta blockers, verapamil, diltiazem, digoxin
angina, variant angina o Antiarrhythmic drugs
Chronic ischemic cardiomyopathy o Neutraceuticals
Catheter ablation
Degenerative Cardiac surgery, especially valve surgery
TAVR, alcohol septal ablation
Lev’s and Lenegre’s diseases
Acute Management of Reversible Causes of
Atrioventricular Block
Recommendations for Acute Management of Reversible Causes of Bradycardia
Attributable to Atrioventricular Block
COR LOE Recommendation
Patients with transient or reversible causes of atrioventricular
block, such as Lyme carditis or drug toxicity, should have medical
therapy and supportive care, including temporary transvenous
I B-NR pacing if necessary, before determination of need for permanent
pacing.
In selected patients with symptomatic second-degree or third-
degree atrioventricular block who are on chronic stable doses of
medically necessary antiarrhythmic or beta-blocker therapy, it is
IIa B-NR reasonable to proceed to permanent pacing without further
observation for drug washout or reversibility.
Acute Management of Reversible Causes of
Atrioventricular Block
Recommendations for Acute Management of Reversible Causes of Bradycardia
Attributable to Atrioventricular Block
Permanent Permanent
Permanent Permanent Permanen t Permanent Permanent Permanent
pacing pacing
pa cing pacing pacing pacing pacing pacing
(Class III: (Class III:
(Class IIa) (Class IIb) (Class IIa) (Class IIa) (Class I) (Class I)
Harm) Harm)
Cardiac
resynchronization therapy
candidate because of HF symptoms?
(LVEF <35%)
Yes GDMT§
No
Infrequent pacing?
Significant comorbidities?
Single chamber
Yes ventricular pacing
No
(Class I)
Permanent
atrial fibrillation?
Single chamber
Yes ventricular pacing
No (Class I)
No
LVEF >50%
Right ventricular pacing lead
Yes
No (Class IIa)
Predicted
pacing <40%?
Right ventricular pacing lead
Yes
(Class IIa)
No
Reversible
or Physiologic
cause
Yes
Treat underlying cause as No
needed, e.g., ischemia
Treatment
effective or not
necessary
Genetic
disorder associated
Yes No with conduction
Observe disease
Yes No
Type
of conduction
disorder
RBBB or fascicular
LBBB
block
Transthoracic Transthoracic
echocardiography echocardiography
(Class I) (Class IIa)
Treat identified
abnormalities
Symptoms
suggestive of intermittent
bradycardia
Yes No
Electrophysiology study
Observe
(Class IIa)
Management of Conduction Disorders
(With 1:1 Atrioventricular Conduction)
Recommendations for Management of Conduction Disorders (With 1:1
Atrioventricular Conduction and Normal PR Intervals)
Syncope,
BBB, and
HV >70ms
Permanent pacing
Yes
(Class I)
No
Alternating
BBB
Permanent pacing
Yes (Class I)
No
Cardiac resynchronization
Yes therapy
No
(Class IIb)
Symptoms
suggest intermittent
AV block?
Yes No
AV block diagnostic
Observation
algorithm†
2018 Bradycardia Guideline
Special Populations
Patients at Risk for Bradycardia During
Noncardiac Surgery or Procedures
Recommendations for Patients at Risk for Bradycardia During Noncardiac Surgery or
Procedures
Shared Decision-Making
Shared Decision-Making
Recommendations for Shared Decision-Making for Pacemaker Implantation in the Setting of
Guideline-Based Indications for Bradycardia Pacing
COR LOE Recommendation
In patients with symptomatic bradycardia or conduction disorder,
clinicians and patients should engage in a shared decision-making
approach in which treatment decisions are based not only on the best
I C-LD available evidence, but also on the patient’s goals of care, preferences,
and values.
In patients with indications for permanent pacing but also with significant
comorbidities such that pacing therapy is unlikely to provide meaningful
III: No clinical benefit, or if patient goals of care strongly preclude pacemaker
C-LD therapy, implantation or replacement of a pacemaker should not be
Benefit performed.
2018 Bradycardia Guideline
Discontinuation of Pacemaker
Therapy
Discontinuation of Pacemaker Therapy