· Lead 2 trace
· ECG components table
· PR interval physiology including pacemaker potentials
· PR interval abnormalities
Parameter |
Normal values |
P wave |
· ≤0.12 seconds · <2.5mm · Positive in II and aVF, biphasic in V1 |
PR interval |
· 0.12 – 0.2 seconds, isoelectric |
QRS complex |
· <0.12 seconds |
Q wave |
· ≤0.04 seconds · ≤2mm, ≤25% height of QRS complex |
ST segment |
· <2mm deviation from isoelectric in V1-2-3 · <1mm deviation from isoelectric elsewhere |
T wave |
· <5mm height |
QT interval |
· Bazett formula: QTc = QT/√(RR) · ≤440 in men, ≤460 in women · > 350ms in both |
Significance |
· Time between excitation of the atrium to excitation of the ventricles · Hence atrial kick · Hence higher cardiac output |
Components |
· Atria (0.5m/s) · AV node (mostly this, 0.05m/s) · Bundle of His (2-4m/s) |
Pacemaker potential of AV node cells |
|
Physiological |
Usually within normal limits · ↑SNS -> ↑cAMP -> ↑slope phase 4 (more than other phases) · ↑Temperature -> ↑pacemaker cell metabolic rate |
Pathological |
Accessory pathway · WPW syndrome · LGL syndrome |
Types |
· First degree: ↑PR interval · Second degree Mobitz 1: ↑PR interval each beat until dropped QRS · Second degree Mobitz 2: intermittent dropped QRS · Third degree: no AV conduction, escape rhythm |
Physiological |
Usually within normal limits · PSNS -> ↓cAMP and ↑K+ conductance -> ↓slope phase 4, ↑hyperpolarisation o E.g. fit athlete · ↓Temp -> ↓pacemaker cell metabolic rate · ↓pO2 -> failure of Na+K+ATPase, unable to repolarize, HCN channel inactive · ↑K+ -> ↑membrane potential -> ↓excitability of conduction system |
Pathological |
· Degeneration of conducting system · Fibrosis · Ischaemia, infarction · Infection: myocarditis, endocarditis · Infiltration · Connective tissue disease |
Medication |
· Beta blockers · Verapamil, diltiazem · Digoxin |
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