850-Arrhythmias (Section 1) Flashcards

1
Q

Normal Conduction

A
  • The conduction of the heart normally begins at the SA-node, located in the right atria
  • The SA-node initializes depolarization of atrial muscle cells
  • The AV-Node, located between the atria and ventricles, is activated and, after a delay, initiates the conduction impulse through the ventricles
  • The Purkinje Fibers carry the signal through the septum to the apex and the rest of the ventricular mass
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2
Q

Interval P-R

-Normal Ranges (per ms) & Pathology

A
  1. Normal range (per ms): 120-200

2. Pathology: Long-heart block (drugs, electrolytes)

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3
Q

Interval QRS

-Normal Ranges (per ms) & Pathology

A
  1. Normal range: 80-120

2. Pathology: Long-conduction abnormalities e.g. bundle branch block

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4
Q

Interval QT

-Normal Ranges (per ms) & Pathology

A
  1. Normal range: (varies with heart value) >450 can lead to ventricular tachycardia
  2. Pathology: Long-repolarisation abnormalities, ion channel-pathies e.g. long QT syndrome
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5
Q

PR Interval

A
  • A time interval that represent AV-node conduction (time impulse travels through the AV-node)
  • Drugs are often used to slow impulses through the AV node.
  • Drugs and disease states may increase time interval or action potential conduction that may lead to blockage of the impulse
  • Need to monitor PR interval with certain drugs
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6
Q

QT and QTc interval

A

-QT interval represents time for ventricular depolarization and repolarization.
-QT interval is rate dependent (i.e., depends on heart rate)
-Should correct with Bazett formula (corrects for HR):
QTc interval = [(QT)/(square root R-R)]

> > > (square root of the RR interval represents heart rate. Most ECG’s that are done will have the QTc calculated for you)«<

  • In general, prolonged QTc interval is considered to be >0.45 secs (450 msec)
  • NEED TO MONITOR FOR DRUGS THAT PROLONG QT INTERVALS TO PREVENT PROARRHYTHMIC EVENTS.
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7
Q

Action potential (blank 1)&raquo_space; Electrical Impulses&raquo_space; Heart Beat&raquo_space; ECG

A

Blank 1: usually generated from SA node

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8
Q

Phase 0

A

depolarization

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9
Q

Phase 1

A

repolarization

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10
Q

Phase 2

A

plateau phase

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11
Q

Phase 3

A

rapid depolarization phase

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12
Q

Phase 4

A

depolarization

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13
Q

Phase 0 (Na+ Dependent & Ca++ Dependent):

A
  • Na+ Dependent: Atrium, Ventricles
  • Ca++ Dependent: SA and AV node

NEED TO KNOW (and how it relates to anti arrhythmic therapy)

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14
Q

Impulse Generation “Leak”

A
  • During Phase 4, a gradual slope (caused by background K+ and Na+ currents) in the potential leads to activation of voltage-gated sodium channels –THRESHOLD POTENTIAL and Phase 0!!! – electrical energy and start of one heart beat.
  • Altering the characteristics of this slope or the sensitivity of sodium channels can alter cardiac pacing (i.e, heart rate)
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15
Q

Slope of Phase 4

A
  • Increase slope, increase automaticity (heart rate)
  • Sympathetic activity increases slope of phase 4 and thus HR.
  • Cholinergic activity decreases slope of phase 4 and thus HR
  • Some antiarrhythmic drugs can change slope of phase 4 and change heart rate
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16
Q

Impulse Generation

A
  • SA node: 60 to 100 beats/minute (most leaky ion currents thus SA node is the primary pacemaker cell in the heart)
  • AV node: 30 to 50 beats/minute
  • Ventricles: < 30 beats/minute

Question 1: Which one has the highest Phase 4 slope?
Question 2: If the SA node does not generate an electrical impulse what would be the heart rate?

17
Q

Effective or Absolute, (phase 2) (ERP) is the

A
  • Longest amount of time when class cannot be depolarized again. The longest input that fails to conduct
    1. Atria 200-270 msecs
    2. Ventricles 200-270 msecs
    3. AV node 280-450 msecs
18
Q

Relative Refractory Periods (RRP)

A

Relative (phase 3, 4) (RRP)
-Time when cells can be depolarized again with a strong enough stimulus. The longest premature coupling interval at which delay in conduction (prolongation of conduction) occurs