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Advanced ECG Interpretation

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1 Advanced ECG Interpretation
Dr. Jeffrey Elliot Field, HBSc. DDS, Fellow, American Dental Society of Anesthesia Diploma, the National Dental Board of Anesthesia. 1 4/19/2017 1

2 OBJECTIVES To get a more in depth knowledge of ECG interpretation.

3 The P-Wave in Detail The normal P-wave: Has a smooth contour
Is monophasic in lead II Is biphasic in lead V1 Has a duration 0f less than 0.12 seconds or 3 small boxes.

4 P-wave Abnormalities Seen in Lead II
In lead II two types of P-wave abnormalities can be seen. Right atrial enlargement is seen as a taller than normal P-wave( increased amplitude) Left atrial enlargement seen as a P-wave with a notch in it.

5 P-Wave Abnormalities Seen In V1
Biphasic P-Waves are seen for both left and right atrial enlargement. For right atrial enlargement the initial portion of the P-wave is larger than the distal portion. Alternatively for left atrial enlargement the initial portion of the P-wave is smaller than the distal portion.

6 P Pulmonale ( right atrial enlargement)
Note the larger initial portion 4/19/2017

7 P Mitrale ( left atrial enlargement)
Note the larger terminal portion 4/19/2017

8 The QRS Complex in Detail
As well as showing ventricular conduction defects, the QRS complex along with ST segment analysis is used to diagnose myocardial oxygen deficits and myocardial infarctions. The QRS complex is also used to diagnose accessory conduction pathways in the heart.

9 S-T Segment Analysis In order to assess the S-T segment we must first define the J-point. The J point in the ECG is the point where the QRS complex joins the ST segment. It represents the approximate end of depolarization and the beginning of repolarization.

10 The Isoelectric Point S-T segments can be elevated, depressed or isoelectric. The J-point is deemed to be isoelectric if the S-T line/segment is not elevated or depressed with respect to the P-Q line/segment. As in the diagram below. See arrows 

11 S-T Changes You can see both S-T elevation and S-T depression on ECG’s. S-T elevation is indicative of a myocardial infarction. So in other words myocardial cell death is occuring. S-T depression is indicative of myocardial ischemia. The myocardial cells are not getting enough oxygen and are at risk of dying.

12 S-T Depression

13 S-T Elevation

14 Myocardial Infarction
Myocardial infarctions can be categorized as follows: -Q-wave MI -Non Q-wave MI 4/19/2017

15 Q-Wave Myocardial Infarction
This is the classic presentation for MI’s. The developing MI is seen as ST segment elevation followed by deepening Q-waves in the leads where ST segment elevation was 1st seen. Q waves are “significant” if they are greater than 1 box in width (longer than 0.04 msec), or are larger than 1/4 of the R wave. Significant Q waves are indicative of myocardial infarction. However signifigant Q-waves in lead III alone are NOT diagnostic of an infarction, even they are otherwise “significant” in size and width. Therefore signifigant Q-waves in lead III are ignored unless other abnormalities are seen. 4/19/2017

16 Note the large Q-waves.

17 Non Q-Wave Myocardial Infarction
In this case you get classic signs and symptoms of an MI(i.e elevated cardiac enzymes and markers and of course physical signs of an MI ( chest pain ,nausea ,vomiting , etc) But non of the usual ECG changes ( i.e. ST segment elevation and deepening Q-waves). In fact sometimes the only clue on the ECG are inverted T-waves. 4/19/2017

18 Accessory Conduction Pathways. Also Called Pre-Excitation Syndromes

19 Pre-excitation Syndromes
These syndromes are characterized by an aberrant conduction pathway that enters the ventricular muscle in addition to the normal pathway. Since these aberrant pathways are shorter they cause ventricular depolarization prior to the normal pathway. There are 2 pre-excitation syndromes Wolf –Parkinson-White Lown-Ganong-Levine Both pathways show shortened P-R intervals of less than 0.20 sec. 4/19/2017

20 Wolf Parkinson White The abberant pathway is the bundle of Kent which bypasses the AV node. This gives a shortened P-R interval ( i.e. less than 0.20 seconds) There is a shoulder on the R-wave of the QRS complex. This shouldered QRS complex is called a Delta-wave and is the result of a fused ( fusion) beat from the normal and aberant pathway. 4/19/2017

21 Wolf Parkinson White Delta Wave  4/19/2017

22 Lown-Ganong-Levine The aberant pathway is the bundle of James which joins the normal pathway above the AV node. Since the abnormal pathway joins the normal pathway Above the AV node rather than within it there is no delta wave but just a shortened PR interval (i.e. less than 0.20seconds) 4/19/2017

23 Importance of Pre-Excitation Syndromes
These can lead to severe tachycardia's. 4/19/2017

24 Bundle Branch Blocks In bundle branch blocks either the right or the left branch is partially ( hemiblocks) or totally blocked. If both right and left bundle branches are blocked, this is termed complete or third degree heart block. Normally both bundle branches depolarize simultaneously but with bundle branch blocks the unblocked side depolarizes first and its impulse then spread to the blocked ventricle . So depolarization of the ventricles is sequential. The major significance of a new BBB is that it may indicate the presence of a previously unknown underlying cardiovascular disease. 4/19/2017

25 Right Bundle Branch Blocks
Conditions that cause this are : -pulmonary embolism -chronic lung disease -cardiomyopathy -atrial and ventricular septal defects -However in some individuals RBBB is seen in perfectly healthy individuals and is a variant of normal. 4/19/2017

26 Right Bundle Branch Block
Right Bundle branch block is seen as 2 R-waves R and R prime with an intervening S-wave in leads V1,V6 and lead 1. The s wave is deep in lead 1 and V1 . This is called R, S, R-prime. 4/19/2017

27 Left Bundle Branch Block
In Contrast to RBBB LBBB is almost always indicative of underlying cardiac pathology. There is no normal variant. Conditions that cause this are : -dilated cardiomyopathy -hypertrophic cardiomyopathy -hypertension -aortic valve disease -coronary artery disease 4/19/2017

28 Left Bundle Branch Block
Left Bundle branch blocks are seen in Leads 1 , V1 and V6 as 2 R-waves. R and R prime without an intervening S-wave. The wave between the R-waves is scooped. R-Rprime 4/19/2017

29 We usually monitor lead 2 but it is good practice to look at lead 1 and 3 as well ( as a minimum)
4/19/2017

30 Clinical Considerations for Bundle Branch blocks
All patients with a bundle branch block should be cleared by their physician prior to any in office anesthesia. Fortunately it is uncommon for a stable right or left bundle branch block to develop into complete heart block. Therefore with physician approval in office anesthesia can be safely performed 4/19/2017

31 Q-T Segment Abnormalities
Q-T segment analysis is very complicated and complete dissertation is out of the scope of this presentation. That being said the Q-T interval is based on or corrected for the heart rate. The equation is: QT corrected=QT/the square root of the R-R interval in seconds.

32 Normal Q-T The normal Q-T corrected interval is different in males and females. < seconds in males and < seconds in females.

33 Shortened Q-T Segment Abnormalities

34 QT Interval Abnormalities
Digoxin toxicity causes a shortened QT interval with a scooping of the ST segment. Note the Q-T segment is only 8 small boxes wide 0.32 seconds divided by the square root of ( 29 X 0.04)( the number of small boxes X 0.04 seconds)= So Q-T corrected is 0.32/1.07=0.30 seconds 4/19/2017

35 Although digoxin treatment toxicity is outside the scope of this lecture suffice it to say that under and over digitalization can lead to severe arrhythmia's and cardiac depression. So if your patient is on digoxin you have to know their digoxin levels and get physician approval to proceed with in office ansthesia.As such these patients may be inappropriate for in office anesthesia. 4/19/2017

36 Other Causes of Short Q-T Intervals
1) familial/genetic short Q-T syndrome 2) Hypercalcemia 3) Hyperthermia

37 Prolonged Q-T Segment Abnormalities

38 Causes of Prolonged Q-T Intervals
1) familial/genetic prolonged Q-T syndrome 2) Hypocalcemia

39

40 Although calcium abnormalities are also outside the scope of this lecture suffice it to say that they can lead to severe arythmia’s and cardiac depression. 4/19/2017

41 Potassium Induced ECG Changes Including T-Wave Abnormalities
Hyperkalemia as it evolves leads to tall peaked T-waves, prolonged P-R interval and a widened QRS complex. Eventually the P-wave is lost and the QRS becomes biphasic Hypokalemia leads to small biphasic flattened T-waves, S-T depression and a prominent U-waves .The U-wave is an extra wave after the T-wave. 4/19/2017

42 Abnormalities in Serum Potassium
Potassium abnormalities are worth dwelling on for a moment as we are likely to encounter them in our day to day practice. Either hypo or hyperkalaemia can lead to severe cardiac events and both need urgent treatment. Normal serum potassium is milliequivalents per litre of blood. 4/19/2017

43

44 4/19/2017

45 The red flags to look for are:
patients on diueretics who loose potassium. Patients on exogenous potassium tablets who can get hyperkalemia. In either of these groups it is worth getting preop electrolytes done. 4/19/2017

46 ECG diagnosis does not have to be difficult as long as you take an orderly and well thought out approach. 4/19/2017

47 PUTTING IT ALL TOGETHER
1) Look at the rhythm. Is it regular or irregular. 2) Determine the rate. Is it normal, fast or slow. 3) Determine the relationship ( if any) between the P-wave and the QRS complexes. 4) Look at the intervals , PR, QRS, QT. 4/19/2017

48 PUTTING IT ALL TOGETHER
5) Finally look at recognizable patterns to sort out a difficult diagnosis: sawtooth P-waves in atrial flutter. a missing QRS complexes in PAC’s. irregularly irregular rhythm for atrial fibrillation. delta waves for WPW. RSR prime for RBBB. RR prime with loss of S in LBBB. Deep Q waves in MI , large T waves in hyperkalemia etc. Missing P-waves in junctional rhythms. 4/19/2017

49 Categorizing Rhythms With Respect To An Interventional Hierarchy
Categorizing Rhythms With Respect To An Interventional Hierarchy . Know when to worry! 4/19/2017

50 4/19/2017

51 Immediate Action Needed
Asystole Ventricular Fibrillation Pulseless Ventricular Tachycardia Third degree heart block Tachyarythmias in which perfussion is compromised 4/19/2017

52 Action Required Within Minutes ( This group is also known as pre-arrest syndromes )
Significant Bradycardia. Runs of unifocal PVC’s ( i.e. triplets , couplets etc.) Multifocal PVC’s. Second degree type 2 heart block ( because it often is the precursor for third degree heart block. Tachyarrhythmia's in which perfusion is not yet compromised. 4/19/2017

53 Referral Required ( prior to dental treatment) With No immediate Action Needed
Any other abnormality noted which the patient was unaware of in their medical history. 4/19/2017

54 Summary You hopefully now understand ECG interpretation.
This can be applied in preoperative intraoperative and post operative patient assessment. You can utilize this knowledge in courses designed to teach arrhythmia treatment such as ILS and ALS and in your emergency simulation courses. 4/19/2017

55 END OF PRESENTATION Thank you for your commitment to continuing education


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