A 67 year old male with no previous cardiac history or risk
factors woke up at midnight with right-sided chest pain. It was the "worst
pain of his life," and it radiated around his ribs, through to his back,
and up into his neck, all on the right side. He was profusely diaphoretic,
nauseated, and he vomited twice. He took some aspirin which gave him some minor
improvement in symptoms. He "toughed out" the night, and when his
pain was still not getting better about 8 hours later, he asked his wife to
take him to the ED.
He arrived at about 8.5 hours after onset of symptoms, still
with severe chest pain, and had this ECG recorded:
There was a baseline ECG available from 3 years ago:
What is your interpretation? What would you do at this
point? See below for interpretations.
Interpretation of presenting ECG:
Sinus tachycardia at about 105 bpm. The computerized QRS
duration is 120ms, qualifying this for an Intraventricular Conduction Delay. It has morphology very similar to LBBB: there is a wide
complex with dominant S waves in the anterior leads, so we presumably can apply the
same rules as full-blown LBBB.
The treating physicians documented that this ECG is "Sgarbossa negative." There is no concordant ST depression in V1-V3, and no ST elevation equal or greater than 5mm. Is there concordant ST elevation? This depends on whether the QRS is mostly positive or mostly negative in lead V5; if positive, then the ST elevation is indeed concordant..
Lead V4 alone would make this ECG "modified Sgarbossa positive"(reference 1, reference 2): it has a 3mm S wave with 2.5mm of ST elevation, making a STE/S ratio of 0.83.
How about lead V5? The S-wave and R-wave are of nearly equal voltage; on the other hand, the S-wave is slightly wider than the R-wave. What matters most? Is it the voltage? Or is it the integral (area under the curve) that matters most? In any case, the difference in voltage and in area is not great, and therefore there should be almost no ST deviation in that lead.
Stated in other words: The "area under the curve" or "integral" is all the area contained between the waveform and the isoelectric line. In LBBB, ST-T is normally discordant to the majority of the QRS, but is that "majority" measure by voltage (in mm of amplitude), or is it best measured by area under the curve? In this case, in V5 the R-wave amplitude is greater, but the S-wave area is greater. In either case, the difference is small.
Thus, leads V4 and V5 are diagnostic of STEMI.
Furthermore, one expects a small R-wave in V1 and V2 in LBBB. Instead, there are Q-waves. There is also a notch on the ascending limb of the S-wave in V2 and also slightly in V3. These are reminiscennt of "Cabrera's sign" (a notch greater than 50 ms on the ascending limb of the S-wave in one of V3-V5). These are signs of previous MI, or of well developed "subacute" acute MI.
All of these ECG findings, along with the clinical scenario, are all but diagnostic of a subacute STEMI in the setting of LBBB.
The treating physicians documented that this ECG is "Sgarbossa negative." There is no concordant ST depression in V1-V3, and no ST elevation equal or greater than 5mm. Is there concordant ST elevation? This depends on whether the QRS is mostly positive or mostly negative in lead V5; if positive, then the ST elevation is indeed concordant..
Lead V4 alone would make this ECG "modified Sgarbossa positive"(reference 1, reference 2): it has a 3mm S wave with 2.5mm of ST elevation, making a STE/S ratio of 0.83.
How about lead V5? The S-wave and R-wave are of nearly equal voltage; on the other hand, the S-wave is slightly wider than the R-wave. What matters most? Is it the voltage? Or is it the integral (area under the curve) that matters most? In any case, the difference in voltage and in area is not great, and therefore there should be almost no ST deviation in that lead.
Stated in other words: The "area under the curve" or "integral" is all the area contained between the waveform and the isoelectric line. In LBBB, ST-T is normally discordant to the majority of the QRS, but is that "majority" measure by voltage (in mm of amplitude), or is it best measured by area under the curve? In this case, in V5 the R-wave amplitude is greater, but the S-wave area is greater. In either case, the difference is small.
Thus, leads V4 and V5 are diagnostic of STEMI.
Furthermore, one expects a small R-wave in V1 and V2 in LBBB. Instead, there are Q-waves. There is also a notch on the ascending limb of the S-wave in V2 and also slightly in V3. These are reminiscennt of "Cabrera's sign" (a notch greater than 50 ms on the ascending limb of the S-wave in one of V3-V5). These are signs of previous MI, or of well developed "subacute" acute MI.
All of these ECG findings, along with the clinical scenario, are all but diagnostic of a subacute STEMI in the setting of LBBB.
Initial troponin I was 50 ng/ml. Cardiology was summoned. They
took him immediately to the cath lab, where they found an acute thrombotic 99%
stenosis of the proximal LAD with TIMI 1 flow. There were also thrombotic
lesions of the mid LAD and D1. They aspirated the thrombi and placed 3 stents
at these lesions. No further troponin data was available.
Here is his ECG later that day:
T wave inversions in the anterolateral leads, consistent with reperfusion. Some ST elevation persists, but no longer meets any criteria. The QRS appears a little bit shorter than previous. |
And here is his ECG the next day:
Still shows T wave inversions with persistent ST elevation. This persistence may portend the development of an LV aneurysm. |
He recovered well and was discharged several days later.
Should thrombolytics be given?
Thrombolytics are still recommended up to 12 hours after the onset of pain. (Sorry, no full text here: this is an analysis of thrombolytic trials from 1983-1993, and found that if pain has been present for 6-12 hours, then a mean of 18 lives were saved per 1000 patients treated with lytics vs. placebo).
The ECG is, in fact, an even better measure of acuteness of a STEMI.
When there is subacute STEMI, the thrombolytic decision must be made carefully with attention to both risk and benefit. This is a large anterior STEMI with persistent pain and ST elevation. There are Q-waves, and the highly elevated troponin I confirms prolonged infarct. ST elevation is still present, however, and T-waves have not yet inverted, so there is still significant salvageable myocardium at risk. Depending on the patient's risk factors for bleeding, and on the door to balloon time for transfer to a PCI institution, thrombolytics may be indicated.
Should thrombolytics be given?
Thrombolytics are still recommended up to 12 hours after the onset of pain. (Sorry, no full text here: this is an analysis of thrombolytic trials from 1983-1993, and found that if pain has been present for 6-12 hours, then a mean of 18 lives were saved per 1000 patients treated with lytics vs. placebo).
The ECG is, in fact, an even better measure of acuteness of a STEMI.
When there is subacute STEMI, the thrombolytic decision must be made carefully with attention to both risk and benefit. This is a large anterior STEMI with persistent pain and ST elevation. There are Q-waves, and the highly elevated troponin I confirms prolonged infarct. ST elevation is still present, however, and T-waves have not yet inverted, so there is still significant salvageable myocardium at risk. Depending on the patient's risk factors for bleeding, and on the door to balloon time for transfer to a PCI institution, thrombolytics may be indicated.
Take Home Points:
- the modified Sgarbossa rule is more sensitive than
the original
- even when the ECG doesn't have a perfect LBBB, if
there is significantly abnormal depolarization with a wide QRS it must still
follow the same rules of appropriate discordance and proportionality
-Signs of old or subacute MI may also be seen in the setting of LBBB
-Signs of old or subacute MI may also be seen in the setting of LBBB
Would you have thrombolized this patient? Say if you were in a rural hospital?
ReplyDeleteMuhammed, in answer to your question, I added a section to the post. Thank you.
DeleteSteve Smith
The articles about the modified Sgarbossa rule state that the ST/S ratio should be less than -0.25 but you had 0.83 in V4.how come that makes it Sgarbossa positive?
ReplyDeleteSorry, we're using the absolute value: the ST elevation is 2.5 mm. The S-wave is (minus) 3.0 mm. A positive number divided by a negative number is a negative number, in this case -0.83. I used the absolute value (0.83).
Delete--Steve Smith
hello doctor
ReplyDeletefirst of all i would like to thank you for taking from your time to share with us your experience, i have several questions : 1 why not considering the loss of normal r wave progression in precordial lead as proof of ongoning ischemia rather than a proof of an ancient MI ? the same thing about Cabrera's sign why taking it as sign of previous MI ?
2 how can we explain the q wave in AVL though it is not a real LBBB ? can we say that Sgarbossa can be used in non specific intraventricular conduction delay in onset of chest pain in order to rule in MI ?
3 i am not english-speaking native so i did not understand the following statement, would you mind reformul it in other words ?
"How about lead V5? The S-wave and R-wave are of nearly equal voltage; on the other hand, the S-wave is slightly wider than the R-wave. What matters most? Is it the voltage? Or is it the integral (area under the curve) that matters most? In any case, the difference in voltage and in area is not great, and therefore there should be almost no ST deviation in that lead. "
merci énormément .
Est ce que vous venez de France? Ou d'autre pays Francophone? De rien!
Delete1. It is in not necessarily old MI, but usually means at least prolonged (sub acute) MI. Sometimes reversible ischemia (not infarction) of the purkinje system can result in anterior Q-waves.
2. I believe that Sgarbossa can be used in non specific IVCD that should have discordant ST-T waves.
3. The "area under the curve" or "integral" is all the area contained between the waveform and the isoelectric line. In LBBB, ST-T is normally discordant to the majority of the QRS, but is that "majority" measure by voltagin (mm of amplitude), or is it best measured by area under the curve? In this case, the R-wave amplitude is greater, but the S-wave area is greater. In either case, the difference is small.
a la prochaine!
Steve Smith
Je suis Algérien, je vous remercie de prendre de votre temps pour me répondre malgré mon Anglais très approximatif
DeleteWhen R and S waves are equal, there is no reason why ST shifts, isn't that ? so the ST elevation is pathologic
thank you very much
Hi,
ReplyDeleteIn my mind, my primary diagnos is aorta dissection type A (AD), with cutting LADs blodflow.
1) Patient said "the worst pain ever felt". Usually AMI patient arent that affected of pain, describing VAS 3-5 (1-10)
2) Patient described a migrating pain, more common in dissection patology.
Before even ongoing with PCI or giving him blood-thinning medication you have to outrule AD. (?!?)
Thank you.
Good idea. Certainly possible. When there is STEMI due to aortic dissection into the coronary ostia, it is far more likely to be RCA, though left main is also possible. With left main, there would be a different ECG pattern, however. It would be even more unlikely to be affecting just the LAD. There would be diffuse subendocardial ischemia (if subtotal). If total left main, then death, cardiogenic shock, simultaneous anterior and posterior MI (LAD and circ). It would be a much different presentation.
DeleteHello,
ReplyDeleteCould you explain to me why a tiny r wave is still present in anterior precordial leads in normal LBBB morphology ?
I've always assumed that QS was the normal morphology of LBBB in anterior leads, as I thought the normal r wave in V1-V2 (in absence of conduction defect) was the "mirror" of the normal q wave in V5-V6, witness of the initial septum depolarization through the left anterior branch (hence its disappearance in LAFB). I therefore wonder where the anterior r wave in LBBB comes from.
Besides, I've just read your article on the modified Sgarbossa rule. If we consider, according to the study, that the ST/S < -0.3 criterion has a sensitivity of 100% (implying a NPV of 100%), then we can ALWAYS use it to rule out MI, which is pretty helpful.
PS : I think you made a mistake in your first "take home point" : the modified Sgarbossa rule is more sensible than the original, not more specific (weighted Scarbossa criteria are actually highly specific).
You are correct: the modified rule is more sensitive, not more specific. It was more accurate overall.
ReplyDeleteThere is a tiny r-wave because the right bundle activates the septum from towards leads V1-V3.