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Examinations in  clinical cardiology

It is a brief early systolic outward thrust , followed by late systolic retraction felt by the palpating finger  when  the LV contracts and rotates  ,  the LV apex and the adjacent  interventricular septum hits against the chest wall. It is usually felt at the 5th left intercostal space just inside the mid clavicular line , lasting less than 30% of systole and  occupying less than 3 square cms area.

Source : Horwitz ,signs and symptoms in clinical cardiology .1985. Lippincot 

Should we always be able to palpate an apical impulse ? 

Not really.If apical impulse is not felt in the sitting posture ,  one has to try in the left lateral position .In  thick chest walled persons it may be impossible to feel the apical impulse in any postion. Many times it is so tiny it lies behind a rib and one will not feel it. In  pericardial effusion also apical impulse is absent.

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Aspirin confusion spreads to clopidogrel !

It all started with 75 mg clopidogrel in CURE study  and others.

It went up to 150, 300, 600, and in some centres 900 mg.

No body knows how much clopidogrel optimally inhibits the platelet.

Aspirin had the same story three decades ago. It started from 40mg went up to 1200mg

and finally settled at 162mgs.

Why this confusion?

 It is because there is no simple platletlet function tests available in bedside.

and also the wide safety margin of this drug.At what level  clopidogrel  is unsafe

is also not clear !

Answers are expected soon .

 

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.The  forgotten “Gem of a study” from lancet 2002 .

The fight between Primary angioplasty and thrombolysis was actually over in 2002 itself. But the cardiology community failed to ,( rather reluctant ) to accept the truth. The issue is being dragged without any useful purpose (for the patient !)  still trying to keep up the non existing superiority of pPCI.

A bolus thrombolytic agent (TPA/RPA) or even streptokinase  can do almost the same if not better than a highly complex procedure called  Primary PCI with lots of logistics issues and most important an unacceptable early procedure related  hazard.

Timely lysis can kick pPCI out of the ring . . . in three aspects with 100% certainty !

1.If symptom to TIMI 2/3 flow in IRA is the true parameter of success .pPCI can never ever come closer to pre hospital lysis.

2.The poor lytics do not differentiate in the efficacy . It simply acts whoever administer it. While results of pPCI are never reproducible and lots of expertise involved.

3.Thrombolytic agents never need to bother  about the complexity of lesions , (or  where is the IRA dilemma ? Is it a CTO or ATO confusion etc ) for the simple reason it doesn’t need to think before acting. It does its job fast.

What did CAPTIM prove ?

  • It proved pPCI has no mortality advantage over pre hospital lysis.
  • Perhaps the most Important conclusion from CAPTIM is pre hospital lysis significantly reduced  number of new onset cardiogenic shock . This alone nullifies the self inflicted pseudoscientific delay wasting the golden hour in the process ! (By the way who fixed the arbitrary acceptable delay conferred to pPCI of I hour .The whole evidence base for this delay to be scrutinised in view of CAPTIM !)

Final message

It is an irony,  a simple intravenous push of a drug (Thrombolytic agent)  very early after an STEMI can save many patients and reduce complication rate .But because it is simple ,it is considered  inferior .

Probably the only role for pPCI is high risk complicated STEMI at presentation or after an attempt of lysis has not stabilised the patient.(Where its referred to as Pharamco Invasive strategy )

2018 update

This post was originally posted in 2008. Now as I see this in 2018 . It is shocking  to know we haven’t  learnt any lesson from this study for 16 years since its published.

In this era of medical  commerce and  simple ,cheap ,and effective treatment can never compete with  sophisticated , glamorous , less effective  treatment modalities !

Read the full version of CAPTIM and comments

Comparison of Angioplasty and Prehospital Thrombolysis in Acute Myocardial Infarction (CAPTIM) study group, are published in the September 14, 2002 issue of theLancet.

Primary angioplasty “no better” than prehospital fibrinolysis: CAPTIM

London, UK – In a finding that would appear to go against the swelling tide of support for primary angioplasty as the treatment of choice for acute MI, investigators comparing primary angioplasty with prehospital administration of alteplase with rescue angioplasty have concluded that the 2 strategies are comparable. The results, from the Comparison of Angioplasty and Prehospital Thrombolysis in Acute Myocardial Infarction(CAPTIM) study group, are published in the September 14, 2002 issue of theLancet.1

“Our findings indicate that primary angioplasty is no better than prehospital fibrinolysis followed by transfer for possible emergency coronary angioplasty in patients presenting within 6 hours of an acute myocardial infarction,” the researchers, led by Dr Eric Bonnefoy and Dr Paul Touboul(Hopital Louis Pradel, Hospices Civils de Lyon, Lyon, France), write.

However, they point out that cessation of funding during the trial resulted in a lower-than-expected enrollment, 840 of 1200 planned patients, reducing their statistical power. “The CI (confidence interval) for the primary end point shows that there could be a real difference in the treatment effects,” they write.

Still, the researchers feel their conclusion is valid. “This was and is for us a very pragmatic question for our care system in France,” Bonnefoy told heartwire. “Is our current management, with prehospital thrombolysis with transfer, in a time when primary angioplasty is promoted as the best-of-the-best treatment, still sufficient? Even if the power of the study is lower than expected, we think that we have our answer, and we can go on with that practice.”

The strategy also means less strain on their cath labs, Bonnefoy added, since only 1 in 4 patients underwent rescue angioplasty. A cost analysis comparing the 2 strategies is currently being carried out.

Earlier thrombolysisPrevious studies comparing primary angioplasty with in-hospital thrombolysis have shown a “definite, albeit modest” benefit of angioplasty over thrombolysis, with lower rates of recurrent infarction and higher patency rates, Bonnefoy et al write. However, it does impose additional treatment delays, and “delay to treatment is an essential consideration for any revascularization strategy.”
In France, where this multicenter trial was carried out, ambulance crews include a physician, and so thrombolysis with intravenous tPA is possible in the prehospital setting. In this trial, they randomized MI patients to either prehospital administration of accelerated alteplase or primary angioplasty and transferred all of the patients to a center where emergency angioplasty could be carried out if it were determined that thrombolysis had not been successful.
The primary end point was a composite of death, nonfatal reinfarction, and nonfatal disabling stroke at 30 days, with analysis by intention to treat.
Of the 840 patients, 419 were randomized to prehospital fibrinolysis and 421 to primary angioplasty. Rescue angioplasty was used “liberally,” they write, in 26% of patients assigned to fibrinolysis.

Time to treatment, as expected, was longer in the primary angioplasty group: the median delay between onset of symptoms and treatment was 130 minutes in the prehospital fibrinolysis group, and time to first balloon inflation was 190 minutes in the angioplasty group.

At 30 days, there was no significant difference in the primary end point between groups. Overall mortality was lower than expected, they note. Deaths were fewer in the prehospital thrombolysis group, but mortality was not significantly different between groups. There was a trend toward less reinfarction and less disabling stroke favoring the primary angioplasty strategy.

CAPTIM: Primary end point

Outcome    

 

Prehospital fibrinolysis    

 

Primary angioplasty    

 

Risk difference (95% CI)    

 

p    

 

Composite end point 8.2% 6.2% 1.96
(-1.53-5.46)
0.29
Mortality 3.8% 4.8% -0.93
(-3.67-1.81)
0.61
Reinfarction 3.7% 1.7% 1.99
(-0.27-4.24)
0.13
Disabling stroke 1.0% 0 1.00
(0.02-1.97
0.12

To download table as a slide, click on slide logo below

Among secondary end points, the researchers noted a nonsignificant trend toward a higher frequency of cardiogenic shockthe most common cause of death in this studyin the primary angioplasty group, noting that cardiogenic shock between randomization and hospital admission occurred only in that group.

The CAPTIM results were first presented at the European Society of Cardiology Congress in September 2001 and reported by heartwire.

 

Strong wordsIn an accompanying commentary, Dr Gregg W Stone (Lenox Hill Heart and Vascular Institute, New York, NY) calls the CAPTIM results “the latest salvo in the ‘primary PTCA vs thrombolytic therapy wars’,” a “well-designed and carried out” trial.2
“Unfortunately,” because of funding issues and slow enrollment, the trial ended before the planned recruitment of 1200 patients that would have been required to show a 40% reduction in the primary end point with primary PTCA, he writes. “Nonetheless, the results demonstrate a trend toward a 24% relative reduction in the occurrence of adverse events favoring the interventional strategy, driven by strong reductions in reinfarction and stroke (which would be expected, after all, to be largely independent of reperfusion time),” Stone notes.
He attributes the lack of mortality benefit from primary angioplasty to the lower-than-expected mortality risk in this population, since the survival benefit of primary angioplasty is seen primarily in the highest-risk patients, the elderly and those with anterior MIs or shock. The lack of mortality benefit, though, “does not diminish the clinical relevance of fewer strokes, reinfarctions, a reduction in urgent revascularization procedures, and the shorter hospital stay” seen with the interventional strategy in this and other studies, he writes.
Perhaps the most novel finding is the reduction in early-onset cardiogenic shock with prehospital thrombolysis, a result that “adds fuel to the fire calling for facilitated primary PTCA trials.” However, several trials of the combined approach to date have shown it to be either inferior to or no better than primary PTCA, he notes. Even in CAPTIM, prehospital thrombolysis was supported by rescue angioplasty in 26% of patients, and Stone speculates these patients may have been “better off” if they had simply been transferred for routine immediate primary PTCA.

“Thus, until the large trials of facilitated PTCA are completed (none of which have even begun enrolling), the best therapy for most patients with evolving AMI should no longer be debated; administer antiplatelet therapy (aspirin, a thienopyridine, and possibly abciximab), withhold thrombolytic therapy, and transfer the patient for primary PTCA, regardless of whether the nearest catheterization suite is 3 floors or 3 hours away,” Stone concludes.

“To do less should no longer be considered standard care. Strong words, yes, but it is time for a wake-up call.”

 

CAPTIM researchers respondAsked to respond, Bonnefoy pointed out that “Dr Stone is surely a primary angioplastician and very convinced, but it’s quite ideological. CAPTIM is quite pragmatic. His arguments are acceptable, but they are not convincing; that is his opinion rather than scientific data.”
Bonnefoy asserts that no study has clearly demonstrated the superiority in terms of mortality of primary angioplasty over prehospital thrombolysis. “And in CAPTIM, we have the surprise and intriguing observation to have lower mortality in the prehospital thrombolysis groupit may be hazard, but it is present.”
Moreover, while high-risk patients may benefit from primary angioplasty, high-risk patients do not represent the majority of the MI population. In patients such as those in the CAPTIM study, he said, “our conclusions are quite valid.”
 

 

 

Sources
  1. Primary angioplasty versus prehospital fibrinolysis in acute myocardial infarction: a randomized study2002; 360:825-829
  2. Primary angioplasty versus “earlier” thrombolysis–time for a wake-up call2002; 360:814-815

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The left atrium always  dilate to pressure overload.And it almost never hypertophies even whne the mean LA pressure raises to high levels. Why ?

1.The atrium basically has little muscle cells to hypertrophy.The left atrial thickness is only 2mm.

They are basically designed to passively fill the ventricles. But this is not always true  physiologically.We

 call it as booster pump and 30% of LV filling is  contributed by active pumping of  left atrium. 

2. The second reason for left atium not gettting hypertrophied  is ,  there are four decompressing exits

(safety  valves) in left atrium  namely, pulmonary viens. In fact it’s a paradox the back pressure across

pulmonary circulationmay result in RV hypertrophy

Inference & potential research areas

If by some mechanism if we can induce hypertophy of left atrium will it be a mechanical advantage for left ventricle in failing hearts .By cell therapy we can convert inert atrial cells into activley contracting cells.

DR.S.Venkatesan, madras medical college,  Chennai, India .

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                                   ACS   is the  most common cardiac emergency .  Management of STEMI is relatively straight forward.  The  only decision that to be taken is the  modality of reperfusion. (Primary PCI   or thrombolysis.) There is no need to risk stratify  STEMI on arrival. All STEMI patients are considered high risk on admission. Whereas  NSTEMI consists of  a heterogeneous  population. They need to be   triaged into low intermediate  or high risk categorizes on arrival.There is two management  approaches for unstable angina .All high risk UA should enter early invasive strategy . And low risk and intermediate risk group will get early conservative management. 

                                       The principle of management of  UA differ from STEMI in a fundamental way , as there is no issue of myocardial salvage in UA .The primary aim is to provide relief from pain and prevent an MI. So in the strict sense there is no time window in unstable angina /NSTEMI.

 

                                       But it is generally considered 48 hours is the time limit for an early invasive approach.If the patient has crossed this time there is apparently no great difference in outcome for conservative and invasive approach. 

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Why should 2b 3a Blockers like abciximab or eptifibatide produce thrombocytopenia ?

After all they  are not designed to kill  the platelets.

But in reality serious thrombocytopenia occur in a significant number of patients after reopro

That may demand platelet infusion

Answer to this question open for posting

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Infective endocarditis  remains a  major cardiac emergency.

Medical management has an initial role and  the many will require some form of surgery

( Mainly valve  replacement). But the surgeons request a realtively stable patients to operate upon as

surgical mortality is high in patients with uncontrolled infection and destabilsed CHF.

Even though there are battery of antibiotics, and volumes of texts written on the medical management

of infective endocarditis the medical therapy fails in bulk of the patients.

We have observed  emprical (Scientific guess work ) therapy has helped many patients .

While rifampicin according to scientific worls it’s useful only in prosthetic valve endocardtis

we have found it quiet useful in all resistant IE patients.

IE being a chronic inflammatory state rifampicin might work 

also as an anti inflammatory or immune   modulator.

This paper was presented in Cardiological society of India , Annual scientific sessions at  Mumbai 2005 . Download PPT

 

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Coronary artery disease has a strong   predilection  to involve proximal segments.

But in a significant population it affects only the distal vascular bed ! What is the extent of this problem ?

This paper was presented in  the annual sessions of Cardiological society of India , Mumbai 2005

Down load presentation

distal-cad-csi-2005

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2b -3a antagonists have revolutinised ACS management .

But the irony is Reo pro is approved for use only  inside cath lab or on the way to cath lab ! when PCI is done . 

If PCI with stenting is planned,  then subsequently cancelled due to  minimal coronary lesion or spontaneous reperfusion  what will be the effect of Abxicimab on outcome ?

Message 1

Abxicimab (Reopro,Faximab)

Useful only if PCI and stenting is done.

Dont use it for regular managment of UA/NSTEMI

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Aberrant cardiac conduction can occur in any of the specialized cardiac conduction tissues. Rate dependent aberrancy is the most common cause of aberrant conduction.

Generally it is thought only supra ventricular impulses can undergo aberrant conduction. But it is not always true.

Many of the ventricular tachycardia which  have inherently wide QRS complex can further widen their QRS width when it conducts fast down stream.This is especially true  in many of the septal VTs and fascicular VT  which  are falsely diagnosed as myocardial VT. These proximal VTs which other wise would have been a narrow QRS VT are converted into wide QRS VT by functional aberration .

Message :

Don’t always think SVT only has a potential to undergo with aberrancy

The VTs also can  behave similarly.

 

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