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Subject: Re: Aspirin (the beat goes on)
Date: Wed, 19 Jun 96 09:42:48 -0500
From: Robert Wolov <wolov@hi*.co*>
To: "Techdiver list" <techdiver@terra.net>

>> 
>>  I was expecting to ear from the experts on this topic. I'm just back from 
>> a trip to France and over there, Aspirin seems to be a standard part of 
>> the treatment of DCS, as standard in fact as pure O2. 
>>
>>  I was reading a new French magazine (Octopus No2, juin-juillet 1996 
>> p14, Jacques Migueres) and the recommended dose seems to be 500 mg (as 
>> long as you don't suffer from allergies). It seems that it can be taken 
>> at the treatment phase but there's no word on a the usefullness of a 
>> preventive dose. It's no good if the your ASA brand contains 
>> "paracetamol" apparently.
>>  
>>  So let me ask the experts again what is the status of aspirin use in the 
>> treatment of DCS in America? Time to phone up DAN?
>
>Until one year ago (more or less), aspirin was also with O2 the standard
>treatment of DCS as recommended by the FEBRAS (belgian part of CMAS). The
>intended effect of aspirin was prevention of blood coagulation (one effect
>of acid acetylsalicilique and not of paracetamol).
>
>It has been supressed because of studies who have shown that aspirin has 
>little
>or no currative effect (it is too late to get the intended effect). Some 
>studies
>showed a preventive effect but at the dosis needed to achieve the result, the
>problems of aspirin outweighted the advantage.


The use of aspirin would seem to have at least "theoretical" advantages 
(there's much in medicine that unfortunately looks good on paper but has 
little effect on the body in practical terms).

Hold onto your socks....<Physiopharmacology Warning!> Doc-Speak about to 
be committed in full public view!! 

We know that micro bubbles (certainly macro bubbles) damages the 
endothelial lining of blood vessels. This physical damage (much like the 
initiating damage of atherosclerotic plaques in hardening of the 
arteries) activates cell membrane phospholipids which form arachidonic 
acid. The arachidonic acid is acted on by cyclooxygenase to form amoungst 
other metabolites, Thromboxane A2 which is a potent vasoconstrictor and 
PLATELET AGGREGATOR. Aspirin blocks the reaction of cyclooxygenase on 
arachidonic acid, therefore lowering the amount of Thromboxane A2 
produced. The body thus tends to limit these small "micro white clots" of 
platelets.

This is the whole reason for taking aspirin *prophylactically* to reduce 
the risk of heart attacks. By taking the aspirin AHEAD of time, you've 
already jumped on blocking the cycloxygenase pathway. Once you've 
triggered the clotting mechanism, and the cat's out of the bag so to 
speak, aspirin has been shown not to be as effective.(though not 
necessarily zero)

Now, with DCI, (by definition the patient is already symptomatic or you 
wouldn't be treating would you?) you already have bubbles, so you are 
already in process damaging the blood vessel linings.

It would seem unlikely that you would get a sufficiently high blood level 
of aspirin at this point, fast enough, in the pathology to do much good. 
But that is SPECULATION ON MY PART and speculation rather than 
experimental/clinical evidence makes for bad science. So, I'd not dismiss 
any of this out of hand.

For the antithrombotic effects of heart attack prevention, very little 
aspirin is needed (something like one tab every other day) so taking a 
tab the morning of a dive at first blush doesn't seem unreasonable.

But, aspirin does have neurotoxic effects. Take it in sufficiently high 
enough doses (like some arthritics do for it's antinflammatory effect) 
and you get ringing in your ears (tinnitus). Now, supposedly divers 
wouldn't be taking aspirin in such high doses that it would have a 
synergistic effect with their O2 deco gases, but theoretically they are 
both hammering on the same system. Just something else to keep in mind.

I wish I read French to see the data. It sounds "interesting" at least. 

Robb Wolov



====================================
CDR Robert B. Wolov, MC, (FS), USNR
Department of Orthopedic Pathology
Armed Forces Institute of Pathology
Washington, DC 20306-6000

wolov@hi*.co* (preferred)
wolov@em*.af*.os*.mi*

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