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Oh boy. In that case, we eagerly await your results. Best of luck.That will have to be studied and I promise to post my peer-reviewed, published results in 3-5 years.
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Oh boy. In that case, we eagerly await your results. Best of luck.That will have to be studied and I promise to post my peer-reviewed, published results in 3-5 years.
I had one just the other night, which is why I brought up this thread. As nausea and vomiting is extremely common in those having an MI it warrants discussion on how to get ASA into them as quickly as possible using alternate methods than PO.
The bottom line is that you are making a big deal out of a problem that doesn't exist.
Because if they're being treated appropriately, by an als provider, we can give them cheap medications so they're not nauseous and they stop vomiting. And in my experience, the amount of true mi patients that are vomiting is much lower than 1/3.Except that is very much exists. 1/3 of MI patients are vomiting. 2/3 have nausea. How does this qualify as "doesn't exist"?
Because if they're being treated appropriately, by an als provider, we can give them cheap medications so they're not nauseous and they stop vomiting. And in my experience, the amount of true mi patients that are vomiting is much lower than 1/3.
I don't actually know who any of you are so I don't actually know how long anyone has been in EMS or if they actually are in EMS at all.Ask yourself a couple of serious questions.
1) How long have I been doing this compared to the people I'm talking to here?
I'll go with the peer-reviewed, published journal articles over anecdotal reports.2) What gives me a better perspective than the people I'm talking to who have been doing this a long time, have more education on the subject and more practical experience dealing with this?
I am obtaining all of my sources from peer-reviewed, published articles. I don't automatically believe someone just because they have a PhD. They would be an appeal to authority which is a logical fallacy.3) What gives me a better perspective than research doctors and PHDs who specialize in this area and apparently haven't found it significant enough to persue?
Nope.If you don't have legitimate answers to all three, you're probably beating a dead horse.
Because there is a difference between being nauseated and being unable to chew and swallow 2 or 3 small pills. Haven't you ever been sick where you've felt like you wanted to puke but were still able to eat some chicken noodle soup? Especially when medics already have easy access to anti-emetics like zofran, it becomes even more of a non issue.Except that is very much exists. 1/3 of MI patients are vomiting. 2/3 have nausea. How does this qualify as "doesn't exist"?
No way. When I feel like I'm gonna puke I can't swallow anything.Because there is a difference between being nauseated and being unable to chew and swallow 2 or 3 small pills. Haven't you ever been sick where you've felt like you wanted to puke but were still able to eat some chicken noodle soup?
Why do you assume I have a medic available? There is one medic available for the three counties that are part of my BLS system. We see the medic so infrequently.Especially when medics already have easy access to anti-emetics like zofran, it becomes even more of a non issue.
That's the plan!But if you wanna spend all that money and go through all that trouble to start studies and get a brand new medical device invented, patented, studied and trialed and eventually approved for use, and then get medical directors to modify their protocols to allow BLS to carry it, by all means go ahead.
We already carry adult and pediatric EpiPens. We also have nasal narcan and PO ASA. We're a "progressive" BLS system.Just remember in a lot of places BLS can't even carry auto injectors and have to rely on assisting patients with their own auto injector.....
The entire medical community once told Louis Pasteur that he could never kill something no one could see.or that you are literally the only one on this thread arguing in favor of this new idea should give you an idea of what the larger medical community's ideas on this will be, and what a steep hill you will have in justifying to others to get this created..
Would you like the name and number of our project medical director? I bet he'd just love to hear from you.You would have time better spent by improving your own system. Your pts deserve more then minimal care.
I'll place more faith in peer-reviewed, published medical articles over most anything else any day of the week. Also, an apostrophe doesn't pluralize a word.Plus, you need to learn not to put all your faith in "peer reviewed study's" . You will learn over time that one study means nothing. You can make a studies outcome say anything you want. The study you posted had 180 pts in it. That is a very low subject matter to study and say this is evidence-based.
Would you like the name and number of our project medical director? I bet he'd just love to hear from you.
You are such a great medical mind. You should be able to handle your own medical director!
I'll place more faith in peer-reviewed, published medical articles over most anything else any day of the week. Also, an apostrophe doesn't pluralize a word.
Why yes, yes in fact I would love to have the name and contact information for your medical director. I think he'd very much like to hear from me on this.Would you like the name and number of our project medical director? I bet he'd just love to hear from you.
I'll place more faith in peer-reviewed, published medical articles over most anything else any day of the week. Also, an apostrophe doesn't pluralize a word.