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Re: nitroglycerine?

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Hi Jill; My docs had mentioned calciium channel blockers, like

nitro, because it is a smoothe muscle relaxer. They said also that

it would relax the sphincer of oddi and reduce the pain of spasms.

I didn't spend a lot of time looking into it and wasn't very

comfortable with it. I had tried antidipressants and didn't like

the way I felt but they did help reduce the pain from spasms. From

what I had learned though, the calcium channel blockers do help

some.

I guess that wasn't much help, just what I had experienced,

Goof luck,

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Jill ,

I have tried the Nito for my SOD. All it did was give me a raging headache. I do

use Levsin .125 mg under the tongue when I have a spasm. It works really well .

Not a cure nor does ot take the pain completely away, but if I catch it in time

it is greater than 80 % effective. Have you ever tried that ?

Lily from Ohio

nitroglycerine?

Hi, all

I went to see a specialist, in Boston, on Wednesday, the 11th. I have mixed

feelings about it and it was topped off by a hospital evacuation for what I

think was a fire drill, just as my appointment was winding down. That,

unfortunately, finished it off. Anyway, after the exam we chatted a bit. One of

his thoughts was that a sphincter is going into spasm (which my own doctor has

thought in the past). His recommendation was 2-fold. He said I should have an

ERCP (last one was many yrs ago) and have an EUS, which I've never had. But,

before going through any testing he suggested trying nitroglycerin. The thought

being that it would relax the sphincter and therefore there should be no more

pain. I never heard of nitro used this way before. Has anyone else? He said if

the nitro works he wouldn't do the testing. I will, naturally, discuss this with

my own doctor in a few weeks and by that time he should have a letter from the

consult. I don't really like the idea of nitro. Apparen! tly, he's used it

successfully. I plan to do some research.

This doctor also seemed to indicate that since no damage has been visible on

scans that that even tho I have pain 24/7 and elevated amylase, that I have

recurrent acute pancreatitis and not chronic. I guess I'm only chronic in

symptoms.

I broached the subject of my mutated cystic fibrosis gene but we never had the

chance to really pursue the subject before the fire alarm went off. I've found

his email address so I've drafted an email to him to get that issue addressed

along with a couple of others.

I'd be interested to hear if anyone has used or knows of anyone that has used

nitroglycerine for sphincter spasms.

Be well,

Jill

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and Jill,

I tried the calcium channel blockers as well,,, no luck with them. I have not

tried the anti depressant route yet. So far the Levsin helps. But I also take

that Clidinuim every 6 hours. That is my life saver.

Lily

Re: nitroglycerine?

Hi Jill; My docs had mentioned calciium channel blockers, like

nitro, because it is a smoothe muscle relaxer. They said also that

it would relax the sphincer of oddi and reduce the pain of spasms.

I didn't spend a lot of time looking into it and wasn't very

comfortable with it. I had tried antidipressants and didn't like

the way I felt but they did help reduce the pain from spasms. From

what I had learned though, the calcium channel blockers do help

some.

I guess that wasn't much help, just what I had experienced,

Goof luck,

------------------------------------------------------------------------------

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I don't know much about CP but when I was in the ER with an

attack a few months back the doctor ordered Nitroglycerin

hoping it would relax the ducts and stop some of the pain but it

didn't work. He said on some people it does have a positive

affect------they must be the lucky ones.

> Hi, all

>

> I went to see a specialist, in Boston, on Wednesday, the 11th. I

have mixed feelings about it and it was topped off by a hospital

evacuation for what I think was a fire drill, just as my

appointment was winding down. That, unfortunately, finished it

off. Anyway, after the exam we chatted a bit. One of his thoughts

was that a sphincter is going into spasm (which my own doctor

has thought in the past). His recommendation was 2-fold. He

said I should have an ERCP (last one was many yrs ago) and

have an EUS, which I've never had. But, before going through any

testing he suggested trying nitroglycerin. The thought being that

it would relax the sphincter and therefore there should be no

more pain. I never heard of nitro used this way before. Has

anyone else? He said if the nitro works he wouldn't do the

testing. I will, naturally, discuss this with my own doctor in a few

weeks and by that time he should have a letter from the consult. I

don't really like the idea of nitro. Apparently, he's used it

successfully. I plan to do some research.

>

> This doctor also seemed to indicate that since no damage has

been visible on scans that that even tho I have pain 24/7 and

elevated amylase, that I have recurrent acute pancreatitis and

not chronic. I guess I'm only chronic in symptoms.

>

> I broached the subject of my mutated cystic fibrosis gene but

we never had the chance to really pursue the subject before the

fire alarm went off. I've found his email address so I've drafted

an email to him to get that issue addressed along with a couple

of others.

>

> I'd be interested to hear if anyone has used or knows of

anyone that has used nitroglycerine for sphincter spasms.

>

> Be well,

> Jill

>

>

>

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Thanks to those that responded to my post about the nitro. I will respond in a

few days but did want to say to Lily that one of my main concerns was headache

since I get 3 day migraines almost every week. I don't really want to add to

that. I'm glad you mentioned the headaches. I asked about side-effects (when I

cornered him outside during the fire drill) and that's the only one he mentioned

but didn't make a big deal of it. It's a big deal to me.

Be well, all

Jill

Re: nitroglycerine?

Jill ,

I have tried the Nito for my SOD. All it did was give me a raging headache.

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Jill,

Heck you don't need to add insult to injury ! Migraines hurt.

Take Care,

Lily from Ohio

Re: nitroglycerine?

Jill ,

I have tried the Nito for my SOD. All it did was give me a raging headache.

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Thanks, Lily. I appreciate your input. I think I'll most likely turn down that

option. Yes, migraines hurt! Will let you know after my appointment in a couple

of weeks. I've been away since Monday morning and just got back. I went to visit

my sister and family in NJ.

Be well,

Jill

Re: nitroglycerine?

Jill,

Heck you don't need to add insult to injury ! Migraines hurt.

Take Care,

Lily from Ohio

----- Original Message -----

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