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Thyroid  (Expert Forum)
 | 
TSH levels and ATD's/Graves/Integral Doc's
Answered by
Mark Lupo, M.D. - Thyroid Nodules, Thyroid Cancer, hyperthyroidism, hypothyroidism, Thyroid Ultrasound
Thyroid & Endocrine Center of Florida Sarasota - FL
Questions in the Thyroid forum are answered by Dr. Mark Lupo. Topics covered include goiter, graves disease, Hashimoto's thyroiditis, hyperthyroid, hypothyroid, thyroid cancers, thyroiditis, and thyroid stimulating hormone (TSH).

TSH levels and ATD's/Graves/Integral Doc's

by jessegirl, Dec 11, 2005 12:00AM
Hi Dr. Mark - I'll try to make this as short as possible, most of my questions have been answered by the CPRN at my Endos. office, but what I still don't understand is my levels.  When my GP first noticed an enlarged thyroid he put me on 15 mg of Methimazole/day.  My levels were .01, when my Endo. increased to 20 mg it stayed at .01, when put back down to 15 mg (only b/c I complained of nausea) it went to 1.9, at 10 mg  my TSH was 2.6.  I'm confused why I was more Hypo w/less medicine, shouldn't it be the other way around?  She actually said I should be taking more, but...  I took myself down to 12.5 mg and now my TSH is 5.0, so I got cut back to 7.5 mg.  I suffer from APC arrythmias also (b/4 GD) and they seem to get better when I'm more Hyper - so I am afraid if I get a throidectomy that I will be one of those "reverse-effect" people that take caffiene to go to sleep and my arrythmias will be worse!

I was also told that my RAI-U was 44% and that combined with eating alot and losing weight is why I was diagnosed w/GD, is there any possibility of a mis-diagnosis?  Other than that, I have none of the listed "triggers".  Also, when I originally went to my GP it was b/c of nausea/dizziness/pressure-type headaches.  Are these symptoms part of GD?  I still experience them daily.  Do you have any patients that used a combo. of medical and alternitive doctors, and do they work-out.  My Endo. says they will not work w/Alt. docs. and patients usually come back to them. Also, does an enlarged thyroid ever decrease?  My antibodies were never taken, will they matter now?

Thank you!

by Mark Lupo, M.D., Dec 11, 2005 12:00AM
The 44% uptake in the absence of thyroid nodules confirms Graves.  Antibodies are not necessary to confirm it in this case.  The TSH takes a while to change, so initially it is not a sensitive way to titrate ATDs -- ie, it stays low until the brain (pituitary/hypothalamus) is comfortable that the thyroid levels are normalizing.  



Headaches are common -- should improve with treatment, if not look into other causes.  I would titrate the methimazole to keep the TSH 1-2.5 range....the tough part is deciding on methimazole for a year or so vs surgery vs radioactive iodine (I-131).  One of the more common things I see is failure to recognize mild Graves eye disease prior to I-131 and then there is a worsening of the eyes -- this is easily avoided with a short course of prednisone.  In most cases I-131 is the safest and most effective treatment of Graves.
Member Comments (6)

by ancientmariner, Dec 12, 2005 12:00AM
To: jessegirl
I noticed that in Dr. Mark's response to you he mentioned the three treatments for Graves: ATDs, surgery or I-131 ablation, and he recommends the latter as being the safest.



I just want to ask you to PLEASE research all of these options before making any decision. I had RAI a few years ago, and went through several years of pure hell. My endo recommended the RAI, saying that the end result would be that I would have to take a pill every morning and I'd be fine. I became very hypo, and was given Synthroid. When he thought I was "normal" again, I did not FEEL normal, and had a number of symptoms that I had never had before in my life (huge weight gain, voice problems, inability to think clearly, concentrate or remember, depression, joint pains, to name a few). But he just told me they couldn't be related to my thyroid. So I started to research for myself. I bought book after book, read article after article. It took many re-readings before some of it would actually become clear and "stick" in my head. Then I found a doctor who would prescribe Armour thyroid and treated my symptoms, not my lab numbers. I am now on 3-12 grains of Armour daily, and finally I am losing weight, I can concentrate, I feel GOOD again.



So please, make sure you find out all you can about the three options, and choose the one that's right for YOU.

by jessegirl, Dec 12, 2005 12:00AM
To: Ancientmariner
Thanks for your comments.  I have been struggling with this decision for almost a year now.  I was getting ready to do RAI when I stumbled upon this web site that led me to Elaine Moore's forum.  Basically I was told that being Hypo T is better than Hyper T (especially with my arrhythmias). I was also told that Hypo T can cause arrhythmias recently, I didn't know that before, so now I'm even more confused about what to do!  My Endo. told me that more of their patients are happy with the results of RAI than not.  I think if I do anything it will be surgery, but then they will only remove all of the thyroid and I will still be Hypo. Uugghh!  Anyway, you can read more of my "story" on Elaine's Forum if you choose.  Go onto about.com, then get to the Hyper/Graves forum under "many questions".  I'd love to hear what you (or anybody that has been through this)would do if you were in my position.  I know there is a lot of sites with people against RAI, but then again, if people had good results, why would they be on these sites seeking help?

by ancientmariner, Dec 13, 2005 12:00AM
To: jessegirl
If I had it to do over again, I would certainly do my research up front, not take the doctor's word as gospel. I would have insisted on additional blood tests for antibodies (TPO and TSI) and I would have insisted that I wanted to try the ATDs for at least a year first. And, I would definitely dump the endo I had and find another doctor. I feel I was rushed into the RAI, and the endo I had was bullying and pompous; he belittled my research efforts and basically made me feel stupid. And all I could do at the time was CRY! I am so angry that other less-invasive options were not presented to me as alternatives, and I am angry that after the RAI made me hypo, he was not willing to effectively treat that. It took a lot of research on my own, and several different doctors before I was able to receive the treatment that I believe will ultimately give me back my life. I have learned more than I ever wanted to know about thyroid, and I know that the synthetic T4 only medicines didn't work for me, but Armour is working!

by jessegirl, Dec 14, 2005 12:00AM
To: ancientmariner
I'm sorry your doctor wasn't much help to you.  I haven't found an Endo. with a personality yet either.  I asked about the antibody test and my Endo's nurse said it was irrellevant b/c my RAI-U test showed me as 44% when the norm is 32%.  What is the controversy surrounding Armour?  I read alot about doctors not prescribing it, etc. , but haven't paid much attention b/c I'm not to that point yet.  I'm Hypo now b/c of Methimazole.  What other options are there besides RAI, surgery and life-long ATD's? Thanks for your feedback.

by ancientmariner, Dec 16, 2005 12:00AM
To: jessegirl
As I understand it, most doctors don't even know what Armour is made from. Even Dr. Bill Law of the AACE stated in a letter to CBS that Armour is made from cow thyroid. That is a misconception that many doctors seem to have; in reality Armour is made from pig thyroids. Doctors also seem to think that the T3 in Armour can be harmful, but our own thyroids, if they work properly, make T3 as well as T4. My doctor told me that T3 can be a problem in people with heart disease, so it's best to start with a low dose and work up gradually until symptoms are gone. But doctors don't read the prescribing information and many start patients at a dose that is too high, which causes all kinds of other problems. Another excuse my old doctor used was that Armour is hard to regulate - it's no harder than Synthroid and possibly easier, because doctors who prescribe Armour routinely seem to go by symptoms rather than labs. The amounts of T4 and T3 in Armour tablets is standardized, and actually has a beter record of consistency that Synthroid.



So, to answer your question, I don't know why doctors don't prescribe Armour more often - one theory is that it's not as profitable as prescribing Synthroid and, in fact, Synthroid's maker Abbott provides financial support to the AACE. I don't know - I have an opinion, but I don't think I'm allowed to voice that in this forum.
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