I was told by the doctor that everything repeated was "normal". I plan to get the test results from him next week and will post those. He told me to keep taking the 50mcg of Levothyroxine as long as I wasn't getting symptoms of hyper and will repeat thyroid labs 6 weeks after starting meds. I did start having irratability and new abdominal cramping the 17th day of dosing, along with muscle aches and palpitations, but alot of the other symptoms have subsided. I will f/u with an endo after the test results come back knowing that my only abnormal lab was my TSH of 6.3. It's all a balancing act and I'm just starting the process and learning much more from this panel than I ever learned in nursing school or being an ICU nurse. The endocrine system is very complex and I realize that now more than ever. Thanks!
With your training and experience I thought you might like to read one of my previous posts about FT3 and FT4 and why test results in the low end of the ranges are not really "normal". Since TSH is a pituitary hormone and affected by so many variables, I have little regard for its use as a diagnostic. At best it is an indicator, to be considered along with symptoms and the "Frees". In my opinion, the best way to treat a thyroid patient is to test and adjust FT3 and FT4 levels with meds, as required to alleviate symptoms. It should be all about symptom relief and not just getting test results somewhere within very broad reference ranges.
The reason the reference ranges for the "Frees" are called "normal", is that they are based on a large population of patients' test results. From that data base the decision was made that about 2.5 % of people would fall out of this "normal" range because they were possibly hypo or hyper. From this decision limits wereplaced at plus and minus two standard deviations (which correlates with plus or minus 2.5%) from the overall average and that was called the "normal" range, supposedly representing people who had no thyroid problems.
After many years of bad experience with this "normal" range for TSH, they finally acknowledged 6 years ago that there were a lot more patients out there with hypo and hyper problems, than previously accepted when they originally established the range.
After excluding from the data base those patients who were suspect for hypo and hyper, they again analyzed the remaining data base and established limits that included 95% of the total data base and called these new limits "normal". This changed the reference range from .5-5.0 down to .3-3.0, which is a huge change. Unfortunately this change hasn't yet been accepted or acknowledged by most labs and doctors.
Also, realize that the reference ranges for the "Frees" were established the same basic way. These ranges have never been reexamined and modified like the range for TSH. I am absolutely convinced that this is the reason why so many hypo people fall into the lower end of the ranges for FT3 and FT4 and are still told they are "normal".
In one my past lives I had a lot of training and experience in statistical analysis. Based on that experience, if I had to estimate what a revised range for FT3 would be if the data base were purged of suspect hypo and hyper people, like was done for TSH,then I would say it the FT3 range should change from 2.3-4.2 pg/dl up to about 3.2-4.3. And FT4 probably would change from .60-1.50ng/dl up to about 1.0-1.55. Quite a difference, huh? Think maybe that is why we hear from so many people that have hypo symptoms, yet they are in the "normal" ranges for the "Frees"? I'd bet my last dollar.
Also, if you haven't read this article, you may find it worthwhile.
http://www.hormonerestoration.com/Thyroid.html
Thank you for the response and I find it amazing how even in the ICU we look at the basic "normal" ranges with the thyroid panel and assume the pt is therapuetic..... and the intensivists will treat according to those "norms" I will be getting my hospital lab records and my f/u lab records from my GP next week. It will be enteresting to see where I fall with the FT3/FT4 results. My GP did say that I am probably on the low end of normal "for me", and did feel that a trial run of medication might help...and IT HAS! I am still having some PVC's, weird pains/rushes through my body and fatigue, with some anxiety on the 18th day of taking my Levo. It's very strange and so hard to explain how you feel to somebody.
The term, "subclinical hypothyroidism" must of come from the excepted reference ranges used for diagnosis. I had really not heard that term until now...when my GP told me he felt I had it. Your explanation of the lab values and the "normal" ranges explained it all very well to me. I was thinking..."am I just a NUT? LOL!!!! " My thyroid panel is "normal"...what's REALLY wrong with me?" (supposed to be plain and simple) It's really not that simple and I have learned alot from this website. Thank you for your time and knowledge....it is much appreciated. I will post my results when I get them.
It took a while just to get the results from my GP on my thyroid labs. I am still waiting for my hospital records (THS,T4,T3) results. According to your analysis on the Free T3,T4 labs....IT"S making sense. These are the results that I have right now.
8/14- doctors visit TSH 3.050
8/15- hospital TSH 6.8
8/19- f/u md TSH 2.240
FT3- 3.2
FT4- 1.2
Anti-Thyroglobulin <20
Anti-TPO-Ab <10.0
All of these reults were prior to taking any thyroid meds. I had alot of PVC' (Premature ventricular Contractions) with slow heart rate 48-52 BPM at rest, and went to the ER. They kept me for 2 days with f/u echo and holter monitor ( All good results, just occasional PVC'S). I'm very athletic...so, they assumed that is why I was so bradycardic. I know different! They couldn't give me a Bet Blocker because my heart rate was too low and sent me out the door with 50mcg of levothyroxine . I must say...I'm NO drama Queen, but the night I went into the ER...I thought I was going to die. I'm on day 24 of the meds. Still get VERY fatigued with Brain fog..palpiations come around lunch and dinner time and last about 30-45 minutes. Resting heart rate is in the 60's with PVC'S now. I get this weird feeling in my chest and stomach and then the low palpiations hit followed with extreme fatigue and flu/like sx's. I HAVE to eat alot to feel good and I do. Otherwise, alot of the hypo symptoms are disapaiting. I know it takes time for the meds to regulate you (IF IT'S EVEN THE RIGHT ONE FOR YOU), and some litaratue states that it might take up to 8 weeks. I f/u with my GP for more labs Oct 2. I wake up every morning and pray I can feel good just to function and deal with my family. I will keep a good attitude and press forward. Any advise would be ppreciated.
Since you started on the 50 mcg of Synthroid 24 days ago, then you should already be over 90% of the maximum level you will see as a result of the meds. So by the time of the next testing on Oct. 2, that should give you a good idea of the total effect on blood levels.
You should realize, however, that symptom changes tend to lag changes in the blood levels of thyroid hormones. Although you should continue to notice improvement, alleviation of your symptoms may take a while, dependent on how long you have been hypo. So all I'm saying is to be patient and not expect all symptoms to disappear overnight when your thyroid hormones get up to the right level.
Glad to hear that you are making progress. Please keep us tuned in.
What is your PROGESTERONE LEVEL? IS it on range?
I must know this before answer your question.
Also, have you checked for your FSH?