Home | About us | Editorial board | Search | Ahead of print | Current issue | Archives | Submit article | Instructions | Subscribe | Contacts | Advertise | Login 
 
Search Article 
  
Advanced search 
  Users Online: 167 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size  

 
Table of Contents
MINI REVIEW
Year : 2012  |  Volume : 16  |  Issue : 8  |  Page : 147-149

Thyrotoxicosis and radioiodine therapy: Does the dose matter?


consultant, Diabetes Day care centre University Hospital of Ayr, Scotland, United Kingdom

Date of Web Publication4-Jan-2013

Correspondence Address:
Andrew Collier
Diabetes Day centre, university hospital Ayr, Scotland
United Kingdom
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2230-8210.104025

Rights and Permissions
   Abstract 

There are 3 treatment options for thyrotoxicosis: Antithyroid drugs, Surgery and radioiodine. The choice of treatment varies geographically. Radioiodine therapy is preferred in the United States. The aim of radioiodine is to destroy sufficient thyroid tissue to cure the hyperthyroidism. There is a lack of consensus towards what dose of radioiodine should be used. Several methods are used to determine the dose. In our practice we administer 400 MBq to patients with Graves and in patients with large multinodular goiter, we would administer 800 MBq.

Keywords: Thyrotoxicosis, radiodine therapy, Dose


How to cite this article:
Collier A. Thyrotoxicosis and radioiodine therapy: Does the dose matter?. Indian J Endocr Metab 2012;16, Suppl S2:147-9

How to cite this URL:
Collier A. Thyrotoxicosis and radioiodine therapy: Does the dose matter?. Indian J Endocr Metab [serial online] 2012 [cited 2020 Nov 30];16, Suppl S2:147-9. Available from: https://www.ijem.in/text.asp?2012/16/8/147/104025

Thyrotoxicosis is a disorder of excess thyroid hormone. The tissue effects of high concentration of thyroid hormones have many clinical manifestations. Two main hormones are synthesized and released by the thyroid gland. Thyroxine (T4) and triiodothyronine (T3). T4 is a prohormone, whereas T3 is biologically active through interaction with specific nuclear receptors that are present in nearly all tissues. Hyperthyroidism, which specifically describes increased thyroid hormone synthesis and secretion, is common in the UK with prevalence of 2% in women and 0.2% in men. Incidence increases with age, is highest in Caucasian populations and in iodine-deficient areas. The most common cause of thyrotoxicosis is Graves' disease, in which auto-antibodies bind to stimulate the thyrotropin receptors found on the surface on the thyroid follicular cells. The next most common cause is autonomous overproduction of thyroid hormones by one or more nodules within the thyroid. The frequency of these forms of thyrotoxicosis varies with iodine intake. Hyperthyroidism has well-known unacceptable consequences including cardiovascular disease, such as atrial fibrillation and heart failure, osteoporosis and reproductive problems. Left untreated, thyrotoxicosis can progress to a thyroid storm. [1],[2]

After biochemical confirmation of thyrotoxicosis, a choice between the 3 treatment types is required: anti thyroid drugs, surgery and radioiodine therapy. The choice of treatment varies significantly geographically. Radio-iodine therapy is preferred in the USA whereas anti-thyroid drugs are favoured in continental Europe and Japan. Radio-iodine can be used as a first line treatment of hyperthyroidism, is the most common form of treatment for Graves' disease in the UK and is the treatment of choice in relapsed cases of thyrotoxicosis. Contraindications include pregnancy or lactation, desire of pregnancy within the next months, suspicion or diagnosis of co-existing thyroid cancer and inability to comply with radiation protection regulations. Radio-iodine is safe, effective, inexpensive and has been used for more than 60 years. [1]

The aim of radioiodine therapy in Graves' disease and in any form of thyrotoxicosis is to destroy sufficient tissue to cure the hyperthyroidism. This process renders the patient either euthyroid or hypothyroid. Radioiodine therapy induces an intense radiation thyroiditis and subsequent fibrosis, thereby destroying the synthetic capacity of the thyroid. There is a lack of consensus towards what dose of radioiodine should be used and whether the aim of treatment is to render the patient euthyroid for a period of time or hypothyroid. [3],[4],[5] Some endocrinologists believe that sustained euthyroidism would clearly be the most desirable outcome but this would appear to be futile. A review from the 1980s stated unequivocally that the goal of radioactive iodine treatment in patients' with Graves' disease should be complete ablation of the gland. [6] This is because eventual hypothyroidism is virtually inevitable. Numerous studies investigating different doses of radioactive iodine activity administered have demonstrated an instance of hypothyroidism of approximately 2-3% many years after therapy. [7],[8]

It is suggested that the radionuclide scan has three main uses in imaging hyperthyroidism: establishing the cause, selection of appropriate radioiodine 131 regimens and follow-up of patients after radioiodine therapy. Several different methods have been used to determine the radioiodine activity that should be administered to thyrotoxic patients. [9] In addition, several factors have been considered as influencing the outcome of radioiodine treatment required. Studies have suggested that patients with larger volume thyroid glands and severe hyperthyroidism are more likely to fail to respond to a single administration of radioiodine. [1] Techniques have been undertaken to assess gland size, either estimated clinically or with imaging and doses have been calculated on the basis of gland size, iodine uptake and sometimes iodine turnover. [10] Many hospitals do not have the resources or facilities to undertake routine radioiodine uptake scans at 4 and 24 h along with detailed radioiodine kinetics calculations. [11] The uses of these methodologies add to the complexity of the procedure and significantly increase the cost related to the therapy. As radioactive iodine therapy is relatively inexpensive, incurring further costs determining the dose of radioiodine that should be administered needs to be justified. [5]

In Ayrshire and Arran, Scotland we have had two District General Hospitals that have historically delivered two different fixed doses of radioiodine to treat thyrotoxic patients. We compared the efficacy of 370 MBq (10 millicuries) with 555 MBq (15 millicuries) radioiodine activities for therapy in patients with Graves' disease over a period of 10 years. We excluded patients with moderate to severe dysthyroid eye disease. We also documented whether these patients had previous treatment with Carbimazole, propylthiouracil and previous radioiodine therapy. Overall, 90% of the patients had a successful outcome from treatment with no significant difference between the higher and lower activities and no difference between the genders. [5] We now administer 400 MBq capsules to all patients with Graves' disease who require radioiodine therapy and continue to have a 90% success rate.

There is no doubt that larger doses of radioiodine (>600 MBq) will lead to a larger percentage of patients becoming euthyroid or hypothyroid more quickly than smaller doses (<400 MBq). [12],[13] Recently, the American Thyroid Association and American Association of Clinical Endocrinologists Taskforce on Hyperthyroidism and Other Causes of Thyrotoxicosis proposed that radiation should be administered in a single dose, typically 370 to 555 MBq, to render the patient with Graves' disease euthyroid. It also recommended that no patient should be treated with a dose less than 370 MBq. [14] There are a number of factors that predict the need for either a second dose (typically given 2-6 months after the initial dose) or a higher initial dose. These include male sex, high free T 4 at diagnosis and a palpable goitre. [8] Larger doses of radioiodine are also required for patients in areas where the iodine content of their diet is high or they are on iodine-containing drugs e.g. amiodarone. Because of the risk of hypothyroidism, thyroid function should be checked every 4-6 weeks. Once euthyroidism has been established annual thyroid function checks are required. [1]

However, larger doses of radioiodine are not without possible complications. The Royal College of Physicians clinical guidelines indicate that although they found no evidence of increased instance of leukaemia, there was a possible increase in small bowel cancer and gastric cancer. [15] The potential benefits using a small radioiodine activity are in line with the international commission on radiological protection recommendations regarding the "linear no threshold" model for radiation risk. [16],[17] Restrictions on behavior of out-patients post-treatment can also be reduced with the administration of a lower activity. When 555 MBq is administered the guidance notes suggest a restriction period of 25 days to ensure that the radiation dose to members of the public is kept below 1 mSv. For activity of 370 MBq, this period can be reduced to 21 days, with obvious benefits to patient, families and carers. [15] Another, potential environmental benefit for administering low activity is the reduction in the release of iodine 131 via sewage system.

There are two further possible theoretical considerations. It is recognized that patients on a low iodine diet are more sensitive to radioiodine therapy. However, compliance with dietary advice is recognized to be poor. [13] In addition, rTSH is known to increase radioiodine uptake and has been used to facilitate radioiodine uptake in thyroid cancers and large thyroid goitres. However, rTSH needs to be administered some hours before the radioiodine and does make a simple treatment regimen much more complex. [18],[19],[20]

It is our practice to administer 400 MBq to patients with Graves' disease. In patients with large goitres, particularly multinodular goitres, we would administer 800 MBq. We would not routinely use carbimazole or propylthiouracil pre-radioiodine to render the patient euthyroid. However, carbimazole or propylthiouracil pre-radioiodine would be considered in a frail elderly patient where there may be a concern regarding a thyroid storm. In patients with thyroid eye disease, we would be resistant to the administration of radioiodine to a smoker. We would prescribe steroid therapy for patients with thyroid eye disease undergoing radioiodine therapy and ensure that they were closely followed-up post treatment in order to deter the progression of the eye disease.

 
   References Top

1.Franklyn JA, Boelaert K. Thyrotoicosis. Lancet 2012;379:1155-66.  Back to cited text no. 1
[PUBMED]    
2.McDermott MT, Kidd GS, Dodson LE Jr, Hofeldt FD. Radioiodine induced thyroid storm. Case report and literature review. Am J Med 1983;75:353-9.  Back to cited text no. 2
[PUBMED]    
3.Peters H, Fischer C, Bogner U, Reiners C, Schleusener H. Radioiodine therapy of Graves' hyperthyroidism: standard vs. calculated 131iodine activity. Results from a prospective, randomized, multicentre study. Eur J Clin Invest 1995;25:186-93.  Back to cited text no. 3
    
4.Leslie WD, Ward L, Salamon EA, Ludwig S, Rowe RC, Cowden EA. A randomized comparison of radioiodine doses in Graves' hyperthyroidism. J Clin Endocrinol Metab 2003;88:978-83.  Back to cited text no. 4
[PUBMED]    
5.Collier A, Ghosh S, Hair M, Malik I, McGarvie J. Comparison of two fixed activities of radioiodine therapy (370 vs. 555MBq) in patients with Graves' disease. Hormones 2009;8:273-8.  Back to cited text no. 5
    
6.Sridama V, McCormick M, Kaplan EL, Fauchet R, DeGroot LJ. Long-term follow-up study of compensated low-dose 131I therapy for Graves' disease. N Engl J Md 1984;311:426-32.  Back to cited text no. 6
[PUBMED]    
7.Cunnien AJ, Hay ID, Gorma CA, Offord KP, Scanlon PW. Radioiodine induced hypothyroidism in Graves' disease: Factors associated with the increasing incidence. J Nucl Med 1982;23:978-83.  Back to cited text no. 7
    
8.Boelaert K, Syed AA, Manji N, Sheppard MC, Holder RL, Gough SC, et al. Prediction of cure and risk of hypothyroidism in patients receiving 1311 for hyperthyroidism. Clin Endocrinol (Oxf) 2009;70:129-38.  Back to cited text no. 8
[PUBMED]    
9.Solomon B, Glinoer D, Lagasse R, Wartofsky L. Current trends in the management of Graves' disease. J Clin Endocrinol Metab1990;70:1518-24.  Back to cited text no. 9
[PUBMED]    
10.de Bruin TW, Croon CD, de Klerk JM, van Isselt JW. Standardized radioiodine therapy in Graves' disease: the persistent effect of thyroid weight and radioiodine uptake on outcome. J Intern Med 1994;236:507-13.  Back to cited text no. 10
[PUBMED]    
11.Berg G, Michanek A, Holmberg E, Nystrom E. Clinical outcome of radioiodine treatment of hyperthyroidism: a follow-up study. J Intern Med 1996;239:165-71.  Back to cited text no. 11
    
12.Santos RB, Romaldini JH, Ward LS. A Randomized Controlled Trial to Evaluate the Effectiveness of 2 Regimens of Fixed Iodine ( 131 I) Doses for Graves Disease Treatment. Clin Nucl Med 2012;3:241-4.  Back to cited text no. 12
    
13.Sztal-Mazer S, Nakatani VY, Bortolini LG, Boguszewski CL, Graf H, de Carvalho GA. Evidence for Higher Success Rates and Successful Treatment Earlier in Graves' Disease with Higher Radioactive Iodine Doses. Thyroid 2012;22:991-5  Back to cited text no. 13
    
14.Bahn Chair RS, Burch HB, Cooper DS, Garber JR, Greenlee MC, Klein I, et al. Hyperthyroidism and other causes of thyrotoxicosis: Management guidelines of the American Thyroid Association and American Association of Clinical Endocrinologists. Thyroid 2011; 21:593-646.  Back to cited text no. 14
[PUBMED]    
15.Royal College of Physicians. Radioiodine in the management of benign thyroid disease. London: Royal College of Physicians Publications; 2007.  Back to cited text no. 15
    
16.Medical and dental guidance notes: A good practice guide on all aspects of ionising radiation in the clinical environment. York: Institute of Physics and Engineering in Medicine; 2002.  Back to cited text no. 16
    
17.ICRP Publication 99, 2006 Low-dose extrapolation of radiation related cancer risk. Annals of the ICRP 35:4. Elsevier, UK.  Back to cited text no. 17
    
18.Nielsen VE, Bonnema SJ, Boel-Jorgensen H, Veje A, Hegedus L. Recombinant human thyrotropin makedly changes the 131I kinetics during 131I therapy of patients with nodular goiter: An evaluation by a randomised double-blinded trail. J Clin Endocrinol Metab 2005;90:79-83.  Back to cited text no. 18
    
19.Pena S, Arum S, Cross M, Magnani B, Pearce EN, Oates ME, et al. 123I thyroid uptake and thyroid size at 24, 48 and 72 hours after the administration of recombinant human thyroid-simulating hormone to normal volunteers. J Clin Endo Metab 2006;91:506-10.  Back to cited text no. 19
[PUBMED]    
20.Huysmans DA, Nieuwlaat WA, Erdtsieck RJ, Schellekens AP, Bus JW. Administration of a single low dose of recombinant human thyrotropin significantly enhances thyroid radioiodide uptake in non-toxic nodular goiter. Clin Endocrinol Metab 2000;85:3592-6.  Back to cited text no. 20
    




 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
    References

 Article Access Statistics
    Viewed1589    
    Printed24    
    Emailed0    
    PDF Downloaded262    
    Comments [Add]    

Recommend this journal