- Research article
- Open Access
- Open Peer Review
Is annual surveillance of all treated hypothyroid patients necessary?
© Viswanath et al; licensee BioMed Central Ltd. 2007
- Received: 08 November 2006
- Accepted: 02 July 2007
- Published: 02 July 2007
Annual surveillance (with thyroid function testing) is widely recommended for the long-term follow-up of treated hypothyroid patients. It is based largely on consensus opinion and there is limited evidence to support the frequency of monitoring. The majority of patients in our hospital based thyroid register are on 18 monthly follow-up.
We carried out a retrospective analysis to see if there is evidence to support more frequent testing. We used a logistic regression model to assess whether any baseline characteristics could be applied to predict an abnormal test.
We identified 2,125 patients with a minimum of 10 years follow-up (89% female, 65% autoimmune hypothyroidism, and mean age at registration 51 years). There were 2 groups: 1182 (56%) had been allocated to 18 monthly follow-up and the rest had annual surveillance. The groups were well matched at baseline. Overall, during follow-up the 12 monthly group had more abnormal tests requiring dose adjustment. However, on logistic regression analysis, people aged less than 60 years, individuals taking < 150 μg thyroxine per day and people on 18 monthly follow-up had less abnormal tests.
18 monthly surveillance may be adequate in the long term follow-up of hypothyroid patients less than 60 years of age on a stable thyroxine dose of 100–150 μg/day where there are robust follow-up mechanisms in place. Implementing this strategy has potential for cost saving.
- Thyroid Stimulate Hormone
- Thyroid Function Test
- Abnormal Test
- Thyroid Stimulate Hormone Level
Hypothyroidism is usually due to primary thyroid failure secondary to chronic autoimmune thyroiditis (Hashimoto's disease) or destructive therapy (radioactive iodine or thyroidectomy). In the United Kingdom the prevalence of overt hypothyroidism in women is at least 1.4 to 1.9% compared to less than 1% in men , and increases with age . Levothyroxine is the standard replacement therapy and treatment is life long, with the aim of restoring patients to a euthyroid state and normalising thyroid stimulating hormone (TSH) concentration. Though the treatment of hypothyroidism is straightforward, data from several studies [3–5] show that only around 60% of patients on thyroxine replacement have normal TSH levels. Thyroxine over replacement is associated with increased risk of atrial fibrillation  and reduction in bone mass in postmenopausal women . In addition a raised TSH level is associated with an unfavourable lipid profile [4, 8].
Hence periodic monitoring of thyroid function tests (TFTs) is essential in the management of patients to judge the response to therapy, patient compliance, and to adjust doses in relation to advancing age. Annual TFT surveillance is widely recommended [9–11]. In the UK, the General Practitioner (GP) contract  effective from April 2004, which financially rewards primary care practices, recommends that patients with hypothyroidism on thyroxine, should have thyroid function tests recorded at least every 15 months. The recommended frequency of testing is based largely on consensus, and there is limited evidence to support this. The majority of patients currently followed up in our hospital based thyroid register are on 18 monthly follow-up. We undertook a retrospective study to see if there is evidence to support more frequent testing.
Grampian Automated Thyroid Register (previously known as Scottish Automated Follow-up Register) has provided follow-up facilities for patients with thyroid disease since 1967, as a joint venture between hospital and primary care. Currently around 20,000 patients are registered on the database. Patients are recalled at a pre-set follow-up interval for TFTs and review by the primary care staff, who provide information on clinical status. The results are reviewed centrally, and if satisfactory, the computer automatically generates a routine recall. If abnormal, the result is reviewed by a thyroid specialist who may recommend a dose change and/or an early review. Written instructions are sent to the GP, reducing the number of patients with abnormal tests requiring review at a hospital based thyroid clinic. After an appropriate intervention, when TFTs are satisfactory, individuals are returned to routine review at the pre-set interval. If they fail to turn up for review, a reminder is sent at 3 and 6 months. Deaths are notified to the thyroid register.
We retrospectively identified hypothyroid patients on thyroxine who had a minimum of 10 years of follow-up on the register. Only patients on 12 monthly and 18 monthly follow-up plans were evaluated. As there were no set guidelines for entering patients on the register, patients were allocated to these follow-up intervals by clinicians on a non-selective basis. We excluded patients who hadn't returned for follow-up for more than 30 months (patients who may have moved away from the region or were non-compliant). Patients with drug-induced hypothyroidism and 11 individuals with inadequate follow-up data were also excluded from the study. The registration details included age, aetiology of hypothyroidism and thyroxine dose at registration. Follow-up information regarding the number of reviews, defaults, changes in thyroxine dose or follow-up interval and the results of the thyroid test at each review was summarised from the database. TFTs undertaken during follow-up were interpreted as hyperthyroid when TSH was suppressed (<0.01 mU/L) and other thyroid hormones were elevated. An elevated TSH (>4 mU/L) with or without a low thyroid hormone concentration was described as a hypothyroid test. The method used for thyroid function testing varied during the study period. Radio-immuno assay (RIA) was used up to1995 (reference range: total T4 70–150 nmol/L, TSH 0.35–3.3 mU/L). From 1995 onwards automated immunoassay was used (Bayer diagnostics, reference range: FT4 10–25 pmol/L, TSH 0.35–3.3 mU/L). Data were anonymised and permission was not required from the Grampian Regional Ethics Committee to carry out this research.
Data were analysed using Student's t-tests, Mann Whitney and chi squared tests as appropriate. To explore the differences in abnormal tests between the follow-up plan logistic regression was used. Covariates adjusted for were gender, autoimmune hypothyroidism (yes or no), age at registration (<25 years, 25 to 60 years, >60 years), thyroxine dose at registration (<100 μg, 100 to 150 μg, >150 μg), thyroid follow-up plan (12 monthly or 18 monthly) and duration of follow-up in years. All analyses were carried out in SPSS.
Comparison of baseline characteristics between the groups
12 monthly FU (n = 943)
18 monthly FU (n = 1182)
Age years mean (SD)
Thyroxine dose at registration (μg/day) mean (SD)
Age < 60 years (n = 1556)
Female (n = 1892)
Autoimmune hypothyroidism (n = 1384)
Mean duration of follow-up (years) mean (SD)
Comparison of follow-up data between the groups
12 monthly (n = 943)
18 monthly (n = 1182)
Total number of reviews
Percentage of early reviews
Percentage of late reviews
Percentage of routine reviews
Total number of tests
Average number of tests per person
Percentage of patients with at least one abnormal test during follow-up
Thyroxine dose changes
The mean thyroxine dose at the time of registration was 131.2 (SD 42.4) μg per day (range 25–300) and around 80% were on 100–150 μg of thyroxine per day. The mean thyroxine dose at last/final review was 127.4 (SD 35.5) μg (median 125, range 25–300). During follow-up, thyroxine dose remained unchanged in 35.4%, and a further 31% and 21% of cases required a dose alteration of 25 μg and 50 μg respectively during long term surveillance. Individuals taking 100–150 μg of thyroxine at registration had fewer dose changes compared to the rest (40.5% vs 14.7%, p < 0.01). Only 62.7% on 18 monthly follow-up required a dose change as opposed to 66.9% on annual surveillance (p < 0.05).
Predictors of abnormal result
95% confidence interval
*Age at registration:
< 25 yrs
> 60 yrs
+Thyroxine dose at registration
Thyroid FU plan
18 monthly interval
It is universally accepted that patients on thyroxine replacement should have regular clinical and biochemical surveillance to ensure compliance and adjust doses in relation to changing requirements. However the ideal screening interval has not been ascertained and there are no published studies on the appropriate frequency of follow-up. Surveillance by annual TFT is recommended by most of the published thyroid guidelines [9–11]. The recommendations are largely based on consensus, and there is limited evidence to support this practice. Vanderpump et al  recommended further audit/study to clarify some of the uncertainties in the follow-up of hypothyroid patients.
Grampian Automated Thyroid Register (GAFUR) was established in 1967 , and is one of the oldest thyroid registers in the world. Thyroid registers improve records, ensure regular reviews, and promote early detection of changes in the patient's clinical status. Thyroid registers have proved to be beneficial in the long-term follow-up of patients with thyroid dysfunction. They are cost-effective  and achieve better biochemical control  in comparison to conventional follow-up. From our thyroid register we were able to identify a large cohort of hypothyroid patients on thyroxine with a minimum of 10 years of follow-up. As expected the majority of patients were women who had developed spontaneous hypothyroidism. As there were no set guidelines, individuals were allocated to either follow-up plan by the referring physician on a non-selective basis. The baseline characteristics were well matched and there did not appear to be any bias in relation to allocation to either group. The system of recall and follow-up was well managed through good co-operation and links between primary care and GAFUR. Individuals in both the groups were compliant with follow-up arrangements. Similar benefits of thyroid registers in maintaining long term surveillance with minimal defaults was reported by Jung et al. in 1991.
During follow-up thyroid function tests were undertaken at each review appointment and 18 monthly follow-up was not associated with an increase in adverse outcomes. On the other hand, patients on annual surveillance were more likely to have an abnormal test. Both the groups were well matched at baseline (table.1) in relation to age and sex distribution, thyroxine dose and duration of follow-up, and we cannot readily account for the difference in outcome. One possible explanation could be physician bias at the time of registration. There were no set guidelines or criteria and it is possible that there was physician bias while allocating individuals to annual screening taking into account factors such as compliance. It is also likely that more frequent testing will find more abnormal results. Another conclusion that can be drawn is that annual surveillance should be recommended as there was an increased chance of detecting an abnormal result. This approach may however lead to unnecessary tests in some individuals as thyroxine dose remained unchanged in 35% of patients during long term follow-up. On the other hand, although 18 monthly surveillance cannot be applied universally, it may be an option in individuals whose thyroxine requirement is less likely to change or have less abnormal tests during follow-up. We undertook further sub-group analysis to identify individuals who may be suitable for less frequent testing.
Patients aged over 60 years at the time of registration were more likely to have an abnormal test during follow-up. This may be due to decreased thyroxine requirements with increasing age. This has been reported in previous studies [17, 18] and probably reflects the progressive decrease in thyroxine degradation rate that occurs with advancing age. The fall in thyroxine requirement with age also corresponds to the loss of lean body mass . Hence people aged over 60 years require annual surveillance.
Individuals taking 100–150 μg/day required fewer dose changes during long term follow-up compared to the rest. We would recommend annual testing in individuals who are on either <100 or >150 μg of thyroxine per day. Once established on the appropriate dose of thyroxine, follow-up interval can be extended to 18 months in individuals aged less than 60 years. There were insufficient patients on the register with a regular follow-up interval of two years to evaluate even less frequent monitoring.
Individuals on annual surveillance had more frequent reviews and required more TFTs compared to the 18 monthly group, and this will have cost implications. The Grampian automated thyroid register currently has over 10,000 registered hypothyroid patients, and the majority are being followed-up 18 monthly. Allocating everyone to annual follow up would mean an extra 3,000 thyroid tests per year. A thyroid function test costs around £15 for the NHS (personal communication with Dr Heather Watson, clinical biochemistry, NHS Grampian on 24/04/06). This would amount to an extra spending of around £45,000 per year without taking into account the cost of additional administrative time for GAFUR and primary care, and inconvenience to the patient. Our study has shown that 18 monthly follow-up may be adequate in the majority of patients under 60 years of age on a stable thyroxine dose of 100–150 μg/day. Implementing these recommendations has potential benefits in terms of savings and reduction in the workload.
The Grampian automated thyroid register was set up in the late 1960s and traditionally TSH and FT4 estimations were undertaken. The recently published UK guidelines  on the use of thyroid function tests recommend TSH estimation alone in the long-term follow-up of treated hypothyroid patients. We are considering changing our practice to achieve additional cost savings in relation to thyroid tests.
Treated hypothyroid patients require regular clinical and biochemical surveillance. Annual surveillance is currently recommended with no evidence to support this practice. Our study has shown that 18 monthly surveillance may be adequate in the long term follow-up of patients less than 60 years of age on a stable thyroxine dose of 100–150 μg/day. Implementing this strategy has potential for cost saving and reduction of workload in health services.
We would like to thank Mr. Robert Wilson, secretary to GAFUR for providing clarification regarding the thyroid care pathway. The Health Services Research Unit is funded by the Chief Scientist Office of the Scottish Executive Health Department. The views expressed are those of the authors.
- Tunbridge WM, Evered DC, Hall R, Appleton D, Brewis M, Clark F, Evans JG, Young E, Bird T, Smith PA: The spectrum of thyroid disease in a community: The Whickham survey. Clin Endocrinol. 1977, 7 (6): 481-493.View ArticleGoogle Scholar
- Vanderpump MP, Tunbridge WM: Epidemiology and prevention of clinical and subclinical hypothyroidism. Thyroid. 2002, 12: 839-847. 10.1089/105072502761016458.View ArticlePubMedGoogle Scholar
- Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, Spencer CA, Braverman LE: Serum TSH, T4, and thyroid antibodies in the United States population (1998 to1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab. 2002, 87: 489-499. 10.1210/jc.87.2.489.View ArticlePubMedGoogle Scholar
- Canaris GJ, Manowitz NR, Mayor G, Ridgway EC: The Colorado thyroid prevalence study. Arch Intern Med. 2000, 160: 526-534. 10.1001/archinte.160.4.526.View ArticlePubMedGoogle Scholar
- Parle JV, Franklyn JA, Cross KW, Jones SR, Sheppard MC: Thyroxine prescription in the community: serum thyroid stimulating hormone level assays as an indicator of under treatment or over treatment. Br J Gen Pract. 1993, 43: 107-109.PubMedPubMed CentralGoogle Scholar
- Sawin CT, Geller A, Wolf PA, Belanger AJ, Baker E, Bacharach P, Wilson PW, Benjamin EJ, D'Agostino RB: Low serum thyrotropic concentration as a risk factor for atrial fibrillation in older people. N Engl J Med. 1994, 331: 1249-1252. 10.1056/NEJM199411103311901.View ArticlePubMedGoogle Scholar
- Faber J, Galloe AM: Changes in body mass during prolonged sub clinical hyperthyroidism due to L-thyroxine treatment: a meta analysis. Eur J Endocrinol. 1994, 130: 350-356.View ArticlePubMedGoogle Scholar
- Franklyn JA, Daykin J, Betteridge J, Hughes EA, Holder R, Jones SR, Sheppard MC: Thyroxine replacement therapy and circulating lipid concentrations. Clin Endocrinol. 1993, 38 (5): 453-459.View ArticleGoogle Scholar
- Vanderpump MP, Ahlquist JA, Franklyn JA, Clayton RN: Consensus statement for good practice and audit measures in the management of hypothyroidism and hyperthyroidism. BMJ. 1996, 313: 539-544.View ArticlePubMedPubMed CentralGoogle Scholar
- Singer PA, Cooper DS, Levy EG, Ladenson PW, Braverman LE, Daniels G, Greenspan FS, McDougall IR, Nikolai TF: Treatment guidelines for patients with hyperthyroidism and hypothyroidism. Standards of Care Committee, American Thyroid Association. JAMA. 1995, 273: 808-812. 10.1001/jama.273.10.808.View ArticlePubMedGoogle Scholar
- AACE Thyroid Task Force: American Association of Clinical Endocrinologists medical guidelines for clinical practice for the evaluation and treatment of hyperthyroidism and hypothyroidism. Endocr Pract. 2000, 8: 457-469.Google Scholar
- New General Medical Services contract 'Investing in General Practice'. British Medical Association. 2003, Annex A: Quality indicators-Hypothyroidism, [http://www.bma.org.uk/ap.nsf/Content/investinggp]
- Hedley AJ, Scott AM, Weir RD, Crooks J: Computer-assisted follow-up register for the North-east of Scotland. BMJ. 1970, 1: 556-558.View ArticlePubMedPubMed CentralGoogle Scholar
- Jones SJ, Hedley AJ, Curtis B, Allison SP, Woolfson AM, Steele R, Bewsher PD, Weir RD: Do we need thyroid follow-up registers? A cost-effective study. Lancet. 1982, 1: 1229-1233. 10.1016/S0140-6736(82)92348-0.View ArticlePubMedGoogle Scholar
- Flynn RW, Morris AD, Jung RT, MacDonald TM, Leese GP: Does an automated thyroid register improve the clinical management of hypothyroid patients? An observational study. Clin Endocrinol. 2005, 63: 116-118. 10.1111/j.1365-2265.2005.02248.x.View ArticleGoogle Scholar
- Jung RT, Scott A, Chong P, Browning M, Waugh N: A new Pick based computer thyroid register based on the national SAFUR requirements for local usage. Health Bull (Edinb). 1991, 49: 244-249.Google Scholar
- Rosenbaum RL, Barzel US: Levothyroxine replacement dose for primary hypothyroidism decreases with age. Ann Int Med. 1982, 96: 53-55.View ArticlePubMedGoogle Scholar
- Sawin CT, Geller A, Hershman JM, Castelli W, Bacharach P: The ageing thyroid: the use of thyroid hormone in older people. JAMA. 1989, 261: 2653-2655. 10.1001/jama.261.18.2653.View ArticlePubMedGoogle Scholar
- Santini F, Pinchera A, Marsili A, Ceccarini G, Castagna MG, Valeriano R, Giannetti M, Taddei D, Centoni R, Scartabelli G, Rago T, Mammoli C, Elisei R, Vitti P: Lean body mass is a major determinant of levothyroxine dosage in the treatment of thyroid diseases. J Clin Endocrinol Metab. 2005, 90: 124-127. 10.1210/jc.2004-1306.View ArticlePubMedGoogle Scholar
- UK Guidelines for the use of thyroid function tests. British Thyroid Association. 2006, [http://www.british-thyroid-association.org/TFT_guideline_final_version_July_2006.pdf]
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6823/7/4/prepub
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