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The investigators aim to establish whether biochemical control during anti-thyroid drug therapy in young people with thyrotoxicosis varies depending upon whether a 'block and replace' or 'dose titration' regimen is used. The investigators will also assess remission rates and the frequency of side-effects in the two treatment groups.
Thyrotoxicosis is an uncommon disorder in childhood and adolescence with a UK incidence around 1 per 100,000 (0-15 years). Most patients with thyrotoxicosis have Graves' disease which develops because of thyrotropin (TSH) receptor stimulation by autoantibodies. Patients with Hashimoto's thyroiditis can also be thyrotoxic in the early phase of the disease and occasionally thyrotoxicosis develops because of activating mutations of the TSH receptor. Many general paediatricians have experience of managing patients with thyrotoxicosis but national guidelines to assist in patient care have not been produced to date.
There is no ideal therapy for thyrotoxicosis in children and adolescents. The three treatment modalities for thyrotoxicosis - anti-thyroid drugs (ATD), surgery and radioiodine all have significant disadvantages. Particular considerations when managing young people include:
Children and adolescents presenting with autoimmune thyrotoxicosis in the UK are usually treated with ATD from diagnosis for 1 - 4 years. Treatment is then stopped and patients who relapse return to ATD or are offered more definitive treatment with surgery or radioiodine. Life-long thyroid hormone replacement will be required if the thyroid gland is removed by surgery or ablated by radioiodine.
Excess thyroid hormone can have a major detrimental impact on cognitive function as well as cardiovascular and skeletal health. The maintenance of a clinically and biochemically euthyroid state is therefore highly desirable. There are two possible approaches when treating patients with ATD.
Both strategies are used by adult endocrinologists but it is unclear which of these approaches is the most appropriate in the young person.
Potential advantages of the 'block and replace' regimen include:
Potential advantages of the dose titration approach include:
This study is a prospective, multi-centre trial which aims to establish which regimen - block and replace or dose titration - is the most appropriate medical therapy for thyrotoxicosis during childhood and adolescence.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Block and Replace | Active Comparator | Carbimazole is commenced in a dose of 0.75 mg/kg/day. The intention is to completely prevent endogenous thyroxine production. Thyroxine is then added in a replacement dose as the thyroid hormone levels fall into the lower half of the laboratory normal range. The principal measure of control during the first 6 months will be thyroid hormone levels rather than TSH. |
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| Dose Titration | Active Comparator | Carbimazole is commenced in a dose of 0.75 mg/kg/day until thyroid hormone levels fall into the local laboratory normal range. The dose is then reduced to 0.25 mg/kg/day with the intention of maintaining the euthyroid state. The principal measure of control during the first 6 months will be thyroid hormone levels rather than TSH. Carbimazole is the preferred treatment because of the increased risk of hepatotoxicity with propylthiouracil but patients who are treated with propylthiouracil can also be recruited and randomised. 1mg of carbimazole is approximately equivalent to 10 mg of propylthiouracil. Drug: Carbimazole 5mg and 20 mg tablets. Administered as a once or twice daily regimen with total daily dose adjusted according to prevailing biochemistry Drug: propylthiouracil 50 mg tablets administered once daily with the dose adjusted according to the prevailing biochemistry. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Block and Replace | Procedure | The primary objective of treatment is to maintain a euthyroid state with TSH and thyroid hormone levels in the local laboratory normal range. Carbimazole is commenced in a dose of 0.75 mg/kg/day (propylthiouracil - for dose see below) with the aim being to completely preventing endogenous thyroxine production. Thyroxine is then added in a low replacement dose as the thyroid hormone levels fall into the lower half of the laboratory normal range. The principle measure of control during the first 6 months will be thyroid hormone levels rather than TSH. Carbimazole is the preferred treatment because of the increased risk of hepatotoxicity with propylthiouracil but patients who are treated with propylthiouracil can also be recruited and randomised. 1mg of carbimazole is approximately equivalent to 10 mg of propylthiouracil. |
| Measure | Description | Time Frame |
|---|---|---|
| Biochemical control as reflected by the stability of blood thyroid stimulating hormone (TSH) concentrations | For each patient, TSH will be determined at each visit: the primary outcome variable is obtained by measuring the proportion of TSH concentrations that are outwith the laboratory normal range (in calculating this value, determinations made within six months of diagnosis are ignored). | 2.5 years |
| Measure | Description | Time Frame |
|---|---|---|
| Remission rates as defined by patients who are biochemically euthyroid at the end of the 4 year study period. | To establish whether the remission rates post therapy in young people with thyrotoxicosis are affected by treatment with a 'block and replace' or 'dose titration' regimen. This will be determined by determining the proportion of individuals who are in remission ie who are biochemically euthyroid off ATD-thyroid drug therapy at the end of the of the study period (4 years). The proportion of subjects in remission following block and replace therapy will therefore be compared with the proportion in remission following dose titration. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Tim Cheetham | Newcastle upon Tyne Hospiatls NHS Foundation Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Royal Aberdeen Children's Hospital | Aberdeen | United Kingdom | ||||
| Birmingham Children's Hospital |
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| Label | URL |
|---|---|
| British Society for Paediatric Endocrinology and Diabetes supports this study | View source |
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| Dose Titration | Procedure | The primary objective of treatment is to maintain a euthyroid state with TSH and thyroid hormone levels in the local laboratory normal range. Carbimazole is commenced in a dose of 0.75 mg/kg/day until thyroid hormone levels fall into the local laboratory normal range. The dose is then reduced to 0.25 mg/kg/day with the intention of maintaining a euthyroid state as reflected by a free thyroxine and TSH within the normal range. Most paediatricians in the UK commence thyrotoxic children on carbimazole rather than propylthiouracil. Carbimazole is the preferred treatment because of the increased risk of hepatotoxicity with propylthiouracil but patients who are treated with propylthiouracil can also be recruited and randomised. The guidelines detailed above can be used in the knowledge that 1mg of carbimazole is approximately equivalent to 10 mg of propylthiouracil. |
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| carbimazole | Drug | Carbimazole 5mg and 20 mg tablets Administered as a once or twice daily regimen with total daily dose adjusted according to prevailing biochemistry |
|
| propylthiouracil | Drug | 50 mg tablets administered once daily with the dose adjusted according to the prevailing biochemistry |
|
| thyroxine | Drug | 25mcg, 50mcg and 100mcg tabletes administered once daily with the dose adjusted according to the prevailing biochemistry |
|
| 4 years |
| The frequency of adverse events on the 2 treatment regimens. | This will be reflected by the number of participants with adverse events and by the proportion of patients changing to a different treatment during the study period. | 3 years |
| Additional measures of biochemical control. | A comparison of the mean and variability of TSH and thyroid hormone concentrations in the 2 treatment groups. | 3 years |
| Birmingham |
| United Kingdom |
| Addebrookes Hospital | Cambridge | United Kingdom |
| Wales College of Medicine | Cardiff | United Kingdom |
| University Hospital | Coventry | United Kingdom |
| Ninewells Hospital | Dundee | United Kingdom |
| Royal Hospital for Sick Children | Edinburgh | United Kingdom |
| Royal Hospital for Sick Children | Glasgow | United Kingdom |
| Hereford Hospital | Hereford | United Kingdom |
| Crosshouse Hospital | Kilmarnock | United Kingdom |
| Alder Hey Children's Hospital | Liverpool | United Kingdom |
| St Bart's Hospital | London | United Kingdom |
| St George's Hospital | London | United Kingdom |
| Royal Manchester Children's Hospital | Manchester | United Kingdom |
| Royal Victoria Infirmary | Newcastle upon Tyne | United Kingdom |
| Norfolk & Norwich University Hospitals | Norwich | United Kingdom |
| Oxford Radcliffe Hospitals | Oxford | United Kingdom |
| Sheffield Children's Hospital | Sheffield | United Kingdom |
| ID | Term |
|---|---|
| D013971 | Thyrotoxicosis |
| D001733 | Bites and Stings |
| ID | Term |
|---|---|
| D006980 | Hyperthyroidism |
| D013959 | Thyroid Diseases |
| D004700 | Endocrine System Diseases |
| D011041 | Poisoning |
| D064419 | Chemically-Induced Disorders |
| D014947 | Wounds and Injuries |
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| ID | Term |
|---|---|
| D003766 | Dental Occlusion |
| D002231 | Carbimazole |
| D011441 | Propylthiouracil |
| D013974 | Thyroxine |
| ID | Term |
|---|---|
| D003813 | Dentistry |
| D009063 | Dental Physiological Phenomena |
| D055688 | Digestive System and Oral Physiological Phenomena |
| D007093 | Imidazoles |
| D001393 | Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D013889 | Thiouracil |
| D014498 | Uracil |
| D011744 | Pyrimidinones |
| D011743 | Pyrimidines |
| D013963 | Thyroid Hormones |
| D006728 | Hormones |
| D006730 | Hormones, Hormone Substitutes, and Hormone Antagonists |
| D024322 | Amino Acids, Aromatic |
| D000598 | Amino Acids, Cyclic |
| D000596 | Amino Acids |
| D000602 | Amino Acids, Peptides, and Proteins |
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