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Table of Contents
REVIEW
Year : 2015  |  Volume : 19  |  Issue : 3  |  Page : 340-346

Anti-thyroid drugs in pediatric Graves' disease


1 Department of Endocrinology, Providence Endocrine and Diabetes Specialty Centre, Kerala, India
2 Department of Pediatric Emergency and PICU, Kamakshi Memorial Hospital, Chennai, Tamil Nadu, India

Date of Web Publication5-Mar-2015

Correspondence Address:
Mathew John
Providence Endocrine and Diabetes Specialty Centre, Trivandrum, Kerala
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2230-8210.152766

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   Abstract 

Graves' disease is the most common cause of hyperthyroidism in children. Most children and adolescents are treated with anti-thyroid drugs as the initial modality. Studies have used Methimazole, Carbimazole and Propylthiouracil (PTU) either as titration regimes or as block and replacement regimes. The various studies of anti-thyroid drug (ATD) treatment of Graves' disease in pediatric patients differ in terms of the regimes, remission rate, duration of therapy for adequate remission, follow up and adverse effects of ATD. Various studies show that lower thyroid hormone levels, prolonged duration of treatment, lower levels of TSH receptor antibodies, smaller goiter and increased age of child predicted higher chance of remission after ATD. A variable number of patients experience minor and major adverse effects limiting initial and long term treatment with ATD. The adverse effects of various ATD seem to more in children compared to that of adults. In view of liver injury including hepatocellular failure need of liver transplantation associated with PTU, the use has been restricted in children. The rate of persistent remission with ATD following discontinuation is about 30%. Radioactive iodine therapy is gaining more acceptance in older children with Graves's disease in view of the limitations of ATD. For individual patients, risk-benefit ratio of ATD should be weighed against benefits of radioactive iodine therapy and patient preferences.

Keywords: Anti-thyroid drugs, Graves′ disease, pediatric


How to cite this article:
John M, Sundrarajan R, Gomadam S S. Anti-thyroid drugs in pediatric Graves' disease. Indian J Endocr Metab 2015;19:340-6

How to cite this URL:
John M, Sundrarajan R, Gomadam S S. Anti-thyroid drugs in pediatric Graves' disease. Indian J Endocr Metab [serial online] 2015 [cited 2020 Nov 26];19:340-6. Available from: https://www.ijem.in/text.asp?2015/19/3/340/152766


   Introduction Top


Graves' disease (GD) is the most common cause of hyperthyroidism in children and is due to the effect of thyroid stimulating hormone (TSH) receptor stimulating antibodies which stimulate the thyroid to produce excess hormones. The incidence of GD is believed to be between 0.1 and 3/100,000 children with a prevalence of 1 in 10,000 children in the United States. [1],[2]

The other causes of hyperthyroidism like toxic nodular goiter, thyroiditis, and activating mutations of TSH receptor are uncommon in pediatric practice. The signs and symptoms of thyrotoxicosis are similar to that of adults, although features such as ophthalmopathy and dermopathy are uncommon. [3],[4] Being a relatively rare disease in pediatric practice, there is a delay in diagnosis compared to that of adults. However, delayed diagnosis may be associated with impaired neurodevelopmental outcome, altered skeletal maturation, including craniosynostosis, advanced bone age, and reduction in school performance. [3],[5]

The various options for treatment of GD in children include antithyroid drugs (ATD), radioactive iodine (RAI), and thyroidectomy. In most centers, the majority of children with GD are initiated on ATD with RAI and surgery being reserved for children who do not achieve sustained remission with ATD. Considering the adverse effects of ATD especially fatal liver injury with propylthiouracil (PTU) and the fact that <30% of children achieve sustained remission with ATD, there is increase in the number of children subjected to RAI. [6],[7] Still, ATD forms the initial therapy for pediatric GD in a significant proportion of subjects. This review focuses on the current use of ATD in children.


   Anti-Thyroid Drugs Top


Anti-thyroid drugs are thionamides which contain a sulfhydryl group and a thiourea moiety within a heterocyclic structure. The common agents that are used as methimazole (MMI), carbimazole, and PTU. These agents are concentrated in the thyroid against a concentration gradient. These agents primarily act by inhibiting thyroid hormone synthesis by inhibiting thyroid peroxidase mediated iodination of tyrosine residues in the thyroglobulin, an important step in the thyroid hormone synthesis. In addition, PTU can block the conversion of T4 to T3 within the thyroid and in peripheral tissues. ATD can also have immunosuppressive effects with reduction in TSH receptor antibody, Intercellular Adhesion Molecule-1, soluble IL-2 and IL-6 receptors. [8]

Initiating and titrating therapy with anti-thyroid drugs

The recommended starting dose is 0.5-1.0 mg/kg/day for MMI and 5-10 mg/kg/day for PTU. [4] In a study comparing low and high dose MMI (<0.5 mg/kg vs. >0.5 mg/kg), more subjects (82%) responded to the higher dose than the lower dose (42%). [9] The medications are initiated at this dose and reduced every 4-8 weeks after documenting resolution of symptoms and thyroid function tests. [10] In most patients with GD, there is early reduction of T3 and T4 to normal levels correlating with resolution of symptoms. Recovery of suppressed TSH to normal levels occurs gradually. Continued suppression of serum TSH in patients with GD during ATD treatment is related to thyroid binding inhibiting immunoglobulin, pre-treatment severity of hyperthyroidism, and time to normalization of serum T 3 and T 4 . [11]

The doses of ATD are progressively reduced and maintained at minimum doses required to maintain a clinical and biochemical euthyroidism (Normal T3 and T4) for a period of 12-24 months. Following that the ATD is discontinued, and patient kept under follow-up for recurrence of symptoms.

In the block and replace method, both ATD and thyroxine are supplemented in an attempt to maintain euthyroidism. However, this approach needs a higher dose of ATD and hence vulnerable to the adverse effects. The rate of remission in this approach is not superior to the traditional approach described above. [12],[13]

Remission with anti-thyroid drugs in paediatric Graves' disease

A patient is considered to be in remission if T3, T4, and TSH remain normal 1 year after discontinuation of antithyroid therapy. [10] The remission rates in adults with GD seem to be variable with studies from US reporting it at 20-30% remission after 12-18 months of medication. [10] The remission rate appears to be higher in Europe and Japan; a long-term European study indicated a 50-60% remission rate after 5-6 years of treatment. [10],[13]

The natural history of untreated GD in children is not well described. The remission rates in children seem to be lower than in adults. The remission rates in various studies are given in [Table 1]. These studies have used various drugs (PTU, MMI or Carbimazole), different drug schedules (titration vs. block and replace regimes), and variable duration of ATD. In various studies lower levels of thyroid hormones (T3 and T4), longer duration of treatment, age group, TSH Rab at presentation, ethnicity, and smaller goiter were associated with increased chances of remission with ATD therapy.
Table 1: Drugs, drug dosage, duration of therapy, remission rates and factors predicting remission in various studies


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The relation between pubertal stages and rates of remission was discussed in various studies. In a study involving 40 patients, remission of GD with relation to puberty has shown that being pre, peri, or post pubertal did not have significant effects on the rate of remission, although the time to remission was longer in the pre pubertal children. During a median follow-up period of 4 years, remission was achieved in 10 of the patients receiving ATD (28%) after 3.76 ± 1.1 year of treatment. No significant associations were found between outcome and age or pubertal stage at diagnosis. Adverse effects were more in pre pubertal children. [22]

In another study of 143 patients, 38% of patients were prepubertal. 20 patients (7 prepubertal, 13 pubertal) reached remission on ATD. Duration of treatment needed to achieve remission was longer in prepubertal (4.2 years) than in pubertal patients (3.1 years) (P = 0.02). The rate of remission was not different between prepubertal (25.9%) and pubertal patients (33.3%) (P = 0.59). There was no difference between adverse effects to ATD between pubertal and pre- pubertal patients. [19]

In French Childhood GD Study Group, a multicenter prospective follow-up of 154 patients who were on MMI for a period of 24 months, followed by a follow-up of 2 years. The overall estimated relapse rate for hyperthyroidism was 59% at 1 year and 68% at 2 years after the end of treatment. The median time to relapse was 8 months. Multivariate survival analysis showed that the risk of relapse was higher for patients of non-Caucasian origin, with high serum thyroid-stimulating hormone receptor antibodies, and high free T4 levels at diagnosis. The risk of relapse decreased with increasing age at onset of disease and duration of the first course of ATD. There was no significant effect of pubertal age on chances of remission in subjects with hyperthyroidism. [17]

In an observational study involving 154 subjects, repeated courses of carbimazole each lasting 2 years were used. Remission was defined as a disease-free for at least 18 months after the completion of each course of ATD treatment. The median duration of follow-up in this study was 10.4 years. Overall estimated remission rates 18 months after the withdrawal of ATD treatment increased with time and were 20%, 37%, 45%, and 49% after 4, 6, 8, and 10 year follow-up, respectively. In a multivariate risk model, baseline high free T4 levels and the presence of other autoimmune disease at diagnosis was associated with a lesser chance of remission. [6]

In one of the largest series of 1138 patients with GD, of the 639 patients who discontinued ATD treatment, 334 (46.2%) achieved a remission, 247 (34.2%) experienced a relapse, and 58 (8.0%) dropped out. The cumulative remission rate increased with the duration of ATD treatment up until 5 years. No significant predictors of a remission were identified. [18]

In various studies, lower thyroid hormone levels, longer duration of treatment, lower levels of TSH receptor antibodies, and smaller goiter predicted higher chance of remission. There was a trend toward higher remission rates in older children with GD on treatment.

Effective duration of anti-thyroid drugs therapy in pediatric Graves' disease

In adults with GD, it is recommended that if MMI is chosen as the primary therapy for GD, the medication should be continued for approximately 12-18 months, then tapered or discontinued if the TSH is normal at that time. [10] A meta-analysis shows the remission rate in adults is not improved by a course of ATDs longer than 18 months. [27]

However, in children, the duration of therapy is controversial. Most studies have used around 24 months of therapy. There are data to support improved remission rates with longer duration of therapy. In Glaser et al., series of 184 pediatric patients treated with ATDs for up to 4 years, remission rates progressively improved from 10% after 1 year to 20% after 3 years and 23% after 4 years of ATD. [16] In the multicenter French Childhood GD Study Group, 154 patients who were on MMI for a period of 24 months, followed by a follow-up of 2 years. In this study, relapse risk decreased with longer duration of the first course of ATD. Furthermore, the estimated relapse rate 2 years after the end of treatment was 83% in patients treated for no more than 24 months, and 60% in patients treated for more than 24 months. [17]

TRAb serves as a marker predicting remission in adults with GD. In a study of 86 children and adolescents with GD treated >3 years, mean TRAb levels decreased with duration of therapy, but even after 13-24 months, TRAbs had normalized in only 3/16 (18.8%) patients. The initial TRAb titer correlated significantly with severity of the initial hyperthyroidism but did not predict the response to therapy as indicated by the dosage of ATD required to control the hyperthyroidism at 6 and 12 months. [28] In another study of 115 children, 38 children (33%) achieved remission after 2 years of ATD therapy. Absence of goiter, lower median TSH receptor antibody levels and lower time required for TSH R Ab normalization were factors associated with a better outcome in pediatric GD. [26] In another small study (n = 17) of subjects with GD, TRAb (TBIAb) was the only factor associated with a lasting remission. [29]

Although it seems that the rates of remission in children are lower than that of adults, there is no definite duration of therapy proposed for children. In studies of pediatric GD, the risk of relapse is reduced with longer duration of therapy with ATD, [16],[17] although 24 months can be considered reasonable before deciding to choose an alternate mode of definitive treatment. [12],[30] Although not compared in the same centers, Asian ethnic patients seem to have a higher rate of remission with ATD. [18],[24],[25] Practitioners planning to continue medications for longer duration should weigh the benefits of ATD against the poor remission rates and adverse effects of ATD.

Does anti-thyroid drugs induced adverse effects occur more commonly in children?

Both PTU and MMI are associated with adverse effects in children and adults. Both medications may cause serious adverse effects such as agranulocytosis and hepatotoxicity. MMI causes cholestatic hepatitis, and PTU causes hepatocellular injury including fulminant hepatic failure. Other serious adverse effects include Steven Johnson Syndrome, thrombocytopenia, neutropenia, and vasculitis. Minor adverse effects include rash, pruritus, arthralgia, hives, nausea, and reduced taste. [2],[3],[8],[10]

Side effects of MMI are dose-related, whereas those of propylthiouracil are less clearly related to dose. [8] In adults, the frequency of adverse effects associated with ATD are skin rash (4-6%), arthralgia (1-5%), gastrointestinal (1-5%), polyarthritis (1-2%), agranulocytosis (0.1-0.5%) with rest of the adverse events described as rare. [8]

In a prospective study of 70 children treated with PTU, 11 children (16%) developed adverse reactions to PTU including skin rash, arthralgia, arthritis with purpura and hematuria, elevated transaminases, and neutropenia. These children were treated with block and replace regimen with a daily dose of 5-7 mg/kg body weight of PTU. [16] In a group of 154 patients followed up for 10 years, only three patients had adverse reactions to ATD necessitating discontinuation of treatment. The incidences of minor reactions were not mentioned in this study. [6]

In a review that compiled the adverse effects of ATD in 500 children, there was an increased incidence of ATD related adverse effects in children: Mild increases in liver enzymes (28%), mild leukopenia (25%), skin rash (9%), granulocytopenia (4.5%), arthritis (2.4%), nausea (1.1%), agranulocytosis (0.4%), and hepatitis (0.4%). Other adverse effects were considered rare. [31] The risk of adverse effects associated with ATD in various studies is shown in [Table 2].
Table 2: Recorded adverse effects of anti-thyroid drugs in children


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There seems to be a difference in adverse reactions to ATD in relation to the pubertal status. In a study of 40 children by Lazar et al., the overall, adverse reactions to ATDs occurred in 35%, with a higher rate among the prepubertal children (71%) than the pubertal (28%) and post pubertal (25%) patients. Major adverse reactions were noted in two children, both prepubertal. [22]

The adverse effects of MMI seem to be dose related. The incidence of agranulocytosis in children is not known although it has been reported in about 0.3% of adult patients taking MMI or PTU. [8],[31]

However, there is little evidence to show that regular routine monitoring of hematological profiles or liver function tests will identify subjects early in the course of illness. The recommendation is to stop MMI and PTU and monitor blood counts if children develop fever, mouth sores, pharyngitis, or feel ill. [8],[30] In 95% of subjects who develop agranulocytosis, it develops within the first 100 days of therapy. [8],[33] While routine monitoring of white blood counts may detect early agranulocytosis, it is not recommended since it is rare and not cost effective.

Most studies show that the incidence of adverse effect of ATD is more common in children than in adults. There is a trend to higher adverse effects in prepubertal children compared to pubertal children. This relative risk benefit ratios should help prioritize treatment options of RAI in children as primary therapy or as a definitive treatment after first cycle of medical treatment.

Propylthiouracil in children

Propylthiouracil (6 propyl-2-thiouracil) was introduced for clinical use in July 1947. It acts by inhibiting the enzyme thyroid peroxidase which adds iodine to the tyrosine residue on thyroxine hormone precursor thyroglobulin. PTU also inhibits the enzyme tetraiodine 5'deiodinase, which converts T4 to T3. [7],[8]

In comparison to MMI and Carbimazole, PTU causes serious liver-related problems. PTU causes hepatocellular necrosis leading to liver transplantation and death. [7] In a review of US FDS Adverse Drug Reporting system, dissimilar hepatotoxicity profile of PTU and MMI in children was analyzed, PTU had a high adjusted reporting ratio for severe liver injury in a group less than 17 year of age. There were 23 cases of severe liver injury with PTU in less than 17 years of age and none with MMI. 4 subjects required liver transplantation. There were 4 cases of mild liver injury with PTU and 1 with MMI. In the same study, a major vasculitis signal was also observed with PTU in comparison to MMI. [34]

In the NICHD, OPPB Workshop in 2008 convened to evaluate PTU safety in children; it was observed that the risk of PTU associated liver transplantation was about 1 in 2000-4000 children. The liver failure associated with PTU was rapidly progressive with a low chance of reversibility. Children are at higher risk of liver failure than adults. The number of children developing reversible PTU-related liver toxicity is 10 fold greater than the number of children who develop liver failure requiring transplantation. Since PTU-induced liver injury is of rapid onset and can be rapidly progressive, serial testing of liver function will not be useful in identifying these subjects. [35] PTU is associated with higher risk of ANCA development and Vasculitis than MMI. PTU and MMI have comparable rates of agranulocytosis which are dose-dependent with MMI and not with PTU. [7]

Propylthiouracil hepatotoxicity has been reported to cause a variety of histological changes including portal and periportal inflammation with eosinophilic, lymphocytic, and plasmacytic infiltration in varying combinations, chronic active hepatitis, and submassive or massive hepatic necrosis. [36] These histological features resemble autoimmune hepatitis type 1 (AIH-1) and is referred to as drug-induced AIH-1. The various postulated for PTU-induced liver damage include inhibition of glucuronyltransferase, reduced bile acid synthesis, and increased oxygen consumption by the hepatocytes. [37],[38]

If PTU is used, it is recommended that PTU should be stopped immediately and liver function be assessed in children who experience anorexia, pruritus, rash, jaundice, light colored stool or dark urine, joint pain, right upper quadrant pain or abdominal bloating, nausea or fatigue. [34] In 2010, FDA added a boxed warning to the drug label for PTU about reports of liver injury and acute liver failure. [39],[40]

Alternatives to anti-thyroid drug therapy: Radioactive iodine and thyroidectomy

Radioactive Iodine therapy is a viable alternative to ATD therapy in children. Introduced more than 60 years back, RAI therapy leads to remission rates in excess of 95%. The aim of RAI therapy is to achieve hypothyroidism. Rare adverse effects include tenderness of the thyroid gland, thyroid storm, and worsening of ophthalmopathy. Experience with RAI is limited in children <5 years. [3],[12],[30] Thyroidectomy (near total or total) is another alternative mode of treatment for pediatric GD. Surgery should be done by high-volume thyroid surgeons and is indicated in children <5 years and those with thyroid gland >80 g in volume. [12],[30],[41]

Role of anti-thyroid drugs in the treatment of Graves's disease in children

Despite the fact that ATD achieves sustained remission in only a third of patients, has longer duration of treatment and the risk of adverse events, ATD still forms the initial treatment modality in a vast majority of children and adolescents of GD. PTU should not be used in children unless in a special situation as bridge therapy for short duration to control hyperthyroidism before surgical treatment in a patient intolerant to MMI. [12],[30]

  • Children et al. has proposed the following as guidance to choosing therapy in subjects with GD. [12],[30] Children <5 years: MMI should be used as first-line treatment till the patient goes into remission. A prolonged duration of therapy may be needed. RAI may be considered when the child is older or if developing adverse effects to ATD. Thyroidectomy is a viable option in experienced hands
  • Children 6-10 years: MMI should be considered as first-line treatment. RAI is a viable option as the child approaches 10 years or if there is a relapse on adequate course of ATD
  • Children >10 years: MMI or RAI therapy can form the first-line treatment. Patients with small goiter and low titer of TSH- R-Ab would be the right candidates for MMI therapy. After 1-2 years of ATD therapy, RAI or a repeat course of ATD would be an option.



   Conclusion Top


Most children and adolescents with GD are treated with ATD as the initial modality. The rate of persistent remission with ATD following discontinuation is in the tune of 30%. ATD are associated with adverse reactions in a minority of subjects including rare but severe adverse effects such as agranulocytosis, liver cell failure, Steven Johnson syndrome, and Vasculitis. The routine use of PTU in children has been restricted due to hepatotoxicity. In patients with relapse after ATD, radio RAI therapy or surgery should be considered as a viable option.

 
   References Top

1.
Lavard L, Ranløv I, Perrild H, Andersen O, Jacobsen BB. Incidence of juvenile thyrotoxicosis in Denmark, 1982-1988. A nationwide study. Eur J Endocrinol 1994;130:565-8.  Back to cited text no. 1
    
2.
Rivkees SA, Mattison DR. Propylthiouracil (PTU) hepatoxicity in children and recommendations for discontinuation of use. Int J Pediatr Endocrinol 2009;2009:132041.  Back to cited text no. 2
    
3.
Bauer AJ. Approach to the pediatric patient with Graves' disease: When is definitive therapy warranted? J Clin Endocrinol Metab 2011;96:580-8.  Back to cited text no. 3
    
4.
Cappa M, Bizzarri C, Crea F. Autoimmune thyroid diseases in children. J Thyroid Res 2010;2011:675703.  Back to cited text no. 4
    
5.
Segni M, Leonardi E, Mazzoncini B, Pucarelli I, Pasquino AM. Special features of Graves' disease in early childhood. Thyroid 1999;9:871-7.  Back to cited text no. 5
    
6.
Léger J, Gelwane G, Kaguelidou F, Benmerad M, Alberti C, French Childhood Graves' Disease Study Group. Positive impact of long-term antithyroid drug treatment on the outcome of children with Graves' disease: national long-term cohort study. J Clin Endocrinol Metab 2012;97:110-9.  Back to cited text no. 6
    
7.
Rivkees SA, Mattison DR. Ending propylthiouracil-induced liver failure in children. N Engl J Med 2009;360:1574-5.  Back to cited text no. 7
    
8.
Cooper DS. Antithyroid drugs. N Engl J Med 2005;352:905-17.  Back to cited text no. 8
    
9.
Slyper AH, Wyatt D, Boudreau C. Effective methimazole dose for childhood Graves' disease and use of free triiodothyronine combined with concurrent thyroid-stimulating hormone level to identify mild hyperthyroidism and delayed pituitary recovery. J Pediatr Endocrinol Metab 2005;18:597-602.  Back to cited text no. 9
    
10.
Bahn 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. Endocr Pract 2011;17:456-520.  Back to cited text no. 10
    
11.
Chung YJ, Lee BW, Kim JY, Jung JH, Min YK, Lee MS, et al. Continued suppression of serum TSH level may be attributed to TSH receptor antibody activity as well as the severity of thyrotoxicosis and the time to recovery of thyroid hormone in treated euthyroid Graves' patients. Thyroid 2006;16:1251-7.  Back to cited text no. 11
    
12.
Rivkees SA. Pediatric Graves' disease: Controversies in management. Horm Res Paediatr 2010;74:305-11.  Back to cited text no. 12
    
13.
Mazza E, Carlini M, Flecchia D, Blatto A, Zuccarini O, Gamba S, et al. Long-term follow-up of patients with hyperthyroidism due to Graves' disease treated with methimazole. Comparison of usual treatment schedule with drug discontinuation vs continuous treatment with low methimazole doses: A retrospective study. J Endocrinol Invest 2008;31:866-72.  Back to cited text no. 13
    
14.
Hamburger JI. Management of hyperthyroidism in children and adolescents. J Clin Endocrinol Metab 1985;60:1019-24.  Back to cited text no. 14
    
15.
Glaser NS, Styne DM. Predictors of early remission of hyperthyroidism in children. J Clin Endocrinol Metab 1997;82:1719-26.  Back to cited text no. 15
    
16.
Glaser NS, Styne DM, Organization of Pediatric Endocrinologists of Northern California Collaborative Graves' Disease Study Group. Predicting the likelihood of remission in children with Graves' disease: A prospective, multicenter study. Pediatrics 2008;121:e481-8.  Back to cited text no. 16
    
17.
Kaguelidou F, Alberti C, Castanet M, Guitteny MA, Czernichow P, Léger J, et al. Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment. J Clin Endocrinol Metab 2008;93:3817-26.  Back to cited text no. 17
    
18.
Ohye H, Minagawa A, Noh JY, Mukasa K, Kunii Y, Watanabe N, et al. Antithyroid drug treatment for graves' disease in children: A long-term retrospective study at a single institution. Thyroid 2014;24:200-7.  Back to cited text no. 18
    
19.
Poyrazoglu S, Saka N, Bas F, Isguven P, Dogu A, Turan S, et al. Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients. J Pediatr Endocrinol Metab 2008;21:745-51.  Back to cited text no. 19
    
20.
Gruñeiro-Papendieck L, Chiesa A, Finkielstain G, Heinrich JJ. Pediatric Graves' disease: Outcome and treatment. J Pediatr Endocrinol Metab 2003;16:1249-55.  Back to cited text no. 20
    
21.
Lippe BM, Landaw EM, Kaplan SA. Hyperthyroidism in children treated with long term medical therapy: Twenty-five percent remission every two years. J Clin Endocrinol Metab 1987;64:1241-5.  Back to cited text no. 21
    
22.
Lazar L, Kalter-Leibovici O, Pertzelan A, Weintrob N, Josefsberg Z, Phillip M. Thyrotoxicosis in prepubertal children compared with pubertal and postpubertal patients. J Clin Endocrinol Metab 2000;85:3678-82.  Back to cited text no. 22
    
23.
Kim WK, Ahn BH, Han HS. The clinical course and prognostic factors to medical treatment of Graves' disease in children and adolescents. Ann Pediatr Endocrinol Metab 2012;17:33-8.  Back to cited text no. 23
    
24.
Song SM, Youn JS, Ko JM, Cheon CK, Choi JH, Yoo HW. The natural history and prognostic factors of Graves' disease in Korean children and adolescents. Korean J Pediatr 2010;53:585-91.  Back to cited text no. 24
    
25.
Bhadada S, Bhansali A, Velayutham P, Masoodi SR. Juvenile hyperthyroidism: An experience. Indian Pediatr 2006;43:301-7.  Back to cited text no. 25
    
26.
Gastaldi R, Poggi E, Mussa A, Weber G, Vigone MC, Salerno M, et al. Graves disease in children: Thyroid-stimulating hormone receptor antibodies as remission markers. J Pediatr 2014;164:1189-94.e1.  Back to cited text no. 26
    
27.
Abraham P, Avenell A, Park CM, Watson WA, Bevan JS. A systematic review of drug therapy for Graves' hyperthyroidism. Eur J Endocrinol 2005;153:489-98.  Back to cited text no. 27
    
28.
Smith J, Brown RS. Persistence of thyrotropin (TSH) receptor antibodies in children and adolescents with Graves' disease treated using antithyroid medication. Thyroid 2007;17:1103-7.  Back to cited text no. 28
    
29.
Mussa GC, Corrias A, Silvestro L, Battan E, Mostert M, Mussa F, et al. Factors at onset predictive of lasting remission in pediatric patients with Graves' disease followed for at least three years. J Pediatr Endocrinol Metab 1999;12:537-41.  Back to cited text no. 29
    
30.
Rivkees SA. Pediatric Graves' disease: Management in the post-propylthiouracil Era. Int J Pediatr Endocrinol 2014;2014:10.  Back to cited text no. 30
    
31.
Rivkees SA, Sklar C, Freemark M. Clinical review 99: The management of Graves' disease in children, with special emphasis on radioiodine treatment. J Clin Endocrinol Metab 1998;83:3767-76.  Back to cited text no. 31
    
32.
Rivkees SA, Stephenson K, Dinauer C. Adverse events associated with methimazole therapy of graves' disease in children. Int J Pediatr Endocrinol 2010;2010:176970.  Back to cited text no. 32
    
33.
Tajiri J, Noguchi S. Antithyroid drug-induced agranulocytosis: How has granulocyte colony-stimulating factor changed therapy? Thyroid 2005;15:292-7.  Back to cited text no. 33
    
34.
Rivkees SA, Szarfman A. Dissimilar hepatotoxicity profiles of propylthiouracil and methimazole in children. J Clin Endocrinol Metab 2010;95:3260-7.  Back to cited text no. 34
    
35.
Hepatic Toxicity Following Treatment for Pediatric Graves' Disease. Meeting: 2008 Oct 28; Eunice Kennedy Shriver National Institute of Child Health and Human Development. Available from: http://www.bpca.nichd.nih.gov/outreach/index.cfm. [Last accessed on 2014 Nov 10].  Back to cited text no. 35
    
36.
Weiss M, Hassin D, Bank H. Propylthiouracil-induced hepatic damage. Arch Intern Med 1980;140:1184-5.  Back to cited text no. 36
    
37.
Benyounes M, Sempoux C, Daumerie C, Rahier J, Geubel AP. Propylthiouracyl-induced severe liver toxicity: An indication for alanine aminotransferase monitoring? World J Gastroenterol 2006;12:6232-4.  Back to cited text no. 37
    
38.
Gürlek A, Cobankara V, Bayraktar M. Liver tests in hyperthyroidism: Effect of antithyroid therapy. J Clin Gastroenterol 1997;24:180-3.  Back to cited text no. 38
    
39.
Available from: http://www.fda.gov/Safety/MedWatch/SafetyInformation/Safety Alerts for Human Medical Products/ucm164162htm. [Last accessed on 2014 Nov 10].  Back to cited text no. 39
    
40.
Rivkees SA. 63 years and 715 days to the "boxed warning": Unmasking of the propylthiouracil problem. Int J Pediatr Endocrinol 2010;2010 :658267.  Back to cited text no. 40
    
41.
Breuer C, Tuggle C, Solomon D, Sosa JA. Pediatric thyroid disease: When is surgery necessary, and who should be operating on our children? J Clin Res Pediatr Endocrinol 2013;5 Suppl 1:79-85.  Back to cited text no. 41
    



 
 
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  [Table 1], [Table 2]


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