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Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease
Graves’ disease (GD) accounts for a large proportion of pediatric hyperthyroidism, and the first-line treatment is antithyroid drug (ATD) therapy. Methimazole (MMI) is effective in most patients but is associated with significant adverse events (AEs). We reviewed the medical records of GD patients (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society for Pediatric Endocrinology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295245/ https://www.ncbi.nlm.nih.gov/pubmed/28203042 http://dx.doi.org/10.1297/cpe.26.1 |
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author | Yasuda, Kie Miyoshi, Yoko Tachibana, Makiko Namba, Noriyuki Miki, Kazunori Nakata, Yukiko Takano, Toru Ozono, Keiichi |
author_facet | Yasuda, Kie Miyoshi, Yoko Tachibana, Makiko Namba, Noriyuki Miki, Kazunori Nakata, Yukiko Takano, Toru Ozono, Keiichi |
author_sort | Yasuda, Kie |
collection | PubMed |
description | Graves’ disease (GD) accounts for a large proportion of pediatric hyperthyroidism, and the first-line treatment is antithyroid drug (ATD) therapy. Methimazole (MMI) is effective in most patients but is associated with significant adverse events (AEs). We reviewed the medical records of GD patients (n = 56) with onset age of <15 yr and investigated the relationship between MMI dose and AEs. The study population comprised 11 male and 45 female patients and the median age at diagnosis was 11 yr. All patients were initially treated with ATDs. Among the 52 patients initially treated with MMI, 20 received a low dose, and 32 received a high dose of MMI (< 0.7 vs ≥ 0.7 mg/kg/day, respectively). AEs occurred in 20% of the patients in the low-dose MMI group, and in 50% patients in the high-dose MMI group (p = 0.031). A greater variety of AEs was observed in the high-dose group. Neutropenia and rash were observed in both groups. With treatment transition to low-dose MMI according to the Japanese Society for Pediatric Endocrinology guidelines, we expect a decrease in the incidence of AEs in future. However, we should be careful as neutropenia and rash can occur independently of the MMI dose. |
format | Online Article Text |
id | pubmed-5295245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Japanese Society for Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
spelling | pubmed-52952452017-02-15 Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease Yasuda, Kie Miyoshi, Yoko Tachibana, Makiko Namba, Noriyuki Miki, Kazunori Nakata, Yukiko Takano, Toru Ozono, Keiichi Clin Pediatr Endocrinol Original Article Graves’ disease (GD) accounts for a large proportion of pediatric hyperthyroidism, and the first-line treatment is antithyroid drug (ATD) therapy. Methimazole (MMI) is effective in most patients but is associated with significant adverse events (AEs). We reviewed the medical records of GD patients (n = 56) with onset age of <15 yr and investigated the relationship between MMI dose and AEs. The study population comprised 11 male and 45 female patients and the median age at diagnosis was 11 yr. All patients were initially treated with ATDs. Among the 52 patients initially treated with MMI, 20 received a low dose, and 32 received a high dose of MMI (< 0.7 vs ≥ 0.7 mg/kg/day, respectively). AEs occurred in 20% of the patients in the low-dose MMI group, and in 50% patients in the high-dose MMI group (p = 0.031). A greater variety of AEs was observed in the high-dose group. Neutropenia and rash were observed in both groups. With treatment transition to low-dose MMI according to the Japanese Society for Pediatric Endocrinology guidelines, we expect a decrease in the incidence of AEs in future. However, we should be careful as neutropenia and rash can occur independently of the MMI dose. The Japanese Society for Pediatric Endocrinology 2017-01-31 2017-01 /pmc/articles/PMC5295245/ /pubmed/28203042 http://dx.doi.org/10.1297/cpe.26.1 Text en 2017©The Japanese Society for Pediatric Endocrinology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Yasuda, Kie Miyoshi, Yoko Tachibana, Makiko Namba, Noriyuki Miki, Kazunori Nakata, Yukiko Takano, Toru Ozono, Keiichi Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease |
title | Relationship between dose of antithyroid drugs and adverse events in
pediatric patients with Graves’ disease |
title_full | Relationship between dose of antithyroid drugs and adverse events in
pediatric patients with Graves’ disease |
title_fullStr | Relationship between dose of antithyroid drugs and adverse events in
pediatric patients with Graves’ disease |
title_full_unstemmed | Relationship between dose of antithyroid drugs and adverse events in
pediatric patients with Graves’ disease |
title_short | Relationship between dose of antithyroid drugs and adverse events in
pediatric patients with Graves’ disease |
title_sort | relationship between dose of antithyroid drugs and adverse events in
pediatric patients with graves’ disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295245/ https://www.ncbi.nlm.nih.gov/pubmed/28203042 http://dx.doi.org/10.1297/cpe.26.1 |
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