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A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice
OBJECTIVE: There are scarce reports regarding the prognosis of a second course of antithyroid drug (ATD) therapy on recurrent Graves' disease (GD). The aim of this study was to assess the long-term remission rate after a second ATD therapy and verify significant clinical predictors of a remissi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321192/ https://www.ncbi.nlm.nih.gov/pubmed/25468954 http://dx.doi.org/10.1530/EJE-14-0704 |
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author | Liu, Xiaomei Qiang, Wei Liu, Xingjun Liu, Lianye Liu, Shu Gao, Aibo Gao, Shan Shi, Bingyin |
author_facet | Liu, Xiaomei Qiang, Wei Liu, Xingjun Liu, Lianye Liu, Shu Gao, Aibo Gao, Shan Shi, Bingyin |
author_sort | Liu, Xiaomei |
collection | PubMed |
description | OBJECTIVE: There are scarce reports regarding the prognosis of a second course of antithyroid drug (ATD) therapy on recurrent Graves' disease (GD). The aim of this study was to assess the long-term remission rate after a second ATD therapy and verify significant clinical predictors of a remission. DESIGN: A prospective randomized clinical trial with long-term follow-up was conducted to evaluate the effects of a second course of ATD therapy. METHODS: A total of 128 recurrent GD patients who had finished a first regular ATD therapy were enrolled in this study, and prescribed methimazole (MMI) treatment with titration regimen. The patients were randomly assigned to two groups when the drug doses were reduced to 2.5 mg daily (qd). Group 1 was discontinued with 2.5 mg qd after about 5 months. Group 2 was continuously reduced to 2.5 mg every other day (qod) after 5 months and then discontinued with 2.5 mg qod after about a further 5 months. The patients were followed for 48 months after drug withdrawal. RESULTS: Of the total number of patients, 97 cases (75.78%) achieved permanent remission at the end of follow-up, with the recurrence of 31 cases (24.22%). The remission rate of group 2 (84.62%) was significantly higher than that of group 1 (66.67%) (P=0.024). Cox regression showed that the hazard ratio for recurrence decreased under a high or high normal TSH level at drug withdrawal. CONCLUSION: A second course of ATD therapy can bring about a satisfying long-term remission on recurrent GD. The drug dose of 2.5 mg qod and a high or high normal TSH level at drug withdrawal may increase the likelihood of permanent remission. |
format | Online Article Text |
id | pubmed-4321192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43211922015-03-09 A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice Liu, Xiaomei Qiang, Wei Liu, Xingjun Liu, Lianye Liu, Shu Gao, Aibo Gao, Shan Shi, Bingyin Eur J Endocrinol Clinical Study OBJECTIVE: There are scarce reports regarding the prognosis of a second course of antithyroid drug (ATD) therapy on recurrent Graves' disease (GD). The aim of this study was to assess the long-term remission rate after a second ATD therapy and verify significant clinical predictors of a remission. DESIGN: A prospective randomized clinical trial with long-term follow-up was conducted to evaluate the effects of a second course of ATD therapy. METHODS: A total of 128 recurrent GD patients who had finished a first regular ATD therapy were enrolled in this study, and prescribed methimazole (MMI) treatment with titration regimen. The patients were randomly assigned to two groups when the drug doses were reduced to 2.5 mg daily (qd). Group 1 was discontinued with 2.5 mg qd after about 5 months. Group 2 was continuously reduced to 2.5 mg every other day (qod) after 5 months and then discontinued with 2.5 mg qod after about a further 5 months. The patients were followed for 48 months after drug withdrawal. RESULTS: Of the total number of patients, 97 cases (75.78%) achieved permanent remission at the end of follow-up, with the recurrence of 31 cases (24.22%). The remission rate of group 2 (84.62%) was significantly higher than that of group 1 (66.67%) (P=0.024). Cox regression showed that the hazard ratio for recurrence decreased under a high or high normal TSH level at drug withdrawal. CONCLUSION: A second course of ATD therapy can bring about a satisfying long-term remission on recurrent GD. The drug dose of 2.5 mg qod and a high or high normal TSH level at drug withdrawal may increase the likelihood of permanent remission. Bioscientifica Ltd 2015-03 /pmc/articles/PMC4321192/ /pubmed/25468954 http://dx.doi.org/10.1530/EJE-14-0704 Text en © 2015 The authors http://creativecommons.org/licenses/by/3.0/deed.en_GB This work is licensed under a Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/deed.en_GB) |
spellingShingle | Clinical Study Liu, Xiaomei Qiang, Wei Liu, Xingjun Liu, Lianye Liu, Shu Gao, Aibo Gao, Shan Shi, Bingyin A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title | A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title_full | A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title_fullStr | A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title_full_unstemmed | A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title_short | A second course of antithyroid drug therapy for recurrent Graves' disease: an experience in endocrine practice |
title_sort | second course of antithyroid drug therapy for recurrent graves' disease: an experience in endocrine practice |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321192/ https://www.ncbi.nlm.nih.gov/pubmed/25468954 http://dx.doi.org/10.1530/EJE-14-0704 |
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