Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2018) 59 P205 | DOI: 10.1530/endoabs.59.P205

SFEBES2018 Poster Presentations Thyroid (27 abstracts)

A second course of antithyroid drug therapy is effective in patients with relapsed Graves’ disease

Khyatisha Seejore 1 , Fozia Nawaz 2 , Katherine Kelleher 2 , Julie Kyaw-Tun 3 , Julie Lynch 1 & Robert D Murray 1,


1Department of Endocrinology, Leeds Centre for Diabetes and Endocrinology, Leeds Teaching Hospitals NHS Trust, Leeds, UK; 2University of Leeds, Leeds, UK; 3Department of Endocrinology and Metabolic Medicine, Calderdale and Huddersfield NHS Foundation Trust, Halifax, UK; 4Division of Cardiovascular and Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds, UK.


Background: Antithyroid drugs (ATDs) are preferred as a first-line treatment for Graves’ disease (GD). However, around 50–60% of patients relapse following treatment withdrawal. Radioactive iodine (RAI) or thyroidectomy is recommended for these patients, however, repeat ATD therapy is a further option, dependent upon patient choice. The long-term efficacy of ATD in relapsed GD has not been robustly established.

Methods: We conducted a retrospective study to assess the prognosis after a second course of ATD and investigate the clinical predictors for remission. Consecutive ATD-treated GD patients with at least three years of follow-up who attended our endocrine service since 2004 were identified and medical records analysed. Remission was defined as maintaining a euthyroid status for at least one year after ATD withdrawal.

Results: 219 patients underwent an initial course of ATD therapy. A total of 129 patients (59%) relapsed upon treatment withdrawal after a mean time of 2.0±2.7 years (range 0–15 years). Seventy-two (58%) patients (70% female, age at diagnosis 43.7±15.0 years) opted for a second course of ATD. Eight patients were lost to follow-up. During 6.1 years (range 1.5–11.7 years) median follow-up, 24 patients (38%) achieved remission, 29 patients (45%) relapsed and 17% (n=11) continued ATD treatment. Male gender (RR=1.88, CI 1.21–2.91) and a large goitre (RR=2.07, CI 1.42–3.02) were independent risk factors for relapse. A higher free T4 level at the time of relapse (mean fT4 36.2±20.7 pmol/l vs 29.6±14.3 pmol/l) was also suggestive of increased risk of relapse following second ATD therapy (P=0.05). Age, smoking status and orbitopathy did not show significant association.

Conclusion: A second course of ATD therapy results in a satisfying long-term remission rate (38%) in GD patients. The best outcomes are in females presenting with lower fT4 level on relapse in the absence of a large goitre.

Volume 59

Society for Endocrinology BES 2018

Glasgow, UK
19 Nov 2018 - 21 Nov 2018

Society for Endocrinology 

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