Significant cardiac disease complicating Graves’ disease in previously healthy young adults
Graves’ disease is associated with tachydysrythmia, cardiac ischaemia and cardiomyopathy – all uncommon in young adults without previous cardiac disease. We present three young individuals who developed cardiac complications after periods of uncontrolled Graves’ disease. Subject 1: A 34-year-old fem...
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doaj-a1b6067af7024b7ba5b62a2d014419782020-11-24T22:07:24ZengBioscientificaEndocrinology, Diabetes & Metabolism Case Reports2052-05732052-05732020-01-01111610.1530/EDM-19-0132Significant cardiac disease complicating Graves’ disease in previously healthy young adultsJ K Witczak0N Ubaysekara1R Ravindran2S Rice3Z Yousef4L D Premawardhana5Section of Endocrinology, Department of Medicine, Prince Phillip Hospital; Centre for Endocrine and Diabetes Sciences, University Hospital of Wales, Heath Park, Cardiff, UKCentre for Endocrine and Diabetes Sciences, University Hospital of Wales, Heath Park, Cardiff, UKCentre for Endocrine and Diabetes Sciences, University Hospital of Wales, Heath Park, Cardiff, UKSection of Endocrinology, Department of Medicine, Prince Phillip HospitalDepartment of Cardiology, University Hospital of Wales, Heath Park, Cardiff, UKCentre for Endocrine and Diabetes Sciences, University Hospital of Wales, Heath Park, Cardiff, UKGraves’ disease is associated with tachydysrythmia, cardiac ischaemia and cardiomyopathy – all uncommon in young adults without previous cardiac disease. We present three young individuals who developed cardiac complications after periods of uncontrolled Graves’ disease. Subject 1: A 34-year-old female had severe thyrotoxic symptoms for weeks. Investigations showed fT4: 98.4 (11–25 pmol/L), fT3: 46.9 (3.1–6.8 pmol/L), TSH <0.01 (0.27–4.2 mU/L) and thyrotrophin receptor antibody (TRAb): 34.8 (<0.9 U//l). She had appropriate treatment but several weeks later she became breathless despite improving thyroid function. Echocardiography showed a pericardial effusion of 2.9 cm. She responded well to steroids and NSAIDs but developed active severe Graves’ orbitopathy after early total thyroidectomy. Subject 2: A 28-year-old male developed thyrotoxic symptoms (fT4: 38 pmol/L, fT3: 13.9 pmol/L, TSH <0.01 (for over 6 months) and TRAb: 9.3 U/L). One month after starting carbimazole, he developed acute heart failure (HF) due to severe dilated cardiomyopathy – EF 10–15%. He partially recovered after treatment – EF 28% and had early radioiodine treatment. Subject 3: A 42-year-old woman who had been thyrotoxic for several months (fT4: 54.3; fT3 >46.1; TSH <0.01; TRAb: 4.5) developed atrial fibrillation (AF) and heart failure. Echocardiography showed cardiomegaly – EF 29%. She maintains sinus rhythm following early total thyroidectomy (EF 50%). Significant cardiac complications may occur in previously fit young adults, who have had uncontrolled Graves’ disease for weeks to months. Cardiac function recovers in the majority, but early definitive treatment should be discussed to avoid Graves’ disease relapse and further cardiac decompensation.https://doi.org/10.1530/EDM-19-0132 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J K Witczak N Ubaysekara R Ravindran S Rice Z Yousef L D Premawardhana |
spellingShingle |
J K Witczak N Ubaysekara R Ravindran S Rice Z Yousef L D Premawardhana Significant cardiac disease complicating Graves’ disease in previously healthy young adults Endocrinology, Diabetes & Metabolism Case Reports |
author_facet |
J K Witczak N Ubaysekara R Ravindran S Rice Z Yousef L D Premawardhana |
author_sort |
J K Witczak |
title |
Significant cardiac disease complicating Graves’ disease in previously healthy young adults |
title_short |
Significant cardiac disease complicating Graves’ disease in previously healthy young adults |
title_full |
Significant cardiac disease complicating Graves’ disease in previously healthy young adults |
title_fullStr |
Significant cardiac disease complicating Graves’ disease in previously healthy young adults |
title_full_unstemmed |
Significant cardiac disease complicating Graves’ disease in previously healthy young adults |
title_sort |
significant cardiac disease complicating graves’ disease in previously healthy young adults |
publisher |
Bioscientifica |
series |
Endocrinology, Diabetes & Metabolism Case Reports |
issn |
2052-0573 2052-0573 |
publishDate |
2020-01-01 |
description |
Graves’ disease is associated with tachydysrythmia, cardiac ischaemia and cardiomyopathy – all uncommon in young adults without previous cardiac disease. We present three young individuals who developed cardiac complications after periods of uncontrolled Graves’ disease. Subject 1: A 34-year-old female had severe thyrotoxic symptoms for weeks. Investigations showed fT4: 98.4 (11–25 pmol/L), fT3: 46.9 (3.1–6.8 pmol/L), TSH <0.01 (0.27–4.2 mU/L) and thyrotrophin receptor antibody (TRAb): 34.8 (<0.9 U//l). She had appropriate treatment but several weeks later she became breathless despite improving thyroid function. Echocardiography showed a pericardial effusion of 2.9 cm. She responded well to steroids and NSAIDs but developed active severe Graves’ orbitopathy after early total thyroidectomy. Subject 2: A 28-year-old male developed thyrotoxic symptoms (fT4: 38 pmol/L, fT3: 13.9 pmol/L, TSH <0.01 (for over 6 months) and TRAb: 9.3 U/L). One month after starting carbimazole, he developed acute heart failure (HF) due to severe dilated cardiomyopathy – EF 10–15%. He partially recovered after treatment – EF 28% and had early radioiodine treatment. Subject 3: A 42-year-old woman who had been thyrotoxic for several months (fT4: 54.3; fT3 >46.1; TSH <0.01; TRAb: 4.5) developed atrial fibrillation (AF) and heart failure. Echocardiography showed cardiomegaly – EF 29%. She maintains sinus rhythm following early total thyroidectomy (EF 50%). Significant cardiac complications may occur in previously fit young adults, who have had uncontrolled Graves’ disease for weeks to months. Cardiac function recovers in the majority, but early definitive treatment should be discussed to avoid Graves’ disease relapse and further cardiac decompensation. |
url |
https://doi.org/10.1530/EDM-19-0132 |
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