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7661 Therapeutic Plasma Exchange as a Bridge Therapy to Total Thyroidectomy in Treatment-Resistant Amiodarone-Induced Thyrotoxicosis
Abstract Disclosure: M. Maher: None. R. McEvoy: None. V. Farnan: None. D.J. Tansey: None. S. McKenna: None. J. O'Connell: None. R. McQuillan: None. M. Griffin: None. J. Lyne: None. C. Magee: None. C. Traynor: None. A. Hudson: None. M.W. O'Reilly: None. A. Agha: None. M. Sherlock: None. C.M...
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Published in: | Journal of the Endocrine Society 2024-10, Vol.8 (Supplement_1) |
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creator | Maher, M McEvoy, R Farnan, V Tansey, D J McKenna, S O’Connell, J McQuillan, R Griffin, M Lyne, J Magee, C Traynor, C Hudson, A O’Reilly, M W Agha, A Sherlock, M Moran, C M |
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Disclosure: M. Maher: None. R. McEvoy: None. V. Farnan: None. D.J. Tansey: None. S. McKenna: None. J. O'Connell: None. R. McQuillan: None. M. Griffin: None. J. Lyne: None. C. Magee: None. C. Traynor: None. A. Hudson: None. M.W. O'Reilly: None. A. Agha: None. M. Sherlock: None. C.M. Moran: None.
Background: Amiodarone-induced thyrotoxicosis (AIT) is challenging to manage where conventional medical treatment fails. We report our experience using therapeutic plasma exchange (TPE) to prepare for salvage thyroidectomy. Clinical Cases: A 53-year-old man was diagnosed with AIT type 2 (FT4 45.3pmol/L, RR 12-22; TSH 0.02mU/L, RR 0.27-4.20) whilst on amiodarone, on a background of lamin A/C cardiomyopathy. He remained thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine. TFTs following 4 TPE sessions showed an improvement in TSH (0.03mU/L) and total T4 (129nmol/L, RR 63-151), despite rising FT4 (91.5pmol/L) and FT3 (12.56pmol/L, RR 2.43-6.01).A 47-year-old man was diagnosed with TRAb-negative AIT type 1 (FT4 51.2pmol/L, TSH 0.03mU/L) on a background of atrial fibrillation treated with amiodarone. He became progressively more thyrotoxic despite carbimazole, prednisolone, lithium and cholestyramine. Following 4 TPE sessions, TFTs demonstrated a reduction in FT4 (42.9pmol/L) and FT3 (10pmol/L, RR 3.1-6.8), along with normalisation of total T4 (155nmol/L, RR 66-181).A 56-year-old female was diagnosed with AIT type 2 (FT4 33.9pmol/L, TSH 0.02mU/L), whilst on amiodarone for ventricular fibrillation. She became rapidly and progressively more thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine (FT4 >100pmol/L). After 5 TPE sessions, TFTs showed a persistently elevated FT4 (>100pmol/L), FT3 (13.1pmol/L), and total T4 (318nmol/L). Lastly, a 65-year-old gentleman was diagnosed with AIT type 2 (FT4 >100pmol/L, FT3 18.4pmol/L, Total T4 >320nmol/L, TSH 100pmol/L. The patient developed acute decompensated heart failure and underwent TPE as a bridge to emergency thyroidectomy. Following 3 TPE sessions, TFTs demonstrated a reduction in FT4 (67.3pmol/L) and Total T4 (223nmol/L). All 4 patients underwent uneventful thyroidectomy and were subsequently rendered euthyroid with thyroxine. Heparin was administered durin |
doi_str_mv | 10.1210/jendso/bvae163.2094 |
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Disclosure: M. Maher: None. R. McEvoy: None. V. Farnan: None. D.J. Tansey: None. S. McKenna: None. J. O'Connell: None. R. McQuillan: None. M. Griffin: None. J. Lyne: None. C. Magee: None. C. Traynor: None. A. Hudson: None. M.W. O'Reilly: None. A. Agha: None. M. Sherlock: None. C.M. Moran: None.
Background: Amiodarone-induced thyrotoxicosis (AIT) is challenging to manage where conventional medical treatment fails. We report our experience using therapeutic plasma exchange (TPE) to prepare for salvage thyroidectomy. Clinical Cases: A 53-year-old man was diagnosed with AIT type 2 (FT4 45.3pmol/L, RR 12-22; TSH 0.02mU/L, RR 0.27-4.20) whilst on amiodarone, on a background of lamin A/C cardiomyopathy. He remained thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine. TFTs following 4 TPE sessions showed an improvement in TSH (0.03mU/L) and total T4 (129nmol/L, RR 63-151), despite rising FT4 (91.5pmol/L) and FT3 (12.56pmol/L, RR 2.43-6.01).A 47-year-old man was diagnosed with TRAb-negative AIT type 1 (FT4 51.2pmol/L, TSH 0.03mU/L) on a background of atrial fibrillation treated with amiodarone. He became progressively more thyrotoxic despite carbimazole, prednisolone, lithium and cholestyramine. Following 4 TPE sessions, TFTs demonstrated a reduction in FT4 (42.9pmol/L) and FT3 (10pmol/L, RR 3.1-6.8), along with normalisation of total T4 (155nmol/L, RR 66-181).A 56-year-old female was diagnosed with AIT type 2 (FT4 33.9pmol/L, TSH 0.02mU/L), whilst on amiodarone for ventricular fibrillation. She became rapidly and progressively more thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine (FT4 >100pmol/L). After 5 TPE sessions, TFTs showed a persistently elevated FT4 (>100pmol/L), FT3 (13.1pmol/L), and total T4 (318nmol/L). Lastly, a 65-year-old gentleman was diagnosed with AIT type 2 (FT4 >100pmol/L, FT3 18.4pmol/L, Total T4 >320nmol/L, TSH <0.01mU/L) on a background of atrial fibrillation that had been treated with amiodarone. FT3 showed a modest reduction (8.2pmol/L) following treatment with carbimazole and prednisolone; however, FT4 remained >100pmol/L. The patient developed acute decompensated heart failure and underwent TPE as a bridge to emergency thyroidectomy. Following 3 TPE sessions, TFTs demonstrated a reduction in FT4 (67.3pmol/L) and Total T4 (223nmol/L). All 4 patients underwent uneventful thyroidectomy and were subsequently rendered euthyroid with thyroxine. Heparin was administered during TPE in all cases. Conclusion: TPE is beneficial as a bridge to thyroidectomy in treatment-resistant AIT. Our cases demonstrate that the biochemical response is variable. Given the possibility for heparin to cause displacement of bound thyroid hormones, Total T4 may be a better biochemical indicator of response than free thyroid hormone(s) for patients on TPE.
Presentation: 6/2/2024</description><identifier>ISSN: 2472-1972</identifier><identifier>EISSN: 2472-1972</identifier><identifier>DOI: 10.1210/jendso/bvae163.2094</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Abstract</subject><ispartof>Journal of the Endocrine Society, 2024-10, Vol.8 (Supplement_1)</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11453412/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11453412/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Maher, M</creatorcontrib><creatorcontrib>McEvoy, R</creatorcontrib><creatorcontrib>Farnan, V</creatorcontrib><creatorcontrib>Tansey, D J</creatorcontrib><creatorcontrib>McKenna, S</creatorcontrib><creatorcontrib>O’Connell, J</creatorcontrib><creatorcontrib>McQuillan, R</creatorcontrib><creatorcontrib>Griffin, M</creatorcontrib><creatorcontrib>Lyne, J</creatorcontrib><creatorcontrib>Magee, C</creatorcontrib><creatorcontrib>Traynor, C</creatorcontrib><creatorcontrib>Hudson, A</creatorcontrib><creatorcontrib>O’Reilly, M W</creatorcontrib><creatorcontrib>Agha, A</creatorcontrib><creatorcontrib>Sherlock, M</creatorcontrib><creatorcontrib>Moran, C M</creatorcontrib><title>7661 Therapeutic Plasma Exchange as a Bridge Therapy to Total Thyroidectomy in Treatment-Resistant Amiodarone-Induced Thyrotoxicosis</title><title>Journal of the Endocrine Society</title><description>Abstract
Disclosure: M. Maher: None. R. McEvoy: None. V. Farnan: None. D.J. Tansey: None. S. McKenna: None. J. O'Connell: None. R. McQuillan: None. M. Griffin: None. J. Lyne: None. C. Magee: None. C. Traynor: None. A. Hudson: None. M.W. O'Reilly: None. A. Agha: None. M. Sherlock: None. C.M. Moran: None.
Background: Amiodarone-induced thyrotoxicosis (AIT) is challenging to manage where conventional medical treatment fails. We report our experience using therapeutic plasma exchange (TPE) to prepare for salvage thyroidectomy. Clinical Cases: A 53-year-old man was diagnosed with AIT type 2 (FT4 45.3pmol/L, RR 12-22; TSH 0.02mU/L, RR 0.27-4.20) whilst on amiodarone, on a background of lamin A/C cardiomyopathy. He remained thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine. TFTs following 4 TPE sessions showed an improvement in TSH (0.03mU/L) and total T4 (129nmol/L, RR 63-151), despite rising FT4 (91.5pmol/L) and FT3 (12.56pmol/L, RR 2.43-6.01).A 47-year-old man was diagnosed with TRAb-negative AIT type 1 (FT4 51.2pmol/L, TSH 0.03mU/L) on a background of atrial fibrillation treated with amiodarone. He became progressively more thyrotoxic despite carbimazole, prednisolone, lithium and cholestyramine. Following 4 TPE sessions, TFTs demonstrated a reduction in FT4 (42.9pmol/L) and FT3 (10pmol/L, RR 3.1-6.8), along with normalisation of total T4 (155nmol/L, RR 66-181).A 56-year-old female was diagnosed with AIT type 2 (FT4 33.9pmol/L, TSH 0.02mU/L), whilst on amiodarone for ventricular fibrillation. She became rapidly and progressively more thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine (FT4 >100pmol/L). After 5 TPE sessions, TFTs showed a persistently elevated FT4 (>100pmol/L), FT3 (13.1pmol/L), and total T4 (318nmol/L). Lastly, a 65-year-old gentleman was diagnosed with AIT type 2 (FT4 >100pmol/L, FT3 18.4pmol/L, Total T4 >320nmol/L, TSH <0.01mU/L) on a background of atrial fibrillation that had been treated with amiodarone. FT3 showed a modest reduction (8.2pmol/L) following treatment with carbimazole and prednisolone; however, FT4 remained >100pmol/L. The patient developed acute decompensated heart failure and underwent TPE as a bridge to emergency thyroidectomy. Following 3 TPE sessions, TFTs demonstrated a reduction in FT4 (67.3pmol/L) and Total T4 (223nmol/L). All 4 patients underwent uneventful thyroidectomy and were subsequently rendered euthyroid with thyroxine. Heparin was administered during TPE in all cases. Conclusion: TPE is beneficial as a bridge to thyroidectomy in treatment-resistant AIT. Our cases demonstrate that the biochemical response is variable. Given the possibility for heparin to cause displacement of bound thyroid hormones, Total T4 may be a better biochemical indicator of response than free thyroid hormone(s) for patients on TPE.
Presentation: 6/2/2024</description><subject>Abstract</subject><issn>2472-1972</issn><issn>2472-1972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkc9KAzEQxhdRUKpP4CUvsDXJptnmJFrqHxAUqecwm8zalN3NkqTS3n1wV7aI3jzNx8z8Pmb4suyS0SnjjF5tsLPRX1UfgEwWU06VOMrOuCh5zlTJj3_p0-wixg2llKlCKCHOss9SSkZWawzQ4zY5Q14aiC2Q5c6soXtHApEAuQ3ODnrc25PkyconaIbGPnhn0STf7onryCogpBa7lL9idDFBl8hN67yF4DvMHzu7NWhHLvmdM37YOs9OamgiXhzqJHu7W64WD_nT8_3j4uYpN2wuRK5qaStWUCWFQqbmls95Vc0UcigLyTnC8NLQsdKyopZGmbmQRjLgtBR0VheT7Hr07bdVi9YMZwZodB9cC2GvPTj9d9K5tX73H5oxMSsE44NDMTqY4GMMWP_AjOrvNPSYhj6kob_TGKjpSPlt_y_gC8mmktY</recordid><startdate>20241005</startdate><enddate>20241005</enddate><creator>Maher, M</creator><creator>McEvoy, R</creator><creator>Farnan, V</creator><creator>Tansey, D J</creator><creator>McKenna, S</creator><creator>O’Connell, J</creator><creator>McQuillan, R</creator><creator>Griffin, M</creator><creator>Lyne, J</creator><creator>Magee, C</creator><creator>Traynor, C</creator><creator>Hudson, A</creator><creator>O’Reilly, M W</creator><creator>Agha, A</creator><creator>Sherlock, M</creator><creator>Moran, C M</creator><general>Oxford University Press</general><scope>TOX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20241005</creationdate><title>7661 Therapeutic Plasma Exchange as a Bridge Therapy to Total Thyroidectomy in Treatment-Resistant Amiodarone-Induced Thyrotoxicosis</title><author>Maher, M ; McEvoy, R ; Farnan, V ; Tansey, D J ; McKenna, S ; O’Connell, J ; McQuillan, R ; Griffin, M ; Lyne, J ; Magee, C ; Traynor, C ; Hudson, A ; O’Reilly, M W ; Agha, A ; Sherlock, M ; Moran, C M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1844-9f6db1309649e198d282bb59e2a73622ea9442bbd6d13f6c9c846c61a207405f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Abstract</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maher, M</creatorcontrib><creatorcontrib>McEvoy, R</creatorcontrib><creatorcontrib>Farnan, V</creatorcontrib><creatorcontrib>Tansey, D J</creatorcontrib><creatorcontrib>McKenna, S</creatorcontrib><creatorcontrib>O’Connell, J</creatorcontrib><creatorcontrib>McQuillan, R</creatorcontrib><creatorcontrib>Griffin, M</creatorcontrib><creatorcontrib>Lyne, J</creatorcontrib><creatorcontrib>Magee, C</creatorcontrib><creatorcontrib>Traynor, C</creatorcontrib><creatorcontrib>Hudson, A</creatorcontrib><creatorcontrib>O’Reilly, M W</creatorcontrib><creatorcontrib>Agha, A</creatorcontrib><creatorcontrib>Sherlock, M</creatorcontrib><creatorcontrib>Moran, C M</creatorcontrib><collection>Oxford University Press Open Access</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the Endocrine Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maher, M</au><au>McEvoy, R</au><au>Farnan, V</au><au>Tansey, D J</au><au>McKenna, S</au><au>O’Connell, J</au><au>McQuillan, R</au><au>Griffin, M</au><au>Lyne, J</au><au>Magee, C</au><au>Traynor, C</au><au>Hudson, A</au><au>O’Reilly, M W</au><au>Agha, A</au><au>Sherlock, M</au><au>Moran, C M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>7661 Therapeutic Plasma Exchange as a Bridge Therapy to Total Thyroidectomy in Treatment-Resistant Amiodarone-Induced Thyrotoxicosis</atitle><jtitle>Journal of the Endocrine Society</jtitle><date>2024-10-05</date><risdate>2024</risdate><volume>8</volume><issue>Supplement_1</issue><issn>2472-1972</issn><eissn>2472-1972</eissn><abstract>Abstract
Disclosure: M. Maher: None. R. McEvoy: None. V. Farnan: None. D.J. Tansey: None. S. McKenna: None. J. O'Connell: None. R. McQuillan: None. M. Griffin: None. J. Lyne: None. C. Magee: None. C. Traynor: None. A. Hudson: None. M.W. O'Reilly: None. A. Agha: None. M. Sherlock: None. C.M. Moran: None.
Background: Amiodarone-induced thyrotoxicosis (AIT) is challenging to manage where conventional medical treatment fails. We report our experience using therapeutic plasma exchange (TPE) to prepare for salvage thyroidectomy. Clinical Cases: A 53-year-old man was diagnosed with AIT type 2 (FT4 45.3pmol/L, RR 12-22; TSH 0.02mU/L, RR 0.27-4.20) whilst on amiodarone, on a background of lamin A/C cardiomyopathy. He remained thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine. TFTs following 4 TPE sessions showed an improvement in TSH (0.03mU/L) and total T4 (129nmol/L, RR 63-151), despite rising FT4 (91.5pmol/L) and FT3 (12.56pmol/L, RR 2.43-6.01).A 47-year-old man was diagnosed with TRAb-negative AIT type 1 (FT4 51.2pmol/L, TSH 0.03mU/L) on a background of atrial fibrillation treated with amiodarone. He became progressively more thyrotoxic despite carbimazole, prednisolone, lithium and cholestyramine. Following 4 TPE sessions, TFTs demonstrated a reduction in FT4 (42.9pmol/L) and FT3 (10pmol/L, RR 3.1-6.8), along with normalisation of total T4 (155nmol/L, RR 66-181).A 56-year-old female was diagnosed with AIT type 2 (FT4 33.9pmol/L, TSH 0.02mU/L), whilst on amiodarone for ventricular fibrillation. She became rapidly and progressively more thyrotoxic despite carbimazole, prednisolone, iodine solution and cholestyramine (FT4 >100pmol/L). After 5 TPE sessions, TFTs showed a persistently elevated FT4 (>100pmol/L), FT3 (13.1pmol/L), and total T4 (318nmol/L). Lastly, a 65-year-old gentleman was diagnosed with AIT type 2 (FT4 >100pmol/L, FT3 18.4pmol/L, Total T4 >320nmol/L, TSH <0.01mU/L) on a background of atrial fibrillation that had been treated with amiodarone. FT3 showed a modest reduction (8.2pmol/L) following treatment with carbimazole and prednisolone; however, FT4 remained >100pmol/L. The patient developed acute decompensated heart failure and underwent TPE as a bridge to emergency thyroidectomy. Following 3 TPE sessions, TFTs demonstrated a reduction in FT4 (67.3pmol/L) and Total T4 (223nmol/L). All 4 patients underwent uneventful thyroidectomy and were subsequently rendered euthyroid with thyroxine. Heparin was administered during TPE in all cases. Conclusion: TPE is beneficial as a bridge to thyroidectomy in treatment-resistant AIT. Our cases demonstrate that the biochemical response is variable. Given the possibility for heparin to cause displacement of bound thyroid hormones, Total T4 may be a better biochemical indicator of response than free thyroid hormone(s) for patients on TPE.
Presentation: 6/2/2024</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1210/jendso/bvae163.2094</doi><oa>free_for_read</oa></addata></record> |
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title | 7661 Therapeutic Plasma Exchange as a Bridge Therapy to Total Thyroidectomy in Treatment-Resistant Amiodarone-Induced Thyrotoxicosis |
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