Comparison of the 2021 EUGOGO guidelines and the 2022 ATA/ETA consensus statement for the management of Graves’ orbitopathy

European Thyroid Journal · 2025 · Europe

Source and licence

Authors
Luigi Bartalena, Daniela Gallo, George J Kahaly et al.
Title
Comparison of the 2021 EUGOGO guidelines and the 2022 ATA/ETA consensus statement for the management of Graves’ orbitopathy
Journal
European Thyroid Journal, 2025
Licence
CC BY 4.0
Changes
Verbatim excerpts; formatting adapted

Full text retrieved 2026-10-27 from Europe PMC · PMC12687763

Licence statement of the original publication

This work is licensed under a Creative Commons Attribution 4.0 International License.

This page reproduces excerpts of the original publication; the original is authoritative. It has not been reviewed by a physician, does not state a recommendation of Medelix and does not replace medical advice. The guideline may have been updated since.

This is a review of another guideline (2021 EUGOGO guidelines (Graves orbitopathy); 2022 ATA/ETA consensus on Graves disease, EUGOGO; ATA/ETA 2022). We do not reproduce that guideline's recommendations here – they belong to the original guideline.

Open the original publication →Full text on Europe PMC

Abstract

Background: In 2021, the European Group on Graves’ orbitopathy (EUGOGO) published clinical practice guidelines for the management of GO, and in 2022, the American and European Thyroid Associations published the ATA/ETA consensus statement on the same topic.

Aims: i) To highlight similarities and differences between the two documents, ii) to suggest possible amendments for future revisions.

Results and conclusions: The two documents show a high degree of concordance as to classification, assessment, and prevention, as well as treatment of mild GO, moderate-to-severe and inactive GO, and sight-threatening GO. The major disagreement regards treatment of moderate-to-severe and active GO. The EUGOGO guidelines, written when teprotumumab was not available outside the USA, indicate intravenous glucocorticoids (IVGC) (with/without mycophenolate) as the first-line treatment, whereas the ATA/ETA consensus statement indicates teprotumumab as the first-line treatment for virtually all phenotypes of moderate-to-severe and active GO, particularly when exophthalmos is predominant. However, also in the ATA/ETA consensus statement, IVGC are the preferred treatment when the goal is GO inactivation and resolution of inflammation, and among the preferred treatments (in combination with orbital radiotherapy) when the goals are inactivation and correction of eye dysmotility. Recent developments to be considered in future revisions of the guidelines/consensus statement include the possible use of biologicals (teprotumumab and tocilizumab) for dysthyroid optic neuropathy, treatment of longstanding inactive GO with teprotumumab, reconsideration of the cautious use of radioactive iodine in patients with moderate-to-severe and active GO concomitantly treated with IVGC (with/without orbital radiotherapy), and use of statins as an adjunct therapy.

Contents of the original publication

The section headings of the original.

  • Format of the two documents
  • Comment
  • Referral of patients with GO to specialized centers
  • Comment
  • Prevention
  • Comment
  • Assessment and classification
  • Comment
  • Management of mild GO
  • Comment
  • Management of moderate-to-severe GO
  • Moderate-to-severe and active GO
  • Comment
  • Moderate-to-severe and inactive GO
  • Comment
  • Management of sight-threatening (very severe) GO
  • Comment
  • Treatment of hyperthyroidism in patients with GO
  • Comment
  • Considerations for revision/amendments of current recommendations
  • Statins
  • Inactive GO
  • DON
  • Treatment of hyperthyroidism
  • Conclusions

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