We noticed you’re blocking ads

Thanks for visiting CRSTEurope. Our advertisers are important supporters of this site, and content cannot be accessed if ad-blocking software is activated.

In order to avoid adverse performance issues with this site, please white list https://crstodayeurope.com in your ad blocker then refresh this page.

Need help? Click here for instructions.

Fundamental in Five | Mar 2018

Managing Thyroid Eye Disease

Timely diagnosis is key to controlling this autoimmune condition.

Thyroid eye disease (TED) is the most common and disfiguring orbital disease in adults. This difficult condition is characterized by autoimmune-mediated inflammation of the orbital soft tissues, extraocular muscles, and eyelids. The majority of patients with TED have autoimmune hyperthyroidism (Graves disease), but, rarely, patients can have hypothyroidism or normal thyroid function.1-4


  • Thyroid eye disease is commonly misdiagnosed; delayed diagnosis can complicate management.
  • Supplements and medical therapy may reduce disease burden and improve outcomes. A novel drug with a new molecular target has shown promise in a clinical trial.
  • In severe cases, surgery may be required to improve orbital and ocular function.

Classically, TED progresses in a standard fashion, with initial signs and symptoms rapidly progressing to a maximal severity (active phase), which then abates to a plateau, improving only slightly from the peak severity (quiescent phase). TED has vision-threatening consequences, but it also causes significant physical deformation, reduces quality of life, and has a far-reaching societal impact.1,3,4

Expansion of orbital soft tissues, including fat and extraocular muscles, induces proptosis, which can be uni- or bilateral. Orbital discomfort, headaches, and periocular deformity are common, and inflammation can occasionally induce optic neuropathy. Extraocular muscle involvement can cause noncomitant strabismus and primary or gaze-evoked diplopia. Eyelid retraction commonly causes lagophthalmos and exposure keratopathy (Figures 1–4).1-8

Figure 1. Atypical example of thyroid eye disease with profound unilateral proptosis, hypotropia, and eyelid retraction.

Figure 2. Another atypical example of thyroid eye disease presenting only with right upper eyelid retraction.

Figure 3. An example of thyroid eye disease with disfiguring proptosis and lower eyelid retraction on both sides (top). A postoperative photograph of the same patient following customized orbital decompression of the medial orbital wall, floor, and lateral walls on both sides (bottom).

Figure 4. Active inflammatory thyroid eye disease with orbital congestion, chemosis, conjunctival and caruncular inflammation, proptosis, esotropia, and eyelid retraction (top). Active thyroid eye disease with bilateral proptosis, hypotropia, and extreme bilateral eyelid retraction (bottom).

Medical therapy for the active phase of TED is a dynamic area of research. Current therapies rely on steroids and radiation, which have safety concerns and limited efficacy. Physicians and scientists have attempted to devise targeted therapies that lessen overall disease burden and potentially reduce the need for surgical intervention. A recent prospective, randomized, controlled trial investigated a novel immunotherapy targeting the insulin-like growth factor-1 receptor (IGF-1R) as a treatment for moderate active TED.1

In that trial, teprotumumab (Horizon Pharma USA/Genmab/Roche), a human monoclonal antibody inhibitor of IGF-1R, was more effective than placebo in reducing inflammation and patient scores on a clinical activity scale.

Surgery can be considered in the disease’s active phase to prevent permanent vision loss, but it is primarily performed only once the disease stabilizes. Customized surgical intervention and surgical techniques are being studied to provide individualized improvement in patient orbital comfort, eyelid function, and appearance.9,10 This article presents five fundamentals of TED and its treatment.

Thyroid eye disease is commonly misdiagnosed

TED is commonly misdiagnosed, not only because of the heterogeneity of presenting symptoms and signs, but also because the thyroid gland symptoms and ocular symptoms can occur at different times. Early in the active phase, symptoms are commonly blamed on dry eye disease, conjunctivitis, or allergic eye disease. In the later stages, patients can be diagnosed with orbital cellulitis, myositis, and even sinusitis. Active phase findings occur rapidly and provide the best options for medical therapy in the disease process.

The active phase of thyroid eye disease provides a narrow window

In most patients, the changing phase of TED lasts between 6 and 18 months. Because of delayed diagnoses and a lack of specialists comfortable with treating TED, patients commonly miss the window when medical management of the disease is most effective. Current medical options for patients in the active phase of TED may lessen the overall disease burden and limit some patients’ severe disfigurement, vision loss, or need for surgical intervention.

Selenium supplementation may lessen the disease burden

Selenium is a trace mineral that functions as an antioxidant, and some serum selenoproteins are known to be lower in patients with autoimmune thyroid disease. Low doses of selenium can be found in some nuts, tuna, and in some oral vitamin supplements. Supplementation of selenium is commonly employed in the treatment of autoimmune thyroid disease, but it has been evaluated in TED only recently. Studies have shown lessened disease activity and improved quality of life in patients in the active phases of TED.11

Targeted therapy has been shown to improve active-phase disease

Medical therapy for active-phase TED remains the most highly researched area. Although corticosteroids and radiation can provide effective blanket treatment for the inflammation, they commonly cause adverse reactions. Therapy that targets ocular and orbital inflammation may allow more effective treatment with fewer adverse events.

In TED, the thyrotropin receptor is a known stimulatory target for pathogenic autoimmune antibodies within the ocular and orbital tissues. There is a known regulatory relationship between IGF-1R and the thyrotropin receptor within orbital fibroblasts. In vitro studies have shown that inhibitory IGF-1R antibodies decreased the stimulatory role of pathogenic thyroid autoantibodies. Teprotumumab recently received breakthrough therapy designation from the US FDA for the treatment of moderate to severe TED.

The 2017 study cited earlier,12 on which I was a coauthor, found that proptosis, clinical activity score, and quality of life were significantly improved in patients receiving tempromumab compared with placebo (See Study in Seconds below). The only significant adverse event was hyperglycemia in some patients, which required adjustment of medication in some patients with diabetes. This was one of the first trials of targeted therapy for TED, and it has opened the door for additional research in active-phase TED.

Study in Seconds

Teprotumumab for Thyroid-Associated Ophthalmopathy

Objective: Evaluated the clinical utility of teprotumumab and assessed the drug against placebo for reduction of clinical activity and proptosis and improvement in quality of life.

Design: Prospective, multicenter, placebo-controlled trial. Following strict inclusion criteria, including evidence of active phase disease, the drug was administered once every 3 weeks for a total of eight doses.

Results: Greater improvement was noted in patients receiving teprotumumab than those receiving placebo at 6 weeks (43% vs 4%, P < .001). An even greater difference was seen at 6 months (69% vs 20%, P < .001). Proptosis, clinical activity score, and quality of life were significantly improved.

Side effects: Hyperglycemia required adjustment of medication in some patients with diabetes.

Smith TJ, Kahaly GJ, Ezra D. Teprotumumab for thyroid-associated ophthalmopathy. N Engl J Med. 2017;376:1748-1761.

Figure 5. Severe right optic disc edema is seen only in advanced cases of thyroid-related compressive optic neuropathy.

Figure 6. Coronal CT scan with classic pattern of extraocular muscle enlargement intensely involving the medial rectus muscles and less so the inferior rectus muscles.

Figure 7. Postoperative coronal CT scan showing strategic removal of the entire medial wall, floor, and lateral wall of the left orbit with prolapse of the orbital contents through the osteotomies.

Customized surgical intervention can be used to rehabilitate patients

Many times, medical therapy may reduce the disease burden in TED but not restore orbital and ocular function to the predisease state (Figures 5 and 6). As a result, rehabilitative surgery may be required. Unless the risk of permanent eye damage is suspected, orbital and periocular surgery should be avoided during the active phase to ensure the stability of surgical results. Surgical techniques and instrumentation have been greatly improved, now allowing surgery to be tailored for each patient. Preoperative orbital volumetric and orbital physiology analysis may provide the adaptive surgeon the ability to better predict surgical outcomes. The introduction of intraoperative surgical navigation and instrumentation, such as piezoelectric bone removal systems, may afford safer, more strategic outcomes with orbital decompression (Figure 7). Algorithms developed for strabismus and eyelid surgery may improve ocular function and appearance.

1. Wiersinga WM, Smit T, et al. Clinical presentation of Graves’ ophthalmopathy. Ophthal Res. 1989;21(2):73-82.

2. Wiersinga WM, Smit T, van der Gaag R, et al. Temporal relationship between onset of Graves’ ophthalmopathy and onset of thyroidal Graves’ disease. J Endocrinol Invest. 1988;11:615-619.

3. Bartley GB. The epidemiologic characteristics and clinical course of ophthalmopathy associated with autoimmune thyroid disease in Olmsted County, Minnesota. Trans Am Ophthalmol Soc. 1994;92:477-588.

4. Stan MN, Bahn RS. Risk factors for development or deterioration of Graves’ ophthalmopathy. Thyroid. 2010;20(7):777-783.

5. Smith TJ, Hegedüs L. Graves’ disease. N Engl J Med. 2016; 375:1552-1565.

6. Bartalena L, Tanda ML. Graves’ ophthalmopathy. N Engl J Med. 2009;360:994-1001.

7. Gould DJ, Roth FS, Soparkar CNS. The diagnosis and treatment of thyroid-associated ophthalmopathy. Aesth Plast Surg. 2012;36:638-648.

8. Bartley GB, Fatrouechi V, Kadrmas EF, et al. Clinical features of Graves’ ophthalmopathy in an incidence cohort. Am J Ophthalmol. 1996;121:284-290.

9. Rootman DB. Orbital decompression for thyroid eye disease. Surv Ophth. 2018;63(1):86-104.

10. Jeffries Jm, Jones RK Currie ZI, et al. Orbital decomopression for thyroid eye disease: methods, outcomes and complications [Published online ahead of print December 15, 2017.] Eye. doi: 10.1038/eye.2017.260.

11. Marcocci C, Kahaly GJ, Krassas GE, et al. Selenium and the course of mild Graves’ orbitopathy. N Engl J Med. 2011;364(20):1920-1931.

12. Smith TJ, Kahaly GJ, Ezra D. Teprotumumab for thyroid-associated ophthalmopathy. N Engl J Med. 2017;376:1748-1761.

Steven M. Couch, MD, FACS
  • Associate Professor of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis
  • couchs@wustl.edu
  • Financial disclosure: None