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Analysis Between the Results of Two Surgical Techniques of Orbital Decompression in Patients With Graves Orbitopathy

Not Applicable
Completed
Conditions
Graves Ophthalmopathy
Interventions
Procedure: Orbital decompression
Registration Number
NCT03278964
Lead Sponsor
University of Sao Paulo General Hospital
Brief Summary

Randomized prospective clinical trial, aiming to compare two techniques of orbital decompression. Patients with Graves orbitopathy in the inactive phase for at least 6 months will be divided in two groups; one group will be submitted to orbital decompression by antro-ethmoidal technique; the other group will be submitted to orbital decompression by lateral wall technique. Patients will be followed up for a period of 6 months after the surgery, and will be evaluated about the effect of orbital decompression on ocular motility, proptosis, ocular surface and quality of life.

Detailed Description

Graves' orbitopathy is the most relevant non-thyroid manifestation of Graves' disease. Its clinical status varies from subclinical to severe deformities. Clinical features include palpebral retraction, exophthalmos, restrictive strabismus, chemosis, ocular surface lesions and optic neuropathy. There are two stages of the disease. There is an active phase in which the inflammatory process is present and the orbital changes evolve. The inactive phase comprises a stable clinical picture regarding the sequelae of the active phase. Orbital decompression surgery is the main treatment procedure for this inactive phase for functional and cosmetic rehabilitation purposes. In the last decades, great advances in the techniques and indication of this surgery have been observed. However, a consensus about the ideal technique does not yet exist. The most commonly used techniques are antro-ethmoidal decompression and lateral wall decompression alone or associated with other walls. The present study will be based on patients with Graves' orbitopathy diagnosis for at least 2 years and who are already in the inactive phase for at least 6 months. There are no prospective studies comparing the 2 main orbital decompression techniques through a detailed analysis of surgical outcomes from computed tomography images, digital photographic images and ocular motility examination. These informations will be collected in the preoperative and postoperative periods. The investigators will evaluate the decompressive potential of each technique calculated by the tomographic images. Participants will be followed up for a period of 6 months after the surgical procedure and the effect of decompression on ocular motility, ocular bulb positioning, ocular surface, vertical palpebral fissure, and the patient's quality of life will also be analyzed. The findings of this work will bring important contribution to the improvement of this surgical procedure of great relevance in the rehabilitation of patients with Graves' orbitopathy.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
42
Inclusion Criteria
  • Diagnosis of Graves orbitopathy for at least 2 years
  • Clinical Activity Score (CAS) < 4 for at least 6 months
  • Agreement with the Informed Consent Form, which will be signed during the selection visit
  • Ability to come to periodic evaluations for 6 months after the orbital decompression
  • Absence of ocular abnormalities such as degenerative myopia, microphthalmia or anophthalmic cavity
  • Absence of orbital abnormalities such as previous fractures or congenital defects
  • Good collaboration for the exams
  • Euthyroidism
  • Exophthalmus ≥ 20 mm in Hertel's exophthalmometry
  • Preoperative clinical evaluation indicating absence of contraindications for a surgical procedure
Exclusion Criteria
  • Myasthenia gravis
  • Pregnancy
  • Previous orbital, strabismus or eyelid surgery
  • Other abnormal eye conditions or symptoms that make it impossible to admit the patient to the study, according to the clinical judgment of the investigator.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Lateral wall techniqueOrbital decompressionPatients in the inactive phase of Graves orbitopathy will be submitted to orbital decompression by lateral wall technique.
Antro-ethmoidal techniqueOrbital decompressionPatients in the inactive phase of Graves orbitopathy will be submitted to orbital decompression by antro-ethmoidal technique.
Primary Outcome Measures
NameTimeMethod
Change in Ocular Motility statusBefore orbital decompression and 1, 3 and 6 months after surgery

Measure by prism and cover, to assess strabismus in the nine positions of gaze

ExophthalmosBefore orbital decompression and 6 months after surgery

Exophthalmos will be measured by Hertel's exophthalmometer and orbital computerized tomography

Secondary Outcome Measures
NameTimeMethod
Digital photography evaluationBefore orbital decompression and 6 months after surgery

Using digital photography, Photoshop and Image J, ductions and versions will be analyzed

Ocular surface evaluationBefore orbital decompression and 6 months after surgery

Assessed by Lysozyme Green, Break-up time, Schirmer I test

Quality of life questionary Quality of life questionaryBefore orbital decompression and 6 months after surgery

GO-QoL form

DiplopiaBefore orbital decompression and 1, 3 and 6 months after surgery

Evaluation by Gorman's Diplopia Table

Volume of the extraocular musclesBefore orbital decompression and 6 months after surgery

Measure by orbital computerized tomography images

Trial Locations

Locations (1)

University of Sao Paulo General Hospital

🇧🇷

São Paulo, Brazil

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