4.6 Article

Evaluation of an Integrated Orbital Tissue Expander in Congenital Anophthalmos: Report of Preliminary Clinical Experience

Journal

AMERICAN JOURNAL OF OPHTHALMOLOGY
Volume 151, Issue 3, Pages 470-482

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2010.09.009

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Funding

  1. RESEARCH TO PREVENT BLINDNESS, INC, NEW YORK, NEW YORK
  2. National Institutes of Health, Bethesda, Maryland [P30-EY014801]
  3. National Institutes of Health to Innovia, LLC, Miami, Florida [NIH-1R43-EY015016-01]
  4. Innovia
  5. Boston Scientific Corp
  6. Small Business Innovation Research (NIH)
  7. Department of Defense

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PURPOSE: To evaluate the effectiveness of an orbital tissue expander designed to stimulate orbital bone growth in an anophthalmic socket. DESIGN: Retrospective, noncomparative, interventional case series. METHODS: SETTINGS: Institutional. STUDY POPULATION: Nine consecutive patients with unilateral congenital anophthalmos. INTERVENTION: The orbital tissue expander is made of an inflatable silicone globe sliding on a titanium T-plate secured to the lateral orbital rim with screws. The globe is inflated by a transconjunctival injection of normal saline through a 30-gauge needle to a final volume of approximately 5 cm(3). Computed tomography scans were used to determine the orbital volume. The data studied were: demographics, prior orbital expansion procedures, secondary interventions, orbital symmetry, and implant-related complications. MAIN OUTCOME MEASURES: The primary outcome measure was the orbital volume change, and the secondary outcome measures were changes in forehead, brow, and zygomatic eminence contour and adverse events. RESULTS: The average patient age at implantation was 41.89 +/- 39.42 months (range, 9 to 108 months). The initial average volume of inflation was 3.00 +/- 0.87 cm(3) (range, 2.0 to 4.0 cm(3)), and the average final volume of 4.33 +/- 0.50 cm(3) (range, 4.0 to 5.0 cm(3)) was achieved. The duration of expansion was 18.89 +/- 8.80 months (range, 4 to 26 months). All patients demonstrated an average increase in the orbital tissue expander implanted orbital volume of 5.112 +/- 2.173 cm(3) (range, 2.81 to 10.38 cm(3)). The average difference between the volume of the implanted and the initial contralateral orbit was 5.68 +/- 2.34 cm(3), which decreased to 2.53 +/- 1.80 cm(3) at the final measurement (P < .001, paired t test). All implants remained inflated except for 2 iatrogenic punctures at the second inflation and 1 that was the result of implant failure. All were replaced. CONCLUSIONS: The integrated orbital tissue expander is safe and effective in stimulating anophthalmic socket bone growth. (Am J Ophthalmol 2011;151:470-482. (C) 2011 by Elsevier Inc. All rights reserved.)

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