April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Suprachoroidal Drainage Devices - Six Months Experience
Author Affiliations & Notes
  • Andre Vicente
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Barbara Borges
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Rita Anjos
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Ana Cabugueira
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • luisa vieira
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Mariana Cardoso
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Arnaldo Dias Santos
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Nuno Silva
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Joana Ferreira
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Fernando Fernandes
    Ophthalmology, Centro Hospitalar Lisboa Central, Lisbon, Portugal
  • Footnotes
    Commercial Relationships Andre Vicente, None; Barbara Borges, None; Rita Anjos, None; Ana Cabugueira, None; luisa vieira, None; Mariana Cardoso, None; Arnaldo Santos, None; Nuno Silva, None; Joana Ferreira, None; Fernando Fernandes, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 6138. doi:
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      Andre Vicente, Barbara Borges, Rita Anjos, Ana Cabugueira, luisa vieira, Mariana Cardoso, Arnaldo Dias Santos, Nuno Silva, Joana Ferreira, Fernando Fernandes; Suprachoroidal Drainage Devices - Six Months Experience. Invest. Ophthalmol. Vis. Sci. 2014;55(13):6138.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To evaluate the clinical outcomes of patients with suprachoroidal drainage devices.

Methods: The authors describe 4 cases of patients presenting with preoperative intraocular pressures (IOP) between 30-40 mmHg, under triple glaucoma medication and history of multiple intraocular surgeries, who underwent suprachoroidal drainage device (StarFlo®) implantation. The following parameters were evaluated: preoperative and postoperative IOP (1 day, 1 week and 1, 3 and 6 months), the use IOP-lowering medication and operative and post-operative complications. IOP reduction in over 30% or <21mmHg was considered relative or absolute success depending on whether this was achieved with or without use of further surgical intervention or medical IOP-lowering treatment, respectively.

Results: At 3 months, there was a reduction in IOP greater than 30% to 3 months post-operative (Baseline IOP: 34 ± 2 mmHg, 3 months IOP: 13 ± 3 mmHg). After this period, IOP-lowering medication was re-started in 2 patients in order to sustain the higher than 30% IOP-lowering reduction. One of the patients with relative success criteria was lost in follow at 3 months. In our last observation, IOP remains lower than preoperative IOP (6 months IOP 13 ± 4 mmHg). No there were no complications during the procedure. A patient presented with hyphema in the first postoperative day, which spontaneously resolved.

Conclusions: Suprachoroidal drainage devices seem to reduce IOP significantly, are technically feasible and have few postoperative complications.

Keywords: 568 intraocular pressure  
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