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A European Study of the Performance and Safety of MINIject in Patients With Medically Uncontrolled Open-angle Glaucoma (STAR-II).
García Feijoó, Julián; Denis, Philippe; Hirneiß, Christoph; Aptel, Florent; Perucho González, Lucía; Hussain, Zubair; Lorenz, Katrin; Pfeiffer, Norbert.
Afiliação
  • García Feijoó J; Departamento de Oftalmologia, Hospital Clinico San Carlos, Universidad Complutense, OFTARED, Madrid, Spain.
  • Denis P; Department of Ophthalmology, Hôpital de la Croix-Rousse, Lyon.
  • Hirneiß C; Klinikum der Universität München, Ludwig-Maximilians-Universität, Munich.
  • Aptel F; Clinique Universitaire d'Ophtalmologie, CHU de Grenoble-Alpes, Grenoble, France.
  • Perucho González L; Departamento de Oftalmologia, Hospital Clinico San Carlos, Universidad Complutense, OFTARED, Madrid, Spain.
  • Hussain Z; iSTAR Medical, Wavre, Belgium.
  • Lorenz K; Department of Ophthalmology, University Medical Center, Johannes Gutenberg-University, Mainz, Germany.
  • Pfeiffer N; Department of Ophthalmology, University Medical Center, Johannes Gutenberg-University, Mainz, Germany.
J Glaucoma ; 29(10): 864-871, 2020 10.
Article em En | MEDLINE | ID: mdl-32769736
ABSTRACT
PRECIS In this European study (STAR-II), MINIject, a novel, ab-interno, supraciliary minimally invasive glaucoma surgery device, effectively lowered intraocular pressure (IOP) and the need for IOP-lowering medications in patients with primary open-angle glaucoma.

PURPOSE:

This study evaluates the safety and performance of a minimally invasive supraciliary glaucoma drainage device (MINIject DO627) for surgical treatment of primary open-angle glaucoma in patients refractory to topical hypotensive medications.

METHODS:

In a prospective, interventional, single-arm, multicenter, European study (STAR-II), MINIject was successfully implanted in a stand-alone procedure in 29 of 31 patients in 8 sites in 3 countries. The primary endpoint was the success rate 6 months after surgery >60% (defined as diurnal IOP ≤21 and >5 mm Hg with ≥20% IOP reduction from baseline, with/without glaucoma hypotensive medication). ClinicalTrials.gov NCT03624361.

RESULTS:

At the 6-month follow-up, the primary endpoint was fulfilled, with 75.9% of patients reaching prospectively defined success. The mean IOP was reduced by 40.2% (9.9 mm Hg) to 14.7±6.0 mm Hg at 6 months from 24.6±3.8 mm Hg at baseline. The use of IOP-lowering medication ingredients was reduced by 63.4% from 2.9±1.2 at baseline to 1.0±1.3. Furthermore, 79.3% of the patients had mean IOP ≤18 mm Hg, 82.8% achieved a ≥20% IOP reduction, and 55.2% were medication free at 6 months. Six device-related serious adverse events were reported in the study eye IOP increase (3/31 patients, 9.7%), and single reports of eye pain, corneal erosion, and chorioretinal folds (1/31, 3.2%), all of which resolved. There was minimal change to corneal endothelial cell density.

CONCLUSION:

Ab-interno supraciliary surgical implantation using MINIject DO627 in a stand-alone procedure significantly lowers IOP by 40% at the 6-month follow-up, while reducing the need for IOP-lowering medication.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glaucoma de Ângulo Aberto / Implantação de Prótese / Implantes para Drenagem de Glaucoma Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glaucoma de Ângulo Aberto / Implantação de Prótese / Implantes para Drenagem de Glaucoma Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha