6533b837fe1ef96bd12a329c

RESEARCH PRODUCT

A European Study of the Performance and Safety of MINIject in Patients With Medically Uncontrolled Open-angle Glaucoma (STAR-II)

Lucia Perucho GonzálezJulian Garcia FeijooChristoph HirneißKatrin LorenzNorbert PfeifferZubair HussainStar-ii InvestigatorsFlorent AptelPhilippe Denis

subject

Adultmedicine.medical_specialtyIntraocular pressureTime Factorsgenetic structuresOpen angle glaucomaGlaucomaOriginal StudiesProsthesis ImplantationTonometry Ocular03 medical and health sciences0302 clinical medicineRefractoryOphthalmologymedicineClinical endpointHumansMinimally Invasive Surgical ProceduresSingle-Blind MethodIn patientEuropean UnionProspective StudiesGlaucoma Drainage ImplantsAdverse effectAntihypertensive AgentsIntraocular PressureAgedAged 80 and overEquipment Safetybusiness.industryIOPMIGSMiddle Agedmedicine.diseaseGlaucoma drainage deviceMINIjecteye diseasesOphthalmologyglaucomaTreatment Outcome030221 ophthalmology & optometryFemalesupraciliarysense organsbusinessGlaucoma Open-Angle030217 neurology & neurosurgery

description

Precis In this European study (STAR-II), MINIject, a novel, ab-interno, supraciliary MIGS device, effectively lowered intraocular pressure (IOP) and the need for IOP-lowering medications in patients with primary open-angle glaucoma. Purpose To evaluate the safety and performance of a minimally invasive supraciliary glaucoma drainage device (MINIject DO627, iSTAR Medical SA, Wavre, Belgium) for surgical treatment of primary open angle glaucoma in patients refractory to topical hypotensive medications. Methods In a prospective, interventional, single-arm, multi-center, European study (STAR-II), MINIject was successfully implanted in a standalone 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 intraocular pressure (IOP) ≤ 21▒mmHg and > 5▒mmHg 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 met with 75.9% of patients reaching prospectively defined success. Mean IOP was reduced by 40.2% (9.9▒mmHg) to 14.7±6.0▒mmHg at 6 months from 24.6±3.8▒mmHg at baseline. The use of IOP-lowering medication ingredients was reduced by 63.4% to 1.0±1.3 from 2.9±1.2 at baseline. Furthermore, 79.3% of patients had mean IOP ≤18▒mmHg, 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 standalone procedure significantly lowers IOP by 40% at 6-month follow-up, while reducing the need for IOP-lowering medication.

https://doi.org/10.1097/ijg.0000000000001632