2020
DOI: 10.1177/1120672120973617
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MRI after successful eyeWatchTM implantation

Abstract: The eyeWatchTM is a new glaucoma drainage device that includes an adjustable mechanism that can vary the resistance to aqueous humor outflow during the postoperative period to reduce the burden of postoperative intraocular pressure (IOP) management. The mechanism contains a magnetic rotor that can be adjusted using an external magnetic control unit. Adjustments of the position of the rotor are performed mostly in the initial postoperative follow-up period in order to reach the target IOP. However, for some pat… Show more

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Cited by 6 publications
(3 citation statements)
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“…POAG is a multi-tissue disease that targets, in ascending order, the TM, the optic nerve head, the lateral geniculate nuclei and the visual cortex [1]. As is known to us, TM dysfunction induces impaired aqueous humor (AH) drainage, elevated IOP and alterations of the optic nerve head and the visual field defects in POAG [2][3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…POAG is a multi-tissue disease that targets, in ascending order, the TM, the optic nerve head, the lateral geniculate nuclei and the visual cortex [1]. As is known to us, TM dysfunction induces impaired aqueous humor (AH) drainage, elevated IOP and alterations of the optic nerve head and the visual field defects in POAG [2][3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…The eyeWatch encompasses a mechanism allowing for selective compression of its internal elastic tube, thus altering its fluidic resistance, which is performed noninvasively using the eyeWatch Pen single use during the surgery or the eyeWatch Pen (office) post-operatively. 20,21 In this small case series we assess the efficacy and safety of eyeWatch device in vitrectomized refractory glaucomatous eyes.…”
Section: Introductionmentioning
confidence: 99%
“…unserem Patienten wurde der EWP verwendet, um die Position wieder auf 0 zu setzen [10]. Somit kann eine cMRT nach Implantation des EWS-Systems durchgeführt werden, den Patienten sollte jedoch mitgeteilt werden, dass sie danach zu einer IOD-Kontrolle kommen müssen.…”
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