ET archive : Treatment at the crossroads (Volume 8 Issue7/8 July/August 2013)
Fitting MIGS techniques inot a new glaucoma treatment paradigm. EuroTimes Volume 8 Issue7/8 July/August 2013
Roibeard O’hEineachain
Published: Friday, July 21, 2017
Tube, or not tube?
MIGS, the new kid on the block

Dramatic improvement in bleb appearance (right) with simple modification of technique (Moorefields Safer Surgery System). Courtesy of Peng T Khaw MD, PhD
In contrast, use of the new MIGS devices involves only a small amount of disturbance of ocular tissues and consequently has much fewer side effects. The iStent® (Glaukos Corporation[see Figure 1]) and the Hydrus™ (Ivantis [see Figure 2]) and the Trabectome® (Neomedix) are all designed to direct aqueous out through Schlemm’s canal. They therefore have a mechanism in common with some more invasive ab externo forms of a Schlemm’s canal surgery, such as viscocanalostomy and canaloplasty. They also share an inherent limitation with those techniques in that they cannot bring pressures below episcleral venous pressure 12 mmHg. On the positive side, the techniques do not result in the creation of a bleb. The iStent is composed of nonferromagnetic titanium and is designed to provide a channel for the outflow of aqueous directly from the anterior chamber to Schlemm’s canal, bypassing the trabecular meshwork. The ab interno device was approved by FDA in 2012 for use with cataract procedures . The FDA trial showed that among patients receiving the implant while undergoing cataract procedures, 73 per cent maintained an IOP of 21 mmHg or lower without medication at 12 months’ followup. That compared to only 50 per cent of those who underwent cataract surgery alone. More recent research by Ike Ahmed MD and his associates demonstrated that two stents can consistently reduce IOP to less than 15 mmHg (G Belovay et al, J Cataract Refract Surg, “Using multiple trabecular micro-bypass stents in cataract patients to treat open-angle glaucoma”, 2012 November; 38:1911-1917).
Manfred Tetz MD, Berlin, reported similar results at this year’s ESCRS Winter Meeting using the new collar-button design of the iStent. At 12 months postoperatively, mean IOP was 14.5 mmHg and the mean number of ocular hypotensive medications patients needed decreased from 1.8 medications preoperatively to 0.3 medications or less at all postoperative time periods The manufacturers of the Hydrus implant describe the device as an intracanalicular scaffold. It is designed for placement into Schlemm’s canal from the inside of the eye. It therefore resembles in design and purpose the Stegmann canal expander, a device implanted by an ab externo approach. However, unlike the ab externo device, the Hydrus has a special injector system and does not require any disturbance of scleral or conjunctival tissue. In a study Dr Tetz presented at the XXX Congress of the ESCRS in Milan last year, patients with mild to moderate openangle glaucoma who were concurrently undergoing cataract surgery underwent implantation of the Hydrus device. At 12 months, washed out IOP was 15.5 mmHg, a decrease of 9.1 mmHg from preoperative washout values. “The results are encouraging. But one little thing remains uncertain with all internally placed implants, did I really hit Schlemm’s canal? And did I put the implant first full-length inside Schlemm’s canal? In most cases with modern implants with the Hydrus and the iStent you're reasonably sure, but with the Grieshaber Stegmann canal expander you implant it from the outside after opening up the canal, so you’re 99 per cent sure that you really placed it in Schlemm’s canal,” Dr Tetz said.
The Trabectome opens access to Schlemm's canal by ablating a portion of the trabecular meshwork of the eye with an electrosurgical hand piece. It received FDA approval in 2004. In a prospective trial by the Trabectome Study Group involving more than 300 patients, the mean IOP fell from preoperative values of 20.0 mmHg to 15.5 mmHg at one year’s follow-up. The mean number of drops patients needed fell from 2.65 ± 1.13 at baseline to 1.29 at one year. (BA Francis et al J Cataract Refract Surg, “Combined cataract extraction and trabeculotomy by internal approach for coexisting cataract and open-angle glaucoma. 2008 Jul;34(7):1096-103). The CyPass (Transcend Medical, Menlo Park, Calif.) uses a different approach, directing the outflow of aqueous into the suprachoroidal space. The CE Mark approved device consists of a tube 6.35mm in length and with an outer diameter of 0.51mm composed of a polyimide material. Like the other MIGS implants it is placed in the eye using an ab interno approach positioned in a superciliary cleft created with the implantation device. The one-year results of the CyCLE study presented at the annual AAO Meeting in Chicago last year revealed that implantation of the device reduced mean IOP by 35 per cent to 16.3 mmHg and a reduced mean medication usage by half. What remains to be seen is whether the device will continue to work over the long-term, Dr Tetz said.
“My current opinion is that the suprachoroidal approach doesn't seem to work well enough in the long-term. I think with a number of studies we have good one-year data and you see that most of the devices close off after one and a half years,” he added. The Xen microfistula implant, AqueSys, is an investigational device delivered through an ab interno incision to create an external subconjunctival filtration pathway, similar to trabeculectomy. It is composed of a soft pliable collagen-derived gelatin material and is placed ab interno through a selfsealing corneal incision and implanted with a 27-gauge needle, visualising the meshwork with a gonio mirror. Therefore, the scleral and conjunctival tissues are left intact. “The AqueSys is actually an MIGS replacement for trabeculectomy. It compares very well because the amount of trauma going to the delicate structures is usually lower and the smaller the trauma area, the less likely it is you will get scarring and closure,” Dr Tetz said.