Retinal cryotherapy, also called cryopexy, seals a retinal break by freezing it from the outside of the eye rather than treating it with light from inside.

Retinal Cryotherapy

It produces the same biological end point as laser retinopexy, a firm chorioretinal adhesion around the break, but the route of delivery and the clinical situations where each is preferred are genuinely different.

Most retina specialists reach for laser first when the break is accessible, and reserve cryotherapy for the situations where laser cannot do the job as well.

Cryotherapy is also, historically, the older of the two techniques, and it remains the default in settings where a laser delivery system is not readily available.


Mechanism

A cryoprobe is applied to the external scleral surface directly over the break, and a freeze-thaw cycle is delivered under indirect ophthalmoscopic visualization to confirm accurate placement.

Ice crystal formation within the retinal pigment epithelium and outer retina disrupts cell membranes, and the wound-healing response that follows produces a chorioretinal scar functionally equivalent to a laser burn.

Unlike laser, where the effect is confined to the point of light absorption, a cryotherapy freeze spreads out somewhat within the tissue, which is one reason the resulting scar tends to be larger and more diffusely pigmented than a laser burn of comparable clinical intent.


Indications

  • Breaks located very far anteriorly, near the ora serrata, where a laser delivery system cannot achieve a direct, centered view
  • Breaks obscured by vitreous hemorrhage or a hazy view that would prevent safe laser aiming but still allow external localization with scleral depression
  • Any break being treated during a scleral buckle procedure, since the sclera is already exposed and cryotherapy avoids an additional separate laser session
  • Breaks in eyes where pupillary dilation or media clarity is poor enough that transpupillary laser delivery is simply not practical

Cryotherapy is generally avoided as a first choice when laser is equally accessible, largely because of its less favorable side-effect profile around pain, inflammation, and the theoretical risk of seeding viable retinal pigment epithelial cells into the vitreous.


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Technique

The surgeon localizes the break externally by indenting the sclera with the cryoprobe tip while watching the corresponding indentation appear internally through the indirect ophthalmoscope.

Freezing is continued until a visible white, ice-ball reaction is seen to surround the break with an adequate margin, then the probe is allowed to thaw fully before it is moved or removed, since pulling on a still-frozen probe can tear the retina it is meant to protect.

Multiple applications are used to encircle a larger tear completely, in the same way a laser barrier requires a confluent ring rather than a single spot.

Most cryotherapy for a routine peripheral break is performed under local or topical anesthesia with sedation as needed, though extensive treatment or a very apprehensive patient occasionally warrants a regional block.


Comparison With Laser Retinopexy

Cryotherapy causes more breakdown of the blood-retinal barrier and a more pronounced postoperative inflammatory response than laser, which translates clinically into more discomfort and a theoretically higher risk of stimulating proliferative vitreoretinopathy when used over a large area.

Laser burns are more discrete and easier to titrate spot by spot, while a cryotherapy freeze is more of an all-or-nothing application over a given area, which is part of why laser is favored whenever direct visualization allows it.

Neither modality treats subretinal fluid, and the same limitation that applies to laser retinopexy applies here: a break with a meaningful cuff of fluid underneath it needs a reattachment procedure, not cryotherapy alone.

Retinal Cryotherapy


Complications

  • Postoperative pain and chemosis, generally more pronounced than after an equivalent laser treatment
  • Choroidal effusion or hemorrhage from vigorous or repeated freeze-thaw cycles over a large area
  • Dispersion of viable retinal pigment epithelial cells into the vitreous cavity, a recognized contributor to proliferative vitreoretinopathy when cryotherapy is used extensively
  • Undertreatment from an inaccurately localized freeze, leaving a gap in the barrier around the break

Follow-Up

Patients are examined within one to two weeks to confirm the treated area has developed a stable, pigmented chorioretinal scar and that no new subretinal fluid has appeared.

New or worsening flashes, a new field defect, or any sense of a curtain progressing across the vision after treatment should prompt an urgent re-examination rather than waiting for the scheduled visit.

As with laser retinopexy, the fellow eye deserves a careful dilated look at the same visit, since the predisposing factors behind one eye’s break are frequently present bilaterally.

Patients should also be counseled that transient floaters and mild discomfort over the treated area are expected for a few days, so that a normal postoperative course is not mistaken for a complication.


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References

  1. Wilkinson CP, Rice TA. Michels’ Retinal Detachment.
  2. American Academy of Ophthalmology. Basic and Clinical Science Course, Section 12: Retina and Vitreous.
  3. Wilkinson CP. Evidence-based analysis of prophylactic treatment of asymptomatic retinal breaks and lattice degeneration. Ophthalmology.
  4. Glaser BM, Vidaurri-Leal J, Michels RG, Campochiaro PA. Cryotherapy during surgery for giant retinal tears and intravitreal dispersion of viable retinal pigment epithelial cells. Ophthalmology.