Conservative Management
Tinted contact lenses (cosmetic CL)
Spontaneous reduction with mydriatics (for iris capture: attempt spontaneous reduction in supine position)
Observation (for mild pupillary distortion with minimal symptoms)
Iris repair surgery is a general term for surgical procedures that repair congenital, traumatic, or postoperative iris defects and damage. This article focuses on suture and reconstruction techniques (pupilloplasty, iridoplasty) that preserve the patient’s own iris tissue.
The choice between iris repair surgery and artificial iris devices depends on the amount and quality of remaining iris tissue. If sufficient iris tissue remains, autologous iris suture is selected; for extensive iris damage or atrophy where suturing is not possible, artificial iris devices (see separate article) are indicated. Iris-fixated IOLs and artificial irises are not yet approved in Japan, and pupil reconstruction using iris suture, which does not require special instruments, is a relatively easy procedure to choose.
Classification of iris injury by site (AAO PPP) 1):
Independent epidemiological data do not exist. Cataract surgery is performed on approximately 1.6 million eyes per year in Japan, and the exact frequency of iris injury complications is unknown, but the prevalence of IFIS is reported to be about 1–2% of all cataract surgeries.
Iris repair is a surgery that reconstructs the pupil by suturing and shaping the patient’s own remaining iris tissue. It is indicated when sufficient iris tissue remains, does not require special instruments, and can be performed without using artificial devices that require regulatory approval in Japan. On the other hand, artificial iris devices are indicated for cases with extensive iris damage or iris atrophy where suturing is impossible (including aniridia). Forcing sutures may only cause iris rupture and unnecessary trauma, so the appropriate indication is important.
| Cause | Typical Findings | Complications |
|---|---|---|
| Congenital coloboma | Inferior (inferotemporal) iris defect, widest at pupillary margin | Microphthalmia, cataract, choroidal coloboma, glaucoma, retinal detachment |
| Traumatic | Iris laceration/iridodialysis, hyphema | Lens dislocation, angle recession, cataract |
| Post-cataract surgery | Pupil distortion/poor transillumination, iris capture | IOL decentration, corneal endothelial damage |
| IFIS sequelae | Iris atrophy, transillumination iris defect | Paralytic mydriasis, increased higher-order aberrations |
Photophobia and glare persist, reducing quality of daily life. An excessively large pupil tends to cause higher-order aberrations and decreased contrast 5). Additionally, irregular pupil leads to persistent monocular diplopia. Difficulty in dilating the pupil during fundus examination may delay early detection of macular and retinal diseases. In congenital coloboma, retinal tears or detachment may occur within the choroidal defect, making regular fundus examinations important.
Congenital Factors
Acquired Factors
The following examinations are necessary for preoperative evaluation of iris suture surgery.
| Examination | Purpose | Details |
|---|---|---|
| Slit-lamp microscopy | Evaluation of iris defect | Location, size, and shape of the defect. Presence of transillumination defects. |
| Anterior segment OCT (AS-OCT) | Detailed evaluation of iris structure and anterior chamber angle | Confirmation of iris thickness, defect extent, and IOL position. |
| Fundus examination | Evaluation of complications | Confirmation of choroidal coloboma, retinal coloboma, and optic nerve coloboma (in congenital cases). |
| Corneal endothelial cell examination | Preoperative baseline | Measurement of corneal endothelial cell density by specular microscopy |
| Intraocular pressure measurement | Confirmation of glaucoma comorbidity | Risk assessment of postoperative intraocular pressure elevation |
| Medication history taking | Identification of drugs causing IFIS | History of α₁-blocker (tamsulosin, etc.) use is most important |
| Systemic examination | Confirmation of congenital syndromes | Evaluation of related diseases such as CHARGE syndrome (heart disease, choanal atresia, hearing loss) |
Preoperative simulation: Using the iris cerclage as a landmark, confirm the location of suture placement and preoperatively assess whether the iris can be brought together without tension during ligation.
This section is the core of this article and details the technique of iris suturing.
Conservative Management
Tinted contact lenses (cosmetic CL)
Spontaneous reduction with mydriatics (for iris capture: attempt spontaneous reduction in supine position)
Observation (for mild pupillary distortion with minimal symptoms)
Iris Suturing (Pupilloplasty)
Indications: Partial iris defect, paralytic mydriasis (sequelae of IFIS or after glaucoma attack), sufficient remaining iris tissue
Suture material: 10-0/9-0 polypropylene (Prolene) suture
Features: No special instruments required, easily selected in Japan
Artificial Iris Device (→ separate article)
Indications: Extensive iris damage, iris atrophy precluding suturing, congenital aniridia
Note: Artificial iris and iris-fixated IOLs are not yet approved in Japan (as of 2024)
Forced suturing risks iris rupture; consider artificial iris devices for extensive damage cases
Choose from the following three methods depending on the situation.
| Knotting Method | Principle | Features |
|---|---|---|
| Siepser slipknot technique2) | Performed only through side ports. The suture on the iris is pulled out with a hook/forceps to form a loop, then the end is passed through the loop twice and tied outside the eye. | High flexibility in knot placement. Care is needed as pulling the suture carelessly can damage the iris. |
| McCannel method3) | A long needle is passed through the main incision to puncture both ends of the iris and the limbus, then a double knot is tied outside the eye. | Easy to perform when the incision and knot placement are close. Simple procedure. |
| SFT method (single-pass four-throw)4) | The end is passed through the loop four times and tied in one go. | Efficient as the knotting operation inside and outside the anterior chamber is completed in one step. |
Conventional methods (incision of the superior healthy pupillary margin or simple suture below the coloboma) often leave pupillary irregularity or deviation. The following are improved techniques.
In cases with extensive iris damage or atrophic iris, forced suturing may only cause iris rupture and unnecessary trauma. Such cases are indications for prosthetic iris devices; refer to the Prosthetic-Iris-Devices article.
If mydriasis of approximately 6 mm or more remains after IOL insertion despite using miotics and iris traction, simultaneous pupilloplasty is indicated. In post-traumatic cases, simultaneous PEA + IOL + iris suture may be performed approximately 2 weeks after injury. However, if the surgery becomes complicated or decision-making is difficult, it is safer to choose a two-stage procedure.
In cases with extensive iris damage or severe iris atrophy, suturing itself may be difficult or impossible. Forced suturing may cause iris rupture and further damage to iris tissue. In such cases, implantation of a prosthetic iris device is an option. In Japan, prosthetic iris devices are currently not approved, so management at specialized facilities is necessary.
The optic cup surrounds the tissue that will become the ocular contents by folding in from above, finally closing at the bottom. If this closure is incomplete during the embryonic period, a typical iris coloboma occurs inferiorly (inferonasally). It may be accompanied by ciliary body coloboma, choroidal coloboma, and optic nerve coloboma. If congenital iris coloboma is associated with zonular deficiency, the lens becomes unstable, making cataract surgery difficult.
In blunt trauma, iridodialysis and sphincter rupture occur due to globe deformation. In penetrating trauma, direct iris damage and prolapse occur.
α₁-adrenergic receptor blockers (e.g., tamsulosin) induce atrophic degeneration of the iris dilator muscle. This degeneration is irreversible and cannot be prevented by preoperative discontinuation of the drug. The degenerated iris is fragile, increasing the risk of intraoperative damage, which may lead to postoperative pupil deformity.
Visual acuity is often good, but if the coloboma extends to the macula, visual acuity becomes poor. Retinal detachment may occur due to retinal tears within or at the edge of the choroidal coloboma, often leading to poor prognosis. When cataract is associated with congenital coloboma, surgery is often difficult due to microphthalmos, zonular deficiency, and poor dilation. Improved surgical techniques for iris coloboma (Cionni method, Ogawa method) have been reported to improve pupil roundness and centration 6)7).
Case reports have reported good outcomes with postoperative corrected visual acuity of 1.0 to 1.2. However, the degree of visual improvement depends on the cause and extent of iris damage and concomitant ocular diseases (e.g., retinal disease, corneal endothelial disorders). The main therapeutic effects of iris repair are often reduction of photophobia and glare, elimination of monocular diplopia, and cosmetic improvement rather than visual acuity improvement. In congenital coloboma involving the macula, there is a limit to visual improvement.