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STAGE III
CATARACT AND REFRACTIVE SURGERY SUBDIVISION
2018
CHAPTER I
INTRODUCTION
Benefits and risks must be considered from each of the procedure so that
secondary IOL implantation could be a reasonable means of improving the functional
acuity in selected aphakic patients. This paper will further discuss about the pre
operative assessment of the eye, classification, surgical techniques, and complications
of various methods of secondary IOL implantation in aphakic eye.
2
CHAPTER II
Secondary IOL implantation refers to IOL insertion at a time remote from the
initial cataract extraction and is performed when primary implantation failed due to
intraoperative complications (such as rupture of the posterior capsule, accidental
aspiration of the capsular bag, etc.) or when cataract extraction was done without lens
implantation at the first instance. Some important issues in secondary IOL
implantation are the location of new IOL placement and the method of fixation in that
location. There are several alternatives for secondary IOL implantation which
depends on preoperative status of the eye. Those lenses are devided into anterior
chamber IOL and posterior chamber IOL : 3,4
1. Angle-supported AC IOL
2. Iris Claw AC IOL
3. Standard capsular bag PC IOL
4. Sulcus placement PC IOL.
5. Peripheral iris suture-fixated PC IOL.
6. Transscleral-fixated PC IOL.
3
There are several issues to consider when deciding which type of IOL to use
for a secondary implantation. Secondary IOL implantation after an ICCE must be
either placed in the anterior chamber, sutured to the iris, or sutured in the posterior
chamber because of the lack of posterior capsular support. After an ECCE that has
left a posterior capsule, the surgeon can, theoretically, implant a PC IOL. However,
even in the rare instances in which the posterior capsule is open, without fused walls,
it is always necessary to have ciliary sulcus placement of secondary posterior
chamber lenses because capsular bag fixation is practically impossible. 1,4
It is important to evaluate some key features of the eye before placing an IOL
into an aphakic eye. Evaluation may include a complete eye examination. Best
corrected visual acuity, the cornea, anterior chamber angle, iris and pupil, posterior
capsule adequacy, posterior segment, and intraocular pressure should be evaluated
carefully before secondary IOL implantation. Gonioscopy, biometry, and endothelial
cell counts should also be done before surgery.3,5,6
4
chamber IOL implantation is possible. Since the footplates of an anterior chamber
lens rest in the recess of an open angle, areas of peripheral anterior synechiae should
be noted and avoided as sites of implantation. Iris and pupil have to be assessed
carefully. The previous iridectomy should be kept away from the path of lens
insertion. 3,4,6
5
CHAPTER III
An anterior chamber IOL has an optic that rests in the anterior chamber and
haptics that rest and fixate in the anterior chamber angle. Gonioscopy is especially
important and valuable to evaluate the anterior chamber angles if an anterior chamber
IOL is contemplated. Because the footplates of an anterior chamber lens rest in the
recess of an open angle, areas of peripheral anterior synechiae should be noted and
avoided as sites of implantation. 3,4 `
Those original designs have since been replaced by lenses with flexible, open-
loop haptics (Kelman multiflex style) that have proved to be safer and have produced
better long-term visual outcomes. Three-point and four-point flexible Kelman style
anterior chamber IOLs are the most frequently used anterior chamber lenses for
secondary implants (Fig. 1). 5,11
6
Figure 1. Kelman AC IOL with flexible 4-point fixation. 5
Despite the flexibility of the multiflex haptics, lens sizing is critical for safe
AC IOL implantation. Many surgeons use the rule of measuring the horizontal
“white-to-white plus one” millimeter (1 mm greater than the measurement of the
corneoscleral junction from 3 to 9 o’clock horizontally) to determine overall AC IOL
diameter. A lens that is too large or implanted in the iris root may cause ocular
discomfort, angle erosion and peripheral anterior synechia. A lens that is too small
will not fixate and may move back and forth, predisposing the patient to progressive
endothelial cell loss and uveitis. 4,9
7
implantation (Fig. 2a). When the anterior hyaloid face is intact but prolapsing into the
anterior chamber, it can usually be pushed posteriorly by a bolus of sodium
hyaluronate. 3,8,9
Once the IOL is already inserted, it can be rotated as necessary to avoid haptic
contact with any pre-existing PAS or the iridectomy (to prevent haptic migration
through it) and until the desired lens position in the angle is achieved correctly. This
is accomplished by gently retracting the distal haptic, rotating the lens, and then
releasing the haptic. This process is repeated as necessary for either haptic until the
desired lens position is achieved. If not already present, a peripheral iridectomy is
made to eliminate the risk of pupillary block. The peripheral iridectomy is typically
made superiorly, far from the lens haptic to minimize haptic prolapse throught
iridectomy. The anterior chamber intraocular lens is released and allowed to slide into
its appropriate anatomic position (Fig 2b). After proper IOL positioning is ensured,
the wound is sutured, the viscoelastic is manually removed and replaced with
balanced salt solution, and the conjunctiva is closed (Fig. 2c).4, 9
a b c
In order to move the IOL further away from the endothelium and to avoid
damage to angle structures, Worst proposed an alternative design for the anterior
chamber intraocular lens in 1977 termed the “iris claw” lens. In this design, the lens is
8
fixated anterior to the iris plane by two diametrically opposing haptic claws that
incarcerate a portion of mid-peripheral iris, where the iris is less vascularized and less
reactive. One of the latest versions of the iris-fixated AC IOL designed is the Artisan
aphakic IOL, which have a substantially different lens design than previous
generations and is associated with fewer complications (Fig. 3).9,13
Iris-claw lens is easy to place and associated with a good visual outcome and
a low incidence of intraoperative and postoperative complications. Artisan aphakic
IOL has been largely used in adult cataract surgery. To ensure proper horizontal
alignment of the lens claws for reliable lens centration, a laser mark can be
preoperatively applied to the iris at the sites where the claws should be anchored,
usually 4 mm off center horizontally at each side of the pupil. 4,14
9
viscoelastic substance, such as sodium hyaluronate (Fig. 4a). After inserting the IOL,
center it, and place the haptics over the laser marks. Place the claws directly over the
laser spots and clip the lens to the iris fold. Anchor the second haptic in the same
manner (Fig. 4b).4,14
After the lens is properly positioned (Fig. 4c), create a superior peripheral
iridectomy then suturing the corneal wound with interrupted 10-0 nylon sutures
Thoroughly irrigate and aspirate the sodium hyaluronate. 4,9,14
Figure 4. Worst iris-claw lens implantation. a. Inserting worst iris-supported claw lens
insertion through a 5.5 mm corneoscleral incision. b. Placing the haptics over the laser
marks. c. Properly positioned iris-claw lens. 4,14
First, the capsular anatomy is inspected, both visually and tactilely, to assess
its integrity. This is initially accomplished by retracting the iris 360 degrees and
determining the extent of intact capsule and zonules. A viscoelastic then is injected to
gently tease open the fused leaflets of the anterior and posterior capsule. Much of this
10
dissection can be performed passively, because the capillary action of the viscoelastic
filling the bag usually separates the capsular surfaces. If resistance is encountered,
careful manipulation with a spatula or microhook may be necessary. If the capsule
cannot be safely reopened, it is best to desist and place a large foldable or one-piece
PMMA IOL in the ciliary sulcus. Once the lens is positioned within the capsular bag,
its centration and stability should be assessed. 9, 15
Secondary PC IOLs are often placed in the unsutured ciliary sulcus because
the capsular bag is usually collapsed and fibrotic at the time of secondary IOL
implantation. The capsular remnants should be thoroughly inspected before lens
insertion. Synechiae between the posterior iris and the capsule are often present and
may lead to decentration or even impede insertion of the loops of the PC IOL. A
viscoelastic device is injected between the iris and anterior capsule; any residual
adhesions are bluntly dissected with the cannula or a spatula, taking care not to tear
the posterior capsule or disinsert the zonules (Fig. 5a). 4,16, 18
The optimal lens for secure sulcus fixation is a large optic (6.5 mm or more),
one-piece polymethyl methacrylate (PMMA) IOL with an overall diameter of 13.5 to
14 mm. However, a foldable IOL with a 6-mm optic and 13-mm overall length allows
insertion through a smaller wound. The IOL power should be reduced by 0.5 to 1.0 D
for sulcus-positioned versus capsular bag PC IOL. The lens can be inserted to the
posterior chamber between the iris and the capsule through a 6-7 mm limbal insicion
(Fig. 5b). Insert the lens into the posterior chamber between the iris and the capsule.
(Fig.5c). 4,16,18
11
Figure 5. PC IOL insertion in the ciliary sulcus. a. Separate any adhesions between the iris
and the capsule. b. Insert the lens into the posterior chamber between the iris and capsule. c.
Retract the iris while the proximal loop is placed in the posterior chamber.4
IOL is inserted through main wound (12 o’clock preferred). Size of main
wound will depend on choice of foldable or nonfoldable IOL. As soon as the lens is
placed into the ciliary sulcus, an intracameral miotic agent (Miochol) is administered
so that the IOL optic can be captured through the pupillary space. Iris capture of the
optic stabilizes the lens and enables better visualization of the haptics, while the
12
haptics remain in the posterior chamber and will be outlined against the posterior
surface of the iris.3,17
Figure 6. McCannel iris suture fixation of a PC IOL. a, Microhook are introduced through two
paracentesis openings and used to elevate the optic above the iris plane, capturing the optic in the pupil
while the haptics remain in the posterior chamber. b, A 10-0 polypropylene suture on a fine long
needle is passed through the paracentesis, penetrates the iris in the periphery just in front of the haptic,
which is indenting the iris stroma, exits the iris as soon as possible after the haptic, and then is driven
up through the peripheral clear cornea. c, Same maneuver is performed under the opposite haptic. d,
With both needles remaining in place behind the haptics, the successful capture of the haptics and
acceptable location of the IOL in the pupil are verified. E, Sutures are tied and cut inside the eye then,
microhook presses the intraocular lens (IOL) optic posteriorly back into the posterior chamber. F,
Pupil is round, and the IOL is well centered.3
The sulcus location is the most closely normal anatomic position of the
crystalline lens. The goal of scleral fixated PC IOL is to have the haptics resting in
13
the ciliary sulcus. Anatomic studies have shown that the ciliary sulcus is 0.83 mm
posterior to the limbus in the vertical meridian and only 0.46 mm posterior to the
limbus in the horizontal meridian. Because of their anatomic location, scleral-fixated
PC IOL have a theoretic advantage over other IOL's with regard to complications..3,9
Many different alternatives have been presented in the literature for placement
of transscleral-fixated PC lenses, either sutured or sutureless. Scleral-sutured lenses
can be sutured by passing the suture needle from the inside to the outside of the eye
(ab interno) and have the advantage of being faster (fig. 7), or by passing the needles
from the outside to inside of the eye (ab externo) that allows more precise needle
placement (fig. 8).9,11
Figure 7. Technique for the ab interno approach. a. The long needles are passed under the iris, aiming
for the inferior ciliary sulcus. Two needle passes are made for each haptic approximately 0.75 mm
posterior to the limbus under previously dissected scleral flaps . b. A second pair of short needle passes
is made under the superior iris for the suture to be tied to the second haptic. c. Girth hitch can be used
to attach the polypropylene suture loop to IOL haptic. This technique is more rapid than tying the
suture to the haptic. The suture can be attached to the IOL haptics before the transscleral needle passes,
14
but the surgeon must avoid tangling the long sutures. d. After exiting the eye under the previously
dissected scleral flaps, the sutures are tied securing the IOL into position. Appropriate suture tension is
important to avoid lens decentration. 3,9
(a) (b)
(c) (d)
Figure 8. Technique for the ab externo approach. a. The long, straight solid needle is passed through
the scleral flap approximately 0.75 mm posterior to the limbus. Inside the eye, the needle should exit at
the ciliary sulcus. A second hollow needle is passed from the opposite side of the eye. b. Solid needle
is “docked” inside the tip of the hollow needle, which has been passed through ciliary sulcus on the
opposite side. After docking, the pair of needles are withdrawn together from the eye, with the solid
needle inside the hollow needle. C. A hook is used to pull the suture out through a superior limbal
wound so that it can be tied to the IOL. D. Suture is cut, and each end is tied to IOL haptic. After the
IOL is placed into position, the scleral sutures must be anchored to the sclera. 3,9
15
glue. The glue has two main components that occur naturally in the blood : fibrinogen
and thrombin, which are kept separate before use. The glue also helps in sealing the
sclerotomy site which would otherwise act as a filtration site and cause hypotony.
The surgical proceduresof glued IOL is shown in figure 9.19
Figure 9. Procedures of glued IOL. a. Create two partial scleral thickness limbus based flaps about 2.5
mm × 2.5 mm, at 3 and 9’o clock position (180° opposite to each other) and sclerotomy done with a 22
G needle about 1 mm behind the limbus underneath the flap. b. A three-piece foldable IOL is then
injected into the eye and a glued IOL forcep, which is an end-opening forcep, introduced from the
sclerotomy site and the tip of the leading haptic is grasped, pulled and externalized beneath the flap. c.
Externalization of the trailing haptic from the other sclerotomy site. d. Two scleral pockets were
created with a 26 G needle in alignment with the sclerotomy wound along the edge of the scleral flap.
e. The haptics were tucked into the scleral pockets. f. The glue (one drop of fibrinogen preparation
followed by a drop of thrombin) was applied under the scleral flap after drying the area and pressed for
nearly one minute and followed by sealing the conjungtiva with the glue. 19
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CHAPTER IV
17
in mind, patient selection is important because a patient with extremely damaged
corneal endothelium could either undergo a secondary lens implantation or a
combined lens implantation and penetrating keratoplasty. 4,9,11
Centering of the IOL optic is technically more difficult when the lens is iris
fixated. Even if the lens is properly centered intraoperatively, decentration may occur,
and the lens may luxate either spontaneously or secondary to trauma if the fixation
bite is too shallow. By adjusting the manipulation procedure and ensuring enough iris
tissue clamped, the complication can be avoided. The size of clamped iris tissue
should be 1.5-2 mm to ensure the IOL fixation and decrease the incidence of lens
dislocation. 9,14
18
The most common postoperative complication after scleral-sutured PC IOL
implantation is persistent CME especially in scleral-sutured PC IOL. There also
appears to be a slightly greater risk of retinal detachment with scleral-sutured PC
lenses which reported to had a 2.7–5.4% risk of retinal detachment. The poor
positioning of the haptics with sutured PC lenses rather than in the ciliary sulcus may
increase the risk of retinal detachment. Also, transscleral sutures ought to increase the
risk of choroidal hemorrhage or effusion particularly in longer time of surgery. 9, 21
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CHAPTER V
CONCLUSION
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