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Ординатура / Офтальмология / Английские материалы / LASIK and Beyond LASIK Wavefront Analysis and Customized Ablation_Boyd_2001

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ALL LASER LASIK WITH THE PULSION FS LASER

Figure 8-5: An uncut section of tissue is pre-programmed to create the hinge for the flap.

Marking the Cornea

-Mark the cornea with appropriate alignment markers.

-Center the eye between the lids and focus the laser.

Preparation

Step 1. Outer Tray.

Position tray with Pulsion PI label facing up, firmly grasp lower left corner and peel lid from left to right to reveal inner tray. Discard lid.

Step 2. Inner Tray.

To preserve sterility, remove inner tray while wearing sterile, powderless surgical gloves and complete steps 2 through 6.

Position inner tray with Pulsion PI label facing up, grasp lower right corner and peel lid from right to left to remove.

Step 3. Inspection.

Remove applanation lens and suction ring assembly from tray, and place onto sterile field. Inspect all parts for damage or disconnection. Do not attempt to use any damaged product.

Figure 8-6: Lid speculum is applied to open the lids to a comfortable position.

Application

Step 4. Applanation Lens.

Grasp applanation lens by the upper rim with the contact lens facing downwards. Slide the applanation lens into the guides located at the bottom of the objective lens assembly on the Pulsion FS Laser. Lock the lens assembly by turning the locking mechanism upward. When the applanation lens is properly seated, a slight click should be heard. (Figure 8-7)

Remove protective cap on applanation lens and inspect through the operating microscope for scratches. A scratched applanation lens should not be used.

Contents

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Section 6

Section 7

Subjects Index

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Figure 8-7. Applanation lens is properly seated.

LASIK AND BEYOND LASIK 121

Chapter 8

 

 

Step 5.

Suction Ring Assembly.

Application

The suction ring assembly serves two func-

Fully depress the syringe plunger and place

tions:

 

the limbal suction ring onto the cornea, centering over

1)

Fixating the globe and

the pupil. Apply a slight downward pressure to the

2)Rigidly coupling the globe to the apring, and then release the plunger allowing the suc-

planation lens. The suction ring assembly consists of a limbal suction ring mounted on the bottom of an actuating cylinder assembly. The suction ring attaches to the limbus by means of low suction applied through a syringe and intraocular pressure increase to around 30 mmHg. (Figure 8-8)

tion ring to firmly affix to the eye. (Figure 8-9).

Step 6. Applanation Procedure

With the eye fixated, the laser’s delivery system must then be properly centered over the suction ring assembly opening (Figure 8-10). This is accomplished by manipulation of the x and y joystick controls located on the laser’s control panel. Once centered over the opening, grasp the two molded levers on the suction ring assembly and gently squeeze to expand the opening in the cylinder wide enough to accommodate the apex of the applanation lens. Slowly lower the delivery device using the z joystick control, gently guiding the applanation lens through the cylinder while holding the suction ring assembly open (Figure 8-11). When the cornea is fully applanated and the lens is well centered in the suction ring assembly, release the molded levers to allow the suction ring assembly to “grip” the applanation lens. The resection may now be initiated. (Figures 8-12, 8-13)

Figure 8-8. The suction ring attaches to the limbus with low suction applied through a syringe.

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Section 7

Subjects Index

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Figure 8-9. Surgeon applies a slight downward pressure to the

Figure 8-10. The laser’s delivery system must be centered over

ring, and then releases the plunger allowing the suction ring to

the suction ring assembly opening.

firmly affix to the eye.

 

122 SECTION II

ALL LASER LASIK WITH THE PULSION FS LASER

Figure 8-11. Surgeon slowly lowers the delivery device using the z joystick control and gently guiding the applanation lens through the cylinder while holding the suction ring.

Releasing the Cornea

When the resection is complete, depress the syringe plunger to release the cornea from suction. Utilize the z joystick on the control panel to raise the delivery device from the eye. Lift the suction ring assembly from the eye, release lens assembly lock and remove the applanation lens by grasping the cone and sliding it away from the objective. Depress the “Home” button on the control panel to raise the delivery device and safely remove the patient from the surgical field. Discard the Pulsion PI components in an appropriate receptacle.

Flap elevation and Excimer Laser Ablation

The patient may be safely switch to the Excimer Laser for Refractive ablation

The corneal flap is lifted superiorly with curved forceps (Figure 8-14); the laser focus is achieved over the pupillary center. At this point, the surgeon can proceed with the ablation of stromal bed (Figures 8-15 and 8-16).

Figure 8-12. Intrastromal resection.

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Section 7

Figure 8-13. Cornea is fully applanated and the lens is well Subjects Index centered in the suction ring

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Figure 8-14. The corneal flap is lifted with curved forceps.

LASIK AND BEYOND LASIK 123

Chapter 8

Figure 8-15. The laser focus is achieved over the pupillary center.

Reposition of the Flap

When the ablation is complete, the corneal flap is replaced onto the stromal bed using the cannula starting superiorly (Figures 8-17 and 8-18). The

Figure 8-16. Surgeon can proceed with the ablation of stromal bed.

cannula is placed underneath the flap and irrigation is completed to clear any remaining debris from the interface as well as allowing BSS under the flap to facilitate “floating” back into its original position. (Figures 8-19 and 8-20)

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Figures 8-17 & 8-18. The corneal flap is replaced onto the stromal bed using the cannula.

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Figures 8-19 & 8-20. The cannula is placed underneath the flap and irrigation is completed to clear any remaining debris from the interface.

124 SECTION II

ALL LASER LASIK WITH THE PULSION FS LASER

Figure 8-21. The Merocel sponge is moistened and squeezed dry and then used to “paint the flap” in the direction of the hinge.

The Merocel sponge is moistened and squeezed dry and then used to “paint the flap” in the direction of the hinge (Figure 8-21).

The flap is inspected to reassure that there are no wrinkles and for proper position by making sure an identical distance between the gutter and keratectomy edge is present all over the flap circumference. Depressing the peripheral “non flap” cornea with closed blunt 0.12 forceps completes a Slade’s striae test. When striae test is positive around the flap edge appropriate apposition has been achieved. During this phase it is recommended to keep a BSS drop over the central corneal epithelium to keep it wet. There is no specific waiting time with this technique, but we recommend waiting 3-5 minutes before removing the speculum.

Figure 8-22. One day Postoperative.

The case is completed by carefully removing the speculum. When doing this step, make sure to lift and close the speculum at the same time to avoid displacement of the flap.

Patient is then instructed to blink normally, and is observed through the microscope. The flap should remain in the same position and appear adhered to the cornea bed.

Postoperative Care

Immediately postoperatively, several drops of an antibiotic are instilled. The eye is not taped or shielded. The patient is asked to follow the home care instructions (Figure 8-22).

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Subjects Index

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LASIK AND BEYOND LASIK 125

LIMITATIONS AND CONTRAINDICATIONS OF LASIK

Chapter 9

LIMITATIONS AND CONTRAINDICATIONS

OF LASIK

Gregg Feinerman, M.D., Tim Peters, M.D., Jason Butler, Kim Nguyen

The belief that any one refractive procedure is best for all ranges of refractive error places patients at risk for a poor outcome. Laser in situ keratomileusis (LASIK), like any surgical procedure, has its limitations. It is essential for the refractive surgeon to understand the limitations of LASIK when performing preoperative exams and counseling patients. During the preoperative assessment the surgeon can identify specific measurements that disqualify patients from LASIK, thus preventing suboptimal postoperative results.

Patient History

At our center we offer LASIK to patients who are at least 18 years of age and have two or more years of refractive stability. The range of correction varies depending on the patient’s corneal thickness and pupil size; but we generally correct between – 12.00 to +4.00 diopters of ametropia with LASIK. The ocular history should include details regarding medications, allergies, and any previous ocular surgery or infection (e.g. Herpes Simplex Virus). Ocular Herpes Simplex is a contraindication to LASIK because the surgery may induce reactivation. Questions regarding recurrent corneal erosion should be addressed, as these patients are more likely to have epithelial adherence problems during surgery. Patients with significant glaucoma should avoid LASIK due to the increased intraocular pressure resulting from the microkeratome. Patients with a history of

prior scleral buckling procedures have an increased risk for inability to achieve proper suction and proper elevation of the intraocular pressure with the suction ring.

Additionally, a thorough medical history should include systemic conditions such as diabetes mellitus, collagen vascular disorders, or pregnancy, as the healing process may be affected. Pregnant or lactating women should postpone LASIK until after their first menstrual period postpartum. Diabetics with unstable blood sugars or significant diabetic retinopathy should be excluded from refractive surgery. Additionally, diabetics may be at higher risk for postoperative infection, epithelial adherence problems, and dry eye. Collagen vascular disease may predispose patients to dry eye and corneal melting.

Patients with inappropriate expectations should be identified preoperatively to avoid postoperative disappointments. For example, patients with amblyopia should be informed that refractive surgery would not improve their best corrected visual acuity. It is also important to address the possibility of nocturnal halos, especially in patients with high correction and/or large pupils.

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Exam

When first examining the patient, it is wise to note the palpebral fissure size. If the patient has very deep-set eyes or narrow palpebral fissures, they should be informed that they might have some intra-

LASIK AND BEYOND LASIK

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Chapter 9

Figure 9-1: Nidek MK 2000 Microkeratome

operative exposure problems. Smaller footprint microkeratomes, such as the Nidek MK 2000 may be helpful in such cases (Fig 9-1). Otherwise, PRK or a possible lateral canthotomy can be discussed in advance so the patient is aware of the possible alternatives. Patients with incomplete eyelid closure are at risk of flap dislocation, and should not undergo refractive surgery. Keratitis Sicca should be diagnosed and treated preoperatively with adequate pre and postoperative artificial tears. Punctal plugs should also be considered preoperatively. Blepharitis should be treated prior to surgery because it may predispose patients to an increased risk for infections or infiltrates.

Computerized corneal topography is performed on all of our refractive surgery candidates to screen for keratoconus, pellucid marginal degeneration, and other corneal disorders (Figs 9-2 & 9-3). It is also helpful to obtain ORBSCAN II topographies in high ametropes because it provides measurements of the anterior chamber depth for phakic intraocular lens implantation. (Fig 9-4)

After completing corneal topography, manual keratometry is measured. The results are compared to the manifest refraction and topographical simulated keratometry to identify lenticular cylinder. It is also important to calculate the theoretical postoperative keratometry prior to surgery in order to prevent the cornea from becoming excessively flat or steep. In myopic treatments we try to avoid creating postoperative corneal curvatures less than 34 diopt-

Figure 9-2: Keratoconus

Note the inferior steepening OS on the keratometric

Contents

 

map with a mean central corneal power of 44.78 D. There is

Section 1

also more than 3.00 D of variability in corneal power over the

 

central 3mm zone. Thinning was found on pachymetry inferi-

Section 2

orly OS.

 

 

 

Section 3

 

 

 

 

Section 4

 

 

Section 5

 

 

Section 6

 

 

Section 7

 

 

Subjects Index

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Figure 9-3: Pellucid Marginal Degeneration

Note the characteristic loop cylinder pattern on this patient with pellucid marginal degeneration.

ers. For hyperopic treatments we do not steepen the cornea beyond 48 diopters. Iatrogenic keratoconus with apical stromal scarring has occurred after hyperopic LASIK when the postoperative curvature exceeds 48 diopters.1

128 SECTION II

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Figure 9-4: ORBSCAN II Corneal Topographer

When reviewing the preoperative keratometry measurements, it is also important to consider that there is an increased likelihood of a buttonhole when performing LASIK on corneas with a preoperative curvature greater than 46 diopters (Fig 9-5). Additionally, there is an increased likelihood of free caps in large flat corneas (corneal curvature is less than 41 diopters) due to the smaller than usual area of applanation as the microkeratome pass is performed. This may be due to the interaction of the suction ring and microkeratome with the globe.2 . Although this data was predominantly determined with the Chiron ACS, it should be kept in mind regardless of the microkeratome used.

Pupil size in dim and room light is carefully measured and recorded. It is helpful to document the nocturnal pupil size with the Colvard Infrared Pupillometer. Patients with large pupils should be counseled regarding pupillary induced optical aberrations such as nocturnal halos, glare, and decreased contrast sensitivity. In our center we pay particular attention to pupil size in myopic patients with greater than 5 mm pupils in room light or 7 mm in dim illumination. This is even more important in those with

Figure 9-5: Buttonhole following LASIK Retroillumination

Figure 9-6: Toric IOL

higher myopic refractive errors (greater than 5 diopters). In hyperopic patients we avoid treating patients with greater than 6 mm pupils in dim illumination because the effective optical zone is smaller.

On slit lamp exam the surgeon should check for corneal dystrophies. For example, patients with anterior basement membrane dystrophy are likely to have shifted corneal epithelium intraoperatively. They are also more likely to suffer from recurrent corneal erosions exacerbated postoperatively. The slit lamp exam should also include an assessment of the lens clarity. In our practice any patient over 50 with lenticular changes is counseled about refractive lensectomy. Significant lenticular changes include more than 2+ nuclear sclerosis, any posterior subcapsular cataract, or cortical changes. A toric IOL is considered in patients with greater than 1.5 diopters of astigmatism (Fig 9-6). Astigmatic keratotomy alone can be considered in patients with more than 2

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LASIK AND BEYOND LASIK

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Chapter 9

Table 1-1

diopters of astigmatism with a spherical equivalent of -0.50 to +0.50 diopters. Where permissible, a phakic intraocular lens (phakic IOL) can be considered in patients younger than 50 that are not candidates for LASIK. If LASIK is contraindicated, phakic IOLs can be offered to patients with hyperopia or moderate to high myopia if the anterior chamber depth is sufficient.

Iatrogenic keratoectasia following LASIK has been reported.3 Thus, it is important to measure the corneal thickness prior to LASIK to help ensure that there is adequate residual stromal bed thickness postoperatively. We measure corneal thickness with the Mentor Pach-Pen instrument (Bio-Rad, Santa Ana California) or the ORBSCAN II topography unit. It is currently accepted that the residual thickness in the stromal bed after LASIK should be at least 200 m, preferably 250 m.4 The residual corneal stromal bed thickness is calculated by first determining the ablation depth with the Munnerlyn formula (Depth of ablation = desired refractive change * optical zone2/3). The calculated ablation depth is added to the thickness of the microkeratome depth plate. Next, the total is subtracted from the patient’s preoperative minimal corneal thickness. This estimate

is useful, but the actual depth of ablation depends on the laser used and type of treatment performed (Table 1-1). For example, cross cylinder ablations (ablations done in plus and minus cylinder) remove less corneal tissue.5 If calculations reveal borderline residual stromal bed thickness, then it should be discussed with the patient prior to primary LASIK. Additionally, the patient is informed that an enhancement may not be possible. The optical zone becomes a limiting factor in higher corrections (Table 1-2). Table 1-3 and Table 1-4 demonstrate a spreadsheet formula created to determine the largest optical zone achievable based on the Munnerlyn Formula, microkeratome depth plate, and a correction/stromal bed limit of 250 m.

Several unique aspects of hyperopic LASIK treatments should be considered preoperatively. Firstly, the hinge location may have an effect on astigmatism. The astigmatic ablation for hyperopia with against the rule astigmatism occurs along the vertical axis (induces steepening along the short axis). For with the rule hyperopia and astigmatism treatments, the astigmatic ablation occurs along the horizontal axis. Thus, the surgeon should consider creating a superior hinge flap when treating hyperopia

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130 SECTION II

LIMITATIONS AND CONTRAINDICATIONS OF LASIK

Table 1-2

Calculation of Ablation Depth Using Munnerlyn Formula

Optical Zone Diameter

 

 

5.5

6.0

6.5

7.0

7.5

 

0.50

5.04

6.00

7.04

8.17

9.38

 

0.75

7.56

9.00

10.56

12.25

14.06

 

1.00

10.08

12.00

14.08

16.33

18.75

 

1.25

12.60

15.00

17.60

20.42

23.44

 

1.50

15.13

18.00

21.13

24.50

28.13

 

1.75

17.65

21.00

24.65

28.58

32.81

 

2.00

20.17

24.00

28.17

32.67

37.50

 

2.25

22.69

27.00

31.69

36.75

42.19

 

2.50

25.21

30.00

35.21

40.83

46.88

 

2.75

27.73

33.00

38.73

44.92

51.56

 

3.00

30.25

36.00

42.25

49.00

56.25

 

3.25

32.77

39.00

45.77

53.08

60.94

 

3.50

35.29

42.00

49.29

57.17

65.63

 

3.75

37.81

45.00

52.81

61.25

70.31

 

4.00

40.33

48.00

56.33

65.33

75.00

 

4.25

42.85

51.00

59.85

69.42

79.69

 

4.50

45.38

54.00

63.38

73.50

84.38

 

4.75

47.90

57.00

66.90

77.58

89.06

Diopters

5.00

50.42

60.00

70.42

81.67

93.75

 

5.25

52.94

63.00

73.94

85.75

98.44

 

5.50

55.46

66.00

77.46

89.83

103.13

 

5.75

57.98

69.00

80.98

93.92

107.81

 

6.00

60.50

72.00

84.50

98.00

112.50

 

6.25

63.02

75.00

88.02

102.08

117.19

 

6.50

65.54

78.00

91.54

106.17

121.88

 

6.75

68.06

81.00

95.06

110.25

126.56

 

7.00

70.58

84.00

98.58

114.33

131.25

 

7.25

73.10

87.00

102.10

118.42

135.94

 

7.50

75.63

90.00

105.63

122.50

140.63

 

7.75

78.15

93.00

109.15

126.58

145.31

 

8.00

80.67

96.00

112.67

130.67

150.00

 

8.25

83.19

99.00

116.19

134.75

154.69

 

8.50

85.71

102.00

119.71

138.83

159.38

 

8.75

88.23

105.00

123.23

142.92

164.06

 

9.00

90.75

108.00

126.75

147.00

168.75

 

9.25

93.27

111.00

130.27

151.08

173.44

 

9.50

95.79

114.00

133.79

155.17

178.13

 

9.75

98.31

117.00

137.31

159.25

182.81

 

10.00

100.83

120.00

140.83

163.33

187.50

Formula: Ablation Depth = (Diopters*((Optical Zone)^2))/3

This chart gives an approximate ablation depth for a given correction and optical zone. Surgeons should consider these calculations a rough estimate of ablation depth. The laser software calculations of ablation depth should also be checked in cases where the calculation results in a residual stromal bed thickness close to 250um.

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Section 4

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Section 7

Subjects Index

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LASIK AND BEYOND LASIK

131