- •Dedication
- •Preface
- •Acknowledgements
- •Contributors
- •Contents
- •1. Minimally Invasive Oculoplastic Surgery
- •1.1 General Points
- •1.2 Lower Lid Entropion
- •1.2.1 Introduction
- •1.2.2 Lower Lid Entropion Sutures
- •1.2.3 Lower Lid Entropion Botulinum Toxin
- •1.3 Lower Lid Ectropion
- •1.3.1 Introduction
- •1.3.2 The Royce Johnson Suture
- •1.3.3 The Pillar Tarsorrhaphy
- •1.4 Distichiasis
- •1.4.1 Introduction
- •1.4.2 Direct Excision of Lashes
- •1.5 Ptosis
- •1.5.1 Introduction
- •1.5.3 Anterior Approach – One Stitch Aponeurosis Repair
- •1.5.4 Supramid Brow Suspension
- •1.6 Lid Retraction
- •1.6.1 Introduction
- •1.6.2 Koornneef Blepharotomy
- •1.6.3 Botulinum Toxin
- •1.7 Lid Tumours
- •1.7.1 Mohs’ Micrographic Surgery
- •1.7.2 Lamella Sparing Tumour Excision
- •References
- •2. Minimally Invasive Conjunctival Surgery
- •2.1 Conjunctival Surgery
- •2.2 Conjunctivochalasis
- •2.2.1 Background of the Disease
- •2.2.2 Indication for Surgery
- •2.2.3 Basic Concept of Surgery
- •2.2.4 Surgical Procedure
- •2.2.5 Postoperative Follow-Up
- •2.3 Pterygium
- •2.3.1 Background of the Disease and the Concept of Minimally Invasive Surgery
- •2.3.2 Indication for Surgery
- •2.3.3 Basic Concept of Surgery
- •2.3.4 Surgical Procedures
- •2.3.5 A Biologic Adhesive for Sutureless Pterygium Surgery
- •2.3.6 Postoperative Follow-Up
- •2.4 Limbal and Conjuntival Dermoids
- •2.4.1 Background of the Disease
- •2.4.2 Basic Concept of Surgery
- •2.4.3 Surgical Procedure
- •2.4.4 Postoperative Follow-Up
- •2.5 Strabismus Surgery
- •2.6 Conclusion
- •References
- •3. Minimally Invasive Lacrimal Surgery
- •3.1 Introduction
- •3.1.1 Causes of Stenoses of the Lacrimal Drainage System
- •3.1.3 General Remarks Regarding Surgical Management
- •3.2 Endonasal Endoscopic (Microscopic) Dacryocystorhinostomy (EDCR)
- •3.2.1 Indication for EDCR
- •3.2.2 Surgical Technique
- •3.2.3 Silicone Stenting for EDCR
- •3.2.2.1 Silicone “Cones” (Lacrimal Duct Stent, Bess, Berlin)
- •3.2.4 Use of Mitomycin C for EDCR
- •3.2.5 Post-Operative Care After EDCR
- •3.2.6 Results of EDCR
- •3.3 Endonasal Endoscopic Laser Dacryocystorhinostomy (ELDCR)
- •3.3.1 Indications for ELDCR
- •3.3.2 Contraindications for ELDCR
- •3.3.3 Surgical Technique for ELDCR
- •3.3.4 Potential Problems with ELDCR
- •3.3.5 Post-Operative Care After ELDCR
- •3.3.6 Results of ELDCR
- •3.4 Dacryoendoscopy with Transcanalicular Laserdacryoplasty (TLDP)
- •3.4.1 Indication for TLDP
- •3.4.2 Contraindication for TLDP
- •3.4.3 Surgical Technique for TLDP
- •3.4.4 Results of TLDP
- •3.5 Microdrill Dacryoplasty (MDP)
- •3.5.1 Indication for MDP
- •3.5.2 Contraindication for MDP
- •3.5.3 MDP Procedure
- •3.5.4 Results of MDP
- •3.6 Balloon Dilatation
- •3.6.1 Indications for Balloon Dilatation
- •3.6.2 Anaesthesia for Balloon Dilatation
- •3.6.3 Surgical Technique with 2 mm or 3 mm Balloon for Incomplete Stenosis
- •3.6.3.1 Post-Operative Care
- •3.6.3.2 Complications
- •3.6.3.3 Results
- •3.6.4.1 Post-Operative Care
- •3.6.4.2 Results
- •3.6.4.3 Complications
- •3.7 Stent Placement
- •3.7.1 Indications for Stent Placement
- •3.7.3 Surgical Technique for Stent Placement
- •3.7.5 Results of Stent Placement
- •References
- •4. Minimally Invasive Corneal Surgery
- •4.1 Penetrating Keratoplasty
- •4.1.1 Introduction
- •4.1.2 Indications
- •4.1.3 Preoperative Evaluation of the Keratoplasty Patient
- •4.1.4 Preparation for Penetrating Keratoplasty
- •4.1.4.1 Eyelid Speculum
- •4.1.4.2 Scleral Fixation Rings
- •4.1.4.3 Large and Fine-Tipped Needle Holder
- •4.1.4.4 Toothed Forceps
- •4.1.4.5 Trephine Blades
- •4.1.4.6 Radial Marker
- •4.1.4.7 Cornea Punch
- •4.1.4.8 Cutting Block
- •4.1.4.9 Scissors
- •4.1.4.10 Cannulas and Blades
- •4.1.5 Preoperative Medications
- •4.1.6 Penetrating Keratoplasty Surgical Procedure
- •4.1.6.1 Placement of the Scleral Fixation Ring
- •4.1.6.2 Marking of the Host Cornea
- •4.1.6.3 Sizing of the Trephine
- •4.1.6.4 Trephination of the Host Cornea
- •4.1.6.5 Trephination of the Donor Cornea
- •4.1.6.6 Removal of the Host Cornea
- •4.1.6.7 Placement of the Donor Cornea Tissue in the Host Stromal Bed
- •4.1.6.8 Placement of the Cardinal Sutures
- •4.1.6.9 Completion of Suturing
- •4.1.6.10 Suture Techniques
- •4.1.6.11 Subconjunctival Medications
- •4.1.7 Intraoperative Complications
- •4.1.7.1 Scleral Perforation
- •4.1.7.2 Damage to the Donor Button
- •4.1.7.4 Posterior Capsule Rupture
- •4.1.7.5 Vitreous Loss
- •4.1.7.6 Anterior Chamber Hemorrhage
- •4.1.7.7 Choroidal Hemorrhage
- •4.1.8 Postoperative Management
- •4.1.8.1 Postoperative Immunosuppressive Regimen
- •4.1.9 Postoperative Complications
- •4.1.9.1 Wound Leaks
- •4.1.9.2 Epithelial Defects
- •4.1.9.3 Suture-Related Problems
- •4.1.9.4 Increased Intraocular Pressure
- •4.1.9.5 Post-Keratoplasty Astigmatism
- •4.1.10.1 Wedge Resections and Compression Sutures
- •4.1.10.2 Relaxing Incisions
- •4.1.10.3 LASIK
- •4.1.10.4 Photorefractive Keratectomy with Mitomycin C
- •4.1.11 Corneal Allograft Rejection
- •4.1.11.1 Host Risk Factors
- •4.1.11.2 Vascularized Corneas
- •4.1.11.3 Prior Graft Loss
- •4.1.11.4 Graft Diameter
- •4.1.11.5 Anterior Synechiae
- •4.1.11.6 Previous Intraocular Surgery
- •4.1.11.7 Herpes Simplex
- •4.1.12 Treatment of Allograft Rejection
- •4.1.13 Large Diameter Penetrating Keratoplasty
- •4.1.14 Summary
- •References
- •4.2 Descemet’s Stripping Endothelial Keratoplasty
- •4.2.1 Introduction
- •4.2.2 Descemet’s Stripping Endothelial Keratoplasty Surgical Technique
- •4.2.2.1 Donor Cornea Preparation
- •4.2.2.2 Host Cornea Preparation
- •4.2.2.3 Insertion of the Donor Cornea
- •4.2.3 Postoperative Medications
- •4.2.4 Donor Dislocation Risks
- •4.2.5 Repositioning Donor Tissue
- •4.2.6 Treatment of Rejection Episodes
- •4.2.7 Visual and Refractive Outcomes
- •4.2.8 Other Complications
- •4.2.9 Summary
- •References
- •4.3 Pterygium
- •4.3.1 Introduction
- •4.3.2 Treatment of Pterygium
- •4.3.3 Surgical Technique
- •4.3.3.1 Removal of the Pterygium
- •4.3.3.2 Harvesting the Conjunctival Autograft
- •4.3.3.3 Securing the Conjunctival Autograft
- •4.3.3.4 Fibrin Glue vs. Nylon Sutures
- •4.3.4 Postoperative Management
- •4.3.5 Recurrent Pterygium
- •4.3.6 Other Techniques in Pterygium Removal
- •4.3.6.1 Bare Scleral Technique
- •4.3.6.2 Adjunctive Agents
- •Mitomycin C
- •Beta-Irradiation
- •4.3.6.3 Amniotic Membrane Transplantation
- •4.3.7 Complications in Pterygium Removal
- •4.3.8 Summary
- •References
- •5. Minimally Invasive Refractive Surgery
- •5.1 Trends in Refractive Surgery
- •5.2 Introduction
- •5.3 Cornea Refractive Surgery
- •5.3.1 Laser In Situ Keratomileusis (LASIK)
- •5.3.1.1 Advances in Flap Creation Technology
- •Microkeratomes
- •Femtosecond Laser
- •5.3.1.2 Technological Advances in Laser Delivery Platforms
- •5.3.1.3 Faster Excimer Lasers
- •5.3.1.4 Reduction of Collateral Thermal Tissue Damage
- •5.3.1.5 Advanced Eye Trackers
- •5.3.2 PRK and Advanced Surface Ablations (ASA)
- •5.3.2.1 Decrease Thermal Load on the Cornea
- •5.3.2.2 Use of Wound-Healing Modulators
- •5.3.2.3 Trend Towards EPI-LASIK
- •5.3.3 Summary
- •5.4 Intraocular Refractive Surgery
- •5.4.1 Phakic Intraocular Lens Surgery
- •5.4.1.1 Advances in Diagnostic Equipment
- •5.4.1.2 Types of Phakic Intraocular Lens
- •5.4.1.3 Kelman-Duet Phakic Intraocular Lens
- •Lens Design
- •Surgical Technique
- •Pre-Operative Preparation
- •Operative Procedure
- •Post-Operative Care
- •Results
- •Refractive Outcomes
- •Corneal Endothelium
- •5.4.1.4 Visian Implantable Collamer Lens
- •Lens Design
- •Surgical Technique
- •Pre-Operative Preparation
- •Operative Procedure
- •Post-Operative Care
- •5.4.1.5 Results
- •5.4.2 Summary
- •5.5 Lens and Cataract Surgery
- •5.5.2 The Ideal MICS Intraocular Lens
- •5.5.2.1 Aspheric Intraocular Lenses
- •5.5.2.2 Toric Intraocular Lenses
- •5.5.2.3 ACRI.LISA 366D and ACRI.LISA TORIC 466TD
- •Lens Design
- •5.5.2.4 Surgical Technique
- •Operative Procedure
- •Post-Operative Care
- •5.5.2.5 Results
- •5.5.3 Summary
- •5.6 The Future: Beyond the Horizon of Refractive Surgery Today
- •Reference
- •6. Minimally Invasive Strabismus Surgery
- •6.1 Introduction
- •6.2 Nonsurgical Treatment
- •6.4 Rectus Muscle Procedures
- •6.4.1 MISS Rectus Muscle Recession
- •6.4.2 MISS Rectus Muscle Plication
- •6.4.3 Parks’ Rectus Muscle Recession
- •6.4.4 Parks’ Rectus Muscle Plication
- •6.4.5 MISS Rectus Muscle Posterior Fixation Suture
- •6.4.7 MISS Rectus Muscle Repeat Surgery
- •6.4.8 MISS Rectus Muscle Transposition Surgery
- •6.5 Oblique Muscle Procedures
- •6.5.1 MISS Inferior Oblique Muscle Recession
- •6.5.2 MISS Inferior Oblique Muscle Plication
- •6.5.3 MISS Superior Oblique Muscle Recession
- •6.5.4 MISS Superior Oblique Muscle Plication
- •6.5.6 Mühlendyck’s Partial Posterior Superior Oblique Tenectomy for Congenital Brown’s Syndrome
- •6.6 Postoperative Handling
- •6.7.1 Intraoperative Complications
- •6.7.2 Postoperative Complications
- •6.8 Suggestions on How to Start Doing MISS
- •6.8.1 Instruments Suitable for MISS
- •6.8.2 Suture Materials Used for MISS
- •6.8.3 General Remarks Regarding MISS Procedures
- •6.8.4 MISS Dose–Response Relationships
- •References
- •7. Minimally Invasive Iris Surgery
- •7.1 Instrumentation
- •7.2 Sutures
- •7.3 Surgical Principles of Iris Suturing
- •7.3.1 Mobilization
- •7.3.2 Intraocular Suturing and Knot Tying
- •7.3.3 Reattachment of Iris to Sclera
- •7.3.4 Pupil Repair
- •7.3.5 Adjunctive Pupil Repair Techniques
- •References
- •8. Minimally Invasive Glaucoma Surgery
- •Introduction
- •8.1.1 Introduction to Deep Sclerectomy
- •8.1.2 Anesthesia
- •8.1.3 Surgical Technique
- •8.1.3.1 Preparation
- •8.1.3.3 Deep Flap Preparation
- •8.1.3.5 Peeling of Schlemm’s Canal and Juxtacanalicular Meshwork
- •8.1.3.6 Drainage Device
- •8.1.3.7 Wound Closure
- •8.1.4 Postoperative Management and Medication
- •8.1.4.1 Medication
- •8.1.4.2 Management
- •8.1.5 Adjunctive Treatments
- •8.1.5.1 Bleb Needling
- •8.1.5.2 Nd:YAG Goniopuncture
- •8.1.6 Complications and Management
- •8.1.6.1 General
- •8.1.6.2 Perioperative Complications
- •8.1.6.3 Early Postoperative Complications
- •8.1.6.4 Late Postoperative Complications
- •Open-Angle Glaucoma
- •Pigmentary Glaucoma
- •Pseudoexfoliation Glaucoma
- •Aphakic Glaucoma
- •Sturge–Weber Syndrome
- •Glaucoma Secondary to Uveitis
- •Congenital and Juvenile Glaucoma
- •Narrow-Angle Glaucoma
- •Posttrauma Angle-Recession Glaucoma
- •Neovascular Glaucoma
- •Narrow-Angle Glaucoma in a Young Patient
- •Pseudophakic Glaucoma with an A/C IOL
- •8.2.1.4 Preoperative Considerations
- •8.2.2 Anesthesia
- •8.2.4 Postoperative Management and Medication
- •8.2.5 Outcomes and Comparison with Other Techniques
- •8.2.6 Complications and Management
- •8.2.6.1 General
- •8.2.6.4 Summary and Key Points
- •References
- •8.3 New Minimally Invasive, Sclerothalamotomy Ab Interno Surgical Technique
- •8.3.1 Introduction to the Sclerothalamotomy Ab Interno
- •8.3.1.1 Indications for the Sclerothalamotomy Ab Interno
- •8.3.2 Anesthesia
- •8.3.3 Surgical Technique
- •8.3.3.1 Preparation
- •8.3.3.2 Diathermy Probe Insertion
- •8.3.4 Postoperative Management and Medication
- •8.3.5 Outcomes and Comparison with Other Techniques
- •8.3.6 Complications and Management
- •8.3.6.1 General
- •8.3.6.3 Conclusions
- •References
- •Type of Glaucoma
- •Stage of Glaucoma
- •Combined Surgery
- •8.4.2 Anesthesia
- •8.4.3 Surgical Technique
- •8.4.3.1 Preparation
- •8.4.3.2 Implantation of the Micro-Bypass Stent
- •8.4.4 Postoperative Management and Medication
- •8.4.5 Outcomes and Combination with Other Techniques
- •8.4.5.1 Trabecular Implant in Refractory Glaucoma Patients
- •8.4.6 Conclusions
- •References
- •9. Minimally Invasive Cataract Surgery
- •10. Minimally Invasive Vitreoretinal Surgery
- •10.1 Introduction
- •10.2 Microincision Vitrectomy
- •10.2.1 Models of Wound Architecture
- •10.2.2 Vitrectomy
- •10.2.3 Adjuncts
- •10.2.4 Common Surgical Techniques
- •10.2.4.1 Macular Surgery
- •10.2.4.2 Proliferative Diabetic Retinopathy
- •10.2.4.3 Retinal Detachment
- •10.2.4.4 Pediatric Vitreoretinal Surgery
- •10.2.5 Complications
- •10.2.6 Future Developments in Minimally Invasive Vitrectomy
- •10.3 Endoscopic Vitreoretinal Surgery
- •10.3.1 Introduction
- •10.3.2 History and Development of Endoscopic Ophthalmic Surgery
- •10.3.3 The Endoscope
- •10.3.4 Applications of Intraocular Endoscopy
- •10.3.4.1 Media Opacity
- •10.3.4.3 PVR and Subretinal Surgery
- •10.3.4.4 Retained Lens Fragments
- •10.3.4.5 Anterior and Retrolental Vitrectomy in Malignant Glaucoma
- •10.3.4.5 Sutured IOL and ECP
- •10.3.5 Limitations and Challenges
- •10.4 Future Directions of Minimally Invasive Vitreoretinal Surgery
- •References
- •INDEX
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4.2.2.1 Donor Cornea Preparation
The technique of donor cornea preparation has been described by Price and Price [10]. In manual donor dissection, a corneoscleral rim is mounted on an artiÞcial anterior chamber (AC) and the chamber is inßated with air or BSS. The tissue is dissected at about 90% stromal depth using a series of three curved blades (DORC International, Zuidland, The Netherlands) [10]. Automated dissection is performed using a Moria CB microkeratome (Moria, Doyleston, PA) and either a 300or a 350-mm head depending on central corneal pachymetry less than or greater than 570-mm [10]. After dissection, the donor is transferred to a cutting block and placed endothelial side up. An 8-, 8.5-, or 9-mm-diameter trephine is used to punch a central corneal button. The button is maintained on the cutting block and covered until ready for use.
4.2.2.2 Host Cornea Preparation
The patient is brought to the operating suite after informed consent has been obtained. Anesthesia is a retrobulbar block (RBB) in most cases. The surgery may be performed under topical monitored anesthesia as well [9]. Attention is directed temporally on the patient and an 8-, 8.5-, or 9 mm trephine is used to mark the recipient corneal epithelium to outline the area from which DescemetÕs membrane is to be removed. Typically the same trephine needed for donor preparation is used. A paracentesis site is made temporally on the recipient with a paracentesis blade. Additional paracenteses are placed around the limbus at locations that will permit the entry of instruments to allow adjustment of the donor graft following placement. The gentian violet marker is used to mark the paracentesis blade so as to make identiÞcation of the paracenteses easy. The anterior chamber is Þlled with viscoelastic (Healon, Advanced Medical Optics, Irvine, CA) to deepen and maintain it. A 5-mm clear corneal temporal incision is made, or a scleral tunnel of the same length is created to minimize induced astigmatism. DescemetÕs membrane is scored along the previously marked epithelial tract using a modiÞed Sinskey hook. DescemetÕs membrane and endothelium are removed from within the scored area using a DescemetÕs stripping instrument to loosen the membrane in the 3 oÕclock position and pull it toward the incision at the 9 oÕclock position. The peeled DescemetÕs membrane is removed from the eye and
laid out across the cornea to ensure it was removed in entirety. The irrigation/aspiration handpiece is then used to remove the remaining viscoelastic from the anterior chamber so that the graft will adhere well.
4.2.2.3 Insertion of the Donor Cornea
The donor cornea is brought onto the operative Þeld on the cutting block and a small amount of Healon is placed on the endothelial surface to protect the endothelium during the folding process. The donor tissue is folded using a forceps (Kelman-McPherson [Katena], Goosey [Moria], or Charlie [Bausch & Lomb]), or any of the surgeonÕs choice into a taco or a burrito shaped conÞguration. The cornea cap is discarded. The edge of the 5 mm cornea or scleral incision is grasped and lifted with a toothed forcep to aid insertion of the tissue. The tissue is inserted into the AC stromal side up and air is injected through the paracentesis to unfold the donor tissue and press it up against the recipient cornea. The cornea/scleral incision is sutured with 10-0 nylon suture, and the knots are buried. If needed, a 27or 30-gauge needle with the tip bent with the needle holder and on a tuberculin syringe, can be inserted into the AC to aid proper positioning of the donor tissue. Care is taken to only grasp the stromal edge of the tissue so as to not damage any endothelial cells. When the surgeon is happy with the placement of the graft, the AC is Þlled with air for 10 min, followed by an exchange of air for BSS. Enough air is maintained in the AC so as to clear the inferior pupil when the patient is in an upright position. A drop of Vigamox (Alcon, Fort Worth, TX) is instilled in the eye. The patient is taken to the recovery room and will lay face up in the recovery room for 30 min to 2 h in order to allow the air to be in contact with the donor cornea and further promote adhesion. We prefer 2 h.
4.2.3 Postoperative Medications
Postoperatively, the authors prefer a combination of topical steroid and cyclosporin A as described earlier for PK. In general, topical prednisolone is prescribed 4Ð8 times daily for an average of 2Ð3 months postoperatively. The prednisolone is tapered by one drop per month until a dose of once daily is obtained. At that time, if the patient is phakic and has experienced no
4 Minimally Invasive Corneal Surgery |
85 |
rejection episodes or developed an IOP steroid response, the topical steroid is changed to loteprednol (Lotemax, Bausch & Lomb, Tampa, FL) one to two times per day. The patient is maintained on a minimum of one drop per day for at least 1 year. All patients receive topical cyclosporine A (Restasis, Allergan, Irvine, CA) twice a day for at least 1 year postoperatively. Many patients may remain on topical immunosuppressive medication for an indeÞnite time period.
4.2.4 Donor Dislocation Risks
Graft dislocation is a complication of DSEK. It is known as the most common postoperative challenge [11]. The incidence of donor detachment of the graft typically is higher when the surgeon performs his or her Þrst DSEK cases. Price and Price described their experience with donor dislocation in the Þrst 200 eyes in which they performed DSEK [11]. The rate of donor dislocation decreased inversely with the number of cases performed [11]. Others have cited similar results with dislocation rates in the literature ranging anywhere from 1 to 25% and higher [11Ð13]. Risk factors for graft dislocation include the entrapment of ßuid between the donor and recipient corneas and rubbing the eye [9]. Techniques to reduce interface ßuid have been described by Price and Terry and include the placement of fenestrations in the mid-peripheral recipient cornea to provide a pathway for ßuid to exit, the use of a LASIK roller to massage the corneal surface to facilitate removal of entrapped ßuid, and scraping the peripheral recipient cornea bed to allow for donor edge adhesion [9]. OÕbrien et al. reported that donor dislocation after DSEK is more common in eyes without an intact lens/iris diaphragm, and/or that underwent extensive tissue manipulation during surgery [12].
4.2.5 Repositioning Donor Tissue
When a clear space can be detected on postoperative slit lamp exam between the donor and recipient tissue, the donor graft has become detached from the recipient. Most donor dislocations are noted within the Þrst week to several weeks following surgery [11, 13]. Stromal edema is visualized over the area of dislocation and the patientÕs vision is often decreased from expected. It is
necessary at this point to reattach the donor tissue. This may be performed in a minor surgery room. The patient is taken to the minor surgery room and laid ßat under the operating microscope. Using sterile technique and a 30-gauge needle on a tuberculin syringe, the AC is Þlled again with air in exchange for anterior chamber ßuid. The donor graft is pressed into approximation with the host stroma. The AC is maintained again at a 100% air Þll for 10 min. The air is then exchanged for BSS as described in the surgical technique above so that the air bubble in the AC will clear the inferior pupil border when the patient sits upright so as to prevent pupillary block. The patient is maintained in the face up position as described previously for 30 min to 2 h to allow good donorÐhost apposition.
4.2.6 Treatment of Rejection Episodes
Endothelial graft rejection is a concern with DSEK. Signs of immunologic rejection at the initial diagnosis include keratic precipitates, diffuse corneal edema, and a combination of both [14]. Epithelial and anterior stromal immunologic reactions are not a concern because these are not transplanted in DSEK [14]. If a rejection episode is conÞrmed or suspected, the patient is placed on topical prednisolone every 1 h while awake along with oral prednisone (1 mg/kg/ day). This dosing regimen is maintained for 1 week and if the rejection episode has been treated successfully, the topical steroid dose is tapered very slowly to four times per day and then maintained at this dosage over a 3Ð4-month period before tapering it down to a maintenance dose of one more drop per day than what the patient had been using when the rejection episode occurred. If the patient had been on topical loteprednol (Lotemax, Bausch & Lomb) at the time of the rejection episode, a switch is made to topical prednisolone and dosed as outlined above. When the patient has demonstrated adequate resolution of the rejection episode, and following the slow taper of prednisolone, the surgeon may choose to switch the patient back to loteprednol at a higher dosing frequency than was being used prior to development of the rejection episode. Topical loteprednol has advantages over prednisolone in a phakic patient in that it has not been cited in the literature to cause cataract. Loteprednol also has an associated lower incidence of an IOP rise. Holland showed an 8% risk of an IOP
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H. M. Skeens and E. J. Holland |
increase in known steroid responders using prednisolone following cornea transplantation compared to a less than 1% increase in those known steroid responders using loteprednol.
Most cases of endothelial graft rejection clear. One study cited a 7% graft failure rate following a graft rejection episode. The patient can be successfully regrafted with DSEK [14].
4.2.7 Visual and Refractive Outcomes
The recovery of useful vision following DSEK occurs usually within weeks [15]. This is in contrast to traditional PK where it may take up to 12 months or longer to achieve a satisfactory visual acuity when large diameter PK is not used. As described in ÒPK,Ó post-PK astigmatism is the most common complication of the full-thickness transplant. As mentioned, PK is considered to be a two step procedure with the Þrst step being the actual cornea transplant itself, followed by a second step that involves correction of the resultant astigmatism. DSEK has been shown to be a Òrefractive neutralÓ cornea transplant [15]. Visual and refractive outcomes of the Þrst 50 cases of a single surgeon were analyzed and mean manifest cylinder as well as mean manifest spherical equivalent were unchanged from preoperative values [15]. Furthermore, at 6 months post DSEK, 62% of patients had ³ 20/40 BCVA and 76% had ³ 20/50 BCVA [15]. Koenig et al. reported a 6-month postoperative BCVA of 20/40 or better in 61.8% of their patients [16].
A hyperopic shift of less than 0.50D has been reported by Price and Price [11], while Koenig et al. reported a hyperopic shift of 1.19 ± 1.32D [16]. Our patients have experienced a hyperopic shift similar to that reported by Koenig. For this reason, when implanting an IOL for a concurrent cataract removal at the time of DSEK, the surgeon should consider implanting an IOL with a refractive error of −1D.
the trabecular meshwork. Air that Þlls the anterior chamber can block the pupil when the patient is in the supine position, but if the air bubble is such that it Þlls less than 50% of the chamber at the end of the procedure, when the patient sits up to eat or go to the bathroom, the air will be in mid-pupil position such that any supine position pupillary block will resolve. Taking care to leave only a 50% air Þll at the end of the case, and having the patient sit upright after 2 h and prior to going home, to ensure that the inferior border of the air bubble clears the inferior pupillary margin, can help prevent pupillary block. Air may also become trapped behind the pupil, shallowing the anterior chamber, and pressing the iris against the endothelium leading to pupillary block. Dilation of the pupil postoperatively with phenylephrine and cyclogyl can add additional protection against pupillary block. If a patient presents with pupillary block due to trapped air, dilating drops should be administered and the patient should be laid back to allow the air to ßoat into the anterior chamber. If this does not work, BSS can be injected into the anterior chamber at the slit lamp to deepen it and force the air from behind the iris. A Yag laser can also be used to make an iridotomy thus providing a channel for aqueous ßow and relieving pupillary block. If the iris has been opposed to the endothelium for an extended period, adhesions may begin to form and the patient may need to be taken back to the operating suite to break the adhesions and deepen the anterior chamber. This should be done immediately to lower the IOP and to preserve endothelial cells.
Central retinal artery occlusion is a rare complication of DSEK. Compression of the retinal vasculature from the high IOP produced during the initial adhesion of the graft with the air bubble is the cause.
As mentioned, graft failure rates reported in the literature range from 0 to 29% with those cases requiring surgical reattachment of a dislocated donor disc having a higher rate of endothelial failure [12].
Endothelial cell loss following DSEK has been reported at 34% at the 6-month postoperative exam and remains stable for the Þrst year [17].
4.2.8 Other Complications |
4.2.9 Summary |
Pupillary block is a potential complication of DSEK. A large amount of air in the anterior chamber can block the ßow of aqueous through the pupil and out
It has been well established that DSEK surgery can preserve and restore the normal recipient cornea, while providing excellent visual acuity within an acceptable
4 Minimally Invasive Corneal Surgery |
87 |
time frame. The avoidance of full-thickness cornea incisions and sutures is a great advantage. Wound dehiscence with expulsion of intraocular contents is not a risk following DSEK. DSEK is associated with itsÕ own complications however, and the cornea surgeon performing this procedure must be aware of how to deal with these potential complications. Fullthickness penetrating keratoplasty is no longer indicated for endothelial dysfunction. DSEK patients regain vision sooner, have minimal to no refractive shift postoperatively, and have an eye that is structurally more sound [9]. As with PK, the long-term success of DSEK will depend on an adequate number of viable endothelial cells in the donor corneal tissue. The most common cause of late PK graft failures is due to low endothelial cell counts [16]. The rapid visual recovery, low morbidity, and minimal effect on the anterior corneal curvature make DSEK the procedure of choice for endothelial dysfunction (Fig. 4.16a, b)
a
b
References
1.Cosar C, Banu M, Sridhar M et al (2002) Indications for penetrating keratoplasty and associated procedures, 1996Ð 2000. Cornea 21:148Ð151
2.Pahor D, Gracner B, Falez M et al (2007) Changing indications for penetrating keratoplasty over a 20-year period, 1985Ð2004. Klin Monatsbl Augenheilkd 224:110Ð114
3.Magovern M, Beauchamp G, McTigue J et al (1979) Inheritance of Fuchs combined dystrophy. Ophthalmology 86:1897Ð1923
4.Rodrigues M, Krachmer J, Hackett J et al (1986) Fuchs corneal dystrophy. A clinicopathologic study of the variation in corneal edema. Ophthalmology 93:789Ð796
5.Adamis A, Filatov V, Tripathi B et al (1993) Fuchs endothelial dystrophy of the cornea. Surv Ophthalmol 38:149Ð168
6.Wilson S, Bourne W (1988) Fuchs dystrophy. Cornea 7: 2Ð18
7.Melles G, Lander F, Beekhuis W et al (1999) Posterior lamellar keratoplasty for a case of pseudophakic bullous keratopathy. Am J Ophthalmol 127:340Ð341
8.Melles G, Wijdh R, Nieuwendaal C (2004) A technique to excise the descemet membrane from a recipient cornea. Cornea 23:286Ð288
9.Price M, Price F (2007) DescemetÕs stripping endothelial keratoplasty. Curr Opin Ophthalmol 18:290Ð294
10.Price M, Price F (2006) DescemetÕs stripping with endothelial keratoplasty. Comparative outcomes with microker- atome-dissected and manually dissected donor tissue. Ophthalmology 113:1936Ð1942
11.Price F, Price M (2006) DescemetÕs stripping with endothelial keratoplasty in 200 eyes. J Cataract Refract Surg 32: 411Ð418
12.OÕBrien P, Lake D, Saw V et al (2008) Endothelial keratoplasty: case selection in the learning curve. Cornea 27: 1114Ð1118
13.Terry M, Shamie N, Chen E et al (2008) A simpliÞed technique to minimize graft dislocation, iatrogenic graft failure, and pupillary block. Ophthalmology 115:1179Ð1186
14.Jordan C, Price M, Trespalacios R et al (2008) Graft rejection episodes after DescemetÕs stripping with endothelial
keratoplasty: part one: clinical signs and symptoms. Br J Ophthalmol 93:387Ð390. doi:10.1136/bjo.2008.140020
15.Price F, Price M (2005) DescemetÕs stripping with endothelial keratoplasty in 50 eyes: a refractive neutral corneal transplant. J Refract Surg 21:339Ð345
16.Koenig S, Covert D, Dupps W et al (2007) Visual acuity, refractive error, and endothelial cell density six months after Descemet stripping and automated endothelial keratoplasty. Cornea 26:670Ð674
17.Terry M, Chen E, Shamie N et al (2008) Endothelial cell loss after DescemetÕs stripping endothelial keratoplasty in a large prospective series. Ophthalmology 115:488Ð496
Fig. 4.16 (a, b) Postoperative photo of a DSEK patient. Courtesy of Edward J. Holland
