*With the exception of programs from the ACCEL series, each of which qualifies for up to 4 Category 1 CME credits.
Volume 51, Issue 13
July 7, 2013
Dry Eye and LASIK Terrence P. O’Brien, MD
Blepharitis Dr. O’Brien
Dry Eye in Graft-Versus-Host Disease Shahzad I. Mian, MD
The following is an abstracted summary, not a verbatim transcript, of the lectures/discussions on this audio program.
Ophthalmology Program Info Accreditation InfoCultural & Linguistic Competency Resources
The goal of this program is to improve the diagnosis and treatment of dry eye and blepharitis. After hearing and assimilating this program, the clinician will be better able to:
1. Elaborate on the effects of laser in situ keratomileusis (LASIK) on corneal nerves and tear production.
2. Identify patients at increased risk and adopt practices to reduce the likelihood of developing dry eye after LASIK.
3. Diagnose and treat anterior and posterior blepharitis.
4. Recognize the signs and symptoms of ocular involvement in graft-versus-host disease (GVHD).
5. Diagnose and manage dry eye in GVHD.
In adherence to ACCME Standards for Commercial Support, Audio-Digest requires all faculty and members of the planning committee to disclose relevant financial relationships within the past 12 months that might create any personal conflicts of interest. Any identified conflicts were resolved to ensure that this educational activity promotes quality in health care and not a proprietary business or commercial interest. For this program, the following has been disclosed: Dr. O’Brien is a consultant for Alcon, Allergan, Bausch & Lomb, NicOx, Rapid Pathogen Screening (RPS), and Santen Pharmaceutical Co. Dr. Mian has received research grant support from Bausch & Lomb. The planning committee reported nothing to disclose. In his lecture, Dr. Mian presents information related to the off-label or investigational use of a therapy, product, or device.
Dry Eye and LASIK
Terrence P. O’Brien, MD, Professor of Ophthalmology and Charlotte Breyer Rodgers Distinguished Chair, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL
Laser in situ keratomileusis (LASIK): cuts through sub-basal plexus of nerves and uncouples neural reflex arc involved in tearing; photorefractive keratectomy (PRK) interferes less with corneal nerves and produces less loss of corneal sensation and tear function
Tear secretion after LASIK: study evaluated tear secretion and corneal sensitivity after LASIK in 48 eyes (Benitez-del-Castillo, 2001); observed large reduction in tear function index (TFI) and corneal sensitivity that did not return to baseline for ≈9 mo; losses greatest at 1 mo
Corneal nerves: provide afferent arm of lacrimal reflex arc and efferent supply of trophic factors; extent of neuronal damage determined by type, depth, and location of injury; damage leads to neurotrophic cornea; regeneration aided by nerve growth factor (NGF) and guidance cues; equal numbers of nerves penetrate cornea in all quadrants; many corneas shown not to regain full sensation for 54 mo after LASIK; recovery slower after hyperopic ablations
LASIK-induced neurotrophic epitheliopathy (LINE): seen in patients without previous dry eye; signs adjacent to flap, less evident at hinge; tear production often normal; resolves 6 to 8 mo after surgery; connection between neurotrophic keratopathy and dry eye disputed; high myopes may have symptoms without signs for years after surgery; studies showed no difference with various hinge positions and no dry eye after retreatment with LASIK
Diagnosis of dry eye: no gold standard test; interpretation of tear film osmolarity unclear; matrix metalloproteinase (MMP)-9 potential marker; changes seen in innervation of corneal nerves in age-related and Sjogren syndrome dry eye; multiple factors lead to lacrimal film instability and loss of goblet cells and mucin, epithelial damage, and apoptosis of cells on ocular surface; pain — study (Belmonte, 2007) suggested dry eye and/or neurotrophic keratopathy caused pain; probably caused by regeneration (amputation neuromas); resprouting of axonal sprouts contribute to hypoesthesia; sprouts and intact nerve fibers regenerate and develop microneuromas that cause hyperalgesia; study in mice showed dry environment after PRK caused more alterations in corneal nerves; patients with LASIK-associated dry eye may not feel symptoms because of corneal hyposensitivity; such patients need obligatory treatment; study of effects of LASIK found clearance of tears decreased, and expression of interleukins, MMP-3, and MMP-9 increased; 1 yr required for normal levels of fluorescein staining
Effects of suction ring: study showed goblet cell density decreased significantly more after femtosecond laser than mechanical LASIK; effect correlated with suction time
Decreased interblink interval: decreases protection of ocular surface; after patient blinks, tear break-up time (TBUT) accelerated and cycle repeats
Risk factors: dryness and inflammation associated with regression of refractive effect; risk factors include high refractive error, ablation depth, low preoperative results from Schirmer test, history of dry eye, female sex, hyperopia, and duration of contact lens wear before surgery
Prevention: identify patients at risk — >40% of patients seek refractive surgery because of dry eye and intolerance of contact lenses; use Ocular Surface Disease Index or other surveys; measure TBUT to evaluate evaporative tear loss; perform slit lamp examination for associated or comorbid inflammation of eyelid margin; important to use lissamine green staining (fluorescein shows only later stages of disease); tear film osmolarity (absolute value of test limited unless extreme hyperosmolarity present); optimize ocular surface before surgery — avoid use of contact lenses; use preservative-free artificial tears; use pulse of topical corticosteroid (4 to 6 wk); eyelid hygiene; punctal plugs; topical azithromycin or tetracycline; course of cyclosporine for some patients (6 to 8 wk); omega-3 essential fatty acids (EFA) supplements; autologous serum tears in some patients; repeat testing for laser vision correction after pretreatment; all tests (eg, wave front analysis, topography, refraction) affected by unstable ocular surface; intraoperatively — avoid excessive use of agents toxic to ocular surface; minimize use of anesthetic (just-in-time anesthesia); use lubricants with low coefficient of friction (eg, hyaluronate, carboxymethylcellulose, carbomers); postoperatively — tape eyes closed and have patients rest for ≈15 min; use topical corticosteroids, eyelid hygiene, autologous serum or plasma; consider NGF for severe dry eye
Treatment: therapeutic algorithm — artificial tears with different viscosities; combination of steroids and cyclosporine; aggressive treatment of eyelid disease; punctal plugs; autologous serum
Treatment of pain: low dose of preservative-free topical lidocaine plus autologous serum possibly helpful; pregabalin (Lyrica) starting at 150 mg per day and increasing to maximum of 600 mg per day; duloxetine (Cymbalta) starting at 30 mg per day, increasing to 120 mg per day; evaluate at 2 mo
Other considerations: blepharitis reported to increase risk for peripheral corneal infiltrates and infectious keratitis; epithelial basement membrane dystrophies associated with recurrent corneal erosions, epithelial ingrowth, regression of effect, and visual alterations after LASIK; systemic diseases — patients with rheumatoid arthritis or systemic lupus erythematosus can have LASIK if treated aggressively; must achieve tight control of disease ≈3 mo before surgery; successful LASIK possible even in patients with Sjogren syndrome and severe preoperative dry eye, low Schirmer test results, and enhanced TBUT if patients treated aggressively (Toda, 2004); use special informed consent
Prevalence: study found ocular discomfort in >1,000 consecutive patients caused by posterior eyelid margin disease in ≈25%, dry eye in ≈20%, and anterior blepharitis in ≈12%; ≥33% of dry eye caused by blepharitis (evaporative tear loss secondary)
Eyelid inflammation: dermatoblepharitis — caused by infection, allergy, connective tissue disease, or other dermatologic disease; eyelid margin disease — anterior inflammation caused by bacterial, viral, or parasitic infection; posterior inflammation caused by disorders of lipid biochemistry
Anterior blepharitis: caused by excessive colonization with bacteria; release of toxins into tear film causes discomfort, irritation, and burning; biofilms contribute to resistance (may form on punctal plugs); bacteria include gram-positive coagulase-negative staphylococci (57%) or Staphylococcus aureus and other gram-positive bacteria; rarely caused by gram-negative bacteria; signs and symptoms — morning crusting; madarosis; collarettes (scales that encircle lash); redness of eyelid margin and conjunctiva; tests — quantitative microbial culture to determine pathogen load; susceptibility testing in recalcitrant cases
Sequelae: some cases with intense inflammation have corneal involvement; study showed cell wall toxin of staphylococci (α-ribitol teichoic acid) caused reaction in peripheral cornea (type III immune-mediated reaction seen with staphylococcal hypersensitivity); intervening clear zone often appears between limbus and infiltrate
Treatment: avoid frequent use of scrubs containing detergent that breaks down meibum into free fatty acids and soaps; use commercial lid scrubs only ≈3 nights per week; SteriLid contains natural tea tree oil derivative (linalool) with antimicrobial and anti-inflammatory activity; effective even against methicillin-resistant staphylococci
Other causes: angular blepharitis not always caused by Moraxella; cylindrical dandruff pathognomonic for blepharitis caused by Demodex folliculorum or Demodex brevis
Posterior disease: pathogenesis of meibomian gland dysfunction (MGD) unclear; bacteria may cause internal hordeolum and chronic MGD because secreted lipases break down meibum; obstructive MGD caused by epithelial hyperplasia, thickened secretions, and cicatricial changes; hypersecretory MGD associated with seborrhea or rosacea; sequelae of chronic inflammation include scarring, loss of goblet cells, and chronic dry eye; telangiectatic vessels appear in eyelid margin; soaps along eyelid margin or lateral or medial canthal areas pathognomonic; meibomian glands highly disordered in severe disease; obstruction caused by deposition of keratin with lipogranulomatous inflammation
Signs and symptoms: toothpaste-like material expressed; dry eye; thickened eyelid margin; filmy or foamy vision; irreversible dragging of meibomian gland orifice posteriorly
Mimics of blepharitis: neoplasia (especially sebaceous cell carcinoma)
Treatment: warm compresses; LipiFlow device available that warms and massages eyelid and has lasting beneficial effect; not all cases caused by infection; among tetracyclines, minocycline most lipophilic, followed by doxycycline and tetracycline; begin treatment with doxycycline; use minocycline for refractory cases; lower doses found to have greater immunomodulatory effect; rotate antibiotic agents or use antiseptics to discourage development of resistance; metronidazole can be used around eye
Antibiotic choice: bacitracin effective against staphylococci and streptococci (only available as ointment); erythromycin ineffective because of resistance; aminoglycosides toxic and delay healing; topical azithromycin — macrolide available for ocular use; concentrated in eyelid; dose, once per night for 6 wk, then every other month; has immunomodulatory and anti-inflammatory effects
Treatment algorithm: topical and systemic antibiotics; corticosteroids; immunomodulatory agents (eg, cyclosporine); grade severity to determine treatment; moderate to severe disease requires multifactorial, protracted approach; omega-3 EFAs help reduce inflammation
Dry Eye in Graft-Versus-Host Disease
Shahzad I. Mian, MD, Associate Professor, Ophthalmology and Visual Sciences; Terry J. Bergstrom Collegiate Professor for Resident Education in Ophthalmology and Visual Sciences, University of Michigan, Kellogg Eye Center, Ann Arbor
Graft-versus-host disease (GVHD): incidence from 10% to 90% (higher with allogeneic tissue and in older recipients); more intense immunosuppressive protocol may increase incidence
Acute GVHD: appears in first 100 days; incidence 35% to 45%; manifestations include maculopapular rash, and involvement of gastrointestinal tract, liver, and (less often) eye; may overlap or recur in chronic stage
Chronic GVHD: incidence 40% to 80%; wider range of organs involved, including eyes; ocular involvement not diagnostic; biopsy diagnosis required or ≥1 diagnostic criterion in another organ
Ocular involvement: features — dry eye, cicatricial conjunctivitis, conjunctivitis sicca, and confluent areas of punctate keratopathy; mild to severe conjunctivitis with membranous features; keratitis with corneal staining; corneal melting with perforation possible in acute and chronic stages; episcleritis, secondary glaucoma, and secondary choroidal detachment reported; chronic phase — may involve external ocular disease, ocular surface disease, and intraocular disease; eyelid margin possibly involved, with MGD, blepharitis, conjunctivitis, and dry eye common; corneal thinning and melting, retinal hemorrhages, cotton wool spots, and nasolacrimal duct obstruction may occur; cataracts develop as result of treatment with steroids
Incidence and risk factors for dry eye disease: incidence >70% to 80% in ocular GVHD; usually occurs after 6 mo; risk factors — condition leading to transplantation; transplantation of allogeneic hematopoietic stem cells; development of systemic disease (especially skin involvement); total body irradiation; aggressive chemotherapy
Pathophysiology: mediated by Th1 helper cells, with infiltration of lacrimal gland and conjunctival surface; destruction of tissue and formation of fibroblasts; altered environment of ocular surface and increased osmolarity; secondary inflammation damages surface further and leads to corneal-epithelial and conjunctival-epithelial irregularities
Diagnosis: history; Ocular Surface Disease Index; measurement of basal production of aqueous tears by Schirmer test (<5 mm indicates dry eye, 6 to 10 mm suggestive of dry eye); corneal fluorescein staining to assess degree of keratitis and detect punctate keratopathy and frank defects; use rose bengal and lissamine green to evaluate patterns of conjunctival staining; TBUT reduced (because of eyelid margin disease); osmolarity provides additional quantitative measurement (absolute value and change over time within single eye and intereye correlation)
Management: lubrication with unpreserved tears; viscosity of tears important; hypo-osmotic tears if osmolarity high; viscoelastic for severe cases; gels and ointments; use of selective muscarinic agonists limited by systemic side effects; environmental modification to control evaporation important, but humidifiers possibly contraindicated because of susceptibility to bronchial infection; moisture goggles; increased blinking
Treatment of blepharitis: warm compresses and eyelid hygiene; oral tetracycline and azithromycin; LipiFlow (no data available for use in GVHD); scleral contact lenses treatment of choice for severe dry eye disease; punctal occlusion with silicon plugs or thermal cautery; smart plugs increase risk for canaliculitis and dacryocystitis
Treatment of ocular surface inflammation: topical corticosteroids — loteprednol (0.3% or 0.5%) has lower risk for ocular hypertension; fluorometholone (drop or ointment); prednisolone for severe inflammation; cyclosporine for mild to moderate disease (low side effect profile with long-term use); tacrolimus ointment on eyelids may reduce MGD and inflammation; more severe disease — autologous serum drops supply anti-inflammatory mediators and growth factors that improve surface and symptoms; dilution varies (20%-50%); higher concentration increases risk for infection of serum tear drops; topical retinoic acid for keratinization (stings); speaker does not use androgens topically because of limited supporting evidence; mucolytics for filamentary keratitis
Prophylaxis: topical cyclosporine (0.5%) before transplantation and continued for ≥6 to 12 mo after transplantation; prophylactic loteprednol under evaluation
Screening: perform eye examinations on all patients before bone marrow transplantation and follow up at 3 mo
Dr. O’Brien, spoke at the 81st Mid-Winter Clinical Conference: Controversies in Ophthalmology, held February 9, 2013, in Los Angeles, CA, and presented by the Research Study Club of Los Angeles (to learn about the 82nd Mid-Winter Clinical Conference, please visit www.researchstudyclub.com/). Dr. Mian addressed the 56th Annual Postgraduate Symposium in Ophthalmology — Advances in Corneal Disease, held March 1 to 2, 2013, in Columbus, OH, and presented by Ohio State University Havener Eye Institute (to learn more about cme activities at Ohio State University, please visit https://ccme.osu.edu. The Audio-Digest Foundation thanks the speakers and the sponsors for their cooperation in the production of this program.
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