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Women of Vision: Are We at Risk for Vision Morbidity? Louise Sclafani, Diana Shechtman,, Melissa Barnett, Lori Glover, (Sue Cotter, Jill Autry at AOA) As ODs we need to place a higher priority on those individuals at increased risk for vision-threatening ocular disease. It has been estimated that the female gender represents 2/3 of all visually compromised individuals due to inherent risk factors and lack of access to healthcare. Our panel will take on this challenge and discuss this population as it relates to the following conditions: optic neuritis/OCT evaluation, AMD/nutritional controversy, psychosocial issues/management options for strabismus or chronic vision impairment', ocular concerns for common systemic pharmaceuticals, safety issues with ophthalmic drugs, and the hormonal influence on ocular surface disease. I. Women and Vision Loss – a. Definitions b. Demographics c. Projections d. Impact of vision loss on women and stakeholders II. Determinants of Eye and Vision Care a. Factors influencing women’s health care b. Access to general medical and eye care III. Improving Population Health a. Reducing health disparities b. Strategies for improving quality of care OCULAR DISEASE AND WOMEN • OPTIC NEURITIS • Decreased vision/visual field over hours or days • Unilateral • Pain on eye movements • Decreased color vision (red cap test) • + RAPD • Visual field defects vary • Swollen disc or no swelling of disc (retrobulbar) • MRI of Brain and Orbits with Flair sequencing • Bloodwork • MULTIPLE SCLEROSIS • Female > Male • 18-45 years old • Optic neuritis th • • Intermittent diplopia (usually 4 nerve) Nystagmus • • • • • • • • • • • • • • • Tingling or numbness in extremities Uhtoff’s sign • Worsening vision with increased body temperature Lhermitte’s sign • Shock-like sensation with neck flexion OPTIC NEURITIS TREATMENT TRIAL (ONTT) Recommends treatment with IV methylprednisolone x 3 days Avoid prednisone orally until AFTER treatment with IV (10-14 days) Hastens visual recovery but not final visual outcome Prolongs time to development of MS Do not use oral steroids alone DIAGNOSING MULTIPLE SCLEROSIS MRI of brain with Flair testing Inspection of CSF for oligoclonal bands Inspection of CSF for increased IgG index VER testing shows increased latency Neurologist Systemic Medications and their Ocular Side Effects • Topamax™ • Topiramate • Tablets • Sprinkle Capsules • FDA Category D • Safety not established < 2 YO • Indications: • Epilepsy • Monotherapy, adjunctive therapy • Migraines • Prophylaxis • Off-label • Bipolar disorder, weight reduction, depression, neuropathic pain • Topamax ™ • Precise Mechanism of Action: not known • Thought to block voltage-dependent sodium channels, augments the activity of the neurotransmitter gamma-aminobutyrate at some subtypes of the GABA-A receptor, antagonizes the AMPA/kainate subtype of the glutamate receptor, and inhibits the carbonic anhydrase enzyme, particularly isozymes II and IV • ??? • Topamax™ • Ocular side effects • Acute myopia and 2° angle closure • May be associated with supraciliary effusion resulting in anterior displacement of the lens and iris • ± mydriasis • Usually within first month • Pediatric population too! • • • • • • • • • • • • • • • • • • • First line treatment is d/c Topamax • Conjunctivitis • Diplopia • Nystagmus • Topamax™ Ocular Changes Associated with Topiramate • Ozturk et al • Current Eye Research, 36(1), 47–52, 2011 • N = 76 eyes • 3 month f/u • Significant myopic shift and an increase in RNFLT were observed • Further studies are warranted Tamoxifen™ Nolvadex Estrogen antagonist Interferes with binding of estradiol to its target tissues Indications • Breast • Ovarian • Pancreatic • Malignant melanoma Tamoxifen™: Ocular Effects Prospective Studies • 1992 study • 20 mg qd • 25 months • 6.3% incidence • #1 – retinopathy • 1999 • 65 patients taking 20 mg qd • 12% incidence • As early as 6 months Tamoxifen™ : Ocular Effects keratopathy • white-yellow subepithelial opacities retinopathy • +/- macular edema cataracts • asc optic neuropathy • Rare Macular holes? • International Ophthalmology 2005; 26(3) • Tamoxifen™ Retinopathy Bilateral yellow-white crystals in ring-like pattern • 13-35 microns • Location is debatable: NFL, RPE, IPL, OPL • Superficial to vasculature macular edema Crystals usually do not resolve with discontinuation of therapy Plaquenil ™ • • • • • • • • • • • Hydroxychloroquine Indications • Malaria • Lupus erythematosus • Rheumatoid arthritis Precise mechanism of action: not known • Acute effects on metabolism of retinal cells Ocular Side Effects • Bilateral ring of RPE depigmentation sparing the fovea Plaquenil ™ Increased risk of retinopathy: • > 5 years use • Cumulative dose > 1000 g • Daily dose > 400 mg/day • Elderly • Kidney or liver disease • Concurrent retinal/macular disease Plaquenil™ Revised recommendations on screening for chloroquine and hydroxychloroquine retinopathy • Ophthalmology. 2011 Feb;118(2):415-22 Screening: • mfERG or SD-OCT or FAF • 10-2 VF (white-on-white) • Repeat promptly if changes • Fundus examination • Fundus photography • Not for screening; may be useful for documentation • No longer: Amsler grid, color vision, FA, etc. Plaquenil™ Baseline examination st • • • Within 1 year of therapy • Counsel patient about risk Annual screening • MINIMAL guidelines • Begin immediately if high risk • Begin after 5 years of use • All patients If toxicity • Consider discontinuing medication • Slow clearing • Visual function may continue to deteriorate • PSEUDOTUMOR CEREBRI PHARMACOTHERAPY AND THE PREGNANT AND NURSING PATIENTS • FDA Pregnancy Categories for Drugs • Stay Informed… • • • • • • • • • • • • • • • • • • • • • • • • • Ophthalmic Drug Facts Epocrates • Pregnancy Categories Drugs@FDA • Drug Package Inserts Websites • LactMed • Drugs and Lactation Database In the Works… Proposed Rule for Pregnancy and Lactation Labeling • FDA • began in 1997 Will eliminate Pregnancy Letter Categories Standardized statements Narrative descriptions • Risk summary • Clinical considerations section • Data • Human • Animal Soft Tissue Infections Penicillins • Augmentin • Dicloxacillin Cephalosporins • Cephalexin • Cefaclor Azithromycin Erythromycin Category B Topical Antibiotics Erythromycin ointment Azasite Tobramycin Dual Acting Anti-Allergy Medications Other Anti-Allergy Medications What Would You Do? New patient • 33 YOF • IOP • 35 mmHg OD and OS • ON thinning • Corresponding VF defect • FHx of POAG The Facts… Up to 30% have ↑IOP during pregnancy Group of UK Ophthalmologists (282) • 25% have pregnant glaucoma patients • • • • • • • • • • • • • • • • Glaucoma and Pregnancy Consider: • No treatment? • IOP often decreases during pregnancy • SLT Brimonidine • Alpha-agonist • Category B • Discontinue if breast feeding • CNS effects in infants due to penetration of BBB Other Glaucoma Medications… Avoid Prostaglandins at all stages of pregnancy • PG important during labor • Potentially • Induce miscarriage • Premature labor Other Category C Medications Beta-blockers • Low MW • Length of fetal exposure to drug may be much longer than adult • Recirculation • Lower blood volume • T1/2 life may be 4-6X longer • Use TXE if needed Carbonic anhydrase inhibitors Pilocarpine MIGRAINES Women>Men; 3:1 Generally starts before 20 years of age Often have family history May have nausea and vomiting, fatigue, photophobia Headaches predominantly on same side;may occasionally switch sides Headache triggers -Stress -Chocolate -Bright lights -Alcohol • • • • • • • • • • • • • -BC pills -Pregnancy MIGRAINE RELATED AURA Flashing lights, heat waves, jagged objects, tunnel vision, colored spots Lasting 15 to 30 minutes May or may not be accompanied by HA Acephalic migraine ACEPHALGIC MIGRAINE Visual symptoms only without onset of HA More typical as patient ages Common in patient with history of classic migraines when younger Flashes of light, scotoma, etc. still last 10-15 minutes with abrupt cessation No headache MACULAR HOLE Progress from Stage 1 to Stage 4 • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • Women 3.3 X greater than Men Older>Younger Idiopathic mostly, occasionally traumatic Best diagnosed with OCT Full-thickness holes generally 20/200 VA Round, dark red colored area in the center of the macula Often with yellow, lipofuscin granules MACULAR HOLE Distinguish from ERM pseudohole • Macular hole perfectly round • Poor vision with macular hole • Positive Watzke-Allen with macular hole • Pseudohole with tortuous surrounding vessels Can follow Stage 1 and 2 holes but get macular OCT for follow-up Amsler grid MACULAR HOLE Why are women more likely to develop holes? Macular hole pathogenesis is thought to be secondary to tangential and anteroposterior vitreomacular traction “Relaxin” theory • Relaxin, a hormone produced during pregnancy, induces matrix metalloproteinases associated with the loss of collagen and glycosaminoglcans in cartilage This process could occur in the vitreous • Premature vitreous syneresis and anomalous PVD MACULAR HOLE SURGERY Vitrectomy with membrane peel (ILM) Gas fluid exchange Face-down positioning for 2 weeks until gas bubble absorbs Watch IOP closely with gas bubble No flying until gas bubble completely resorbs Can use silicone oil but need second surgery Thyroid Eye Disease Graves Disease Excess secretion of thyroid hormone th th Usually in 4 -5 decade F>M Most common cause of proptosis in adults Thyroid ophthalmopathy • 10-25% of cases no evidence of thyroid dysfunction Risk Factors Smoking Gender Radioiodine Genetics Clinical Manifestations of Thyroid Ophthalmopathy Eyelid retraction Soft tissue involvement Proptosis Restrictive thyroid myopathy Dysthyroid optic neuropathy • • • • • • • • • • • • • • • Thyroid associated dermopathy Optic Neuropathy Current Treatment Smoking cessation Artificial tears, etc. Steroids • Usually need high dose Orbital radiotherapy Orbital decompression Other surgeries Rule out Thyroid Disease If… Superior limbic keratoconjunctivitis Chronic dacryoadenitis Lagophthalmos Globe subluxation Acanthosis nigricans Central Serous Chorioretinopathy (CSC) I. Introduction Case presentation Serous detachment of neurosensory retina in macular area A. Blister-like with shallow & round edges B. Loss of foveal light reflex II. Clinical picture A. Acute presentation B. Unilateral C. Males>>Female (2:10) D. Young 20-50 years old E. Type A personality III. Related conditions Systemic VKH Lupus Organ transplants Sleep apnea H. Pylori Pregnancy Drugs Viagra Steroids Pseudoephedrine Sorafenib III. Symptoms A. Acute symptoms B. Blurred vision C. Relative scotoma or metamorphopsia D. Color desaturation IV. Pathophysiology: Leakage from choriocapillaries through the RPE V. The woman & ICSC Why would a woman be affected? Related conditions pregnancy : resolve 1-2M s/p delivery lupus Clinical characteristics Most resolve spontaneously Good recovery of final VA Subretinal precipitates may be seen in as many as 50% of cases Older patients VI. Natural history A. Spontaneous resolution in most cases (~3-6 months) B. AS many as 50% may be recurrent (common within 1st yrs after initial presentation) VII. Management/Treatment Options A. B. C. D. E. Role of OCT imaging FA/ICG Autoflourescence Most cases are managed with careful routine observation If treatment is necessary photocoagulation or photodynamic therapy are viable options. PDT is more commonly implemented in chronic/recurrent cases F. Consider differential diagnosis of associated CNV in non characteristic cases VIII. AMD Management A. Lutein B. O3 Hormone Influence on Ocular Surface Disease 1. Intrinsic factors a. Female gender b. Older age c. Changing hormone levels / decreased androgens d. Hormone replacement therapy 2. Extrinsic factors a. Contact lens wear b. Postmenopausal estrogen therapy 3. 4. 5. 6. c. Medications d. Vitamin A deficiency Autoimmune disorders a. Rheumatoid Arthritis b. Sjogren’s Syndrome c. Systemic Lupus Erythematous d. Irritable bowel syndrome e. Crohn’s disease Thyroid disease a. Grave’s disease b. Hyperthyroidism c. Hypothyroidism Diabetes Treatments a. Gene therapy to treat dry eye related hormonal diseases b. New molecules to target the core mechanisms of dry eye disease. c. Anti-inflammatory / immune-modulatory drugs d. Secretagogues e. Lubricants f. Hormones g. Autologous serum Adult Strabismus – Scope of the Problem II. Types of Patients Adult onset Childhood onset III. Spectrum of Patient Concerns Diplopia Visual confusion Poor stereopsis Anomalous head posture Psychosocial concerns – Quality of Life IV. Clinical Evaluation V. Eye Alignment Motor Fusion Sensory Fusion Management Goals Treatment options Lenses Prism Vision therapy Surgery