Corneal Complications of Aesthetic Procedures: A CME Publication
Corneal Complications of Aesthetic Procedures: A CME Publication
25
 A CME Publication
Accreditation
Vindico Medical Education is accredited
by the Accreditation Council for Continuing
Medical Education to provide continuing
medical education for physicians.
Credit Designation
Vindico Medical Education designates
this enduring material for a maximum of
1.25 AMA PRA Category 1 Credit(s)™.                                                                                   Volume 5 • Number 3 • October 2019
Physicians should claim only the credit
commensurate with the extent of their
                                                    Corneal Complications of
participation in the activity.
continued from page 1                       Although special cleaners are avail-       perming, especially for those in
Lash extensions are a popular trend,        able for lash extensions, many of the      whom lash extensions have become
but they can damage the natural lashes      ingredients in the cleaners are toxic to   problematic.10 Perming involves curl-
if applied incorrectly, potentially         the corneal surface, the lashes, and the   ing the lashes upwards by breaking
causing ocular surface problems.4           skin in the periorbital area.10            the sulfur bonds in the lash follicles
Although consumers undergoing eye-                                                     to recreate them in a bent fashion,
lash extensions should use a licensed       Lash Strips                                resulting in curly lashes.10 However,
professional who is certified to apply          When consumers become intol-           the process of perming typically in-
the lashes, most eyelash applications       erant of lash extensions or develop        volves several ingredients, some of
are performed at beauty/nail salons         allergic reactions to their key com-       which can lead to blepharokerati-
where employees are not certified           ponents, they may try an at-home           tis or a chemical burn if the perm-
to perform the task.4 The glues used        process of gluing a strip of artificial    ing chemical seeps onto the corneal
with these individually applied lashes      lashes onto their eyelids. The glue        surface.8,10,12 Ingredients frequently
often contain latex and formalde-           used with these at-home false lashes       used in lash perming include AMP-
hyde, which can negatively affect the       is typically applied 1 to 2 mm above       acrylates/allyl methacrylate copo-
tear film in patients allergic to these     the natural lash line, where new lash      lymer, carbomer, glycerin, sodium
substances,5 leading to periorbital         growth occurs.10 Consumers are sup-        hydroxide, phenoxyethanol, hydro-
erythema, chemosis, and permanent           posed to remove the false eyelashes        lyzed collagen, panthenol, tocoph-
lash loss.5 If a consumer is allergic to    every night.10 However, this step          eryl acetate, benzoic acid, dehydro-
latex and the person applying the lash      concurrently strips away new lash          acetic acid, potassium sorbate, and
extensions is unaware of this fact, the     growth, thins the natural lashes, and      sodium benzoate.10
latex in the fixative could lead to al-     interferes with their protective pur-
lergic blepharoconjunctivitis.6,7 Simi-     pose against surface irritants.6,10        Lash Dying
larly, the gel pads used during the lash                                                  Lash dying or tinting is another
application process may contain latex       Lash Embellishment                         beauty option that consumers use to
and a variety of adhesives, which can           Lash embellishment is a beauty         darken their lashes to make them ap-
potentially lead to ocular irritation       trend whereby users apply rhine-           pear more prominent. This coloring
and allergic dermatitis.6-8 Eyelashes       stones, feathers, and other adornments     process is often performed in salons
that are excessively long or thick may      to the lashes with fine wires or glues.5   by hair and nail technicians who are
alter the air dynamics as well as fun-      These can create trauma to the natu-       not familiar with orbital anatomy.8
nel pollen and pollution onto the cor-      ral lash and lash root, leading to per-    Many dyes have harsh components,
neal surface instead of repelling these     manent lash loss due to the weight of      including hydrogen peroxide, syn-
environmental elements.9                    the objects attached as well as to the     thetic coal tar, and histamine.8,10 Ul-
    The interest in obtaining longer        tugging and manipulation.10 If a user      timately, these coloring agents may
lashes with extensions creates a vi-        attaches decorative feathers to their      lead to an allergic reaction in patients
cious cycle—persons must return to a        eyelashes and they have an allergy to      sensitive to these components.8,10 To
salon every few weeks for a “refill,” as    feathers, this may create the perfect      perform eyelash tinting properly,
20% to 30% of human lashes are lost         venue for allergic conjunctivitis.10       the dye should first be tested on the
during that period due to natural turn-     Similarly, the use of trendy glued-on      skin,8 and then the consumer should
over.7,10 This not only creates a cost      LED lights to the upper eyelid margin      be seated at a 45-degree angle after
burden, but it may exacerbate dry eye       can affect the growth of new lashes.10     the dye is applied to the lashes to
disease, blepharitis, and meibomian         The weight of these lights can lead to     avoid getting colorant into the eye.10
gland dysfunction.6,7,10 As patients aim    traction alopecia, particularly because    Unfortunately, these 2 steps are fre-
to retain their lash extensions, they be-   users must apply a copious amount          quently not performed.
come hesitant to wash their eyelids.10      of glue to keep them on.10,11 Stripping
Consequently, debris accumulates at         off the lights can remove natural, new     Makeup and Ocular
the base of the lashes, which can lead      eyelash growth.10                          Surface Disease
to blepharitis, foreign body sensation,                                                   The use of makeup, with its many
or a Demodex folliculorum infestation,      Lash Perming                               ingredients, may lead to exacerbation
with progressive worsening of the per-         Another lash trend toward which         of OSD and overall eye discomfort.3
son's ocular surface disease (OSD).10       consumers are gravitating is lash          Most patients do not link the use of
  4                                                                          Volume 5 • Number 3 • October 2019
about their use of beauty products        3.    O’Dell LE, et al. Poster presented       15. National Environmental Health
and cosmetic procedures.                        at: ARVO 2017; May 6-11, 2017;               Association.       https://www.neha.
                                                Baltimore, MD. Poster A0420.                 org/sites/default/files/publications/
    I believe an important pearl is to
                                                https://iovs.arvojournals.org/article.       position-papers/NEHA_Policy_
teach patients to read beauty product           aspx?articleid=2638663&resultCli             Statement_Microblading_FINAL.
ingredient labels as closely as they            ck=1. Accessed July 31, 2019.                pdf. Accessed August 20, 2019.
may read food ingredient labels. For      4.    Mukamal R. https://www.aao.org/          16. Bussel II, et al Ophthalmol-
example, teaching patients about the            eye-health/tips-prevention/eyelash-          ogy        Times.       https://www.
presence of prostaglandins (indicated           extension-facts-safety.    Accessed          ophthalmologytimes.com/modern-
with prost in an ingredient name) can           August 19, 2019.                             medicine-cases/cosmetic-eyeliner-
make them aware of this substance,        5.    Avitzur O. https://www.consumer-             tattoo-risk-factor-ocular-surface-
which may cause periorbital pigmen-             reports.org/cro/2013/05/eyelash-             disease. Accessed July 10, 2019.
tation, along with a negative effect on         extensions-can-pose-health-risks/        17. Choi M. https://www.livinghealthy.
                                                index.htm. Accessed July 10, 2019.
meibomian glands.24 In patients with                                                         com/articles/itchy-eyes-why-
chronic blepharitis and dry eye, pa-      6.    Amano Y, et al. Cornea.                      your-manicure-is-the-most-likely-
                                                2012;31(2):121-5.                            culprit. Accessed July 10, 2019.
tients or their ophthalmologists should
                                          7.    Whelan C. https://www.healthline.        18. Shanmugam S, et al. Contact Der-
look for products with benzalkonium
                                                com/health/eyelash-extension-side-           matitis. 2012;67(5):309-10.
chloride (BAK), which may aggravate             effects. Accessed August 20, 2019.
their underlying ocular surface prob-                                                    19. Whitelocks S. https://www.daily-
                                          8.    Masud M, et al. Med Hypoth-
lem.24 Patients also should look for                                                         mail.co.uk/femail/article-2510576/
                                                esis Discov Innov Ophthalmol.
eye beauty products that are free of                                                         Woman-gets-platinum-eye-jewelry-
                                                2019;8(2):96-103.
                                                                                             implanted-optic-membrane.html.
parabens, which are preservatives that    9.    Amador GJ, et al. J R Soc Interface.         Accessed July 15, 2019.
could irritate the ocular surface.10            2015;12(105):20141294.
                                                                                         20. American Academy of Ophthal-
    Ophthalmologists need to keep in      10.   Matossian C. Presented at: ASCRS
                                                                                             mology. https://www.aao.org/eye-
mind that beauty-related procedures             2019; May 4, 2019; San Diego, CA.
                                                                                             health/news/eyeball-jewelry. Ac-
and products can be causes, mas-                Course #IC-111.
                                                                                             cessed August 20, 2019.
queraders, or exacerbators of OSD.        11.   Matossian C, et al. Ophthalmology
                                                Management. 2016;20(April):30-3.         21. Saldanha MJ, et al. Can J Ophthal-
                                                                                             mol. 2016;51(4):e115-e116.
References                                12.   Cherney K. https://www.healthline.
                                                com/health/lash-lift-side-effects.       22. Leung TG, et al. J Ophthalmic In-
1. Sorvino C. https://www.forbes.com/
                                                Accessed August 20, 2019.                    flamm Infect. 2013;3(1):39.
   sites/chloesorvino/2017/05/18/self-
   made-women-wealth-beauty-gold-         13.   Robaei       D.     Ophthalmology.       23. American Academy of Ophthal-
   mine/#27d371652a3a.       Accessed           2018;125(5):641.                             mology.        https://www.aao.org/
   July 10, 2019.                         14.   Wesley N. https://www.mdedge.                eye-health/tips-prevention/eyeball-
2. Starr CE, et al. In: Ocular Surface          com/dermatology/article/57216/               tattoos-are-even-worse-than-they-
   Diseases, Disorders, & Dysfunc-              pigmentation-disorders/cosmetic-             sound. Accessed August 20, 2019.
   tions. Thorofare, NJ: Vindico Medi-          tattooing-and-ethnic-skin. Accessed      24. Mocan MC, et al. J Glaucoma.
   cal Education; 2017;3(4):1-6.                August 20, 2019.                             2016;25(9):770-4.
  6                                                                             Volume 5 • Number 3 • October 2019
T    he corneal pe-
     riphery repre-
sents a unique im-
                                                Marginal keratitis generally pres-
                                            ents with 1 or multiple small infil-
                                            trates, with a small, clear, intervening
                                                                                       Phlyctenular Keratitis
                                                                                           Phlyctenular keratitis is thought
                                                                                       to occur as a response to antigens
munologic        zone.                      space between the limbus and the           released by infectious organisms. It
Proximity to sys-                           infiltrate, which is thought to occur      was initially described in children
temic      vasculature Julie Schallhorn,    because of the diffusion dynamics          with tuberculosis, but staphylococcal
on the limbal side            MD, MS        of the immune complex deposition.8         blepharitis and meibomitis are more
makes this portion of the cornea ac-        The infiltrates may occur anywhere,        commonly seen today.9-12 It has also
cessible to inflammatory cells, anti-       but they are typically found at loca-      been reported in the setting of helmin-
bodies, and inflammatory mediators.1        tions of overlap between the eyelid        thic infections and rosacea and occurs
Due to the junction between the lim-        margin and the limbus.8 There often        more commonly in children.13,14
bal blood supply and the avascular          is overlying epithelial ulceration, but        Phlyctenules can be limited to
central cornea, immune mediators            the epithelium may be intact in some       the conjunctiva, where they present
and antibodies can collect in the           cases.8 Examination of the eyelids         as raised nodules on a background
peripheral stroma causing disease,          and lashes often reveals blephari-         of conjunctival injection, usually in
whereas the central cornea remains          tis with scurf, lid margin crusting,       the nasal/temporal limbus. The lack
unaffected.1 The limbus also houses         or ulceration and may demonstrate          of deep episcleral injection and the
a population of antigen-presenting          meibomitis.8 Typically, the infiltrates    characteristic boring pain separate
cells that are effective at recruiting a    are culture-negative (so-called sterile    phlyctenular keratitis from scleritis.8
cellular immune response.1 However,         infiltrates), but cultures from the eye-   When involving the cornea, phlycte-
this can result in the unique inflam-       lids and conjunctiva yield high levels     nules generally appear as a white foci
matory patterns of crescentic inflam-       of Staphylococcus species.8                of inflammation, leading a wedge-
mation that is often seen in peripheral         In the setting of ulceration, and      shaped patch of injection or vascular-
corneal diseases.2                          especially if the patient has a his-       ization (Figure 1). There can be ulcer-
                                            tory of contact lens wear, the infil-      ation overlying the inflammation, with
Marginal Keratitis                          trate should be cultured to rule out       the lesion requiring a culture to differ-
    Marginal keratitis, also called         an infectious etiology. After culture,     entiate it from infectious keratitis.
staphylococcal marginal keratitis or        my patients are started on a broad-            Chronic phlyctenular disease can
staphylococcal hypersensitivity kerati-     spectrum topical antibiotic, such as       have a meandering pattern of vascular-
tis, is thought to arise from the deposi-   a fourth-generation fluoroquinolone,       ized, scarred cornea leading from the
tion of immune complexes within the         4 times per day. In classic cases          limbus to the central cornea.8 This is
peripheral corneal stroma in response       without a history of contact lens          thought to occur from repeated bouts
to antigens from lid bacteria.3 This        wear, some practitioners will also         of inflammation at the head of the le-
causes the attraction of inflammatory       start a mild topical steroid, such as      sion, leading the phlyctenule further
cells, resulting in the appearance of an    fluorometholone 0.1%, at the same          onto the cornea with each relapse.8
infiltrate.3 As macrophages ingest the      time. In atypical cases or those with          The clinical sequelae of phlyc-
immune complexes and neutrophils            a history of contact lens wear, ste-       tenules, particularly in the pediatric
disgorge cytotoxic enzymes, ulcer-          roids should not be given prior to         population where it is more common,
ation of the overlying epithelium can       obtaining culture results.8 Treatment      can be severe.15 Significant corneal
form.3,4 Marginal keratitis has also        also involves addressing underlying        involvement can result in corneal
been reported in the setting of numer-      blepharitis. Patients generally bene-      scarring and irregular astigmatism,
ous other conditions, including ocular      fit from a regimen of lid hygiene and      inducing amblyopia in younger chil-
rosacea, syphilis, graft-versus-host        warm compresses, although compli-          dren.15 If ulceration occurs, treatment
disease, and leukocytoclastic vascu-        ance with these measures can often         involves obtaining a culture to rule
litis, and atypical or severe cases re-     be suboptimal and many patients            out infection, and a topical antibi-
quire further investigation.5-7             will experience repeat episodes.8          otic—generally a fourth-generation
  Ocular Surface Diseases, Disorders, & Dysfunctions ®                                                                        7
fluoroquinolone or polymyxin/trime-
                                             Figure 1. Corneal                            Figure 2. Peripheral
thoprim—is used until the epithelium
                                                       Phylectenule                                 Ulcerative
is healed, in addition to use of a topi-                                                            Keratitis Without
cal steroid.1 Lesions are generally re-                                                             Scleritis
sponsive to steroids, requiring appli-
cation no more than 4 times per day.1
Patients with ocular rosacea or mei-
bomitis also benefit from the addition
of an oral macrolide or tetracycline
antibiotic.16 In young children, eryth-
romycin is preferred to the tetracy-
clines.16 In my experience, some pa-
tients require chronic topical steroids      Source: Courtesy of Gerami Seitzman, MD.     Source: Julie Schallhorn, MD, MS.
to control their disease. In such cases,
topical 0.03% tacrolimus ointment
has been shown to be of benefit.17,18      cornea may be markedly thinned, and          there are any positive findings on
Children with phlyctenular disease         perforation may occur.2 There may            patients’ review of systems, consider
should be followed closely to prevent      be associated scleritis in concomitant       referral to a rheumatologist for further
scarring, loss of vision, and steroid-     systemic vasculitic disease.2                evaluation. Patients presenting with
induced ocular complications.1                 Approximately 50% of the oc-             what appears to be PUK should also
                                           currences of PUK are associated              undergo a laboratory culture to rule
Peripheral Ulcerative                      with a systemic vasculitic disease.20        out infection. In cases of suspected
Keratitis                                  The most common systemic asso-               viral etiology, polymerase chain reac-
    Peripheral ulcerative keratitis        ciation is rheumatoid arthritis, but         tion should be performed.24 Numerous
(PUK) is a severe, vision-threatening      numerous other autoimmune etiolo-            infectious pathogens, including Acan-
disease in which ulceration of the epi-    gies have been implicated, includ-           thamoeba and herpes, can masquer-
thelium and progressive keratolysis of     ing granulomatosis with polyangiitis         ade as PUK, thus differentiation is of
the stroma result in severe peripheral     (GPA; formerly known as Wegener’s            the utmost importance to provide the
corneal thinning, with a risk of per-      granulomatosis), polyarteritis nodosa,       proper treatment.19,24,25
foration and secondary infection.1,19      Cogan’s syndrome, systemic lupus                 The diagnosis of noninfectious
The exact pathogenic mechanisms            erythematosus, relapsing polychon-           PUK should always prompt a workup
are unknown but are thought to be the      dritis, eosinophilic granulomatosis          for systemic vasculitic diseases (Ta-
development of an immune response          with polyangiitis (formerly known as         ble).26 This is essential, given the fre-
against a corneal or epithelial antigen.   Churg-Strauss syndrome), Behcet’s            quency of concurrent systemic dis-
However, cell-mediated cytotoxicity        disease, inflammatory bowel dis-             ease and the life-threatening nature
may also play a role.1,19 This results     ease, and scleroderma.1,21,22 Infectious     of these diseases.26 It is especially
in the deposition of antibody–antigen      causes have also been implicated in          critical to properly diagnose patients
complexes within the peripheral stro-      PUK, including varicella zoster and          with GPA as a cause of PUK because
ma, complement activation, and an in-      herpes simplex, acanthamoeba, fun-           patients with GPA and eye involve-
flux of T cells, macrophages, and neu-     gal infections, many bacterial species,      ment are at a significantly increased
trophils.1 Neutrophil activation results   syphilis, tuberculosis, and others.1,19      risk of mortality—up to 50% at
in the release of cytotoxic enzymes,           Patients should undergo a thor-          5 months—without treatment.26
which degrade the epithelium and col-      ough review of systems, with special             Patients with PUK without associ-
lagen fibers, resulting in ulceration      attention focused on the musculoskel-        ated scleritis who have a negative sys-
and thinning.1 The associated limbal       etal, skin, and respiratory systems to       temic workup and no other attributable
vasculature may demonstrate a vaso-        evaluate symptoms of any other auto-         causes of PUK are usually associated
occlusive vascultitis.2                    immune disease.21,23 Specifically for        with a diagnosis of Mooren’s ulcer.8
    The presenting appearance of PUK       relapsing polychondritis, the practitio-     An association between Mooren’s
is peripheral crescentic ulceration,       ner should inquire about patients’ ten-      ulcer and hepatitis C infection has
with thinning in the absence of an         derness over cartilaginous processes,        been reported.27 Thus, patients with
infectious infiltrate (Figure 2).2 The     including the nose and pinna.21,23 If        a diagnosis of Mooren’s ulcer should
     8                                                                                                  Volume 5 • Number 3 • October 2019
undergo evaluation for hepatitis C.27                               Any keratoconjunctivitis sicca or sec-     Summary
There have also been reports of asso-                               ondary Sjogren’s syndrome should              With a thorough patient examina-
ciation of Mooren’s ulcer with expo-                                also be addressed, as this can contrib-    tion and history and an understand-
sure to helminths, although the patho-                              ute to further melting.1                   ing of the underlying pathophysiol-
genic mechanisms remain unclear.28                                      Perforation of the cornea in an        ogy of corneal diseases, clinicians
    In patients with a negative infec-                              acute setting can often be managed         should be able to differentiate the
tious workup, treatment should be                                   with topical cyanoacrylate glue until      numerous peripheral corneal auto-
initiated with high-dose oral cor-                                  the systemic disease can be brought        immune diseases and provide the
ticosteroids, generally prednisone                                  under control, which is the preferred      appropriate treatment. Proper diag-
1 mg/kg.21,23 Patients taking oral non-                             method of treating perforations in pa-     nosis of these diseases is extremely
steroidal anti-inflammatory drugs or                                tients with active disease (Figure 3).23   important, as they often are harbin-
aspirin or have a history of peptic                                 Patients with large perforations that      gers of severe systemic diseases.
ulcer disease should begin peptic ul-                               are unresponsive to glue require
cer prophylaxis with an oral proton                                 urgent tectonic grafting.23 In these       References
pump inhibitor or H2-blocker.21 In                                  cases, all attempts should be made         1.      Dana MR, et al.                    Cornea.
hyperacute cases, intravenous pulse                                 to get the systemic disease under                  2000;19(5):625-43.
steroids may be necessary.21 Patients                               control as rapidly as possible or          2.      Foster CS. J Fr                  Ophtalmol.
should be transitioned to systemic                                  further melting of the tectonic graft              2013;36(6):526-32.
immunomodulatory therapy from                                       will occur.29                              3.      Ficker L, et al. Eye (Lond).
oral steroids in most cases.21 Mul-                                     Areas of PUK can induce signifi-               1989;3(Pt 2):190-3.
tidisciplinary care with rheumatol-                                 cant irregular astigmatism.30 When the     4.      Jayamanne DG, et al. Eye (Lond).
ogy is essential to ensure appropriate                              disease has been stabilized, treatment             1997;11(Pt 5):618-21.
patient management. During active                                   with large-diameter scleral lenses can     5.      Martinez JA, et al. Am J Ophthal-
disease, topical and systemic anticol-                              often provide excellent vision as well             mol. 1989;107(4):431-3.
lagenase adjuvant measures, includ-                                 as the treatment of concurrent kerato-     6.      Dai E, et al. Cornea. 2007;26(6):756-8.
ing oral doxycycline, oral high-dose                                conjunctivitis sicca.30 Patients who are   7.      Li Yim JF, et al. Clin Exp Ophthal-
vitamin C, and topical 20% n-acetyl-                                not candidates for contact lenses may              mol. 2007;35(3):288-90.
cysteine, may be helpful but should                                 undergo tectonic grafting for the treat-   8.      Krachmer JH, et al (eds). Cornea.
not be used as a stand-alone therapy.8                              ment of astigmatism.29                             Philadelphia, PA: Elsevier; 2011.
     Ocular Surface Diseases, Disorders, & Dysfunctions ®                                                                      9
9.    Lahiri K, et al. Pediatr Infect Dis J.   16. Culbertson WW, et al. Ophthalmol-      23. Messmer EM, et al. Surv Ophthal-
      2015;34(6):675.                              ogy. 1993;100(9):1358-66.                  mol. 1999;43(5):379-96.
10. Neiberg MN, et al. Optometry.              17. Yoon CH, et al.             Cornea.    24. Praidou A, et al. Cornea.
    2008;79(3):133-7.                              2018;37(2):168-71.                         2012;31(5):570-1.
                                                                                          25. Vignesh AP, et al. Taiwan J Oph-
11. Suzuki T. Cornea. 2012;31 Suppl            18. Kymionis GD, et al. Cornea.                thalmol. 2016;6(4):204-5.
    1:S41-4.                                       2012;31(8):950-2.                      26. Tarabishy AB, et al. Surv Ophthal-
12. Suzuki T, et al. Am J Ophthalmol.          19. Moreira AT, et        al.   Cornea.        mol. 2010;55(5):429-44.
    2005;140(1):77-82.                             2003;22(6):576-7.                      27. Wilson SE, et al. Ophthalmology.
13. Blaustein BH, et al. Optometry.            20. Knox Cartwright NE, et al. Cornea.         1994;101(4):736-45.
    2001;72(3):179-84.                             2014;33(1):27-31.                      28. van der Gaag R, et al. Br J Ophthal-
                                                                                              mol. 1983;67(9):623-8.
14. Doan S, et al. J Ophthalmic In-            21. Galor A, et al. Rheum Dis Clin         29. Lohchab M, et al. Surv Ophthal-
    flamm Infect. 2013;3(1):38.                    North Am. 2007;33(4):835-54, vii.          mol. 2019;64(1):67-78.
15. Rodriguez-Garcia A, et al. Eye             22. Shiuey Y, et al. Int Ophthalmol        30. Ding Y, et al. Surv Ophthalmol.
    (Lond). 2016;30(3):438-46.                     Clin. 1998;38(1):21-32.                    2019;64(2):162-74.
Episcleritis and Scleritis                     vessels, whereas the vessels in scle-      Patient Workup
continued from page 1                          ritis will not blanch.3 Moreover, use          If the patient has positive find-
A large cohort study of patients in            of the red-free filter on the slit lamp    ings on review of systems or frequent
northern California found the in-              can be helpful in distinguishing vas-      recurrences, a workup for an associ-
cidence to be 41/100,000 person-               cular engorgement of the superficial       ated systemic disease and possibly a
years and the prevalence to be                 episcleral layers of the episclera         biopsy should be considered.4 Labo-
52.6/100,000 person-years.3 Extrapo-           from the involvement of the deeper         ratory workup should be directed
lated to the population of the United          visceral layer in scleritis (Figure 2).1   and guided by the patient’s history
States, we would expect 120,000 new                Episcleritis is usually idiopathic,    and review of systems rather than
cases of episcleritis every year in the        but it may be associated with sys-         a “shotgun” approach to testing.6
United States.3 Because of its self-           temic disease in approximately one-        For instance, findings of lower back
limiting nature, the true incidence            third of patients.4 Jabs et al5 found      stiffness or pain that is worse in the
and prevalence may be difficult to             an association with rheumatoid             morning and gets better with activ-
quantify, as many patients may not             arthritis in 11.1% of patients with        ity should prompt testing for HLA-
seek attention or may be treated by            episcleritis. In another study, atopy      B27.6 Laboratory investigations for
their primary care physician.3                 (12%) was the most commonly as-            episcleritis and scleritis are shown in
                                               sociated systemic disease.4 The            the Table.
Classification of Episcleritis                 study authors found no correlation             In addition, nearly half of patients
    Episcleritis is classified as sim-         between the number of recurrences,         with episcleritis will have a concur-
ple or nodular. Simple episcleritis            laterality, or type of episcleritis and    rent underlying eye disease such as
is most common and characterized               the presence of associated systemic        rosacea, keratoconjunctivitis sicca, or
by sectoral or diffuse vascular con-           disease.4 Of note, 2 patients in the       atopic keratoconjunctivitis.4 A thor-
gestion of the episcleral vessels.1            study were found to have previously        ough examination of the ocular sur-
Nodular episcleritis presents with a           undiagnosed systemic vasculitides,         face, including lids as well as palpebral
discrete, elevated area of inflamed            including granulomatosis with poly-        and bulbar conjunctiva, is essential
episcleral tissue (Figure 1).3 Episcle-        angiitis and Cogan’s syndrome.4            because treatment of these conditions
ritis can be distinguished from scle-          Thus, obtaining a thorough history         will often resolve the episcleritis.4
ritis by the presence of straight ves-         and review of systems is important
sels rather than criss-cross vessels           for each patient presenting with           Treatment
in the deep episcleral plexus, which           episcleritis, with a special focus on         Because episcleritis is often self-
causes a bluish-red color when vas-            symptoms of atopy, inflammatory,           limited, treatment may not be required.
cular congestion occurs in scleritis.1         and collagen vascular diseases.            Jabs et al5 found that 16.7% of cases
Use of 10% phenylephrine will re-              This should be repeated annually,          of episcleritis spontaneously remit-
sult in blanching of the episcleral            or optimally with each recurrence.4        ted without treatment. However, for
  10                                                                                    Volume 5 • Number 3 • October 2019
patients with persistent inflamma-               systemic complications.3 The esti-           complain about mild to moderate
tion or symptomatic disease, treat-              mated annual incidence of scleritis          dull pain that can be worse at night
ment may be justified and should                 in the United States is 10,500 new           and can be referred to other parts of
be aimed at any underlying condi-                cases per year, with a prevalence of         the face, including the cheek, jaw,
tion (eg, removal of allergens or                5.2/100,000 person-years.3 Scleri-           and face.9 In my experience, some
treatment of dry eye).4 Iced arti-               tis typically affects women in their         patients, such as those who are al-
ficial tears and cold compresses                 fourth to sixth decade of life and is        ready taking systemic anti-inflam-
are often the only treatment that                rare in children.3                           matory medications, may not have
is needed.4 Topical nonsteroidal                     Structural and vascular character-       pain. Keratitis and uveitis can also
anti-inflammatory drugs (NSAIDs)                 istics of the sclera explain its predis-     be present and usually portend a
are not better than artificial tears in          position to inflammatory conditions.9        poorer prognosis.10
treating episcleritis.7 In contrast,             The sclera is avascular, obtaining
topical corticosteroids resulted in              nutrition from the choroid as well           Nodular Scleritis
improvement in 50% of cases.5                    as episcleral vascular networks, with            Nodular anterior scleritis pres-
Topical fluorometholone 0.1% or                  artery-to-artery anastomoses, where          ents with a localized, elevated nod-
prednisolone acetate 1% is gener-                blood oscillates rather than circu-          ule on the sclera that is immobile
ally effective.5 Less than 20% of pa-            lates.9 This leads to reduced circula-       and firm, with surrounding inflam-
tients with episcleritis may require             tion and clearance of antigens, allow-       mation.5 These patients should be
oral NSAIDs for control, and oral                ing the inflammation to persist.9            monitored for progression to necro-
corticosteroid use or immunosup-                     Watson’s and Hayreh’s classifi-          tizing anterior scleritis.5
pressive therapy is usually not re-              cation of scleritis into anterior and
quired.8 Over-the-counter NSAIDs,                posterior forms is useful in deter-          Necrotizing Scleritis
such as naproxen and ibuprofen,                  mining severity as well as choosing              In necrotizing anterior scleri-
are effective and well tolerated.6               the appropriate treatment.1 Ante-            tis, vasculitis leads to closure of
Both selective and nonselective                  rior scleritis is further subdivided         the deep episcleral plexus, result-
cyclooxygenase inhibitors have                   into diffuse, nodular, and necrotiz-         ing in necrosis of the scleral tissue
demonstrated an 80% success rate                 ing with inflammation and without            (Figure 4).11 This can lead to ex-
in the treatment of episcleritis.8               inflammation (scleromalacia per-             posure of the underlying uveal tis-
                                                 forans), with diffuse scleritis being        sue, causing a blue discoloration to
Scleritis                                        the most common subtype.1                    the eye (Figure 5).11 The pain and
   Scleritis is an ocular inflamma-                                                           tenderness in these patients tend to
tion that involves the opaque outer              Diffuse Anterior Scleritis                   be more severe than in other types
eye wall and may include the epi-                   Diffuse anterior scleritis is char-       of scleritis.11 In addition, patients
sclera, cornea, and underlying uvea.1            acterized by generalized inflamma-           may be more likely to experi-
The disease is typically character-              tion of the sclera and is typically in-      ence ocular complications, such
ized by severe ocular pain and is as-            sidious in onset (Figure 3).9 Patients       as keratitis, uveitis and elevated
sociated with significant ocular and             with anterior scleritis will often           intraocular pressure.11
  Ocular Surface Diseases, Disorders, & Dysfunctions ®                                                                  11
Other Forms of Scleritis                   Table. Laboratory Testing for Episcleritis And Scleritis
   The most severe form of scleri-
                                            Diagnostic Test                                      Purpose
tis—scleromalacia         perforans—is
                 11                         Antineutrophil cytoplasmic           Can suggest granulomatosis
also the rarest. Typically seen in
                                            antibodies (ANCAs)                   with polyangiitis
patients with rheumatoid arthritis,
obliterative arteritis in the deep epi-     Antinuclear antibodies (ANAs)        Can suggest systemic lupus
                                                                                 erythematosus, rheumatoid arthritis,
scleral plexus may cause necrosis                                                mixed connective tissue disease,
without pain, redness, or other signs                                            polymyositis/dermatomyositis, but the
of inflammation.11                                                               positive predictive value is low, so it
   Posterior scleritis involves in-                                              has questionable utility)
flammation posterior to the rectus          Urinalysis                           May reveal microscopic hematuria in
muscle insertions and can be diffuse                                             systemic vasculitis; helpful in identifying
or nodular.5 Patients with posterior                                             additional renal abnormalities that
                                                                                 can point to further areas for
scleritis tend to be younger than                                                diagnostic testing
those with anterior scleritis, and dis-
ease is often bilateral.5 Due to the an-    Chest X-ray, computed                Sarcoidosis
                                            tomography imaging
atomic location of the inflammation,
patients may experience more severe         Fluorescent treponemal               Syphilis (rapid plasma reagin [RPR] or
                                            antibody absorption test,            venereal disease research laboratory
vision loss due to serous retinal de-
                                            enzyme immunoassay test              [VDRL] testing should be obtained as
tachments, optic nerve edema, or            (EIA), treponema pallidum            well for confirmation)
chorioretinal granulomas.12 A B-            particle agglutination assay
scan ultrasound can be helpful in           (TPPA), microhemagglutination
                                            assay for Treponema pallidum
making the diagnosis, with thick-
                                            antibodies (MHA-TP)
ening of the posterior coats ⬎2 mm
                                            Interferon-gamma-release assay Tuberculosis
and a “T-sign” caused by edema of
Tenon’s space and the optic nerve.12        Lyme serology                        Should be performed in patients from
                                                                                 endemic areas with a history of tick
                                                                                 bite or rash consistent with disease;
Infectious and Systemic Causes                                                   positive results should be confirmed
of Scleritis                                                                     with Western blot testing
    Up to 50% of patients with scle-        HLA-B27                              Seronegative spondyloarthropathies
ritis will have an associated infec-
tious or rheumatic disease.13 The           Complete blood count (CBC)           Helpful prior to starting
                                                                                 systemic therapy
most common infectious cause is
herpes zoster, and the most com-            Comprehensive metabolic panel        Helpful in identifying renal issues
                                                                                 associated with vasculitis and possible
mon rheumatic disease association                                                hepatitis; helpful prior to starting
is rheumatoid arthritis.13 Although                                              systemic therapy
most patients have the systemic dis-
                                           Source: Sanjay Kedhar, MD.
ease before the diagnosis of scleri-
tis, it is important to note that 14%      in necrotizing scleritis, with 50% to     obtaining a complete blood count,
of patients in one study received a        80% having an underlying systemic         comprehensive metabolic panel, an-
diagnosis after initial evaluation for     condition.13,14 Because a significant     tineutrophil cytoplasmic antibodies
scleritis, and 8% of those undiag-         portion of patients with scleritis will   (ANCA), syphilis serologies, urinal-
nosed initially developed a systemic       have an associated systemic disease       ysis, and chest radiograph.14 Mea-
disease during follow-up.13 System-        (some life-threatening), a laboratory     suring antineutrophil cytoplasmic
ic vasculitides (especially granulo-       workup is warranted in all patients       antibodies, assessing for granuloma-
matosis with polyangiitis) were 3          who do not carry an established diag-     tosis with polyangiitis, is crucial for
times more likely to be diagnosed          nosis.14 The workup should be guided      the initial workup for scleritis. In ad-
as a result of the initial evaluation      by the history, review of systems,        dition, cytoplasmic ANCA-positive
than rheumatic diseases.1 The risk         and physical examination.14 All pa-       patients may be more refractory to
of systemic autoimmune disease in-         tients should be tested for systemic      treatment and more likely to need
creases with severity and is greatest      vasculitis, which should include          immunosuppressive therapy, even
  12                                                                                      Volume 5 • Number 3 • October 2019
methotrexate to be effective for con-    importance because prognosis, as-         12. McCluskey PJ, et al. Ophthalmol-
trolling scleritis in approximately      sociation with systemic disease,              ogy. 1999;106(12):2380-6.
50% of patients. In another study,       and treatment will differ. Episcle-       13. Akpek EK, et al. Ophthalmology.
azathioprine was found to be ap-         ritis is benign, self-limited, and            2004;111(3):501-6.
proximately 20% less effective.27        rarely associated with systemic           14. Sainz de la Maza M, et al. Ophthal-
                                                                                       mology. 2012;119(1):43-50.
Mycophenolate mofetil success-           disease.4 Scleritis carries signifi-
                                                                                   15. Doshi RR, et al. Surv Ophthalmol.
fully controlled inflammation in         cant ocular and systemic morbidity
                                                                                       2013;58(6):620-33.
49% of patients with scleritis within    and should always be investigated,
                                                                                   16. Liesegang TJ. Ophthalmology.
6 months of treatment, tracking          with special attention to systemic
                                                                                       1991;98(8):1216-29.
closely to the overall effectiveness     vasculitis. A high index of suspi-
                                                                                   17. Reynolds MG, et al. Am J Ophthal-
in other ocular inflammatory diseas-     cion is necessary for the recogni-            mol. 1991;112(5):543-7.
es.28 Tumor necrosis alpha inhibi-       tion of posterior scleritis as well as    18. Sainz de la Maza M, et al. Ophthal-
tors have been shown to be effective     performing a complete evaluation              mology. 2012;119(1):51-8.
in the treatment of active anterior      of patients for infection or systemic     19. McMullen M, et al. Can J Ophthal-
scleritis, with infliximab achieving     autoimmune disease.                           mol. 1999;34(4):217-21.
quiescence in 80% of patients, with                                                20. Albini TA, et al. Ophthalmology.
60% being able to taper oral predni-     References                                    2005;112(10):1814-20.
sone down to 10 mg or less per day.29    1. Watson PG, et al. Br J Ophthalmol.     21. Sohn EH, et al. Ophthalmology.
Adalimumab may also be effective,            1976;60(3):163-91.                        2011;118(10) 1932-7.
but etanercept should be avoided         2. Read RW, et al. Ophthalmology.         22. Cheung CM, et al. Ophthalmology.
because it has been shown to be              1999;106(12) 2377-9.                      2012;119(1):59-65.
less effective for ocular inflamma-      3. Honik G, et al. Cornea.                23. Beardsley RM, et al. Expert Opin
tion.30 Rituximab holds promise for          2013;32(12):1562-6.                       Pharmacother. 2013;14(4)411-24.
cases of refractory scleritis, with 9    4. Akpek EK, et al. Ophthalmology.        24. McCluskey PJ, et al. Arch Ophthal-
of 12 patients achieving a reduction         1999;106(4):729-31.                       mol. 1987;105(6):793-7.
in inflammation or 50% reduction in      5. Jabs DA, et al. Am J Ophthalmol.       25. Jabs DA, et al. Am J Ophthalmol.
                                             2000;130(4):469-76.                       2000;130(4):492-513.
steroid use in one study.31 Alkylating
                                         6. Sieper J, et al. Ann Rheum Dis.        26. Gangaputra S, et al. Ophthalmol-
agents, such as cyclophosphamide
                                             2002;61 Suppl 3:iii8-18.                  ogy. 2009;116(11):2188-98.e1.
and chlorambucil have also been
                                         7. Lyons CJ, et al. Eye (Lond).           27. Prasadhika S, et al. Am J Ophthal-
used successfully in severe cases.32
                                             1990;4(Pt 3):521-5.                       mol. 2009;148(4):500-9.e2.
    I believe that the surgical man-
                                         8. Kolomeyer AM, et al. Ocul Immu-        28. Daniel E, et al. Am J Ophthalmol.
agement of patients with scleritis is                                                  2010;149(3):423-32.
                                             nol Inflamm. 2012;20(4):293-9.
not common. However, surgery may                                                   29. Sen HN, et al. Can J Ophthalmol.
                                         9. Watson PG, et al. Exp Eye Res.
be necessary for the repair of scleral       2004;78(3):609-23.                        2009;44(3):e9-12.
or corneal defects or to aid in diag-                                              30. Levy-Clarke G, et al. Ophthalmol-
                                         10. Sainz de la Maza M, et al. Ophthal-
nosis via biopsy.                            mology. 1997;104(1):58-63.                ogy. 2014;121(3):785-96.e3.
                                         11. Watson PG. In: Duane’s Clinical       31. Suhler EB, et al. Ophthalmology.
Summary                                      Ophthalmology. Rev ed. Philadel-          2014;121(10):1885-91.
    Distinguishing between episcle-          phia, PA: Lippincott Williams &       32. Pujari SS, et al. Ophthalmology.
ritis and scleritis is of paramount          Wilkins; 1992:1-43.                       2010;117(2):356-65.
EXPERT INTERVIEW
Recent reports indicated that                                    ocular events.3 In clinical trials of dupilumab for AD, in
dupilumab therapy for patients with                              addition to having a previous history of conjunctivitis,
moderate to severe atopic dermatitis                             a greater baseline AD severity was associated with in-
can be associated with ocular side                               creased incidence of conjunctivitis.3 In a real world cohort
effects. What are these side effects?                            of 142 dupilumab-treated patients, 7 of 12 (58%) who de-
                                                                 veloped conjunctivitis had other atopic conditions.5 Nine
                                                 Kenneth A.
    Ocular side effects are common in pa-        Beckman, MD,    (75%) had severe baseline AD.5 Three of these patients
tients treated with dupilumab for atopic             FACS        developed severe conjunctivitis, whereas the 3 patients
dermatitis (AD), which received US Food and Drug Ad-             with less than severe AD at baseline developed mild (n=1)
ministration approval for AD in 2017.1,2 Conjunctivitis          or moderate (n=2) conjunctivitis.5 In another series of
incidence was similar in dupilumab and placebo groups            13 patients with conjunctivitis, 8 (62%) had severe AD at
in clinical trials for other indications.3 In addition to con-   baseline and 4 (31%) had a history of conjunctivitis.8 On-
junctivitis, blepharitis, dry eye, photophobia, and keratitis    treatment conjunctivitis was severe in 3 of the 8 (38%)
have also been observed following dupilumab treatment            patients with severe baseline AD, but no patient with mod-
for patients with AD.4-6 Flare-ups of existing ocular sur-       erate baseline AD developed conjunctivitis, although 1 de-
face conditions have also been reported, including poten-        veloped severe blepharitis.8 More research is needed, and
tial recurrence of herpes virus infections.4 Case reports        all patients taking dupilumab should be considered at risk
have noted goblet cell scarcity in affected patients.7 The       for OSD until more evidence is acquired.4
term dupilumab-induced ocular surface disease has been
proposed to accommodate the spectrum of ocular surface           What steps should be taken to manage ocular
manifestations that may be observed.6                            events associated with dupilumab therapy?
Is the initial presentation of these patients different              Clinicians managing patients with AD should be
from those with ocular surface disease who are not               aware of the increased risk for OSD associated with this
being treated with dupilumab?                                    disease.6 Referral for an eye examination before starting
                                                                 treatment can help confirm that timely therapy is pro-
   Many of these patients already have ocular surface            vided.3 Eye care specialists must ensure that complete
disease (OSD) due to the severity of their AD.3 In my            health and medication histories are acquired.3 Education
practice, most patients with AD have lid margin disease,         is as important for the clinicians as it is for the patients.
dry eye, and severe allergic conjunctivitis before dupil-        A baseline eye examination is warranted before starting
umab treatment. Those conditions tend to worsen after            dupilumab therapy.3 Lid margin disease treatments, such
starting dupilumab therapy. I initially investigate patients     as lid hygiene, warm compresses, and artificial tears, can
with AD as I would for any other patient with OSD. Also,         be helpful.3,6 However, when OSD flares, it is difficult
when dermatologists want to know their patient’s ocular          to treat and usually requires several medications.6 Anti-
surface status before starting dupilumab therapy, a full         inflammatory agents, including steroids, cyclosporine,
dry eye workup is also performed.                                and lifitegrast, may be used to treat OSD.6
                                                                     In my experience, patients with AD do not want to stop
Are there any patient factors associated with the                dupilumab therapy, despite the development of OSD, be-
development of ocular events in those treated with               cause dupilumab is effective in treating AD. Many of these
dupilumab for atopic dermatitis?                                 patients are young. In addition to being miserable from
                                                                 dermatitis, they are self-conscious of their appearance.
  Persons with underlying OSD at the time of treat-              Most patients are willing to adhere to any ocular therapy
ment initiation may be more vulnerable to subsequent             regimen rather than discontinue dupilumab treatment.
  Ocular Surface Diseases, Disorders, & Dysfunctions ®                                                                     15
        VINDICO
        medical education
CASE PRESENTATION
Dupilumab-Induced Ocular Surface Disease
Laura M. Periman, MD; Laura K. Green, MD; Brede A. Skillings, MD
A     41-year-old man
      with a history
of atopic dermatitis,
                                                                                      tears. The oral prednisone was de-
                                                                                      creased to 10 mg daily. At the 4-week
                                                                                      follow-up, the patient noted moderate
for which he is treat-                                                                improvement in his ocular and eyelid
ed with dupilumab,                                                                    symptoms. There was significant im-
presented with com-                                                                   provement in examination findings,
                           Laura M. Periman, Laura K. Green, MD   Brede A. Skillings,
plaints of bilateral eye          MD                                     MD           specifically regarding dermatitis, ec-
irritation, mucoid dis-                                                               tropion, erythema, and injection of the
charge, photophobia, and tearing approximately 6 weeks            tarsal conjunctiva (Figure 4). He was then started on
after starting dupilumab. He described his pain level as a        oral doxycycline 100 mg daily (which was decreased to
9 out of 10 in severity. He had been treated with topical         50 mg daily due to gastrointestinal issues), as well as
and oral steroids, artificial tears, and warm compresses          prednisolone acetate 1% twice daily in both eyes, and
for the past 2 years. He was taking oral prednisone con-          continued on the previous regimen. After 6 weeks, the
tinuously for the past 9 months, with a dosage of 13 mg           patient reported continued improvement and was as-
daily at the time of visit. Due to his severe atopic der-         ymptomatic. The oral steroids, followed by the topical
matitis, multiple attempts to taper the oral prednisone           steroids, were then tapered. The patient was continued
failed. While taking oral prednisone, he developed ste-           on a regimen of pimecrolimus 1% cream twice daily,
roid-induced diabetes mellitus.                                   desonide 0.5% cream once daily, and petroleum jelly
                                                                  administered to the lateral canthus.
Examination
    The patient’s best-corrected visual acuity was 20/20          Discussion
in both eyes. His pupils, intraocular pressure, and con-              Atopic dermatitis is a T-cell–mediated, chronic in-
frontational visual fields were within normal limits. The         flammatory skin disease.1 Dupilumab was US Food and
eyelid examination was notable for bilateral dermatitis           Drug Administration-approved in 2017 for the treatment
of the periocular skin, erythema, 3+ meibomian gland              of moderate to severe atopic dermatitis and has since
dysfunction, vascularization of the lid margins, and ec-          been approved for moderate to severe asthma and chronic
tropion of the lower lids (Figures 1-3). There also was           rhinosinusitis with nasal polyposis.2 Clinical trials re-
a right upper lid chalazion, which the patient reports as         ported conjunctivitis as an adverse event more frequently
being present for 2 months. The conjunctiva showed 1+             in patients treated with dupilumab compared with pla-
chemosis, 1+ injection, 3+ papillary conjunctivitis, and          cebo.3 Since then, articles describing the risk factors;
keratinization of the lower lid tarsal surface bilaterally.       varying presentations, including periocular dermatitis;
The corneal examination was notable for trace superfi-            and possible treatment options have been published.4,5
cial punctate keratitis. The remainder of the examination             Dupilumab blocks interleukin (IL)-4 and IL-13.1
was within normal limits. A Schirmer’s test with anes-            Interleukin-4 is an important cytokine involved in the
thesia was normal at 18 mm and 19 mm in the right and             allergic TH2 cell response, whereas IL-13 plays a key
left eyes, respectively, at 5 minutes.                            role in goblet cell differentiation.1 The mechanism of
                                                                  ocular inflammation related to dupilumab is poorly un-
Treatment                                                         derstood, and further research is needed to elucidate
   The patient insisted on maintaining the dupilum-               the immunopathophysiology. However, given that IL-
ab because it had significantly improved eczema on                13 blockade may result in decreased goblet cell den-
the rest of his body, so he was initiated on desonide             sity, the immunoregulatory capacity of the ocular sur-
0.5% cream and pimecrolimus 1% cream twice daily                  face may also decrease, resulting in more aggressive
to the eyelids as well as frequent warm compresses,               Th1 and Th17 inflammation, which is more typical of
lid hygiene, and frequent preservative-free artificial            dry eye disease.6,7 Immunosuppressive medications
  Ocular Surface Diseases, Disorders, & Dysfunctions ®                                                                                   17
Figure 1. Patient With Atopic Dermatitis Figure 2. Patient With Atopic Dermatitis
 The patient has atopic dermatitis, with significant eyelid erythema,     Close-up photograph of the patient in Figure 1, with significant
 thickening, keratinization, and ectropion.                               eyelid erythema, thickening, keratinization, and ectropion.
 Source: Laura K. Green, MD.                                              Source: Laura K. Green, MD.
  Photograph shows the patient with palpebral conjunctival injection      The patient’s external findings improved after antibiotic, steroid,
  and inflammation.                                                       and nonsteroidal interventions as described.
  Source: Laura K. Green, MD.                                             Source: Laura K. Green, MD.
CME Posttest
1. Which of the following statements is false regarding                           6. All the following are effective treatments for adults suffering from
   lash extensions?                                                                  infected phlyctenules with ulceration except:
   A. They are a popular trend.                                                      A. Fourth-generation fluoroquinolone
   B. The glues used often contain latex and formaldehyde.                           B. Polymyxin/trimethoprim
   C. The latex in the fixative could lead to allergic blepharoconjunctivitis        C. Topical steroid
      in allergic individuals.                                                       D. Oral erythromycin
   D. Even if applied incorrectly, they do not damage the
      natural eyelashes.                                                          7. The most common systemic association of peripheral ulcerative
                                                                                     keratitis is _________.
2. Which of the following statements is true regarding lash strips?                  A. Scleroderma
   A. The glue used with at-home false lashes is typically applied                   B. Lupus erythematosus
      1 to 2 mm above the natural lash line.                                         C. Rheumatoid arthritis
   B. Consumers are not supposed to remove the false eyelashes                       D. Polyarteritis nodosa
      every night.
   C. Using false eyelashes on a regular basis has no effect on new               8. All the following are side effects that can occur with dupilumab
      lash growth.                                                                   therapy for atopic dermatitis except:
   D. Regular use of false eyelashes enhances the protection against                 A. Conjunctivitis
      surface irritants.
                                                                                     B. Blepharitis
3. Which of the following statements is true regarding the treatment                 C. Glaucoma
   of episcleritis?                                                                  D. Dry eye
   A. 86.7% of cases spontaneously resolve without treatment.
                                                                                  9. When ocular surface disease flares in patients taking dupilumab
   B. Topical nonsteroidal anti-inflammatory drugs are not better than
                                                                                     for atopic dermatitis, which of the following is likely to be
      artificial tears in treating episcleritis.
                                                                                     least effective?
   C. Use of topical corticosteroids has resulted in improvement in
      肁90% of cases.                                                                 A. Steroids
   D. Oral corticosteroid use or immunosuppressive therapy is                        B. Artificial tears
      usually required.                                                              C. Cyclosporine
                                                                                     D. Lifitegrast
4. What is the therapeutic failure rate for oral NSAIDs in patients with
   noninfectious anterior scleritis?                                              10. A 43-year-old woman with a history of atopic dermatitis, which
   A. 8%                                                                              is treated with dupilumab, presents with complaints of bilateral
                                                                                      eye irritation, mucoid discharge, photophobia, and tearing
   B. 18%
                                                                                      approximately 4 weeks after starting dupilumab. She described
   C. 28%                                                                             her pain level as 9 out of 10 in severity. She had been treated with
   D. 38%                                                                             topical and oral steroids, artificial tears, and warm compresses
                                                                                      for the past 3 years. She has been taking oral prednisone 15 mg
5. Tumor necrosis alpha inhibitors have been shown to be effective in                 for the past 7 months. Best-corrected visual acuity was 20/20 in
   the treatment of active anterior scleritis, with infliximab achieving              both eyes. Her pupils, intraocular pressure, and confrontational
   quiescence in __% of patients.                                                     visual fields were within normal limits. The eyelid examination
   A. 90                                                                              was notable for bilateral dermatitis of the periocular skin,
                                                                                      erythema, 3+ meibomian gland dysfunction, vascularization of
   B. 80
                                                                                      the lid margins, and ectropion of the lower lids. The conjunctiva
   C. 70                                                                              showed 1+ chemosis, 1+ injection, 3+ papillary conjunctivitis, and
   D. 60                                                                              keratinization of the lower lid tarsal surface bilaterally. The corneal
                                                                                      examination was notable for trace superficial punctate keratitis.
                                                                                      Schirmer’s test was normal bilaterally. Your treatment regimen
                                                                                      should include all the following except:
                                                                                      A. Desonide 0.5% cream and pimecrolimus 1% cream twice daily
                                                                                      B. Warm compresses and lid hygiene
                                                                                      C. Frequent preservative-free artificial tears
                                                                                      D. Increase prednisone to 30 mg daily
18
Volume 5 • Number 3
*Time spent on this activity: Hours                  Minutes                                               Function within an interprofessional team to continually assess practice patterns to
                                                                                                             ensure they align with the latest evidence-based care.
                                                                                                             This activity validated my current practice(s)
                                                                                                                                                                                                  Y N
                                                                                                                                                                                                  Y N
                                                                                                                                                                                                          3
                                                                                                                                                                                                          3
                                                                                                                                                                                                                4
                                                                                                                                                                                                                4
(Includes reading articles and completing the learning assessment and evaluation.)                           Other planned changes to practice (please provide below):
This information MUST be completed in order for the quiz to be scored.
                                                                                                             If you do not intend to make changes to your practice, please indicate why:
           THE MONOGRAPH AND TEST EXPIRE OCTOBER 10, 2020
                                                                                                          8. The following are barriers I face most often in my current practice
PRINT OR TYPE                                                                                                 that impact my ability to provide optimal care:                               Y=Yes N=No 4=N/A
                                                                                                             Lack of applicable evidence-based guidelines for my current practice/patients         Y N 4
                                                                                                             Lack of time to stay up-to-date on the latest evidence-based care                     Y N 4
Last Name                                         First Name                                 Degree          Lack of systems-based coordination of care involving an interprofessional team        Y N 4
                                                                                                             Access to clinical trials                                                             Y N 4
                                                                                                             Integrating/utilizing electronic health records                                       Y N 4
                                                                                                             Implementing value-based metrics/quality measures                                     Y N 4
Mailing Address                                                                                              Insurance/financial restrictions                                                      Y N 4
                                                                                                             Lack of patient engagement                                                            Y N 4
                                                                                                             Lack of patient adherence/compliance to therapy                                       Y N 4
City                                                                        State            Zip Code
                                                                                                          9. How confident are you in your ability to manage your patients with ocular surface disease?
                                                                                                             ❏ Extremely Confident
                                                                                                             ❏ Very Confident
Date of Birth (used for tracking credits ONLY)
                                                                                                             ❏ Somewhat Confident
                                                                                                             ❏ Not at All Confident
                                                                                                             ❏ Does Not Apply
Phone Number                                      FAX Number
                                                                                                          10. What educational topics would be of value to you for future CME activities? Please be specific.
*E-mail Address
                                                                                                          11. Please indicate your degree:
                                                                                                              ❏ MD/DO                    ❏ PA                           ❏ Other Health Care
Activity Evaluation                                                                                           ❏ PharmD/RPh               ❏ RN/BSN/MSN                   ❏ Industry
Your evaluation of this activity is extremely important, as it allows us to plan for future educational       ❏ NP                       ❏ PhD                          ❏ Other:________________________
programs. Please take a moment to answer the following questions:
                                                                                                          12. Please indicate your primary specialty:
1. How many years have you been treating patients with ocular surface disease?                                ❏ General Ophthalmology                        ❏ Pharmacy
   ❏ 1 to 9      ❏ 10 to 20         ❏ 21 to 30        ❏ More than 30        ❏ N/A                             ❏ Retina/Vitreous                              ❏ Nursing
                                                                                                              ❏ Cornea/External Disease                      ❏ Industry
2. Approximately how many patients with ocular surface disease do you see per month?                          ❏ Glaucoma                                     ❏ Other:________________________________
   ❏ 1 to 9       ❏ 10 to 30        ❏ 31 to 50        ❏ More than 50       ❏ N/A
                                                                                                          13. Please indicate your primary professional/practice setting:
3. Please rate the overall educational quality of this activity (from 1 = Poor; 5 = Excellent).               ❏ Office/Private Practice                  ❏ Hospital
   ❏1               ❏2                 ❏3                 ❏4                  ❏5                              ❏ Research                                 ❏ Academic
                                                                                                              ❏ Residency                                ❏ Fellowship
4. Do you believe this program:                                                  Y=Yes N=No 4=N/A             ❏ Urgent Care                              ❏ Fed/State Govt.
   Achieved its identified educational goals and learning objectives?                    Y N 4                ❏ Pharmacy                                 ❏ Industry
   Covered content that is relevant and will be useful to your practice?                 Y N 4                ❏ Administration                           ❏ Other:________________________________
   Increased your awareness of gaps in evidence-aligned care?                            Y N 4
   Advanced your knowledge of practice changes that may improve gaps                                      * Required field
   in patient care within your health care system?                                       Y N 4
   Will increase your competence in managing these patients?                             Y N 4
   Aspired you to engage/coordinate care within your health care
   system to improve health care delivery?                                               Y N 4              Please return the CME Registration Form before the test expires to:
   Used teaching methods and educational formats that were effective for learning?       Y N 4
   Will improve your ability to communicate with patients/caregivers?                    Y N 4                                              Vindico Medical Education
   Provided you with resources to use in your practice and/or with your patients?        Y N 4                                                      PO Box 36
   Addressed and provided strategies for overcoming barriers to optimal patient care? Y N 4                                                 Thorofare, NJ 08086-0036
   *Was presented objectively and was free of commercial bias?                           Y N 4                                               or Fax to: 856-384-6680
   *If you indicated that the activity was not free of commercial bias, please provide additional
   comments here:                                                                                                                            Questions about CME?
                                                                                                             Contact us at CME@VindicoCME.com or Call us at 856-994-9400 ext. 504
                                                                                             Y=Yes N=No
5. Future activities concerning this subject matter are necessary.                                Y N
                                                                                                                                                               OFFICE USE ONLY
6. Approximately what percentage of the activity’s content was NEW to you?                                                                                   Enduring material: Other
   ❏ 0%           ❏ 25%              ❏ 50%              ❏ 75%              ❏ 100%                                                       October 10, 2019                                        OSN-J845
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                     VINDICO
                     medical education