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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5200_Библиотеки_им_академика_М_И_Перельмана
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NonsteroidalAntiinflammatoryDrugs
Ketorolac0.5%solution
(Acular)Dosing:1dropQID
Stingingandburning,cornealedema,
iritis,ocularirritationorinflammation
Usewithcautionin
patientswithaspirin
sensitivitiesandpatients
withbleedingdisorders
orthosereceiving
anticoagulanttherapy.
Labeling:donot
administerwhilewearing
contactlenses.
Vasoconstrictors(Decongestants)
Naphazoline0.0125%or
0.03%solutions(ClearEyes)
and0.1%solution(AK-Con)
Dosing:1-2dropsinthe
affectedeye(s),uptoQID
Stinging,blurredvision,mydriasis,
redness,punctatekeratitis,increased
IOP
Narrow-angle
glaucomaNarrowanglewithout
glaucoma
Useshouldbelimitedto
72h.
Containsbenzalkonium
chloride;usewith
contactlensesnot
addressedinlabeling.
0.1%solutionrequiresa
prescription.
Tetrahydrozoline0.05%
solution(VisineAdvanced
Relief,MurineforRedEyes,
ClearEyesTripleAction,
GoodSense,Opti-Clear)
Dosing:1-2dropsuptoQID
Stinging,blurredvision,mydriasis,
redness,punctatekeratitis,increased
IOP
Narrow-angle
glaucomaNarrowanglewithout
glaucoma
Useshouldbelimitedto
72h.Contains
benzalkoniumchloride;
usewithcontactlenses
not
addressedinlabeling
TopicalCorticosteroids
Dexamethasone0.1%solution
(AK-Dex,Decadron)or0.1%
suspension(Maxidex)
Dosing
Solution:1-2dropseveryhour
duringthedayandq2hatnight
initially,reducedto1dropq4h
withfavorableresponse
Suspension:1-2dropslessthan
fourtosixtimesadayinmild
disease;hourlyinsevere
disease
IOPelevation,lossofvisualacuity,
cataractformation,secondaryocular
infection,globeperforation,stinging
andburning
Dendritickeratitis
Fungaldisease
Viraldiseaseofthe
corneaand
conjunctiva
Mycobacterialeye
infection
Labeling:wait15min
followingadministration
beforeinsertingcontact
lenses.
Fluorometholone0.1%
ointmentorsuspension(FML,
Flarex)or0.25%suspension
(FMLForte)
Dosing
Ointment:0.5inchribbonone
toTID;
duringinitial24-48h,dosing
may
beincreasedtoq4h.
Suspension:1dropBIDto
QID;during
IOPelevation,glaucoma,posterior
subcapsularcataractformation,
delayedwoundhealing
Dendritickeratitis
Vacciniaand
varicella
Fungaldisease
Viraldiseaseofthe
corneaand
conjunctiva
Mycobacterialeye
infection

initial24-48h,dosingmaybe
increasedtoq4h.
Loteprednol0.2%or0.5%
suspension
(Alrex,Lotemax)Dosing
0.2%solution:1dropinthe
affected
eye(s)QID
0.5%solution:1-2dropsinthe
affectedeye(s)QID
IOPelevation,lossofvisualacuity,
cataractformation,secondaryocular
infection,globeperforation,stinging
andburning,dryeye,itching,
photophobia
Dendritickeratitis
Fungaldisease
Viraldiseaseofthe
corneaand
conjunctiva
Mycobacterialeye
infection
Ifneeded,dosingofthe
0.5%solutioncanbe
increasedto1dropevery
hourduringthefirst
weekoftherapy.
Labeling:wait15min
followingadministration
beforeinsertingcontact
lenses.
Prednisolone0.12%or1%
suspension(PredMild,
Omnipred,PredForte)or1%
solution
Dosing
Solution:2dropsQID
Suspension:1-2dropsBIDto
QID;dosemaybeincreased
duringthe
initial24-48h.
IOPelevation,cataractformation,
delayedwoundhealing,secondary
ocularinfection,acuteuveitis,globe
perforation,stingingandburning,
conjunctivitis
Dendritickeratitis
Fungaldisease
Viraldiseaseofthe
cornea
andconjunctiva
Mycobacterialeye
infectionAcute,
purulent,untreated
eyeinfections
Labeling:wait15min
followingadministration
beforeinsertingcontact
lenses.
IOP,increasedintraocularpressure.
MastCellStabilizers
The mastcell stabilizers (bepotastine,cromolyn, lodoxamide, andnedocromil) inhibit hypersensitivity
reactionsandpreventtheincreaseincutaneousvascularpermeabilitythataccompaniesallergicreactions.
These agents may be helpful for patients with allergic conjunctivitis. Ocular adverse events include
transientburning,stingingor discomfort,pruritus,blurred vision,dryeyes,tastealteration,andforeign
bodysensation(seeTable16.3).
Antihistamine/MastCellStabilizer
Severalproducts(azelastine,epinastine,ketotifen,andolopatadine)havethecombinedpropertiesofan
antihistamineandamastcellstabilizer,providingimmediatereliefofitchingandlong-termsuppression
ofhistaminerelease.Ketotifenisavailablewithoutaprescription.Theseagentsaregivenonceortwicea
dayandhaveanadverseeffectprofilesimilartotheantihistaminesandmastcellstabilizers(seeTable
16.3).
NonsteroidalAntiinflammatoryOphthalmicDrugs
Theophthalmicnonsteroidalantiinflammatorydrug(NSAID)ketorolacmaybeusefulfortreatingtheitch
associated with allergic conjunctivitis. The NSAIDs inhibit the biosynthesis of prostaglandin by
decreasingtheactivityoftheenzymecyclooxygenase.Ketorolacisadministered1dropfourtimesaday
intotheaffectedeye.Itshouldbeusedwithcautioninpatientswithaspirinsensitivitiesandpatientswho
havebleedingdisordersorarereceivinganticoagulanttherapybecauseophthalmicNSAIDsareabsorbed
systemically.Adverseeventsincludetransientstingingandburning,irritationandinflammation,corneal

edema,andiritis(seeTable16.3).
Vasoconstrictors(Decongestants)
Vasoconstrictoreyedrops (naphazolineandtetrahydrozo-line)mayofferrelieftopatientswithallergic
conjunctivitis. With the exception of the higher-strength (0.1%) naphazoline solution, these agents are
available without a prescription. Adverse effects include stinging, blurred vision, mydriasis, and
increased redness; punctate keratitis and increased intraocular pressure (IOP) may also occur. These
agentsarecontraindicatedinpatientswithnarrow-angleglaucomaoranarrowanglewithoutglaucoma.
Reboundcongestionmayoccurwithextendeduseoftheseagents;useshouldbelimitedtoamaximumof
72hours(seeTable16.3).
TopicalCorticosteroids
Topical corticosteroids have been shown to reduce inflammation in allergic conjunctivitis. Low-dose
corticosteroid therapy can be used at infrequent intervals for short-term periods (1–2 weeks) (AAO,
2018b). Long-term use of topical corticosteroids is associated with severe adverse effects including
ocularinfection,cataractformation,andglaucoma(Orayetal.,2016)(seeTable16.3).
SelectingtheMostAppropriateAgent
Treatment of bacterial conjunctivitis is aimed at eradicating the offending organism. Cultures are not
indicatedunlesstheinfectiondoesnotresolvewithfirst-linetherapy(Table16.4andFigure16.1).
There is conflicting information about the use of soft contact lenses while taking ophthalmic
medicationsthatcontainthepreservativebenzalkoniumchloride.Thispreservative,whichisinmanyof
the ophthalmic antihistamines, mast cell stabilizers, NSAIDs, vasoconstrictors, and topical steroids
reviewedinthissection,maybeabsorbedbycontactlenses.Whilenoproductsidentifycontactlensuse
as an absolute contraindication to therapy, some (e.g., cromolyn, lodoxamide, and nedocromil) have
warningsadvisingagainsttheuseofcontactlensesduringtherapy;othersadvisepatientstowait10to15
minutesafteradministeringthemedicationbeforereinsertingcontactlenses(seeTable16.3).Regardless
oftheetiology,contactlenswearersshouldrefrainfromwearingcontactlensesduringanacutecaseof
conjunctivitis.
BacterialConjunctivitis
The treatmentof bacterial conjunctivitis is aimed at theorganisms S. aureus, S. pneumoniae, and H.
influenzae.First-linetreatmentsinclude5to7daysoftherapywitherythromycinointment(twiceorthree
timesdaily)orpolymyxinB–trimethoprimsolution(1dropevery3–4hours).Therapyselectioncanbe
basedonpatientpreferenceforointmentorsolution.Ifbacterialconjunctivitisdoesnotresolvewithfirstlinetherapy,thepatientshouldbereferredtoaneyecareprofessionalsothatculturesmaybetakentorule
outC.trachomatis.The ophthalmic fluoroquinolones withimproved gram-positive organism coverage
(besifloxacin,gatifloxacin,levofloxacin,ormoxifloxacin)canbeusedassecond-linetherapy.
Gonococcalinfectionrequiresimmediatetreatment.Ceftriaxoneplusazithromycinisrecommendedfor
adultsandchildrenwhoweighatleast45kg;childrenwhoweighlessthan45kgandneonatesshould
receiveareduceddoseofceftriaxone.Inadultsandchildrenatleast8yearsold,C.trachomatisinfection

istreatedwithazithromycinordoxycycline.Azithromycinshouldbeusedinchildrenwhoweighatleast
45kgbutarelessthan8yearsold,whileneonatesandchildrenwhoweighlessthan45kgshouldreceive
erythromycinbaseorerythromycinethylsuccinate.
Seasonal(HayFever)Conjunctivitis
Steps should be taken to minimize exposure to the offending allergen. The ophthalmic antihistamines
alcaftadineoremed-astinecanbeusedasfirst-linetherapyformildseasonalconjunctivitis.Ifsymptom
controlisinadequate,abriefcourse(1–2weeks)ofalow-potencytopicalcorticosteroidcanbeaddedto
theregimen.Iftheconditionispersistent,amastcellstabilizeror,preferably,anagentwithantihistamine
andmast cell stabilizer properties (azelastine, epinastine, ketotifen, or olopatadine) can be used. The
ophthalmicNSAIDketorolacshouldbe reserved forthird-linetherapy, as itisgenerallyless effective
than the ophthalmic antihistamines (Abelson et al., 2015). Many of these agents can be stored in the
refrigeratorandprovide acoolingsensationandsymptomaticreliefuponinstillation.Patientsmayalso
benefit from the use of cool compresses and artificial tears (which dilute allergens and help manage
coexistingteardeficiency).
TABLE16.4
RecommendedOrderofTreatmentforConjunctivitis
Order Agent Comments
BacterialConjunctivitis(nongonococcal,nonchlamydial)
Firstline Erythromycinointmentor
Bacitracin-polymyxinBointment
Ointmentstendtocausea
greaterdegreeofblurry
visionthansolutions.
Second
line
Ophthalmicfluoroquinolone(besifloxacin,gatifloxacin,levofloxacin,or
moxifloxacin)solution
Theremainingophthalmic
fluoroquinolonesdonot
providegoodstaphylococcal
coverage.
Seasonal(HayFever)Conjunctivitis
Firstline Topicalantihistamine(alcaftadineoremedastine) Minimizationofexposureto
theoffendingallergen,cool
compresses,andartificial
tearsmayalsobehelpful.
Second
line
Additionofabriefcourseoflow-potencytopicalcorticosteroidtothefirstlineagent
or
Forrecurrentorpersistentdisease:aproductwithantihistamine/mastcell
stabilizerproperties(azelastine,epinastine,ketotifen,orolopatadine)
Third
line
Ophthalmicketorolac
Vernal/AtopicConjunctivitis
Firstline Topicalantihistamineororalantihistamineormastcellstabilizer Minimizationofexposureto
theoffendingallergen,cool
compresses,andartificial
tearsmayalsobehelpful.
Second Foracuteexacerbations:additionofabriefcourseoflow-potencytopical

line corticosteroidtothefirst-lineagent
ViralConjunctivitis
Firstline Topicalantihistaminesor
Artificialtearsor
Coldcompresses
Thereisnoeffective
treatmentforviral
conjunctivitis;treatmentis
forsymptommitigation.
Second
line
Inseverecases:alow-potencytopicalcorticosteroid Useofthetopical
corticosteroidsshouldnot
exceed2wk.
GiantPapillaryConjunctivitis
Mild
disease
Oneormoreofthefollowing:replacecontactlensesmorefrequently,
decreasecontactlenswearingtime,increasethefrequencyofenzyme
treatment,usepreservative-freelenscaresystems,switchtodisposable
lenses,administermastcellstabilizer,changethecontactlenspolymer
Moderate
orsevere
disease
Sameasmilddiseaseand Discontinuationofcontact
lenswearforseveralweeks
orabriefcourseoftopical
corticosteroidtreatment
Vernal/AtopicConjunctivitis
Similar to seasonal conjunctivitis, general treatment measures for vernal/atopic conjunctivitis include
minimizingexposuretotheoffendingallergenanduseofcoolcompressesandartificialtears.Thetopical
antihistamines (alcaftadine or emedastine), oral antihistamines, or mast cell stabilizers (bepotastine,
cromolyn, lodoxamide, or nedocromil) can be used as first-line agents for the treatment of vernal or
atopicconjunctivitis.Forpatientswithacuteexacerbations,atopicalcorticosteroidcanbeaddedtothe
first-lineagentforcontrolofseveresymptoms.

FIGURE16-1Treatmentalgorithmforconjunctivitis.
IOPincreasedintraocularpressure
ViralConjunctivitis
There is no effective treatment for viral conjunctivitis; patients should be informed of the risk of
spreadingtheinfectiontotheothereye(inunilateralinfection)ortootherpeople.Topicalantihistamines,
artificial tears, or cool compresses can be used to relieve symptoms. In severe cases of adenoviral
keratoconjunctivitis with marked chemosis or lid swelling, epithelial sloughing, or membranous
conjunctivitis,topicalcorticosteroidscanbehelpfulinreducingsymptomsandpreventingscarring.

GiantPapillaryConjunctivitis
Management of giant papillary conjunctivitis centers around identifying and modifying the causative
entity.Treatmentofmildgiantpapillaryconjunctivitisduetocontactlensusecanconsistofoneormore
ofthe following:more frequentreplacementof contactlenses, reduction incontactlenswearingtime,
increase inthefrequencyofenzyme treatment,use ofpreservative-free lenscaresystems,switching to
disposable daily-wear lenses, administration of a mast cell stabilizer, and change of the contact lens
polymer (AAO, 2018b). In moderate or severe giant papillary conjunctivitis due to contact lens use,
discontinuationofcontactlensuseforseveralweeksorabriefcourseoftopicalcorticosteroidtherapy
maybenecessary.
MonitoringPatientResponse
Ifsymptomsbegintoimprovewithin48hours,nofollow-upisneeded.Ifthereis noimprovement,the
patientshouldbereferredtoaneyecareprofessionalforevaluation.
PatientEducation
Itisimportanttoinstructpatientswithbacterialorviralconjunctivitis towashtheir handscarefullyto
preventspreadinginfection.Organismsinbacterialconjunctivitisremainactive(andcontagious)for24
to48hoursaftertherapybegins,whilepatientswithviralconjunctivitiscanremaincontagiousforupto
14days.Patientsshouldbetaughthowtoapplythemedicationintheinneraspectofthelowereyelid.The
tip ofthe container should nottouchthe eyelashes,asit maycontaminatethemedicationandresultin
therapy failure or reinfection. Patients should not share eye medications because this can spread the
infection. To improve the effectiveness of an ophthalmic antibiotic, crusted eyelids should be gently
cleansedbeforeinstillingmedication.Regardlessoftheetiology,contactlenswearersshouldrefrainfrom
wearingcontactlensesduringanacutecaseofconjunctivitis.
DRYEYEDISEASE:KERATOCONJUNCTIVITISSICCA
Keratoconjunctivitis sicca,commonlyreferred toasdryeyedisease(DED)or dry eye syndrome,isa
common ophthalmologic abnormality involving bilateral disruption of tear film on the ocular surface.
EstimatesoftheprevalenceofdryeyeintheUnitedStatesrangefrom10%to20%,withtheprevalence
markedlyhigherforindividualsovertheageof80yearscomparedtothoseyoungerthan60yearsofage
(19.0% vs. 8.4%) (Moss et al., 2000). DED can occur intermittently or as a chronic condition that
becomes a self-perpetuatingsyndrome.While themajorityofpatientswithDEDexperiencenon-sightthreatening ocular irritationandintermittentlyblurred vision,patients withsevereDEDare atriskfor
severe visionloss duetoocular surfacekeratinization,cornealscarring,andcornealulceration(AAO,
2018c).
Causes
DED is a multifactorial disease. It can be the result of decreased tear production, increased tear
evaporation,oracombinationofthesefactors(Craigetal.,2017).Inaddition,decreasedtearsecretion
andclearance initiate an inflammatory response on theocular surface, and research suggests thatthis

inflammationplaysaroleinthepathogenesisofDED(Leeetal.,2018).
Risk factors for DED include advanced age, female gender, and a history of laser-assisted in situ
keratomileusis surgery. Individuals with concomitant inflammatory conditions (rosacea, lupus,
sarcoidosis, or rheumatoid arthritis), systemic viral infections (hepatitis C, human immunodeficiency
virus/ acquired immunodeficiency syndrome, or Epstein-Barr virus), or conditions such as MGD
blepharitis, Sjögrensyndrome,Parkinson’sdisease,andBell palsyarealso atincreased riskforDED.
Symptoms caused by dry eye may be exacerbated by environmental factors such as wind, reduced
humidity,cigarettesmoke,andheatingandair-conditioning(Calogneetal.,2017).Systemicmedications
such as antihistamines, diuretics, anticho-linergics, antidepressants, beta blockers, antipsychotics,
menopausalhormonetherapy,oralcontraceptives,andisotretinoincanalsoexacerbatedryeyesymptoms
(AAO,2018c;Clayton,2018).
Pathophysiology
Tears are composedofthree layers: a mucuslayer produced bygobletcells, whichcoats thecornea,
allowingthetear toadheretotheeye;amiddle aqueouslayerproducedbythelacrimalglands,which
providesmoistureandsuppliesoxygenandnutrientstothecornea;andanouterlipidfilmlayerproduced
bythemeibomianglands,whichsealsthetearfilmontheeyeandpreventsevaporation.Theouterlipid
filmlayerisreplenishedbyeyelidblinking,whichrelubricatesandredistributesthelipidlayeracrossthe
ocularsurface.Theocularsurfaceandtear-secretingglandsfunctionasanintegratedunittomaintainthe
tear supply and to clear used tears. Aging, ocular surface diseases (such as herpes simplex virus
keratitis), surgeriesthatdisruptthetrigeminalafferentsensorynerves,systemicinflammatorydiseases,
and systemic diseases and medications that disrupt the efferent cholinergic nerves that stimulate tear
secretioncandisruptthisfunctionalunitandresultinanunstableandpoorlymaintainedtearfilm(AAO,
2018c;Pfulgfelder&dePaiva,2017).Decreasedtearsecretionandclearanceleadstoaninflammatory
responseontheocularsurface,whichisalsobelievedtoplayaroleinDED.
DiagnosticCriteria
Family practitioners should always refer patients reporting dry eye to an ophthalmologist if there is
moderatetoseverepain,visionloss,cornealinfiltrationorulceration,ornoresponsetotherapy(AAO,
2018c). Making the diagnosis of DED, particularly the mild form, can be difficult because of the
unpredictable correlation between reported symptoms and clinical signs and the relatively poor
sensitivity/specificity of existing diagnostic tests (AAO,2018c). Because mostdry eyeconditions are
chronic,repeatobservationwillallowamoreaccurateclinicaldiagnosisofDED.
SignsandsymptomsofDEDincludeadryeyesensation,ocularirritation,redness,burning,stinging,a
foreign body or gritty sensation, blurred vision, photophobia, contact lens intolerance, an increased
frequencyofblinking,and,paradoxically,increasedtearing(AAO,2018c;NationalEyeInstitute[NEI],
2019). DED symptoms tend to worsenin dry climates, in the wind, duringair travel, withprolonged
visualefforts(e.g.,readingorcomputeruse),andtowardtheendoftheday(AAO,2018c).
A physical examination (including a test of visual acuity, an external examination, and slit-lamp
biomicroscopy)shouldbeperformedtodocumentthesignsofDED;toassessthequality, quantity, and
stabilityofthetearfilm;andtoruleoutothercausesofocularirritation(AAO,2018c).Evaluativetools
(the Dry Eye Questionnaire 5 or Ocular Surface Disease Index) can be utilized to screen for DED;
positivesymptomscoresshouldtriggeramoredetailedexamination,whichmayincludefluoresceintear

break-uptime,tear osmolaritytesting, or ocular surfacestaining (Craiget al.,2017).Individuals with
moderate to severe dry eye who have a family history of autoimmune disorders and/or signs and
symptomsofanautoimmunedisordershouldbeevaluatedforanunderlyingautoimmunedisorder.
InitiatingDrugTherapy
Beforestartingdrugtherapy,thepatientshouldtrynonpharma-cologicinterventionssuchasenvironmental
control (increasing air humidity, avoiding drafts and cigarette smoke) and scheduling regular breaks
during computer use and reading. Unfortunately, these interventions result in limitedeffectiveness and
producefew lastingimprovements inDED symptoms.Exogenous medicalfactors that cancause DED
(i.e., blepharitis, meibomianitis)shouldbeaddressed,andprescriptionmedicationsthatcanexacerbate
DEDsymptomsshouldbediscontinuedwhenpossible.
IfthenonpharmacologicinterventionsfailtoeliminateDED symptoms,drugtherapyis appropriate.
Table16.5givesinformationaboutthedrugsusedtotreatDED.
GoalsofDrugTherapy
ThegoalsoftherapyinDEDaretorelievediscomfort,maintainandimprovevisualfunction,andreduce
or prevent structural damage (AAO, 2018c). Therapy should attempt to normalize tear volume and
composition so that the eye tissues are properly lubricated, nourished, and protected, resulting in
improvedpatientsatisfactionandclinicaloutcomes.
ArtificialTearsandLubricants
ArtificialtearsandlubricantscanbeusedaspalliativetherapiestorelieveDEDsymptoms.Designedto
mimic the composition of natural tears, artificial tears contain lipids, water with dissolved salts and
proteins,andmucin.Artificialtearsandlubricantsareover-the-counterproducts,availableinavarietyof
formulations(emulsions,gels,ointments).Ointmentsandgelsmaymaketheeyelidsstickyandblurvision
andareoftenusedonlyatbedtime.
For patients with mild DED, use of artificial tears four times daily plus a lubricating ointment at
bedtimemaybeuseful.Astheseverityofdryeyeincreases,administrationofartificialtearscanincrease
tohourly.Preservative-freepreparationsshouldbeusedifthepatientappliestearsmorethanfourtimesa
day(AAO,2018c).
CholinergicAgonists
The cholinergic agonists pilocarpine and cevimeline are indicated for the treatment of dry mouth in
patientswithSjögrensyndrome. Theseagentsbindtomuscarinicreceptors,stimulatingsecretionofthe
salivaryandsweatglands and improvingtear function. However, these agents are more effective for
treatingdrymouthcomparedtodryeye.Themainadverseeventwiththeseagentsisexcessivesweating,
reported in 18% to 40% of patients. The use of these agents is contraindicated in patients with
uncontrolledasthmaandwhenmiosisisundesirable(acuteiritis,narrow-angleglaucoma).
FattyAcidSupplements

Supplementation with n-3 fatty acids has been reported to provide benefits in DED due to their
antiinflammatoryactivityandhasbeenrecommendedbyclinicians(Serhanetal.,2008).However,there
isnodefinitiveevidencesupportingfattyacidsupplementationinthemanagementofDED,andalarge,
multicenter, double-blind clinical trial failed to demonstrate the effectiveness of n-3 fatty acid
supplementationinpatientswithmoderatetosevereDED(Asbelletal.,2018).
TopicalCyclosporine
Cyclosporineophthalmicemulsionhasbeenreportedtoincrease aqueoustearproductionanddecrease
ocular irritation symptoms in patients with DED. It prevents T cells from activating and releasing
cytokines that incite the inflammatory component of dry eye. Adverse effects include ocular burning,
conjunctivalhyperemia,discharge,itching,andblurredvision.
Lifitegrast
Lifitegrast is a lymphocyte function-associated antigen-1 (LFA-1) antagonist. The exact mechanism of
actionoflifitegrastinDEDisnotknown,thoughlifitegrastblockstheinteractionofcellsurfaceproteins
LFA-1 and intercellular adhesion molecule-1 and may inhibit T cell–related inflammation in DED.
Adverseeffectsincludetastealterationanddecreasedvisualacuity.
TopicalCorticosteroids
TopicalcorticosteroidshavebeenshowntoreduceinflammationinDEDbyreducingcytokinelevelsin
theconjunctivalepithelium.Low-dosecorticosteroidtherapycanbeusedatinfrequentintervalsforshortterm (2 weeks) suppression of irritation secondary to inflammation (AAO, 2018c). Long-term use of
topical corticosteroids is associated with severe adverse effects, including ocular infection, cataract
formation,andglaucoma(Cutoloetal.,2019).
SelectingtheMostAppropriateAgent
AgentselectionisdeterminedbytheseverityofDEDandtheunderlyingpathophysiology(Table16.6).
First-LineTherapy
ForpatientswithmildDED,theuseofatearsubstitutefourtimesadayisappropriate.Formoderateor
severeDED,artificialtearscanbeusedasoftenashourly,althoughadministrationthatfrequentlymaybe
cumbersome.Preservative-freepreparationsshouldbeusedifthepatientusestearsmorethanfourtimes
aday.Alubricatingointmentappliedatbedtimemayalsobeuseful.
ApatientwithDEDandunderlyingSjögrensyndromemaybenefitfromtherapywithoralpilocarpine5
mgfourtimesdailyororalcevimeline30mgthreetimesdaily.
TABLE16.5
OverviewofDryEyeDiseaseAgents
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