3 tonometry and ocular

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    r mon arnarr mon arnar

    With acknowled ements toWith acknowled ements to

    Dr RobertDr Robert HarperHarper

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    B k r n h n in r i n I PB k r n h n in r i n I P

    Glaucoma is characterized by raised IOP, opticneuro a y an amage caus ng v sua e

    loss traditional view

    progressive optic neuropathy, with a typicallycupped, pale optic disc and a characteristic loss of

    sensitivity to light Sponsel in 1980s

    a variable combination of raised IOP, optic discchanges and visual field loss Quigley in 1990s

    Randomised controlled trial evidence 2000+

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    Theories of optic nerve damage

    Reduced blood flow/vascular dysregulation

    laminar plates

    Current view: RGC death is causes b a o tosisand remodelling of the optic nerve head, mediatedby mechanical forces, ischaemia and reperfusion

    injury (IOP and OBF implicated in these issues)

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    Age

    IOP

    Race

    Diabetes Mellitus

    Hypertension

    M o ia Corneal thickness

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    Background: IOP at presentation:Background: IOP at presentation:

    epidemiologyepidemiology

    Study No POAG % with

    normal IOP

    Des Moines, USA 189 68

    Ferndale, Wales 20 35Framingham, USA 40 52

    Baltimore, USA 194 59

    Beaver Dam, USA 104 32Roscommon, Ireland 41 37

    Blue Mountains, Aus 108 75

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    .

    IOP 16-21mmHg ~ 2.5x

    IOP 22-29mmHg ~ 13x

    Baltimore Eye Study 1991

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    ac groun : str ut on oac groun : str ut on o

    Av=15.7 mmH

    SD=2.7 mmHg

    -

    str ut on s ewe

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    Background: IOP and clinical trialsBackground: IOP and clinical trials

    Key randomised glaucoma trialsOHTS, EMGT, CNTGS, CIGTS, AGIS, EGPS

    Lowering IOP exerts a favourable influence on the

    development and progression of glaucoma Lower IOP means better rotection

    Lowering IOP does not always stop progression

    -

    reduction/progression relationship

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    summarysummary

    Multi-centre study, 1636 patients with OHT- mm g - yrs, compar ng convers on

    rate to glaucoma in Rx versus No Rx

    Conversion 4.4% in Rx group and ~9% incontrol rou i.e. no Rx

    >90% of OHT pts did not convert after 5 years

    , ,predictors for conversion to POAG

    CCT was a risk factor for POAG conversion

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    stu y summarystu y summary

    First treatment versus no treatment RCT in

    Population screening 44K 255 pts recruited

    Randomised to IOP or no Rx~

    IOP reduction reduced progression risk by

    ~

    Lower risk patients and no treatment option

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    Typical tonometry referral criteriaTypical tonometry referral criteria

    Contact applanation tonometry

    IOP >22mmHg with disc changes

    IOP >35mmHg (urgent)

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    e ear est tonometer

    a pat on

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    n entat on tonometers

    If a plunger of known weight is rested

    indentation should (?) be proportional to

    Note: ocular rigidity/facility of aqueousoutflow (see separate lecture on

    tonometr

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    Plunger may be connected to lever arm and

    scale (e.g. Schitz) or to electronic recordingsystem (e.g. Mueller)

    From Henson (1983)

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    c otz

    The footplate is rested on the cornea and the

    plunger is free to indent the cornea. A varietyof weights may be used to minimise errorsdue to corneal rigidity (use with tables)

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    Normal weight (knurled knob above

    footplate) = 5.5grams giving total of 16.5grams to be supported by cornea. Additionalweights are 7.5, 10, 15 g

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    n entat on

    Shiotz o

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    sa vantages

    50g)

    Difficult to disinfect note also CJD risk ?

    Displacement of aqueous

    Effect of corneal ri idit on readin

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    vantages

    Cheap Portable

    Can measure ocular tension of eye

    w scarre cornea

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    pp anat on tonometrypp anat on tonometry

    Imbert-Fick law IOP = tonometer weight (g) / area (mm2)

    Method of choice for tonometry (currently)

    Constant area, variable force

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    Gambs Cone just touching cornea

    3.06 mm black square

    3.06 mm diameter

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    Difficulty with Gambs

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    o mann tonometero mann tonometer

    Applanation diameter 3.06 mm

    very e u sp ace .

    bending force = surface tension

    1 gm equiv to 10 mmHg-

    - SD of differences

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    o mann Doubling prism to separate images by 3.06

    mm

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    , .comparing calibrate new

    instruments.

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    Ad

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    Advantages

    cheap

    comfortable (apart from anaesthetic)

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    sa vantages

    cannot be delegated

    contact w t cornea s g t c ance oabrasion)

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    rrorsrrors

    Lids touching the probe ( IOP)

    ur ace ens on orce a ere m n ma

    Prolon ed contact IOP

    Corneal astigmatism (>3DC)

    Incorrect vert cal al gnment ( IOP)

    Calibration s stematic or random or Observer errors ( or IOP)

    Meniscus width (usually IOP)

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    en scus w ten scus w t

    Thickness of flourescein ring Ideal ~ 1/10th diameter cone (0.3mm*)

    ~2mmHg

    .

    ~0.35 mmHg

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    er ns

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    Hand held

    A l h r Portable

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    NonNon--contact applanation tonometrycontact applanation tonometry First NCT designed by Grolman and introduced by

    American Optical in 1972 r nc p e was cons ere as ear y as y r c

    Zeiss

    Reichert (formerly American Optical) NCT II and

    Keeler Pulsair EasyEye

    Nidek NT-2000/4000

    -

    Canon TX-10

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    pr nc p epr nc p e r g na rects an a r-pu towar s t e cornea -

    point of applanation detected by optical system, time

    electronically (time relates to the IOP)

    Later enerations measure air- ulse ressure at

    applanation Keeler Pulsair is hand-held and can be used in any

    pos t on - creates rampe a r pu se w c automat ca yapplanates cornea at alignment. Optical system detects

    .generation instrument is Pulsair EasyEye

    Modern NCTs use lower ulse ressure than theoriginal Reichert instrument

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    m tat onsm tat ons Some NCT advantages could become limitations

    if the user is unaware of the errors that can beintroduced in estimating IOP

    See variations in IOP in slides below

    Essential to take at least 3-4 readings per eye inorder to balance out the effect of the ocular pulse

    NCTs can provide clinically meaningful measuresof IOP which equate to those obtained by theGoldmann instrument

    NCT has not replaced GAT as the technique ofchoice in the hospital setting

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    actors a ect ngactors a ect ng s ort terms ort term

    Time of Day (diurnal range) Normal ~3-6 mmHg

    Glaucoma avera e ~13 mmH

    Diurnal variation in plasma cortisol (?)

    - ,

    Repeat tonometry and phasing

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    Typical IOP Diurnal Variation in Normals,

    showing nocturnal dip.

    25

    15

    10IO

    5

    0 2 4 6 8 10 12 14 16 18 20 22 0 2 4 6 8 10 12

    Time of Day (Hours)

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    actors a ect ngactors a ect ng s ort terms ort termArterial pulse

    -

    Drinking/Fluid intake

    Water and coffee +3 mmHg in 20 min alcohol -3mmHg in 5 min

    Contraction of extra/intraocular muscle IOP

    Accommodation

    Blinking and lid squeezing

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    actors a ect ngactors a ect ng s ort terms ort termBlood pressure, exertion, posture

    sitting to supine 1-6 mmHg increase

    nvers on ncreases++ o - mm g

    aerobic exercise can lower IOP

    straining can increase IOP

    ti ht collar or neck tie 4mmH holding breath

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    ystem c an ocu ar seaseystem c an ocu ar seaseSystemic disease

    association between raised IOP/Glaucoma andsystemic hypertension and DM

    the secondary glaucomas!

    anterior uveitis and retinal detachments

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    Lee at al. The corneal thickness and intraocular pressure story: where are we

    now? Clin ExpOphthalmol 2002; 30: 334-337

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    ornea t c ness anornea t c ness anPost PRK

    7

    5

    6

    Hg)

    3

    4

    tion(m

    1

    2

    O

    Predu

    0

    0 25 50 75 100 125 150 175

    I

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    ar y correct on actorar y correct on actorCCT

    (mm)

    10mm

    Hg

    15mm

    Hg

    20mm

    Hg

    25mm

    Hg

    30mm

    Hg

    . + . + . + . + . + .

    0.48 +2.2 +2.6 +2.9 +3.3 +3.6

    . . . . . .

    0.52 -0.4 -0.2 +0.0 +0.1 +0.30.54 -1.6 -1.5 -1.4 -1.3 -1.2

    0.56 -2.8 -2.8 -2.8 -2.8 -2.7

    0.58 -3.9 -4.0 -4.1 -4.1 -4.2

    Additive correction (in mmHg) to be added to IOPrea ngs a eren s or eve s o a er

    Ehlers et al, 1975).

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    ornea t c nessornea t c ness

    Knowledge of CCT provides information on

    an n v ua s r s an a ows correc on o

    IOP (OHTS, Brandt 2004)

    No single correction factor is agreed upon. - .

    difference from an average CCT is suggested

    European Glaucoma Society (2003)

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    Choose based on

    Validity/Precision

    issues

    Ease of use

    Value for money

    ppearance

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    eve opments n tonometryeve opments n tonometry

    Ocular Res onse AnalyserTonopen

    neumatonometry

    Pascal D namic Contour tonometer

    Integrated tonometer/pachymeter unit

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    cu ar esponse na ysercu ar esponse na yser

    Reichert ORA

    Bi-directional dynamic

    Corneal hysteresis:

    corneal rigidity,

    Clinical trials awaited

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    Pascal Dynamic Contour TonometryPascal Dynamic Contour Tonometry

    Based on principle of contour

    Contour tip concave, with

    with contact surface

    va ues c a me to e c oserto true manometric levelscompared to GAT

    1Kniestedt et al, Archives of Ophthalmology 2004

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    onopenonopen

    Applanation device with small footprint-

    abnormalities

    A sterile cover must be over the tip

    button until CAL appears in the window

    Ensure atient has anaesthetic, entl taTonopen against cornea. Final averagedreading (of usually 4 6) displayed

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    neumatonometerneumatonometerResistance to air flow

    varies with IOP

    3mm diameter area

    Back pressure in air

    resistance to air flow

    Force applied adjusts to maintain

    constant area of applanation

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    Overcomes some of the problems

    Measures

    IOP (mmHg) ulse am litude

    (mmHg)

    ulse volume (l) pulse rate (/min)

    ocular blood flow

    (l/min)OBF tonometerOBF tonometer

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    cont nuous recor ngcont nuous recor ng

    14

    Hg

    13

    IOPm

    12

    11

    10

    Time (sec)

    1 2 3 4 5 6

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    cu ar oo ow onometercu ar oo ow onometer

    Earl studies su estedhelpful in vascularaetiolo of POAG/NTG

    Benefit of OBF now

    Still affected by cornel

    c ness more anGAT?)

    --

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    --

    Distribution of IOP

    Normal and Glaucoma

    Distribution of POBF

    Normal and Glaucoma

    16

    18

    20

    20

    25

    10

    12

    14

    15

    4

    6

    8

    5

    10

    0

    2

    8 12 16 20 24 28 32 36 400

    100 400 700 1000 1300 1600 More

    IOPPOBF

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    natomy ys o ogy onatomy ys o ogy o The eye receives its blood supply from 2 sources of

    the ophthalmic artery: Ciliary arteries

    Central retinal artery

    Ciliary supply accounts for 95% of total OBF

    Intraorbital (pial arteries and CRA)

    Pre-laminar (posterior ciliary arteries)

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    pt c nerve oo supp ypt c nerve oo supp y

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    et o s o assess nget o s o assess ng

    Angiography

    Laser doppler velocimetry

    Laser doppler flowmetry

    Heidelberg Retina Flowmetry (HRF)

    Laser speckle phenomenonue e en op cs

    Retinal vessel analyser

    ornea empera ure Colour Doppler imaging

    er p era oo ow

    See Flammer et al, Prog Ret Eye Res 2002, 21:359-93.

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    n g aucoman g aucomaeren ec n ques measure eren aspec s o

    ocular blood circulation and numerous studies have

    -groups (see Flammer et al review, 2002)

    .

    There is reduced OBF in glaucoma that involves differentarts of the e e includin the o tic nerve head retinal

    circulation, the retrobulbar and peripheral blood flow

    The reduced OBF appears more pronounced in patients

    w t The effect of reduced OBF is more pronounced under

    . .

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    oss e causes o re uct onoss e causes o re uct on

    Increased resistance to OBF

    Anatomical variations

    Vascular dysregulation

    ecrease per us on pressure

    Due to increased IOP

    Due to decreased BP

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    an per us on pressurean per us on pressureOcular perfusion pressure (OPP) cannot be

    Estimate:

    OPP=2/3 mean arterial BP minus IOP

    Medical thera directed towards

    increasing OPP

    qu va en re uc ons may no g ve esame increase in OPP

    Perfusion ressure and POAGPerfusion ressure and POAG

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    Tielsch et al (1995) Arch Ophthalmol 113:216-221