Ординатура / Офтальмология / Английские материалы / Oxford American Handbook of Ophthalmology_Tsai, Denniston, Murray_2011
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xx SYMBOLS AND ABBREVIATIONS
RD |
retinal detachment |
RE |
right eye |
RES |
recurrent erosion syndrome |
RF |
rheumatoid factor |
RGP |
rigid gas permeable (of contact lenses) |
RK |
refractive keratectomy |
RNA |
ribonucleic acid |
RNFL |
retinal nerve fiber layer |
ROP |
retinopathy of prematurity |
ROS |
review of systems |
RP |
retinitis pigmentosa |
RPE |
retinal pigment epithelium |
RPR |
rapid plasma reagin |
RRD |
rhegmatogenous retinal detachment |
RS |
respiratory system |
rtPA |
recombinant tissue plasminogen activator |
SBP |
systolic blood pressure |
SBS |
shaken baby syndrome |
SC |
subcutaneous |
SCC |
squamous cell carcinoma |
sec |
second(s) |
SF |
short-term fluctuation |
SF6 |
sulfur hexafluoride |
SH |
social history |
Si |
silicone (of oil) |
SINS |
surgery-induced necrotizing scleritis |
SITA |
Swedish interactive threshold algorithm |
SLE |
systemic lupus erythematosus |
SLK |
superior limbic keratoconjunctivitis |
SLP |
scanning laser polarimetry |
SLT |
selective laser trabeculoplasty |
SO |
superior oblique |
SR |
superior rectus |
SRF |
subretinal fluid |
SUN |
Standardization of Uveitis Nomenclature (group) |
SVC |
superior vena cava |
SVP |
spontaneous venous pulsation |
SWAP |
short-wavelength automated perimetry |
TB |
tuberculosis |
TED |
thyroid eye disease |
TEN |
toxic epidermal necrolysis |
TFT |
thyroid function tests |
TG |
triglyceride |
SYMBOLS AND ABBREVIATIONS xxi
TI |
transillumination defects |
TINU |
tubulointerstitial nephritis with uveitis |
TLT |
titanium:sapphire laser trabeculoplasty |
TM |
trabecular meshwork |
TNF |
tumor necrosis factor |
tPA |
tissue plasminogen activator |
TPHA |
treponema pallidum hemagglutination assay |
TRD |
tractional retinal detachment |
TSH |
thyroid-stimulating hormone |
TTT |
transpupillary thermotherapy |
UA |
urinalysis |
UC |
ulcerative colitis |
U+E |
urea and electrolytes |
UGH |
uveitis–glaucoma–hyphema syndrome |
URTI |
upper respiratory tract infection |
US |
ultrasound |
UV |
ultraviolet |
V1,2,3 |
ophthalmic, maxillary, and mandibular divisions of CN V |
VA |
visual acuity |
VCC |
variable corneal compensator |
VDRL |
venereal disease research laboratory test |
VEGF |
vascular endothelial growth factor |
VEP |
visual-evoked potential |
VF |
visual field |
VHL |
von Hippel–Lindau syndrome |
VKC |
vernal keratoconjunctivitis |
VKH |
Vogt–Koyanagi–Harada syndrome |
VOR |
vestibulo-ocular reflex |
VSD |
ventricular septal defect |
VZV |
varicella zoster virus |
WHO |
World Health Organization |
XX-linked
XD |
X-linked dominant |
yr |
year |
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xxiii
Orthoptic abbreviations
ACS |
alternating convergent strabismus |
ADS |
alternating divergent strabismus |
AHP |
abnormal head posture |
ARC |
abnormal retinal correspondence |
BD |
base down (of prism) |
BI |
base in (of prism) |
BO |
base out (of prism) |
BU |
base up (of prism) |
BSV |
binocular single vision |
CC |
Cardiff cards |
CI |
convergence insufficiency |
Conv XS |
convergence excess |
CSM |
central, steady, and maintained (quality of fixation) |
CT |
cover test |
DVD |
dissociated vertical deviation |
DVM |
delayed visual maturation |
Ecc fix |
eccentric fixation |
Eesophoria
ET |
esotropia |
E(T) |
intermittent esotropia |
FCPL |
forced choice preferential looking |
FL/FLE |
fixing with left eye |
FR/FRE |
fixing with right eye |
Hhyperphoria
HT |
hypertropia |
Ho |
hypophoria |
HoT |
hypotropia |
KP |
Kay’s pictures |
LCS |
left convergent strabismus |
LDS |
left divergent strabismus |
MLN |
manifest latent nystagmus |
MR |
Maddox rod |
MW |
Maddox wing |
NPA |
near point of accommodation |
NPC |
near point of convergence |
NRC |
normal retinal correspondence |
o/a |
overaction |
Obj |
objection |
xxiv ORTHOPTIC ABBREVIATIONS
Occ |
occlusion |
OKN |
optokinetic nystagmus |
PCT |
prism cover test |
PFR |
prism fusion range |
PRT |
prism reflection test |
RCS |
right convergent strabismus |
RDS |
right divergent strabismus |
Rec |
recovery |
SG |
Sheridan Gardiner test |
Sn |
Snellen chart |
SP |
simultaneous perception |
Supp |
suppression |
u/a |
underaction |
VOR |
vestibulo-ocular reflex |
Xexophoria
XT |
exotropia |
X(T) |
intermittent exotropia |
More complex variations for intermittent strabismus include:
R(E)T |
intermittent right esotropia predominantly controlled |
RE(T) |
intermittent right esotropia predominantly manifest |
Adjust according to whether:
R (right), L (left), or A (alternating)
ET (esotropia), XT (exotropia), HT (hypertropia), or HoT (hypotropia).
These abbreviations are in common usage and are approved by the American Academy of Ophthalmology
Chapter 1 |
1 |
|
|
Clinical skills
Obtaining an ophthalmic history 2 Assessment of vision: acuity (1) 5 Assessment of vision: acuity (2) 7
Assessment of vision: clinical tests in children and tests of binocular status 9
Assessment of vision: contrast and color 11 Biomicroscopy: slit-lamp overview 13 Biomicroscopy: use of the slit lamp 15 Anterior segment examination (1) 17
Additional techniques for anterior segment examination 18 Anterior segment examination (2) 19
Gonioscopy 20
Posterior segment examination (1) 22 Posterior segment examination (2) 24 Pupillary examination 27
Ocular motility examination (1) 29 Ocular motility examination (2) 31 Visual fields examination 33 Lids/ptosis examination 34
Orbital examination 36 Nasolacrimal system examination 38 Refraction: outline 40
Refraction: practical hints 42 Focimetry 44
2CHAPTER 1 Clinical skills
Obtaining an ophthalmic history
One of the first and most vital skills acquired by those involved in eye care is the accurate and efficient taking of an ophthalmic history. In ophthalmology clinical examination is very rewarding, probably more so than in any other specialty. However, this is additional to, rather than instead of, the history.
Apart from the information gained, a rapport is established which should help the patients to tolerate the relatively invasive ophthalmic examination. The patients are also more likely to accept any subsequent explanation of diagnosis and ongoing management if they know they have been listened to.
Presenting illness (PI)
Why are they here?
The patient’s initial illness (i.e., complaint) often helps to direct additional questioning and examination. Routine eye care referral has a valuable role in screening for asymptomatic disease (notably glaucoma) but may generate unnecessary referrals for benign variants (e.g., anomalous discs, early lens opacities).
History of presenting illness (HPI)
The analysis of most ophthalmic problems center around general questions regarding the onset, precipitants, associated features (e.g., pain, redness, discharge, photophobia, etc.), duration, relieving factors, recovery, and specific questions of the presenting illness (i.e., complaints) (Box 1.1). Even after clinical examination, further information may be needed to include or rule out diagnoses.
Although some of these processes can be formalized as algorithms, their limitations should be recognized; they cannot compare to the multivariate processing, recognition of exceptions, and calculation of diagnostic probabilities subconsciously practiced by an experienced clinician.
Past ophthalmic history (POH)
The background for each presentation is important. Inquire about previous surgery/trauma, previous/concurrent eye disease, and refractive error. The differential diagnosis of an acute red eye will be affected by knowing that the patient had complicated cataract surgery 2 days previously or has a 10-year history of recurrent acute anterior uveitis, or even that the patient wears contact lenses.
Past medical history (PMH)
Similarly, consider the entire patient. Ask generally about any medical problems. In addition, inquire specifically about relevant conditions that they may have forgotten to mention. The patients presenting with recurrently itchy eyes may not mention that they have eczema or asthma. Similarly, if they have presented with a vascular event, ask specifically about diabetes, hypertension, and hypercholesterolemia.
OBTAINING AN OPHTHALMIC HISTORY 3
Box 1.1 Obtaining the history of the presenting illness (HPI)—an example
Patient presenting with loss of vision
Did the event occur suddenly or gradually?
Sudden loss of vision is commonly associated with a vascular occlusion (e.g., AION, CRAO, CRVO) or bleeding (e.g., vitreous hemorrhage, “wet” macular degeneration). Gradual loss of vision is commonly associated with degenerations or depositions (e.g., cataract, macular dystrophies or “dry” macular degeneration, corneal dystrophies).
Is the vision loss associated with pain?
Painful blurring of vision is most commonly associated with anterior ocular processes (e.g., keratitis, anterior uveitis), although orbital disease, optic neuritis, and giant cell arteritis may also cause painful loss of vision.
Is the problem transient or persistent?
Transient loss of vision is commonly due to temporary/subcritical vascular insufficiency (e.g., giant cell arteritis, amaurosis fugax, vertebrobasilar artery insufficiency), whereas persistent loss of vision suggests structural or irreversible damage (e.g., vitreous hemorrhage, macular degeneration).
Does the problem affect one or both eyes?
Unilateral disease may suggest a local (or ipsilateral) cause. Bilateral disease may suggest a more widespread or systemic process.
Is the vision blurred, dimmed or distorted?
Blurring or dimming of vision may be due to pathology anywhere in the visual pathway from cornea to cortex; common problems include refractive error, cataract, and macular disease. Distortion is commonly associated with macular pathology, but again may arise from high refractive error (high ametropia/astigmatism) or other ocular disease.
Where is the problem with their vision?
A superior or inferior hemispheric field loss suggests a corresponding inferior or superior vascular event involving the retina (e.g., retinal vein occlusion) or optic disc (e.g., segmental AION). Peripheral field loss may indicate retinal detachment (usually rapidly evolving from far periphery), optic nerve disease, chiasmal compression (typically bitemporal loss), or cortical pathology (homonymous hemianopic defects). Central blurring of vision suggests diseases of the macula (positive scotoma: a “seen” spot) or optic nerve (negative scotoma: an unseen defect).
When is there a problem?
For example, glare from headlights or bright sunlight is commonly due to posterior subcapsular lens opacities.
4CHAPTER 1 Clinical skills
Family history (FH)
This is relevant both to diseases with a significant genetic component (e.g., retinitis pigmentosa, some corneal dystrophies) and to infectious conditions (e.g., conjunctivitis, TB, etc.).
Social history (SH)
Ask about smoking and alcohol intake if relevant to the ophthalmic disease (e.g., vascular event or unexplained optic neuropathy, respectively). Consider the social context of the patients. Will they be able to manage hourly drops? Can they even take the top off the bottle?
Drugs and allergies
Ask about concurrent medication and any allergies to previous medications (e.g., drops), since these may limit your therapeutic options. In addition to actual allergies, consider contraindications (e.g., asthma or chronic obstructive pulmonary disease [COPD] and B-blockers).
ASSESSMENT OF VISION: ACUITY (1) 5
Assessment of vision: acuity (1)
Measuring visual acuity (VA)
Box 1.2 An approach to measuring visual acuity
Select (and document) |
Consider age, language, literacy, |
|
appropriate test: |
general faculties of patient |
|
Check distance acuity |
Unaided with distance prescription |
|
(for each eye): |
with pinhole (if <20/30) |
|
Check near acuity (for each eye) |
Unaided with near prescription |
|
(where appropriate): |
|
|
Selecting the appropriate clinical test
Table 1.1 Tests of visual acuity
Patient |
Distance |
Near |
Adult: literate
Adult: illiterate
Children: age3 years
Children: age2 years
Babies/infants
Snellen |
Test type N chart |
LogMAR |
|
Illiterate E Landholt ring
Sheridan-Gardiner (single optotype)
Sheridan-Gardiner (single optotype) Sonsken-Silver (multiple optotype)
Kay picture test (single optotype) Multiple picture test
Reduced
Sheridan-Gardiner
Reduced Kay picture test
Clinical tests: fix and follow, objection to occlusion, picking up fine objects
Preferential looking tests: Keeler, Teller, Cardiff cards
Electrodiagnostic tests: Visual-evoked potential (VEP) response to alternating checkerboard of varying frequency
