A presentation covering all aspects of Trachoma, one of the oldest infectious disease which is one of the leading causes of preventable blindness. Present day scenario and management.
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TRACHOMA- DIAGNOSIS AND MANAGEMENT
1. Dr. Arvind K. Morya, MBBS, MS(Gold Medalist),MNAMS
Glaucoma,Phaco(MICS), Cornea and refractive, Strabismus
Paediatric Ophthalmology and Medical Retina Services
Department of Ophthalmology, AIIMS Jodhpur
2. Introduction
Trachoma comes from Greek word trachoma
(τράχωμα) meaning “roughness”.
Trachoma was well known as an infectious ocular
disease and documented as “ophthalmia”.
The history of this disease began as early as 8000
B.C.
3. Trachoma
Trachoma, one of the oldest infectious eye diseases,
is the world’s leading cause of preventable blindness.
Repeated infections of the conjunctivae with
Chlamydia trachomatis can lead to trichiasis, corneal
opacity and blindness.
An estimated 325 million people live in at-risk areas.
Trachoma blinds one person every 15 minutes.
4. EPIDEMIOLOGY
Endemic in 42 countries - causing visual impairment
in 1.9 million people.
Leading cause of infectious Blindness globally
Infective Trachoma (TF/TI) – Follicles in upper tarsal
conjunctiva – upto10 years of age
Trachomatous Trichiasis(TT) – Scarring leading to
Trichiasis – After 15 years of age
Spread- direct contact/ through flies
7. MODES OF INFECTION:
•Direct spread by air-borne
or water-borne modes
•Vector transmission by flies
•Material transfer through
contaminated fingers,
clothes, bedding etc
8. PREDISPOSING
FACTORS:
•Age: commonly in
infancy & childhood,
but age no bar
•Sex: more in females
•Climate: dry & dusty
weather favors
•Socio-economic status:
more in poor classes
due to unhygenic
conditions,
overcrowding,
unsanitary conditions,
flies, lack of education
etc
•Environmental:
exposure to dust,
irritants, smoke,
9. CLINICAL PROFILE
• Incubation period: 5-21 days, mostly
insidious onset
• Clinical course:
• Pure trachoma is mild & symptomless, often
neglected
• If superimposed with bacterial infection,
presents with typical bacterial conjunctivitis
11. Corneal signs:
• Superficial keratitis
• Herbert follicles
• Pannus
• Corneal ulcer
• Herbert Pits
• Corneal opacity
12. • Active disease, predominantly follicles
• At least 5 or more follicles in upper palpebral
conjunctiva
TF (Trachomatous
Inflammation –
Follicular)
• Pronounced inflammatory thickening of upper palpebral
conjunctiva obscures > half of normal deep tarsal
vessels
TI (Trachomatous
Inflammation –
Intense)
• Presence of scarring in tarsal cunjunctiva
• Seen as white bands or sheets of fibrosis
TS (Trachomatous
Scarring)
• When at least 1 eyelash rubs the ocular surface
• Evidence of recently removed trichiatic eyelashes
TT (Trachomatous
Trichiasis)
• Easily visible corneal opacity present in pupillary area
• Causes significant visual impairment
CO - Corneal
Opacity
WHO Classification (FISTO)
18. Grade for upper eyelid Entropion
Minimal Apparent migration of meibomian glands
Conjunctivalization of lid margin
Lash-globe contact on up gaze
Moderate Lash-globe contact in primary position
Thickening of tarsal plate
Lid retraction
Severe Lid retraction causing incomplete closure
Gross lid distortion
Metaplastic lashes
Presence of keratin plaques
20. Investigations
Accurate estimation of infection
1. DNA based NAAT
2. rRNA based NAAT
In-vivo confocal microscopy : Hu et al IVCM
GRADING FOR INFLAMMATORY AND
SCARRING CHANGES
21. Nucleic acid amplification tests
Nucleic acid amplification test (NAAT) that targets
the cryptic DNA plasmid of chlamydia (Amplicor;
Roche Diagnostics, Indianapolis, IN).
A second-generation rRNA-based NAAT with an
additional target capture step (Aptima Combo 2;
Gen-Probe, San Diego, CA) has been shown to be
among the most sensitive and specific of the NAATs
for the detection of chlamydia.
Because of its superior sensitivity, the RNA test is a
logical gold standard test against which to compare
other tests for their ability to predict ocular
chlamydia.
23. A.INFLAMMATORY INFILTRATE : SEEN AS MULTIPLE BRIGHT WHITE NUCLEI.
THE MEAN INFLAMMATORY CELL DENSITY OF 3 RANDOMLY SELECTED
VOLUME SCANS IS CALCULATED
B.B. DENDRITIFORM CELLS ( DCs) : present or absent , present when >/= 1 dcs
per volume scaned
C.C . Tissue oedema : present or absent
D.D papillae : present or absent .
25. Trachoma
Recurrent infection in childhood (1-9 years)
Trichiasis in adulthood (>15 years)
Corneal opacity/ blindness
(painful)
A,F,E
S- surgery
26. Active infection
Antibiotic of choice for treating
active trachoma is Azithromycin
Children -20 mg/kg in a single
dose
Adults - single dose of 1 g
Also available in eye drops and
ointment form.
Azithromycin can safely be used
in all age groups and does not
have the side effects associated
with the earlier drug of choice
tetracycline.
Topical Azithromycin eye drops -
infants
29. How to treat?
Minor Trichiasis: 5 or less trichiatic lashes,
not threatening cornea
Epilation- Mechanical epilation is usually the
first-line treatment, especially for a few isolated
lashes.
Recurrence is common.
30. Electrolysis
Involves inserting a probe into
each individual follicle under slit
lamp or operating microscope
magnification.
After local anesthetic is
infiltrated into the eyelid, the
probe is inserted along a hair
shaft .
Electrical charge is applied until
bubbling is seen at the root of
the hair shaft.
If the hair shaft and bulb pull
freely, the treatment is
successful.
31. Cryotherapy
After local anesthetic is injected, the probe is
applied to the treatment area using a coupling
gel .
The cold treatment is then initiated, with the
thermocouple set to -20 to -30 degrees Celsius.
A frost-ball will propagate, and slight traction on
the probe will cause eyelid distraction, thus
confirming thermocoupling.
32. The coupling is held for 5 seconds and then allowed
to thaw.
This process is repeated, thus completing the double-
freeze thaw technique.
Clinical whitening indicates adequate follicle
destruction
Side effects- eyelid notching, entropion, eyelid
edema, canalicular scarring, herpes zoster
reactivation, symblepharon and eyelid pigmentary
changes.
33. Argon Laser treatment
The argon beam is generally titrated based on the
pigmentation of the cilia, with suggested laser
settings varying between 300 mW/0.5 s/50 µm and
1,200 mW/0.2 to 0.5 s/50 to 100 µm.
The beam is directed 2 to 3 mm below the lash
base, coaxial to the lash.
Repetitive burns are required for follicle destruction.
34. Side effects—primarily short-lived edema and
erythema—are minimal as compared to more
destructive modalities.
35. Surgical techniques
Include eyelid wedge resection, horizontal
blepharotomy, tarsal fracturing and eyelid splitting.
36. How to treat?
More than 5 trichiatic lashes/
threatening the cornea/ associated
entropion
Corrective eyelid margin/ entropion surgery
based on degree of entropion
37. WHO Recommendation
WHO recommends entropion surgery in any
trichiasis
‘to avoid loss to follow up in patients with minor
trichiasis’
38. Degree of entropion?
Globe lash contact- in upgaze only / primary
gaze
Eyelid margin changes- keratinization/
metaplastic lashes
Lagophthalmos- inability to close the eyelid
on gentle or forced closure
Tarsal thickening
40. Choice of surgery
Signs Surgery
Globe lash
touch only
Anterior lamellar
repositioning-
Contact in upgaze
only
Greyline split in
addition-
Contact in primary
gaze
Eyelid
margin
changes
Eyelid margin rotation
surgeries with tarsal/
bilamellar split
Bilamellar tarsal
rotation,
Posterior lamellar
tarsal rotation
Lagophthalm
os
Posterior lamellar
advancement
Absent on forced
closure
Posterior lamellar
grafting
Persists on forced
closure
49. Strategies for prevention of trachoma
Global Elimination
of Trachoma –
GET 2020 program
WHO Goal
- Eliminate
trachoma
by 2020
India is
signatory to
GET2020
50. History
In 1997, WHO launched the WHO Alliance for the
Global Elimination of Trachoma by the year 2020
(GET2020).
GET
strengthens
national
capacity by
Epidemiological
Assessment
Monitoring
surveillance
Project Evaluation
Resource
mobilization
52. Target
Elimination of trachoma as a public health problem:
Persons > 15 years of age suffering from TT “unknown to
the health system”
(< 0.2% in each district, approximately 1 case per 1000 total
population)
Children 1-9 years of age suffering from TF/TI < 5% in each
district, sustained for at least two years in the absence of
ongoing antibiotic mass treatment, in each formerly endemic
district
Presence of a health system able to identify and manage
new trachomatous trichiasis cases
Through defined strategies
With appropriate financial resources to implement those
strategies
53. State Prevalence rate
of active
infection
(1959-63 survey)
Prevalence rate
of active
infection
(86-89 Survey)
Burden of active
infection
TRA in 2006
Haryana 79.1 (Punjab) 3.8 4.0
Rajasthan 74.1 4.2 7.8
Gujarat 56.0 4.8 0.9
Punjab 79.1 6.9 5.5
Western UP /
Uttaranchal
68.1 9.5 9.8
Trachoma burden in India
Prevalence studies needed to assess the true burden in the
community and to ascertain whether trachoma has ceased to be a
public health problem
54. Prevalence of TT in India is 3.5 per 1000 in 15+ population
(Age & Sex Standardized)
Prevalence of Trachomatous
Trichiasis
in India (2014-17)
WHO Criteria For Elimination: Less than 2/1000 in 15+ population
55. Trachoma Elimination in India:
Recommendations
Central Task force & Monitoring committee of trachoma
elimination programme:
Central Task Force at national level for policy planning,
strategy for implementation for elimination of Trachoma from
the country by the year 2020
Monitoring Committee for monitoring and reporting of
Trachoma cases in states for elimination of Trachoma from
the country by the year 2020.
56. No. T-12011/37/2017-Ophth.
Ministry of Health and Family Welfare
Directorate General of Health Services
Ophthalmology Section
Nirman Bhawan, New Delhi
Dated 22.3.2018
Subject: Formation of Central Task Force at national level for policy planning and strategy
Implementation for elimination of Trachoma from the country by the year 2020.
It has been decided with the approval of competent authority to form a Central Task Force
at national level for policy planning and strategy implementation for elimination of Trachoma from
the country by the year 2020. The composition of the Task Force is as under:
S.No. Name Position
1 Dr. B.D.Athani, DGHS, Dte.GHS Chairperson
2 Dr. Promila Gupta, Addl. DG, Dte.GHS Member
3 Dr. (Prof.) Atul Kumar, Chief, Dr. R.P.Centre for Ophthalmic Sciences,
AIIMS, New Delhi & Advisor (Ophth.), GOI
Member
4 Dr. (Prof.) Praveen Vashisht, Dr. R.P.Centre for Ophthalmic Sciences,
AIIMS, New Delhi
Member
Secretary
5 Dr. V. Rajshekhar, Eye Surgeon and AC(NPCB), MoH&FW Member
6 Dr. Vivek Gupta, Assistant Prof. of Community Ophthalmology, Dr.
R.P. Centre for Ophthalmic Sciences, AIIMS, New Delhi
Member
7 Dr. Noopur Gupta, Assistant Prof. of Ophthalmology, Dr. R.P. Centre
for Ophthalmic Sciences, AIIMS, New Delhi
Member
8 Dr. S.K. Jain, Addl. Director (NCDC), Neglected Tropical Diseases
(NTD)
Member
9 Dr. Patanjali Dev, Adviser, WHO SEARO (Ophthalmology) Member
10 Dr. Ahmed Jamsheed Mohamed, Regional Advisor NTDC, WHO
Regional Office for SEA, New Delhi.
Member
11 Dr. Rashmi Shukla, National Professional Officer,Neglected Tropical
Diseases,WHO Country Office for India, New Delhi
Member
12 Dr. Nicole, Seguy, WHO India Member
57. No. T-12011/37/2017-Ophth.
Ministry of Health and Family Welfare
Directorate General of Health Services
Ophthalmology Section
Nirman Bhawan, New Delhi
Dated 22.3.2018
Subject: Formation of Central Task Force at national level for policy planning and strategy
Implementation for elimination of Trachoma from the country by the year 2020.
It has been decided with the approval of competent authority to form a Central Task Force
at national level for policy planning and strategy implementation for elimination of Trachoma from
the country by the year 2020. The composition of the Task Force is as under:
S.No. Name Position
1 Dr. B.D.Athani, DGHS, Dte.GHS Chairperson
2 Dr. Promila Gupta, Addl. DG, Dte.GHS Member
3 Dr. (Prof.) Atul Kumar, Chief, Dr. R.P.Centre for Ophthalmic Sciences,
AIIMS, New Delhi & Advisor (Ophth.), GOI
Member
4 Dr. (Prof.) Praveen Vashisht, Dr. R.P.Centre for Ophthalmic Sciences,
AIIMS, New Delhi
Member
Secretary
5 Dr. V. Rajshekhar, Eye Surgeon and AC(NPCB), MoH&FW Member
6 Dr. Vivek Gupta, Assistant Prof. of Community Ophthalmology, Dr.
R.P. Centre for Ophthalmic Sciences, AIIMS, New Delhi
Member
7 Dr. Noopur Gupta, Assistant Prof. of Ophthalmology, Dr. R.P. Centre
for Ophthalmic Sciences, AIIMS, New Delhi
Member
8 Dr. S.K. Jain, Addl. Director (NCDC), Neglected Tropical Diseases
(NTD)
Member
9 Dr. Patanjali Dev, Adviser, WHO SEARO (Ophthalmology) Member
10 Dr. Ahmed Jamsheed Mohamed, Regional Advisor NTDC, WHO
Regional Office for SEA, New Delhi.
Member
11 Dr. Rashmi Shukla, National Professional Officer,Neglected Tropical
Diseases,WHO Country Office for India, New Delhi
Member
12 Dr. Nicole, Seguy, WHO India Member
59. Acknowledgements
Special thanks to Dr. Rachna Meel, Dr. Noopur
Gupta, Dr. Rashmi Singh, Dr. Talvir Sidhu for Anterior
lamellar repositioning video and Trabut procedure
video.
Special thanks to Dr. Hunter Yuen for bilamellar
tarsal rotation video.
Postgraduate Dr. Sonalika Gogia, Ms. Diksha and
Ms. Neha for providing their inputs for making this
presentation
For any queries, contact us at:
[email protected]
Editor's Notes
Rrna more sensitive than dna based 100% SENSITIVITY AND SPECIFICITY
INFLAMMATORY INFILTRATE : SEEN AS MULTIPLE BRIGHT WHITE NUCLEI. THE MEAN INFLAMMATORY CELL DENSITY OF 3 RANDOMLY SELECTED VOLUME SCANS IS CALCULATED
B. DENDRITIFORM CELLS ( DCs) : present or absent , present when >/= 1 dcs per volume scaned
C . Tissue oedema : present or absent
D papillae : present or absent .