TRACHOMA DISEASE.
Trachoma is the leading cause of eye problems like
blindness among people worldwide. This disease is associated with poor hygiene
and inadequate sanitation.
Chronic granulomatous
kerato-conjuvtitis. Is caused by chlamydia trachomatics. Affect most children
age who can develop blind at later age.This disease can spread by conjuctival
sectrections by towels,flies,and finger.
Begins in early childhood with repeated infection of
the conjunctiva by Chlamydia trachomatis, the causative agent. This
triggers recurrent episodes of chronic conjunctival inflammation (active
trachoma Conjunctival scarring, which is believed to be immunopathologically
mediated, develops progressively over many years. The scar may contract,
pulling the eyelids in
(entropion), resulting in contact between the eyelashes and the eye
(trichiasis). This damages the cornea, and blinding opacification often follows.
active trachoma and 7.6 million with sight-threatening trichiasis requiring
surgery
Trachoma is the leading infectious cause of
blindness worldwide. It is a considerable public health problem,afflicting some
of the poorest regions of the globe, predominantly in sub-Saharan Africa and
Asia. In 2003, the WHO estimated that there were 84 million people having
Symptoms and Signs.
Clinically, trachoma is subdivided into Active (early) and (late-stage) disease.
Active disease is more commonly found in children.
The individual may have minimal symptoms of ocular irritation and a slight watery discharge. In
more severe cases, there may be
photophobia and copious
watering. However, it is not uncommon to find asymptomatic individuals
with significant conjunctival inflammation.
Active disease is characterized by a
chronic, recurrent follicular conjunctivitis, most prominently involving the
upper tarsal conjunctiva Follicles are collections of lymphoid cells subjacent to
the conjunctival epithelium.
They range from 0.2 to 2 mm in diameter, but only
those greater than 0.5 mm are considered significant in the WHO classification
scheme.Intense cases are characterized by the presence of papillary
hypertrophy. When mild, there is engorgement of the small vessels appearing as
small red dots with surrounding oedema within the tarsal conjunctiva. In more
severe.
Pathophysiology
of Trachoma
The Stimulus for Inflammation
and Scarring in Trachoma
Chronic inflammation is a central event in the
development of scar tissue in many human diseases. The ocular surface is no
exception; inflammation leads to scarring in conditions such as mucus membrane
pemphigoid and Stevens – Johnson syndrome. Clinically, active trachoma is
characterized by episodes of chronic conjunctivitis. In children, the median
duration has been estimated to be 36 weeks, and in adults, 7 weeks [35] . It
seems likely that this chronic, recurrent inflammatory process results in the
development of conjunctival scarring. Long-term epidemiological studies
examining the development of scarring have identified a sub-group of people who
have. severe inflammatory trachoma (TI) on repeated examination.
These
individuals are at greatest risk of developing scarring and trichiasis in later
life What is driving inflammation in trachoma? There is a consensus in the
literature that, for the majority of people,serial reinfection of the
conjunctiva by C. trachomatis is the major stimulant to the development
of the cicatricial complications, although direct microbiological evidence
for this from long-term epidemiological studies is very limited . In primate
models, conjunctival scarring only developed after many episodes of C.
trachomatis reinfection . An alternative view, which may be true for a
minority, is that the infection becomes persistent,driving the inflammation .
for this is limited.
The signs of trachomatous inflammation can often be found in the absence of
detectable C. trachomatis. One possible explanation for this is that
other nonchlamydial bacterial pathogens could also be provoking an inflammatory
response. Such pathogens are more commonly
found in individuals with conjunctival scarring and inflammation compared to
controls, particularly where trichiasis is also present.
In adults with trachomatous scarring, the conjunctival epithelium is atrophic,
often only one cell thick and goblet cells are lost [1] . The loose
sub-epithelial stroma (normally collagen types I and III) is replaced with a thick
scar of collagen type V. Along the conjunctival basement membrane, collagen
type IV is laid down.
These new fibers are orientated vertically, and are firmly attached to the
posterior surface of the tarsal plate, causing distortion [1] . Biopsies from
some scarred individuals have an inflammatory infiltrate dominated by T-cells, corresponding
to clinical conjunctival inflammation,which is frequently observed in people
with established trichiasis.
glands and a chronic inflammatory infiltrate
In vitro studies suggest that the organism may
transform into a persistent nonreplicating form when stressed, although,
evidence for this has not been found in vivo. From studies on monkeys, it has
been found that conjunctival inflammation develops in response to chlamydial
Heat Shock Protein60 (HSP60), which is found within live whole organisms . Heat
shock proteins are found in both eukaryotic and prokaryotic cells, and have
extensive sequence homology; they are induced when a cell is under stress.
It has been
suggested that the chronic inflammatory reaction in trachoma could be partly an
autoimmune reaction to the human equivalent of HSP60; however, the evidence
This has led
to the suggestion that at least in the late stages of the disease,they could promote
disease progression, and are highly likely to contribute to the corneal
pathology.
III, and IV (normally found in the stroma) and
deposition of new type V [13].
The tarsal plate is usually of normal thickness, but
there is often atrophy of the meibomian
ummary for the Clinician
■ Blinding trachoma is the end-stage of a chronic |
Trachoma
Control
The SAFE
Strategy.
Trachoma is a major public health problem in many endemic
countries, and controlling it requires a “public health” approach that goes
beyond the ophthalmology clinic. Many countries have had organized control
programs for decades.
These have taken different approaches to prevent the
blinding disease, which have met with
variable success. To meet this challenge, in 1998 the World Health Assembly
resolved to eliminate blinding trachoma by the year 2020 [89] . The Global
Alliance for the Elimination of Blinding Trachoma (GET2020) was formed, which
includes representatives from the WHO,
national blindness control programs from endemic countries, NGOs working in the
field, industry, and academics. The GET2020 alliance recognized the importance
of a multifaceted approach to controlling trachoma by adopting and promoting
the SAFE Strategy. The four
components of SAFE are Surgery
for trichiasis, Antibiotics
for infection, Facial
cleanliness, and Environmental
improvements to reduce transmission. In the following sections, supporting
evidence and important issues around the implementation of the SAFE Strategy
will be
reviewed.
ummary for the Clinician
■ The SAFE Strategy is being implemented by |
Conclusion.
Trachoma remains the commonest infectious cause of blindness
worldwide, and in many endemic regions, it is second only to cataract. During
the last few decades,
real progress has been made in controlling the disease.Trachoma was endemic in
Europe 100 years ago, where it declined in the face of general improvements in
living standards: less crowding, improved sanitation and water supply. Similar
improvements have happened or are happening in parts of currently endemic
countries.However, for many communities, it may take many decades for these
general improvements to arrive and have an impact on trachoma. Therefore, it is
necessary to actively implement the SAFE Strategy as the best validated
approach to the prevention of blindness from trachoma. (SEE DIABETIC CONDITION)
- CORONA VIRUS
- MONKEY POX
- VAGINAL DRYNESS
- FIBROID
- INFERTILITY
- OVULATION CYCLE
- OVARIAN CANCER
- VAGINAL BACTERIA
- MALE INFERTILITY
- BEST DAYS OF CONCIEVING
- MUCUS AFTER OVULATION
- FOODS FOR ERECTILE FUNCTIONS
- PREGNANCY ANEMIA
- DO AND DONT DURING PREGNANCY
- ERECTILE DYSFUNCTION
- U.T.I IN PREGNANCY
- STROKE RISK
- EAT THIS NOT THAT
- HOOKWORMS INFECTION
- OMEGA 3 BENEFITS
- FASTING
- WEIGHT LOSS TIPS
- vitiligo
- ABORTION
- DENGUE VIRUS
- EBORA VIRUS
- FEVER
- URINARY TRACT INFECTION
- HOSPITAL INFECTIONS
- WEST NILE VIRUS
- YELLOW FEVER
- EYE DISEASE
- ZIKA VIRUS
- STRESS
- IRON DEFFICIENCE
- INSOMNIA (SLEEPING PROBLEMS)
- HEART PROBLEMS
- COMPONENTS OF BLOOD
- BLOOD DISORDER
- LABORATORY TEST OF BLOOD DISORDER
- BONE MARROW EXAMINATION
- BLOOD ANEMIA
- ANIMAL BITES
- EYE BURN
- CHOCKING
- HEAT STROKE
- SMOKE EFFECTS
- SNAKE BITE
- MALARIA VACCINE
- BEST WAY TO SLEEP A CHILD
- CHILD FEVER REDUCING
- ELEPHANTIASIS
- WOMEN BEARDS
- DATES
- PAPAYA FRUITS
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