Glaucoma is the second leading cause of blindness worldwide according to the WHO. It is a group of eye diseases that damage the optic nerve and causes vision loss, usually due to increased intraocular pressure. There are two main types - open-angle glaucoma which is most common, and closed-angle glaucoma which is more urgent. Detection involves measuring eye pressure, examining the optic nerve and retina, and visual field testing. Treatment goals are to lower eye pressure through medications, laser trabeculoplasty, or surgery such as trabeculectomy or tube shunt implantation to slow disease progression.
Congenital Glaucoma is one of the most common causes of irreversible childhood blindness. This presentation covers this topic in detail that can aid physicians in effective patient care.
PS: The slides in the preview look skewed, download the presentation to view the font used in Office 2012 and upwards.
Congenital Glaucoma is one of the most common causes of irreversible childhood blindness. This presentation covers this topic in detail that can aid physicians in effective patient care.
PS: The slides in the preview look skewed, download the presentation to view the font used in Office 2012 and upwards.
INTRODUCTION
ETIOLOGY
RISK FACTORS
PATHOPHYSIOLOGY
CLASSIFICATION
CLINICAL FEATURES
DIAGNOSTIC MEASURES
MANAGEMENT
Medical
Surgical
Nursing
CONCLUSION
BIBLIOGRAPHY
POST TEST
some people are affected with this problem they want to know about the glaucoma causes, risk factor, pathophysiology, signs and symptoms, treatment and complication, etc and they get more knowledge and they will avoid the complication especially loss of vision.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
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The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
2. GLAUCOMA- Definition
Glaucoma can be considered a generic
name for a group of diseases causing optic
neuropathy ( disc cupping ) and visual field
loss usually , but not always, in the
presence of raised IOP, it is increasingly
being realised that other factors- such as
optic nerve head perfusion, are
concomitantly responsible for optic
neuropathy in adult glaucoma.
3. EPIDEMIOLOGY
Glaucoma is the second leading cause of blindness in the world, according to the
World Health Organization.
As of 2010, there were 60.5 million people in the world with glaucoma.
By 2020, the prevalence is projected to increase to 79.6 million worldwide .
On the basis of population based studies from India ,estimated that 11.2 million
person affected with Glaucoma. Among them 6.48 million with POAG,2.54
million with PACG,2.28 million with secondary glaucoma.
References:
1.QuigleyHA,BromanAT.(2006) “The number of people with glaucoma worldwide in 2010 and 2020”,Br J
Ophthalmol;90(3):262-267
2.George R,Ramesh S Ve,Vijaya L.(2010) “Glaucoma in India:Estimated Burden of Disease” J Glaucoma;19:391-
397
3. Kingman, Sharon (2004). "Glaucoma is second leading cause of blindness globally". Bulletin of the World
Health Organization 82 (11): 887–888.
4. THE HEALTHY EYE
• Light rays enter the eye
through the cornea, pupil
and lens.
• These light rays are
focused directly onto the
retina, the light-sensitive
tissue lining the back of the
eye.
• The retina converts light
rays into impulses; sent
through the optic nerve to
your brain, where they are
recognized as images.
5. Aqueous Humor Dynamics
In the front of the eye is a space called the anterior chamber.
A clear fluid ,called aqueous humor produce from ciliary body ,passes
through pupil to enter into anterior chamber and nourishes the nearby
tissues. The fluid leaves the anterior chamber at the angle where the
cornea and iris meet, called trabecular meshwork. From there it drains
into Canal of Schlemm which inturn opens into aqueous veins and
reabsorbed.
6. Sometimes the aqueous humor passes slowly or blocked through
the meshwork drain. Then the fluid builds up, the pressure inside
the eye rises(IOP-Increased intraocular pressure). Unless the
pressure at the front of the eye is controlled, it can damage the optic
nerve and cause vision loss. This is the main cause of Glaucoma.
IOP & GLAUCOMA
7. TYPES OF GLAUCOMA
Two main categories of glaucoma:
• Open-angle glaucoma: the most common form of glaucoma -
(the most common form that affects approximately 95% of
individuals)
• Closed-angle glaucoma: a less common and more urgent form
of glaucoma.
Other Types of glaucoma:
Normal-Tension Glaucoma
Congenital glaucoma
Secondary glaucoma
8. OPEN-ANGLE Glaucoma:
• Trabecular meshwork becomes less efficient at draining aqueous
humor.
• Intraocular pressure (IOP) builds up, which leads to damage of
the optic nerve.
• Damage to the optic nerve occurs at different eye pressures
among different patients.
• Typically, glaucoma has no symptoms in its early stages.
9. CLOSED -ANGLE(or narrow-angle) glaucoma:
• The drainage angle of
trabecular meshwork
becomes blocked by the iris.
• IOP builds up very fast.
• Symptoms include severe
eye or brow pain, redness of
the eye, decreased or blurred
vision.
• Must be treated as a medical
Emergency-should visit
ophthalmologist immediately.
11. NORMAL-TENSION Glaucoma
Normal-tension glaucoma occurs when there is damage to the optic nerve
detected in patient who has completely normal Inter Ocular Pressure (IOP).It has
the same characteristics of POAG. Lowering eye pressure through medication
sometimes slows the progress of the disease, but this type of glaucoma may
worsen despite low pressure. Treatment is generally the same as for open-angle
glaucoma with high eye pressure.
OPTIC CUP PRODUCED IN RETINA
12. CONGENITAL Glaucoma
Congenital Glaucoma results as a condition from birth.Children are born
with conditions.such as abnormal development of anterior chember
angle which prohibt the normal drainage of fluid from the eyes,which
cause an increase in pressure within the eye, subsequent retinal and
optical disc damage.
13. Secondary Glaucoma
Glaucoma can develop as a complication from other conditions
including:
Eye injuries
Uveitis (internal eye inflammation)
Pigment dispersion
Diabetes (Neovascular glaucoma)
Steroid use
Normal vision Glaucoma affected vision
14. Detection of Glaucoma
Regular glaucoma check-ups include two routine eye tests:
1.Tonometry – eye pressure test IOP
2.Ophthalmoscopy --using a magnifying instrument
(ophthalmoscope) and a light source.
Additional tests:
Perimetry : The perimetry test is also called a visual field test.
Gonioscopy : is a painless eye test that checks if the angle where the iris
meets the cornea is open or closed, showing if either open angle or closed
angle glaucoma is present.
15. Tonometry measures intraocular pressure either by the force required to
flatten a constant area of the cornea (e.g. Goldmann tonometry) or by
the area flattened by a constant force.
Goldmann tonometer: Stationary device requires anesthesia drops, requires contact
with cornea and is attached to a slit lamp – usually is used by an Ophthalmologist.
TONOMETRY
16. Non-contact tonometry or air-puff tonometry:
This type of tonometer uses a rapid air pulse to applanate the cornea. Intraocular
pressure is estimated by detecting the force of the air jet at the instance of applanation.
In most cases a stationary unit,
Does not require anesthetic drops
TONOMETRY
17. Tono-pen - is a portable electronic, digital pen-like instrument that
determines IOP by making contact with the cornea, after use of
topical anesthetic eye drops – tip covers are used between the
patients.
TONOMETRY
18. The newest Advancement in tonometry is DIATON TONOMETER –
It measures intraocular pressure (IOP) through the Eyelid.
TONOMETRY
20. OPTHALMOSCOPY
Eye drops may be placed in the eyes to dilate the pupils.
Special magnifying lenses are used to examine the retina and optic nerve
for damage.
Normal optic nerve Suspicious Optic Nerve
21. Slit Lamp & Gonioscopy
A special microscope called a slit lamp is used to examine the structures of
the eye.
A gonioscopy lens may be used to view the drainage angle.
22. PERIMETRY OR VISUAL FIELD TEST
Perimetry is an essential method used to determine if there is any loss of the visual field .
Peripheral (side) vision is tested with a perimeter.
23. GLAUCOMA TREATMENT
The goal is to decrease the eye pressure
The three main categories of treatment are:
1. Medication
2. Laser trabeculoplasty
3. Conventional surgery
Unfortunately, these treatments will not
reverse any existing damage but they can
slow the progression of the disease
24. DRUGS THAT DECREASE AQUEOUS PRODUCTION
I. Beta-Blockers [Timolol]
-Mechanism: Act on ciliary body to production of aqueous humor
-Administration: Topical drops to avoid systemic effects
-Side Effects: Cardiovascular (bradycardia), bronchoconstriction , depression
II. Alpha-2 Adrenergic Agonists [Brimonidine]
-Mechanism: production of aqueous humor
-Administration: Topical drops
-Side Effects: Lethargy, fatigue, dry mouth.
III. Carbonic Anhydrase Inhibitors [Acetazolamide]
-Mechanism: Blocks CAI enzyme production of bicarbonate ions (transported to
posterior chamber, carrying osmotic water flow), thus production of
aqueous humor
-Administration: Oral, topical
-Side Effects: kidney stones, possible (rare) aplastic anemia
25. DRUGS THAT INCREASE AQUEOUS OUTFLOW
I. Nonspecific Adrenergic Agonists [epinephrine)
-Mechanism: uveoscleral outflow of aqueous humor
-Administration: Topical drops
-Side Effects: Can precipitate acute attack in patients with narrow iris-corneal angle,
headaches, cardiovascular arrhythmia, tachycardia
II. Parasympathomimetics [Pilocarpine]
-Mechanism: contractile force of ciliary body muscle, outflow via TM
-Administration: Topical drops or gel.
-Side Effects: Headache, induced miopia.
III. Prostaglandins [latanoprost]
-Mechanism: May uveoscleral outflow by relaxing ciliary body muscle
-Administration: Topical drops
-Side Effects: Iris color change
26. Generally recommended for patients with open angle glaucoma that continues
to progress despite use of medications.
During ALT (Argon laser trabeculoplasty), an Argon laser beam is directed at
the trabecular meshwork.
If the laser is successful, changes occur in the trabecular meshwork that enable
it to drain fluid more effectively.
Laser trabeculoplasty
27. Conventional surgery
Conventional surgery (filtering microsurgery) involves creating a drainage hole
with the use of a small surgical tool.
This new opening allows the intraocular fluid to bypass the clogged drainage
canals and flow out of this new, artificial drainage canal.
29. Advancement-Trabectome surgery
Trabectome surgery increases the amount of fluid exiting the eye.
The tip of the Trabectome removes the strainer-like tissue (trabecular
meshwork) that reduces flow into the natural drainage system.
Studies indicate that Trabectome usually lowers the eye pressure by about
30%, while also decreasing the number of glaucoma eye drops that need to
be taken.
30. TUBE SHUNT IMPLANTATION
Tubes or glaucoma shunts are devices that are implanted in the eye and provide an
artificial alternative drainage site for fluid from the eye.
Most shunt devices look somewhat like a computer mouse.
Usually, a small incision is made near the top of eye underneath the conjunctiva.
The tube which extends from the body of the device, is inserted into the eye's anterior
chamber.
32. REFERENCES
1. Casson, Robert J; Chidlow, Glyn; Wood, John PM; Crowston, Jonathan G; Goldberg,
Ivan (2012). "Definition of glaucoma: Clinical and experimental concepts". Clinical &
Experimental Ophthalmology 40 (4): 341–349.
2. QuigleyHA,BromanAT.(2006) “The number of people with glaucoma worldwide in
2010 and 2020”,Br J Ophthalmol;90(3):262-267.
3.George R,Ramesh S Ve,Vijaya L.(2010) “Glaucoma in India:Estimated Burden of
Disease” J Glaucoma;19:391-397.
4. Kingman, Sharon (2004). "Glaucoma is second leading cause of blindness globally".
Bulletin of the World Health Organization 82 (11): 887–888.
5. Kingman, Sharon (2004). "Glaucoma is second leading cause of blindness globally".
Bulletin of the World Health Organization 82 (11): 887–888.
6. Anderson DR.(1989), “Glaucoma: the damage caused by pressure”. XLVI Edward
Jackson Memorial Lecture. Am J Ophthalmol;108:485–495.
33. REFERENCES
7. Smith G, Atchison DA,(1997): The Eye and Visual Optical Instruments. Cambridge:
Cambridge University Press 46(10):15-45.
8. Andrew Iwach, MD (GREG): Trabeculectomy with Intraoperative Sponge 5-Flourouracil.
Ophthalmology 1996 Jun;103(6):963-970.
9. http://eyewiki.aao.org/Medical_Management_for_Primary_Open_Angle_Glaucoma
10. Schwartz K, Budenz D,(2004): Current management of glaucoma. Curr Opin
Ophthalmol 15:119-140.
34. Sincere thanks to Dr. Debojyoti Chakrabarty, the Head of the P.G. Dept. of
Zoology, Barasat Govt. College for his valuable suggestions and providing
infrastructure facilities.
Thanks to Dr. Tuhin Kumar Saha, Dr. Madhumita Manna,
Dr. Debjani Sarkar, Dr. Sanjay Podder, Dr. Srikanta Guria, Dr.Tanaya Dey for
providing encouragements and various help during the entire period of study.
Thanks to my seniors of SEM-III.
Grateful thanks also to the non teaching stuffs of our department
Lastly, the co-operation received from the classmates is also acknowledged.
ACKNOWLEDGEMENT