This document discusses surgical treatments for dry eye disease (DED), including lacrimal occlusive devices and tarsorrhaphy. Punctal plugs are described as the most common lacrimal occlusive device used to reduce tear clearance by blocking the puncta. Absorbable plugs dissolve within days while non-absorbable silicone or acrylic plugs can last permanently. Complications include extrusion, granulation, and biofilm formation. Tarsorrhaphy involves suturing the eyelids together to reduce exposure and evaporation; it can be temporary or permanent. The document outlines different tarsorrhaphy techniques and potential complications such as trichiasis, granuloma, and
Ischemic optic neuropathy constitutes one of the major causes of blindness or seriously impaired vision among the middle-aged and elderly population.
Ischemic optic neuropathy is due to acute ischemia of the optic nerve. it can be classified into two, depending upon the part of the optic nerve involved:
1.Anterior ischemic optic neuropathy (AION)
-AION is due to acute ischemia of the front (anterior) part of the optic nerve (also called optic nerve head), which is supplied mainly by the posterior ciliary arteries.
-AION is divided into two types, depending on what causes it:
1.Arteritic AION: This is the most serious type and is due to a disease called giant cell arteritis or temporal arteritis.
2. Non-arteritic AION: This is the usual, most common type, with many different causes but not associated with giant cell arteritis.
2.Posterior ischemic optic neuropathy (PION). -
-PION is a much less common type. It is due to acute ischemia of the back (posterior) part of the optic nerve, located some distance behind the eyeball; this part of the optic nerve is NOT supplied by the posterior ciliary arteries
(Hayreh, 2009)
Ischemic optic neuropathy constitutes one of the major causes of blindness or seriously impaired vision among the middle-aged and elderly population.
Ischemic optic neuropathy is due to acute ischemia of the optic nerve. it can be classified into two, depending upon the part of the optic nerve involved:
1.Anterior ischemic optic neuropathy (AION)
-AION is due to acute ischemia of the front (anterior) part of the optic nerve (also called optic nerve head), which is supplied mainly by the posterior ciliary arteries.
-AION is divided into two types, depending on what causes it:
1.Arteritic AION: This is the most serious type and is due to a disease called giant cell arteritis or temporal arteritis.
2. Non-arteritic AION: This is the usual, most common type, with many different causes but not associated with giant cell arteritis.
2.Posterior ischemic optic neuropathy (PION). -
-PION is a much less common type. It is due to acute ischemia of the back (posterior) part of the optic nerve, located some distance behind the eyeball; this part of the optic nerve is NOT supplied by the posterior ciliary arteries
(Hayreh, 2009)
Retinal vasculitis refers to the inflammation of the retinal vessel resulting in evident clinical manifestations i.e. vascular sheathing, leakage and occlusion. This presentation covers the etiology, pathogenesis, clinical features, diagnosis and management of this spectrum of retinal disease.
Retinal vasculitis refers to the inflammation of the retinal vessel resulting in evident clinical manifestations i.e. vascular sheathing, leakage and occlusion. This presentation covers the etiology, pathogenesis, clinical features, diagnosis and management of this spectrum of retinal disease.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
3. The definition of DED by the TFOS DEWS 2:
Multifactorial disease:
Loss of homeostasis of the tear film,
Ocular symptoms,
Tear film instability,
Hyper-osmolarity,
Ocular surface inflammation and damage,
Neurosensory abnormalities.
4.
5. Why We Should Treat
DED?
Mild and Severe DED
in QoL similar to Mild
Psoriasis and Moderate- Severe
Angina.
6.
7. Surgical Options for DED
1- To reduce the tear clearance. (punctal/ canallicular occlusion)
2- To supply tear lake. (artificial tear reservoirs, surgery of the
salivatory gland)
3- To reduce the area of exposed. (tarsorrhaphy, induced ptosis)
4- To treat conditions associated with DED. (LSCT, AMT)
8. Lacrimal Occlusive Devices
• Punctal Plugs: Easily visible and removable without much difficulty.
• Canalicular Plugs:
Not visible,
Extrusion unlikely,
Increasing the risk of migration ,
Difficulty in localizing their position without ultrasound.
10. Indications
Any condition that would benefit from aqueous retention on the ocular
surface, including:
• Dry eye stage 2, 3
• Symptomatic contact lens wear
• DED related to refractive surgery
• ADDE secondary to a variety of systemic diseases ( Sjogren ,GVHD,
Autoimmune diseases) / After control of ocular surface inflammation.
11. Indications
• Superior limbic keratoconjunctivitis (SLK)
• Any corneal irregularities or scarring that affect tear stability
• Lid palsy or lid closure abnormalities
• Toxic Epitheliopathy
12. Contraindications/ Controversy
• Allergy to any of the materials.
• Lacrimal outflow obstruction.
• Ectropion.
• Active ocular infection.
• Ocular surface inflammation. (pro-inflammatory
cytokines )
Inflammation should be treat prior to insertion of PPs.
13. Absorbable Devices
• “Test” devices.
• Collagen-based plugs, absorbs within 4 to 7 days.
At 4 c or under, Atelocollagen dissolves. It turns into a white colored gel at
body temperature.
• Certain polymer-based plugs last for 3 days to 6 months.
14. Non-Absorbable Devices
• Non-absorbable or “permanent” plugs are often silicone-based.
• Made of long-lasting materials : silicone, teflon, hydroxyethyl
methacrylate (HEMA), polycaprolactone (PCL) .
16. The criteria for designing the PPs :
Purpose of application. (tear retention or drug delivery)
Required length of retention. (short-term or long-term)
Patient compliance.
Commercial value.
17. Types of PPs
1-Umbrella. Easy to spot and remove.
2-Slanted or low profile cap. Comfort, extra stability.
3-Tapered. Exerts extra force horizontally to keep the
PPs in place.
18. 4-Reservoir. Captures and holds tears, reduce FB
sensation and increase comfort.
5-Perforated PPs. Central lumen; in treating punctal
stenosis and partial occlusion.
19.
20. Some PPs coated with a "slick"
surface for easier insertion.
Soft, pliable PPs increase
comfort and conform more
readily to the shape of the tear
drainage channels.
21. Older people benefit from soft PPs
with aging, tear drainage channels
enlarge and muscular lining less
elastic.
In this case, softer punctal plugs
are more likely to stay in place than
harder ones.
22. Canalicular Plugs
• Horizontal and Vertical / Temporary and Permanent.
• Temporary made of animal collagen and last for 4–14 days.
• Temporary extended/ Permanent last from 2 to 6 months. Made of different
materials such as glycolic acid with trimethylene carbonate, and polydioxanone
(PDS).
• The diameter of the plug is more important than its length.
23.
24.
25.
26.
27.
28. Complications of Punctal Plugs
• Extrusion:
Hard PPs (silicone PPs) are more likely to dislodged and
fall out.
Hard PPs tend to trigger complications.
Even in soft PPs, complications occur if finishing of the
edge is not satisfactory or the figuration tends to
stimulate tissues.
29. • Granulation:
Granulation is the most frequently observed complication of PPs.
Large plug size was the major risk factor leading to granuloma formation.
mucosal dissection by the plug edges necrosed tissue
pyogenic granuloma PP extrusion
30. • Biofilm formation.
Punctal silicone plugs contaminated with microbes.
In more than 50% of cases, staphylococcus.
Acrylic plugs may portend a lower risk of infection than silicone plugs.
Carefully monitor these plugs.
32. • Insoluble lacrimal canaliculus plugs associated with complications
such as infections (canaliculitis, dacryocystitis) and inflammations
• No serious complications associated with lacrimal canaliculus
collagen plugs.
33. PPs as Controlled Drug Delivery Implants
• PPs advantages :
• in loss of drug and/or formulation,
• in lacrimal drainage of drug,
• Patient compliance,
• in costs.
Latanoprost, Olopatadine, Cyclosporine-a
34. Punctal Cauterization
• Cautery,
• Diathermy ,
• Argon laser.
Today, disposable, hand-held thermal cautery is the most widely
used method.
35.
36. • Very few complications with cauterization:
• Epiphora
• Recanalization
Superficial cauterization have a higher rate of recanalization, and
that deeper surgical procedures may increase the success rate.
37. Irreversible Obstrauction of the Lacrimal Punctum
or Canaliculs
By Surgery:
1- Suturing the lacrimal punctum
Removal of the punctal epithelium.
Diathermy and excision.
2- Suturing the canaliculus
3- Excision of the canaliculus
By Glue:
• Acrylate glue.
• Pressure over the lacrimal fossa.
• Can exert toxic effects.
• Complications: canaliculitis,
dacryolithiasis, dacryocystitis,
dilatation of a canaliculus
40. Tarsorrhaphy
Ocular surface exposure,
Evaporation of the tear film
the traumatic effect of the moving lids on the healing epithelium.
Indications:
Persistent epithelial defects.
Severe dry eye that is refractory to medical Tx and punctal occlusion.
Exposure keratopathy.
41. There are four basic
types of tarsorrhaphy
• 1-Short-duration tarsorrhaphy
without sutures.
Tape, adhesive glue (lasts for a few
days), or Levator paralysis by
botulinum toxin injection.
• Induced Ptosis
1- Ptosis induced by botulinum toxin
* About 6-8 weeks
2- Ptosis induced by implantation of gold
weights
* Well tolerated.
* Complications: Displacement of the
implant and anterior bulging .
42. • 2-Temporary suture tarsorrhaphy, with or
without a bolster. (Blepharorrhaohy)
Various suture materials (e.g. Catgut, Silk,
Nylon, or Prolene) can be used. A suture
tarsorrhaphy may last up to 4 to 6 weeks.
45. • 4-The most extensive type of tarsorrhaphy is mobilization of skin or tarsal
plate flaps:
Lids are split into anterior and posterior lamellae. Either lamella can be resected
in the upper or lower lid and filled with advancement of the opposite lamella.
The “tongue and groove” method , tarsal flap of one lid is inserted between the
lamellae of the other lid.
It is difficult to reverse these tarsorrhaphies at a later date.
46.
47.
48. Complications after Tarsorrhaphy
Localized trichiasis and distichiasis.
Pyogenic granuloma of the eyelid.
Lid margin deformities.
Focal cellulitis.
Premature separation.
Cheese-wiring of the sutures, skin breakdown.
Entropion after lysis of a permanent tarsorrhaphy.