This document discusses various surgical procedures for glaucoma management. It provides details on laser trabeculoplasty, incisional surgery such as filtering procedures, laser iridotomy, glaucoma drainage devices, and cyclodestructive procedures. Laser trabeculoplasty involves applying laser energy to the trabecular meshwork to lower intraocular pressure. Filtering surgery involves creating a fistula to allow aqueous humor to drain from the anterior chamber. Laser iridotomy is used to treat pupillary block glaucoma by creating an iridotomy. Glaucoma drainage devices provide an alternative drainage pathway through a tube. Cyclodestructive procedures aim to reduce aqueous production by ablating the ciliary body. The
A surgical procedure featuring a partial thickness scleral flap that creates a fistula between AC and subconjunctival space for filtration of aqueous and creation of conjunctival bleb in an effort to lower IOP
A surgical procedure featuring a partial thickness scleral flap that creates a fistula between AC and subconjunctival space for filtration of aqueous and creation of conjunctival bleb in an effort to lower IOP
Brainstem
Last part of brain
The medulla oblongata or simply medulla is a long stem-like structure which makes up the lower part of the brainstem.[1] It is anterior and partially inferior to the cerebellum. It is a cone-shaped neuronal mass responsible for autonomic (involuntary) functions, ranging from vomiting to sneezing.[2] The medulla contains the cardiac, respiratory, vomiting and vasomotor centers, and therefore deals with the autonomic functions of breathing, heart rate and blood pressure as well as the sleep wake cycle.
During embryonic development, the medulla oblongata develops from the myelencephalon. The myelencephalon is a secondary vesicle which forms during the maturation of the rhombencephalon, also referred to as the hindbrain.
The bulb is an archaic term for the medulla oblongata.[1] In modern clinical usage, the word bulbar (as in bulbar palsy) is retained for terms that relate to the medulla oblongata, particularly in reference to medical conditions. The word bulbar can refer to the nerves and tracts connected to the medulla, and also by association to those muscles innervated, such as those of the tongue, pharynx and larynx.
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Title: Sense of Smell
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 primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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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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
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3. INDICATIONS:
• WHEN MEDICAL THERAPY FAILS TO ARREST VISUAL FIELD LOSS
• A NON COMPLIANT PATIENT
• PATIENT WHO CAN'T COME FOR REPEATED REVIEW
• IF MEDICATION ALONE CAN'T CONTROL IT.
6. CHOICE OF SURGERY:-
OPEN ANGLE GLAUCOMA
LASER TRABECUOPLASTY
INCISIONAL THERAPY
CLOSE ANGLE GLAUCOMA
LASER IRIDOTOMY
LASER GONIOPLASTY /PERIPHERAL
IRIDOPLASTY
PERIPHERAL IRIDECTOMY
OTHER
GLAUCOMA DRAINAGE DEVICES
CILIARY BODY ABLATION PROCEDURESS
7. LASER TRABECULOPLASTY
• LTP IS A TECHNIQUE WHERE LASER ENERGY IS APPLIED TO THE T.M IN DISCRETE
SPOTS,USUALLY COVERING 180’TO 360’ / TREATMENT
VARIOUS MODALITIES:
ARGON LASER TRABECULOPLASTY(ALT)
DIODE LASER TRABECULOPLASTY
SELECTIVE LASER TRABECULOPLASTY(SLT)
8. MECHANISMS:
• TREATED AREA OF TM –MAY SHRINK—CAUSING STRETCHING OF ADJACENT
AREAS-
• TM- RELEASES IL1 ß& TNF A INCREASING OUTFLOW FACILITY THROUGH
INDUCTION OF SPECIFIC MATRIX METALLOPROTEINASES.
9. INDICATIONS:
• POAG
• PIGMENTARY GLAUCOMA
• EXFOLIATION SYNDROME
• STEROID INDUCED GLAUCOMA
LESS RESPONSIVE TO
APHAKIC & PSEUDOPHAKIC
EYES THAN PHAKIC EYES
IT LOWERS DOWN IOP BY 20-25 %
IT IS NOT EFFECTIVE FOR TREATING UVEITIC
GLAUCOMA.
10. TECHNIQUE:
ALT
• 50ΜM –0.1 SEC
• THROUGH A GONIOLENS AT THE ANT.
NONPIGMENTED & POST. PIGMENTED EDGE OF
THE TM.
• (300-1000MW)
• APPLIED 360’ BUT EFFECTIVE 180’(40-50
APPLICATIONS)
SLT
• FDA APPROVED ---LASER TARGETS
INTRACELLULAR MELANIN.
• A FREQUENCY DOUBLED Q SWITCHED ND:YAG
LASER WITH-- 400ΜM SPOT SIZE TO DELIVER
0.4-1.0 MJ OF ENERGY FOR 0.3 NS.
A DIODE LASER: A 75µm WITH A POWER SETTING 600-
1000MW FOR 0.1 SEC.
11. COMPLICATIONS:
• TRANSIENT RISE OF IOP
• IT HAS REPORTED TO INCREASE 50-60 MMHG
• LOW GRADE IRITIS
• PREVENTION:
• IF TREATED AT 180 ‘/SESSION
• TOPICAL ANTI INFLAMMATORY DRUGS FOR 4-7
DAYS
12. INCISIONAL SURGERY:
• TRADITIONALLY REFERRED AS FILTERS.
• MORE ACCURATE TO CALL IT AS FISTULIZING PROCEDURES.
• GOAL:- TO CREATE A NEW PATHWAY (FISTULA) THAT ALLOWS AQUEOUS HUMOR TO FLOW OUT OF THE
ANTERIOR CHAMBER THROUGH THE SURGICAL OPENING IN THE SCLERA & INTO THE SUBCONJUNCTIVAL
& SUB TENON SPACES.
14. MECHANISM OF ACTION:
• DRAINAGE FISTULA:- MECHANISM IS TO CREATE AN OPENING OR FISTULA AT THE LIMBUS .
• IT ALLOWS A DIRECT COMMUNICATION BETWEEN THE ANTERIOR CHAMBER & SUBCONJUC SPACE.
• IT BYPASSES THE TRABECULAR MESH WORK , SCHLEM CANAL & COLLECTING CHANNELS .
• AQUEOUS GET ABSORBED BY SURROUNDING TISSUES & DRAINS WITH TEARS THROUGH NLD
15. FILTERING BLEB:
• CHARACTERISED BY ELEVATION OF CONJUNCTIVA AT THE SURGICAL SITE .
• THE CLINICAL APPEARANCE & FUNCTION OF BLEB VARIES IN:
REGARD TO EXTENT , ELEVATION & VASCULARITY.
17. LIMBAL STAB INCISION:
• PARACENTESIS SITE: SELF HEALING, BEVELED INCISION AT THE LIMBUS
• SITE:TEMPORALLY AT THE HORIZONTAL MERIDIAN OR IN THE INFERIOR –TEMPORAL QUADRANT.
19. FISTULIZING TECHNIQUES:
FULL THICKNESS:
• COMPLICATED BY EXCESSIVE AQ FILTERATION.
• PROLONGED FLAT AC , CORNEAL
DECOMPENSATION,SYNECHIAE
FORMATION,CATARACTS.
• ENDOPHTHALMITIS .
PARTIAL THICKNESS:
• SUGGESTED BY SUGAR (1961)
• WAS POPULARIZED BY CAIRNS (1968)
• THIS TECHNIQUE WAS KNOWN AS
TRABECULECTOMY.
20. 1- Aqueous flow incut ends of
schlemm canals
2-cyclodialysis
3-through the scleral flaps
4-through the CT subst of
scleral flap
5-around the margins of
scleral flap.
31. CORTICOSTEROIDS
• PREVENT BLEB FAILURE
• IT MODULATE WOUND HEALING PROCESS
• INHIBITS CELL ATTACHMENT & PROLIFERATION.
• STILL THE INCIDENCE OF BLEB FAILURE IS HIGH
IN: GLAUCOMA IN APHAKIA & PSEUDOPHAKIA&
NEOVASCULAR. GLAUCOMA
32. 5-FLUOROURACIL
• PYRIMIDINE ANALOG ANTIMETABOLITE WHICH
BLOCK DNA SYNTHESISTHROUGH THE
INHIBITION OF THYMIDYLATE SYNTHESIS
SHOWN TO INHIBIT FIBROBLAST
PROLIFERATION IN CELL CULTURE.
• PROTOCOL- SUB CONJ INJECTION.. 5 MG TWICE
DAILY FOR 7 DAYS & THEN ONCE FOR 7 DAYS.
• COMPLICATIONS-CONJUNCTIVAL WOUND
LEAKS,CORNEAL EPITHELIAL DEFECTS.
• SUCCESS REPORTED IN -5 MG 5 FU FOR 7-14
DAYS.
MITOMYCIN C
• ANTINEOPLASTIC ANTIBIOTIC FROM
STREPTOMYCIN CAESPITOSUS.
• A SPONGE SOAKED IN 0.5 MG/ML TO THE
SUBCONJUNCTIVAL TISSUES FOR 5 MINUTES
• RETROSPECTIVE STUDIES 0.2 MG /ML APPLIED FOR
2 MINS .
33. COMPLICATIONS:
EARLY
• INFECTION
• HYPOTONY
• SHALLOW/FLAT AC
• HYPHEMA
• CME
• TRANSIENT IOP RISE
• CHOROIDAL EFFUSION
• SUPRACHOROIDAL HAEMMORHAGE
• PERSISTENT UVEITIS
LATE
• LEAKAGE OR FAILURE OF THE FILTERING BLEB
• CATARACT
• BLEBITIS
• BLEB MIGRATION
• HYPOTONY
• PTOSIS
• EYELID RETARACTION
34. LASER IRIDOTOMY
• INDICATION:-PRESENCE OF PUPILLARY BLOCK
Therapeutic
TO PREVENT
PUPILLARY BLOCK
Diagnostic
PATENT IRIDOTOMY
FAILS TO CHANGE THE
PERIPHERALIRIS
CONFIGURATION
35. CONTRAINDICATIONS:
• RUBEOSIS IRIDIS
• PATIENTS ON ANTI COAGULANTS, ASPIRIN
PREOP EVALUATION
• CLOUDY CORNEA TREATMENT
• SHALLOW CHAMBER
• ENGORGED IRIS
• PRETREATMENT WITH PILOCARPINE
• APRACLONIDINE/BRIMONIDINE TO BLUNT IOP
SPIKES.
36.
37. TECHNIQUE:
ARGON LASER
• COLOUR OF THE IRIS
ND:YAG LASER
• Q SWTCHED LASER
• REQUIRES FEWER PULSES
• NOT EFFECTED BY IRIS COLOUR
• INITIAL SETTINGS 2-8MJ
Spot size Power time
50um 800-
1000mw
0.1 sec
38. COMPLICATIONS:
ARGON LASER
• LOCALISED LENS OPACITY
• ACUTE RISE IN IOP
• EARLY IRIDOTOMY
• POSTERIOR SYNECHIAE
• CORNEAL/RETINAL BURNS
ND:YAG LASER
• DISRUPTION OF THE ANTERIOR LENS CAPSULE
• CORNEAL ENDOTHELIUM
• BLEEDING
• POST OP IOP SPIKE
• INFLAMMATION
39. INCISIONAL IRIDECTOMY:
• CHANDLER
• SITE: SUPERIOR QUADRANTS FORNIX/LIMBUS BASE
• A 3MM TO 4MM INCISION IS MADE INTO THE AC & 1 TO 1.5 MM BEHIND THE CL JUNCTION.
41. LASER GONIOPLASTY/PERIPHERAL IRIDOPLASTY
• GOALS: IT IS A TECHNIQUE TO DEEPEN THE ANGLE.
• PRIMARILY USED IN ANGLECLOSURE GLAUCOMA RESULTING FROM PLATEAU IRIS.
• STROMAL BURNS ARE CREATED IN THE PERIPHERAL IRIS TO CAUSE CONTRACTION & FLATTENING.
44. GLAUCOMA DRAINAGE DEVICE :
• THESE DEVICES HAVE BEEN DEVELOPED THAT AID ANGLE FILTRATION BY SHUNTING AQUEOUS TO A SITE
AWAY FROM THE LIMBUS.
• IT INVOLVES PLACING A TUBE IN THE
ANTERIOR CHAMBER
CILIARY SULCUS
THROUGH THE PARS PLANA INTO THE VITREOUS CAVITY.
45. DEVICES:
VALVED
• AHMED (NEW WORLD MEDICAL)
NON VALVED
• MOLTENO (MOLTENO
OPHTHALMIC,DUNEDIN,NEWZEALAND)
• BAERVELDT (ABBOTT MEDICAL OPTICS)
50. TECHNIQUE:-
• SITE: SUPEROTEMPORAL QUADRANT IS PREFFERED OVER THE SUPERONASAL QUADRANT.
• VALVED DEVICES MUST BE PRIMED
• EXTRAOCULAR PLATE BETWEEN THE VERTICAL & HORIZONTAL RECTUS MUSCLE.
• TUBE PORTION OF THE DEVICE IS ROUTED 1 OF 3 WAYS
ANTERIOR ENTER THE ANTERIOR CHAMBER
PSEUDOPHAKIC EYES CILIARY SULCUS
VITRECTOMY THROUGH PARS PLANA FOR POSTERIOR
IMPLANTATION
53. TRANSSCLERAL CP
• IN 1961 WEEKEND & ASSOCIATES- XENON ARC PHOTO COAGULATION OVER THE CILIARY BODY
• IN 1969 VUCICEVIC & ASSOCIATES –USE OF RUBY LASERS
• IN 1984 BECKMANN & WAELTERMANN – RUBY LASER
54. INSTRUMENTS
ND YAG
• WAVELENGTH OF 1064NM
• TRAVERSE THE SCLERA WITH LOW ABSORPTION &
SCATTER.
• MAY BE OPERATED AS PULSED, FREE RUNNING,
THERMAL MODE ,OR A CONTINUOUS WAVE MODE
• MAY BE DELIVERED NONCONTACT , SLIT LAMP OR A
CONTACT PROBE
SEMICONDUCTOR DIODE LASERS
• RANGE OF 750-850 NMS
• DO NOT TRAVERSE THE SCLERA AS EFFECIENTLY
AS ND :YAG LASER
55.
56.
57.
58.
59. COMPLICATIONS:-
EARLY:
• UVEITIS & HYPHEMA
• DELLEN
• LOSS OF CENTRAL VISION
• OCULAR DECOMPRESSION RETINOPATHY
LATE:
• LATE FAILURE OF FILTRATION
• A LEAKING FILTERING BLEB