Peritoneal dialysis by Dr. Basil TumainiBasil Tumaini
Peritoneal dialysis by Dr. Basil Tumaini, prepared for nephrology lecture during the residency in Internal medicine at Muhimbili University of Health and Allied Sciences
Peritoneal dialysis by Dr. Basil TumainiBasil Tumaini
Peritoneal dialysis by Dr. Basil Tumaini, prepared for nephrology lecture during the residency in Internal medicine at Muhimbili University of Health and Allied Sciences
Renal Replacement Therapy: modes and evidenceMohd Saif Khan
Renal replacement therapy is a supportive care often required in critically ill patients who develop acute renal failure and its complications. Complexity arises when such patients become hemodynamically unstable and pose special challenge to critical care clinicians in ICU to carefully choose dialytic modality to tackle volume and solute overload. This presentation is about short description of modalities of RRT and current evidence regarding initiation, dose and type of modality.
A very simple yet comprehensive presentation to understand the concept of CRRT and its implementation in Intensive Care Unit. Intended for the very beginners in ICU. After going through the presentation you will be able to say "Now I know it!"
RENAL DIALYSIS.
RRT
Renal Replacement Therapy.
Dialysis is the artificial process of eliminating waste (diffusion) and unwanted water (ultra filtration) from the blood.
Dialysis is a procedure that cleans and filters the blood. It rids the body of harmful wastes and extra salt and fluids. It also controls blood pressure and helps our body keep the proper balance of chemicals such as potassium, sodium, and chloride.
Dialysis is a Greek word meaning "loosening from something else".
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
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
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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
3. Dialysis is a process whereby the solute composition of a solution,
A, is altered by exposing solution A to a second solution, B, through
a semipermeable membrane until they reach equilibrium
Water molecules and low-molecular-weight solutes in the two solutions can
pass through the membrane pores and intermingle, but larger solutes
(such as proteins) cannot pass through the semipermeable barrier,
and the quantities of high-molecular-weight solutes on either
side of the membrane will remain unchanged.
9. • DIFFUSION DEPENDS ON VELOCITY
IT REFERS TO SOLUTE
OSMOSIS REFERS TO MOVEMENT OF WATER
ULTRAFILTRATION(CONVECTION)-REFERS TO SOLVENT DRAG.IT REFERS
TO BOTH SOLUTE AND WATER
FACTORS- OSMOTIC PRESSURE
-MEMBRANE PRESSURE DIFFERENCE(TMP)
10.
11. Hydrostatic ultrafiltration
a. Transmembrane pressure.
The rate of ultrafiltration will depend on the total pressure difference
across the membrane (calculated as the pressure in the blood
compartment minus the pressure in the dialysate compartment).
b. Ultrafiltration coefficient (KUF). It is the permeability of dialyzer
membranes to water and is a function of membrane thickness and
pore size.
KUF is defined as the number of milliliters of fluid per hour that will be
transferred across the membrane per mm Hg pressure gradient
across the membrane.
12. The number of ml/hour of water the dialyzer can remove for every 1
mm Hg rise in TMP
E.g. a HF with KUF of 1 can remove 100ml/hour with
TMP of 100
For volumetric machines HF with KUF above 4 should be used to give
accurate results
17. Why is ultrafiltration needed for water in presence
of diffusion for solutes inspite of osmosis?
Hemofiltration and hemodiafiltration. Whereas diffusive removal of a solute
depends on its size, all ultrafiltered solutes below the membrane pore size are
removed at approximately the same rate. This principle has led to use of a
technique called hemofiltration, whereby a large amount of ultrafiltration (more
than is required to remove excessive fluid) is coupled with infusion of a
replacement fluid in order to remove solutes.
Although hemodialysis and hemofiltration often show comparable
removal of small solutes such as urea (MW 60), hemofiltration can
effect much higher removal of larger, poorly diffusible solutes, such as
inulin (MW 5,200). Sometimes hemodialysis and hemofiltration are
combined. The procedure is then called hemodiafiltration.
18. NEED OF COUNTERCURRENT MECHANISM
If the blood and dialysate were left in static contact with each
other via the membrane, the concentration of permeable
waste products in the dialysate would become equal to that in
the blood, and no further net removal of waste products would
occur.
In Dialysis, concentration equilibrium is prevented, and the concentration
gradient between blood and dialysate is maximized, by continuously refilling the
dialysate compartment with fresh dialysis solution and by replacing dialyzed
blood with undialyzed blood.
The purpose of “countercurrent” flow is to maximize the concentration
difference of waste products between blood and dialysate in all parts of the
dialyzer.
19. solute blood dialysate direction
UREA high zero To Dx
OTHER TOXINS high zero To Dx
Sodium 135-140 135-140 NO
Potassium Above 5 1.4-3.0 To Dx
Magnesium Above 1 0.5-1.0 To Dx
glucose +/-140 (8) 180 (10) +/-
chloride 100-119 100-119 NO
Ionized Calcium 4.5-5 mg/dl
2-2.5mEq/L
5-6 mg/dl
2.5-3 mEq/L
+/-
23. In this case, the flow rate of the cleared
stream is simply 60% of the inlet flow rate. If the inlet flow rate
is 400 mL/min, the flow rate of the cleared stream would be
0.60 × 400 = 240 mL/min, and the flow rate of the unchanged
stream would be 160 mL/min. Thus, a dialyzer extraction ratio
of 60% translates into a dialyzer clearance of 0.6 × blood inflow
rate , or 240 mL/min.
24.
25. Effect of dialyzer blood flow rate on
clearance
we see that when blood flow is very low,
50 mL/min, the blood in the dialyzer is cleaned very well,
due to a long residence time in the dialyzer, and the outlet
SUN is only 1 mg/dL, with an extraction ratio of 99%. However,
the amount of blood cleared is limited by the flow rate
of 50 mL/min; although 99% of the blood is cleared, 99% of
50 mL/min is a low number
26. When the blood flow rate is
increased, the blood is only partially cleared of urea due to
less time spent in the dialyzer, but even though the extraction
ratio falls as blood flow rate is increased, the volume
of blood cleared of urea nitrogen keeps increasing as the
blood flow rate is increased. Ultimately, when blood flow
rate is very high, 20 L/min, the clearance in this particular
example is 600 mL/min, even though only 3% of the inlet
SUN is removed.
27. Diffusion and Backdiffusion
Movement of
molecules from the
blood side is called
Clearance or
diffusion
Movement of
molecules from the
Dialysate side is
called
BackDiffusion
Removal of Toxins
Removal of excess
K+
Backdiffusion of
Bicarbonate
Glucose and
Calcuim
28. Transmembrane
pressure (TMP) =
Positive pressure in Blood side + Negative
pressure in Dialysate side in mmHg
Maximum UF
Higher
pressure
Lower UF
Lower
pressure
29. The
magnitude
of net
filtration in
Haemodialys
is is
determined
by
1- The
hydraulic
permeability
of the
dialyzer
2-The
surface
area of the
membrane,
and by the
geometry
of the
dialyzer .
3-the
hydrostatic
and
oncotic
forces
acting on
the blood
and
dialysate
sides of
30. The K0A, mass transfer area coefficient
If the extraction ratio remained constant at 60%, a doubling of the
blood flow rate would double the clearance.
However, removal efficiency falls at higher blood flow rates, and so the
clearance does not increase with QB in a 1:1 ratio.
Ultimately, at very high blood flow rate, the clearance will plateau. The
theoretical maximum clearance of a dialyzer ( for a given solute) at
infinite blood and dialysate flow rates is called the K0A and has units of
mL/min.
31. Urea diffuse from Plasma and Blood , creatinine less and Phosphate
Much less
-
8%
-
13%
32. Effect of erythrocytes
urea diffuses into and out of erythrocytes quickly.
For example, if the outlet plasma urea nitrogen level is 40 mg/dL, the
urea concentration in erythrocytes will have been reduced to
about that level also.
When calculating the removal rate of creatinine or phosphorus in mg/min
or mmol/min, one needs to use the plasma flow rate instead of the blood
flow rate.
33. Effect of dialysis solution flow rate
Dialyzer clearance of urea (and other solutes) depends on the dialysis solution flow rate as
well.
A faster dialysis solution flow rate increases the efficiency of diffusion of urea from blood
to dialysate although the effect is usually modest.
The usual dialysis solution flow rate is 500 mL/min.
A flow rate of 800 mL/min will increase urea clearance by about 5%–8% when a
highefficiency dialyzer is used and when the blood flow rate is greater than 350 mL/min.
The optimum dialysis solution flow rate is 1.5–2.0 times the blood flow rate.
34. Dialysate delivered at a rate of 500ml/min
◦ 120 liters of dialysate / 4-hoursession
Concentrated solutions mixed with water
Usually 1:34 or 1:40
Conductivity is a measurement of electric conductivity of Na to check
if dilution is correct
With proper dilution conductivity = 13-15
Serious hyponatremia or hypernatremia occurs if dilution is incorrect
35. H+ neutralized by Na HCO3 in the body
Acetate
◦ Transformed in LIVER to HCO3 (10-15 min)
◦ BUT is a potent vasodilator
Hypotension especially with liver disease
Acetate intolerance in high flux dialyzers
Bicarbonate
◦ Immediately neutralizes H+
◦ BUT precipitates Calcium salts (CaCO3)
Should be delivered separately as NaHCO3
Short life span of machine
Needs a strong post dialysis acid rinse (citric acid)
36. Attempts are made to increase the surface area of contact
between dialysate and dialyzer
• The Hollow fiber
◦ The parallel plate dialyzer
37. ◦ Surface area.
◦ Low flux vs high flux.
◦ Biocompatibility.
◦ Technique of manufacture including hemo- adsorption.
38. Cellulose membrane (Cuprophan)
◦ Is the first membrane to be used
◦ Contains free hydroxyl radicals
◦ They are bio-incompatible (BIC)
They are able to activate complement a inflammatory reaction a
chronic inflammation a protein catabolism + anorexia + malnutrition
a Cardiovascular accidents
Cause dialysis relatedAmyloidosis
Increased incidence of infection
Rapid loss of residual kidney function
◦ Cuprophan is BIC BUT this effect can be abolished after 2nd
use
39. Substituted Cellulose
◦ Chemically bonding the free hydroxyl group
Cellulose di acetate
Cellulose Triacetate
◦ Addition of a synthetic material to cellulose
Hemophane (semi synthetic)
Synthetic modified cellulose (SMC)
Synthetic material
◦ Contains no cellulose
Polysolphone
PMMA
PAN
40. Ability of the dialyzer to clear urea from
blood
The more clearance the better the dialyzer
Clearance can be calculated in vivo=
Qb x [BUN ART – BUNVEN]
BUNART
Clearance is closely related to the surface area
41.
42. HF with a high urea clearance
◦ They contain pores bigger in number and size
◦ Must be with bicarbonate dialysis
◦ They perform more adequate dialysis
◦ Clearance of bigger molecules toxins e.g. (B2 microglobulin)
◦ expensive
43.
44. The more the patient’s weight the larger surface area (and clearance)
you need
Patients with increased weight gain (volume overload) need adialyzer
with high KUF