This document discusses chronic kidney disease and hemodialysis. It provides information on assessing kidney function, the causes and treatment of chronic kidney disease, and preparing patients for renal replacement therapies like hemodialysis and peritoneal dialysis. It describes the dialysis process, equipment used, and some potential acute complications of hemodialysis treatment.
Postoperative care is the care you receive after a surgical procedure. The type of postoperative care you need depends on the type of surgery you have, as well as your health history. It often includes pain management and wound care. Postoperative care begins immediately after surgery.
Postoperative care is the care you receive after a surgical procedure. The type of postoperative care you need depends on the type of surgery you have, as well as your health history. It often includes pain management and wound care. Postoperative care begins immediately after surgery.
Acute kidney injury is common among hospitalized patients. It affects some 3–7% of patients admitted to the hospital and approximately 25–30% of patients in the intensive care unit.
Topics Covered:
Basic kidney physiology (just enumeration).
Manifestations of renal impairment.
AKI vs. CRF , definitions, causes and their classifications (in brief) .
Clinical evaluation of a case of renal failure.
indications for renal replacement therapy.
Approach for real-Life patient with renal impairment: group-case discussion.
A 33-year old man with polyuria and polydipsiaUsama Ragab
Clinical case uncovered (CCU) series
Endocrinology and diabetes
Case number 11: A 33-year old man with polyuria and polydipsia
Medical case presentation of polyuria
This presentation comprises of congenital anomalies of kidney and urinary tract made concise and in depth for PG preparation. It contains all important topics of the regarding subject covered in detail.
Acute kidney injury is common among hospitalized patients. It affects some 3–7% of patients admitted to the hospital and approximately 25–30% of patients in the intensive care unit.
Topics Covered:
Basic kidney physiology (just enumeration).
Manifestations of renal impairment.
AKI vs. CRF , definitions, causes and their classifications (in brief) .
Clinical evaluation of a case of renal failure.
indications for renal replacement therapy.
Approach for real-Life patient with renal impairment: group-case discussion.
A 33-year old man with polyuria and polydipsiaUsama Ragab
Clinical case uncovered (CCU) series
Endocrinology and diabetes
Case number 11: A 33-year old man with polyuria and polydipsia
Medical case presentation of polyuria
This presentation comprises of congenital anomalies of kidney and urinary tract made concise and in depth for PG preparation. It contains all important topics of the regarding subject covered in detail.
End-stage renal disease is a condition in which the kidneys no longer function normally and required excellent medical and nursing care for the managing this condition.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
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
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
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
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
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
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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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
2. Case -1Case -1
Diabetic for 20 yrs, work up showed CrDiabetic for 20 yrs, work up showed Cr
1.0, urine with +++ protein.1.0, urine with +++ protein.
Report from previous yr showing theReport from previous yr showing the
same results.same results.
Does he have chronic kidney disease?Does he have chronic kidney disease?
3. Case 2Case 2
21 yr old male , admitted with road traffic21 yr old male , admitted with road traffic
accident , developed renal failure requiringaccident , developed renal failure requiring
dialysis during the hospital stay.dialysis during the hospital stay.
He is undergoing dialysis treatment, 15He is undergoing dialysis treatment, 15thth
dialysis on the 40dialysis on the 40thth
hospital stay.hospital stay.
He has no significant medical history andHe has no significant medical history and
a routine checkup done a month prior toa routine checkup done a month prior to
admission was showing normal urineadmission was showing normal urine
analysis and renal function.analysis and renal function.
4. Case 3Case 3
A 82 yr old , urine Cr 1.2, urine analysisA 82 yr old , urine Cr 1.2, urine analysis
normal. He is only 50 kg wtnormal. He is only 50 kg wt
Doctor calculated GFR beforeDoctor calculated GFR before
administering antibiotic and it was lessadministering antibiotic and it was less
than 50ml/minute.than 50ml/minute.
What would you tell his son if he ask youWhat would you tell his son if he ask you
about his kidney function?.about his kidney function?.
5. Case 4Case 4
50 yr old diabetic with normal urine50 yr old diabetic with normal urine
analysis and no microalbuminuria ,withanalysis and no microalbuminuria ,with
serum Cr 0.8.(done 2 weeks beforeserum Cr 0.8.(done 2 weeks before
hospital admission).hospital admission).
Admitted with fever and urosepsis withAdmitted with fever and urosepsis with
hypotension- Cr 2.6, urine with plenty ofhypotension- Cr 2.6, urine with plenty of
pus cells , RBC and +++ protein.pus cells , RBC and +++ protein.
6. Calculation of GFRCalculation of GFR
(140-age) x weight (in kg)(140-age) x weight (in kg)
72 x P72 x PCrCr
For females multiply the result by 0.85For females multiply the result by 0.85
7.
8.
9.
10. Management of CKDManagement of CKD
Treatment of reversible causes .Treatment of reversible causes .
Preventing the progression of renalPreventing the progression of renal
disease.disease.
Treatment of complications of CKD .Treatment of complications of CKD .
Treatment of complications of ESRD.Treatment of complications of ESRD.
Identifying and preparing pts for RRTIdentifying and preparing pts for RRT
11. Reversible causesReversible causes
Decreased renal perfusion.Decreased renal perfusion.
RASRAS
Diuretic use.Diuretic use.
Hypotension –drugs, cardiogenic.Hypotension –drugs, cardiogenic.
Sepsis.Sepsis.
Drugs which lower GFR –ACEI,NSAID.Drugs which lower GFR –ACEI,NSAID.
12. Reversible causes -contdReversible causes -contd
Nephrotoxic drugsNephrotoxic drugs
Avoid nephrotoxic drugs in pts with CKD,Avoid nephrotoxic drugs in pts with CKD,
IV contrast, NSAID, Aminoglycosides.IV contrast, NSAID, Aminoglycosides.
amphoterecin etcamphoterecin etc
13. Reversible causes -contdReversible causes -contd
Urinary tract obstructionUrinary tract obstruction
BPH and outlet obstructionBPH and outlet obstruction
Kidney stone and obstruction.Kidney stone and obstruction.
14. Slowing rate of progression of CKDSlowing rate of progression of CKD
By reducing the intraglomerular HTN.By reducing the intraglomerular HTN.
BP control <130/80.BP control <130/80.
Reduced protein intake.Reduced protein intake.
Lowering cholestrol.Lowering cholestrol.
Smoking cessation.Smoking cessation.
15. Treatment of complications of CKDTreatment of complications of CKD
Volume overload-Volume overload-
Hyperkalemia.Hyperkalemia.
Metabolic acidosis.Metabolic acidosis.
Hyperphosphatemia.Hyperphosphatemia.
Secondary hyperparathyroidism.Secondary hyperparathyroidism.
HTNHTN
Anemia.Anemia.
Dyslipedemia.Dyslipedemia.
16. Treatment of complications ofTreatment of complications of
ESRDESRD
Uremic bleeding.Uremic bleeding.
Malnutrition.Malnutrition.
Pericarditis.Pericarditis.
Thyroid dysfunction.Thyroid dysfunction.
Uremia and uremic symptoms.Uremia and uremic symptoms.
17. Choices of RRTChoices of RRT
Transplantation.Transplantation.
Hemodialysis.Hemodialysis.
Peritoneal Dialysis.Peritoneal Dialysis.
18. TransplantationTransplantation
Not all pts appropriate candidate.Not all pts appropriate candidate.
Improve quality of life.Improve quality of life.
Donor availability main problem.Donor availability main problem.
Living related, living unrelated andLiving related, living unrelated and
Cadaveric donors.Cadaveric donors.
Details later….Details later….
19. Hemodialysis.Hemodialysis.
Home verus in-center therapy.Home verus in-center therapy.
Usual maintenance dialysis 3Usual maintenance dialysis 3
times/week,each session 4 hrs.times/week,each session 4 hrs.
Long nocturnal hemodialysis.- usually 5-6Long nocturnal hemodialysis.- usually 5-6
nights per week, each session 8-10 hrs.nights per week, each session 8-10 hrs.
Short daily dialysis at home- gainingShort daily dialysis at home- gaining
popularity.popularity.
20. Peritoneal dialysis.Peritoneal dialysis.
At home dialysis.At home dialysis.
Very convenient for pt’s who wish to work.Very convenient for pt’s who wish to work.
For pt’s who wish to travel.For pt’s who wish to travel.
For very young children and infants.For very young children and infants.
For pt’s with severe cardiovascular illness.For pt’s with severe cardiovascular illness.
For pt’s with difficult vascular access.For pt’s with difficult vascular access.
21. Contraindications to PDContraindications to PD
Unsuitable peritoneum- due to priorUnsuitable peritoneum- due to prior
surgery, malignancy.surgery, malignancy.
Hernia.Hernia.
Poorly controlled diabetes.Poorly controlled diabetes.
Back pain may get worse.Back pain may get worse.
22. Contra indications for dialysis.Contra indications for dialysis.
No absolute contraindications.No absolute contraindications.
Pt’s with advanced disease in an organPt’s with advanced disease in an organ
system other than kidneys usually excluded ( egsystem other than kidneys usually excluded ( eg
–end stage heart disease, liver disease etc).–end stage heart disease, liver disease etc).
Pts with advanced malignancy.Pts with advanced malignancy.
Un co-operative patients.Un co-operative patients.
23. Preparation for hemodialysis.Preparation for hemodialysis.
Access placement.Access placement.
3 types of access- primary A-V fistula,3 types of access- primary A-V fistula,
A-V graft.A-V graft.
double lumen cuffeddouble lumen cuffed
tunneled catheter.tunneled catheter.
24. Primary A-V fistula.Primary A-V fistula.
Usually on non-dominant upper extremity.Usually on non-dominant upper extremity.
End –to-side vein-to-artery anastomosis.End –to-side vein-to-artery anastomosis.
Usually wrist (radio-cephalic) or upper armUsually wrist (radio-cephalic) or upper arm
(brachio -cephalic OR brachio-basilic).(brachio -cephalic OR brachio-basilic).
Better to do it 6 months prior to anticipatedBetter to do it 6 months prior to anticipated
dialysis.dialysis.
25. A-V graftA-V graft
By anastomosing a synthetic conduitBy anastomosing a synthetic conduit
between artery and vein.between artery and vein.
Usually a polytetrofluroethylene (PTFE)Usually a polytetrofluroethylene (PTFE)
graft.graft.
26. A-V graftA-V graft
Straight fore arm- radio-cephalic.Straight fore arm- radio-cephalic.
Looped fore arm- brachio-cephalic.Looped fore arm- brachio-cephalic.
Straight upper arm -brachial –axillary.Straight upper arm -brachial –axillary.
Looped upper arm – axillary –axillary.Looped upper arm – axillary –axillary.
27. Complications of graft/ fistulaComplications of graft/ fistula
Infection.Infection.
Thrombosis.Thrombosis.
Aneurysm – in 3-5%.Aneurysm – in 3-5%.
Hand ischemia due to steal ,more (6%)inHand ischemia due to steal ,more (6%)in
brachiocephalic.brachiocephalic.
High output heart failure ( pt’s with severeHigh output heart failure ( pt’s with severe
heart failure should be excluded fromheart failure should be excluded from
having permanent access.)having permanent access.)
28. Tunneled cuffed catheter.Tunneled cuffed catheter.
Mostly from IJ.Mostly from IJ.
Can be used immediately.Can be used immediately.
Usually in pt’s with no access, or in pt’sUsually in pt’s with no access, or in pt’s
with failed access.with failed access.
Infection most common, severeInfection most common, severe
complication.complication.
Can get clotted too.Can get clotted too.
29. Preparation for PDPreparation for PD
Insert PD catheter 2-3 weeks prior toInsert PD catheter 2-3 weeks prior to
initiation of PD.initiation of PD.
Two type of PD.- CAPD,CCPD.Two type of PD.- CAPD,CCPD.
If pt choose CCPD, buy machine earlyIf pt choose CCPD, buy machine early
etc.etc.
30. Indications to start dialysis.Indications to start dialysis.
Pericarditis/ pericardial effusion, pleuritis.Pericarditis/ pericardial effusion, pleuritis.
Neurological dysfunction- encephalopathy,Neurological dysfunction- encephalopathy,
psychiatric disturbances, seizure etc.psychiatric disturbances, seizure etc.
Bleeding diathesis due to uremia.Bleeding diathesis due to uremia.
Fluid overload refractory to diuretics.Fluid overload refractory to diuretics.
Hyperkalemia refractory to treatment.Hyperkalemia refractory to treatment.
31. Indications.Indications.
Metabolic acidosis refractory to treatment.Metabolic acidosis refractory to treatment.
Hyper phosphatemia and hypocalcemiaHyper phosphatemia and hypocalcemia
refractory to treatment.refractory to treatment.
Deterioration in nutritional statusDeterioration in nutritional status
accompanied by nausea, vomiting.accompanied by nausea, vomiting.
Refractory anemia.Refractory anemia.
Otherwise unexplained decline inOtherwise unexplained decline in
functioning.functioning.
32. Hemodialysis.Hemodialysis.
Pts blood pumped through the dialysisPts blood pumped through the dialysis
machine to remove waste products andmachine to remove waste products and
excess water.excess water.
36. Diffusion.Diffusion.
Primary means of waste removal.Primary means of waste removal.
Depends on - concentration of solute,Depends on - concentration of solute,
membrane surface area, porosity andmembrane surface area, porosity and
thickness of membrane, size of solutethickness of membrane, size of solute
,flow rate of blood and dialysate,flow rate of blood and dialysate
Usual blood flow – 300-500mlUsual blood flow – 300-500ml
Usual dialysate flow – 500 -800 mlUsual dialysate flow – 500 -800 ml
37. Convective TransportConvective Transport
Most important for large solutes .Most important for large solutes .
By high rate of fluid transport, solutesBy high rate of fluid transport, solutes
dragged along with fluid.dragged along with fluid.
38. Fluid removal.Fluid removal.
By hydrostatic pressure gradientBy hydrostatic pressure gradient
generated by the dialysis machine.generated by the dialysis machine.
The TMP cause fluid to cross from highThe TMP cause fluid to cross from high
pressure blood compartment to lowpressure blood compartment to low
pressure dialysate compartment.pressure dialysate compartment.
40. Difft category of dialyzersDifft category of dialyzers
Type of membrane .Type of membrane .
Synthetic, cellulose, substitutedSynthetic, cellulose, substituted
cellulose etc.cellulose etc.
41. DialyzerDialyzer
Blood volume capacityBlood volume capacity
Usually 60-120 ml ( blood lines 100-Usually 60-120 ml ( blood lines 100-
150 ml)150 ml)
Surface area- Large surface area –betterSurface area- Large surface area –better
clearance.clearance.
42. DialyzerDialyzer
Ultrafiltration coefficient- Low KUf lowUltrafiltration coefficient- Low KUf low
permeability of water,so higher TMP topermeability of water,so higher TMP to
achieve UF and vice versa.achieve UF and vice versa.
But newer machines with controlled UF.But newer machines with controlled UF.
43. Dialyzer.Dialyzer.
Usually reported as small solute clearanceUsually reported as small solute clearance
and large solute clearance ,and at difftand large solute clearance ,and at difft
blood flows.blood flows.
Usually we use small clearance one forUsually we use small clearance one for
first dialysis, and large clearance one forfirst dialysis, and large clearance one for
large pts.large pts.
44. DialyzerDialyzer
Capacity to reuse.Capacity to reuse.
Sterilization – usually by ethylene oxide,Sterilization – usually by ethylene oxide,
but pts with allergies can use the onesbut pts with allergies can use the ones
with gamma irradiation, steamwith gamma irradiation, steam
autoclaving.autoclaving.
46. Dialysis tubings.Dialysis tubings.
Arterial line carry blood from pt to theArterial line carry blood from pt to the
dialyzer.dialyzer.
Venous line carry dialyzed blood back toVenous line carry dialyzed blood back to
patient.patient.
47. Dialysis machine.Dialysis machine.
Blood pump to move blood betweenBlood pump to move blood between
patient and dialyzer.patient and dialyzer.
A delivery system to transport dialysisA delivery system to transport dialysis
solution.solution.
Monitoring devices –pressure monitors,Monitoring devices –pressure monitors,
venous air trap and air detector,temptvenous air trap and air detector,tempt
sensor etcsensor etc
49. Hypotension.Hypotension.
Rapid fluid removalRapid fluid removal
Inaccurate dry weight.Inaccurate dry weight.
Cardiac- arrhythmias,pericardial effusion.Cardiac- arrhythmias,pericardial effusion.
Intake of antihypertenisives.Intake of antihypertenisives.
Low Hb, low sugar.Low Hb, low sugar.
Intake of meals immediately before or duringIntake of meals immediately before or during
dialysis.dialysis.
Low sodium dialysate.Low sodium dialysate.
Reaction to dialyzer membrane (not now)Reaction to dialyzer membrane (not now)
50. Treatment of hypotensionTreatment of hypotension
Place pt in trendelenburg position.Place pt in trendelenburg position.
Stop UF.Stop UF.
Reduce blood flow.Reduce blood flow.
Give saline.Give saline.
Further treatment based on etiology.Further treatment based on etiology.
51. Disequilibrium syndrome.Disequilibrium syndrome.
First described in 1962.First described in 1962.
Neurological symptoms of varyingNeurological symptoms of varying
severity.severity.
New pts just being started on dialysis atNew pts just being started on dialysis at
greater risk.greater risk.
Predisposing factors – increased BUN,Predisposing factors – increased BUN,
extremes of age, severe MA, preexistingextremes of age, severe MA, preexisting
seizure disorder.seizure disorder.