national institute of kidney disease and urology (nikdu)
Dialysis access refers to the creation of an entrance way into the bloodstream so that the blood can be cleansed by the dialysis procedure. It is well established that dialysis cannot be provided without access.
The attainment and maintenance of a single reliable, long-lasting dialysis access with minimal complications continue to be challenging.
Achievement of such an access is associated with optimal patient clinical outcomes, superior quality of life, and minimal costs.
Although large efforts are spent for creating fistula as the primary access, use of Hemodialysis Vascular catheters are still the major access on the first Hemodialysis session and after 4 month whether we would like it or not.
"USRDS 2013"
Complication on avf play significant number of hospitalization & morbidity. Despite fistula first campaign are still beneficial for most patient, gathering knowlege to prevent complication are important.
By the end of the module, you will be able to:
Define Arterio Venous Fistula and Arterio Venous Graft
Identify Complications and Management
Familiarise and use the Pre Needling Cannulation Tool
Although large efforts are spent for creating fistula as the primary access, use of Hemodialysis Vascular catheters are still the major access on the first Hemodialysis session and after 4 month whether we would like it or not.
"USRDS 2013"
Complication on avf play significant number of hospitalization & morbidity. Despite fistula first campaign are still beneficial for most patient, gathering knowlege to prevent complication are important.
By the end of the module, you will be able to:
Define Arterio Venous Fistula and Arterio Venous Graft
Identify Complications and Management
Familiarise and use the Pre Needling Cannulation Tool
Endovenous Ablation of Varicose Veins. Treat painful varicose veins by Laser ...Saurabh Joshi
Varicose Veins is a very common medical condition affecting more than 30 % of the population. If left untreated, this can cause painful skin ulceration and a significant loss of quality of life.
Treatment is an office procedure, a small needle prick is all that is needed to position the Laser / RFA fiber within the vein and treat this disease once and for all.
Find out more and contact Dr.Joshi for details.
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.
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
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
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
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.
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
These lecture slides, by Dr Sidra Arshad, offer a quick overview of 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 leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
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. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
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
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.
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
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...
Vascular access in Haemodialysis (2).pptx
1.
2. • It is well established that dialysis cannot be provided without
access.
• The attainment and maintenance of a single reliable, long-
lasting dialysis access with minimal complications continue to
be challenging.
• Achievement of such an access is associated with optimal
patient clinical outcomes, superior quality of life, and minimal
costs.
3. • Dialysis access planning should start in CKD stage IV (glomerular filtration
rate [GFR] 15–30 mL/min), when education about CKD and modalities of
RRT should be discussed.
• The rate of decline of GFR over time is perhaps the best predictive guide to
timely referral and access placement.
• The components required for patient-focused access planning are as
follows:
1. Timely and appropriate referral;
2. Education (above);
3. Patient history and physical examination;
4. Supportive investigations.
4. Hemodialysis Access
Dialysis access refers to the creation of an
entrance way into the bloodstream so that the
blood can be cleansed by the dialysis procedure.
6. Types of Hemodialysis Access:
Among 4,07,811 U.S. end-stage
renal disease patients undergoing
hemodialysis :
64.2% are dialyzed through AVFs
18.5% through AVG
19.5% through hemodialysis
catheters
https://www.ajronline.org/doi/full/10.2214/AJR.15.14650
7. Change in type of vascular access during the first year of dialysis among ESRD patients
starting via hemodialysis in 2013 quarterly:
(a) type of vascular access in use (cross-sectional)
(b) longitudinal changes in vascular access use and other outcomes,
Data Source: Special
analyses, USRDS ESRD
Database. Data from
January 1, 2013 to May
30, 2016
CROWNWeb, Consolidated
Renal Operations in a Web-
enabled Network; ESRD, end-
stage renal disease; HD,
hemodialysis; PD, peritoneal
dialysis.
2017 Annual Data Report Volume 2, Chapt
8. Preparation for Hemodialysis Access:
Ideally before dialysis an venous access should be made:
• – Fistula should be placed 6 months prior to start dialysis
• – Graft should be placed 3-6 weeks prior to start dialysis
• – Venous catheter can be used instantly
10. What is a fistula or AVF?
An arteriovenous fistula is a connection between an artery and a vein
surgically created for hemodialysis by the vascular surgeon.
It is the preferred access of all the types of hemodialysis access and is
often referred to as the “gold standard.”
This access results in an extra pressure and extra blood to flow into the
vein, which helps to enlarge and strengthen the vein.
11. Preparation for Access
Before an access is made, patient is evaluated by a vascular surgeon
for
– vein mapping with an doppler ultrasound
– Vessel with a 2-2.5 mm and above diameter are acceptable for
fistula.
– US also help to determine course of the veins
– Blood lab tests for anesthetic and surgical fitness
12. Main Features Addressed by Duplex Ultrasound Vascular
Examination
Arterial System
• Artery size from the axilla to hand including the palmer arch
• Dual arteries in upper arm, i.e., high bifurcation
• Degree of arterial wall calcification
• Arterial stenotic lesions
• Blood flow at defined segments
Venous System
• Detailed venous anatomy in arm and leg as needed
• Vein size mapping from wrist to axilla
• Vein patency and presence or lack of stenosis
• Patency and flow pattern of subclavian vein
• Presence of diving venous branch at antecubital fossa
13. What is an arteriovenous fistula?
An AV fistula allows a higher rate of blood to flow
back and forth from the vein to a dialysis machine.
Untreated veins cannot withstand repeated needle
insertions, because they would collapse under
strong suction.
14.
15. Hemodialysis Access
• There are only about ten sites
in the body where an AV fistula
or graft can be made.
They are commonly located in
the
• – Arm (non-dominate forearm
or upper arm)
• – Leg
• – Neck
17. Different fistula: Radiocephallic
End to side anastomosis of radial artery and
forearm cephalic vein, Brescia- Cimino fistula
(proximal forearm).
Original fistula created by Dr. James Cimino in
1966.
Technically simple
Distal patency rates at one year are
approximately 50% to 80%.
The use of this distal access site preserves
more proximal vessels for subsequent attempts
at creating a fistula.
Ref: Types of Arteriovenous Fistulas Michael Segal; Erion Qaja. Last Update: March 16, 2019.
18. Proximal forearm AVF:
• Anastomosis between
proximal radial artery and
median antecubital vein
24. Maturation of the fistula:
Rule of 6s includes:
– The flow should be greater than 600 mL per minute
– Greater than 6 mm diameter
– Less than 6 mm below the skin
– At least 6 cm of the vein for cannulation
– expected maturation at 6 weeks
_
Ref: Types of Arteriovenous Fistulas Michael Segal; Erion Qaja. Last Update: March 16, 2019.
27. Assessment of AV Access by Physical Examination
• Pulse:
• Thrill:
• Arm elevation: to assess the outflow tract(if fails to collapse-
indicates -the downstream stenosis)
• Pulse augmentation: to evaluate the inflow segment(if pulse does
not augment –indicates accessory outflow pathway)
32. AV Fistula: Advice to the patients
Listen – Check for Bruit
Feel – Check for “thrill.”
Ask the patient –
– not to squeeze an access arm with elastic, a
watch, or by carrying something across it.
– To visit whenever there is chills or a fever.
33. Caring for Your AV Fistula
• Daily care of AV fistula is essential for it’s proper functioning
• Look – Check for
– signs of infection, such as
• – swelling,
• – redness,
• – warmth and
• – drainage, as well as
• – bleeding, peeling of the skin over the access or bulging areas.
34. NKF Recommended AVF cannulation Policy
Clinical exam by an experienced nurse has been able to predict AVF
maturity 80% of the time.
Fistula First Initiative advises 3 level of Cannulation competence
(CCHT, PCT III)
Only an expert cannulator is authorized to cannulate a new AVF.
35. Advantages of AVFs
The gold standard for vascular access because –
– it provides adequate blood flow,
– lasts a long time, usually 20 plus years
– has a lower complication rate than other types of access.
It is done as minor outpatient surgery
Usually take 6 to 12 weeks to develop
Fewer infections & thrombus than grafts and catheters
Pt can take Bath
36. Disadvantages of AVFs
May require another temporary type of access during the
healing and maturation phase
Maturation may be delayed, or it may fail to mature
Visible as a bulge under the skin
Not always possible for all patients
Needles are required to access the AV fistula for
hemodialysis
37. “ Fistula First, Catheter Last”
Goal
Increase AVF rate in appropriate HD patients to 60% by
2009
Decease long term(>90days) catheter rate to <10%
AVF is most cost effective, lasts longest, needs less
intervention and has lowest complication.
38. K/DOQI recommendation
Care under a Nephrologist.
Dialysis education at CKD 4( GFR <30).
Avoid phlebotomy/BP check in the non-dominant arm once CKD 4.
Fistula placement 6-12 months before anticipated HD.
43. Primary Failure
• HD fistula maintenance study (Prospective observational study) primary failure 40%
• AVF 47-60% VS. AVG. 19-40%
• BC 32%
• BB 21%
• Upper arm AVF 15%
• In one retrospective study on >16K patients , 27% of AVF group VS 17% of AVG group needed
another access, in one year.
44. AVF or Graft
5year patency for AVF and
AVG are similar
Higher patency for AVF after 2
years.
AVF less successful than AVG
in elderly female and with DM.
50. Does
fistula
Exercise
help?
Hemodialysis International, Oct 20,2015 by
Nestor Fontsere.
After one month by clinical exam 94.7% in the
exercise group VS 80.6% ( p-0.009)in non-
exercise group had a more mature fistula.
After one month by Doppler, 81.6% in exercise
group versus 74.2% in non-exercise group (p-
0.459) had a more mature fistula.
54. Catheter
Once a catheter is placed, needle insertion is not necessary.
Though Catheters are not ideal for permanent access, but they
are useful to start hemodialysis immediately & will work for
several weeks or months while fistula / graft matures.
Catheterization should be carried out in operating theatre or
high-dependency care areas, always using a fully aseptic
technique.
55. Catheter
Dialysis catheters are
artificial indwelling
transcutaneous
conduits that
are used to access the
venous space for renal
replacement therapy
(RRT).
Ref: http://meditechdevices.com/duraflow-acute-hemodialysis-catheter/
69. Disadvantage of
Catheter
Highest infection rate
Direct line to the heart contributes to more serious life
threatening infections
Clots more frequently
Often difficult to obtain sufficient blood flow to allow for
effective removal of waste materials through dialysis
Bathing and swimming are not recommended due to infection
risks
70.
71.
72.
73. Complication during jugular /
subclavian catheterization:
• Common :
Minor hematoma formation at
insertion site
Local infection
Arterial (carotid, subclavian,
vertebral) puncture
Arrhythmias,
74. Complication during jugular /
subclavian catheterization:
• Rare Complications:
Major hematoma compressing
airway
Major trauma to large vessels
with hemorrhage
Cardiac perforation with
tamponade
Pneumothorax or hemothorax
(diagnosis via chest radiograph)
Thoracic duct injury, usually associated with
left subclavian
or internal jugular approach (diagnosis
established by the
presence of chyle in pleural fluid)
Sepsis
Venous air embolism
Nerve injury
Venous thrombosis and pulmonary emboli
76. EQUIPMENTS :
• Other instruments:
• Sterile mask, gloves, and
gown
• Sterile drapes
• Monitors (ECG, pulse ox
imeter & BP)
• Peripheral IV with infusion
• Suture material
• Scalpel / BP blade – 15 no
Sterile gauze
Syringes
Disinfectant (2% chlorhex idine, iodine
solution)
Gallipot
0.9% normal saline
Heparin
Needle holder
Sponge holding forceps
77. EQUIPMENTS :
• Seldinger needle :
designed for single wall
puncture
• – small in diameter,
• – thin walled,
• – short beveled
• – very sharp.
• – Hub clear
80. Procedure:
Obtain informed written consent
Choose the site for insertion
Position the patient
Put on your gloves and gown.
Clean and drape the site: The iodine solution should be applied vigorously to an area
of skin approximately 30cm in diameter, in a circular motion from centre to
periphery for at east 30 seconds. Do not use a forward and backward movement.
repeat this step three times using a new swab for each application
allow the antiseptic to air dry, do not wipe or blot
81. Procedure:
Draw 5 ml of lidocaine; raise a bleb on the skin with a 27-gauge
needle.
Infiltrate local anesthetic all around the site, working down
toward the vein. Pull back on the plunger before injecting each
time to ensure that you don’t inject into
the vein.
open the dialysis catheter Kit, Flush each port of the catheter
with saline or heparinized saline (1:10), and close off each line
82. Procedure:
The length of the catheter planned to be
inserted should be noted prior to insertion
and documented
Attach a syringe to the 18/19 G needle,
keeping the beveled surface along Numeric
marking on syringe.
Catheterization with tip at desired position
Dressing
85. Anatomical consideration
Rt Femoral vein catheterization:
Find the arterial pulse and enter
the skin 1 cm medial to this, at a
45° angle to the vertical and
heading parallel to the artery.
Advance slowly, aspirating all
the time, until you enter the vein
86. Anatomical
consideration
• Rt subclavian vein
Catheterization:
Pt positioning
Selection of puncture site
Puncture
Wire advancement with
angled tip toward the heart
95. The white tube of DEATH
• 9% bacteremia annually ($22-45K/episode)
• 30% complications/yr. ( malfunction )
• 51% annual mortality in patients who exclusively use CVC
• Increase MI, CHF, PVD, CVA
• Lower flow rate, poor Kt/V
• Poor quality of life
• Up to 40% central venous stenosis ( Subclavian 50%, IJ 10%), may preclude
future AVF.
98. Graft
AV graft is the second most common vascular access of
choice in hemodialysis patients
Arteriovenous graft is a surgically created anastomosis
between an artery and vein via prosthetic conduit. The
conduit can be straight or looped and placed
superficially under skin for easy cannulation
The graft becomes an artificial vein that can be used
repeatedly for needle placement and blood access during
hemodialysis
99. AV Graft
Location: Grafts can be placed in arm or leg but most are
placed in the forearm
Grafts can be used after 3-6 weeks of placement
Indications –
• – Small, weak or hypoplastic peripheral vein
• – obesity
• – severe arterial occlusive disease .
100. AV Graft material:
Biological
Synthetic – polytetrafluorethylene (PTFE) , Dacron, silicon, and
polyurethane.
Polytetrafluoroethylene (PTFE) grafts are preferred over
biological and other synthetic grafts due to low thrombosis risk,
longer patency, ease of implantation, and low risk of disintegration
with infection.
Ref: Comparative study of use of Diastat versus standard wall PTFE grafts in upper arm hemodialysis
access.Almonacid PJ, Pallares EC, Rodriguez AQ, Valdes JS, Rueda Orgaz JA, Polo JR Ann Vasc Surg. 2000
Nov; 14(6):659-62.
101. AV Graft material, newer options:
• The HeRO Graft
(Hemodialysis Reliable
Outflow) HeRO Graft is
the only fully
subcutaneous AV access
clinically proven to
maintain long-term
access for catheter-
dependent patients with
central venous stenosis.
Ref: Merit Medical dialysis devices
102. AV Graft material, newer options:
• TEVG (Tissue Engineered Vascular Graft)
:
• Built to tolerate hemodynamic loads, heal
and remodel in response to needle sticks,
resist infection, no post operative
maturation period.
• Currently the major draw back is cost
effectiveness.
The Tissue-Engineered Vascular Graft—Past, Present, and Future; Tissue Eng Part B Rev. 2016 Feb 1; 22(1): 68–100.
doi: 10.1089/ten.teb.2015.0100
103. Types of AVGs depending on
location:
• Straight
forearm
(radial
artery to
cephalic
vein)
108. ePTFE Graft
Thrombosis
Identified by flow, pressure, duplex scan
RCT failed to show usefulness of preemptive
angioplasty .
High frequency of early AVG restenosis after
angioplasty.
Stent grafts prevent AVG restenosis better than
balloon angioplasty, but do not prevent AVG
thrombosis.
109. Advantages of Graft
Implanted during minor outpatient surgery
Can be used within 3-4 weeks
Initial high blood flow rates
Less primary failure than AVFs
110. Disadvantages of Graft
Usually only lasts 3-5 years
More likely to get infected than AVF
More likely to have infection & blood clots than an AVF
Longer bleeding time than an AVF after dialysis needles
are removed
114. The Centers for Disease Control Core Interventions
for Dialysis Bloodstream Infection (BSI) Prevention
115.
116. Variations in clinical definitions of CRBSIs:CDC
• Clinical manifestations and at least one positive peripheral blood culture and no
other apparent source, with either positive semiquantitative (>15 CFU/catheter
segment) or quantitative (>10 CFU/catheter segment) culture, whereby the same
organism is isolated from the catheter segment and a peripheral blood sample.
Simultaneous quantitative cultures of blood samples with a ratio of ≥3 : 1 (catheter
vs. peripheral). A differential period of catheter culture vs. peripheral blood culture
positivity of at least 2 hours.
OR
• The isolation of the same organism from semiquantitative or quantitative culture
segment and from blood with accompanying symptoms of bacteremia and no other
apparent source of infection.
117. Variations in clinical definitions of CRBSIs:IDSA
• Bacteremia or fungemia in a patient with an intravascular catheter with at least one
positive blood culture and with clinical manifestations of infections and no apparent
source for the bacteremia except the catheter.
AND
• One of the following must be present:
i) A positive semiquantitative (>15 CFU/ catheter segment) or quantitative (>103
CFU/catheter segment) culture whereby the same organism is isolated from the
catheter segment and peripheral blood.
ii) Simultaneous quantitative blood culture with a >5 : 1 ratio catheter versus
peripheral.
iii) Differential time period of catheter culture versus peripheral blood culture.
118. Variations in clinical definitions of CRBSIs: KDOQI
• Definite: Same organism from a semiquantitative culture of the catheter
tip (>15 CFU/catheter segment) and from a blood culture in a symptomatic
patient with no other apparent source of infection.
• Probable: Defervescence of symptoms after antibiotic treatment with or
without removal of the catheter in the setting where blood culture
confirms an infection, but the catheter tip does not or vice versa in a
symptomatic patient with no other apparent source of infection.
• Possible: Defervescence of symptoms after antibiotic treatment or after
removal of catheter in the absence of laboratory confirmation of
bloodstream infection in a symptomatic patient with no other apparent
source of infection.
119.
120.
121.
122.
123.
124.
125.
126. Journal
Food and Drug Administration Task Force. Precautions
necessary with centralvenous catheters. FDA Drug
Bulletin, July 1989:15– 16.
Scott WL. Centralvenous catheters: an overview of Food
and Drug Administration activities. Surg OncolClin North
Am 1995; 4:377–392.
Oncology Nursing Society. Access Device Guidelines:
Recommendations for Nursing Practice and Education.
Pittsburgh, PA: Oncology Nursing Press, 1996.
NationalAssociation of Vascular Access Networks.
NAVAN Position Statement. J Vasc Access Devices
1998;3:8–10
Inference:
“the catheter tip should not be placed in or
allowed to migrate into the heart”
a catheter tip should not be positioned
within the right atrium.
the tip of a PICC should be positioned within
the lower third of the superior vena cava
(SVC), close to the junction of the SVC and
right atrium
127. Journal:
Infusion Nurses Society. Standards of
Practice. J Intrav Nurs 2000; 23(suppl):6S
NationalKidney Foundation. K/
DOQI Clinical Practice Guidelines for
Vascular Access. Am J Kidney Dis 2001;
37(suppl1):S137–S181.
Central Venous Catheter Tip Position: A
Continuing Controversy
J Vasc Interv Radiol 2003; 14:527–534
Inference:
“central catheters should have the distal tip dwelling in the vena
cava”
· for tunneled (cuffed) catheters - states that the tip should be
positioned at the SVC/right atrial junction or into the right
atrium to ensure optimal blood flow.
· For nontunneled hemodialysis catheters, position the catheter
tip at the SVC/atrial junction or in the SVC.
The majority of central venous catheters used for routine
applications should be positioned with the distal tip in the SVC.
However, to achieve optimal performance of a hemodialysis or
pheresis catheter, it may be necessary to position the tip within
the upper right atrium
130. Catheter exit site review:
CVCs should be reviewed for signs of infection at each
haemodialysis treatment or whenever accessed
The insertion site should be examined by the clinician
for erythema, exudate, tenderness, pain, redness,
swelling, suture integrity and catheter position
131. Hemodialysis
• Hemodialysis circulates blood through a machine
outside the body to remove toxins and excess fluid &
then pumps the cleansed blood back into the body.