This document summarizes the history and developments in vascular access for hemodialysis. It discusses key milestones like the first hemodialysis in 1924, the Quinton-Scribner shunt in 1960, and the Brescia-Cimino fistula in 1966. It then compares arteriovenous fistulas, grafts, and catheters and their primary failure rates, infection risks, and longevity. The document outlines criteria for successful fistulas and grafts and factors that can lead to stenosis. It also discusses strategies to prevent stenosis and reduce catheter use, such as earlier patient referral and education on permanent access options.
Vascular access in Haemodialysis (2).pptxMithunAhmed5
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.
Buttonhole Cannulation Technique Power PointKelley Stanley
My BSN Capstone project done on buttonhole technique cannulation for arteriovenous fistulas. Study of the facts, the evidence, an intervention plan, evaluation plan, and a disemmination plan for buttonhole technique implementation to an outpatient hemodialysis unit.
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"
Vascular access in Haemodialysis (2).pptxMithunAhmed5
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.
Buttonhole Cannulation Technique Power PointKelley Stanley
My BSN Capstone project done on buttonhole technique cannulation for arteriovenous fistulas. Study of the facts, the evidence, an intervention plan, evaluation plan, and a disemmination plan for buttonhole technique implementation to an outpatient hemodialysis unit.
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"
Future of RF Ablation: Continuous or Segmental?Vein Global
By: Alan M. Dietzek, MD, RVT, RPVI, FACS
Visit VeinGlobal at http://www.veinglobal.com/ for more presentations and videos on this topic, or for more information on venous disease news, education and research.
Endovascular and surgical treatment of pulmonary embolism 26.11.17Ivo Petrov
Interventional treatment (thrombus fragmentation and supraselective fibrinolysis) of high and intermediate risk patients with pulmonary embolism.
Protocols of intervention, results, clinical cases provided
Abstract del Dr. Hector Ferral acerca del manejo endovascular de la CCSVI en pacientes portadores de Esclerosis Múltiple.
El Dr. Ferral se licenció en Medicina en la ciudad de Mexico, Universidad Anahuac (1979-1985)
Residencia en Medicina Interna: Instituto nacional de Nutricion 1986-1988
Residencia en Radiologia: Instituto nacional de Nutrición: 1988-1991
Fellowship en Intervencionismo: Universidad de Minnesota, Minneapolis : 1991-1993
Attending, Profesor asociado: Lousiana State University, New Orleans: 1995-2000
Attending: Profesor Asociado: University of Texas, San Antonio: 2000-2003
Attending: Profesor de Radiologia: Jefe del Servicio de Intervencionismo, Rush University, Chicago: 2004-2011
Attending: North Shore University: Evanston, Chicago Dic. 2011 a la fecha
más información en www.cdyte.com
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
- 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
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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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
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.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
6. Burdens in vascular access
Ivan D. Maya et al: AJKD 2008 (University of Alabama at Birmingham)
>20% of dialysis patients hospitalizations:
access related
Adjusted mortality: 40 ~ 70% greater for
catheter > AV shunt
Fistula prevalence: USA < Europe/Japan
75% of US patients initiate dialysis with a
catheter
7. Choices in vascular access
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Feature Fistula Graft Catheter
Primary failure rate % 20 ~ 50 10 ~ 20 <5
Time to 1st use (W) 4 ~ 12 2~ 3
Immediate
Need to intervene VL Mod H
Qb Excel Excel Mod
Thrombosis rate VL Mod H
Infection rate VL Mod VH
Longevity ~ 5Y ~ 2Y <1Y
8. Vascular access monitoring
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
PE: absent thrill, abnormal bruit, distal
edema, pulsating swelling aneurysm (F) or
pseudo-aneurysm (G)
Dialysis abnormality: difficult puncture,
aspiration of clots, prolonged bleeding from
needle site
Unexplained decrease in Kt/V
9. Vascular access surveillance
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Static dialysis venous pressure (DVP): Ratio of
DVP to systolic BP > 0.5: inaccurate predictor
Access blood flow: < 600mL/min(G) or <400-500
mL/min(F)
A decrease in Qa > 33% from baseline WD paulson et al: KI 81:
132-142, 2010
Doppler ultrasound: peak systolic velocity (PSV)
ratio > 2/1
Dynamic DVP and recirculation: less useful
Flow and change in flow(Qa and DVP) early in a
dialysis session by monthly flow surveillance:
inaccurate predictor
Sunanda et al: ALKD 52: 930-938, 2008 (N=176)
11. What is a successful fistula?
Allon et al, KI 62: 1109-24, 2002
Caliber large enough
Blood flow rate: access Qb > dialysis Qb by at least 100
ml/min to avoid vein collapse and re-circulation
mean dialysis Qb:
400 ml/M (USA) 300 ml/M(Europe)
200 ml/M(Japan)
Vein wall hypertrophy enough
Superficial enough
12. How is a successful fistula?
Allon et al, KI 62: 1109-24, 2002
Experience ( >12 procedures) of the surgeon
Site of fistula:
primary failure rate: 66% in forearm; 41% upper arm
Pre-operative sonographic vascular mapping:
age, DM, race, BMI
Hand exercise ?
Anti-platelet agents for 3 ~ 6 W
Kaufman et a, Semin dial 13: 40-46, 2000
13. Pre-operative vascular mapping
Allon et al, KI 62: 1109-24, 2002
Mapping with ultrasonography or venography
Criteria for placement of a shunt:
Minimum vein diameter: 0.25cm (AVF)
Minimum vein diameter: 0.40cm (AVG)
Minimum artery diameter: 0.20cm
Draining vein or central vein: lack of stenosis, sclerosis, or
thrombosis
A change of planned surgical procedure: 31%
Order of preference of vascular access to be
placed: Distal F > Proximal F > Proximal
transposed brachio-basilic F > Upper extremity
G> Thigh G> Unusual G (Necklace, chest wall)
14. Assessment of fistula maturation
Allon et al, KI 62: 1109-24, 2002
Post-operative sonographic measurement at
2M:
A: minimum vein diameter: >0.4cm
B: Access Qb> 500ml/min
A or B: 70%
A+B: 95%
neither: 33%
Time interval for dialysis use: 2 ~ 4M
15. AF fistulas: primary failure
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
High primary failure rate: 20 ~ 50%
Steal syndrome: 1 ~ 4%
Post-operative ultrasound to evaluate
maturation: 4 ~ 8 W after surgery
Ultrasound criteria for maturity:
Fistula diameter ≧ 0.4cm
Access flow ≧ 500mL/min
Distance from skin ≦ 0.5cm
16. Primary failure
Primary failure rate : early thrombosis or
failure to mature adequately (Juxta-anastomotic
stenosis/Large accessory veins/Excessively deep fistula )
Primary survival ( intervention-free): time from
access placement to initial intervention
Cumulative survival ( assisted ) : time from
access placement to permanent failure
Primary or cumulative survival at 1 year:
Oliver et al, KI 60: 1532-39, 2001
F > G: if primary failure
excluded F = G: if primary failure
included
17. Effect of clopidogrel on early
failure of AVFs for HD
Multicenter randomized controlled trial: N= 877
Clopidogrel: 300mg loading dose/75mg/D for 6 weeks
Inclusion criteria: upper extremity AVF/start HD within 6 M
Primary outcome: unassisted AVF patency at 6W
Secondary outcome: AVF dialysis suitability ( Use of AVF with 2
needles at Q-b ≧>300 ml/min for 8 sessions this began ≧ 120 days
after AVF creation)
Clopidogrel group: 37% lower risk of thrombosis(RR 0.46
p=0.018); Forearm(RR 0.53); upper arm(RR 0.89)
A surprising high primary failure in both
groups(61%/59%) →more than reducing early fistula
thrombosis in required Dember LM et al: JAMA 299:
2164-71, 2008
18. Anti-platelet agents for fistula
Study N Intervention/Duration Thrombosis (%)
Intervention Control
Andrassy et al 92 Aspirin 500mg/D x 4W 4 23
1974
Grontoft et al 36 Ticlopidine 250mg/D x 4W 11 47
1985
Grontoft et al 260 Ticlopidine 250mg/D x 4W 12 19
1998
Dember et al 877 Clopidegrel 300mg/D(L) 12 19
2008 75mg/D x 6W
DOPPS: N= 2815: aspirin to reduce significantly lower risk of final AVF failure
19. AV fistulas: late failure
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Late fistula failure by stenosis
60% at venous outlet
25% at arterial anastomosis
5% at central vessels
A large aneurysm,
rarely
Thrombosed fistula requires thrombectomy with
48 Hr
Primary patency rate after:
27 ~ 81% at 6M; 18 ~ 70% at 12M
21. AV grafts: graft failure
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Graft failure:
~ 80% thrombosis
~ 20% infection
A large pseudo-aneurysm,
rarely
Underlying stenosis in most thrombosed grafts:
~ 60% Venous
anastomosis 15% venous
outlet 10%
central veins
10% intragraft
5% arterial anastomosis
22. AV grafts: graft failure
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Intervention-free patency after elective
angioplasty: 70 ~ 85% at 3M; 20 ~ 40% at 12M
Intervention-free patency after thrombectomy:
33 ~ 63% at 3M; 10 ~ 39% at 6M
Stents may prolong patency in selected grafts:
elastic lesion
No clear advantage of bovine or cadaveric human
vein grafts over PTFE grafts
Polyurethane grafts (Vectra): can be cannulated
within 24 Hr
23. Vascular access stenosis: VNH
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
VNH: venous neo-intimal hyperplasia (SMC +
micro-F + microvessels)
Hemo-dynamic turbulence: an shear forces
Dialysis needle injury
Surgical vascular damage
PTFE
Uremia
Vascular damage from angioplasty
Expression of genes for cytokines
Local anti-proliferative drug delivery system:
Human study in progress
24. Preventive strategy for VNH
Strategy Mechanism of action Used in AVF
model
Mechanical design
Tapered graft and pre-cuffed graft geometry at anastomosis Y
Deculluarized xenograft elastic mismatch between graft/vessel Y
Biological reagents
Antisense ODNs inhibit DNA transcription N
Decoy(E2F) inhibit cell cycle progression Y
Gene transfer
VEGF promote endothelialization N
C-type natriuretic peptide inhibit proliferation via cGMP Y
Cell based therapy
Endothelial progenitor cells promote endothelialization of graft surface Y
Endothelial cell implant promote endothelial function Y
Small molecule drugs
Rapamycin inhibit protein translation Y
Paclitaxel inhibit mitosis by stabilizing microtubules Y
Dypiridamole inhibit phosphodiesterase activity Y
Imatinib inhibit PDGF receptor activity N
Irradiation induce DNA damage Y
ODN: antisense oligonucleotide Li Li Christi et al: KI 74 1247-61, 2008(University of Utah, USA)
28. Definition of CRB
Public Health Agency of Canada
Definite CRB diagnosis:
1> blood cultures from both
catheter lumen and a peripheral vein grow
the same organism
2>Colony count in catheter (C) ≧ 5
~ 10X colony count in vein (V)
or C ≧ V, 2 Hours earlier
False positive diagnosis: colonization if
from only one lumen
29. Diagnosis of CRB
Probable CRB diagnosis: ≧2 positive blood
culture ( blood culture/catheter tip:+/- or -/+
) + no evidence of a source of infection
other than catheter
Possible CRB diagnosis: negative or single
blood culture + no evidence of a source of
infection other than catheter , but fever
↓after catheter removal
Catheter culture( positive ): CRB 63%
30. Catheter-related bacteremia (CRB)
Similar rates but different average time
tunneled: 1/1000 catheter-days
non-tunneled: 1.54/1000 catheter-days
(p=0.98) Cuevas et al, JASN 1999
tunneled: 66.2 days
non-tunneled: 20.6 days
35% of patients within 3 months
48% of patients within 6 months
31. Risk factors for CRB
Femoral route
Duration of catheter use ( FVC: 5D; JVC: 3 ~ 4W)
Nasal/skin colonization with S.A.
Poor personal hygiene:
Povidone-iodine/Mupirocin over exit site of
catheter
Use of occlusive transparent dressing
DM
Immuno-suppression
Low albumin; high ferritin
33. Use rate of HD permanent
catheter < 10%
NKF-K/DOQI guidelines
34. CQI process to reduce catheter rates
in incident patients: a call to action
1. Discuss with referral sources about
criteria for referral: GFR≦ 30 ml/min
2. Refer patients and family to educational classes about treatment options
that should include PD, transplantation, etc: GFR ≦ 20 ml/min
3.Explicitly discuss with patients and family the need for a permanent
access at a GFR ≦ 20 ml/min
4.Track success of surgical outcomes by surgeon
Refer back to surgeon in 6-8 weeks if fistula is not maturing
5.Provide full disclosure of catheter related risks to patients and family
who refuse surgery for permanent access
6.Weaning of a medi-alert bracelet to protect one arm from veni-puncture
7.Classify requests to hospitals for access placement as urgent
RM Hakim et al: K 76: 1040-1048, 2009
35. Prophylaxis of CRB
Nasal mupirocin or 5-D course of oral
RIF/3M: S.A. carrier (50% in HD )who
have a previous catheter-related bacteremia
caused by S.A. and continue to need HD
catheter ongoing
by IDSA: Infectious Diseases Society of America
Prophylaxis of exit site colonization by mupirocin
or polysporin( Bacitracin+gramicidin+polymyxin
B) ointment at exit site
Lock therapy: GM/Citrate; Taurolidine/Citrate
36. Vancomycin plus Gentamicin in febrile HD
Life-threatening infection by β-lactam resistant
GPC or MRSA
GPC infection+ serious allergy to β-lactam
antibiotics
Antibiotic-associated colitis unresponsive to
Metronidazole or that is life-threatening
Prophylaxis of endocarditis in high-risk Patients:
Presence of central venous dialysis catheter
Alternative:Vancomycin plus 3rd cephalosporin
Rationale: mixed bacteremia 9.8 ~ 12.2%
37. Clinical approach to (tunneled) CRB
Ivan D. Maya et al: AJKD 2008(University of Alabama at Birmingham)
Vancomycin/Ceftazidime or GM
/Antibiotic lock
Negative culture Positive culture Positive culture
X 5D Fever resolve in 2-3D Fever persists
Catheter(-)
CNS GNB CPS Candida ECHO
Stop Metastatic
Catheter(+) Workup: bone
Keep lock Catheter(-) Catheter(-) Anti Duration
Anti: 3W Anti: 3W Fluconazole 6-8W
Guidewire Consider 2W
exchange ECHO/bone scan
38. Catheter removal ?
Non-cuffed Cuffed
Exit site infection Yes No
Tunnel infection Yes Yes
Catheter-related Yes S.A.: Yes
bacteremia(CRB) CNS: No ?
Enterococcus: Yes
39. Antibiotic dosing in HD patients
Systemic antibiotics
Vancomycin 20mg/Kg loading during last one hour ; 500 mg TIW
Gentamicin 1mg/Kg (maximum <100mg) TIW
Ceftazidime 1G TIW
Cefazolin 20mg/Kg TIW
Daptomycin 6mg/Kg TIW
Antibiotic lock: volume of solution(ml)
Vancomycin/Ceftazidime /Heparin: 1.0 /0.5/0.5
Vancomycin/Heparin: 1.0/1.0
Ceftazidime/Heparin: 1.0/1.0
Cefazolin/Heparin: 1.0/1.0
40. Tunnel infection
CDC guideline:
Erythema, tenderness, and induration in
tissues overlying the catheter + > 2cm from the exit site
Public Health Agency of Canada:
Definite:
1> Purulent discharge from tunnel
2> Erythema, tenderness, induration(2/3) at
tunnel with a positive culture from serous discharge
Probable: Erythema, tenderness,
induration(2/3) at tunnel with serous discharge, but
negative culture /no discharge, but lack of alternative
Possible:
Erythema, tenderness, induration(2/3) at tunnel , but
42. Exit site infection
CDC guideline:
Erythema, tenderness, and induration or purulence in
tissues overlying the catheter within 2cm from the exit
site
Public Health Agency of Canada:
Definite:
1> Purulent discharge at exit site
2> Erythema, tenderness, induration(2/3) at exit site
with a positive culture from serous discharge
Probable: Erythema, tenderness, induration(2/3) at
exit site with serous discharge, but negative culture /no
discharge, but lack of alternative
Possible: Erythema, tenderness,
induration(2/3) at exit site , but alternative cause cannot be
ruled out
44. AVG infection
30-day infection rate: 6%
Risk factors:
femoral route
poor hygiene
repetitive cannulations
perigraft hematoma formation
prolonged postdialysis bleeding from graft
repeat surgical revisions
HIV status(30%), DM, low albumin, high ferritin
transient bacteremia from distal site or CRB
45. AVG infection: S/S
Local pain, irritation, tenderness
Redness, warmth
Diffuse or local swelling
Skin breakdown
Serous or purulent discharge
Leukocytosis, fever
46. Sub-clavian vein obstruction
CVC placed for > 2 ~ 3 weeks:
40 ~ 50%
If infected:
75%
PTA+/- stent
Veno-venous bypass surgery
Access ligantion
47.
48. Antibiotic-heparin lock therapy
If Vancomycin: 2.0 mg/ml; Ceftazidime:
2.0 mg/ml plus heparin 5000IU/ml, each
concentration > 100µg/ml will persist > 21
days.
Cefazolin, Vancomycin: 10mg/ml;
Ceftazidime, Ciprofloxacin: 10mg/ml;
Gentamycin: 5mg/ml
No benefit to UK instillation as an adjunct
to antibiotic lock
49. Antibiotic lock: indications
Catheterretained during an episode of
catheter-related bacteremia
O’Grady et al, MMWR Morb Mortal Wkly Rep 51: 1-29,
2002
Historyof multiple catheter-related
bacterremias despite optimal aseptic
technique
Mernet et al, Clinical Infect Dis 32: 1249-72, 2001
51. Ideal lock solution for prophylaxis
Prophylaxis of bio-film formation → CRB↓
1> Cidal activity against a broad spectrum
of GPC/GNB/Fungi
2> Low likelihood of promoting
antibiotic resistant bacteria
3> Compatible with
catheter material and anticoagulant agent
4> Safe if inadvertently instilled
52. Potential antimicrobial lock solutions
Michael Allon: AJKD 44: 2004
1st 2nd 3rd 4th
殺菌 低阻 質合
安全
GM 40mg/dl /Citrate OK No OK OK
30% Citrate OK OK OK OK
70% Isopropyl alcohol OK OK OK No
Taurolidine OK OK OK No
53. CRB prevalence: per 1000 days
4.5
4
3.5
3
2.5 Heparin lock
2 Antimicrobial lock
1.5
1
0.5
0
Dogra Mcintyre Kim Nori Saxena
55. Antibiotic lock: barriers
All randomized trials: F-U for < 6M
Selection of antibiotic resistant infection if
longer use
Systemic toxicity from leaks into
circulation 10-fold lower concentration of
GM: 4 ~ 5 mg/mL
Economic
FDA not approved