SlideShare una empresa de Scribd logo
1 de 53
Catheter related
infections
Dr. Nadia Mohsen Abdu Ibrahim
Specialist of Nephrology
New Mansoura General Hospital
HD Catheter related
Complications
 Mchanical
(Dysfunction)
 Infectious
Dialysis catheter
related infections Local site
infection
Exit , insertion
site infection
Tunnel infection
CRBSI
non Cuffed, non Tunneled
Catheters (Temporary)
Short.
More ridgid.
< 3wks for IJ.
<5 days for femoral
Exit site= insertion
site
No tunnel
Cuffed Tunneled
Catheters
(Permanent)• Softer
• Sheath for insertion,
Dacron cuff.
• 1 year –Indefinite
• Exit site, insertion site,
tunnel
N.B Up until 6 weeks following
tunneled catheter placement
the insertion site and exit site
may be considered
contiguous; after healing has
completed they may be
considered distinct.
Agarwal, Anil K, Asif Arif. NephSAP.
Interventional Nephrology, ASN. 361-375.2009.
Magnitude of the problem
The risk of bacteremia in dialysis patients with
dialysis catheters has been estimated to be
approximately 10 times higher than the risk of
bacteremia in patients with AV fistulas
catheter-dependent hemodialysis patients have a
two- to threefold higher risk of infection-related
hospitalization and infection-related death, as
compared to patients undergoing dialysis via a
fistula or graft .
Host factors
• Chronic illness (DM)
• Immune deficiency
neutropenia
• Malnutrition
• Hypoalbuminemia
• Extremes of age
• Iron overload
• Previous BSI
Catheter factors
• Type (Nontunneled )
• location (Femoral )
• duration of catheterization
(Prolonged )
• Barrier Precautions during
insertion (Submaximal; “mask,
cap, sterile gloves, gown, large
drape”
• Skill of the catheter inserter
• Catheter- site care
• thrombosis (increased
manipulation of the catheter
• presence of septic foci
elsewhere .
Risk Factors
The deposition of biofilm (on external & internal
surface of vascular catheters) is thought to play
an important role in the colonization process.
produced by a combination of host factors (eg,
fibrinogen and fibrin) and microbial products
(eg, glycocalyx or "slime"), and can be present
24 hours following catheter insertion
From: Mermel L, Rhode Island Hospital
POTENTIAL ROUTES OF INFECTION
All sources of infection
are potential targets
for prevention
Routes of infection
colonization from the skin
 Skin of patient and hands of healthcare workers on insertion or
manipulation
 Migration from the skin along the outside of the catheter into the
bloodstream.
 skin commensals: Staphylococcus aureus and coagulase-negative
staphylococci, are often isolated from colonized catheters and
patients with CRBSIs
 The Dacron cuff in tunneled catheters with fibrosis, in time may
create a mechanical barrier to migration of bacteria from the skin
along the outside of the catheter.
intraluminal or hub contamination
secondary seeding from a bloodstream infection
 Hematogenous seeding can occur during a
bloodstream infection originating from another focus
of infection, often from a gastrointestinal site
 The secondary seeding of CVCs may result in a
relapse of the bloodstream infection due to the same
organism.
contamination of the infusate or additives, such
as a contaminated heparin flush (Rare, Epidemic)
Causative organisms
Organism
(1) Gram-positive cocci
Staph. aureus
coagulase negative staph
Meticillin-resistant Staphylococcus aureus
Enterococcus faecalis
(3) Gram-negative bacilli
Pseudomonas aeruginosa
Enterobacter cloacae
Escherichia coli
Acinetobacter species
Serratia marcesens
Klebsiella pneumonia
(3) Polymicrobial
(4) Candida species
40 to
80 %
Non-
staphylococcal
dialysis CRBSIs
Causative organisms
CRBIs
 Gram-positive organisms are responsible for most
dialysis catheter-related infections. Coagulase-
negative staphylococcal and S. aureus together
account for 40 to 80 % of cases in most studies .
 S. aureus infection is commonly associated with
significant morbidity and mortality , and usually
complicated by metastatic infections : infective
endocarditis, septic arthritis, septic emboli,
osteomyelitis, epidural abscess and severe sepsis,
have been reported.
Local site infections
Generally are due to the same organisms, commonly . S.
aureus and P. aeruginosa
CRBSI
diagnostic approach and
management
 clinical evaluation
 microbiologic confirmation
(cultures)
CRBSI ,, Def
CRBSI should be suspected in any dialysis patient
with a hemodialysis catheter and signs and/or
symptoms of a bloodstream infection, particularly
when there is NO clinical evidence for an alternate
source of infection
(eg, productive cough, dysuria, foot infection, diarrhea, or skin rash) and focused physical
examination (eg,lung auscultation or inspection of the feet).
(NKF K/DOQI, 2006)
National Kidney Foundation/ Kidney Disease Outcomes Quality Initiative. 2006 Updates Clinical Practice Guidelines and
Recommendations.
1. Clinical evaluation
fever, chills, hemodynamic instability, changes
in mental status, catheter dysfunction( (+ or -)
signs of local site infection, don’t reflect CRBSI)
2. Microbiological evaluation
(Bl. Culture )
 should be obtained before antibiotics are administered.
 Bl. Sample
 two : drawn from a peripheral vein & drawn from the
dialysis catheter or
 two drawn from separate peripheral sites.
or
 two separate samples from dialysis catheter (if blood
cannot be obtained from a peripheral vein) , drawn 10 to 15
minutes
N.B avoid withdraw sample during HD session : it is unlikely that there is a
meaningful difference between samples drawn from peripheral veins and
those drawn from catheters since systemic blood is circulating through the
dialysis system.
3. Empiric systemic Antibiotics
For Gram-positive coverage
 Vancomycin
( iv in a dose of 20 mg/kg, should be given as a loading
dose during the last 60 minutes of the dialysis session,
followed by 500 mg in the last 30 to 60 minutes of
subsequent dialysis sessions)
 Daptomycin (for patients with vancomycin allergy)
( iv at a dose of 9 mg/kg (for patients using high-
permeability dialyzers) or 7 mg/kg (for patients using
low-permeability dialyzers) during the last 30 minutes of
each dialysis session
For Gram-negative coverage
 Gentamicin ?? or Ceftazidime (iv 2 gm, should be
given after each hemodialysis session)
4. Bl. Culture and sensitivity results
positive blood cultures
 +ve culture of the same organism from both the catheter tip
and peripheral vein.
colony count from the catheter at least 5-fold greater than that obtained from the peripheral
vein if quantitative blood cultures are used. Alternatively, catheter cultures should become
positive at least 2 hours earlier than the simultaneously drawn peripheral blood cultures (ie,
differential time to positivity
 +ve culture of the two samples drawn from catheter lumen
at separate times (10 to 15 minutes) are positive.
Intraluminal catheter colonization
 if +ve catheter-drawn blood cultures & -ve peripheral blood
cultures
Heparin provides a suitable growth medium for microorganisms and a positive result
will likely indicate ‘lock’ colonisation as opposed to ‘catheter’ colonisation
5. Treatment Tailor
• Once the culture and sensitivity have been
identified, the antibiotic regimen should be
modified accordingly
Staphylococcus
Methicillin-resistant Staphylococcus
continue Vancomycin, Patients with vancomycin allergy can be
treated with daptomycin
Methicillin-sensitive staphylococcus
 Vancomycin should be substituted with cefazolin (a first-
generation cephalosporin) ( iv 20 mg/kg after each dialysis
session)
 for penicillin-allergic patients → Vancomycin is the preferred
N.B Cefazolin is preferred due in part to the observation that the
widespread use of vancomycin has been associated with an
increasing incidence of infections due to vancomycin-resistant
enterococci. In addition, cefazolin is as or more effective than
vancomycin for ttt of methicillin-sensitive staph. infections
Repeat culture (after 48 to 72 of therapy) → if
remain +ve → (prolonged S. aureus bacteremia)
 (TEE; echocardiograms) should be done to all
patients and to check for signs and symptoms of a
metastatic infection (e.g infective endocarditis)
Vancomycin-resistant
enterococcus
 treated with daptomycin
(6 mg/kg when it is infused following a dialysis session
in inpatients.,, at a dose of 7 mg/kg (for patients using
low-flux dialyzers) or 9 mg/kg (for patients using high-
flux dialyzers) during the last 30 minutes of each
dialysis session.
 This higher dose is required to compensate for
intra-dialytic Daptomycin removal (dialysable)
Gram-negative organisms
Aminoglycosides?? (risk of aminoglycoside
ototoxicity) and ceftazidime (third-generation
cephalosporins ) preferred for longer-term
treatment.
in resistance to ceftazidime, however ,
aminoglycosides or carbapenems may be alternate
choices.
Candidemia
 The isolation of candida requires catheter removal
and treatment with Amphotericin B & Azoles
( Fluconazole )
 Fluconazole has an excellent safety profile, oral 800
mg (12 mg/kg) loading dose, then 400 mg (6 mg/kg)
orally daily
6. Monitoring
Repeat blood cultures 48 to 96 hours after the
institution of treatment. If these repeat blood cultures
remain positive→
1) catheter removal
2) additional evaluation for a metastatic infection or
endocarditis
7. Duration of therapy
The optimal duration of antimicrobial therapy remains
uncertain.
A. uncomplicated catheter-related bacteremia: (all signs of
infection rapidly resolve and follow-up blood cultures after
three or more days of appropriate therapy are negative)
• if the infected catheter has been removed and replaced with a
new catheter or salvaged and treated with an antibiotic lock
solution → ttt continues for two to three weeks.
• due to S. aureus → ttt for four weeks
B. complicated catheter related bacteremia: (evidence of a
metastatic infection or when follow up blood cultures remain
positive, we advise at least six weeks of therapy.
Patients with osteomyelitis, we advise treatment for 6 to 8
weeks.
Algorithm for Suspected catheter related bacteremia (CRBSI)
8. Catheter management
As a general role
ESNT Vascular Access Guidelines
 All Dialysis patients with CRBSIs are
administered systemic antimicrobial therapy and
Immediate catheter removal followed by
placement of a temporary non-tunneled catheter
for short-term dialysis access.
 After –ve culture results new, tunneled dialysis
catheter can be inserted.
since the catheter is both the source of the infection
and the vascular access necessary for providing
ongoing dialysis →
 indication for catheter removal
 Catheter exchange over a guide wire, with
Antibiotic lock
 Catheter Salvage, with antibiotic lock
Salvage should be used only as a treatment of last resort,
associated with a 5-fold higher risk of treatment failure ,
up to 8-fold in cases with S. aureus CRBSI.
Catheter Removal
should be done immediately , in the following
circumstances
 Temporary non-cuffed dialysis with CRBSI
 Severe sepsis
 Hemodynamic instability
 Evidence of metastatic infection
 Accompanying exit-site or tunnel infection,(purulence)
 If fever and/or bacteremia persist 48 to 72 hours after
initiation of antibiotics to which the organism is
susceptible
 Difficult-to-cure pathogens, [s. aureus, pseudomonas,
candida and fungi, or multiply-resistant bacterial
pathogens]
9. Catheter tip culture
 Routine culturing of catheter tips is not
recommended
 considered for confirming pathogen & measuring the
effectiveness of interventions
Guidewire catheter exchange
is a reasonable option for patients whom immediate removal of
the cuffed catheter is not feasible
 Exclude indications for catheter removal
 the patient can be started on broad-spectrum iv antibiotics
without immediate catheter removal.
 If the fever resolves within 2 to 3 days (ie, by the next dialysis
session), the infected catheter can be exchanged over a
guidewire for a new catheter.
 It is not necessary to routinely confirm –ve culture results before
catheter exchange as long as the patient is asymptomatic (ie, no
fever or chills).
 Retrospective studies suggest that catheter exchange over a guidewire
is associated with a cure rate similar to that observed with catheter
removal while reducing the number of access procedures required.
Tanriover B, Carlton D, Saddekni S, et al. Bacteremia associated with tunneled dialysis catheters:
Comparison of two treatment strategies. Kidney Int. 2000; 57:2151–2155. [PubMed: 10792637]
Catheter colonization
Management :
• Repeat to confirm (blood cultures from a peripheral
vein)
• Exchange catheter over a guide wire is preferred
• Salvage & antibiotic lock therapy (without systemic
therapy) if removal is not feasible
• follow up blood cultures
Antibiotic lock (Antibiotic/ heparin
solution
 If the tunneled dialysis catheter is salvaged
 The goal is to sterilize the catheter lumens from bacteria
present in biofilms
 It is a mixture of an anticoagulant ( heparin ) and high
concentrations of an antibiotic in a small volume. prepared
immediately before being instilled into each catheter lumen
at the end of each dialysis session
 for the duration of (3 weeks)
 if fever or bacteremia persists despite this approach →
Infected catheters should be removed
 Vancomycin / ceftazidime / heparin : Vancomycin (1 mL of
5 mg/mL in normal saline solution) plus ceftazidime (0.5 mL
of 10 mg/mL in normal saline solution) plus heparin (0.5 mL
of 1,000 U/mL solution)
 Vancomycin / heparin : Vancomycin (1 mL of 5 mg/mL in
normal saline solution) plus heparin (1 mL of 1000 U/mL
solution)
 Ceftazidime / heparin: Ceftazidime (1 mL of 10 mg/mL in
normal saline solution) plus heparin (1 mL of 1000 U/mL
solution)
 Cefazolin / heparin : Cefazolin (1 mL of 10 mg/mL in normal
saline solution) plus heparin (1 mL of 1000 U/mL solution)
Ethanol Lock
 The biofilm can prevent antibiotics penetration to
the surface of the inner lumen of the catheter.
 Ethanol locks have been proven to be effective in
this setting (catheter salvage in CRBSIs)
 Preparation:
1. Draw up 3.5mL of alcohol 100% (ethanol) and 1.5mL sterile
water for injection in a 10mL syringe (makes a total of 5mL
of 70%)
2. The dwell time for an ethanol lock is four hours. The ethanol
lock should be repeated daily by clinicians for 4-5 days
3. The clinician should flush the CVC pre and post ethanol lock
with sodium chloride 0.9%. Post flushing of the line should
only occur after the alcohol volume has been withdrawn
from the CVC at the conclusion of the four hour dwell time.
Contraindications
 If the patient is unstable
 +ve exit site or tunnel infection
 If the patient is pregnant or breast feeding
 If the pathogen is a Stap. aureus, multi-resistant
organism , fungaemia (including candidaemia).
1. Exit site
2. Insretion site
3. Tunnel
Exit site infection
 Def: Infection confined to the erea of exit site with purulent
discharge, or erythema, tenderness, or indurations (within 2cm
of the skin at the exit site) [Agarwal, Anil K, Asif Arif. NephSAP. Interventional Nephrology, ASN.
361-375. 2009]
 site drainage cultures and blood cultures should be
obtained.
Management
 Uncomplicated exit site infections (without systemic
signs of infection, -ve blood cultures, no purulence) →
topical antibiotic agents based on swab culture results
(mupirocin 2% & and polysporin ointment for S. aureus
infection and ketoconazole or lotrimin ointment for
Candida infection), With antibiotic lock.
 Complicated exit site infections (that do not resolve
with these interventions and/or accompanied by
purulent drainage ) → systemic antibiotics for ≤7 days.
If failure of systemic antibiotics occurs → immediate
catheter removal
Insertion site infection
 Insertion site infection of tunneled catheters should
prompt catheter removal
(guidewire catheter exchange is not appropriate as it can lead
to bacteremia and septic emboli)
 Cultures (exudate, blood cultures )
 if bloodstream infection is excluded (-ve blood
cultures) → systemic antimicrobial therapy for ≤7
days is sufficient
Tunnel infection (pocket)
 Def: erythema, tenderness, and induration
overlying the subcutaneous tunnel tract (which
extends for ≥2 cm from the exit site). + or − signs
of exit site (NKF K/DOQI, 2006)
N.B neutropenic patients may complain of pain in the
absence of erythema or swelling .
 Managemet :
 catheter removal; (in some circumstances incision
and drainage may also be appropriate).
 +or – excision, drainage of the tunnel site
 systemic antibiotics administered for ≤7 days
 Educate healthcare workers and provide training for
the insertion and maintenance of catheters
 Maximal Barrier Precautions ( during Insertion and
handling)
 Patient education
 Skin Antisepsis (chlorhexidine is preferred)
 Catheter Site Dressing Regimens
 Antimicrobial Lock Solutions
 Bundles and Checklists
Central Line Insertion Checklist -Adults
Operator:________________________________________Date:_______________________
RN Assisting:____________________________________ Room/Location:______________
Safety Pause:
 Correct Patient  Correct Procedure
 Correct Site  Verbal agreement from all members of the team.
In order to eliminate central line associated blood stream infections, we will be following the
Central Line Insertion Procedure Checklist based on CDC Guidelines.
Prior to the Procedure:
1. Hand Hygiene done with Chlorhexidine Gluconate (CHG) 2% surgical hand scrub and water or waterless
alcohol based gel before patient contact and before donning sterile gloves.
YES
2. Cleanse Site with 2% CHG with sponge 1.5mL.
YES
3. Disinfect Site with a back and forth friction scrub, utilizing 2% CHG wand 10.5mL for 30 seconds and
allow to dry completely before catheter insertion.
YES
4. Maximum Barriers Did the operator wear:
YES Cap/Bouffant
YES Mask
YES Sterile Gown
YES Sterile Gloves
YES Patient draped with full body sterile sheet.
During the procedure:
5. YES Operator(s) maintained the sterile field.
6. YES Personnel assisting wore a cap, mask and donned gloves appropriately.
After the procedure:
6. Sterile dressing applied immediately by the operator.
YES
QUALITY IMPROVEMENT
THIS FORM IS NOT PART OF THE PATIENT'S PERMANENT RECORD.
Please return the form to your Nurse Manager. If a step has was not followed, please note and
the Nurse Manager will follow up with the physician.
 AVF first , Prepare your patient in
advance
 Pay attention To this
Thank you
Thank you

Más contenido relacionado

La actualidad más candente

3. central line associated blood stream infection
3. central line associated blood stream infection3. central line associated blood stream infection
3. central line associated blood stream infection
ChartwellPA
 
Guideline Update For The Management Of Intravenous Catheter Related Infections
Guideline Update For The Management Of Intravenous Catheter Related InfectionsGuideline Update For The Management Of Intravenous Catheter Related Infections
Guideline Update For The Management Of Intravenous Catheter Related Infections
nels1937
 

La actualidad más candente (20)

Catheter associated blood stream infections
Catheter associated blood stream infectionsCatheter associated blood stream infections
Catheter associated blood stream infections
 
3. central line associated blood stream infection
3. central line associated blood stream infection3. central line associated blood stream infection
3. central line associated blood stream infection
 
cath infection
cath infectioncath infection
cath infection
 
CATHETER RELATED BLOOD STREAM INFECTIONS
CATHETER RELATED BLOOD STREAM INFECTIONSCATHETER RELATED BLOOD STREAM INFECTIONS
CATHETER RELATED BLOOD STREAM INFECTIONS
 
Prevention of blood stream infection
Prevention of blood stream infectionPrevention of blood stream infection
Prevention of blood stream infection
 
Infection prevention-dialysis-settings
Infection prevention-dialysis-settingsInfection prevention-dialysis-settings
Infection prevention-dialysis-settings
 
Prevention of Central Line Associated Blood Stream Infection (CLABSI )[compa...
Prevention of Central Line Associated Blood Stream Infection  (CLABSI )[compa...Prevention of Central Line Associated Blood Stream Infection  (CLABSI )[compa...
Prevention of Central Line Associated Blood Stream Infection (CLABSI )[compa...
 
CLABSI/CRBSI PREVENTION BUNDLE CARE FOR NURSES
CLABSI/CRBSI PREVENTION BUNDLE CARE FOR NURSESCLABSI/CRBSI PREVENTION BUNDLE CARE FOR NURSES
CLABSI/CRBSI PREVENTION BUNDLE CARE FOR NURSES
 
Catheter Associated Urinary Tract Infection (CAUTI)
Catheter Associated Urinary Tract Infection (CAUTI)Catheter Associated Urinary Tract Infection (CAUTI)
Catheter Associated Urinary Tract Infection (CAUTI)
 
Catheter related _infections .. dr Osama Elshahat
Catheter related _infections .. dr Osama ElshahatCatheter related _infections .. dr Osama Elshahat
Catheter related _infections .. dr Osama Elshahat
 
Diagnosis and management of central line infections
Diagnosis and management of central line infectionsDiagnosis and management of central line infections
Diagnosis and management of central line infections
 
Guideline Update For The Management Of Intravenous Catheter Related Infections
Guideline Update For The Management Of Intravenous Catheter Related InfectionsGuideline Update For The Management Of Intravenous Catheter Related Infections
Guideline Update For The Management Of Intravenous Catheter Related Infections
 
CLABSI
CLABSICLABSI
CLABSI
 
Central Line Associated Blood Stream Infections( CLABSI)
Central Line Associated Blood Stream Infections( CLABSI)Central Line Associated Blood Stream Infections( CLABSI)
Central Line Associated Blood Stream Infections( CLABSI)
 
Vascular access
Vascular accessVascular access
Vascular access
 
CR-BSI
CR-BSICR-BSI
CR-BSI
 
Catheter associated uti
Catheter associated utiCatheter associated uti
Catheter associated uti
 
Tunneled Hemodialysis Catheter-Related Infections.pptx
Tunneled Hemodialysis Catheter-Related Infections.pptxTunneled Hemodialysis Catheter-Related Infections.pptx
Tunneled Hemodialysis Catheter-Related Infections.pptx
 
Infection control for_hemodialysis_facilities
Infection control for_hemodialysis_facilitiesInfection control for_hemodialysis_facilities
Infection control for_hemodialysis_facilities
 
Dr mohammed abdelgawad crbsi
Dr mohammed abdelgawad   crbsiDr mohammed abdelgawad   crbsi
Dr mohammed abdelgawad crbsi
 

Destacado

Preventing Catheter Associated Bloodstream Infection
Preventing Catheter Associated Bloodstream InfectionPreventing Catheter Associated Bloodstream Infection
Preventing Catheter Associated Bloodstream Infection
Stingray67
 
Hemodialysis Dr. Sanaa Kamal
Hemodialysis Dr. Sanaa KamalHemodialysis Dr. Sanaa Kamal
Hemodialysis Dr. Sanaa Kamal
subauday
 
IV Cannula Infection
IV Cannula InfectionIV Cannula Infection
IV Cannula Infection
AYM NAZIM
 
Infective endocarditis prophylaxis
Infective endocarditis prophylaxisInfective endocarditis prophylaxis
Infective endocarditis prophylaxis
drninadphade
 

Destacado (15)

Educational Series | Prevention of Central Venous Catheter-Related Bloodstrea...
Educational Series | Prevention of Central Venous Catheter-Related Bloodstrea...Educational Series | Prevention of Central Venous Catheter-Related Bloodstrea...
Educational Series | Prevention of Central Venous Catheter-Related Bloodstrea...
 
Preventing Catheter Associated Bloodstream Infection
Preventing Catheter Associated Bloodstream InfectionPreventing Catheter Associated Bloodstream Infection
Preventing Catheter Associated Bloodstream Infection
 
Infection control guidelines for Prevention of Peripheral Venous Catheter (PV...
Infection control guidelines for Prevention of Peripheral Venous Catheter (PV...Infection control guidelines for Prevention of Peripheral Venous Catheter (PV...
Infection control guidelines for Prevention of Peripheral Venous Catheter (PV...
 
Contamination and antimicrobial prophylaxis in Peritoneal Dialysis
Contamination and antimicrobial prophylaxis in Peritoneal DialysisContamination and antimicrobial prophylaxis in Peritoneal Dialysis
Contamination and antimicrobial prophylaxis in Peritoneal Dialysis
 
CLABSI Prevention
CLABSI PreventionCLABSI Prevention
CLABSI Prevention
 
Temporary vascular access for hemodialysis
Temporary vascular access for hemodialysisTemporary vascular access for hemodialysis
Temporary vascular access for hemodialysis
 
Hemodialysis Dr. Sanaa Kamal
Hemodialysis Dr. Sanaa KamalHemodialysis Dr. Sanaa Kamal
Hemodialysis Dr. Sanaa Kamal
 
IV Cannula Infection
IV Cannula InfectionIV Cannula Infection
IV Cannula Infection
 
Atlas of dialysis vascular access
Atlas of dialysis vascular accessAtlas of dialysis vascular access
Atlas of dialysis vascular access
 
Intravenous catheter
Intravenous catheterIntravenous catheter
Intravenous catheter
 
ANTISEPTIC
ANTISEPTICANTISEPTIC
ANTISEPTIC
 
Intracatheters
IntracathetersIntracatheters
Intracatheters
 
Cannula And Infection
Cannula And InfectionCannula And Infection
Cannula And Infection
 
Infective endocarditis prophylaxis
Infective endocarditis prophylaxisInfective endocarditis prophylaxis
Infective endocarditis prophylaxis
 
Central line associated bloodstream infections
Central line associated bloodstream infectionsCentral line associated bloodstream infections
Central line associated bloodstream infections
 

Similar a Catheter related infections- DR Nadia Mohsen

MANAGEMENT OF INFECTIONS IN
MANAGEMENT OF INFECTIONS INMANAGEMENT OF INFECTIONS IN
MANAGEMENT OF INFECTIONS IN
NeurologyKota
 
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
AYM NAZIM
 
Role of medical thoracoscopy in treatment of parapneumonic
Role of medical thoracoscopy in treatment of parapneumonicRole of medical thoracoscopy in treatment of parapneumonic
Role of medical thoracoscopy in treatment of parapneumonic
Mohamed M.Kamel MBBCh, MSc, MD
 

Similar a Catheter related infections- DR Nadia Mohsen (20)

Catheter
CatheterCatheter
Catheter
 
Eman anan
Eman ananEman anan
Eman anan
 
crbsi2.ppt
crbsi2.pptcrbsi2.ppt
crbsi2.ppt
 
MANAGEMENT OF INFECTIONS IN
MANAGEMENT OF INFECTIONS INMANAGEMENT OF INFECTIONS IN
MANAGEMENT OF INFECTIONS IN
 
Catheter Related Blood Stream Infection (CRBSI) - (Diagnosis & Management Ste...
Catheter Related Blood Stream Infection (CRBSI) - (Diagnosis & Management Ste...Catheter Related Blood Stream Infection (CRBSI) - (Diagnosis & Management Ste...
Catheter Related Blood Stream Infection (CRBSI) - (Diagnosis & Management Ste...
 
catheterrelatedinfectionsatmeda-final1-171127225448.pdf
catheterrelatedinfectionsatmeda-final1-171127225448.pdfcatheterrelatedinfectionsatmeda-final1-171127225448.pdf
catheterrelatedinfectionsatmeda-final1-171127225448.pdf
 
crbsi 1.pptx
crbsi 1.pptxcrbsi 1.pptx
crbsi 1.pptx
 
Gram positive sepsis
Gram positive sepsisGram positive sepsis
Gram positive sepsis
 
Diagnosis of ventilator associated pneumonia
Diagnosis of ventilator associated pneumoniaDiagnosis of ventilator associated pneumonia
Diagnosis of ventilator associated pneumonia
 
CLABSI.pptx
CLABSI.pptxCLABSI.pptx
CLABSI.pptx
 
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
Guidelineupdateforthemanagementofintravenouscatheterrelated 12639283169308-ph...
 
Hydatid cyst disaese
Hydatid cyst disaeseHydatid cyst disaese
Hydatid cyst disaese
 
Hickman Catheter- An overview. Details about Hickman, insertion, care, mainte...
Hickman Catheter- An overview. Details about Hickman, insertion, care, mainte...Hickman Catheter- An overview. Details about Hickman, insertion, care, mainte...
Hickman Catheter- An overview. Details about Hickman, insertion, care, mainte...
 
Ventilator associated pneumonia
Ventilator associated pneumoniaVentilator associated pneumonia
Ventilator associated pneumonia
 
Neutropenic sepsis.pptx
Neutropenic sepsis.pptxNeutropenic sepsis.pptx
Neutropenic sepsis.pptx
 
hospital acquired infection HAI
hospital acquired infection HAIhospital acquired infection HAI
hospital acquired infection HAI
 
CIED POCKET INFECTION.pptx
CIED POCKET INFECTION.pptxCIED POCKET INFECTION.pptx
CIED POCKET INFECTION.pptx
 
Sidcrbsi
SidcrbsiSidcrbsi
Sidcrbsi
 
Role of medical thoracoscopy in treatment of parapneumonic
Role of medical thoracoscopy in treatment of parapneumonicRole of medical thoracoscopy in treatment of parapneumonic
Role of medical thoracoscopy in treatment of parapneumonic
 
Disseminated fungal infections 2015
Disseminated fungal infections  2015Disseminated fungal infections  2015
Disseminated fungal infections 2015
 

Más de FarragBahbah

Modified therapeutic plasma-exchange
Modified therapeutic plasma-exchangeModified therapeutic plasma-exchange
Modified therapeutic plasma-exchange
FarragBahbah
 
Hussein drug therapy in aki 3 osama alshahat 2 pptx
Hussein drug therapy in aki 3 osama alshahat 2 pptxHussein drug therapy in aki 3 osama alshahat 2 pptx
Hussein drug therapy in aki 3 osama alshahat 2 pptx
FarragBahbah
 
Pres ln master class 21 oct 2019
Pres ln master class 21 oct 2019 Pres ln master class 21 oct 2019
Pres ln master class 21 oct 2019
FarragBahbah
 
Fluid management in pd patient
Fluid management in pd patientFluid management in pd patient
Fluid management in pd patient
FarragBahbah
 
Membranous nephropathy 22 october 2019, prof. hussein sheashaa
Membranous nephropathy 22 october 2019, prof. hussein sheashaaMembranous nephropathy 22 october 2019, prof. hussein sheashaa
Membranous nephropathy 22 october 2019, prof. hussein sheashaa
FarragBahbah
 
Toxicology emergency dr.farrag megahed
Toxicology  emergency dr.farrag megahedToxicology  emergency dr.farrag megahed
Toxicology emergency dr.farrag megahed
FarragBahbah
 
Interstial nephr mohamed abdallah
Interstial nephr mohamed abdallahInterstial nephr mohamed abdallah
Interstial nephr mohamed abdallah
FarragBahbah
 
Fasting ramadan nephrology prospective prof. osama el shahate
Fasting ramadan nephrology prospective prof. osama el shahateFasting ramadan nephrology prospective prof. osama el shahate
Fasting ramadan nephrology prospective prof. osama el shahate
FarragBahbah
 
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
FarragBahbah
 
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحاتالدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
FarragBahbah
 
Parathyroidectomy alshimaa
Parathyroidectomy  alshimaaParathyroidectomy  alshimaa
Parathyroidectomy alshimaa
FarragBahbah
 

Más de FarragBahbah (20)

Pd aki 2019
Pd aki 2019Pd aki 2019
Pd aki 2019
 
Modified therapeutic plasma-exchange
Modified therapeutic plasma-exchangeModified therapeutic plasma-exchange
Modified therapeutic plasma-exchange
 
Hussein drug therapy in aki 3 osama alshahat 2 pptx
Hussein drug therapy in aki 3 osama alshahat 2 pptxHussein drug therapy in aki 3 osama alshahat 2 pptx
Hussein drug therapy in aki 3 osama alshahat 2 pptx
 
Pres ln master class 21 oct 2019
Pres ln master class 21 oct 2019 Pres ln master class 21 oct 2019
Pres ln master class 21 oct 2019
 
Fluid management in pd patient
Fluid management in pd patientFluid management in pd patient
Fluid management in pd patient
 
Membranous nephropathy 22 october 2019, prof. hussein sheashaa
Membranous nephropathy 22 october 2019, prof. hussein sheashaaMembranous nephropathy 22 october 2019, prof. hussein sheashaa
Membranous nephropathy 22 october 2019, prof. hussein sheashaa
 
Dialysis in aki
Dialysis in akiDialysis in aki
Dialysis in aki
 
Dkd master class
Dkd master class Dkd master class
Dkd master class
 
Gn master class
Gn master classGn master class
Gn master class
 
Ibrahim
IbrahimIbrahim
Ibrahim
 
Aya elsaeid 1
Aya elsaeid 1Aya elsaeid 1
Aya elsaeid 1
 
Toxicology emergency dr.farrag megahed
Toxicology  emergency dr.farrag megahedToxicology  emergency dr.farrag megahed
Toxicology emergency dr.farrag megahed
 
Interstial nephr mohamed abdallah
Interstial nephr mohamed abdallahInterstial nephr mohamed abdallah
Interstial nephr mohamed abdallah
 
Fasting ramadan nephrology prospective prof. osama el shahate
Fasting ramadan nephrology prospective prof. osama el shahateFasting ramadan nephrology prospective prof. osama el shahate
Fasting ramadan nephrology prospective prof. osama el shahate
 
Ramadan fasting &amp; kidney disease may 2019
Ramadan fasting &amp; kidney disease may 2019Ramadan fasting &amp; kidney disease may 2019
Ramadan fasting &amp; kidney disease may 2019
 
Diet managment in ramadan dr doaa hamed
Diet managment in ramadan  dr doaa hamedDiet managment in ramadan  dr doaa hamed
Diet managment in ramadan dr doaa hamed
 
Vascular access 2019
Vascular access 2019Vascular access 2019
Vascular access 2019
 
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
الرعاية-الغذائية-لمرضي-الكلي-كوبري-القبة-يناير-2019
 
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحاتالدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
الدليل الإرشادي لمرضي القصور الكلوي د.دعاء حامد .د.اسامه الشحات
 
Parathyroidectomy alshimaa
Parathyroidectomy  alshimaaParathyroidectomy  alshimaa
Parathyroidectomy alshimaa
 

Último

The basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptxThe basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptx
heathfieldcps1
 
Spellings Wk 3 English CAPS CARES Please Practise
Spellings Wk 3 English CAPS CARES Please PractiseSpellings Wk 3 English CAPS CARES Please Practise
Spellings Wk 3 English CAPS CARES Please Practise
AnaAcapella
 

Último (20)

The basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptxThe basics of sentences session 3pptx.pptx
The basics of sentences session 3pptx.pptx
 
How to Give a Domain for a Field in Odoo 17
How to Give a Domain for a Field in Odoo 17How to Give a Domain for a Field in Odoo 17
How to Give a Domain for a Field in Odoo 17
 
Micro-Scholarship, What it is, How can it help me.pdf
Micro-Scholarship, What it is, How can it help me.pdfMicro-Scholarship, What it is, How can it help me.pdf
Micro-Scholarship, What it is, How can it help me.pdf
 
Spellings Wk 3 English CAPS CARES Please Practise
Spellings Wk 3 English CAPS CARES Please PractiseSpellings Wk 3 English CAPS CARES Please Practise
Spellings Wk 3 English CAPS CARES Please Practise
 
Mehran University Newsletter Vol-X, Issue-I, 2024
Mehran University Newsletter Vol-X, Issue-I, 2024Mehran University Newsletter Vol-X, Issue-I, 2024
Mehran University Newsletter Vol-X, Issue-I, 2024
 
Holdier Curriculum Vitae (April 2024).pdf
Holdier Curriculum Vitae (April 2024).pdfHoldier Curriculum Vitae (April 2024).pdf
Holdier Curriculum Vitae (April 2024).pdf
 
Making communications land - Are they received and understood as intended? we...
Making communications land - Are they received and understood as intended? we...Making communications land - Are they received and understood as intended? we...
Making communications land - Are they received and understood as intended? we...
 
Application orientated numerical on hev.ppt
Application orientated numerical on hev.pptApplication orientated numerical on hev.ppt
Application orientated numerical on hev.ppt
 
Single or Multiple melodic lines structure
Single or Multiple melodic lines structureSingle or Multiple melodic lines structure
Single or Multiple melodic lines structure
 
Unit-V; Pricing (Pharma Marketing Management).pptx
Unit-V; Pricing (Pharma Marketing Management).pptxUnit-V; Pricing (Pharma Marketing Management).pptx
Unit-V; Pricing (Pharma Marketing Management).pptx
 
HMCS Max Bernays Pre-Deployment Brief (May 2024).pptx
HMCS Max Bernays Pre-Deployment Brief (May 2024).pptxHMCS Max Bernays Pre-Deployment Brief (May 2024).pptx
HMCS Max Bernays Pre-Deployment Brief (May 2024).pptx
 
Towards a code of practice for AI in AT.pptx
Towards a code of practice for AI in AT.pptxTowards a code of practice for AI in AT.pptx
Towards a code of practice for AI in AT.pptx
 
Sociology 101 Demonstration of Learning Exhibit
Sociology 101 Demonstration of Learning ExhibitSociology 101 Demonstration of Learning Exhibit
Sociology 101 Demonstration of Learning Exhibit
 
How to setup Pycharm environment for Odoo 17.pptx
How to setup Pycharm environment for Odoo 17.pptxHow to setup Pycharm environment for Odoo 17.pptx
How to setup Pycharm environment for Odoo 17.pptx
 
Introduction to Nonprofit Accounting: The Basics
Introduction to Nonprofit Accounting: The BasicsIntroduction to Nonprofit Accounting: The Basics
Introduction to Nonprofit Accounting: The Basics
 
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
TỔNG ÔN TẬP THI VÀO LỚP 10 MÔN TIẾNG ANH NĂM HỌC 2023 - 2024 CÓ ĐÁP ÁN (NGỮ Â...
 
Spatium Project Simulation student brief
Spatium Project Simulation student briefSpatium Project Simulation student brief
Spatium Project Simulation student brief
 
How to Create and Manage Wizard in Odoo 17
How to Create and Manage Wizard in Odoo 17How to Create and Manage Wizard in Odoo 17
How to Create and Manage Wizard in Odoo 17
 
Key note speaker Neum_Admir Softic_ENG.pdf
Key note speaker Neum_Admir Softic_ENG.pdfKey note speaker Neum_Admir Softic_ENG.pdf
Key note speaker Neum_Admir Softic_ENG.pdf
 
ICT Role in 21st Century Education & its Challenges.pptx
ICT Role in 21st Century Education & its Challenges.pptxICT Role in 21st Century Education & its Challenges.pptx
ICT Role in 21st Century Education & its Challenges.pptx
 

Catheter related infections- DR Nadia Mohsen

  • 1. Catheter related infections Dr. Nadia Mohsen Abdu Ibrahim Specialist of Nephrology New Mansoura General Hospital
  • 2.
  • 3. HD Catheter related Complications  Mchanical (Dysfunction)  Infectious
  • 4. Dialysis catheter related infections Local site infection Exit , insertion site infection Tunnel infection CRBSI
  • 5. non Cuffed, non Tunneled Catheters (Temporary) Short. More ridgid. < 3wks for IJ. <5 days for femoral Exit site= insertion site No tunnel Cuffed Tunneled Catheters (Permanent)• Softer • Sheath for insertion, Dacron cuff. • 1 year –Indefinite • Exit site, insertion site, tunnel N.B Up until 6 weeks following tunneled catheter placement the insertion site and exit site may be considered contiguous; after healing has completed they may be considered distinct. Agarwal, Anil K, Asif Arif. NephSAP. Interventional Nephrology, ASN. 361-375.2009.
  • 6.
  • 7. Magnitude of the problem The risk of bacteremia in dialysis patients with dialysis catheters has been estimated to be approximately 10 times higher than the risk of bacteremia in patients with AV fistulas catheter-dependent hemodialysis patients have a two- to threefold higher risk of infection-related hospitalization and infection-related death, as compared to patients undergoing dialysis via a fistula or graft .
  • 8. Host factors • Chronic illness (DM) • Immune deficiency neutropenia • Malnutrition • Hypoalbuminemia • Extremes of age • Iron overload • Previous BSI Catheter factors • Type (Nontunneled ) • location (Femoral ) • duration of catheterization (Prolonged ) • Barrier Precautions during insertion (Submaximal; “mask, cap, sterile gloves, gown, large drape” • Skill of the catheter inserter • Catheter- site care • thrombosis (increased manipulation of the catheter • presence of septic foci elsewhere . Risk Factors
  • 9. The deposition of biofilm (on external & internal surface of vascular catheters) is thought to play an important role in the colonization process. produced by a combination of host factors (eg, fibrinogen and fibrin) and microbial products (eg, glycocalyx or "slime"), and can be present 24 hours following catheter insertion
  • 10. From: Mermel L, Rhode Island Hospital POTENTIAL ROUTES OF INFECTION All sources of infection are potential targets for prevention
  • 11. Routes of infection colonization from the skin  Skin of patient and hands of healthcare workers on insertion or manipulation  Migration from the skin along the outside of the catheter into the bloodstream.  skin commensals: Staphylococcus aureus and coagulase-negative staphylococci, are often isolated from colonized catheters and patients with CRBSIs  The Dacron cuff in tunneled catheters with fibrosis, in time may create a mechanical barrier to migration of bacteria from the skin along the outside of the catheter.
  • 12. intraluminal or hub contamination secondary seeding from a bloodstream infection  Hematogenous seeding can occur during a bloodstream infection originating from another focus of infection, often from a gastrointestinal site  The secondary seeding of CVCs may result in a relapse of the bloodstream infection due to the same organism. contamination of the infusate or additives, such as a contaminated heparin flush (Rare, Epidemic)
  • 13. Causative organisms Organism (1) Gram-positive cocci Staph. aureus coagulase negative staph Meticillin-resistant Staphylococcus aureus Enterococcus faecalis (3) Gram-negative bacilli Pseudomonas aeruginosa Enterobacter cloacae Escherichia coli Acinetobacter species Serratia marcesens Klebsiella pneumonia (3) Polymicrobial (4) Candida species 40 to 80 % Non- staphylococcal dialysis CRBSIs
  • 14. Causative organisms CRBIs  Gram-positive organisms are responsible for most dialysis catheter-related infections. Coagulase- negative staphylococcal and S. aureus together account for 40 to 80 % of cases in most studies .  S. aureus infection is commonly associated with significant morbidity and mortality , and usually complicated by metastatic infections : infective endocarditis, septic arthritis, septic emboli, osteomyelitis, epidural abscess and severe sepsis, have been reported. Local site infections Generally are due to the same organisms, commonly . S. aureus and P. aeruginosa
  • 15.
  • 16. CRBSI diagnostic approach and management  clinical evaluation  microbiologic confirmation (cultures)
  • 17. CRBSI ,, Def CRBSI should be suspected in any dialysis patient with a hemodialysis catheter and signs and/or symptoms of a bloodstream infection, particularly when there is NO clinical evidence for an alternate source of infection (eg, productive cough, dysuria, foot infection, diarrhea, or skin rash) and focused physical examination (eg,lung auscultation or inspection of the feet). (NKF K/DOQI, 2006) National Kidney Foundation/ Kidney Disease Outcomes Quality Initiative. 2006 Updates Clinical Practice Guidelines and Recommendations.
  • 18. 1. Clinical evaluation fever, chills, hemodynamic instability, changes in mental status, catheter dysfunction( (+ or -) signs of local site infection, don’t reflect CRBSI)
  • 19. 2. Microbiological evaluation (Bl. Culture )  should be obtained before antibiotics are administered.  Bl. Sample  two : drawn from a peripheral vein & drawn from the dialysis catheter or  two drawn from separate peripheral sites. or  two separate samples from dialysis catheter (if blood cannot be obtained from a peripheral vein) , drawn 10 to 15 minutes N.B avoid withdraw sample during HD session : it is unlikely that there is a meaningful difference between samples drawn from peripheral veins and those drawn from catheters since systemic blood is circulating through the dialysis system.
  • 20. 3. Empiric systemic Antibiotics For Gram-positive coverage  Vancomycin ( iv in a dose of 20 mg/kg, should be given as a loading dose during the last 60 minutes of the dialysis session, followed by 500 mg in the last 30 to 60 minutes of subsequent dialysis sessions)  Daptomycin (for patients with vancomycin allergy) ( iv at a dose of 9 mg/kg (for patients using high- permeability dialyzers) or 7 mg/kg (for patients using low-permeability dialyzers) during the last 30 minutes of each dialysis session For Gram-negative coverage  Gentamicin ?? or Ceftazidime (iv 2 gm, should be given after each hemodialysis session)
  • 21. 4. Bl. Culture and sensitivity results positive blood cultures  +ve culture of the same organism from both the catheter tip and peripheral vein. colony count from the catheter at least 5-fold greater than that obtained from the peripheral vein if quantitative blood cultures are used. Alternatively, catheter cultures should become positive at least 2 hours earlier than the simultaneously drawn peripheral blood cultures (ie, differential time to positivity  +ve culture of the two samples drawn from catheter lumen at separate times (10 to 15 minutes) are positive. Intraluminal catheter colonization  if +ve catheter-drawn blood cultures & -ve peripheral blood cultures Heparin provides a suitable growth medium for microorganisms and a positive result will likely indicate ‘lock’ colonisation as opposed to ‘catheter’ colonisation
  • 22. 5. Treatment Tailor • Once the culture and sensitivity have been identified, the antibiotic regimen should be modified accordingly
  • 23. Staphylococcus Methicillin-resistant Staphylococcus continue Vancomycin, Patients with vancomycin allergy can be treated with daptomycin Methicillin-sensitive staphylococcus  Vancomycin should be substituted with cefazolin (a first- generation cephalosporin) ( iv 20 mg/kg after each dialysis session)  for penicillin-allergic patients → Vancomycin is the preferred N.B Cefazolin is preferred due in part to the observation that the widespread use of vancomycin has been associated with an increasing incidence of infections due to vancomycin-resistant enterococci. In addition, cefazolin is as or more effective than vancomycin for ttt of methicillin-sensitive staph. infections
  • 24. Repeat culture (after 48 to 72 of therapy) → if remain +ve → (prolonged S. aureus bacteremia)  (TEE; echocardiograms) should be done to all patients and to check for signs and symptoms of a metastatic infection (e.g infective endocarditis)
  • 25. Vancomycin-resistant enterococcus  treated with daptomycin (6 mg/kg when it is infused following a dialysis session in inpatients.,, at a dose of 7 mg/kg (for patients using low-flux dialyzers) or 9 mg/kg (for patients using high- flux dialyzers) during the last 30 minutes of each dialysis session.  This higher dose is required to compensate for intra-dialytic Daptomycin removal (dialysable)
  • 26. Gram-negative organisms Aminoglycosides?? (risk of aminoglycoside ototoxicity) and ceftazidime (third-generation cephalosporins ) preferred for longer-term treatment. in resistance to ceftazidime, however , aminoglycosides or carbapenems may be alternate choices.
  • 27. Candidemia  The isolation of candida requires catheter removal and treatment with Amphotericin B & Azoles ( Fluconazole )  Fluconazole has an excellent safety profile, oral 800 mg (12 mg/kg) loading dose, then 400 mg (6 mg/kg) orally daily
  • 28. 6. Monitoring Repeat blood cultures 48 to 96 hours after the institution of treatment. If these repeat blood cultures remain positive→ 1) catheter removal 2) additional evaluation for a metastatic infection or endocarditis
  • 29. 7. Duration of therapy The optimal duration of antimicrobial therapy remains uncertain. A. uncomplicated catheter-related bacteremia: (all signs of infection rapidly resolve and follow-up blood cultures after three or more days of appropriate therapy are negative) • if the infected catheter has been removed and replaced with a new catheter or salvaged and treated with an antibiotic lock solution → ttt continues for two to three weeks. • due to S. aureus → ttt for four weeks B. complicated catheter related bacteremia: (evidence of a metastatic infection or when follow up blood cultures remain positive, we advise at least six weeks of therapy. Patients with osteomyelitis, we advise treatment for 6 to 8 weeks.
  • 30. Algorithm for Suspected catheter related bacteremia (CRBSI)
  • 31.
  • 32.
  • 33. 8. Catheter management As a general role ESNT Vascular Access Guidelines  All Dialysis patients with CRBSIs are administered systemic antimicrobial therapy and Immediate catheter removal followed by placement of a temporary non-tunneled catheter for short-term dialysis access.  After –ve culture results new, tunneled dialysis catheter can be inserted.
  • 34. since the catheter is both the source of the infection and the vascular access necessary for providing ongoing dialysis →  indication for catheter removal  Catheter exchange over a guide wire, with Antibiotic lock  Catheter Salvage, with antibiotic lock Salvage should be used only as a treatment of last resort, associated with a 5-fold higher risk of treatment failure , up to 8-fold in cases with S. aureus CRBSI.
  • 35. Catheter Removal should be done immediately , in the following circumstances  Temporary non-cuffed dialysis with CRBSI  Severe sepsis  Hemodynamic instability  Evidence of metastatic infection  Accompanying exit-site or tunnel infection,(purulence)  If fever and/or bacteremia persist 48 to 72 hours after initiation of antibiotics to which the organism is susceptible  Difficult-to-cure pathogens, [s. aureus, pseudomonas, candida and fungi, or multiply-resistant bacterial pathogens]
  • 36. 9. Catheter tip culture  Routine culturing of catheter tips is not recommended  considered for confirming pathogen & measuring the effectiveness of interventions
  • 37. Guidewire catheter exchange is a reasonable option for patients whom immediate removal of the cuffed catheter is not feasible  Exclude indications for catheter removal  the patient can be started on broad-spectrum iv antibiotics without immediate catheter removal.  If the fever resolves within 2 to 3 days (ie, by the next dialysis session), the infected catheter can be exchanged over a guidewire for a new catheter.  It is not necessary to routinely confirm –ve culture results before catheter exchange as long as the patient is asymptomatic (ie, no fever or chills).  Retrospective studies suggest that catheter exchange over a guidewire is associated with a cure rate similar to that observed with catheter removal while reducing the number of access procedures required. Tanriover B, Carlton D, Saddekni S, et al. Bacteremia associated with tunneled dialysis catheters: Comparison of two treatment strategies. Kidney Int. 2000; 57:2151–2155. [PubMed: 10792637]
  • 38. Catheter colonization Management : • Repeat to confirm (blood cultures from a peripheral vein) • Exchange catheter over a guide wire is preferred • Salvage & antibiotic lock therapy (without systemic therapy) if removal is not feasible • follow up blood cultures
  • 39. Antibiotic lock (Antibiotic/ heparin solution  If the tunneled dialysis catheter is salvaged  The goal is to sterilize the catheter lumens from bacteria present in biofilms  It is a mixture of an anticoagulant ( heparin ) and high concentrations of an antibiotic in a small volume. prepared immediately before being instilled into each catheter lumen at the end of each dialysis session  for the duration of (3 weeks)  if fever or bacteremia persists despite this approach → Infected catheters should be removed
  • 40.  Vancomycin / ceftazidime / heparin : Vancomycin (1 mL of 5 mg/mL in normal saline solution) plus ceftazidime (0.5 mL of 10 mg/mL in normal saline solution) plus heparin (0.5 mL of 1,000 U/mL solution)  Vancomycin / heparin : Vancomycin (1 mL of 5 mg/mL in normal saline solution) plus heparin (1 mL of 1000 U/mL solution)  Ceftazidime / heparin: Ceftazidime (1 mL of 10 mg/mL in normal saline solution) plus heparin (1 mL of 1000 U/mL solution)  Cefazolin / heparin : Cefazolin (1 mL of 10 mg/mL in normal saline solution) plus heparin (1 mL of 1000 U/mL solution)
  • 41. Ethanol Lock  The biofilm can prevent antibiotics penetration to the surface of the inner lumen of the catheter.  Ethanol locks have been proven to be effective in this setting (catheter salvage in CRBSIs)  Preparation: 1. Draw up 3.5mL of alcohol 100% (ethanol) and 1.5mL sterile water for injection in a 10mL syringe (makes a total of 5mL of 70%) 2. The dwell time for an ethanol lock is four hours. The ethanol lock should be repeated daily by clinicians for 4-5 days 3. The clinician should flush the CVC pre and post ethanol lock with sodium chloride 0.9%. Post flushing of the line should only occur after the alcohol volume has been withdrawn from the CVC at the conclusion of the four hour dwell time.
  • 42. Contraindications  If the patient is unstable  +ve exit site or tunnel infection  If the patient is pregnant or breast feeding  If the pathogen is a Stap. aureus, multi-resistant organism , fungaemia (including candidaemia).
  • 43.
  • 44. 1. Exit site 2. Insretion site 3. Tunnel
  • 45. Exit site infection  Def: Infection confined to the erea of exit site with purulent discharge, or erythema, tenderness, or indurations (within 2cm of the skin at the exit site) [Agarwal, Anil K, Asif Arif. NephSAP. Interventional Nephrology, ASN. 361-375. 2009]
  • 46.  site drainage cultures and blood cultures should be obtained. Management  Uncomplicated exit site infections (without systemic signs of infection, -ve blood cultures, no purulence) → topical antibiotic agents based on swab culture results (mupirocin 2% & and polysporin ointment for S. aureus infection and ketoconazole or lotrimin ointment for Candida infection), With antibiotic lock.  Complicated exit site infections (that do not resolve with these interventions and/or accompanied by purulent drainage ) → systemic antibiotics for ≤7 days. If failure of systemic antibiotics occurs → immediate catheter removal
  • 47. Insertion site infection  Insertion site infection of tunneled catheters should prompt catheter removal (guidewire catheter exchange is not appropriate as it can lead to bacteremia and septic emboli)  Cultures (exudate, blood cultures )  if bloodstream infection is excluded (-ve blood cultures) → systemic antimicrobial therapy for ≤7 days is sufficient
  • 48. Tunnel infection (pocket)  Def: erythema, tenderness, and induration overlying the subcutaneous tunnel tract (which extends for ≥2 cm from the exit site). + or − signs of exit site (NKF K/DOQI, 2006) N.B neutropenic patients may complain of pain in the absence of erythema or swelling .  Managemet :  catheter removal; (in some circumstances incision and drainage may also be appropriate).  +or – excision, drainage of the tunnel site  systemic antibiotics administered for ≤7 days
  • 49.
  • 50.  Educate healthcare workers and provide training for the insertion and maintenance of catheters  Maximal Barrier Precautions ( during Insertion and handling)  Patient education  Skin Antisepsis (chlorhexidine is preferred)  Catheter Site Dressing Regimens  Antimicrobial Lock Solutions  Bundles and Checklists
  • 51. Central Line Insertion Checklist -Adults Operator:________________________________________Date:_______________________ RN Assisting:____________________________________ Room/Location:______________ Safety Pause:  Correct Patient  Correct Procedure  Correct Site  Verbal agreement from all members of the team. In order to eliminate central line associated blood stream infections, we will be following the Central Line Insertion Procedure Checklist based on CDC Guidelines. Prior to the Procedure: 1. Hand Hygiene done with Chlorhexidine Gluconate (CHG) 2% surgical hand scrub and water or waterless alcohol based gel before patient contact and before donning sterile gloves. YES 2. Cleanse Site with 2% CHG with sponge 1.5mL. YES 3. Disinfect Site with a back and forth friction scrub, utilizing 2% CHG wand 10.5mL for 30 seconds and allow to dry completely before catheter insertion. YES 4. Maximum Barriers Did the operator wear: YES Cap/Bouffant YES Mask YES Sterile Gown YES Sterile Gloves YES Patient draped with full body sterile sheet. During the procedure: 5. YES Operator(s) maintained the sterile field. 6. YES Personnel assisting wore a cap, mask and donned gloves appropriately. After the procedure: 6. Sterile dressing applied immediately by the operator. YES QUALITY IMPROVEMENT THIS FORM IS NOT PART OF THE PATIENT'S PERMANENT RECORD. Please return the form to your Nurse Manager. If a step has was not followed, please note and the Nurse Manager will follow up with the physician.
  • 52.  AVF first , Prepare your patient in advance  Pay attention To this