Infectious Complications of PD: Peritonitis and Exit Site / Tunnel Infections Franz Schaefer Pediatric Nephrology Division Center for Pediatric and Adolescent.

Slides:



Advertisements
Similar presentations
AKI in Pediatrics Patrick D. Brophy MD Associate Professor
Advertisements

EXPERIENCE WITH DIFFICULT CAPD CATHETER INSERTION Dr.Sunil Shroff Dept. of Urology & Transplantation, Sri Ramachandra Medical College & Research Institution,
G. Simonetti and F. Schaefer Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University of Heidelberg, Germany Management of High and.
THE CHOICE OF DIALYSIS ACCES CONTROVERSY AND EVIDENCE
Infection Control Issues in the Dialysis Setting
Non-Infectious Complications
Peritoneal dialysis Dr Ejaz Ahmed.
Dr. Leonid Feldman Nephrology and Hypertension Division Assaf Harofeh Medical Center November, 2007 Peritoneal Dialysis.
Infectious complications of hemodialysis catheters
Management of children with CKD in a DGH M Shenoy Consultant Paediatric Nephrologist RMCH Nephrology for the General Paediatrician Meeting Manchester.
PERITONITIS PREVENTION Baxter. Germ Warfare!!! 1.2 Continuing Education Units.
MANUAL CATHETER ASSOCIATED BLOOD STREAM INFECTION (CABSI) SURVEILLANCE
RENAL REPLACEMENT THERAPY
Le malattie immunitarie aumentano il rischio di complicanze infettive? Gianfranca Cabiddu Divisione Nefrologia Azienda Ospedaliera Brotzu- Cagliari.
Peritoneal Dialysis PD Access. Peritoneal Dialysis Peritoneal Catheters  PD catheter is patients lifeline  Several advances have made access safer and.
Infections in PD Prevention and Management
Feast or Famine: Survival and Chronic Kidney Disease Kerin Worley and Deb Gipson UNC Chapel Hill April, 2004.
MRSA and VRE. MRSA  1974 – MRSA accounted for only ____of total staph infections  1995 – MRSA accounted for _____ of total staph infections  2004 –
Gerard Dou, The Dropsical Woman, 1663, Louvre, Paris Peer Report: Dialysis Care & Outcomes in the U.S., 2014 Executive Summary.
Update in Home Peritoneal Dialysis Care
Complications of Dialysis
Outcome of patients started on PD as first line therapy, Saira Usama, Jamal S. Alwakeel, Ahmad H. Mitwalli, Abdulkareem Alsuwaida, Akram Askar, King Khalid.
ETHNIC DISPARITIES IN KIDNEY TRANSPLANTATION: REPLACEMENT OF RENAL FUNCTION IN ROMA („GYPSIE“) MINORITY IN CROATIA Milica Kljak University Hospital Centre.
| 1| 1Peer Report: Dialysis Care & Outcomes in the U.S., 2014 | Mortality Peer Report: Dialysis Care & Outcomes in the U.S., 2014 Mortality.
ANZDATA Registry Annual Report 2013 Philip Clayton CHAPTER 9 KIDNEY DONATION 2013 Annual Report - 36th Edition PERITONEAL DIALYSIS CHAPTER 6.
Antibiotic Prophylaxis in Chronic Renal Failure Hemodialysis Gregory A. Chambers, PA-S Lock Haven University February 25, 2009.
A Comparison of Sevelamer and Calcium-Based Phosphate Binders on Mortality, Hospitalization, and Morbidity in Hemodialysis: A Secondary Analysis of the.
Chapter 5 Peritoneal Dialysis 2014 ANZDATA Registry 37th Annual Report Data to 31-Dec-2013 ANZDATA gratefully acknowledges the contributions of the Peritoneal.
July 2009 Feasibility and Efficacy of Optimal Peritoneal Dialysis Catheter Placement Using a Laparoscopic Technique Introduction or Purpose Peritoneal.
UKRR – HES linkage James Fotheringham Sheffield Kidney Institute.
Current Issues in PD Peritonitis. Baxter Healthcare Objectives Participants Will Review  Current Issues Related to Peritonitis  Current Treatment Recommendations.
2015 ANNUAL DATA REPORT V OLUME 2: E ND -S TAGE R ENAL D ISEASE Chapter 8: Pediatric ESRD.
2015 ANNUAL DATA REPORT V OLUME 2: E ND -S TAGE R ENAL D ISEASE Chapter 10: Dialysis Providers.
’10 slides on peritoneal dialysis in older CKD patients’
EVC 2015 – Vascular Access Maurizio Gallieni Nephrology and Dialysis Unit – Ospedale San Carlo Borromeo University of Milano, Italy Type of PD catheter.
Providing Quality in Peritoneal Dialysis Annette Butler and Mark Denton.
Caspofungin prophylaxis vs placebo, followed by preemptive Tx for invasive candidiasis (IC) in ICU pts: MSG-01 study Multi-centre, double-blind, phase.
1 PERITONEAL DIALYSIS. 2 How Does PD Clean the Blood? Diffusion – passage of particles in solution across a semi- permeable membrane from an area of greater.
Prevalence of Bacteremia in Low Risk Patients with Sickle Cell Disease and Fever Shashidhar Marneni, MD Fellow(1 st Year) Pediatric Emergency Medicine.
Complications of PD Peter Rutherford Medical Director Senior Lecturer in Nephrology.
Long Term Peritoneal Dialysis In Children – Frequent Complications Conclusions: Peritoneal Dialysis is the method of choice for pediatric patients, with.
Infection following KTP 신장내과 R3 김경엽. Infections Infections Leading cause of morbidity and mortality in the early posttransplant period Leading cause of.
신장내과 이지연 Peritoneal dialysis-related infection ISPD guidelines 2010 update.
Fungal Peritonitis (FP) Constantinos J. Stefanidis “P. and A. Kyriakou” Children’s Hospital Athens, Greece.
World Kidney Day 2016: Kidney Disease & Children
Figure 10.1 Dialysis unit counts, by unit affiliation, 2011–2014
First-year death rates by modality figure 8
West Midlands Renal Peer Review
Figure 3.1 First-year mortality rates in incident dialysis patients, by incident year & month Patients aged 18 years or older. Peer Report Dialysis.
Principles of dialysis
Volume 85, Issue 4, Pages (April 2014)
F.H. Bender, J. Bernardini, B. Piraino  Kidney International 
December 31st point prevalent counts by modality figure 3.1
Hospital admissions per patient, by modality figure 5
Complications of Dialysis
PD Catheters Care Plan Kate Oh. The type of material of PD catheter Catheters are made either of polyurethane or silicone rubber Exit-site, antibiotic.
CHAPTER 6 PERITONEAL DIALYSIS Fiona Brown Aarti Gulyani
Adjusted relative mortality risk
Outcomes with trisodium citrate 30% vs heparin as catheter-locking solution (all catheters) in patients on hemodialysis Variable TSC, n (%) Heparin, n.
Volume 85, Issue 4, Pages (April 2014)
بنام خداوند جان و خرد بنام خداوند جان و خرد.
F.H. Bender, J. Bernardini, B. Piraino  Kidney International 
Cause Specific Death Rates for All Dialysis Patients
Microbiology and outcomes of peritonitis in North America
E. Tacconelli  Clinical Microbiology and Infection 
Bradley A. Warady, Mwaffek Bashir, Lynn A. Donaldson 
Stock and Flow of Peritoneal Dialysis Patients Australia
Peritonitis treatment algorithm.
Stock and Flow of Peritoneal Dialysis Patients Australia
Stock and Flow of Haemodialysis Patients Australia
Presentation transcript:

Infectious Complications of PD: Peritonitis and Exit Site / Tunnel Infections Franz Schaefer Pediatric Nephrology Division Center for Pediatric and Adolescent Medicine University of Heidelberg, Germany Download Presentation at:

Reasons for Hospitalizations

Reasons for Change of Dialysis Modality* Percent NAPRTCS, 2006 * Other than transplantation

Causes of Death for Prevalent Pediatric PD Patients ( ) USRDS, 2004 Mortality per 1000 patient years at risk

Prevention of Peritonitis Catheter-related factors Prevention of exit-site and tunnel infections Direct tunnel downward or use swan-neck catheter Use double-cuff catheters Use exit-site mupirocin Timely replacement of the catheter for catheter-related peritonitis Contamination Experienced nursing personnel Avoidance of spiking technology Long training period Training protocols Antibiotic prophylaxis Preoperative antibiotics at catheter insertion Contamination at time of exchange Dialysate leak at catheter exit site Invasive procedures Exit site mupirocin Warady & Schaefer, In: Chap. 24, Pediatric Dialysis, 2004

Peritonitis: Diagnostic Criteria Cloudy effluent Dialysate WBC count >100/uL >50% polymorphonuclear leukocytes Positive culture

Peritonitis: Effluent Cloudiness

Peritonitis: Source of Infection Unknown: 70 % ! Episodes (%)

Spectrum of Causative Organisms Schaefer et al. Kidney Int 2007

Regional Distribution of Culture Results Schaefer et al. Kidney Int 2007

If the patient presents with: -No fever -Mild or no abdominal pain -No risk factors for severe infection Glycopeptide (e.g. vancomycin, 30 mg/l cont. or 30 mg/kg q.5-7 days) and Ceftazidime (continuous 125 mg/L or 250 mg/L o.d.) If any of the following is present: -Fever, severe abdominal pain, age <2 yrs -History of MRSA infection or carrier -Recent or current exit site/tunnel infection Initiate empiric therapy Peritoneal effluent evaluation Cell count and differential Gram stain, culture Cloudy effluent Cefazolin (250/125 mg/l) and Ceftazidime (continuous 125 mg/L or 250 mg/L o.d.) EMPIRIC THERAPY

Cefazolin/ Ceftazidime Glycopeptide/ Ceftazidime Any Treatment Gram positive5/90 (5.6%)4/129 (3.1%)9/219 (4.1%) Gram negative4/56 (7.1%)12/65 (18.5%) 16/121 (13.2%) * Culture negative4/92 (4.4%)2/59 (3.4%)6/151 (4.0%) Any culture result13/238 (5.5%)18/253 (7.1%)31/491 (6.3%) Clinical Response Failure after 72h Empiric Antibiotic Treatment Warady et al. JASN 2007; 18:2172

Risk of Day 3 Clinical Response Failure Odds ratio (95% Cl)P Gram-negative causative organism 3.61 ( )P <0.001 Intermittent ceftazidime administration (only gram-negative) 6.65 (2.07 – 21.4)P <0.005 APD modality: 'dry day' vs. 'wet day' 2.53 ( )P <0.01 Exit site score >2 (only gram-positive) 5.46 ( )P <0.05 No effect: choice of empiric therapy, risk assignment

In vitro Resistance Predicts Empiric Therapy Failure Odds ratio 95% CI Gram-positive Gram-negative

In vitro Sensitivities by Gram

Schaefer et al. Kidney Int 2007 In vitro Resistance Rates

Final Outcome Outcome PD Continued PD DiscontinuedTotal TemporaryPermanent Full functional recovery (89%) Ultrafiltration problems (3.3%) Adhesions (3.1%) Uncontrolled infection (2.5%) Secondary fungal peritonitis 0044(0.8%) General therapy failure 0066 (1.3%) Total431 (89%)12 (3%)39 (8%)482 (100%)

Outcome by Causative Organism Rate of successful outcome (%)

Risk of Incomplete Functional Recovery OR (95% CI)P Disease Severity Score day (1.72 – 7.84)< Straight vs. curled catheter 2.70 (1.24 – 5.87)< Exit-site score 1.34 (1.05 – 1.71)< Pseudomonas on culture 3.57 (1.11 – 11.5)< 0.05 No effect: choice of empiric therapy, risk assignment

Monitor local staphylococcal methicillin, gram-negative ceftazidime resistance patterns Cefazolin OR Glycopeptide and Aminoglycoside OR (continuous) Ceftazidime Initiate empiric therapy Peritoneal effluent evaluation Cell count and differential Gram stain, culture Cloudy effluent Revised Guideline: Empiric Antibiotic Therapy

Revised Guideline: Modification for Culture Negative Episodes If improved clinically: Continue 1st generation cephalosporin or glycopeptide for 14 days Discontinue aminoglycoside after 3 days Add/continue ceftazidime after 3 days If not improved clinically: Remove catheter

Exit Site Infection

Diagnosis of Exit-Site Infection The diagnosis of a catheter exit-site infection should be made in the presence of a purulent discharge from the sinus tract or marked pericatheter swelling, redness and/or tenderness with or without a pathogenic organism cultured from the exit-site. Infectious symptoms should be rated according to an objective scoring system. GUIDELINE 14 Warady, Schaefer et al., Peritonitis Guidelines, PDI, 2000

Exit-Site Scoring System 0 Points 1 Point 2 Points SwellingnoExit only (<0.5 cm)Including part of or entire tunnel Crustno 0.5 cm Rednessno 0.5 cm Pain on pressurenoSlightSevere SecretionnoSerousPurulent Schaefer F. et al. J Am Soc Nephrol 10: , 1999 a Infection should be assumed with a cumulative exit-site score of 4 or greater.

Causative Organisms at Exit Site % of 58 episodes

Therapy of Exit Site Infection Usually oral Usually upon culture results Grampositive usually penicillinase- resistant penicillin or cefalexin Length of therapy at least two weeks One-stage catheter replacement for refractory ESI

Exit-site infection rate Tunnel infection rate Peritonitis rate0.170 Nasal Carriers Noncarriers S.Aureus Infection Rate Luzar et al, NEJM, 1990

Nasal S.Aureus Decontamination Piraino B, J Am Soc Nephrol, 1998 S. aureus Peritonitis, Episodes / y

Options for Prevention of Exit-Site Infections

Topical S.Aureus Prophylaxis

Warady et al., Peritonitis Guidelines, PDI 2000 Prophylaxis for S. Aureus Nasal Carriage Nasal culture every 2-4 wks until positive x 1 or negative x 6 If negative x 6: no prophylaxis needed If positive Mupirocin intra-nasally BID x 5 d every 4 wks Mupirocin at exit site daily

Exit Site and Peritonitis Exit site co-colonization is associated with 2-fold likelihood of peritonitis treatment failure 3-fold likelihood of catheter exchange Schaefer et al. Kidney Int 2007 Pseudomonas peritonitis is associated with Use of saline or soap for cleansing (p twice per week (p<0.005) Use of exit site mupirocin (p<0.005) Being United States resident (OR 2.95, p<0.01)

Indications for Catheter Removal Failure to respond to appropriate antibiotics within 5 days Fungal peritonitis Peritonitis with exit site/tunnel infection Recurrent peritonitis Chronic exit site infection

International Pediatric PD Network