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 Peritonitis
 Exit site infections
 Tunnel Infections
Incidence
 1.1 -1.3 episodes per-patient year in the US I 1980s and early
1990s
 Rate has fallen 0.2 to 0.6 per-patient year
Hand book of dialysis fifth edition
 Seventy episodes of bacterial peritonitis occurred in 45
patients (0.17 episodes/patient-year), and 123 ESI/TI
occurred in 60 patients (0.29 episodes/patient-year).
A survey of peritonitis and exit-site and/or tunnel infections in Japanese children on PD
Pediatric Nephrology June 2006, Volume 21, Issue 6, pp 828–834
 A prospective study of 501 peritonitis episodes in 44 pediatric
dialysis centers located in 14 countries that examined peritonitis
etiology, efficiency of opinion-based management guidelines, and
final outcomes.
 Between October 2001 and December 2004, a total of 548
peritonitis episodes were recorded in 392 pediatric patients, that
is, 1.4±0.8 episodes per patient
Worldwide variation of dialysis-associated peritonitis in children
Kidney InternationalVolume 72, Issue 11, 1 December 2007, Pages 1374-1379
PATHWAYS OF INFECTION
 Intraluminal
 Periluminal
 Bowel source
 Hematogenous
 Transvaginal
HOST DEFENSES
 Dialysis solution pH and
osmolality
 Peritoneal dialysis calcium
levels
Gram positive organisms
 40- 50%
 S aureus
 Coagulase negative
staphylococcal
Gram negative organisms
20-30%
 pseudomonas
 Ecoli
Fungi ~ 2-4%
Mycobacterium ~ 1%
Polymirobial growth 10%
Culture negative 15%
Handbook of dialysis 5th edition
•Culture-negative
incidence varied
significantly from 11%
in North America to
67% in Mexico
•Argentina and North
America had the
highest rate of Gram-
negative episodes.
Worldwide variation of dialysis-associated peritonitis in children
Kidney InternationalVolume 72, Issue 11, 1 December 2007, Pages 1374-1379
At least two of the following three findings
1. Sign and symptoms' of peritoneal inflammation
2. Cloudy peritoneal fluid with an elevated peritoneal fluid
count (>100/mcL) with 50% neurtrophils
2. Demonstration of bacteria in peritoneal effluent by gram
stain or culture
Li PK, Szeto CC, Piraino B, de Arteaga et al. ISPD peritonitis recommendations: 2016 update on prevention
and treatment. Perit Dial Int. 2016;36:481–508
 Abdominal pain – 79 - 88 %
 Fever (greater than 37.5ºC) – 29 - 53 %
 Nausea or vomiting – 31 - 51 %
 Cloudy effluent – 84 percent
 Hypotension – 18 %
Clinical manifestations and diagnosis of peritonitis in peritoneal dialysis: Uptodate
Author: John M Burkart, MD
 Peritoneal fluid for cell count and differential, gram
stain and culture.
 Complete blood count and blood cultures.
CONSENSUSGUIDELINES FORTHE PREVENTIONANDTREATMENTOF CATHETER-RELATED INFECTIONS
AND PERITONITIS IN PEDIATRIC PATIENTS RECEIVING PERITONEAL DIALYSIS: 2012 UPDATE
 The loading dose:
CAPD IP or IV
APD  IV or IP peritoneal dwell left in place for atleast 4-
6hr
 Maintenance antimicrobial dose
Doses added in each exchange or intermittent dose once
daily
APD CAPD or added to day time dwell
APD on day dry schedule CAPD or low volume day time
dwell time
APD  higher doses
 The recommendation of increasing dose by 25%in patient with
residual renal function is removed from the latest version
 IP aminoglycoside should preferably be administered as daily
intermittent dosing
 Treatment of IP aminoglycoside for over 3 weeks should be
avoided
 Vancomycin should also be administered intermittently.Trough
vancomycin level >15 μg/mL.
The new ISPD peritonitis guideline Cheuk Chun Szeto Renal ReplacementTherapyv olume 4,
Article number: 7 (2018)
 Vancomycin should not be given into amino-acid based
solution
 When used in combination, they should preferably be
injected to different bags of PD solution
 Tobudic S, PoepplW, Kratzer C,Vychytil A, Burgmann H. Comparative in vitro antimicrobial activity of
vancomycin, teicoplanin, daptomycin and ceftobiprole in four different peritoneal dialysis fluids. Eur J Clin
Microbiol Infect Dis. 2012;31:1327–34
 Temporary use of hypertonic exchanges and short dwell
times may be needed to maintain adequate fluid removal
 Screening for malnutrition
 Blood glucose monitoring with appropriate adjustments of
insulin dosage
 Perforated ulcer
 Pancreatitis
 Appendicitis
 Diverticulitis
 Oral nystatin or fluconazole be considered at the time of
antibiotic administration
 Accidental intraluminal contamination
 Before invasive dental procedures
 Before procedures involving the gastrointestinal or
genitourinary tract
Incidence : ~1 episode in every
24-48 patient-months
Etiology: S.aureus, P, aeruginosa
Pathogenesis: Nasal carriage of
S. aureus is risk factor
Uncomplicated catheter exit-site infections
Oral antibiotic therapy
 score of 4 or greater
 2 or greater with pathogenic organism on culture
 no tunnel involvement
 Duration2 -3 weeks
Catheter tunnel infections
Oral, intraperitoneal, or intravenous
 If MRSA is the causative agent, intraperitoneal or
intravenous glycopeptide therapy is indicated.
 Duration should be 2 – 4 weeks .
 Systemic prophylactic antibiotics immediately prior to
catheter insertion
 Antibiotic prophylaxis before other invasive procedures
 Catheter exit site care with daily topical application of
antibiotic (mupirocin or gentamicin) cream or ointment.
 Prompt treatment of exit site and tunnel infection
 Disconnect systems with a “flush before fill” design be
used for CAPD
Infections in peritonial dialysis
Infections in peritonial dialysis

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Infections in peritonial dialysis

  • 1.
  • 2.  Peritonitis  Exit site infections  Tunnel Infections
  • 3. Incidence  1.1 -1.3 episodes per-patient year in the US I 1980s and early 1990s  Rate has fallen 0.2 to 0.6 per-patient year Hand book of dialysis fifth edition
  • 4.  Seventy episodes of bacterial peritonitis occurred in 45 patients (0.17 episodes/patient-year), and 123 ESI/TI occurred in 60 patients (0.29 episodes/patient-year). A survey of peritonitis and exit-site and/or tunnel infections in Japanese children on PD Pediatric Nephrology June 2006, Volume 21, Issue 6, pp 828–834
  • 5.  A prospective study of 501 peritonitis episodes in 44 pediatric dialysis centers located in 14 countries that examined peritonitis etiology, efficiency of opinion-based management guidelines, and final outcomes.  Between October 2001 and December 2004, a total of 548 peritonitis episodes were recorded in 392 pediatric patients, that is, 1.4±0.8 episodes per patient Worldwide variation of dialysis-associated peritonitis in children Kidney InternationalVolume 72, Issue 11, 1 December 2007, Pages 1374-1379
  • 6. PATHWAYS OF INFECTION  Intraluminal  Periluminal  Bowel source  Hematogenous  Transvaginal HOST DEFENSES  Dialysis solution pH and osmolality  Peritoneal dialysis calcium levels
  • 7. Gram positive organisms  40- 50%  S aureus  Coagulase negative staphylococcal Gram negative organisms 20-30%  pseudomonas  Ecoli Fungi ~ 2-4% Mycobacterium ~ 1% Polymirobial growth 10% Culture negative 15% Handbook of dialysis 5th edition
  • 8. •Culture-negative incidence varied significantly from 11% in North America to 67% in Mexico •Argentina and North America had the highest rate of Gram- negative episodes. Worldwide variation of dialysis-associated peritonitis in children Kidney InternationalVolume 72, Issue 11, 1 December 2007, Pages 1374-1379
  • 9. At least two of the following three findings 1. Sign and symptoms' of peritoneal inflammation 2. Cloudy peritoneal fluid with an elevated peritoneal fluid count (>100/mcL) with 50% neurtrophils 2. Demonstration of bacteria in peritoneal effluent by gram stain or culture Li PK, Szeto CC, Piraino B, de Arteaga et al. ISPD peritonitis recommendations: 2016 update on prevention and treatment. Perit Dial Int. 2016;36:481–508
  • 10.  Abdominal pain – 79 - 88 %  Fever (greater than 37.5ºC) – 29 - 53 %  Nausea or vomiting – 31 - 51 %  Cloudy effluent – 84 percent  Hypotension – 18 % Clinical manifestations and diagnosis of peritonitis in peritoneal dialysis: Uptodate Author: John M Burkart, MD
  • 11.  Peritoneal fluid for cell count and differential, gram stain and culture.  Complete blood count and blood cultures.
  • 12.
  • 13.
  • 14. CONSENSUSGUIDELINES FORTHE PREVENTIONANDTREATMENTOF CATHETER-RELATED INFECTIONS AND PERITONITIS IN PEDIATRIC PATIENTS RECEIVING PERITONEAL DIALYSIS: 2012 UPDATE
  • 15.
  • 16.
  • 17.  The loading dose: CAPD IP or IV APD  IV or IP peritoneal dwell left in place for atleast 4- 6hr  Maintenance antimicrobial dose Doses added in each exchange or intermittent dose once daily APD CAPD or added to day time dwell APD on day dry schedule CAPD or low volume day time dwell time APD  higher doses
  • 18.
  • 19.  The recommendation of increasing dose by 25%in patient with residual renal function is removed from the latest version  IP aminoglycoside should preferably be administered as daily intermittent dosing  Treatment of IP aminoglycoside for over 3 weeks should be avoided  Vancomycin should also be administered intermittently.Trough vancomycin level >15 μg/mL. The new ISPD peritonitis guideline Cheuk Chun Szeto Renal ReplacementTherapyv olume 4, Article number: 7 (2018)
  • 20.  Vancomycin should not be given into amino-acid based solution  When used in combination, they should preferably be injected to different bags of PD solution  Tobudic S, PoepplW, Kratzer C,Vychytil A, Burgmann H. Comparative in vitro antimicrobial activity of vancomycin, teicoplanin, daptomycin and ceftobiprole in four different peritoneal dialysis fluids. Eur J Clin Microbiol Infect Dis. 2012;31:1327–34
  • 21.  Temporary use of hypertonic exchanges and short dwell times may be needed to maintain adequate fluid removal  Screening for malnutrition  Blood glucose monitoring with appropriate adjustments of insulin dosage
  • 22.  Perforated ulcer  Pancreatitis  Appendicitis  Diverticulitis
  • 23.  Oral nystatin or fluconazole be considered at the time of antibiotic administration  Accidental intraluminal contamination  Before invasive dental procedures  Before procedures involving the gastrointestinal or genitourinary tract
  • 24.
  • 25. Incidence : ~1 episode in every 24-48 patient-months Etiology: S.aureus, P, aeruginosa Pathogenesis: Nasal carriage of S. aureus is risk factor
  • 26.
  • 27. Uncomplicated catheter exit-site infections Oral antibiotic therapy  score of 4 or greater  2 or greater with pathogenic organism on culture  no tunnel involvement  Duration2 -3 weeks
  • 28. Catheter tunnel infections Oral, intraperitoneal, or intravenous  If MRSA is the causative agent, intraperitoneal or intravenous glycopeptide therapy is indicated.  Duration should be 2 – 4 weeks .
  • 29.  Systemic prophylactic antibiotics immediately prior to catheter insertion  Antibiotic prophylaxis before other invasive procedures  Catheter exit site care with daily topical application of antibiotic (mupirocin or gentamicin) cream or ointment.  Prompt treatment of exit site and tunnel infection  Disconnect systems with a “flush before fill” design be used for CAPD