TREATMENT OF PERITONEAL DIALYSIS (PD) RELATED PERITONITIS. General Principles

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WA HOME DIALYSIS PROGRAM (WAHDIP) GUIDELINES General Principles 1. PD related peritonitis is an EMERGENCY early empiric treatment followed by close review is essential 2. When culture results and sensitivities are known, antimicrobial therapy should be adjusted to narrow-spectrum agents as appropriate 3. Intraperitoneal (IP) administration is superior to intravenous (IV) dosing in treatment of peritonitis 4. Intermittent and continuous dosing are equally efficacious 5. Selection of antimicrobials must be made in light of both patient s and program s history of micro-organisms and susceptibilities 6. Aminoglycosides, cephalosporins and vancomycin can be mixed in the same dialysis bag without loss of bioactivity 7. Some common definitions for peritonitis can be found below: a. Recurrent an episode that occurs within four weeks of completion of therapy of a prior episode but with different organism b. Relapsing an episode that occurs within four weeks of completion of therapy of a prior episode with the same organism or one sterile episode (relapsing episodes should NOT be counted as another peritonitis when calculating peritonitis rates) c. Repeat an episode that occurs more than four weeks after completion of therapy of a prior episode with the same organism d. Refractory failure of the effluent to clear after five days of appropriate antimicrobials e. Catheter Related Peritonitis peritonitis in conjunction with an exit-site or tunnel infection with the same organism or one site sterile A senior Renal Physician MUST be contacted if there are any questions pertaining to the treatment of PD related peritonitis Page 1 of 7

INITIAL EMPIRIC MANAGEMENT OF PD RELATED PERITONITIS All PD patients who present with a cloudy PD drain bag require IMMEDIATE antimicrobial treatment 1. Send the whole bag of cloudy PD fluid for laboratory testing (Gram stain, MC&S, WCC & differential) 2. Commence antimicrobial treatment covering Gram-positive, Gram-negative organisms and yeast Gram-positive coverage Gram-negative coverage Yeast coverage Intra-peritoneal vancomycin Intra-peritoneal gentamicin Oral nystatin As a single STAT dose 2 grams As a single STAT dose 40 mg < 60kg 80 mg > 60 kg 1 tablet/capsule (500,000 units) QID for duration of IP therapy Both intra-peritoneal antimicrobials to be placed in the same bag and left to dwell for a minimum of 6 hours 1. Monitor patient s clinical condition clarity of PD fluid, abdominal pain, fluid status 2. Follow up results of microbiological testing 3. Liaise with Renal Physician to determine appropriate subsequent management Patients receiving more than one dose of gentamicin or vancomycin should have plasma levels monitored for adequacy and non-toxicity. Page 2 of 7

SUBSEQUENT MANAGEMENT OF PD RELATED PERITONITIS: DIRECTED BY CULTURE RESULTS Gram-positive isolate or culture negative Continue vancomycin treatment for Gram-positive organisms. Otherwise treat as directed by the results of culture and susceptibilities in consultation with a specialist, if necessary. Culture negative Stop gentamicin Continue IP vancomycin Dose: 2 grams Duration: 14 days Staphylococcus species Corynebacterium species Stop gentamicin Continue IP vancomycin or as directed Dose: 2 grams Duration: 21 days Enterococcus Streptococcus species Continue IP vancomycin or as directed Dose: 2 grams Duration: 21 days Continue IP gentamicin 40 mg Frequency: each day Duration: 7 days Stop IP gentamicin Continue IP vancomycin or as directed Duration: 14 days Polymicrobial Gram +ve (without ESI/tunnel infection) Based on susceptibilities Frequency: as advised Duration: as advised Page 3 of 7

SUBSEQUENT MANAGEMENT OF PD RELATED PERITONITIS: DIRECTED BY CULTURE RESULTS Gram-negative isolates Treatment should be directed by the results of culture and susceptibilities in consultation with a specialist, if necessary Pseudomonas aeruginosa Gram-negative organism (E.coli, Proteus or Klebsiella) - single species isolated Stop IP vancomycin and IP gentamicin If susceptible, commence oral ciprofloxacin 500 mg and IP cefepime or IP ceftazidime 1 gram Frequency: daily Duration: 21 days Stop IP vancomycin and IP gentamicin If susceptible, commence oral ciprofloxacin 500 mg and IP cephazolin or IP cefepime or IP ceftazidime 1 gram as per susceptibility Frequency: daily Duration: 14 to 21 days Stenotrophomonas Stop IP vancomycin and IP gentamicin Consult with an Infectious Disease physician/microbiologist in every case Polymicrobial Gramnegative peritonitis Commence IV piperacillin/tazobactam and IP amoxycillin Continue IP gentamicin as per susceptibility Doses: as advised Frequency: as advised Duration: 14 days Page 4 of 7

SUBSEQUENT MANAGEMENT OF PD RELATED PERITONITIS High-risk peritonitis Please contact renal physician (may warrant PD catheter removal) Staphylococcus aureus (MSSA or MRSA) with exit site /tunnel infection Seriously consider catheter removal in refractory exit site infection (ESI) Pseudomonas aeruginosa with exit site /tunnel infection Fungal peritonitis Seriously consider catheter removal in refractory ESI IMMEDIATE catheter removal required Consult with an Infectious Diseases physician Adjuvant Treatment commence antifungal therapy for 10-14 days after catheter removal Polymicrobial Gramnegative enteric organisms Mycobacterial peritonitis Consider enteric source and investigate source of contamination Systemic antimicrobial therapy usually required Seriously consider catheter removal Consult with an Infectious Diseases physician Page 5 of 7

INDICATIONS FOR CATHETER REMOVAL FOR PERITONEAL DIALYSIS- RELATED INFECTIONS Refractory peritonitis Relapsing peritonitis Refractory exit-site and tunnel infection Fungal peritonitis Catheter removal may also be considered for repeat peritonitis mycobacterial peritonitis multiple enteric organisms STABILITY OF ANTIMICROBIALS The stability of antimicrobials will vary with different PD solutions. Please check the manufacturer s recommendations with regard to antimicrobial stability in PD solutions. It is also important to consider drug compatibility if adding more than one antimicrobial into a PD solution. REFERENCES Therapeutic Guidelines: Antibiotic Version 14 2010 ISPD Guidelines, Peritoneal Dialysis-Related Infections Recommendations: 2010 Update ISPD Position Statement on Reducing the Risks of Peritoneal Dialysis-Related Infections: 2011 Kam-Tao P; Szeto C; Piraino B; Bernardini J; Figueiredo A; Gupta A; Johnson D; Kuijper E; Lye W; Salzer W; Schaefer F; Struijk D. ISPD Guidelines/ Recommendations Peritoneal Dialysis-Related Infections Recommendations:2010 Update. Peritoneal Dialysis International 2010 30 pp393-423 Wong P; Lo K; Tong G; Chan S; Lo M; Mak S; Wong A. Prevention of fungal peritonitis with nystatin prophylaxis in patients receiving CAPD. Peritoneal Dialysis international 2007 27 pp531-536 CARI Guidelines: Treatment of peritoneal dialysis-associated fungal peritonitis 2004 CONSULTATION Infectious Diseases Physicians can be contacted for consultation on the following numbers: Fremantle Hospital (08) 9431 3333 Royal Perth Hospital (08) 9224 2244 Sir Charles Gairdner Hospital (08) 9346 3333 Page 6 of 7

These guidelines were prepared by the Western Australian Committee for Antimicrobials of the Western Australian Therapeutics Advisory Group ACKNOWLEDGEMENTS WATAG gratefully acknowledges the following contributors to these Guidelines, Members of the WA Committee on Antimicrobials - Anna Allman, Duncan McLellan, John Dyer, Kerry Fitzsimons, Paul Ingram, Rebecca McCann, Ronan Murray, Michelle Porter, Matt Rawlins, Owen Robinson, Tom Snelling and Helen Van Gessel Kathy Irwin and Lesley Gregory for overseeing the development; Prof. Neil Boudville, Gerrie Vandepeer and Adriana Viola for research and assessment of evidence. Page 7 of 7