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Part 8: PD Peritonitis |
Department of Microbiology, Research Centre of Infection and Immunology, The University of Hong Kong, Hong Kong SAR, PR China
Correspondence to: K.Y. Yuen, Department of Microbiology, The University of Hong Kong, 4/F University Pathology Building, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong SAR, PR China. hkumicro{at}hkucc.hku.hk
As the survival of patients with end-stage renal failure has improved,
their exposure to antibiotics has also increased. Infections, especially
peritoneal dialysis–related peritonitis, are unavoidable because of
lapses in technique and the slow worsening of systemic and peritoneal defense
associated with aging and dialysis. The selective pressure inherent in the use
of antibiotics shapes the pattern of antibiotic resistance in the bacteria
causing peritonitis and extraperitoneal infections, and vice versa.
Renal function–preserving and non-ototoxic regimens that
incorporate double β-lactams (first- and third-generation cephalosporins)
for peritonitis have increased the selective pressure in favor of
methicillin-resistant staphylococci (MRS) and extended-spectrum
β-lactamase (ESBL)–producing Enterobacteriaceae. Attempts to use
the fluoroquinolones as alternatives to β-lactams was met with rocketing
quinolone resistance. The high incidence of MRS led many nephrologists to use
empiric vancomycin—until the début of vancomycin-resistant
enterococci. The recent emergence of heterogeneous and high-level vancomycin
resistance in staphylococci (which are especially prevalent in patients on
dialysis) calls for further prudence in the use of vancomycin.
The coming challenges are ESBL-producing Enterobacteriaceae with
carbapenemase, multi-resistant Pseudomonas, and highly virulent
community-acquired methicillin-resistant Staphylococcus aureus with
Panton–Valentine leukocidin. Antibiotic auditing programs and meticulous
patient training by nurses are the only available defense at the moment. Novel
approaches such as antibiotic-impregnated Tenckhoff catheters, biocompatible
dialysis fluid, and peritoneal immuno-augmentation strategies are eagerly
awaited.
KEY WORDS: Antibiotic resistance; antibiotic control; vancomycin-resistant Staphylococcus aureus; vancomycin-resistant enterococci; extended-spectrum beta-lactamase; carbapenemase; peritonitis.
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