Intraperitoneal Vancomycin Plus Either Oral Moxifloxacin or Intraperitoneal Ceftazidime for the Treatment of Peritoneal Dialysis-Related Peritonitis: A Randomized Controlled Pilot Study

Am J Kidney Dis. 2017 Jul;70(1):30-37. doi: 10.1053/j.ajkd.2016.11.008. Epub 2016 Dec 24.

Abstract

Background: Intraperitoneal administration of antibiotics is recommended as a first treatment for managing peritoneal dialysis (PD)-related peritonitis. However, the efficacy of oral administration of quinolones has not been well studied.

Study design: Randomized controlled pilot study.

Setting & participants: 80 eligible patients with PD-related peritonitis from Peking University First Hospital (40 in each arm).

Intervention: Intraperitoneal vancomycin, 1g, every 5 days plus oral moxifloxacin, 400mg, every day (treatment group) versus intraperitoneal vancomycin, 1g, every 5 days plus intraperitoneal ceftazidime, 1g, every day (control group).

Outcomes: The primary end point was complete resolution of peritonitis, and secondary end points were primary or secondary treatment failure.

Measurements: PD effluent white blood cell count.

Results: Baseline demographic and clinical characteristics of the 2 groups were comparable. There were 24 and 22 Gram-positive organisms, 6 and 7 Gram-negative organisms, 9 and 10 culture-negative samples, and 1 and 1 fungal sample in the treatment and control groups, respectively. Complete resolution of peritonitis was achieved in 78% and 80% of cases in the treatment and control groups, respectively (OR, 0.86; 95% CI, 0.30-2.52; P=0.8). There were 3 and 1 cases of relapse in the treatment and control groups, respectively. Primary and secondary treatment failure rates were not significantly different (33% vs 20% and 10% vs 13%, respectively). In each group, there was 1 peritonitis-related death and 6 transfers to hemodialysis therapy. During the 3-month follow-up period, 7 and 3 successive episodes of peritonitis occurred in the treatment and control groups, respectively. Only 2 adverse drug reactions (mild nausea and mild rash, respectively) were observed in the 2 groups.

Limitations: Sample size was relatively small and the eligibility ratio was low. Also, the number of peritonitis episodes was low, limiting the power to detect a difference between groups.

Conclusions: This pilot study suggests that intraperitoneal vancomycin with oral moxifloxacin is a safe, well-tolerated, practical, and effective first-line treatment for PD-related peritonitis. Larger adequately powered clinical trials are warranted.

Keywords: Intraperitoneal vancomycin; PD-related peritonitis; complete cure; continuous ambulatory peritoneal dialysis (CAPD); empirical antibiotic regimen; intraperitoneal ceftazidime; oral moxifloxacin; oral quinolones; peritoneal dialysis (PD); randomized clinical trial; renal failure.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Anti-Bacterial Agents / administration & dosage*
  • Ceftazidime / administration & dosage*
  • Drug Therapy, Combination
  • Female
  • Fluoroquinolones / administration & dosage*
  • Humans
  • Male
  • Middle Aged
  • Moxifloxacin
  • Peritoneal Dialysis / adverse effects*
  • Peritoneum
  • Peritonitis / drug therapy*
  • Peritonitis / etiology*
  • Pilot Projects
  • Prospective Studies
  • Vancomycin / administration & dosage*

Substances

  • Anti-Bacterial Agents
  • Fluoroquinolones
  • Vancomycin
  • Ceftazidime
  • Moxifloxacin