Background., Azithromycin is an azalide antibiotic with a similar antibacte
rial spectrum to erythromycin but with greater gram-negative activity. Azit
hromycin displays a favorable pharmacokinetic profile, with improved absorp
tion and higher sustained tissue concentrations compared with erythromycin.
This results in a prolonged elimination half-life, suggesting a potential
for treating continuous ambulatory peritoneal dialysis (CAPD) peritonitis.
Objective:This study aimed to define the potential role of azithromycin in
treating CAPD peritonitis.
Design:The pharmacokinetics and peritoneal dialysis (PD) clearance of azith
romycin were studied following a single 500-mg oral dose of azithromycin. B
lood and dialysate samples were taken over a 10-day period and assayed usin
g high-pressure liquid chromatography.
Setting: The study took place within the Renal Unit at Southend Hospital NH
S Trust, a district general hospital in the United Kingdom.
Patients: Eight patients with oliguric end-stage renal failure without peri
tonitis maintained on CAPD (3 x 2 L/day). *
Results: Peak plasma concentrations occurred at 2 3 hours with 0.35 - 1.35
mug/mL (mean 0.75). The mean elimination half-life was 84.55 hrs, and plasm
a clearance was 21.93 L/hour. This compares with values of greater than 40
hours and 40.8 L/hour reported in healthy volunteers. After 8 hours, the me
an dialysate concentration was 0.07 mug/mL; PD clearance was 0.06 L/hr.
Conclusion: Azithromycin is not substantially removed by CAPD in the absenc
e of peritonitis and cannot be recommended for widespread use in this setti
ng at present. However, the successful use of azithromycin in CAPD peritoni
tis, due possibly to an intracellular drug transport mechanism, has been re
ported. Future research should address this possibility.