My. Munar et al., CYCLOSPORINE AND VANCOMYCIN DISPOSITION DURING CONTINUOUS VENOVENOUS HEMODIAFILTRATION, The Annals of pharmacotherapy, 29(4), 1995, pp. 374-377
OBJECTIVE: To report cyclosporine and vancomycin disposition during co
ntinuous venovenous hemodiafiltration (CVVHD) in a 41-year-old heart t
ransplant patient while in the intensive care unit at a primary and te
rtiary care teaching hospital. CASE SUMMARY: The patient received a 60
-mg infusion of cyclosporine over 24 hours and vancomycin 1 g over 1 h
our. Blood samples subsequently were collected and analyzed using whol
e blood monoclonal radioimmunoassay and fluorescence polarization immu
noassay, respectively. Blood samples were measured every hour from the
arterial and venous lines of the apparatus, as were ultrafiltrate dru
g concentrations. Drug clearance rates into the ultrafiltrate subseque
ntly were calculated. DISCUSSION: Measurements of ultrafiltrate detect
ed no cyclosporine. A slight variation existed between arterial and ve
nous drug concentrations, which was not statistically significant (p >
0.05, paired Student's t-test). Analysis of vancomycin samples reveal
ed a steady decline of drug concentration, with 4.75% of the dose elim
inated in the ultrafiltrate, Vancomycin arterial and venous concentrat
ions decreased from 24.4 and 23.3 mg/L to 15.7 and 12.3 mg/L, respecti
vely. CONCLUSIONS: Vancomycin is eliminated by CVVHD and it may be nec
essary for these patients to receive the drug more frequently. In cont
rast, cyclosporine is not removed effectively by CVVHD; therefore, rep
lacement doses are not warranted.