Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu klinické zkoušky, srovnávací studie, časopisecké články
PubMed
18613859
DOI
10.1111/j.1365-2710.2008.00932.x
PII: JCP932
Knihovny.cz E-zdroje
- MeSH
- acetylglukosaminidasa moč MeSH
- amikacin aplikace a dávkování farmakokinetika farmakologie MeSH
- antibakteriální látky aplikace a dávkování farmakokinetika farmakologie MeSH
- biologické markery krev MeSH
- časové faktory MeSH
- cystatin C MeSH
- cystatiny krev MeSH
- cystická fibróza krev farmakoterapie MeSH
- dítě MeSH
- dospělí MeSH
- hodnoty glomerulární filtrace * MeSH
- intravenózní infuze MeSH
- kreatinin krev moč MeSH
- ledviny účinky léků patologie MeSH
- lidé MeSH
- mladiství MeSH
- monitorování léčiv MeSH
- předškolní dítě MeSH
- ROC křivka MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- srovnávací studie MeSH
- Názvy látek
- acetylglukosaminidasa MeSH
- amikacin MeSH
- antibakteriální látky MeSH
- biologické markery MeSH
- CST3 protein, human MeSH Prohlížeč
- cystatin C MeSH
- cystatiny MeSH
- kreatinin MeSH
BACKGROUND AND OBJECTIVE: Monitoring of renal function in cystic fibrosis (CF) patients is essential. The dosage regimen of amikacin is regularly modified according to the patient's glomerular filtration rate (GFR). The aim of the study was to evaluate the use of cystatin C (CyC) for monitoring amikacin therapy along with other markers of renal tubular and glomerular function, and damage [N-acetyl-beta-d glucosaminidase (NAG), creatinine level and creatinine clearance]. METHODS: We compared the GFR, estimated from the serum concentrations of creatinine (Cockcroft-Gault formula) and CyC (Grubb's formula). Seventy-one patients (mean age 12 years; range 4-28 years) with CF were treated by intermittent intravenous infusion of amikacin. Tubular nephrotoxicity was investigated by measurement of urine NAG/urine creatinine ratio (U-NAG/U-creatinine). Concentrations of all markers were measured before starting amikacin therapy and at days 3, 5, 7, 10 and 12. Fluorescence polarization analysis, turbidimetry, enzymatic phototometric creatinine deaminase method and fluorimetry were used for determination of serum amikacin, serum CyC, creatinine and urine NAG activity. Receiver operating characteristic (ROC) analysis was performed to assess the influence of GFR estimated from serum creatinine and serum CyC for the prediction of amikacin clearance during aminoglycoside therapy. RESULTS: Significant differences in the rate of U-NAG/U-creatinine were noted before and after treatment with amikacin (P < 0.001). Serum creatinine levels and creatinine clearance at the end of amikacin therapy (12th day) did not show any significant differences in comparison with the levels measured before the start of therapy (0th day). At days 5, 7, 10 and 12, serum CyC levels showed a significant elevation (P < 0.001), and CyC clearance showed a significant decrease (P < 0.001) in comparison with the levels measured at day 0. The ratio of amikacin clearance/creatinine clearance decreased with therapy whereas the amikacin clearance/CyC and amikacin clearance/CyC clearance increased. CONCLUSION: We showed that the rate of U-NAG/U-creatinine is a suitable marker for monitoring tubular nephrotoxicity in CF patients. Serum creatinine and estimated creatinine clearance are modest predictors of GFR in CF patients. CyC appears to be a better marker of GFR than serum creatinine concentration or creatinine clearance in our study. Serum CyC levels and CyC clearance showed greater ability to predict amikacin clearance during therapy than creatinine clearance.
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