Aims: The objective of this study was to confirm the compatibility of ethanol and 4% trisodium citrate (TSC) for potential use as a catheter locking solution. Methods: Increasing concentrations of ethanol were combined with 4% TSC in glass test tubes and stored at 37degreesC over 72 hours. Each tube was visually inspected to determine the highest compatible concentration. To confirm visual compatibility, HPLC analysis was used to compare the concentration of TSC in control solutions (n = 6) to solutions containing both TSC and the highest concentration of ethanol that was visually compatible (n = 6). Compatibility in carbothane hemodialysis catheters was then confirmed in vitro. Results: Results of the compatibility tests indicated that 30% ethanol was the maximum concentration visually compatible with 4% TSC. Ethanol concentrations of 35% or above form a crystalline precipitate in the glass test tubes within 72 hours. HPLC analysis showed no difference in the concentration of TSC in the control solutions compared to the TSC/ethanol solutions when incubated in glass test tubes. A slight, but statistically significant increase in the TSC concentration (1.27%; p < 0.0001) was observed when the ethanol/TSC solution was incubated in carbothane hemodialysis catheters. This slight increase may be due to ethanol absorption into the catheter polymer. Further studies are underway to determine if an ethanol/TSC lock affects the mechanical properties of these carbothane hemodialysis catheters. Conclusions: We conclude that 30% ethanol is compatible with 4% trisodium citrate in carbothane hemodialysis catheters in vitro. Until the lock's affect on carbothane hemodialysis catheters is known, it cannot yet be recommended for clinical use.
机构:
Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Maloney, Sara E. E.
Grayton, Quincy E. E.
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Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Grayton, Quincy E. E.
Wai, Christine
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Univ N Carolina, UNC Kidney Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Wai, Christine
Uriyanghai, Unimunkh
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Univ N Carolina, UNC Kidney Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Uriyanghai, Unimunkh
Sidhu, Jasleen
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Univ N Carolina, UNC Kidney Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Sidhu, Jasleen
Roy-Chaudhury, Prabir
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Univ N Carolina, UNC Kidney Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Roy-Chaudhury, Prabir
Schoenfisch, Mark H. H.
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Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
Univ N Carolina, Eshelman Sch Pharm, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
机构:
Stanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USAStanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA
Pieroni, Kevin P.
Nespor, Colleen
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Childrens Home Pharm, Palo Alto, CA USAStanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA
Nespor, Colleen
Poole, Robert L.
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Childrens Home Pharm, Palo Alto, CA USA
Lucile Packard Childrens Hosp Stanford, Dept Pharm, Palo Alto, CA 94304 USAStanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA
Poole, Robert L.
Kerner, John A., Jr.
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Stanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA
Childrens Home Pharm, Palo Alto, CA USAStanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA
Kerner, John A., Jr.
Berquist, William E.
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Stanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USAStanford Univ, Sch Med, Div Gastroenterol Hepatol & Nutr, Dept Pediat, Palo Alto, CA 94304 USA