Construction method of kidney transplantation anti-infection drug dosage prediction model
A construction method and dose prediction technology, applied in the construction of the dose prediction model of anti-infective drugs for kidney transplantation, and in the field of dose prediction models for individualized drug regimens of anti-infective drugs for kidney transplantation, which can solve the problem of unclear models and pharmacokinetics of people without kidney transplantation. Kinetics and other issues, to achieve accurate drug treatment, reduce the risk of adverse reactions, and improve the effectiveness of the effect
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[0060] Example 1 Take daptomycin as an example to illustrate the dose prediction model of anti-infective drugs for kidney transplantation
[0061] Previous studies have found that the pharmacokinetics of daptomycin are characterized by low fat solubility and high plasma protein binding. It is mainly cleared through the kidneys (52%), and the drug is excreted in the urine in its original form. The bactericidal effect of daptomycin is dose-dependent, and its pharmacodynamics is most closely related to the maximum plasma concentration (C max ) to the minimum inhibitory concentration MIC ratio, and the plasma concentration-time curve (AUC 0-24h ) ratio of the area under the MIC. For the treatment of complex skin and soft tissue infections, blood infections, and endocarditis, the FDA recommended dose is 4-6mg / kg / 24h, but if the creatinine clearance rate is less than 30mL / min, the recommended dose is 4-6mg / kg / 48h, but the pharmacokinetic characteristics of different patients vary...
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